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EC number: 201-148-0 | CAS number: 78-83-1
- 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

Immunotoxicity
Administrative data
- Endpoint:
- immunotoxicity, other
- Remarks:
- in vitro
- Type of information:
- experimental study
- Adequacy of study:
- other information
- Reliability:
- 4 (not assignable)
- Rationale for reliability incl. deficiencies:
- secondary literature
Data source
Reference
- Reference Type:
- secondary source
- Title:
- Immunotoxicological evaluation of environmental chemicals utilizing the mouse lymphocyte mitogenesis test
- Author:
- Sakazaki, H. et al.
- Year:
- 2 001
- Bibliographic source:
- Journal of Health Sciences, 47(3), pp. 258-271; cited in OECD SIDS "Isobutanol", Final September 2004
Materials and methods
- Principles of method if other than guideline:
- Immunotoxicity - Lymphocyte Mitogenesis Test
- GLP compliance:
- not specified
Test material
- Reference substance name:
- 2-methylpropan-1-ol
- EC Number:
- 201-148-0
- EC Name:
- 2-methylpropan-1-ol
- Cas Number:
- 78-83-1
- Molecular formula:
- C4H10O
- IUPAC Name:
- 2-methylpropan-1-ol
Constituent 1
Test animals
- Species:
- mouse
- Strain:
- Balb/c
- Remarks:
- and C3H/He
- Sex:
- male
Administration / exposure
- Vehicle:
- water
- Remarks:
- or DMSO (max. 0.3 %)
- Duration of treatment / exposure:
- 96 h
- Frequency of treatment:
- continous
Doses / concentrations
- Remarks:
- Doses / Concentrations:
10e-9 to 10e-3 mol/L
- Control animals:
- yes, concurrent vehicle
- Details on study design:
- B cells were isolated from the spleen of male C3H/He mice following injection of 10 ml of RPMI-1640 medium into the spleen. T cells were isolated from the spleen of male BALB/C mice in a similar manner. The cells were flushed out of the spleen using a syringe and the suspended cells were removed from the connective tissue, washed, and counted with a hematocytometer. The cells were dispensed into 96-well microplates at 10e-5 cells/well in 200 µL RPMI-1640 medium containing 5 mM HEPES, 50 PM 2-mercaptoethanol, 100 IU/mI penicillin, 50 µg/ml streptomycin, 0.18% NaHC03, and 10% fetal calf serum. Mitogenic stimuli for the B and T cells were provided by addition of 100 µg/ml lipopolysaccharide or 200 µg/ml concanavalin A, respectively. The test chemical was added to stimulated cells and incubations proceeded for 96 hours at 37' C in a 5% C02 atmosphere. At the end of the exposure period, the total amount of DNA in the grown cells was determined by the ethidium bromide fluorescence method. The control cells were treated in the same manner as the treated cells with the exception that no test chemical was added (only vehicle) . A cell growth curve was plotted against test chemical concentration and a concentration for 50% growth inhibition (IC50) was determined .
Results and discussion
Effect levels
- Key result
- Dose descriptor:
- other: inhibition of mitogenic actitivity
- Basis for effect level:
- other: Isobutanol showed no inhibition of mitogenic activity in stimulated B and T cells in the concentration range tested.
- Remarks on result:
- not measured/tested
Applicant's summary and conclusion
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