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Diss Factsheets
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EC number: 285-480-1 | CAS number: 85099-25-8
- 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
Acute Toxicity: oral
Administrative data
- Endpoint:
- acute toxicity: oral
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 1979
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Provides basic data; some details missing including dose levels.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 979
- Report date:
- 1979
Materials and methods
Test guideline
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- The test substance was administered to groups of male and female Sprague Dawley rats by oral gavage and observed for a period of 14 days.
- GLP compliance:
- no
- Test type:
- standard acute method
- Limit test:
- no
Test material
- Details on test material:
- Polycat 8CAS 98-94-2 (cyclohexyldimethylamine), N,N-dimethylcyclohexylamine (DMCHA)purity not indicated Lot # 79-507-CJLiquid
Constituent 1
Test animals
- Species:
- rat
- Strain:
- Sprague-Dawley
- Sex:
- male/female
- Details on test animals or test system and environmental conditions:
- - Age: no data - Weight at study initiation: 110 g- Housing: During the observation period the rats were housed in stainless steel hanging cages with up to two rats of the same sex and dosage group per cage.
Administration / exposure
- Route of administration:
- oral: gavage
- Vehicle:
- not specified
- Details on oral exposure:
- MAXIMUM DOSE VOLUME APPLIED: 0.63ml/kg.
- Doses:
- Dosages ranged from 0.25 to 0.63ml/kg.
- No. of animals per sex per dose:
- 10/sex/dose
- Control animals:
- no
- Details on study design:
- ADMINISTRATION: - Doses: 0.25-0.63 ml/kg - Doses per time period: single - Post dose observation period: 14-daysEXAMINATIONS: mortality/clinical signs limited necropsy on all animals that died and on up to 3/sex/treatment of the survivors
- Statistics:
- No information provided
Results and discussion
- Preliminary study:
- Not relevant
Effect levelsopen allclose all
- Key result
- Sex:
- male/female
- Dose descriptor:
- LD50
- Effect level:
- > 272 - < 289 mg/kg bw
- Remarks on result:
- other: Originally reported in ml/kg; mg/kg bw determined using a density of 0.849 g/cm3.
- Sex:
- male
- Dose descriptor:
- LD50
- Effect level:
- 289 mg/kg bw
- 95% CL:
- > 221 - < 340
- Remarks on result:
- other: originally reported as 0.34 ml/kg bw, 95% confidence interval 0.26-0.40
- Sex:
- female
- Dose descriptor:
- LD50
- Effect level:
- 272 mg/kg bw
- 95% CL:
- > 238 - < 306
- Remarks on result:
- other: Originally reported as 0.32 ml/kg, 95% confidence interval 0.28-0.36
- Mortality:
- - Number of deaths at each dose: not specified - Time of death: within 24 hours, and a few delayed deaths
- Clinical signs:
- decreased activity, ataxia, jerks, tremors, dyspnea, clonic convulsions, salivation and squinting. These signs usually lasted less than 24 hours.
- Body weight:
- No information provided.
- Gross pathology:
- (a) in the majority of animals that died: gastric lesions, suggestive of irritation, were observed, including red linear mucosal streaks or red discoloration of mucosa. An occasional erosion and one example of mucosal oedema was also observed. (b) in some animals that survived: thin connective tissue adhesions in stomach serosa and varios adnexal structures were found in some animals. Mucosal keratinization of stomach was found in one animal.
- Other findings:
- No additional information provided
Any other information on results incl. tables
Gross examination of animals dying acutely or survivors at the end of the 14 day observation period, suggested that Polycat 8 was irritating to the stomach under the conditions of this study.
Applicant's summary and conclusion
- Interpretation of results:
- Category 3 based on GHS criteria
- Conclusions:
- Under the conditions of this study, the LD50 of the test substance was found to be between 272 and 289mg/kg bw. Based on this result, the test substance was considered to be a Category 3 toxicant and should have the signal word Danger and the hazard statement, H301: Toxic if swallowed associated with it. According to Directive 67/548/EEC, the test substance should be classified as Harmful and have the risk phrase R22: Harmful if swallowed associated with it.
- Executive summary:
In a study conducted in 1979, the test substance, cyclohexyldimethylamine (DMCHA) was evaluated for its ability to induce toxicity when administered to male and female Sprague Dawley rats via oral gavage. The concentration administered ranged from 0.25 to 0.63 ml/kg. Following a single administration, the animals were observed for a 14 day post-exposure period.
Rats treated with DMCHA exhibited decreased activity, ataxia, jerks, tremors, dyspnea, clonic convulsions, salivation and squinting. These signs usually lasted less than 24 hours. Most deaths occurred within 24 hours after treatment although a few delayed deaths also occurred.
Gross examination of animals dying acutely and survivors at the end of the 14-day recovery period suggested that DMCHA, administered under the conditions of this study, was irritating to the stomach.
Under the conditions of this study, the LD50 of the test substance was found to be between 272 and 289mg/kg bw. Based on this result, the test substance was considered to be a Category 3 toxicant and should have the signal word Danger and the hazard statement, H301: Toxic if swallowed associated with it. According to Directive 67/548/EEC, the test substance should be classified as Harmful and have the risk phrase R22: Harmful if swallowed associated with it.
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.
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