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EC number: 940-029-4 | CAS number: 1474044-86-4
- 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
Eye irritation
Administrative data
- Endpoint:
- eye 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 the O.E.C.D. test guideline 405 with GLP compliance.
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 405 (Acute Eye 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-ylmethyl 2-ethyl-2,5-dimethylhexanoate
- Reference substance name:
- Neodecanoic acid, oxiranylmethyl ester
- IUPAC Name:
- Neodecanoic acid, oxiranylmethyl ester
- Test material form:
- other: Colorless liquid at room temperature.
- Details on test material:
- As per IUCLID5 Sections 1.1. 1.2. 1.4. and 4.1. for 2,3-epoxypropyl neodecanoate, REACH Registration: 01-2119431597-33-0000.
Constituent 1
Constituent 2
Test animals / tissue source
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or tissues 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 eight to ten weeks old on study Day 1 and weighted approximately 1.8 - 2.6 kg. Rabbits were housed in floor-pens, each accommodating one animal throughout the acclimatisation and experimental phases of the study. Wood chips were provided as floor litter.
The animal holding room was designed to permit at least 10 air changes per hour and to maintain environmental conditions of 16 to 22°C and approximately 40-80% Relative Humidity. The room was illuminated by fluorescent strip-lights for twelve hours daily (typically 06:00 to 18:00 hours).
SQC TRB Rabbit Diet 9603 (pelleted) from Harlan Tekiad, 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.
Test system
- Vehicle:
- unchanged (no vehicle)
- Controls:
- no
- Amount / concentration applied:
- 0.1 ml
- Duration of treatment / exposure:
- 3 days
- Observation period (in vivo):
- 3 days
- Number of animals or in vitro replicates:
- 3
- Details on study design:
- One dose consisting of 0.1 mL of undiluted test substance, dispensed from a syringe, was instilled into the left conjunctival sac of the New Zealand White rabbits The lower eyelid was gently prised away from the eyeball to create a receptacle for the dose. After instillation the eyelids were held closed for a few seconds to prevent loss of the dose. The right eye remained untreated and served as a control to the treated eye. The day of dosing was designated as Day 1. The condition of the treated eyes were assessed for a period of at least three days to ensure the test substance did not cause ocular damage. Ocular changes were assessed and recorded immediately, half an hour, one and four hours after treatment on Day 1 and 24, 48 and 72 hours after dosing.
At examinations carried out 24 hours after treatment, 2% aqueous fluorescein solution was applied to the cornea and then washed out with water for irrigation. The comeal surface was then illuminated by an ultraviolet source and inspected for areas of absorption of the fluorescing dye that indicate epithelial disruption.
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- conjunctivae score
- Remarks:
- Redness
- Basis:
- mean
- Remarks:
- of 3 animals.
- Time point:
- other: one hr
- Score:
- ca. 0.7
- Max. score:
- 1
- Reversibility:
- fully reversible within: 24 hr
- Irritation parameter:
- conjunctivae score
- Remarks:
- Redness
- Basis:
- mean
- Remarks:
- of three animals.
- Time point:
- other: 4 hr
- Score:
- ca. 0.7
- Max. score:
- 1
- Reversibility:
- fully reversible within: 24 hr
- Irritation parameter:
- chemosis score
- Basis:
- mean
- Remarks:
- of three animals.
- Time point:
- other: 4 hr
- Score:
- ca. 0.3
- Max. score:
- 1
- Reversibility:
- fully reversible within: 24 hr
- Irritant / corrosive response data:
- Reactions in one rabbit eye were resricted to slight conjunctival reddening and production of an ocular discharge immediately after dosing but these reactions had resolved half an hour later. For the other two rabbits conjunctival redness persisted to the four hour post dosing assessment but had resolved by Day 2. The presence of a slight discharge from the eye was noted for both animals on Day I and the conjunctivae for one rabbit were slightly swollen. No iridial or corneal changes were apparent in any of the three treated eyes.
- Other effects:
- No observations indicative of systemic toxicity or ill health were noted for any rabbits during the course of the study.
Applicant's summary and conclusion
- Interpretation of results:
- not irritating
- Remarks:
- Migrated information Criteria used for interpretation of results: expert judgment
- Conclusions:
- Instillation of the test substance into the conjunctival sac of three rabbits caused transient conjunctival changes that resolved within 24 hours. The iris and cornea were overtly unaffected by instillation of the test article. Therefore, the test substance is not an eye irritant.
- Executive summary:
The test substance, 2,3-epoxypropyl neodecanoate was accessed for eye irritational potential in an O.E.C.D. test guideline 405 study. Instillation of the test substance into the conjunctival sac of three rabbits caused transient conjunctival changes that resolved within 24 hours. The iris and cornea were overtly unaffected by instillation of the test article. Therefore, the test substance is not an eye irritant. It is anticipated that Neononanoic acid glycidyl ester will also be a non-eye irritant.
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