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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: - | CAS number: -
- 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:
- read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- weight of evidence
- Reason / purpose for cross-reference:
- assessment report
- Reason / purpose for cross-reference:
- read-across source
- Duration:
- 24 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 100 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- other: a solution containing 100 mg/L test item in dilution water
- Basis for effect:
- mobility
- Key result
- Duration:
- 48 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 100 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- other: a solution containing 100 mg/L test item in dilution water
- Basis for effect:
- mobility
- Duration:
- 24 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 100 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- other: a solution containing 100 mg/L test item in dilution water
- Basis for effect:
- mobility
- Duration:
- 48 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 100 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- other: a solution containing 100 mg/L test item in dilution water
- Basis for effect:
- mobility
- Results with reference substance (positive control):
- The 24h- EC50 of potassium dichromate was tested in a current reference test. The value was determined as 1.7 mg/L, lying within the demanded range of 0.6 - 1.7 mg/L.
- Validity criteria fulfilled:
- yes
- Conclusions:
- The following results were determined for the test item:
24 h-NOEC = 100 mg/L
48 h-NOEC = 100 mg/L
24 h-EC50 > 100 mg/L
48 h-EC50 > 100 mg/L - Executive summary:
The study was performed as a limit test at 100 mg/L following OECD Guideline 202 and GLP. Twenty daphnia were exposed to the test item for 48 hours in a static test system. After 24 and 48 hours, the immobilised daphnia were counted. The treatment showed no significant immobilisation. 5 % of the daphnia were immobilised in the control, 10 % were immobilised in the treatment. The 24h- EC50 of potassium dichromate was tested in a current reference test. The value was determined as 1.7 mg/L, lying within the demanded range of 0.6 - 1.7 mg/L. At the start and at the end of the experiment, the content of the test item in the test solution was determined using titration. The recovery after 48 hours was 95 % of the start concentration, the correlation between nominal and measured concentration was 116 % at the start and 111 % at the end. Therefore, the determination of the biological results was based on the nominal concentration. The following results were determined for the test item:
24 h-NOEC = 100 mg/L
48 h-NOEC = 100 mg/L
24 h-EC50 > 100 mg/L
48 h-EC50 > 100 mg/L
The source substance contains the major organic moieties of the target substance. Therefore, this study shows that no acute toxicity to invertebrates can be attributed to the organic moieties of the target substance.
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- weight of evidence
- Reason / purpose for cross-reference:
- assessment report
- Reason / purpose for cross-reference:
- read-across source
- Duration:
- 24 h
- Dose descriptor:
- EC50
- Effect conc.:
- 9 500 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Key result
- Duration:
- 48 h
- Dose descriptor:
- EC50
- Effect conc.:
- 4 400 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Duration:
- 48 h
- Dose descriptor:
- EC100
- Effect conc.:
- > 10 000 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Duration:
- 48 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 2 500 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Details on results:
- - Behavioural abnormalities: The surviving animals in 5 and 10 g/L are very weak by the end of the test, while the vitality of the animals in all other concentrations (up to 2.5 g/L) resemble the control animals.
See also table 1. - Results with reference substance (positive control):
- no reference substance used in the study
- Reported statistics and error estimates:
- none
- Validity criteria fulfilled:
- yes
- Conclusions:
- The test item is not acute toxic for daphnia.
- Executive summary:
The test item was tested in a study according to OECD Guideline 202 and GLP. The following EC50 values were obtained:
EC50(24h) = 9500 mg/L
EC50(48h) = 4400 mg/L
The surviving animals in 5 and 10 g/L are very weak by the end of the test, while the vitality of the animals in all other concentrations(up to 2.5 g/L) resemble to the control animals.
The source substance contains the major organic moieties of the target substance. Therefore, this study shows that no acute toxicity to invertebrates can be attributed to the organic moieties of the target substance.
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- weight of evidence
- Reason / purpose for cross-reference:
- read-across source
- Reason / purpose for cross-reference:
- assessment report
- Duration:
- 48 h
- Dose descriptor:
- EC50
- Remarks:
- soft water, clone C
- Effect conc.:
- 1.57 mg/L
- Nominal / measured:
- meas. (initial)
- Conc. based on:
- element (total fraction)
- Basis for effect:
- mobility
- Duration:
- 48 h
- Dose descriptor:
- EC50
- Remarks:
- soft water, clone A
- Effect conc.:
- 0.79 mg/L
- Nominal / measured:
- meas. (initial)
- Conc. based on:
- element (total fraction)
- Basis for effect:
- mobility
- Duration:
- 48 h
- Dose descriptor:
- EC50
- Remarks:
- moderate-hard water, clone C
- Effect conc.:
- 6.06 mg/L
- Nominal / measured:
- meas. (initial)
- Conc. based on:
- element (total fraction)
- Basis for effect:
- mobility
- Duration:
- 48 h
- Dose descriptor:
- EC50
- Remarks:
- moderate-hard water, clone A
- Effect conc.:
- 2.77 mg/L
- Nominal / measured:
- meas. (initial)
- Conc. based on:
- element (total fraction)
- Basis for effect:
- mobility
- Duration:
- 48 h
- Dose descriptor:
- EC50
- Remarks:
- hard water, clone C
- Effect conc.:
- 5.83 mg/L
- Nominal / measured:
- meas. (initial)
- Conc. based on:
- element (total fraction)
- Basis for effect:
- mobility
- Duration:
- 48 h
- Dose descriptor:
- EC50
- Remarks:
- hard water, clone A
- Effect conc.:
- 3.64 mg/L
- Nominal / measured:
- meas. (initial)
- Conc. based on:
- element (total fraction)
- Basis for effect:
- mobility
- Conclusions:
- In general, D. magna clones were more sensitive to zinc in soft water relative to hard water. In addition, a significant genetic variability concerning zinc toxicity was shown. The least sensitive clone had the following EC50 (48 h) values: 259 µg/L (soft water), 1060 µg/L (moderate-hard water), 962 µg/L (hard water). The most sensitive clone had the following EC50 (48 h) values: 131 µg/L (soft water), 457 µg/L (moderate-hard water), 601 µg/L (hard water). This result is also relevant for the target substance, which contains 16.5 % zinc ions.
- Executive summary:
D. magna clones were exposed to single-metal solutions of varying concentration at two or three levels of water hardness (soft, moderate–hard and hard) for periods ranging from 12–96 h (12 h increments). EC50 values for each metal-, genotype-, water hardness-, exposure period-combination were determined for (i) total metal concentration and (ii) the free hydrated metal ion concentration (predicted using geochemical speciation modeling) and compared using analysis of covariance with environment (water hardness) and genotype (clone) as fixed factors and exposure time as a covariate. Substantial genetic variability occurred in both essential (Zn, Cu) and non essential (Cd, U) metals.
Concerning Zinc, the least sensitive clone had the following EC50 (48 h) values: 259 µg/L (soft water), 1060 µg/L (moderate-hard water), 962 µg/L (hard water). The most sensitive clone had the following EC50 (48 h) values: 131 µg/L (soft water), 457 µg/L (moderate-hard water), 601 µg/L (hard water). This result is also relevant for the target substance, which contains 16.5 % zinc ions. To account for the Zn content of 16.5 %, these values were converted to the target substance.
As a result, the least sensitive clone had the following EC50 (48 h) values: 1.57 mg/L (soft water), 6.06 mg/L (moderate-hard water), 5.83 mg/L (hard water). The most sensitive clone had the following EC50 (48 h) values: 0.79 mg/L (soft water), 2.77 mg/L (moderate-hard water), 3.64 mg/L (hard water).
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- weight of evidence
- Reason / purpose for cross-reference:
- read-across source
- Reason / purpose for cross-reference:
- assessment report
- Duration:
- 48 h
- Dose descriptor:
- EC50
- Remarks:
- pH 8, DOC 7.49 mg/L, Ca 52.7 mg/L
- Effect conc.:
- 19.94 mg/L
- Nominal / measured:
- meas. (initial)
- Conc. based on:
- element (dissolved fraction)
- Basis for effect:
- mobility
- Duration:
- 48 h
- Dose descriptor:
- EC50
- Remarks:
- pH 7.3, DOC 2.53 mg/L, Ca 5 mg/L
- Effect conc.:
- 2.15 mg/L
- Nominal / measured:
- meas. (initial)
- Conc. based on:
- element (dissolved fraction)
- Basis for effect:
- mobility
- Conclusions:
- Both inorganic and organic Zn complexation reduces Zn2+ activity and thus also reduce toxicity. Inorganic complexation (i. e. ZnCO3) is relatively straightforward, while dissolved organic matter (DOM) vary much in their zinc-binding characteristics. Therefore, for unknown samples, it is suggested to assume that the DOM consists of a fixed fraction of chemically active fulvic acid, i.e., 61 %, which is the mean of optimal %AFA of the five abovementioned samples with which Zn titration studies were performed. This result is also relevant for the target substance, which contains 16.5 % zinc ions.
- Executive summary:
Zinc toxicity to Daphnia magna was evaluated in a series of experiments with spiked natural surface waters. The eight selected freshwater samples had varying levels of bioavailability modifying parameters: pH (5.7–8.4), dissolved organic carbon (DOC, 2.48–22.9 mg/L), Ca (1.5–80 mg/L), Mg (0.79–18 mg/L), and Na (3.8–120 mg/L). In those waters, acute zinc toxicity (expressed as 50% effective concentrations [EC50]) varied up to 9-fold for the D. magna (48-h EC50 from 354 to 3290 µg Zn/L). Both inorganic and organic Zn complexation reduces Zn2+ activity and thus also reduce toxicity. Inorganic complexation (i. e. ZnCO3) is relatively straightforward, while dissolved organic matter (DOM) vary much in their zinc-binding characteristics. Therefore, for unknown samples, it is suggested to assume that the DOM consists of a fixed fraction of chemically active fulvic acid, i.e., 61%, which is the mean of optimal %AFA of the five abovementioned samples with which Zn titration studies were performed. This result is also relevant for the target substance, which contains 16.5 % zinc ions. Accounting to the Zn content of 16.5 %, this corresponds to EC 50 values between 2.15 and 19.94 mg/L for the target substance.
Referenceopen allclose all
Main Study
Immobilities
In the control, none of the daphnia died or showed any signs of abnormal behaviour throughout the test (see table below).
Table a: Immobilities
Nominal Concentration in mg/L |
Immobility 24 hours |
Immobility 48 hours |
||||||||
abs. |
in % |
abs. |
in % |
|||||||
0 |
0 |
0 |
0 |
1 |
5 |
0 |
0 |
0 |
1 |
5 |
100 |
0 |
1 |
0 |
0 |
5 |
0 |
1 |
1 |
0 |
10 |
pH and O2, Temperature
The pH values in the test media and the control ranged from 7.5 to 7.7. The concentration of dissolved oxygen stayed above 8.1 mg/L throughout the test. Temperature range was 23.0 – 24.8oC. The details are given in the following tables:
Table :b pH and O2-values
Nominal Concentration in mg/L |
pH |
O2-Concentration in mg/L |
||
0 h |
48 h |
0 h |
48 h |
|
0 |
7.6 |
7.6 |
8.6 |
8.1 |
100 |
7.5 |
7.7 |
8.4 |
8.2 |
Table c: Temperature
Temperature inoC |
||
0 h |
24 h |
48 h |
23.0 |
23.4 |
24.8 |
table 1: Immobilisation rate, skinnings an no. of animals which are trapped at the surface after 48 h
Control | 625 [mg/L] | 1250 [mg/L] | 2500 [mg/L] | 5000 [mg/L] | 10000 [mg/L] | |
Immobilisation [%], 24 h | 0 | 0 | 0 | 0 | 0 | 60 |
Immobilisation [%], 48 h | 0 | 0 | 0 | 0 | 85 | 90 |
Skinnings [%], 48 h | 100 | 100 | 100 | 100 | 75 | 50 |
animals trapped at thesurface [%], 48 h | 0 | 0 | 0 | 0 | 5 | 0 |
The target substance contains 16.5 % Zn ions. Therefore, the hazard value for Zn ion is converted to the target substance considering a Zn content of 16.5 % as worst-case value.
EC50 (Zn ion) = 0.259 mg/L
EC50 (target substance) = 0.259/0.165 = 1.57 mg/L
EC50 (Zn ion) = 0.131 mg/L
EC50 (target substance) = 0.131/0.165 = 0.79 mg/L
EC50 (Zn ion) = 1.06 mg/L
EC 50 (target substance) = 1.06/0.165 = 6.06 mg/L
EC50 (Zn ion) = 0.457 mg/L
EC 50 (target substance) = 0.457/0.165 = 2.77 mg/L
EC50 (Zn ion) = 0.962 mg/L
EC 50 (target substance) = 0.962/0.165 = 5.83 mg/L
EC50 (Zn ion) = 0.601 mg/L
EC50 (target substance) = 0.601/0.165 = 3.64 mg/L
The target substance contains 16.5 % Zn ions. Therefore, the hazard value for Zn ion is converted to the target substance considering a Zn content of 16.5 % as worst-case value.
EC50 (Zn ion) = 3.29 mg/L
EC 50 (target substance) = 3.29/0.165 = 19.94 mg/L
EC50 (Zn ion) = 0.354 mg/L
EC 50 (target substance) = 0.354/0.165 = 2.15 mg/L
Description of key information
Read-Across: WoE, FF6, OECD 202, GLP, D. magna, 48 h, EC50 = 4400 mg/L
Read-Across: WoE, Blancolen, OECD 202, GLP, D. magna, 48 h, EC50 = > 100 mg/L, NOEC = 100 mg/L
Read-Across: WoE, Zn ion, D. magna, 48 h, EC50 = 0.79 mg/L (converted to the target substance taking into account the Zn content of 16.5 % at the most)
Read-Across: WoE, Zn ion, D. magna, 48 h, EC50 = 2.15 mg/L (converted to the target substance taking into account the Zn content of 16.5 % at the most)
Key value for chemical safety assessment
Fresh water invertebrates
Fresh water invertebrates
- Effect concentration:
- 0.79 mg/L
Additional information
Read-across - FF6
The test item was tested in a study according to OECD Guideline 202 and GLP. The following EC50 values were obtained:
EC50(24h) = 9500 mg/L
EC50(48h) = 4400 mg/L
The surviving animals in 5 and 10 g/L are very weak by the end of the test, while the vitality of the animals in all other concentrations (up to 2.5 g/L) resemble to the control animals.
The source substance contains the major organic moieties of the target substance. Therefore, this study shows that no acute toxicity to invertebrates can be attributed to the organic moieties of the target substance.
Read-across - Blancolen
The study was performed as a limit test at 100 mg/L following OECD Guideline 202 and GLP. Twenty daphnia were exposed to the test item for 48 hours in a static test system. After 24 and 48 hours, the immobilised daphnia were counted. The treatment showed no significant immobilisation. 5 % of the daphnia were immobilised in the control, 10 % were immobilised in the treatment. The 24h-EC50 of potassium dichromate was tested in a current reference test. The value was determined as 1.7 mg/L, lying within the demanded range of 0.6 - 1.7 mg/L. At the start and at the end of the experiment, the content of the test item in the test solution was determined using titration. The recovery after 48 hours was 95 % of the start concentration, the correlation between nominal and measured concentration was 116 % at the start and 111 % at the end. Therefore, the determination of the biological results was based on the nominal concentration. The following results were determined for the test item:
24 h-NOEC = 100 mg/L
48 h-NOEC = 100 mg/L
24 h-EC50 > 100 mg/L
48 h-EC50 > 100 mg/L
The source substance contains the major organic moieties of the target substance. Therefore, this study shows that no acute toxicity to invertebrates can be attributed to the organic moieties of the target substance.
Read-across - Zn ion
Barata 1998
D. magna clones were exposed to single-metal solutions of varying concentration at two or three levels of water hardness (soft, moderate–hard and hard) for periods ranging from 12–96 h (12 h increments). EC50 values for each metal-, genotype-, water hardness-, exposure period-combination were determined for (i) total metal concentration and (ii) the free hydrated metal ion concentration (predicted using geochemical speciation modeling) and compared using analysis of covariance with environment (water hardness) and genotype (clone) as fixed factors and exposure time as a covariate. Substantial genetic variability occurred in both essential (Zn, Cu) and non essential (Cd, U) metals.
Concerning Zinc, the least sensitive clone had the following EC50 (48 h) values: 259 µg/L (soft water), 1060 µg/L (moderate-hard water), 962 µg/L (hard water). The most sensitive clone had the following EC50 (48 h) values: 131 µg/L (soft water), 457 µg/L (moderate-hard water), 601 µg/L (hard water). This result is also relevant for the target substance, which contains 16.5 % zinc ions. To account for the Zn content of 16.5 %, these values were converted to the target substance.
As a result, the least sensitive clone had the following EC50 (48 h) values: 1.57mg/L (soft water), 6.06 mg/L (moderate-hard water), 5.83 mg/L (hard water). The most sensitive clone had the following EC50 (48 h) values: 0.79 mg/L (soft water), 2.77 mg/L (moderate-hard water), 3.64 mg/L (hard water).
De Schamphelaere 2005
Zinc toxicity to Daphnia magna was evaluated in a series of experiments with spiked natural surface waters. The eight selected freshwater samples had varying levels of bioavailability modifying parameters: pH (5.7–8.4), dissolved organic carbon (DOC, 2.48–22.9 mg/L), Ca (1.5–80 mg/L), Mg (0.79–18 mg/L), and Na (3.8–120 mg/L). In those waters, acute zinc toxicity (expressed as 50% effective concentrations [EC50]) varied up to 9-fold for the D. magna (48-h EC50 from 354 to 3290 mg Zn/L). Both inorganic and organic Zn complexation reduces Zn2+ activity and thus also reduce toxicity. Inorganic complexation (i. e. ZnCO3) is relatively straightforward, while dissolved organic matter (DOM) vary much in their zinc-binding characteristics. Therefore, for unknown samples, it is suggested to assume that the DOM consists of a fixed fraction of chemically active fulvic acid, i.e., 61%, which is the mean of optimal %AFA of the five abovementioned samples with which Zn titration studies were performed. This result is also relevant for the target substance, which contains 16.5 % zinc ions. Accounting to the Zn content of 16.5 %, this corresponds to EC50 values between 2.15 and 19.94 mg/L for the target substance.
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.