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Diss Factsheets
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EC number: 203-643-7 | CAS number: 109-06-8
- 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
![](https://echa.europa.eu/o/diss-blank-theme/images/factsheets/A-REACH/factsheet/print_toxicological-information.png)
Repeated dose toxicity: oral
Administrative data
- Endpoint:
- chronic toxicity: oral
- Type of information:
- experimental study
- Adequacy of study:
- supporting study
- Reliability:
- 4 (not assignable)
- Rationale for reliability incl. deficiencies:
- other: English summary of a Russian non-guideline study. No or very limited information on design and methods of the study.
Data source
Reference
- Reference Type:
- secondary source
- Title:
- Pathomorphology of the central nervous system during the chronic poisoning of rats with α-picoline
- Author:
- Polilei, S.A.
- Year:
- 1 969
- Bibliographic source:
- Tr.Krasnoyarsk Gos. Med. Inst. 9(1), 80-85, 1969 (Russ) cited in Chem.Abstr, Vol 75
Materials and methods
- Principles of method if other than guideline:
- The test substance was given orally for 6 month to rats. After the exposure period, animals were decapitated. Brain and spinal cord were examined histopathologically.
- GLP compliance:
- no
- Limit test:
- no
Test material
- Reference substance name:
- 2-methylpyridine
- EC Number:
- 203-643-7
- EC Name:
- 2-methylpyridine
- Cas Number:
- 109-06-8
- Molecular formula:
- C6H7N
- IUPAC Name:
- 2-methylpyridine
- Details on test material:
- - Name of test material (as cited in study report): α-picoline
Constituent 1
Test animals
- Species:
- rat
Administration / exposure
- Route of administration:
- oral: unspecified
- Duration of treatment / exposure:
- 6 months
Doses / concentrations
- Remarks:
- Doses / Concentrations:
0.0025, 0.01 or 0.05 mg/kg bw
Basis:
no data
- Control animals:
- no
Examinations
- Sacrifice and pathology:
- Brain and spinal cord were examined histopathologically
Results and discussion
Results of examinations
- Details on results:
- - Functional and dystrophic changes in cells of the 1st, 2nd, 3rd, and 5th layer of the cerebral cortex, but also of the sub-cortex were observed. At the dose of 0.0025 mg/kg bw these changes were mostly functional but single neurons of the thalamo-hypothalamnic region showed swelling, chromatolysis, wrinkling, and hyperchromatosis.
- By raising the dose of the test substance, dystrophic changes in all parts of the brain increase, and become most pronounced in the 3rd group of rats.
- Chronic intoxication of animals with the test substance is accompanied by vascular disturbances aggravating neuronal and glial lesions. Chronically intoxicated rats of the 3rd group showed a relatively constant demyelination of nerve pathways in the brain.
Target system / organ toxicity
- Critical effects observed:
- not specified
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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