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EC number: 214-300-6 | CAS number: 1120-21-4
- Life Cycle description
- Uses advised against
- Endpoint summary
- Appearance / physical state / colour
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- Boiling point
- Density
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- Additional information on environmental fate and behaviour
- Ecotoxicological Summary
- Aquatic toxicity
- Endpoint summary
- Short-term toxicity to fish
- Long-term toxicity to fish
- Short-term toxicity to aquatic invertebrates
- Long-term toxicity to aquatic invertebrates
- Toxicity to aquatic algae and cyanobacteria
- Toxicity to aquatic plants other than algae
- Toxicity to microorganisms
- Endocrine disrupter testing in aquatic vertebrates – in vivo
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- Toxicological Summary
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- Acute Toxicity
- Irritation / corrosion
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- Repeated dose toxicity
- Genetic toxicity
- Carcinogenicity
- Toxicity to reproduction
- Specific investigations
- Exposure related observations in humans
- Toxic effects on livestock and pets
- Additional toxicological data
![](https://poisoncentres.echa.europa.eu/o/diss-blank-theme/images/factsheets/A-REACH/factsheet/print_ecotoxicological-information.png)
Short-term toxicity to aquatic invertebrates
Administrative data
Link to relevant study record(s)
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- key study
- Study period:
- The study was conducted between 04 August and 08 August.
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Remarks:
- GLP guideline study.
- Justification for type of information:
- A discussion and report on the read across strategy is given as an attachment in IUCLID Section 13.
- Reason / purpose for cross-reference:
- read-across: supporting information
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 202 (Daphnia sp. Acute Immobilisation Test)
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EU Method C.2 (Acute Toxicity for Daphnia)
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Analytical monitoring:
- yes
- Vehicle:
- no
- Test organisms (species):
- Daphnia magna
- Details on test organisms:
- The test was carried out using 1st instar Daphnia magna derived from in-house laboratory cultures.
Adult Daphnia were maintained in 150 mL glass beakers containing Elendt M7 medium in a temperature controlled room at approximately 20 °C. The lighting cycle was controlled to give a 16 hours light and 8 hours darkness cycle with 20 minute dawn and dusk transition periods. Each culture was fed daily with a mixture of algal suspension (Desmodesmus subspicatus) and Tetramin® flake food suspension. Culture conditions ensured that reproduction was by parthenogenesis. Gravid adults were isolated the day before initiation of the test, such that the young daphnids produced overnight were less than 24 hours old. These young were removed from the cultures and used for testing. The diet and diluent water are considered not to contain any contaminant that would affect the integrity or outcome of the study. - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 48 h
- Nominal and measured concentrations:
- Nominal: 10 and 100 mg/L.
- Details on test conditions:
- Procedure
Due to the low aqueous solubility and complex nature of the test item, for the purposes of the study the test medium was prepared as a Water Accommodated Fraction (WAF) of the test item.
Previous studies conducted on similar test items (e.g. Harlan Study Number 41304080) indicated that a 23-Hour stirring period followed by a 1-Hour standing period was sufficient to ensure that the maximum dissolved test item concentration was obtained in a Water Accommodated Fraction (WAF), as no significant increase in dissolved carbon was obtained by extending the stirring period to 96 hours.
Definitive Test
The following loading rates were assigned to the definitive test: 10 and 100 mg/L.
Experimental Preparation
Nominal amounts of test item (23 and 230 mg) were each separately added to the surface of
2.3 liters of test water to give the 10 and 100 mg/L loading rates respectively. After the addition of the test item, the test water was stirred by magnetic stirrer using a stirring rate such that a vortex was formed to give a dimple at the water surface. The stirring was stopped after 23 hours and the mixtures allowed to stand for 1 hour. A wide bore glass tube, covered at one end with Nescofilm was submerged into the vessel, sealed end down, to a depth of approximately 5 cm from the bottom of the vessel. A length of Tygon tubing was inserted into the glass tube and pushed through the Nescofilm seal. Microscopic inspection of the WAFs showed no micro-dispersions or undissolved test item to be present. The aqueous phase or WAF was removed by mid-depth siphoning (the first approximate 75-100 mL discarded) to give the 10 and 100 mg/L loading rate WAFs.
Total Organic Carbon (TOC) analysis was performed on the test solutions at 0 and 48 hours.
Exposure Conditions
In the definitive test 100 mL nominal volume conical flasks containing approximately 130 mL of test preparation were used. At the start of the test 5 daphnids were placed in each test and control vessel at random, in the test preparations. Four replicate test and control vessels were prepared. The test vessels were then sealed to reduce loss through volatilization and maintained in a temperature controlled room at approximately 21 °C with a photoperiod of 16 hours light (398 to 481 lux) and 8 hours darkness with 20 minute dawn and dusk transition periods. The daphnids were not individually identified, received no food during exposure and the test vessels were not aerated.
The control group was maintained under identical conditions but not exposed to the test item.
The test preparations were not renewed during the exposure period.
Data from the control group was shared with similar concurrent studies.
Evaluations
Test Organism Observations
Any immobilization or adverse reactions to exposure were recorded at 24 and 48 hours after the start of exposure. The criterion of effect used was that Daphnia were considered to be immobilized if they were unable to swim for approximately 15 seconds after gentle agitation. - Reference substance (positive control):
- yes
- Remarks:
- potassium dichromate
- Key result
- Duration:
- 48 h
- Dose descriptor:
- EL50
- Effect conc.:
- > 100 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Remarks on result:
- other: The toxicity cannot be attributed to a single component or a mixture of components, but to the test item as a whole.
- Details on results:
- Total Organic Carbon Analysis
Total Organic Carbon (TOC) analysis of the test preparations at 0 and 48 hours showed no significant differences in the amount of carbon present within the 10 and 100 mg/L loading rate WAF test vessels when compared to the control vessels. Therefore, given the background level of carbon in the control vessels and also the low level of carbon in the test vessels, it was considered that all the results were around the limit of quantification of the analytical method.
The dissolved test item may have been one or several components of the test item. Given that toxicity cannot be attributed to a single component or mixture of components but to the test item as a whole, the results were based on nominal loading rates only.
Immobilization Data
There was no immobilization in 20 daphnids exposed to concentrations of 10 and 100 mg/L loading rate WAF for a period of 48 hours. Inspection of the immobilization data gave the following results:
The 24 h EL50 was > 100 mg/L Loading Rate WAF
The 48 h EL50 was > 100 mg/L Loading Rate WAF
The No Observed Effect Loading rate after 24 and 48 hours exposure was 100 mg/L loading rate WAF. - Results with reference substance (positive control):
- A positive control (Harlan Study Number 41400711) used potassium dichromate as the reference item at concentrations of 0.32, 0.56, 1.0, 1.8 and 3.2 mg/L.
Exposure conditions for the positive control were similar to those in the definitive test.
Analysis of the immobilization data by the maximum-likelihood probit method (Finney, 1971*) at 24 hours and by the trimmed Spearman-Karber method (Hamilton et al 1977**) at 48 hours based on the nominal test concentrations gave the following results:
The 24 h EC50 was 0.87 mg/L with 95 % confidence limits of 0.75 – 1.0 mg/L.
The 48 h EC50 was 0.71 mg/L with 95 % confidence limits of 0.65 – 0.78 mg/L.
The NOEC was 0.56 mg/L and the LOEC was 1.0 mg/L.
The No Observed Effect Concentration is based upon less than 10% immobilization at this concentration.
The results from the positive control with potassium dichromate were within the normal range for this reference item. - Reported statistics and error estimates:
- An estimate of the EL50 values was given by inspection of the immobilization data.
- Validity criteria fulfilled:
- yes
- Conclusions:
- Measured acute (short-term) toxicity data are available for Shell GTL Solvent G215 (Hydrocarbons, C12-C15, n-alkanes, isoalkanes, <2% aromatics) to the freshwater invertebrate Daphnia magna. The test was conducted under static (no renewal of the test media) conditions in accordance with OECD Test Guideline 202 and method C2 of EC Regulation No. EC 440/2008. Appropriate modifications to the test and media preparation procedures were made to take account of the test substance containing multiple constituents, having low solubility in water and being potentially volatile. No effects on mobility of D. magna were observed after 48 hours exposure to the test medium prepared as a water-accommodated fraction (WAF) at loading rates up to 100 mg/l; 48-hour EL50 >100 mg/l, NOELR ≥100 mg/l. Samples of the control and the 10 and 100 mg/l loading rate WAFs were taken at 0 and 48 hours for Total Organic Carbon (TOC) analysis. Given the background level of carbon in the control vessels and also the low level of carbon in the test vessels, it was considered that all the results were around the limit of quantification of the analytical method. The results of the test are considered to be reliable.
- Executive summary:
Introduction
A study was performed to assess the acute toxicity of the test item to Daphnia magna. The method followed was designed to be compatible with the OECD Guidelines for Testing of Chemicals (April 2004) No 202, "Daphnia sp., Acute Immobilisation Test" referenced as Method C.2 of Commission Regulation (EC) No. 440/2008.
Methods…….
Due to the low aqueous solubility and complex nature of the test item, for the purposes of the test, the test medium was prepared as a Water Accommodated Fraction (WAF).
In the definitive test, twenty daphnids (4 replicates of 5 animals) were exposed to Water Accommodated Fractions (WAFs) of the test item at nominal loading rates of 10 and 100 mg/L for 48 hours at a temperature of approximately 21°C under static test conditions. The number of immobilized Daphnia and any adverse reactions to exposure were recorded after 24 and 48 hours.
Results…….
Samples of the control and the 10 and 100 mg/L loading rate WAFs were taken at 0 (fresh media) and 48 hours (old media) for Total Organic Carbon (TOC) analysis. Given the background level of carbon in the control vessels and also the low level of carbon in the test vessels, it was considered that all the results were around the limit of quantification of the analytical method.
Given that the toxicity cannot be attributed to a single component or a mixture of components, but to the test item as a whole, the results were based on nominal loading rates only.
Exposure of Daphnia magna to the test item gave EL50values of greater than 100 mg/L loading rate WAF. The No Observed Effect Loading Rate was 100 mg/L loading rate WAF.
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- key study
- Study period:
- March 1997
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: The study was conducted according to a standard guideline without deviations from the protocol and was conducted under GLP guidelines.
- Justification for type of information:
- A discussion and report on the read across strategy is given as an attachment in IUCLID Section 13.
- Reason / purpose for cross-reference:
- read-across: supporting information
- Qualifier:
- according to guideline
- Guideline:
- other: ISO (1990) Proposal to TC147/SC5/WG2: Determination of acute lethal toxicicty to marine adult copepods (Arcartia tonsa Dana)
- Deviations:
- no
- GLP compliance:
- yes
- Analytical monitoring:
- no
- Vehicle:
- no
- Details on test solutions:
- A water accommodated fraction was prepared for each treatment loading. Test substance was added to test medium and stirred for approximately 20 hours, then allowed to stand for approximately 1 hour before withdrawing an aliquot by siphon from the middle of the aqueous phase to avoid either floating or settled test substance. Seawater used in the study was UV sterilized, filtered to 0.2 um, and obtained from Scapa Flow, Orkney, UK.
- Test organisms (species):
- other: Arcartia tonsa
- Details on test organisms:
- Test organisms were 19 days old at test initiation.
- Test type:
- static
- Water media type:
- saltwater
- Limit test:
- no
- Total exposure duration:
- 48 h
- Post exposure observation period:
- None
- Test temperature:
- 19.6 to 21.7 degrees C
- pH:
- 8.00 to 8.02
- Dissolved oxygen:
- 97 to 99%
- Salinity:
- 33.7‰ (3.4%)
- Nominal and measured concentrations:
- Nominal treatment levels included the control and 1000, 3000, 3204, 5596, and 10000 mg/L.
- Details on test conditions:
- Test vessels were covered 100 ml borosilicate glasss crystallizing dishes containing 50 ml of test medium. 18 to 21 organisms were tested per treatment level and 38 organisms were tested in the control. No more than 11 organisms were added to a test vessel.
- Reference substance (positive control):
- yes
- Remarks:
- 3,5-dichorophenol
- Duration:
- 24 h
- Dose descriptor:
- LL50
- Effect conc.:
- > 10 000 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality
- Key result
- Duration:
- 48 h
- Dose descriptor:
- LL50
- Effect conc.:
- > 10 000 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality
- Details on results:
- Mortality results for the definitive test:
Nominal Copepod Total
Loading Mortality Mortality
(mg/L) (@ 24, 48 hrs)* (%)
Control 0, 1 3
1000 2, 3 17
3000 0, 0 0
3204 0, 1 5
5596 1, 1 5
10,000 0, 1 5
*38 organisms tested in the control and 18 to 21 organisms tested in the treatment levels - Results with reference substance (positive control):
- The 48-hour LC50 value for 3,5-dichlorophenol was 0.78 mg/L, which compared to the historical laboratory mean concentration of 0.68 mg/L.
- Reported statistics and error estimates:
- Statistical analyses were not conducted as 50% motality was not reached.
- Validity criteria fulfilled:
- yes
- Conclusions:
- Water accommodated fractions (WAFs) of the test substance did not produce 50% mortality with Arcartia tonsa at loading levels ranging between 1000 and 10,000 mg/L after a 48-hour exposure. Therefore, the 48-hour LL50 is reported as >10,000 mg/L.
- Executive summary:
Water accommodated fractions (WAFs) of the test substance did not produce 50% mortality with Arcartia tonsa at loading levels ranging between 1000 and 10,000 mg/L after a 48-hour exposure. Therefore, the 48-hour LL50 is reported as >10,000 mg/L. Although the three highest loading levels demonstrated a low degree of mortality, the reported mortality was eqivalent to the control. The 17% mortality reported in the 1000 mg/L loading level was the highest mortality reported in any of the treatment levels, but as this occurred in the lowest level and the treatment levels above it demonstrated either no mortality or mortality that was comparable to the control, the mortality in the lowest loading level is not considered significant.
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- key study
- Study period:
- March to November 1993
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: This robust summary has a reliability rating of 1 because the study followed a standard guideline, followed GLP guidelines, and was conducted without deviations that would invalidate the study.
- Justification for type of information:
- A discussion and report on the read across strategy is given as an attachment in Section 13.
- Reason / purpose for cross-reference:
- read-across: supporting information
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 202 (Daphnia sp. Acute Immobilisation Test)
- Deviations:
- no
- GLP compliance:
- yes
- Analytical monitoring:
- yes
- Details on sampling:
- An equilabration study was conducted prior to the study to determine the length of time needed to develop water accommodated fractions (WAFs) at the 1000 mg/L loading level. The aqueous phase of the WAF was analyzed after 1, 24, 48, and 96 hours of stirring. In all samples, the quantity of test substance in solution was less than the limit of detection (0.5 mg/L). Further analysis of test substance in test media a loading level of 1 g/L also showed no detectable amounts of test substance. Consequently, analysis of treatment solutions from the definitive study were not conducted.
- Vehicle:
- no
- Test organisms (species):
- Daphnia magna
- Details on test organisms:
- Organisms used in the test were from a laboratory culture were less than 24 hour old. The source of the culture was from ICI Brixham Laboratory from I.R.Ch.A., France.
- Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 48 h
- Post exposure observation period:
- None
- Hardness:
- 206 mg/L CaCO3
- Test temperature:
- 18 to 19 degrees C
- pH:
- 6.9 to 7.4
- Dissolved oxygen:
- 9.0 to 9.1 mg/L
- Salinity:
- Reshwater medium
- Nominal and measured concentrations:
- The nominal loading rates were 10, 30, 100, 300, and 1000 mg/L. A control was also tested.
- Details on test conditions:
- The study was conducted in closed test systems that were not renewed during the study. The test systems used were 150 ml glass Erlenmeyer flasks. The control and treatment levels were evaluated in replicate test systems. Ten organisms, less than 24 hours old, were exposed in each of the control and treatment solution flasks and were not fed during the study.
- Reference substance (positive control):
- no
- Duration:
- 24 h
- Dose descriptor:
- EL50
- Effect conc.:
- > 1 000 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Duration:
- 24 h
- Dose descriptor:
- LL0
- Effect conc.:
- 1 000 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Key result
- Duration:
- 48 h
- Dose descriptor:
- LL50
- Effect conc.:
- > 1 000 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Duration:
- 48 h
- Dose descriptor:
- LL0
- Effect conc.:
- 1 000 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Details on results:
- There was no immobility reported in any of the treatment solutions and control at test termination.
- Reported statistics and error estimates:
- None
- Validity criteria fulfilled:
- yes
- Conclusions:
- The water accommodated fraction (WAF) of the test substance did not produce a 50% effect (immobility) with Daphnia magna at a loading of 1000 mg/L after a 48-hour exposure. Therefore, the 48-hour LL50 is reported as >1000 mg/L. There was no mortality at the 1000 mg/L loading level after 48 hours. Therefore, the 48-hour LL0 for mortality is reported as 1000 mg/L. There was also no mortality in the control.
- Executive summary:
The water accommodated fraction (WAF) of the test substance did not produce a 50% effect (immobility) with Daphnia magna at a loading of 1000 mg/L after a 48-hour exposure. Therefore, the 48-hour LL50 is reported as >1000 mg/L. There was no mortality at the 1000 mg/L loading level after 48 hours. Therefore, the 48-hour LL0 for mortality is reported as 1000 mg/L. There was also no mortality in the control.
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- key study
- Study period:
- October 1990
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: This robust summary has a reliability rating of 2 because only limited analyses accompanied the study. However, the study generally followed a standard guideline and GLP, and was conducted without deviations that would invalidate the study.
- Justification for type of information:
- A discussion and report on the read across strategy is given as an attachment in Section 13.
- Reason / purpose for cross-reference:
- read-across: supporting information
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- EPA OPPTS 850.1020 (Gammarid Acute Toxicity Test)
- Deviations:
- no
- GLP compliance:
- yes
- Analytical monitoring:
- yes
- Details on sampling:
- The water accommodated fraction prepared at 10000 mg/L and the control used on Day 3 of the study were analyzed. Both samples were analyzed upon preparation and after 24 hours.
- Vehicle:
- no
- Details on test solutions:
- Individual treatment solutions were prepared by adding accurately weighed test substance, to 1.0 L of natural seawater in erlenmeyer flasks. The stock solutions were thoroughly mixed and the phases were allowed to separate for 24 hours. The Water Accommodated Fraction (WAF) was then drawn off the mixing vessel into the test vessels.
- Test organisms (species):
- other: Chaetogammarus marinus
- Details on test organisms:
- Test organisms were cultured in the laboratory prior to use in the test. They had a mean length of 4.2 mm. During the test, each test organism was fed a few Artemia nauplii per day.
- Test type:
- semi-static
- Water media type:
- saltwater
- Limit test:
- yes
- Total exposure duration:
- 96 h
- Post exposure observation period:
- None
- Hardness:
- No data
- Test temperature:
- 15.0 degrees C (mean)
- pH:
- 7.8 to 7.9 for new solutions and 7.7 to 8.0 for 24-hour old solutions.
- Dissolved oxygen:
- 7.7 to 9.1 mg/L for new solutions and 6.8 to 8.5 mg/L for 24-hour old solutions.
- Salinity:
- 33.7‰ (3.4%)
- Nominal and measured concentrations:
- Nominal treatment levels included the control and 10,000 mg/L. Measured concentrations were determined only for the treatment level on day 3 for the freshly prepared treatment solution and after 24 hours upon renewal. The 10,000 mg/L treatment solution analytical results were only reported for the normal paraffinic constituents, which totaled greater than the limit of detection (0.004 mg/L) in the freshly prepared exposure solution and at the limit of detection, 0.004 mg/L, in the 24-hour old exposure solution. The purpose of the analyses was to demonstrate that components of the test substance were in solution, because no effects were demonstrated in the study.
- Details on test conditions:
- Test vessels were closed scintillation vials filled with approximately 20 ml of test solution. Twenty replicates each of the treatment and control were tested, each containing 1 test organism. The test organisms were gently transferred daily to vials with freshly prepared WAF. Lighting was 16 hrs light and 8 hrs dark.
- Reference substance (positive control):
- no
- Key result
- Duration:
- 96 h
- Dose descriptor:
- LL50
- Effect conc.:
- > 1 000 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality
- Duration:
- 96 h
- Dose descriptor:
- NOELR
- Effect conc.:
- 1 000 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality
- Duration:
- 96 h
- Dose descriptor:
- NOELR
- Effect conc.:
- 1 000 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- other: Swinning behavior and food uptake
- Details on results:
- Mortality results for the definitive test:
Nominal Crustacean Total
Loading Mortality Mortality
(mg/L) (@ 24, 48, 72, 96 hrs)* (%)
Control 0, 0, 0, 0 0
10,000 0, 0, 0, 0 0
Mortality results for the range-finding test:
Nominal Crustacean Total
Loading Mortality Mortality
(mg/L) (@ 24, 48, 72, 96 hrs)* (%)
Control 0, 0, 0, 0 0
1 0, 0, 0, 0 0
100 0, 0, 0, 0 0
1000 0, 0, 0, 0 0
*20 organisms tested at each of the control and treatment levels - Reported statistics and error estimates:
- Statistical analyses were not conducted.
- Validity criteria fulfilled:
- yes
- Conclusions:
- The water accommodated fraction (WAF) of the test substance did not produce a 50% effect (mortality) with Chaetogammarus marinus at a loading of 10,000 mg/L after a 96-hour exposure. Therefore, the 96-hour LL50 is reported as >10,000 mg/L. There was no mortality at the 10,000 mg/L loading level after 96 hours. Therefore, the 96-hour NOELR for mortality is reported as 10,000 mg/L. There was also no mortality in the control.
- Executive summary:
The water accommodated fraction (WAF) of the test substance did not produce a 50% effect (mortality) with Chaetogammarus marinus after 96 hours at a loading of 10,000 mg/L, the only treatment level tested. Therefore, the 96-hour LL50 is reported as >10,000 mg/L. There was no mortality at the 10,000 mg/L loading level after 96 hours and no effects on swimming and feeding behavior were observed. Therefore, the 96-hour NOELR for these endpoints is reported as 10,000 mg/L. There was also no mortality in the control during the study. The control and treatment solutions were renewed every 24 hours. Analytical results showed that the treatment solution contained components of the test substance and that their combined concentration was greater than the limit of detection of the test substance, based on one sample from a freshly prepared WAF for day 3. The only components of the test substance quantitated were the normal paraffins. Threrefore, the analytical data do not characterize the solubility of the test substance from the 10,000 mg/L loading, but only serve to demonstrate that components of the test substance were in solution. The concentration of the test substance from the day three 24-hour old sample was reported at the limit of detection. The low analytical results are to be expected because of the very low water solubility of the components of the test substance. The day 3 analyses were conducted because no effects were observed during the first two days of the study and confirmation of exposure to the test substance was needed.
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- key study
- Study period:
- 1986 to 1987
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: The study has a reliability of 2 because it was conducted according to a standard guideline, but was not conducted under GLP guidelines and the report contains little information on water quality parameters.
- Justification for type of information:
- A discussion and report on the read across strategy is given as an attachment in IUCLID Section 13.
- Reason / purpose for cross-reference:
- read-across: supporting information
- Qualifier:
- according to guideline
- Guideline:
- other: As described in: The evaluation of the hazards of harmful substances carried by ships. Joint group of experts on the scientific aspects of marine pollution - GESAMP - reports and studies no. 17, 1982.
- Deviations:
- no
- GLP compliance:
- no
- Analytical monitoring:
- yes
- Details on sampling:
- 100 ml samples of the aqueous exposure phase were sampled for paraffin content.
- Vehicle:
- no
- Details on test solutions:
- The test solutions were prepared by stirring the test substance (100 and 1000 mg/L; each loading was far in excess of water solubility, which was cited as approximately 0.05 mg/L), with water for 24 hours. After stirring, the two phases in each solution were allowed to stand and separate for 4 hours. The aqueous phase was removed from the bottom of the mixing vessel through a stopcock. The aqueous phase was then used in the definitive study and the analyses. Exposure solutions were renewed daily.
- Test organisms (species):
- other: Chaetogammarus marinus
- Details on test organisms:
- The test organisms were from a laboratory culture, approximately 5mm long. The laboratory culture was maintained under standardized conditions and fed Fucus sp. Housing included shelter for concealment.
- Test type:
- semi-static
- Water media type:
- saltwater
- Limit test:
- no
- Total exposure duration:
- 96 h
- Post exposure observation period:
- None
- Test temperature:
- 15 degrees C
- pH:
- 7.5 to 8.3
- Dissolved oxygen:
- Most test solutions were saturated with oxygen, with the exception of a few test solutions that were lower than saturation but >6.5 mg/L.
- Salinity:
- 2.8%
- Nominal and measured concentrations:
- The nominal loading levels were 100 and 1000 mg/L, which each measured <0.005 mg/L at test initiation.
- Details on test conditions:
- A test system consisted of 10 organisms placed in 1000 ml of treatment solution contained in a glass beaker and covered with glass to minimize volatile losses. The control and treatment solutions were prepared in duplicate.
- Reference substance (positive control):
- no
- Key result
- Duration:
- 96 h
- Dose descriptor:
- LL50
- Effect conc.:
- > 1 000 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality
- Remarks on result:
- other: Water accommodated fractions up to a 1000 mg/L loading did not produce mortality after a 96-hour exposure.
- Validity criteria fulfilled:
- yes
- Conclusions:
- Water accommodated fractions (WAFs) of the test substance did not produce mortality to Chaetogammarus marinus due to the low water solubility of the test substance. The limit of detection was 0.005 mg/L and the test substance was not detected in samples from each of the exposure solutions. The saturated exposure solutions at four different loadings up to 1000 mg/L did not produce mortality in the test organisms after a 96-hour exposure. Therefore, the 96-hour LL50 = >1000 mg/L. The solubility of the test substance is noted in the report as 0.05 mg/L.
- Executive summary:
Water accommodated fractions (WAFs) of the test substance did not produce mortality to Chaetogammarus marinus due to the low water solubility of the test substance. The limit of detection was 0.005 mg/L and the test substance was not detected in samples from each of the exposure solutions. The saturated exposure solutions at four different loadings up to 1000 mg/L did not produce mortality in the test organisms after a 96-hour exposure. Therefore, the 96-hour LL50 = >1000 mg/L. The solubility of the test substance is noted in the report as 0.05 mg/L.
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- key study
- Study period:
- 1986 to 1987
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: The study has a reliability of 2 because it was conducted according to a standard guideline, but was not conducted under GLP guidelines and the report contains little information on water quality parameters.
- Justification for type of information:
- A discussion and report on the read across strategy is given as an attachment in IUCLID Section 13.
- Reason / purpose for cross-reference:
- read-across: supporting information
- Qualifier:
- according to guideline
- Guideline:
- other: As described in: The evaluation of the hazards of harmful substances carried by ships. Joint group of experts on the scientific aspects of marine pollution - GESAMP - reports and studies no. 17, 1982.
- Deviations:
- no
- GLP compliance:
- no
- Analytical monitoring:
- yes
- Details on sampling:
- 100 ml samples of the aqueous exposure phase were sampled for paraffin content.
- Vehicle:
- no
- Details on test solutions:
- The test solutions were prepared by stirring the test substance (0.56, 1.0, 100, and 1000 mg/L; each loading was far in excess of water solubility, which was cited as approximately 0.05 mg/L), with water for 24 hours. After stirring, the two phases in each solution were allowed to stand and separate for 4 hours. The aqueous phase was removed from the bottom of the mixing vessel through a stopcock. The aqueous phase was then used in the definitive study and the analyses.
- Test organisms (species):
- Daphnia magna
- Details on test organisms:
- The test organisms were less than 24 hours old and born of adults aged approximately 3 weeks. The adults were from a laboratory culture, maintained under standardized conditions.
- Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 48 h
- Post exposure observation period:
- None
- Test temperature:
- 20 degrees C
- pH:
- 7.5 to 8.3
- Dissolved oxygen:
- Most test solutions were saturated with oxygen, with the exception of a few test solutions that were lower than saturation but >6.5 mg/L.
- Nominal and measured concentrations:
- The nominal loading levels were 0.56, 1.0, 10, and 100 mg/L, which each measured <0.003 mg/L at test initiation.
- Details on test conditions:
- A test system consisted of 10 organisms placed in 250 ml of treatment solution contained in a glass beaker and covered with glass to minimize volatile losses. Control and treatment solutions were prepared in duplicate.
- Reference substance (positive control):
- no
- Key result
- Duration:
- 48 h
- Dose descriptor:
- EL50
- Effect conc.:
- > 1 000 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Remarks on result:
- other: Water accommodated fractions up to a 1000 mg/L loading did not produce immobility after a 48-hour exposure.
- Validity criteria fulfilled:
- yes
- Conclusions:
- Water accommodated fractions (WAFs) of the test substance did not produce immobility to Daphnia magna due to the low water solubility of the test substance. The limit of detection was 0.003 mg/L and the test substances was not detected in samples from each of the exposure solutions. The saturated exposure solutions at four different loadings up to 1000 mg/L did not produce immobility in the test organisms after a 48-hour exposure. Therefore, the 96-hour EL50 = >1000 mg/L. The solubility of the test substance is noted in the report as 0.05 mg/L.
- Executive summary:
Water accommodated fractions (WAFs) of the test substance did not produce immobility to Daphnia magna due to the low water solubility of the test substance. The limit of detection was 0.003 mg/L and the test substance was not detected in samples from each of the exposure solutions. The saturated exposure solutions at four different loadings up to 1000 mg/L did not produce immobility in the test organisms after a 48-hour exposure. Therefore, the 96-hour EL50 = >1000 mg/L. The solubility of the test substance is noted in the report as 0.05 mg/L.
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- key study
- Study period:
- 1986 to 1987
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: The study has a reliability of 2 because it was conducted according to a standard guideline, but was not conducted under GLP guidelines and the report contains little information on water quality parameters.
- Justification for type of information:
- A discussion and report on the read across strategy is given as an attachment in IUCLID Section 13.
- Reason / purpose for cross-reference:
- read-across: supporting information
- Qualifier:
- according to guideline
- Guideline:
- other: As described in: The evaluation of the hazards of harmful substances carried by ships. Joint group of experts on the scientific aspects of marine pollution - GESAMP - reports and studies no. 17, 1982.
- Deviations:
- no
- GLP compliance:
- no
- Analytical monitoring:
- yes
- Details on sampling:
- 100 ml samples of the aqueous exposure phase were sampled for paraffin content.
- Vehicle:
- no
- Details on test solutions:
- The test solutions were prepared by stirring the test substance (100 and 1000 mg/L; each loading was far in excess of water solubility, which was cited as approximately 0.05 mg/L), with water for 24 hours. After stirring, the two phases in each solution were allowed to stand and separate for 4 hours. The aqueous phase was removed from the bottom of the mixing vessel through a stopcock. The aqueous phase was then used in the definitive study and the analyses. Exposure solutions were renewed daily.
- Test organisms (species):
- Americamysis bahia (previous name: Mysidopsis bahia)
- Details on test organisms:
- The test organisms were from a laboratory culture, approximately 4 weeks old and 6 mm long. The laboratory culture was maintained under standardized conditions and fed Artemia nauplii.
- Test type:
- semi-static
- Water media type:
- saltwater
- Limit test:
- no
- Total exposure duration:
- 96 h
- Post exposure observation period:
- None
- Test temperature:
- 20 degrees C
- pH:
- 7.5 to 8.3
- Dissolved oxygen:
- Most test solutions were saturated with oxygen, with the exception of a few test solutions that were lower than saturation but >6.5 mg/L.
- Salinity:
- 2.8%
- Nominal and measured concentrations:
- The nominal loading levels were 100 and 1000 mg/L, which each measured <0.005 mg/L at test initiation.
- Details on test conditions:
- A test system consisted of 1 organism placed in 20 ml of treatment solution contained in a closed glass scintillation vial. Ten individual systems for the control and each treatment level were prepared.
- Reference substance (positive control):
- no
- Key result
- Duration:
- 96 h
- Dose descriptor:
- LL50
- Effect conc.:
- > 1 000 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality
- Remarks on result:
- other: Water accommodated fractions up to a 1000 mg/L loading did not produce mortality after a 96-hour exposure.
- Validity criteria fulfilled:
- yes
- Conclusions:
- Water accommodated fractions (WAFs) of the test substance did not produce mortality to Mysidopsis bahia (new name: Americamysis bahia) due to the low water solubility of the test substance. The limit of detection was 0.005 mg/L and the test substance was not detected in samples from each of the exposure solutions. The saturated exposure solutions at four different loadings up to 1000 mg/L did not produce mortality in the test organisms after a 96-hour exposure. Therefore, the 96-hour LL50 = >1000 mg/L. The solubility of the test substance is noted in the report as 0.05 mg/L.
- Executive summary:
Water accommodated fractions (WAFs) of the test substance did not produce mortality to Mysidopsis bahia (new name: Americamysis bahia) due to the low water solubility of the test substance. The limit of detection was 0.005 mg/L and the test substance was not detected in samples from each of the exposure solutions. The saturated exposure solutions at four different loadings up to 1000 mg/L did not produce mortality in the test organisms after a 96-hour exposure. Therefore, the 96-hour LL50 = >1000 mg/L. The solubility of the test substance is noted in the report as 0.05 mg/L.
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 1986 to 1987
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: The study has a reliability of 2 because it was conducted according to a standard guideline, but was not conducted under GLP guidelines and the report contains little information on water quality parameters.
- Qualifier:
- according to guideline
- Guideline:
- other: As described in: The evaluation of the hazards of harmful substances carried by ships. Joint group of experts on the scientific aspects of marine pollution - GESAMP - reports and studies no. 17, 1982.
- Deviations:
- no
- GLP compliance:
- no
- Analytical monitoring:
- yes
- Details on sampling:
- 100 ml samples of the aqueous exposure phase were sampled for paraffin content.
- Vehicle:
- no
- Details on test solutions:
- The test solution was prepared by stirring the test substance (1000 mg/L; the loading was far in excess of water solubility, which was cited as less than 0.05 mg/L), with water for 24 hours. After stirring, the two phases were allowed to stand and separate for 24 hours. The aqueous phase was removed from the bottom of the mixing vessel through a stopcock. The aqueous phase was then used in the definitive study and the analyses. Exposure solutions were renewed daily.
- Test organisms (species):
- other: Chaetogammarus marinus
- Details on test organisms:
- The test organisms were from a laboratory culture, approximately 5mm long. The laboratory culture was maintained under standardized conditions and fed Fucus sp. Housing included shelter for concealment.
- Test type:
- semi-static
- Water media type:
- saltwater
- Limit test:
- yes
- Total exposure duration:
- 96 h
- Post exposure observation period:
- None
- Test temperature:
- 15 degrees C
- pH:
- 7.5 to 8.3
- Dissolved oxygen:
- Most test solutions were saturated with oxygen, with the exception of a few test solutions that were lower than saturation but >6.5 mg/L.
- Salinity:
- 2.8%
- Nominal and measured concentrations:
- The nominal loading level was 1000 mg/L, which measured <0.005 mg/L at test initiation.
- Details on test conditions:
- A test system consisted of 10 organisms placed in 1000 ml of treatment solution contained in a glass beaker and covered with glass to minimize volatile losses. The control and treatment solution were prepared in duplicate.
- Reference substance (positive control):
- no
- Key result
- Duration:
- 96 h
- Dose descriptor:
- LL50
- Effect conc.:
- > 1 000 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality
- Remarks on result:
- other: The water accommodated fraction of a 1000 mg/L loading did not producemortality after a 96-hour exposure.
- Validity criteria fulfilled:
- yes
- Conclusions:
- The water accommodated fraction (WAF) of the test substance did not produce mortality to Chaetogammarus marinus due to the low water solubility of the test substance. The limit of detection was 0.005 mg/L. The saturated exposure solution at a loading of 1000 mg/L did not produce mortality in the test organisms after a 96-hour exposure. Therefore, the 96-hour LL50 = >1000 mg/L. The solubility of the test substance is noted in the report as between 0.05 mg/L and 0.004 mg/L.
- Executive summary:
The water accommodated fraction (WAF) of the test substance did not produce mortality to Chaetogammarus marinus due to the low water solubility of the test substance. The limit of detection was 0.005 mg/L. The saturated exposure solution at a loading of 1000 mg/L did not produce mortality in the test organisms after a 96-hour exposure. Therefore, the 96-hour LL50 = >1000 mg/L. The solubility of the test substance is noted in the report as between 0.05 mg/L and 0.004 mg/L. The solubility of the test substance is noted in the report as between 0.05 mg/L and 0.004 mg/L.
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 1986 to 1987
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: The study has a reliability of 2 because it was conducted according to a standard guideline, but was not conducted under GLP guidelines and the report contains little information on water quality parameters.
- Qualifier:
- according to guideline
- Guideline:
- other: As described in: The evaluation of the hazards of harmful substances carried by ships. Joint group of experts on the scientific aspects of marine pollution - GESAMP - reports and studies no. 17, 1982.
- Deviations:
- no
- GLP compliance:
- no
- Analytical monitoring:
- yes
- Details on sampling:
- 100 ml samples of the aqueous exposure phase were sampled for paraffin content.
- Vehicle:
- no
- Details on test solutions:
- The test solution was prepared by stirring the test substance (1000 mg/L; the loading was far in excess of water solubility, which was cited as less than 0.05 mg/L), with water for 24 hours. After stirring, the two phases were allowed to stand and separate for 24 hours. The aqueous phase was removed from the bottom of the mixing vessel through a stopcock. The aqueous phase was then used in the definitive study and the analyses.
- Test organisms (species):
- Daphnia magna
- Details on test organisms:
- The test organisms were less than 24 hours old and born of adults aged approximately 3 weeks. The adults were from a laboratory culture, maintained under standardized conditions.
- Test type:
- static
- Water media type:
- freshwater
- Limit test:
- yes
- Total exposure duration:
- 48 h
- Post exposure observation period:
- None
- Test temperature:
- 20 degrees C
- pH:
- 7.5 to 8.3
- Dissolved oxygen:
- Most test solutions were saturated with oxygen, with the exception of a few test solutions that were lower than saturation but >6.5 mg/L.
- Nominal and measured concentrations:
- The nominal loading level was 1000 mg/L, which measured <0.005 mg/L at test initiation.
- Details on test conditions:
- A test system consisted of 10 organisms placed in 250 ml of treatment solution contained in a glass beaker and covered with glass to minimize volatile losses. The control and treatment solution were prepared in duplicate.
- Reference substance (positive control):
- no
- Key result
- Duration:
- 48 h
- Dose descriptor:
- EL50
- Effect conc.:
- > 1 000 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Remarks on result:
- other: The water accommodated fraction of a 1000 mg/L loading did not produce immobility after a 48-hour exposure.
- Validity criteria fulfilled:
- yes
- Conclusions:
- The water accommodated fraction (WAF) of the test substance did not produce immobility to Daphnia magna due to the low water solubility of the test substance. The limit of detection was 0.005 mg/L and the test substance was not detected in samples from the highest exposure solution. The saturated exposure solution at a loading of 1000 mg/L did not produce immobility in the test organisms after a 48-hour exposure. Therefore, the 96-hour EL50 = >1000 mg/L. The solubility of the test substance is noted in the report as between 0.05 mg/L and 0.004 mg/L.
- Executive summary:
The water accommodated fraction (WAF) of the test substance did not produce immobility to Daphnia magna due to the low water solubility of the test substance. The limit of detection was 0.005 mg/L and the test substance was not detected in samples from the highest exposure solution. The saturated exposure solution at a loading of 1000 mg/L did not produce immobility in the test organisms after a 48-hour exposure. Therefore, the 96-hour EL50 = >1000 mg/L. The solubility of the test substance is noted in the report as between 0.05 mg/L and 0.004 mg/L.
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 1986 to 1987
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: The study has a reliability of 2 because it was conducted according to a standard guideline, but was not conducted under GLP guidelines and the report contains little information on water quality parameters.
- Qualifier:
- according to guideline
- Guideline:
- other: As described in: The evaluation of the hazards of harmful substances carried by ships. Joint group of experts on the scientific aspects of marine pollution - GESAMP - reports and studies no. 17, 1982.
- Deviations:
- no
- GLP compliance:
- no
- Analytical monitoring:
- yes
- Details on sampling:
- 100 ml samples of the aqueous exposure phase were sampled for paraffin content.
- Vehicle:
- no
- Details on test solutions:
- The test solution was prepared by stirring the test substance (1000 mg/L; the loading was far in excess of water solubility, which was cited as less than 0.05 mg/L), with water for 24 hours. After stirring, the two phases were allowed to stand and separate for 24 hours. The aqueous phase was removed from the bottom of the mixing vessel through a stopcock. The aqueous phase was then used in the definitive study and the analyses. Exposure solutions were renewed daily.
- Test organisms (species):
- Americamysis bahia (previous name: Mysidopsis bahia)
- Details on test organisms:
- The test organisms were from a laboratory culture, approximately 4 weeks old and 6 mm long. The laboratory culture was maintained under standardized conditions and fed Artemia nauplii.
- Test type:
- semi-static
- Water media type:
- saltwater
- Limit test:
- yes
- Total exposure duration:
- 96 h
- Post exposure observation period:
- None
- Test temperature:
- 20 degrees C
- pH:
- 7.5 to 8.3
- Dissolved oxygen:
- Most test solutions were saturated with oxygen, with the exception of a few test solutions that were lower than saturation but >6.5 mg/L.
- Salinity:
- 2.8%
- Nominal and measured concentrations:
- The nominal loading level was 1000 mg/L, which measured <0.005 mg/L at test initiation.
- Details on test conditions:
- A test system consisted of 1 organism placed in 20 ml of treatment solution contained in a closed glass scintillation vial. Ten individual systems for the control and treatment level were prepared.
- Reference substance (positive control):
- no
- Key result
- Duration:
- 96 h
- Dose descriptor:
- LL50
- Effect conc.:
- > 1 000 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality
- Remarks on result:
- other: The water accommodated fraction of a 1000 mg/L loading did not produce mortality after a 96-hour exposure.
- Validity criteria fulfilled:
- yes
- Conclusions:
- The water accommodated fraction (WAF) of the test substance did not produce mortality to Mysidopsis bahia (new name: Americamysis bahia) due to the low water solubility of the test substance. The limit of detection was 0.005 mg/L and the test substance was not detected in samples from highest exposure solution. The saturated exposure solution at a loading of 1000 mg/L did not produce mortality in the test organisms after a 96-hour exposure. Therefore, the 96-hour LL50 = >1000 mg/L. The solubility of the test substance is noted in the report as between 0.05 mg/L and 0.004 mg/L.
- Executive summary:
The water accommodated fraction (WAF) of the test substance did not produce mortality to Mysidopsis bahia (new name: Americamysis bahia) due to the low water solubility of the test substance. The limit of detection was 0.005 mg/L and the test substance was not detected in samples from highest exposure solution. The saturated exposure solution at a loading of 1000 mg/L did not produce mortality in the test organisms after a 96-hour exposure. Therefore, the 96-hour LL50 = >1000 mg/L. The solubility of the test substance is noted in the report as between 0.05 mg/L and 0.004 mg/L.
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- key study
- Study period:
- 1986 to 1987
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: The study has a reliability of 2 because it was conducted according to a standard guideline, but was not conducted under GLP guidelines and the report contains little information on water quality parameters.
- Justification for type of information:
- A discussion and report on the read across strategy is given as an attachment in IUCLID Section 13.
- Reason / purpose for cross-reference:
- read-across: supporting information
- Qualifier:
- according to guideline
- Guideline:
- other: As described in: The evaluation of the hazards of harmful substances carried by ships. Joint group of experts on the scientific aspects of marine pollution - GESAMP - reports and studies no. 17, 1982.
- Deviations:
- no
- GLP compliance:
- no
- Analytical monitoring:
- yes
- Details on sampling:
- 100 ml samples of the aqueous exposure phase were sampled for paraffin content.
- Vehicle:
- no
- Details on test solutions:
- The test solution was prepared by stirring the test substance (1000 mg/L; the loading was far in excess of water solubility, which was cited as 0.004 mg/L), with water for 24 hours. After stirring, the two phases were allowed to stand and separate for 24 hours. The aqueous phase was removed from the bottom of the mixing vessel through a stopcock. The aqueous phase was then used in the definitive study and the analyses. Exposure solutions were renewed daily.
- Test organisms (species):
- other: Chaetogammarus marinus
- Details on test organisms:
- The test organisms were from a laboratory culture, approximately 5mm long. The laboratory culture was maintained under standardized conditions and fed Fucus sp. Housing included shelter for concealment.
- Test type:
- semi-static
- Water media type:
- saltwater
- Limit test:
- yes
- Total exposure duration:
- 96 h
- Post exposure observation period:
- None
- Test temperature:
- 15 degrees C
- pH:
- 7.5 to 8.3
- Dissolved oxygen:
- Most test solutions were saturated with oxygen, with the exception of a few test solutions that were lower than saturation but >6.5 mg/L.
- Salinity:
- 2.8%
- Nominal and measured concentrations:
- The nominal loading level was 1000 mg/L, which measured <0.005 mg/L at test initiation.
- Details on test conditions:
- A test system consisted of 10 organisms placed in 1000 ml of treatment solution contained in a glass beaker and covered with glass to minimize volatile losses. The control and treatment solution were prepared in duplicate.
- Reference substance (positive control):
- no
- Key result
- Duration:
- 96 h
- Dose descriptor:
- LC50
- Effect conc.:
- > 0.004 mg/L
- Nominal / measured:
- estimated
- Conc. based on:
- test mat.
- Basis for effect:
- mortality
- Remarks on result:
- other: No effects were reported in a saturated exposure solution. The limit of detection is noted as 0.005 mg/L and the solubility is reported as 0.004 mg/L.
- Key result
- Duration:
- 96 h
- Dose descriptor:
- LL50
- Effect conc.:
- > 1 000 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality
- Remarks on result:
- other: The water accommodated fraction of a 1000 mg/L loading did not produce mortality after a 96-hour exposure.
- Validity criteria fulfilled:
- yes
- Conclusions:
- The water accommodated fraction (WAF) of the test substance did not produce mortality to Chaetogammarus marinus due to the low water solubility of the test substance. The limit of detection was 0.005 mg/L and the test substance was not detected in samples from the highest exposure solution. The saturated exposure solution at a loading of 1000 mg/L did not produce mortality in the test organisms after a 96-hour exposure. Therefore, the 96-hour LL50 = >1000 mg/L. The solubility of the test substance is noted in the report as 0.004 mg/L, which is approximately the limit of detection. Consequently, the EC50 is reported as >0.004 mg/L.
- Executive summary:
The water accommodated fraction (WAF) of the test substance did not produce mortality to Chaetogammarus marinus due to the low water solubility of the test substance. The limit of detection was 0.005 mg/L and the test substance was not detected in samples from the highest exposure solution. The saturated exposure solution at a loading of 1000 mg/L did not produce mortality in the test organisms after a 96-hour exposure. Therefore, the 96-hour LL50 = >1000 mg/L. The solubility of the test substance is noted in the report as 0.004 mg/L, which is approximately the limit of detection. Consequently, the EC50 is reported as >0.004 mg/L.
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- key study
- Study period:
- 1986 to 1987
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: The study has a reliability of 2 because it was conducted according to a standard guideline, but was not conducted under GLP guidelines and the report contains little information on water quality parameters.
- Justification for type of information:
- A discussion and report on the read across strategy is given as an attachment in IUCLID Section 13.
- Reason / purpose for cross-reference:
- read-across: supporting information
- Qualifier:
- according to guideline
- Guideline:
- other: As described in: The evaluation of the hazards of harmful substances carried by ships. Joint group of experts on the scientific aspects of marine pollution - GESAMP - reports and studies no. 17, 1982.
- Deviations:
- no
- GLP compliance:
- no
- Analytical monitoring:
- yes
- Details on sampling:
- 100 ml samples of the aqueous exposure phase were sampled for paraffin content.
- Vehicle:
- no
- Details on test solutions:
- The test solution was prepared by stirring the test substance (1000 mg/L; the loading was far in excess of water solubility, which was cited as 0.004 mg/L), with water for 24 hours. After stirring, the two phases were allowed to stand and separate for 24 hours. The aqueous phase was removed from the bottom of the mixing vessel through a stopcock. The aqueous phase was then used in the definitive study and the analyses.
- Test organisms (species):
- Daphnia magna
- Details on test organisms:
- The test organisms were less than 24 hours old and born of adults aged approximately 3 weeks. The adults were from a laboratory culture, maintained under standardized conditions.
- Test type:
- static
- Water media type:
- freshwater
- Limit test:
- yes
- Total exposure duration:
- 48 h
- Post exposure observation period:
- None
- Test temperature:
- 20 degrees C
- pH:
- 7.5 to 8.3
- Dissolved oxygen:
- Most test solutions were saturated with oxygen, with the exception of a few test solutions that were lower than saturation but >6.5 mg/L.
- Nominal and measured concentrations:
- The nominal loading level was 1000 mg/L, which measured <0.005 mg/L at test initiation.
- Details on test conditions:
- A test system consisted of 10 organisms placed in 250 ml of treatment solution contained in a glass beaker and covered with glass to minimize volatile losses. The control and treatment solution were prepared in duplicate.
- Reference substance (positive control):
- no
- Key result
- Duration:
- 48 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 0.004 mg/L
- Nominal / measured:
- estimated
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Remarks on result:
- other: No effects were reported in a saturated exposure solution. The limit of detection is noted as 0.005 mg/L and the solubility is reported as 0.004 mg/L.
- Key result
- Duration:
- 48 h
- Dose descriptor:
- EL50
- Effect conc.:
- > 1 000 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Remarks on result:
- other: The water accommodated fraction of a 1000 mg/L loading did not produce immobility after a 48-hour exposure.
- Validity criteria fulfilled:
- yes
- Conclusions:
- The water accommodated fraction (WAF) of the test substance did not produce immobility to Daphnia magna due to the low water solubility of the test substance. The limit of detection was 0.005 mg/L and the test substance was not detected in samples from the highest exposure solution. The saturated exposure solution at a loading of 1000 mg/L did not produce immobility in the test organisms after a 48-hour exposure. Therefore, the 96-hour EL50 = >1000 mg/L. The solubility of the test substance is noted in the report as 0.004 mg/L. The solubility of the test substance is noted in the report as 0.004 mg/L, which is approximately the limit of detection. Consequently, the EC50 is reported as >0.004 mg/L.
- Executive summary:
The water accommodated fraction (WAF) of the test substance did not produce immobility to Daphnia magna due to the low water solubility of the test substance. The limit of detection was 0.005 mg/L and the test substance was not detected in samples from the highest exposure solution. The saturated exposure solution at a loading of 1000 mg/L did not produce immobility in the test organisms after a 48-hour exposure. Therefore, the 96-hour EL50 = >1000 mg/L. The solubility of the test substance is noted in the report as 0.004 mg/L, which is approximately the limit of detection. Consequently, the EC50 is reported as >0.004 mg/L.
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- key study
- Study period:
- 1986 to 1987
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: The study has a reliability of 2 because it was conducted according to a standard guideline, but was not conducted under GLP guidelines and the report contains little information on water quality parameters.
- Justification for type of information:
- A discussion and report on the read across strategy is given as an attachment in IUCLID Section 13.
- Reason / purpose for cross-reference:
- read-across: supporting information
- Qualifier:
- according to guideline
- Guideline:
- other: As described in: The evaluation of the hazards of harmful substances carried by ships. Joint group of experts on the scientific aspects of marine pollution - GESAMP - reports and studies no. 17, 1982.
- Deviations:
- no
- GLP compliance:
- no
- Analytical monitoring:
- yes
- Details on sampling:
- 100 ml samples of the aqueous exposure phase were sampled for paraffin content.
- Vehicle:
- no
- Details on test solutions:
- The test solution was prepared by stirring the test substance (1000 mg/L; the loading was far in excess of water solubility, which was cited as 0.004 mg/L), with water for 24 hours. After stirring, the two phases were allowed to stand and separate for 24 hours. The aqueous phase was removed from the bottom of the mixing vessel through a stopcock. The aqueous phase was then used in the definitive study and the analyses. Exposure solutions were renewed daily.
- Test organisms (species):
- Americamysis bahia (previous name: Mysidopsis bahia)
- Details on test organisms:
- The test organisms were from a laboratory culture, approximately 4 weeks old and 6 mm long. The laboratory culture was maintained under standardized conditions and fed Artemia nauplii.
- Test type:
- semi-static
- Water media type:
- saltwater
- Limit test:
- yes
- Total exposure duration:
- 96 h
- Post exposure observation period:
- None
- Test temperature:
- 20 degrees C
- pH:
- 7.5 to 8.3
- Dissolved oxygen:
- Most test solutions were saturated with oxygen, with the exception of a few test solutions that were lower than saturation but >6.5 mg/L.
- Salinity:
- 2.8%
- Nominal and measured concentrations:
- The nominal loading level was 1000 mg/L, which measured <0.005 mg/L at test initiation.
- Details on test conditions:
- A test system consisted of 1 organism placed in 20 ml of treatment solution contained in a closed glass scintillation vial. Ten individual systems for the control and treatment level were prepared.
- Reference substance (positive control):
- no
- Key result
- Duration:
- 96 h
- Dose descriptor:
- LC50
- Effect conc.:
- > 0.004 mg/L
- Nominal / measured:
- estimated
- Conc. based on:
- test mat.
- Basis for effect:
- mortality
- Remarks on result:
- other: No effects were reported in a saturated exposure solution. The limit of detection is noted as 0.005 mg/L and the solubility is reported as 0.004 mg/L.
- Key result
- Duration:
- 96 h
- Dose descriptor:
- LL50
- Effect conc.:
- > 1 000 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality
- Remarks on result:
- other: The water accommodated fraction of a 1000 mg/L loading did not produce mortality after a 96-hour exposure.
- Validity criteria fulfilled:
- yes
- Conclusions:
- The water accommodated fraction (WAF) of the test substance did not produce mortality to Mysidopsis bahia (new name: Americamysis bahia) due to the low water solubility of the test substance. The limit of detection was 0.005 mg/L and the test substance was not detected in samples from the highest exposure solution. The saturated exposure solution at a loading of 1000 mg/L did not produce mortality in the test organisms after a 96-hour exposure. Therefore, the 96-hour LL50 = >1000 mg/L. The solubility of the test substance is noted in the report as 0.004 mg/L, which is approximately the limit of detection. Consequently, the EC50 is reported as >0.004 mg/L.
- Executive summary:
The water accommodated fraction (WAF) of the test substance did not produce mortality to Mysidopsis bahia (new name: Americamysis bahia) due to the low water solubility of the test substance. The limit of detection was 0.005 mg/L and the test substance was not detected in samples from the highest exposure solution. The saturated exposure solution at a loading of 1000 mg/L did not produce mortality in the test organisms after a 96-hour exposure. Therefore, the 96-hour LL50 = >1000 mg/L. The solubility of the test substance is noted in the report as 0.004 mg/L, which is approximately the limit of detection. Consequently, the EC50 is reported as >0.004 mg/L.
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- key study
- Study period:
- 1986 to 1987
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: The study has a reliability of 2 because it was conducted according to a standard guideline, but was not conducted under GLP guidelines and the report contains little information on water quality parameters.
- Justification for type of information:
- A discussion and report on the read across strategy is given as an attachment in IUCLID Section 13.
- Reason / purpose for cross-reference:
- read-across: supporting information
- Qualifier:
- according to guideline
- Guideline:
- other: As described in: The evaluation of the hazards of harmful substances carried by ships. Joint group of experts on the scientific aspects of marine pollution - GESAMP - reports and studies no. 17, 1982.
- Deviations:
- no
- GLP compliance:
- no
- Analytical monitoring:
- yes
- Details on sampling:
- 100 ml samples of the aqueous exposure phase were sampled for paraffin content.
- Vehicle:
- no
- Details on test solutions:
- The test solution was prepared by stirring the test substance (1000 mg/L; the loading was far in excess of water solubility, which was cited as less than 0.004 mg/L), with water for 24 hours. After stirring, the two phases were allowed to stand and separate for 24 hours. The aqueous phase was removed from the bottom of the mixing vessel through a stopcock. The aqueous phase was then used in the definitive study and the analyses. Exposure solutions were renewed daily.
- Test organisms (species):
- other: Chaetogammarus marinus
- Details on test organisms:
- The test organisms were from a laboratory culture, approximately 5mm long. The laboratory culture was maintained under standardized conditions and fed Fucus sp. Housing included shelter for concealment.
- Test type:
- semi-static
- Water media type:
- saltwater
- Limit test:
- yes
- Total exposure duration:
- 96 h
- Post exposure observation period:
- None
- Test temperature:
- 15 degrees C
- pH:
- 7.5 to 8.3
- Dissolved oxygen:
- Most test solutions were saturated with oxygen, with the exception of a few test solutions that were lower than saturation but >6.5 mg/L.
- Salinity:
- 2.8%
- Nominal and measured concentrations:
- The nominal loading level was 1000 mg/L, which measured <0.005 mg/L at test initiation.
- Details on test conditions:
- A test system consisted of 10 organisms placed in 1000 ml of treatment solution contained in a glass beaker and covered with glass to minimize volatile losses. The control and treatment solution were prepared in duplicate.
- Reference substance (positive control):
- no
- Key result
- Duration:
- 96 h
- Dose descriptor:
- LC50
- Effect conc.:
- > 0.003 mg/L
- Nominal / measured:
- estimated
- Conc. based on:
- test mat.
- Basis for effect:
- mortality
- Remarks on result:
- other: No effects were reported in a saturated exposure solution. The limit of detection is noted as between 0.005 mg/L and the solubility is reported as between 0.004 and 0.002 mg/L.
- Key result
- Duration:
- 96 h
- Dose descriptor:
- LL50
- Effect conc.:
- > 1 000 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality
- Remarks on result:
- other: The water accommodated fraction of a 1000 mg/L loading did not produce mortality after a 96-hour exposure.
- Validity criteria fulfilled:
- yes
- Conclusions:
- The water accommodated fraction (WAF) of the test substance did not produce mortality to Chaetogammarus marinus due to the low water solubility of the test substance. The limit of detection was 0.005 mg/L. The saturated exposure solution at a loading of 1000 mg/L did not produce mortality in the test organisms after a 96-hour exposure. Therefore, the 96-hour LL50 = >1000 mg/L. The solubility of the test substance is noted in the report as between 0.004 mg/L and 0.002 mg/L, which is approximately the limit of detection. Consequently, the EC50 is reported as >0.003 mg/L.
- Executive summary:
The water accommodated fraction (WAF) of the test substance did not produce mortality to Chaetogammarus marinus due to the low water solubility of the test substance. The limit of detection was 0.005 mg/L. The saturated exposure solution at a loading of 1000 mg/L did not produce mortality in the test organisms after a 96-hour exposure. Therefore, the 96-hour LL50 = >1000 mg/L. The solubility of the test substance is noted in the report as between 0.004 mg/L and 0.002 mg/L, which is approximately the limit of detection. Consequently, the EC50 is reported as >0.003 mg/L.
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- key study
- Study period:
- 1986 to 1987
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: The study has a reliability of 2 because it was conducted according to a standard guideline, but was not conducted under GLP guidelines and the report contains little information on water quality parameters.
- Justification for type of information:
- A discussion and report on the read across strategy is given as an attachment in IUCLID Section 13.
- Reason / purpose for cross-reference:
- read-across: supporting information
- Qualifier:
- according to guideline
- Guideline:
- other: As described in: The evaluation of the hazards of harmful substances carried by ships. Joint group of experts on the scientific aspects of marine pollution - GESAMP - reports and studies no. 17, 1982.
- Deviations:
- no
- GLP compliance:
- no
- Analytical monitoring:
- yes
- Details on sampling:
- 100 ml samples of the aqueous exposure phase were sampled for paraffin content.
- Vehicle:
- no
- Details on test solutions:
- The test solution was prepared by stirring the test substance (1000 mg/L; the loading was far in excess of water solubility, which was cited as less than 0.004 mg/L), with water for 24 hours. After stirring, the two phases were allowed to stand and separate for 24 hours. The aqueous phase was removed from the bottom of the mixing vessel through a stopcock. The aqueous phase was then used in the definitive study and the analyses.
- Test organisms (species):
- Daphnia magna
- Details on test organisms:
- The test organisms were less than 24 hours old and born of adults aged approximately 3 weeks. The adults were from a laboratory culture, maintained under standardized conditions.
- Test type:
- static
- Water media type:
- freshwater
- Limit test:
- yes
- Total exposure duration:
- 48 h
- Post exposure observation period:
- None
- Test temperature:
- 20 degrees C
- pH:
- 7.5 to 8.3
- Dissolved oxygen:
- Most test solutions were saturated with oxygen, with the exception of a few test solutions that were lower than saturation but >6.5 mg/L.
- Nominal and measured concentrations:
- The nominal loading level was 1000 mg/L, which measured <0.005 mg/L at test initiation.
- Details on test conditions:
- A test system consisted of 10 organisms placed in 250 ml of treatment solution contained in a glass beaker and covered with glass to minimize volatile losses. The control and treatment solution were prepared in duplicate.
- Reference substance (positive control):
- no
- Key result
- Duration:
- 48 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 0.003 mg/L
- Nominal / measured:
- estimated
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Remarks on result:
- other: No effects were reported in a saturated exposure solution. The limit of detection is noted as between 0.005 mg/L and the solubility is reported as between 0.004 and 0.002 mg/L.
- Key result
- Duration:
- 48 h
- Dose descriptor:
- EL50
- Effect conc.:
- > 1 000 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Remarks on result:
- other: The water accommodated fraction of a 1000 mg/L loading did not produce immobility after a 48-hour exposure.
- Validity criteria fulfilled:
- yes
- Conclusions:
- The water accommodated fraction (WAF) of the test substance did not produce immobility to Daphnia magna due to the low water solubility of the test substance. The limit of detection was 0.005 mg/L and the test substance was not detected in samples from the highest exposure solution. The saturated exposure solution at a loading of 1000 mg/L did not produce immobility in the test organisms after a 48-hour exposure. Therefore, the 96-hour EL50 = >1000 mg/L. The solubility of the test substance is noted in the report as between 0.004 mg/L and 0.002 mg/L, which is approximately the limit of detection. Consequently, the EC50 is reported as >0.003 mg/L.
- Executive summary:
The water accommodated fraction (WAF) of the test substance did not produce immobility to Daphnia magna due to the low water solubility of the test substance. The limit of detection was 0.005 mg/L and the test substance was not detected in samples from the highest exposure solution. The saturated exposure solution at a loading of 1000 mg/L did not produce immobility in the test organisms after a 48-hour exposure. Therefore, the 96-hour EL50 = >1000 mg/L. The solubility of the test substance is noted in the report as between 0.004 mg/L and 0.002 mg/L, which is approximately the limit of detection. Consequently, the EC50 is reported as >0.003 mg/L.
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- key study
- Study period:
- 1986 to 1987
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: The study has a reliability of 2 because it was conducted according to a standard guideline, but was not conducted under GLP guidelines and the report contains little information on water quality parameters.
- Justification for type of information:
- A discussion and report on the read across strategy is given as an attachment in IUCLID Section 13.
- Reason / purpose for cross-reference:
- read-across: supporting information
- Qualifier:
- according to guideline
- Guideline:
- other: As described in: The evaluation of the hazards of harmful substances carried by ships. Joint group of experts on the scientific aspects of marine pollution - GESAMP - reports and studies no. 17, 1982.
- Deviations:
- no
- GLP compliance:
- no
- Analytical monitoring:
- yes
- Details on sampling:
- 100 ml samples of the aqueous exposure phase were sampled for paraffin content.
- Vehicle:
- no
- Details on test solutions:
- The test solution was prepared by stirring the test substance (1000 mg/L; the loading was far in excess of water solubility, which was cited as less than 0.004 mg/L), with water for 24 hours. After stirring, the two phases were allowed to stand and separate for 24 hours. The aqueous phase was removed from the bottom of the mixing vessel through a stopcock. The aqueous phase was then used in the definitive study and the analyses. Exposure solutions were renewed daily.
- Test organisms (species):
- Americamysis bahia (previous name: Mysidopsis bahia)
- Details on test organisms:
- The test organisms were from a laboratory culture, approximately 4 weeks old and 6 mm long. The laboratory culture was maintained under standardized conditions and fed Artemia nauplii.
- Test type:
- semi-static
- Water media type:
- saltwater
- Limit test:
- yes
- Total exposure duration:
- 96 h
- Post exposure observation period:
- None
- Test temperature:
- 20 degrees C
- pH:
- 7.5 to 8.3
- Dissolved oxygen:
- Most test solutions were saturated with oxygen, with the exception of a few test solutions that were lower than saturation but >6.5 mg/L.
- Salinity:
- 2.8%
- Nominal and measured concentrations:
- The nominal loading level was 1000 mg/L, which measured <0.005 mg/L at test initiation.
- Details on test conditions:
- A test system consisted of 10 organisms placed in 1000 ml of treatment solution contained in a glass beaker and covered with glass to minimize volatile losses. The control and treatment solution were prepared in duplicate.
- Reference substance (positive control):
- no
- Key result
- Duration:
- 96 h
- Dose descriptor:
- LC50
- Effect conc.:
- > 0.003 mg/L
- Nominal / measured:
- estimated
- Conc. based on:
- test mat.
- Basis for effect:
- mortality
- Remarks on result:
- other: No effects were reported in a saturated exposure solution. The limit of detection is noted as between 0.005 mg/L and the solubility is reported as between 0.004 and 0.002 mg/L.
- Key result
- Duration:
- 96 h
- Dose descriptor:
- LL50
- Effect conc.:
- > 1 000 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality
- Remarks on result:
- other: The water accommodated fraction of a 1000 mg/L loading did not produce mortality after a 96-hour exposure.
- Validity criteria fulfilled:
- yes
- Conclusions:
- The water accommodated fraction (WAF) of the test substance did not produce mortality to Mysidopsis bahia (new name: Americamysis bahia) due to the low water solubility of the test substance. The limit of detection was 0.005 mg/L and the test substance was not detected in samples from the highest exposure solution. The saturated exposure solution at a loading of 1000 mg/L did not produce mortality in the test organisms after a 96-hour exposure. Therefore, the 96-hour LL50 = >1000 mg/L. The solubility of the test substance is noted in the report as between 0.004 mg/L and 0.002 mg/L, which is approximately the limit of detection. Consequently, the EC50 is reported as >0.003 mg/L.
- Executive summary:
The water accommodated fraction (WAF) of the test substance did not produce mortality to Mysidopsis bahia (new name: Americamysis bahia) due to the low water solubility of the test substance. The limit of detection was 0.005 mg/L and the test substance was not detected in samples from the highest exposure solution. The saturated exposure solution at a loading of 1000 mg/L did not produce mortality in the test organisms after a 96-hour exposure. Therefore, the 96-hour LL50 = >1000 mg/L. The solubility of the test substance is noted in the report as between 0.004 mg/L and 0.002 mg/L, which is approximately the limit of detection. Consequently, the EC50 is reported as >0.003 mg/L.
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- key study
- Study period:
- 1986 to 1987
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: The study has a reliability of 2 because it was conducted according to a standard guideline, but was not conducted under GLP guidelines and the report contains little information on water quality parameters.
- Justification for type of information:
- A discussion and report on the read across strategy is given as an attachment in IUCLID Section 13.
- Reason / purpose for cross-reference:
- read-across: supporting information
- Qualifier:
- according to guideline
- Guideline:
- other: As described in: The evaluation of the hazards of harmful substances carried by ships. Joint group of experts on the scientific aspects of marine pollution - GESAMP - reports and studies no. 17, 1982.
- Deviations:
- no
- GLP compliance:
- no
- Analytical monitoring:
- yes
- Details on sampling:
- 100 ml samples of the aqueous exposure phase were sampled for paraffin content.
- Vehicle:
- no
- Details on test solutions:
- The test solution was prepared by stirring the test substance (1000 mg/L; the loading was far in excess of water solubility, which was cited as 0.002 mg/L), with water for 24 hours. After stirring, the two phases were allowed to stand and separate for 24 hours. The aqueous phase was removed from the bottom of the mixing vessel through a stopcock. The aqueous phase was then used in the definitive study and the analyses. Exposure solutions were renewed daily.
- Test organisms (species):
- other: Chaetogammarus marinus
- Details on test organisms:
- The test organisms were from a laboratory culture, approximately 5mm long. The laboratory culture was maintained under standardized conditions and fed Fucus sp. Housing included shelter for concealment.
- Test type:
- semi-static
- Water media type:
- saltwater
- Limit test:
- yes
- Total exposure duration:
- 96 h
- Post exposure observation period:
- None
- Test temperature:
- 15 degrees C
- pH:
- 7.5 to 8.3
- Dissolved oxygen:
- Most test solutions were saturated with oxygen, with the exception of a few test solutions that were lower than saturation but >6.5 mg/L.
- Salinity:
- 2.8%
- Nominal and measured concentrations:
- The nominal loading level was 1000 mg/L, which measured <0.005 mg/L at test initiation.
- Details on test conditions:
- A test system consisted of 10 organisms placed in 1000 ml of treatment solution contained in a glass beaker and covered with glass to minimize volatile losses. The control and treatment solution were prepared in duplicate.
- Reference substance (positive control):
- no
- Key result
- Duration:
- 96 h
- Dose descriptor:
- LC50
- Effect conc.:
- > 0.002 mg/L
- Nominal / measured:
- estimated
- Conc. based on:
- test mat.
- Basis for effect:
- mortality
- Remarks on result:
- other: No effects were reported in a saturated exposure solution. The limit of detection is noted as 0.005 mg/L and the solubility is reported as 0.002 mg/L.
- Key result
- Duration:
- 96 h
- Dose descriptor:
- LL50
- Effect conc.:
- > 1 000 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality
- Remarks on result:
- other: The water accommodated fraction of a 1000 mg/L loading did not produce mortality after a 96-hour exposure.
- Validity criteria fulfilled:
- yes
- Conclusions:
- The water accommodated fraction (WAF) of the test substance did not produce mortality to Chaetogammarus marinus due to the low water solubility of the test substance. The limit of detection was 0.005 mg/L. The saturated exposure solution at a loading of 1000 mg/L did not produce mortality in the test organisms after a 96-hour exposure. Therefore, the 96-hour LL50 = >1000 mg/L. The solubility of the test substance is noted in the report as 0.002 mg/L, which is approximately the limit of detection. Consequently, the EC50 is reported as >0.002 mg/L.
- Executive summary:
The water accommodated fraction (WAF) of the test substance did not produce mortality to Chaetogammarus marinus due to the low water solubility of the test substance. The limit of detection was 0.005 mg/L. The saturated exposure solution at a loading of 1000 mg/L did not produce mortality in the test organisms after a 96-hour exposure. Therefore, the 96-hour LL50 = >1000 mg/L. The solubility of the test substance is noted in the report as 0.002 mg/L, which is approximately the limit of detection. Consequently, the EC50 is reported as >0.002 mg/L.
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- key study
- Study period:
- 1986 to 1987
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: The study has a reliability of 2 because it was conducted according to a standard guideline, but was not conducted under GLP guidelines and the report contains little information on water quality parameters.
- Justification for type of information:
- A discussion and report on the read across strategy is given as an attachment in IUCLID Section 13.
- Reason / purpose for cross-reference:
- read-across: supporting information
- Qualifier:
- according to guideline
- Guideline:
- other: As described in: The evaluation of the hazards of harmful substances carried by ships. Joint group of experts on the scientific aspects of marine pollution - GESAMP - reports and studies no. 17, 1982.
- Deviations:
- no
- GLP compliance:
- no
- Analytical monitoring:
- yes
- Details on sampling:
- 100 ml samples of the aqueous exposure phase were sampled for paraffin content.
- Vehicle:
- no
- Details on test solutions:
- The test solution was prepared by stirring the test substance (1000 mg/L; the loading was far in excess of water solubility, which was cited as 0.002 mg/L), with water for 24 hours. After stirring, the two phases were allowed to stand and separate for 24 hours. The aqueous phase was removed from the bottom of the mixing vessel through a stopcock. The aqueous phase was then used in the definitive study and the analyses.
- Test organisms (species):
- Daphnia magna
- Details on test organisms:
- The test organisms were less than 24 hours old and born of adults aged approximately 3 weeks. The adults were from a laboratory culture, maintained under standardized conditions.
- Test type:
- static
- Water media type:
- freshwater
- Limit test:
- yes
- Total exposure duration:
- 48 h
- Post exposure observation period:
- None
- Test temperature:
- 20 degrees C
- pH:
- 7.5 to 8.3
- Dissolved oxygen:
- Most test solutions were saturated with oxygen, with the exception of a few test solutions that were lower than saturation but >6.5 mg/L.
- Nominal and measured concentrations:
- The nominal loading level was 1000 mg/L, which measured <0.005 mg/L at test initiation.
- Details on test conditions:
- A test system consisted of 10 organisms placed in 250 ml of treatment solution contained in a glass beaker and covered with glass to minimize volatile losses. The control and treatment solution were prepared in duplicate.
- Reference substance (positive control):
- no
- Key result
- Duration:
- 48 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 0.002 mg/L
- Nominal / measured:
- estimated
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Remarks on result:
- other: No effects were reported in a saturated exposure solution. The limit of detection is noted as 0.005 mg/L and the solubility is reported as 0.002 mg/L.
- Key result
- Duration:
- 48 h
- Dose descriptor:
- EL50
- Effect conc.:
- > 1 000 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Remarks on result:
- other: The water accommodated fraction of a 1000 mg/L loading did not produce immobility after a 48-hour exposure.
- Validity criteria fulfilled:
- yes
- Conclusions:
- The water accommodated fraction (WAF) of the test substance did not produce immobility to Daphnia magna due to the low water solubility of the test substance. The limit of detection was 0.005 mg/L and the test substance was not detected in samples from the highest exposure solution. The saturated exposure solution at a loading of 1000 mg/L did not produce immobility in the test organisms after a 48-hour exposure. Therefore, the 48-hour EL50 = >1000 mg/L. The solubility of the test substance is noted in the report as 0.002 mg/L, which is approximately the limit of detection. Consequently, the EC50 is reported as >0.002 mg/L.
- Executive summary:
The water accommodated fraction (WAF) of the test substance did not produce immobility to Daphnia magna due to the low water solubility of the test substance. The limit of detection was 0.005 mg/L and the test substance was not detected in samples from the highest exposure solution. The saturated exposure solution at a loading of 1000 mg/L did not produce immobility in the test organisms after a 48-hour exposure. Therefore, the 48-hour EL50 = >1000 mg/L. The solubility of the test substance is noted in the report as 0.002 mg/L, which is approximately the limit of detection. Consequently, the EC50 is reported as >0.002 mg/L.
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- key study
- Study period:
- 1986 to 1987
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: The study has a reliability of 2 because it was conducted according to a standard guideline, but was not conducted under GLP guidelines and the report contains little information on water quality parameters.
- Justification for type of information:
- A discussion and report on the read across strategy is given as an attachment in IUCLID Section 13.
- Reason / purpose for cross-reference:
- read-across: supporting information
- Qualifier:
- according to guideline
- Guideline:
- other: As described in: The evaluation of the hazards of harmful substances carried by ships. Joint group of experts on the scientific aspects of marine pollution - GESAMP - reports and studies no. 17, 1982.
- Deviations:
- no
- GLP compliance:
- no
- Analytical monitoring:
- yes
- Details on sampling:
- 100 ml samples of the aqueous exposure phase were sampled for paraffin content.
- Vehicle:
- no
- Details on test solutions:
- The test solution was prepared by stirring the test substance (1000 mg/L; the loading was far in excess of water solubility, which was cited as 0.002 mg/L), with water for 24 hours. After stirring, the two phases were allowed to stand and separate for 24 hours. The aqueous phase was removed from the bottom of the mixing vessel through a stopcock. The aqueous phase was then used in the definitive study and the analyses. Exposure solutions were renewed daily.
- Test organisms (species):
- Americamysis bahia (previous name: Mysidopsis bahia)
- Details on test organisms:
- The test organisms were from a laboratory culture, approximately 4 weeks old and 6 mm long. The laboratory culture was maintained under standardized conditions and fed Artemia nauplii.
- Test type:
- semi-static
- Water media type:
- saltwater
- Limit test:
- yes
- Total exposure duration:
- 96 h
- Post exposure observation period:
- None
- Test temperature:
- 20 degrees C
- pH:
- 7.5 to 8.3
- Dissolved oxygen:
- Most test solutions were saturated with oxygen, with the exception of a few test solutions that were lower than saturation but >6.5 mg/L.
- Salinity:
- 2.8%
- Nominal and measured concentrations:
- The nominal loading level was 1000 mg/L, which measured <0.005 mg/L at test initiation.
- Details on test conditions:
- A test system consisted of 10 organisms placed in 1000 ml of treatment solution contained in a glass beaker and covered with glass to minimize volatile losses. The control and treatment solution were prepared in duplicate.
- Reference substance (positive control):
- no
- Key result
- Duration:
- 96 h
- Dose descriptor:
- LC50
- Effect conc.:
- > 0.002 mg/L
- Nominal / measured:
- estimated
- Conc. based on:
- test mat.
- Basis for effect:
- mortality
- Remarks on result:
- other: No effects were reported in a saturated exposure solution. The limit of detection is noted as 0.005 mg/L and the solubility is reported as 0.002 mg/L.
- Key result
- Duration:
- 96 h
- Dose descriptor:
- LL50
- Effect conc.:
- > 1 000 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality
- Remarks on result:
- other: The water accommodated fraction of a 1000 mg/L loading did not produce mortality after a 96-hour exposure.
- Validity criteria fulfilled:
- yes
- Conclusions:
- The water accommodated fraction (WAF) of the test substance did not produce mortality to Mysidopsis bahia (new name: Americamysis bahia) due to the low water solubility of the test substance. The limit of detection was 0.005 mg/L. The saturated exposure solution at a loading of 1000 mg/L did not produce mortality in the test organisms after a 96-hour exposure. Therefore, the 96-hour LL50 = >1000 mg/L. The solubility of the test substance is noted in the report as 0.002 mg/L, which is approximately the limit of detection. Consequently, the EC50 is reported as >0.002 mg/L.
- Executive summary:
The water accommodated fraction (WAF) of the test substance did not produce mortality to Mysidopsis bahia (new name: Americamysis bahia) due to the low water solubility of the test substance. The limit of detection was 0.005 mg/L and the test substance was not detected in samples from the highest exposure solution. The saturated exposure solution at a loading of 1000 mg/L did not produce mortality in the test organisms after a 96-hour exposure. Therefore, the 96-hour LL50 = >1000 mg/L. The solubility of the test substance is noted in the report as 0.002 mg/L, which is approximately the limit of detection. Consequently, the EC50 is reported as >0.002 mg/L.
Referenceopen allclose all
Validation Criteria
The test was considered to be valid given that none of the control daphnids showed immobilization or other signs of disease or stress and that the oxygen concentration at the end of the test was ≥3 mg/L in the control and test vessels.
Water Quality Criteria
Temperature was maintained at approximately 21°C throughout the test, while there were no treatment related differences for oxygen concentration or pH.
Vortex Depth Measurements
The vortex depth was recorded at the start and end of the mixing period and was observed to be a dimple at the water surface on each occasion.
Observations on Test Item Solubility
Observations on the test media were carried out during the mixing and testing of the WAFs.
At the start of the mixing period the 10 and 100 mg/L loading rates were observed to be clear colorless water columns with globules of test item at the surface. After 23 hours stirring and the 1-Hour settlement period, the 10 and 100 mg/L loading rates were observed to be clear colorless solutions. Microscopic inspection of the WAFs showed no micro-dispersions or undissolved test item to be present. After siphoning and for the duration of the test, the 10 and 100 mg/L loading rates were observed to be clear, colorless solutions.
Description of key information
There is data available for this substance. Additionally, key data is available for structural analogues Hydrocarbons, C12-C15, n-alkanes, isoalkanes, <2% aromatics; Hydrocarbons, C11-C14, n-alkanes, isoalkanes, cyclics, <2% aromatics, Decane, Undecane, Hydrocarbons, C11-C14, n-alkanes, <2% aromatics, Dodecane, Tridecane, Tetradecane. The data is read across to this substance based on analogue read across and a discussion and report on the read across strategy is provided as an attachment in IUCLID Section 13. Key information is summarised below:
Hydrocarbons, C12-C15, n-alkanes, isoalkanes, <2% aromatics presented a 48-h EL50 for Daphnia magna of >100 mg/L (WAF) based on mobility.
Hydrocarbons, C11-C14, n-alkanes, isoalkanes, cyclics, <2% aromatics presented a 48-h LL50 for Daphnia magna of >1,000 mg/L (WAF) based on mortality.
Hydrocarbons, C11-C14, n-alkanes, isoalkanes, cyclics, <2% aromatics presented a 96-h LL50 for Chaetogammarus marinus of >10,000 mg/L (WAF) based on mortality.
Decane presented a 96-h LL50 for Chaetogammarus marinus of >1,000 mg/L (WAF) based on mortality.
Decane presented a 96-h EL50 for Daphnia magna of >1,000 mg/L (WAF) based on mobility.
Decanepresented a 96-h LL50 for Mysidopsis bahia of >1,000 mg/L (WAF) based on mortality.
Undecane presented a 96-h LL50 for Chaetogammarus marinus of >1,000 mg/L (WAF) based on mortality.
Undecane presented a 96-h EL50 for Daphnia magna of >1,000mg/L (WAF) based on mobility.
Undecane presented a 96-h LL50 for Mysidopsis bahia of >1,000 mg/L (WAF) based on mortality.
Hydrocarbons, C11-C14, n-alkanes, <2% aromatics presented a 48-h LL50 for Arcartia tonsa of >10,000 mg/L (WAF) based on mortality.
Dodecane presented a 96-h LL50 for Chaetogammarus marinus of >1,000mg/L (WAF) based on mortality.
Dodecane presented a 96-h EL50 for Daphnia magna of >1,000 mg/L (WAF) based on mobility.
Dodecane presented a 96-h LL50 for Mysidopsis bahia of >1,000 mg/L (WAF) based on mortality.
Tridecane presented a 96-h LL50 for Chaetogammarus marinus of >1,000 mg/L (WAF) based on mortality.
Tridecane presented a 96-h EL50 for Daphnia magna of >1,000 mg/L (WAF) based on mobility.
Tridecane presented a 96-h LL50 for Mysidopsis bahia of >1,000 mg/L (WAF) based on mortality.
Tetradecane presented a 96-h LL50 for Chaetogammarus marinus of >1,000 mg/L (WAF) based on mortality.
Tetradecane presented a 96-h EL50 for Daphnia magna of >1,000 mg/L (WAF) based on mobility.
Tetradecane presented a 96-h LL50 for Mysidopsis bahia of >1,000 mg/L (WAF) based on mortality.
Key value for chemical safety assessment
Additional information
The normal paraffin substances, including n-decane, n-undecane, n-dodecane, n-tridecane, n-tetradecane, and other substances including Hydrocarbons, C11-C14, n-alkanes, <2% aromatics; Hydrocarbons, C11-C14, n-alkanes, isoalkanes, cyclics, <2% aromatics; and Hydrocarbons, C12-C15, n-alkanes, isoalkanes, <2% aromatics, are not expected to demonstrate acute invetebrate toxicity based on results of studies with freshwater and marine invertebrates, including Daphnia magna, Chaetogammarus marinus, Mysidopsis bahia and Arcartia tonsa. Each of these substances has been shown not to demonstrate effects, as measured by immobility or mortality in 48- or 96-h toxicity studies at the highest loading levels tested, which have ranged from 100 to 10,000 mg/L. Only for n-nonane, experimental concentrations could me measured and 96-h LC50 and 48-h EC50 below 100 mg/L were determined.
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