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Diss Factsheets
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EC number: 812-724-1 | CAS number: 106705-37-7
- 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: inhalation
Administrative data
- Endpoint:
- acute toxicity: inhalation
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: Acceptable, well-documented study report equivalent or similar to OECD guideline (403): pre-GLP.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 964
- Report date:
- 1964
Materials and methods
Test guideline
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 403 (Acute Inhalation Toxicity)
- Deviations:
- yes
- Remarks:
- No analytical concentration measurements.
- GLP compliance:
- no
- Test type:
- standard acute method
- Limit test:
- yes
Test material
- Reference substance name:
- Neodecanoic acid
- EC Number:
- 248-093-9
- EC Name:
- Neodecanoic acid
- Cas Number:
- 26896-20-8
- Molecular formula:
- C10H20O2
- IUPAC Name:
- 2-ethyl-2,5-dimethylhexanoic acid
Constituent 1
Test animals
- Species:
- other: mouse, rat, and guinea pig
- Strain:
- other: Swiss, Wistar, and Hartley
- Sex:
- male
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: no data provided
- Age at study initiation: no data provided
- Weight at study initiation: no data provided
- Fasting period before study: 3-4 hours
- Housing: groups
- Diet (e.g. ad libitum): ad libitum
- Water (e.g. ad libitum): ad libitum
- Acclimation period: 14 days
Administration / exposure
- Route of administration:
- inhalation: vapour
- Type of inhalation exposure:
- whole body
- Vehicle:
- other: unchanged (no vehicle)
- Details on inhalation exposure:
- GENERATION OF TEST ATMOSPHERE / CHAMBER DESCRIPTION
- Exposure apparatus: stainless steel gassing chamber
- Exposure chamber volume: 500 l
- Method of holding animals in test chamber: n/a
- Source and rate of air: forced room air
- Method of conditioning air: glass bubblers - Analytical verification of test atmosphere concentrations:
- no
- Duration of exposure:
- 6 h
- Concentrations:
- 3 mg/l nominal concentration
- No. of animals per sex per dose:
- 10 males per species
- Control animals:
- no
- Details on study design:
- - Duration of observation period following administration: 14 days (or other?) Every 30 minutes during exposure and daily thereafter for 14 days
- Necropsy of survivors performed: yes
- Other examinations performed: clinical signs, body weight,organ weights - Statistics:
- No data analyzed.
Results and discussion
Effect levelsopen allclose all
- Sex:
- male
- Dose descriptor:
- LC50
- Effect level:
- > 3 mg/L air (nominal)
- Exp. duration:
- 6 h
- Remarks on result:
- other: mice and rats
- Sex:
- male
- Dose descriptor:
- LC50
- Effect level:
- < 3 mg/L air (nominal)
- Exp. duration:
- 6 h
- Remarks on result:
- other: guinea pig
- Mortality:
- 2 guinea pigs died on the 2nd day, 1 on the 13th, and 2 on the 14th post exposure.
All mice and rats survived. - Clinical signs:
- other: No significant signs of respiratory irritation were noted. Alopecia and some weight loss were noted in the guinea pigs during the 14-day observation period.
- Body weight:
- Not analyzed.
- Gross pathology:
- No significant findings.
Applicant's summary and conclusion
- Interpretation of results:
- other:
- Remarks:
- Criteria used for interpretation of results: EU
- Conclusions:
- The acute inhalation LC50 for isononanol is >3 mg/l for mice and rats.
- Executive summary:
Neodecanoic acid was administered via a vapor inhalation to 10 each of mice, rats, and guinea pigs at the nominal concentration of 3 mg/l for 6 hours. Clinical observations were made every 30 minutes during the exposure and daily thereafter for 14 days. No significant signs of respiratory irritation were noted. Alopecia and some weight loss were noted in the guinea pigs during the 14-day observation period. Two guinea pigs died on the 2nd day, 1 on the 13th, and 2 on the 14th post exposure. All mice and rats survived. Based on these data it is concluded that the LC50 for mice and rats is greater than 3 mg/l.
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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