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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
Dermal absorption
Administrative data
- Endpoint:
- dermal absorption in vitro / ex vivo
- Type of information:
- experimental study
- Adequacy of study:
- supporting study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Non guideline study. GLP-status unknown. Published abstract in peer reviewed literature.
Data source
Reference
- Reference Type:
- publication
- Title:
- Dermal Absorption of Pyridine and Some Methyl Pyridines In Vitro
- Author:
- Wilkinson, S.C., Williams, F.M.
- Year:
- 2 001
- Bibliographic source:
- Toxicology 168 (2001) 1
Materials and methods
- Principles of method if other than guideline:
- The absorption of the test substance through human skin was studied in vitro using dermatomed human breast skin (280 µm) to assess the dermal absorption hazard of this compound and to identify physicochemical influences on absorption
- GLP compliance:
- not specified
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): 2-methyl pyridine (MPYR)
Constituent 1
Test animals
- Species:
- other: Dermatomed human breast skin (280 µm)
Administration / exposure
- Details on in vitro test system (if applicable):
- - Dermatomed human breast skin (280 µm) was mounted in Scott Dick flow through diffusion cells.
- Minimal Essential Medium Eagle (pH 7.4) was pumped beneath the skin at 1.5 mL/h and at 32 °C for 24 h.
- The test compound was applied to the skin (0.64 cm2) undiluted (10 µL) or in aqueous vehicle (200 µL, 3 mg/mL).
- Charcoal filters were placed above the skin to trap volatilized test compounds.
- Concentrations of test compounds in receptor fluids were determined by Gas Chromatography.
- Steady-state flux (J), apparent kp, time to steady state and total absorption (% of applied dose) were calculated from cumulative absorption time curves.
Results and discussion
Any other information on results incl. tables
Dermal absorption parameters for 2-methylpyridine
Undiluted:
- Steady-state flux = 822 ± 222 nmol/cm2 per h, apparent kp = 0.8 ± 0.2E−4 cm/h, Time to steady-state = 0.55 ± 0.15 h
- Total absorption = 0.49 ± 0.14 %
Aqueous solution:
- Steady-state flux = 686 ± 129 nmol/cm2 per h, apparent kp = 213.0 ± 40.0E−4 cm/h, Time to steady-state = 0.39 ± 0.08 h
- Total absorption = 5.56 ± 1.18 %
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.