Registration Dossier
Registration Dossier
Data platform availability banner - registered substances factsheets
Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.
The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.
Diss Factsheets
Use of this information is subject to copyright laws and may require the permission of the owner of the information, as described in the ECHA Legal Notice.
EC number: 205-460-8 | CAS number: 141-13-9
- Life Cycle description
- Uses advised against
- Endpoint summary
- Appearance / physical state / colour
- Melting point / freezing point
- Boiling point
- Density
- Particle size distribution (Granulometry)
- Vapour pressure
- Partition coefficient
- Water solubility
- Solubility in organic solvents / fat solubility
- Surface tension
- Flash point
- Auto flammability
- Flammability
- Explosiveness
- Oxidising properties
- Oxidation reduction potential
- Stability in organic solvents and identity of relevant degradation products
- Storage stability and reactivity towards container material
- Stability: thermal, sunlight, metals
- pH
- Dissociation constant
- Viscosity
- Additional physico-chemical information
- Additional physico-chemical properties of nanomaterials
- Nanomaterial agglomeration / aggregation
- Nanomaterial crystalline phase
- Nanomaterial crystallite and grain size
- Nanomaterial aspect ratio / shape
- Nanomaterial specific surface area
- Nanomaterial Zeta potential
- Nanomaterial surface chemistry
- Nanomaterial dustiness
- Nanomaterial porosity
- Nanomaterial pour density
- Nanomaterial photocatalytic activity
- Nanomaterial radical formation potential
- Nanomaterial catalytic activity
- Endpoint summary
- Stability
- Biodegradation
- Bioaccumulation
- Transport and distribution
- Environmental data
- 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
- Toxicity to other aquatic organisms
- Sediment toxicity
- Terrestrial toxicity
- Biological effects monitoring
- Biotransformation and kinetics
- Additional ecotoxological information
- Toxicological Summary
- Toxicokinetics, metabolism and distribution
- Acute Toxicity
- Irritation / corrosion
- Sensitisation
- 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
Short-term toxicity to aquatic invertebrates
Administrative data
Link to relevant study record(s)
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 12 Sept. 2000 - 10 Nov. 2000
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- guideline study with acceptable restrictions
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 202 (Daphnia sp. Acute Immobilisation Test)
- Deviations:
- yes
- Remarks:
- slightly modified/adapted to the kind of test substance (poorly water soluble and volatile).
- GLP compliance:
- yes (incl. QA statement)
- Specific details on test material used for the study:
- Batch N°20070036
Expiry date 31-Mar-2001 - Analytical monitoring:
- yes
- Details on sampling:
- Performed at t=0 and t=48 hours
- Vehicle:
- no
- Details on test solutions:
- As the test substance is poorly water soluble, the test substance was tested using the aqueous extracts from the test substance. For this purpose, suspensions of the test substance were prepared in dilution water. For this purpose, the test substance was weighed into the glass vessels with the respective amount of water used for the preparation of the aqueous extracts. The test substance was introduced into the dilution water whilst shaking an a shaking machine (approx 130 rpm) for 24h at room temperature. It is assumed that during that time equilibration between the test substance and the water was achieved. Thereafter, the suspensions were filtered through filter paper which was previously rinsed thoroughly with ultrapure water (Seral, „Purelab Plus") in order to eliminate possible soluble impurities from the filter material. The filtered extracts were used directly for the test without any further dilution steps.
- Test organisms (species):
- Daphnia magna
- Details on test organisms:
- Daphnia magna STRAUS of laboratory bred (originally derived from Dr. Knie, LWA Düsseldorf) were used for the test. The animals used for the test were not older than 24h.
- Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 48 h
- Remarks on exposure duration:
- The incubation period was 48h.
- pH:
- As a control the pH was measured at the beginning of the test and after 48h.
- Nominal and measured concentrations:
- 1st main Test (Nominal; (aqueous extracts)) : 1 mg/L, 2 mg/L, 4 mg/L, 8 mg/L, and 10 mg/L loading rates
2nd main Test (Nominal; (aqueous extracts)) : 0.25 mg/L, 0.5 mg/L, 1 mg/L, 2 mg/L, 4 mg/L, and 8 mg/L loading rates - Details on test conditions:
- - As the test substance exhibits partial adsorptive properties the aqueous extracts of the test substance were transferred into the respective test vessels, and after approx. 1 hour, the aqueous extracts were replaced by a second part of the aqueous extract. By that measure the surfaces of the glass walls were saturated with the test substance, and losses due to adsorption avoided.
As the test substance contains volatile components the test was performed in closed bottles. For this purpose, the aqueous extracts of test substance were filled into the test vessels (100 mL-carboys ) up to the neck, and after introducing of the animal the vessels were closed with the glass-stoppers. By this measure any gas-phase was avoided.
- Four parallel test solutions with 5 animals were prepared for each concentration, respectively.
- As a control the pH was measured at the beginning of the test and after 48h. The daphnia were not fed during the test. - Reference substance (positive control):
- no
- Key result
- Duration:
- 48 h
- Dose descriptor:
- EL50
- Effect conc.:
- 0.9 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Remarks on result:
- other: Loading Rate
- Details on results:
- SCREENING TEST:
A screening test was performed in order to find out the concentration range of the test substance for the main test. Three concentrations of the test substance were used: 1.0 mg/L, 10 mg/L and 100 mg/L (Loading Rated). After 48 hours the immobilisation observed was 0, 10 and 100% respectively.
1st MAIN TEST:
Based on the results of the screening test, the following concentrations were tested: 1mg/L, 2mg/L, 4 mg/L, 8 mg/L and 10 mg/L (Loading Rates). After 48 hours the immobilisation observed was 85, 100, 100, 100 and 100% respectively. In contrary to the screening test there was a higher inhibitory effect at the lowest concentration of 1 mg/L. Therefore a second main test was performed using two lower concentrations.
2nd MAIN TEST:
The following nominal concentrations were tested: 0.25 mg/L, 0.5 mg/l, 1 mg/L, 2 mg/L, 4 mg/L and 8 mg/L (Loading rate). After 48 hours the immobilisation observed was 0, 5, 75, 100, 100, and 100% respectively.
TOC analyses performed with the test solutions of the 1st main test at 0 hour and 48 hours showed that the organic matter of the test substance remained constant (See "Any other information on results incl. tables" for details). For this reason, the results of the test were based on the nominal concentrations (i.e. loading rates). - Validity criteria fulfilled:
- yes
- Conclusions:
- The LC50 (48h) value has been determined to be equal to 0.9 mg/L under these test conditions.
- Executive summary:
„FARENAL" was tested for acute toxicity towards Daphnia according to OECD 202, Part I. In order to investigate the influence of the test substance towards the daphnia the swinuning behaviour of the animals was recorded. As the test substance is poorly water soluble, the test substance was tested using the aqueous extracts from the test substance (termed eluates hereafter). Under the conditions used for the test, immobilisation of the daphnia was observed at nominal concentrations >0.5 mg/L. The following effective loadings (EL-values) were calculated on basis of the nominal concentrations being tested:
Inhibition Values t24h Standard Deviation (%) 95% Confidence-Level (%) EL0 0.4 mg/L 14 45 EL50 1.2 mg/L 10 32 EL100 3.8 mg/L 17 53 Inhibition Values t48h Standard Deviation (%) 95% Confidence-Level (%) EL0 0.3 mg/L 15 49 EL50 0.9 mg/L 9 30 EL100 2.8 mg/L 13 43 Within TOC-analyses performed with the test solutions (definitive test) only very small arnounts of the test substance were dissolved in the aqueous phase (in maximum only 2.5 mg/L representing 31% of the nominal concentration at the highest concentration [8 mg/L, definitive test] being tested). Recoveries at the three lowest concentrations could not be determined at all, and, regarding the very low measured TOC-values, „recovery rates" at the two highest concentrations being tested should not be given. Within TOC-analyses performed with the test solutions (ls t main test) at to and teil, it could be shown, that the organic matter of the test substance remained constant in the aqueous phase. For this reason, the results of this test are based on the nominal concentrations tested.
Reference
TOC values determined within 1st Main Test
Nominal Concentrations / Loading Rates (mg/L) |
Mean Values of measured values t0h, (mg/L TOC) | Mean Values t0h, measured Values, net - Blank (mg/L TOC) | Mean Values of measured values t48h, (mg/L TOC) | Mean Values t48h, measured Values, net - Blank (mg/L TOC) | % Recovery (Mean Value) |
Blank | 0 | 0 | 0.11 | 0 | - |
1 | (4.42)* | (4.42)* | 0.68 | 0.57 | (12.9) - ignored due to error of 0h determination |
2 | 0.66 | 0.66 | 0.79 | 0.68 | 102.6 |
4 | 1.68 | 1.68 | 2.10 | 1.98 | 118.0 |
8 | 2.61 | 2.61 | 3.10 | 2.99 | 114.3 |
10 | 3.53 | 3.53 | 4.31 | 4.19 | 118.7 |
* Value too high, attributed to either an impurity in the test flask or in the flask for preparation of the eluate.
TOC values determined within 2nd Main Test
Nominal Concentrations / Loading Rates (mg/L) |
Mean Values of measured values t0h, (mg/L TOC) | Mean Values t0h, measured Values, net - Blank (mg/L TOC) | Mean Values of measured values t48h, (mg/L TOC) | Mean Values t48h, measured Values, net - Blank (mg/L TOC) | % Recovery (Mean Value) |
Blank | 0.8 | 0 | 0.61 | 0 | - |
0.5 | 0.06 | -0.73 | 0.08 | -0.53 | - |
1 | 0.53 | -0.26 | 0.56 | -0.05 | - |
2 | 0.27 | -0.52 | 1.20 | 0.59 | - |
4 | 2.36 | 1.57 | 1.67 | 1.06 | 67.3 |
8 | 2.63 | 1.83 | 2.04 | 1.43 | 78.1 |
According to the study report, regarding the very low measured TOC values, recovery rates should not be given for this test. From the measured TOC-value at the nominal concentration of 8mg/L and the known carbon content (73.13%) including the % purity of the test substance (91.5%) and the chemical formula of the test substance (C14H26O), a maximum water solubility of the test substance of 2.50 mg/L was calculated.
The water solubility value of 2.5 mg/L, estimated in the study report, is higher than the subsequently determined water solubility of 0.67 mg/L (Foster and Thomas, 2015). Some aldehydes are susceptible to autoxidation to the corresponding carboxylic acid. Therefore, the higher measured concentrations observed in the daphnia study test solutions may reflect some degradation of the parent aldehyde during the 24 hour equilibration period. Given, that this would reflect the stability of the test substance in real-world conditions, the test is considered reliable with restrictions and suitable for assessing the hazard of the registered substance. Given that the TOC method of analysis has a low sensitivity (approximately 1 mg/l), accurate measured concentrations of the test item were not possible, particularly for the test solutions prepared at the lower nominal concentration loading rates. Furthermore, in main test 2, the blank solutions had measured TOC values that were higher than those obtained for the lower nominal concentrations (see results for 0.5, 1 and 2 mg/L above) confounding the issue. Therefore it was considered appropriate to based the effect results on the nominal concentrations (loading rates). This was supported by the fact that in main test 2, the TOC analysis demonstrated that the organic matter of the test substance remained constant.
Description of key information
Effective Loading EL50 value of 0.9 mg/L.
Key value for chemical safety assessment
Fresh water invertebrates
Fresh water invertebrates
- Effect concentration:
- 0.9 mg/L
Additional information
The acute toxicity towards daphnia was studied under static conditions for 48 hours (Lebertz, 2001). The test was conducted using completely filled and stoppered vessels and the test vessels preconditioned using solutions of the test substance to minimise, respectively, losses due to volatility and adsorption. Total Organic Carbon (TOC) analysis performed at 0 and 48 hours in one of the main tests showed that the organic matter of the test substance remained constant in the aqueous phase.
As the test substance is poorly soluble, the test substance was tested using aqueous extracts of suspensions of the test substance prepared in dilution water from loading rates of 0.25, 0.5, 1, 2, 4 and 8 mg/L loading rates (final test). The suspensions were shaken for 24 hours at room temperature and then filtered through filtered paper which was previously rinsed through with ultrapure water in order to eliminate possible soluble impurities from the filter material. The filtered extracts were used directly for the test without any further dilution steps.
TOC analysis showed that the maximum concentration achieved was approximately 2.5 mg/L. This is higher than the subsequently determined water solubility of 0.67 mg/L (Foster and Thomas, 2015). Some aldehydes are susceptible to autoxidation to the corresponding carboxylic acid. Therefore, the higher measured concentration observed may reflect some degradation of the parent aldehyde during the 24 hour equilibration period. Given, that this would reflect the stability of the test substance in real-world conditions, the test is considered reliable with restrictions and suitable for assessing the hazard of the registered substance.
Given that the TOC method of analysis has a low sensitivity (approximately 1 mg/l), accurate measured concentrations of the test item were not possible particularly for the solutions prepared at the lower nominal concentration loading rates. Given also that TOC analysis for the higher test concentrations demonstrated that the organic matter of the test substance remained constant, it was considered justifiable to base the effects on the loading rates.Information on Registered Substances comes from registration dossiers which have been assigned a registration number. The assignment of a registration number does however not guarantee that the information in the dossier is correct or that the dossier is compliant with Regulation (EC) No 1907/2006 (the REACH Regulation). This information has not been reviewed or verified by the Agency or any other authority. The content is subject to change without prior notice.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.