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EC number: 299-966-6 | CAS number: 93918-85-5
- 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
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Guideline study, non-GLP, no measurement of test substance concentration
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 002
- Report date:
- 2002
Materials and methods
Test guidelineopen allclose all
- 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:
- no
Test material
- Reference substance name:
- Laurylmercaptobutyronitrile
- IUPAC Name:
- Laurylmercaptobutyronitrile
- Details on test material:
- - Name of test material (as cited in study report): Laurylmercaptobutyronitril.
- Substance type: Mono-constituent
- Physical state: Liquid
- Analytical purity: 99%
- Storage condition of test material: Room temperature at about 20 °C, in the dark away from direct sunlight
Constituent 1
Sampling and analysis
- Analytical monitoring:
- no
Test solutions
- Vehicle:
- no
- Details on test solutions:
- - Method: A supersaturated dispersion of the test substance at a nominal loading rate of 100 mg/L was prepared by weighing 49 mg of substance in to 500 mL medium. The dispersion was ultrasonicated for 15 minutes followed by 48 hours of intense stirring at room temperature in the dark. The supersaturated dispersion was then filtered under reduced pressure through a 0.45 µm membrane. The filtrate was used directly.
- Evidence of undissolved material (e.g. precipitate, surface film, etc): Solution remained clear and colorless throughout test.
Test organisms
- Test organisms (species):
- Daphnia magna
- Details on test organisms:
- TEST ORGANISM
- Common name: water flea
- Strain: Strauss
- Source: Internal stock, strain originally supplied by University of Sheffield/UK
- Age at study initiation: 6-24 hours, not first brood progeny
- Feeding during test: no
ACCLIMATION
- Acclimation period: Organisms raised in same conditions as test, no acclimation period
Study design
- Test type:
- static
- Water media type:
- freshwater
- Limit test:
- yes
- Total exposure duration:
- 48 h
Test conditions
- Hardness:
- 250 mg CaCO3/L
- Test temperature:
- 20 - 21 °C
- pH:
- 7.7 - 7.9
- Dissolved oxygen:
- 8.3 - 8.5 mg/L
- Nominal and measured concentrations:
- Nominal loading rate: 100 mg/L
- Details on test conditions:
- TEST SYSTEM
- Test vessel: 100 mL glass beakers filled with 50 mL test medium
- Type: Open
- Aeration: no. Test medium aerated to oxygen saturation prior to test.
- No. of organisms per vessel: Ten
- No. of vessels per concentration (replicates): Two
- No. of vessels per control (replicates): Two
TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: Reconstituted test water. Purified water containing the following analytical grade salts:
CaCl2∙2H2O: 294 mg/L
MgSO4∙7H2O: 123 mg/L
NaHCO3: 65 mg/L
KCl: 5.8 mg/L
- Alkalinity:0.8 mM
- Ca/mg ratio: 4:1
- Culture medium different from test medium: No
OTHER TEST CONDITIONS
- Photoperiod: 16h light: 8h darkness, 30 minute transition periods
- Light intensity: 200 - 1200 lux
EFFECT PARAMETERS MEASURED (with observation intervals if applicable) :
Immoblization and other signs of intoxication at 24 and 48 hours.
TEST CONCENTRATIONS
- Spacing factor for test concentrations: None
- Justification for using less concentrations than requested by guideline: Limit test
- Range finding study: Yes. No toxicity found at any dose tested
- Results used to determine the conditions for the definitive study: Yes, limit test based on lack of toxicity. - Reference substance (positive control):
- yes
- Remarks:
- Potassium dichromate tested annually
Results and discussion
Effect concentrations
- Duration:
- 48 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 100 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- other: Water soluble fraction
- Basis for effect:
- mobility
- Remarks on result:
- other: No immobilization or other toxic effects observed.
- Details on results:
- - Behavioural abnormalities: none
- Other biological observations: none
- Mortality of control: none
- Other adverse effects control: none
- Effect concentrations exceeding solubility of substance in test medium: yes
- other: No immobilization or other mortality observed in control or exposed organisms after 48 hours. - Results with reference substance (positive control):
- Results not available
Applicant's summary and conclusion
- Validity criteria fulfilled:
- yes
- Conclusions:
- The 48-hr EC50 of laurylmercaptobutyronitrile to Daphnia magna was >100 mg/L (nominal loading rate). No toxicity was observed from a water soluble fraction prepared at 100 mg/L
- Executive summary:
Toxicity of laurylmercaptobutyronitrile to D. magna was assessed in a limit test conducted according to OECD 202. The test substance was not fully soluble at the limit of 100 mg/L, so a water-soluble fraction was made. Test substance (100 mg/L) was sonicated in reconstituted test water for 15 minutes, stirred for 48 hours, and filtered to 0.45 µm under reduced pressure. No immobilization or sublethal effects were observed in controls or test solutions. Test substance concentrations were not analytically determined. The 48-hour EC50 of laurylmercaptobutyronitrile is >100 mg/L.
The test was conducted according to an internationally accepted guideline but was not GLP compliant. Test substance concentrations were not analytically confirmed. This test is considered reliable with restrictions. It is suitable for Risk Assessment, Classification & Labeling, and PBT Analysis.
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.
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