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EC number: 221-975-0 | CAS number: 3302-10-1
- 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
Endpoint summary
Administrative data
Description of key information
3,5,5 -trimethylhexanoic acid did not induce skin sensitisation in a guinea-pig maximisation test. No cases of skin sensitisation have been observed in two large companies producing 3,5,5 -trimethylhexanoic acid and no cases are reported in the literature.
There is no information available on respiratory sensitising effects of 3,5,5 -trimethylhexanoic acid.
Key value for chemical safety assessment
Skin sensitisation
Link to relevant study records
- Endpoint:
- skin sensitisation: in vivo (non-LLNA)
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 1994
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- comparable to guideline study with acceptable restrictions
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 406 (Skin Sensitisation)
- Principles of method if other than guideline:
- guinea pig maximisation test, unclear if according to guidelines
- GLP compliance:
- not specified
- Type of study:
- guinea pig maximisation test
- Justification for non-LLNA method:
- Study has been performed before REACH regulation came into force
- Species:
- guinea pig
- Strain:
- Hartley
- Sex:
- female
- Details on test animals and environmental conditions:
- no details provided
- Route:
- intradermal
- Vehicle:
- not specified
- Concentration / amount:
- 1-5%
- Day(s)/duration:
- no data
- Adequacy of induction:
- not specified
- Route:
- epicutaneous, occlusive
- Vehicle:
- petrolatum
- Concentration / amount:
- not provided
- Day(s)/duration:
- no data
- Adequacy of induction:
- not specified
- No.:
- #1
- Route:
- epicutaneous, semiocclusive
- Vehicle:
- unchanged (no vehicle)
- Concentration / amount:
- no data
- Day(s)/duration:
- 24 h
- Adequacy of challenge:
- not specified
- No. of animals per dose:
- 20-25
- Details on study design:
- no data
- Challenge controls:
- no data
- Positive control substance(s):
- not specified
- Positive control results:
- Positive results have been shown for several substances, e.g. acrylic monomere or potassium dichromate
- Key result
- Reading:
- other: overall result
- Group:
- test chemical
- Dose level:
- pure substance
- Clinical observations:
- no data provided
- Remarks on result:
- no indication of skin sensitisation
- Remarks:
- no further information provided
- Reading:
- other: overall result
- Group:
- negative control
- Dose level:
- not indicated
- Clinical observations:
- no data provided
- Remarks on result:
- no indication of skin sensitisation
- Reading:
- other: overall result
- Group:
- positive control
- Dose level:
- <=25%
- Clinical observations:
- no data provided
- Remarks on result:
- positive indication of skin sensitisation
- Interpretation of results:
- GHS criteria not met
- Conclusions:
- The test substance was reported to be not sensitising in this study.
- Executive summary:
The test substance was not sensitising in a guinea pig maximisation test (no details reported) (Cronin, 1994).
Reference
Result: negative (no further details provided)
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed (not sensitising)
- Additional information:
In vitro data:
Skin sensitisation in vitro has not been investigated as there is sufficient information available for the submission substance.
Animal data:
3,5,5-trimethylhexanoic acid did not induce skin sensitisation in a guinea pig maximisation test. This assay has been performed according to a generally accepted methodology. No indication for skin sensitisation was obtained. This negative result is supported by the findings of the OECD Toolbox profiler which did not indicate an alert for skin sensitising properties.
Human experience (chapter 7.10.4):
No cases of sensitisation in workers were observed by the occupational medicine department of Hoechst AG and BASF AG, two major producers of 3, 5, 5-trimethylhexanoic acid, during many years of production and further processing of the test substance (BASF 1997; Hoechst 1997; cited in BG Chemie, 2005).
Further,the Information Network of Departments of Dermatology for the surveillance and scientific evaluation of contact allergies in Germany, stated that there are no data on the sensitizing potential of isononanoic acid, and deemed it unlikely that the chemical has any allergenic potential (IVDK 1997; cited in BG Chemie, 2005).
Overall, 3, 5, 5-trimethylhexanoic acid is not likely to have sensitizing properties.
Respiratory sensitisation
Endpoint conclusion
- Endpoint conclusion:
- no study available
Justification for classification or non-classification
Based on the negative findings in a guinea-pig maximisation test and the experience with 3,5,5 -trimethylhexanoic acid from the workplace it is concluded that the submission substance 3,5,5-trimethylhexanoic acid does not cause skin sensitisation and has not to be classified as skin sensitiser according to Regulation (EC) No 1272/2008.
There is no information available on respiratory sensitising effects of 3,5,5 -trimethylhexanoic acid.
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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