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Diss Factsheets
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EC number: 215-542-5 | CAS number: 1330-61-6
- 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
Acute Toxicity: oral
Administrative data
- Endpoint:
- acute toxicity: oral
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- study well documented, meets generally accepted scientific principles, acceptable for assessment
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 971
- Report date:
- 1971
Materials and methods
Test guideline
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- Animals were treated with a single dose and observed during 14 days.
- GLP compliance:
- no
- Test type:
- standard acute method
- Limit test:
- no
Test material
- Reference substance name:
- Isodecyl acrylate
- EC Number:
- 215-542-5
- EC Name:
- Isodecyl acrylate
- Cas Number:
- 1330-61-6
- Molecular formula:
- C13H24O2
- IUPAC Name:
- 2-methyloctyl prop-2-enoate
- Test material form:
- other: liquid
Constituent 1
Test animals
- Species:
- rat
- Strain:
- Wistar
- Sex:
- male
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: Mellon Institute
- Age at study initiation: 3 - 4 weeks
- Weight at study initiation: 90 - 120 g
- Diet (e.g. ad libitum): Rockland diets
- Water (e.g. ad libitum): ad libitum
Administration / exposure
- Route of administration:
- oral: gavage
- Vehicle:
- unchanged (no vehicle)
- Details on oral exposure:
- undiluted substance
- Doses:
- 20, 10 and 5 ml/kg
- No. of animals per sex per dose:
- 5
- Control animals:
- no
- Details on study design:
- no
- Statistics:
- no
Results and discussion
Effect levels
- Sex:
- male
- Dose descriptor:
- LD50
- Effect level:
- 9 486 mg/kg bw
- Remarks on result:
- other: original data: 10.7 ml/kg
- Remarks:
- LD50 (mg/kg) = LD50 (ml/kg) x density x 1000 = 10.7 x 0.8866 x 1000 = 9486 mg/kg
- Mortality:
- 20.0 ml/kg: 5/5 animals died on day 0, 1 ,1 ,3 and 5
10.0 ml/kg: 2/5 animals died on day 2 and 3
5.0 ml/kg: 0/5; all animals survived - Clinical signs:
- other: Prostrate and heavy breathing within one hour; sluggish at 24 hours, slightly sluggish 5 min after dose.
- Gross pathology:
- Congestion throught thee lungs and the abdominal viscera in the victims; livers mottled.
- Other findings:
- no
Any other information on results incl. tables
Dosage; ml/kg |
Dead / Dosed |
Days to Death |
Weight Change |
Signs and/or Sympthoms |
20.0 |
5/5 |
0,1,1,3,5 |
- |
Prostrate and heavy breathing within one hour; sluggish at 24 hours, slightly sluggish 5 min after dose. |
10.0 |
2/5 |
2,3 |
67 to 73 |
|
5.0 |
0/5 |
- |
68 to 91 |
Applicant's summary and conclusion
- Interpretation of results:
- GHS criteria not met
- Conclusions:
- Based on the results on this acute study, an oral LD50 of 9486 mg/kg was calculated in rats.
- Executive summary:
In this study, rats were treated orally with isodecyl acrylate a single dose of 5, 10 or 20 ml/kg.
This study was conducted as a range-finding test according to the method described by Smyth HF Jr. and Carpenter CP (1948).
All animals treated with 20 ml/kg died in the 5 days after administration. Two animals died at the dose of 10 ml/kg on day 2 and 3.A LD50 value of approx. 9486 mg/kg bw (10,7 ml/kg) was determined.
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