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EC number: 680-602-3 | CAS number: 98133-47-2
- 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
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 11 Sept 2017 - 02 Feb 2018
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 018
- Report date:
- 2018
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 202 (Daphnia sp. Acute Immobilisation Test)
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
Test material
- Reference substance name:
- 3-(acetyloxy)-1-{[3-(acetyloxy)propyl]carbamoyl}-2,2-dimethylpropyl acetate
- Cas Number:
- 98133-47-2
- Molecular formula:
- C15H25NO7
- IUPAC Name:
- 3-(acetyloxy)-1-{[3-(acetyloxy)propyl]carbamoyl}-2,2-dimethylpropyl acetate
- Test material form:
- liquid: viscous
Constituent 1
- Specific details on test material used for the study:
- - Lot No.: 75518
- Purity: 95.7%
- Expiration date: September 19, 2018
Sampling and analysis
- Analytical monitoring:
- yes
- Details on sampling:
- Samples of stock solution and test solutions were taken to determine the actual test item concentrations in comparison to the nominally applied concentrations. Samples of test solutions were taken at the start (0 hour) and end (48 h) of exposure.
Test solutions
- Vehicle:
- no
- Details on test solutions:
- Based on the results of a preliminary non-GLP range finding test, a nominal limit concentration of 100mg/L was tested in the definitive test.
A stock solution was prepared at a nominal loading rate of 100 mg/L by adding 50 mg of the test item to 500 mL of the test medium. This stock solution (S1) was slowly stirred (500 rpm) for 10 minutes at ambient temperature in the dark. Thereafter this stock solution was left to settle for 20 minutes. The stock solution was visually examined for undissolved/particulate matter in the free water column. Visual inspection of the flask showed a clear solution without Tyndall effect.
The stock solution S1 was prepared once to prepare the test solutions. The volume of the stock solution was large enough to prepare the test concentrations and all analytical samples.
Test organisms
- Test organisms (species):
- Daphnia magna
- Details on test organisms:
- Species: Daphnia magna STRAUS (clone M10), cultured at ECT Oekotoxikologie GmbH since December 22, 2011.
Origin: The organisms were originally supplied by KU Leuven, Belgium.
Age of parental daphnids: less than 35 d
Age of exposed daphnids at the beginning of the test: less than 24 h
Study design
- Test type:
- static
- Water media type:
- freshwater
- Remarks:
- Elendt medium M4
- Limit test:
- yes
- Total exposure duration:
- 48 h
Test conditions
- Hardness:
- Water hardness: 254 mg/LCaCO3
- Test temperature:
- target: 18 to 22°C, constant within a range of 2°C
actual: 19.9 to 20.9°C - pH:
- 7.7 to 7.8
- Dissolved oxygen:
- 8.3 to 8.6 mg/L
- Nominal and measured concentrations:
- Nominal: 100 mg/L
Geometric Mean Measured: 96.1 mg/L - Details on test conditions:
- - Based on the results of a preliminary non-GLP range finding test, the following nominal limit concentration was tested in the definitive test: 100 mg/L.
- The test period (exposure of test organisms to the test solutions in a static system) was 48 hours.
- Additionally, daphnids were exposed under control conditions (non-treated test medium without solvent).
- Four replicates were used for the test item concentration and the control. Each replicate vessel contained five daphnids.
- Glass beakers (nominal 60 mL), covered with watch glasses, were used as test vessels. The test vessels were filled-up as far as operationally possible as a means of reducing the overall headspace.
- Volume of test solution per test vessel: 57-60 mL
- Test medium: medium M4 (OECD 2004)
- Adjustment of pH in the medium: none
- Application of test item: test item dissolved in Medium M4 applied once at the beginning of the test - Reference substance (positive control):
- yes
- Remarks:
- Potassium dichromate (K2Cr2O7)
Results and discussion
Effect concentrations
- Key result
- Duration:
- 48 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 100 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Details on results:
- Analytical Findings: The test item concentration was stable during the test period, with 93.5% of the initially measured concentration found in the aged solution.
Biological findings: In this limit test no immobilities were observed in control or in the limit concentration of 100 mg test item/L. It is therefore concluded that the EC50 of the test item is higher than the limit concentration tested (nominal: 100 mg test item/L). This corresponds to a geometric mean measured D-Panthenyltriacetate concentration of 96.1 mg/L - Results with reference substance (positive control):
- The most recent reference test with potassium dichromate performed in a separate study (Study No. IDA1705) resulted in an EC50(24 h) of 1.29 mg/L.
According to the OECD guideline No. 202 (OECD, April 2004) EC50(24 h)-values for potassium dichromate obtained from different laboratories should range between 0.6 mg/L and 2.1 mg/L.
The toxicity of the reference item is within this range. Therefore the results of this reference test are acceptable and the test conditions are reliable and the sensitivity of the test system could be demonstrated. - Reported statistics and error estimates:
- In this limit test no immobilities were observed in control or in the limit concentration of 100 mg test item/L. A statistical evaluation for differences between treatment and control was therefore not required and was not performed.
Any other information on results incl. tables
Validity of the test - All validity criteria were fulfilled as required by the test guideline:
Required | Found |
immobilised daphnids in the control: <=10% |
0% |
dissolved oxygen concentration in control and test vessels at the end of the test: => 3mg/L |
=> 8.3mg/L |
Signs of disease or stress, for example, discoloration or unusual behaviour such as trapping at surface of water, did not exceed 10 per cent of the daphnids in the controls.
Applicant's summary and conclusion
- Validity criteria fulfilled:
- yes
- Conclusions:
- In a study to determine the acute toxicity of D-Panthenyltriacetate to the water flea Daphnia magna, no immobilities were observed in a limit test performed at a concentration of 100 mg test item/L.
It is therefore concluded that the 48h EC50 of the test item is higher than the limit concentration tested (nominal: 100 mg test item/L). This corresponds to a geometric mean measured D-Panthenyltriacetate concentration of 96.1 mg/L
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