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Diss Factsheets
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EC number: 210-959-9 | CAS number: 626-67-5
- 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
Specific investigations: other studies
Administrative data
- Endpoint:
- specific investigations: other studies
- Type of information:
- experimental study
- Adequacy of study:
- other information
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Meets generally accepted scientific standards, well documented and acceptable for assessment.
Data source
Reference
- Reference Type:
- publication
- Title:
- Effect of tobacco smoke compounds on the plasma membrane of cultured human lung fibroblasts.
- Author:
- Thelestam, M., Curvall, M., Enzell, C.R.
- Year:
- 1 980
- Bibliographic source:
- Toxicology, 15, 203-217
Materials and methods
- Principles of method if other than guideline:
- Cultured human fibroblasts were incubated with N-methylpiperidine, a solvent alone and a positive control reference. Liberation of uridine nucleotides through the cell membrane was the basis for assessment of the membrane damaging capability of the test substance, in comparison with the negative and positive reference.
- GLP compliance:
- not specified
- Type of method:
- in vitro
Test material
- Reference substance name:
- N-Methyl Piperidine
- IUPAC Name:
- N-Methyl Piperidine
Constituent 1
Administration / exposure
- Details on exposure:
- Cultured human fibroblasts (line MRC-5, 10xE5 cells/cm², labelled with ³H uridine) were incubated with N-methylpiperidine (2480 mg/L, 30 min at 37°C in TRIS-buffered 0.15 mM saline) and solvent alone. Additionally a positive control reference (Scraping with a rubber policeman) was applied. Liberation of uridine nucleotides through the cell membrane was the basis for assessment of the membrane damaging capability of the test substance, in comparison with the negative and positive reference.
After incubation the solution containing leaked radioactive marker was removed and centrifuged (1000 g, 10 min, 4°C) and radioactivity in 0.1 mL aliquots of the supernatant was measured by liquid scintillation. A maximal release of the radioactivity was obtained by treating control cells for 30 min with 0.06 M sodium borate buffer (pH 7.8) and scraping with a rubber policeman. This treatment ruptured the cell membranes leaving the nuclei intact. The following expression was used to calculate the relative leakage of the radioactive marker:
(experimental release - spontaneous release)/ (maximal release - spontaneous release) x 100.
The spontaneous release of the nucleotide marker during incubation for 30 min at 37°C was 3-7 per cent of the maximal release. - Duration of treatment / exposure:
- 30 min
Doses / concentrations
- Remarks:
- Doses / Concentrations:
2480 mg/L
Basis:
no data
Examinations
- Examinations:
- Determination of the leakage of the radioactive marker.
Results and discussion
- Details on results:
- N-Methyl Piperidine was classified as a substance with strong membrane damaging potential, based on the strong liberation of uridine nucleotides of 80%.
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.