Registration Dossier
Registration Dossier
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: 239-370-5 | CAS number: 15337-18-5
- 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:
- 06 September to ****
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 202 (Daphnia sp. Acute Immobilisation Test)
- Deviations:
- yes
- Remarks:
- see below
- Qualifier:
- according to guideline
- Guideline:
- EU Method C.2 (Acute Toxicity for Daphnia)
- Deviations:
- yes
- Remarks:
- see below
- Principles of method if other than guideline:
- The following deviations from study plan occurred:
- The study plan states that the test will be conducted at a temperature range of 18-22 °C, however, during the definitive test, temperatures of 23 °C were recorded. Given that no adverse effects were observed, this was considered not to have had an impact on the outcome or integrity of the test.
- The study plan states that 20 daphnids will be added to each test concentration (4 replicates of 5), however, during the definitive test, no daphnia were observed to be present in replicates 1 to 3 of the 50% v/v saturated solution test group at 24 or 48 hours. Although this was a deviation to the study plan, given that no toxicity was observed in the higher concentration of 100% v/v saturated solution, this was considered not to have had an impact on the outcome or integrity of the test. - GLP compliance:
- yes (incl. QA statement)
- Specific details on test material used for the study:
- CAS RN: 15337-18-5
Physical state/Appearance: Yellow viscous liquid
Purity: 96.6% - Analytical monitoring:
- yes
- Details on sampling:
- Samples were taken from the control and each test group from the bulk test preparation at 0 hours and from the pooled replicates at 48 hours for quantitative analysis. Duplicate samples were taken and stored frozen for further analysis if necessary.
Preparation of Test Samples
The test samples were thawed with the aid of sonication before being filtered through 0.45 µm cellulose acetate filters. - Vehicle:
- no
- Details on test solutions:
- A nominal amount of test item (550 mg) was dispersed in 11 liters of test water with the aid of propeller stirring at approximately 1500 rpm for 48 hours. After 48 hours the stirring was stopped and any undissolved test item was removed by filtration through a 0.2 µm Sartorius Sartopore filter (first approximate 2 liters discarded in order to pre-condition the filter) to give a 100% v/v saturated solution. A series of dilutions was made from this saturated solution to give further test concentrations of 6.25, 12.5, 25 and 50 % v/v saturated solution.
- Test organisms (species):
- Daphnia magna
- Details on test organisms:
- The test was carried out using first instar Daphnia Magna Straus taken from in-house laboratory cultures, maintained in Elendt M7 medium in a temperature controlled room at 18 to 22 °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. 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:
- other: Reconstituted water (ISO medium)
- Limit test:
- no
- Total exposure duration:
- 48 h
- Post exposure observation period:
- Immobilization and any adverse reactions to exposure were recorded after 24 and 48 hours.
- Hardness:
- 250 mg/L as CaCO3
- Test temperature:
- 22 ºC to 23 ºC
- pH:
- 7.9 to 8.1
- Dissolved oxygen:
- 8.4 to 8.7 mg O2/L
- Nominal and measured concentrations:
- Definitive test: 6.25, 12.5, 25, 50 and 100% v/v saturated solution.
- Details on test conditions:
- As in the range-finding test, 150 mL glass jars containing approximately 100 mL of test preparation were used. At the start of the test five 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 covered and maintained in a temperature controlled room maintaining the water temperature at 22 to 23 °C, with a photoperiod of 16 hours light (between 200 and 1200 Lux) and 8 hours darkness with 20 minute transition periods. The daphnids were not individually identified, received no food during exposure and the test vessels were not aerated.
The control group was concurrently maintained under identical conditions, but was not exposed to the test item.
The test solutions were not renewed during the exposure period. - Reference substance (positive control):
- yes
- Remarks:
- potassium dichromate
- Key result
- Duration:
- 48 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 100 other: % v/v saturated solution
- Nominal / measured:
- nominal
- Conc. based on:
- other: (geom. mean) as zinc (equivalent to 0.071 mg/L as test item)
- Basis for effect:
- mobility
- Key result
- Duration:
- 48 h
- Dose descriptor:
- NOEC
- Effect conc.:
- > 100 other: % v/v saturated solution
- Nominal / measured:
- nominal
- Conc. based on:
- other: (geom. mean) as zinc (equivalent to 0.071 mg/L as test item)
- Basis for effect:
- mobility
- Details on results:
- Measured test concentrations in the maximum tested saturation level at 0 and 48 hour during the definitive test were determined to be 0.0091 mg/L as zinc (equivalent to 0.085 mg/L as test item) and 0.0064 mg/L as zinc (equivalent to 0.059 mg/L as test item), respectively. The geometric mean measured test concentration was determined to be 0.0076 mg/L as zinc (equivalent to 0.071 mg/L as test item).
At the start and throughout the test all control and test solutions were observed to be clear colorless solutions.
No immobilization was observed in 20 daphnids exposed to test concentrations up to and including test concentrations of 100% v/v saturated solution for a period of 48 hours. No sub-lethal effects of exposure were observed throughout the test.
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 equal to or greater than 3 mg/L in the control and test vessels. - Results with reference substance (positive control):
- Exposure of Daphnia magna to the reference item, potassium dichromate, gave the following results:
24-hour EC50: 0.61 mg/L;
48-hour EC50: 0.54 mg/L;
No Observed Effect Concentration (NOEC): 0.32 mg/L
Lowest Observed Effect Concentration (LOEC): 0.56 mg/L
The results from the positive control with potassium dichromate were within the normal ranges for this reference item. - Validity criteria fulfilled:
- yes
- Conclusions:
- The acute toxicity of the test item, zinc bis (dipentyldithiocarbamate) (oil free), to the freshwater invertebrate Daphnia magna was investigated over a 48-hour period. The 48-hour EC50 was determined to be greater than 100% v/v saturated solution (>0.0076 mg/L as zinc; equivalent to >0.071 mg/L as test item). The No Observed Effect Concentration was 100% v/v saturated solution (0.0076 mg/L as zinc; equivalent to 0.071 mg/L as test item).
No toxic effects were observed at exposure concentrations up to and including the limit of saturation in the test medium. - Executive summary:
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", and Method C.2 of Commission Regulation (EC) No. 440/2008. A preliminary media preparation trial indicated that a saturated solution method of preparation was the most appropriate for this test item.
Following a preliminary range-finding test, twenty daphnids (4 replicates of 5 animals) were exposed to an aqueous solution of the test item at nominal concentrations of 6.25, 12.5, 25, 50 and 100% v/v saturated solution for 48 hours at a temperature of 22 ºC to 23 ºC under static test conditions. Immobilization and any adverse reactions to exposure were recorded after 24 and 48 hours. An initial test was conducted, however, an inconsistent immobilization pattern was observed hence the test was repeated.
Measured test concentrations in the maximum tested saturation level at 0 and 48 hour during the definitive test were determined to be 0.0091 mg/L as zinc (equivalent to 0.085 mg/L as test item) and 0.0064 mg/L as zinc (equivalent to 0.059 mg/L as test item), respectively. The geometric mean measured test concentration was determined to be 0.0076 mg/L as zinc (equivalent to 0.071 mg/L as test item).
Exposure of Daphnia magna to the test item gave EC50 values of greater than 100% v/v saturated solution (>0.0076 mg/L as zinc; equivalent to >0.071 mg/L as test item). This study showed that there were no toxic effects at exposure concentrations up to and including the limit of saturation in the test medium. The No Observed Effect Concentration was 100% v/v saturated solution (0.0076 mg/L as zinc; equivalent to 0.071 mg/L as test item).
Reference
Cumulative Immobilization Data and Observations in the Definitive Test
Nominal |
24 Hours |
|||||||||
Cumulative Immobilized Daphnia |
Observations |
|||||||||
R1 |
R2 |
R3 |
R4 |
Total |
% |
R1 |
R2 |
R3 |
R4 |
|
Control |
0 |
0 |
0 |
0 |
0 |
0 |
5 N |
5 N |
5 N |
5 N |
6.25 |
0 |
0 |
0 |
0 |
0 |
0 |
5 N |
5 N |
5 N |
5 N |
12.5 |
0 |
0 |
0 |
0 |
0 |
0 |
5 N |
5 N |
5 N |
5 N |
25 |
0 |
0 |
0 |
0 |
0 |
0 |
5 N |
5 N |
5 N |
5 N |
50 |
0 |
* |
* |
* |
0 |
0 |
5 N |
* |
* |
* |
100 |
0 |
0 |
0 |
0 |
0 |
0 |
5 N |
5 N |
5 N |
5 N |
Nominal |
48 Hours |
|||||||||
Cumulative Immobilized Daphnia |
Observations |
|||||||||
R1 |
R2 |
R3 |
R4 |
Total |
% |
R1 |
R2 |
R3 |
R4 |
|
Control |
0 |
0 |
0 |
0 |
0 |
0 |
5 N |
5 N |
5 N |
5 N |
6.25 |
0 |
0 |
0 |
0 |
0 |
0 |
5 N |
5 N |
5 N |
5 N |
12.5 |
0 |
0 |
0 |
0 |
0 |
0 |
5 N |
5 N |
5 N |
5 N |
25 |
0 |
0 |
0 |
0 |
0 |
0 |
5 N |
5 N |
5 N |
5 N |
50 |
0 |
* |
* |
* |
0 |
0 |
5 N |
* |
* |
* |
100 |
0 |
0 |
0 |
0 |
0 |
0 |
5 N |
5 N |
5 N |
5 N |
N = Normal
R1– R4= Replicates 1 to 4
*No daphnids observed, no impact as no effects observed at the higher concentration of 100% v/v saturated solution
Description of key information
The acute toxicity of the test item to the freshwater invertebrate Daphnia magna has been investigated and based on the geometric mean measured test concentrations gave a 48-Hour EC50 value of greater than 0.0076 mg/L as zinc (equivalent to 0.071 mg/L as test item). The No Observed Effect Concentration was 0.0076 mg/L as zinc (equivalent to 0.071 mg/L as test item) mg/L. This study showed that there were no toxic effects at saturation.
Key value for chemical safety assessment
Fresh water invertebrates
Fresh water invertebrates
- Effect concentration:
- 0.007 mg/L
Additional information
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.

EU Privacy Disclaimer
This website uses cookies to ensure you get the best experience on our websites.