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EC number: 295-322-3 | CAS number: 91995-60-7
- 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:
- migrated information: read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: GLP compliant, comparable to guideline study with acceptable restrictions.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 991
- Report date:
- 1991
Materials and methods
Test guideline
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 403 (Acute Inhalation Toxicity)
- GLP compliance:
- yes
- Test type:
- standard acute method
- Limit test:
- yes
Test material
- Reference substance name:
- 2-methoxy-2-methylbutane
- EC Number:
- 213-611-4
- EC Name:
- 2-methoxy-2-methylbutane
- Cas Number:
- 994-05-8
- Molecular formula:
- C6H14O
- IUPAC Name:
- 1,1-dimethylpropyl methyl ether
- Details on test material:
- - Name of test material (as cited in study report): identification number: LF-9128 (TA 691)
- Physical state: a clear, colorless liquid
- Stability at test conditions: stable
- Storage: refrigerated (approximately 3°C).
Constituent 1
Test animals
- Species:
- rat
- Strain:
- Sprague-Dawley
- Sex:
- male/female
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: Charles river Breeding lab. Inc., Portage, MI
- Weight at study initiation: 225-319 gram
- Housing: individually in stainless steel cages, exposure in 1m3 glass and stainless steel chambers (Unifab, Kalamazoo, MI)
- Diet: ad libitum
- Water: ad libitum
- Acclimation period: approximately 3 weeks
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 20.5
- Humidity (%): 36.2
- Photoperiod (hrs dark / hrs light): 12/12
Administration / exposure
- Route of administration:
- inhalation: vapour
- Type of inhalation exposure:
- whole body
- Vehicle:
- other: unchanged (no vehicle)
- Details on inhalation exposure:
- The animals were exposed for 4 hours to a test atmosphere generated from a single batch of the test article. The generation system consisted of a glass column packed with glass beads. The test article was delivered at a constant rate from a glass reservoir. Compressed air entered at the bottom of the glass bead column and test article entered approximately at the middle of the column. The resultant vapour entered the chamber supply air duct and was carried into the top of the chamber. The test article was completely vapourized with only a slight discolouration of the glass beads. The amount of residue on the beads was too small to measure.
The exposure was conducted in 1m3 glass and stainless steel chambers (Unifab, Kalamazoo, MI). - Analytical verification of test atmosphere concentrations:
- yes
- Remarks:
- the test article vapour concentration was monitored by IR
- Duration of exposure:
- 4 h
- Concentrations:
- 5400 mg/m³
- No. of animals per sex per dose:
- 5
- Control animals:
- no
- Details on study design:
- Five male and five female Sprague-Dawley rats were assigned to a single group, which was exposed in a 1 m3 exposure chamber to a mean TAME vapour concentration of 5,400 mg/m3 for 4 hours. The rats were clinically observed immediately after removal from the chamber, approximately 2 to 3 hours after the exposure and at least once per day during the 14-day post exposure observation period. Rats were weighed before the exposure, one week later and before necropsy.
Examinations performed: clinical observations, body weights, gross necropsy. - Statistics:
- Statistical analyses were used to analyse the results: calculation of standard deviations.
Results and discussion
Effect levels
- Sex:
- male/female
- Dose descriptor:
- LC50
- Effect level:
- > 5 400 mg/m³ air
- Exp. duration:
- 4 h
- Mortality:
- No mortality was observed.
- Clinical signs:
- other: In clinical observations, rales were seen in all rats immediately following the exposure. The rales were present in 7/10 animals about 2 hours after the exposure, but 3 ¼ hours later all rats appeared normal. Redness around the nose in 7/10 rats, salivat
- Body weight:
- All rats gained weight during the study.
- Gross pathology:
- Necropsy revealed external haemorrhagic lung foci in the lungs in seven rats. However, mostly these foci were comparable in size and number to control rat foci, with the exception of one female rat that had numerous foci. One male that had a diffuse red area on its lungs. Six rats had enlarged mandibular lymph nodes.
Applicant's summary and conclusion
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.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.

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