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EC number: 247-979-2 | CAS number: 26761-45-5
- 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
Skin irritation / corrosion
Administrative data
- Endpoint:
- skin irritation: in vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: The study was conducted according to an O.E.C.D. Testing Guideline under the GLP regulations.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 998
- Report date:
- 1998
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
- Deviations:
- no
- GLP compliance:
- yes
Test material
- Reference substance name:
- 2,3-epoxypropyl neodecanoate
- EC Number:
- 247-979-2
- EC Name:
- 2,3-epoxypropyl neodecanoate
- Cas Number:
- 26761-45-5
- Molecular formula:
- C13H24O3
- IUPAC Name:
- (oxiran-2-yl)methyl 2,2-dimethyloctanoate
- Test material form:
- other: Liquid at room temperature.
- Details on test material:
- As per IUCLID5 Sections 1.1, 1.2. and 1.4.
Constituent 1
- Specific details on test material used for the study:
- See IUCLID Section 1.2 and 1.4
Test animals
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or test system and environmental conditions:
- New Zealand White rabbits of the Crl:NZW/Kbl.BR strain were obtained from Charles River UK Ltd, Margate. The animals were examined and weighed on the day of arrival. The rabbits were in a body weight range of 2.45 to 2.69 kg on the day prior to dosing. The rabbits were approximately eleven to fourteen weeks old on Day 1 of the study. Rabbits were housed in floor-pens, each accommodating one animal throughout the acclimatisation and experimental phases of the study. Each pen had a minimum floor area of 0.6 sq m. Wood chips were provided as floor litter. Each batch of wood chips was analysed for specific contaminants.
SQC TRB Rabbit Diet 9603 (pelleted) from Harlan Teklad, Bicester was freely available to the animals at all times. Each batch of diet had been analysed for specific constituents. Mains water was provided, ad libitum, via water bottles attached to the pen walls, The water had been periodically analysed for specific contaminants. No contaminants were present in diet, bedding or water at levels which might interfere with achieving the objective of the study.
The holding room was designed to permit at least 10 air changes per hour and to maintain environmental conditions of 16 to 22°C. Humidity was not actively controlled but was expected to remain within the range 40-80% Relative Humidity. Recordings of maximum and minimum temperature and humidity were made twice daily and any minor deviations from the expected ranges were noted in the study data. The room was illuminated by fluorescent strip-lights for twelve hours daily.
The condition of the animals was assessed daily throughout an acclimatisation period of at least one week. A clinical inspection was performed prior to study commencement to ensure the animals were suitable for the test procedures. Healthy animals, weighing not more than 4.0 kg, were arbitrarilyallocated to the study on the day prior to commencement of treatment.
Test system
- Type of coverage:
- semiocclusive
- Preparation of test site:
- shaved
- Vehicle:
- unchanged (no vehicle)
- Controls:
- no
- Amount / concentration applied:
- 0.5 mL of undiluted test substance.
- Duration of treatment / exposure:
- 4 hours
- Observation period:
- 15 days
- Number of animals:
- 3
- Details on study design:
- The animals were prepared for treatment with test substance with electric clippers that were used to remove all hair from an area of the dorsum measuring not less than l0x8cm. The dermal test site, a 30 x 20 mm area on the clipped dorsum of the three New Zealand White rabbits was subject to application of 0.5 mL of undiluted 2,3-epoxypropyl neodecanoate. The applied dose was spread uniformly over the designated area and then covered by a dense gauze patch (30 x 20 mm). This in turn was covered by a larger gauze patch (40 x 40 mm) and an open weave, elasticated adhesive bandage “Steroban” from Steroplast Ltd, Bredbury which was wrapped firmly around the torso to secure the applied dose in the correct position. The dressing was considered to be semi-occlusive. The dressing was removed after four hours. The test site was lightly brushed clean of any solid residues and swabbed with moist cotton wool. The site location was marked on the dorsum with indelible ink after completion of the cleansing process. A detailed account of any clinical signs of ill health or systemic toxicity was maintained. The conditions of the dermal test sites were recorded immediately after removal of the patches and dressings. The condition of all dermal test sites was recorded one hour, 24, 48 and 72 hours after removal of the patch and dressing. Further observations were recorded on Day 8 and Day 15. Inflammatory skin reactions were graded from 0 - 4 for erythema, eschare and oedema.
Results and discussion
In vivo
Results
- Irritation parameter:
- primary dermal irritation index (PDII)
- Basis:
- mean
- Time point:
- other: 72 hours
- Score:
- 0.7
- Max. score:
- 0.7
- Reversibility:
- fully reversible within: 15 d
- Irritant / corrosive response data:
- The only evidence of skin irritation observed in the study was an erythema score of 1 for two animals at 72 hours and a score of 1 for one animal at the 24 hr observation time.
Any other information on results incl. tables
Tables showing the individual animal dermal reactions and Group mean dermal scores are attached below.
Applicant's summary and conclusion
- Interpretation of results:
- not irritating
- Remarks:
- Migrated information Criteria used for interpretation of results: EU
- Conclusions:
- Based on the dermal observations made during this study 2,3-epoxypropyl neodecanoate is not irritating to rabbit skin under the experimental conditions
- Executive summary:
Under the conditions of an O.E.C.D. 404 Testing Guideline study undiluted 2,3 -epoxypropyl neodecanoate was not irritating to rabbit skin following four hr of exposure.
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