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Diss Factsheets
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EC number: 202-796-7 | CAS number: 99-87-6
- 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: inhalation
Administrative data
- Endpoint:
- acute toxicity: inhalation
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- accepted calculation method
Data source
Reference
- Reference Type:
- other: Unpublished report
- Title:
- Unnamed
- Year:
- 1 962
Materials and methods
Test guideline
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- - Principle of test:
Rats were exposed to atmospheres saturated with 9.7 mg /L of pcymene for a period of 5 hours. A "lethal concentration time value (LCt)" was calculated based on the "shortest period of exposure causing death", where the concentration was expressed as mg/l and time as minutes.
- Parameters analysed / observed: Clinical signs and mortality were recorded. - GLP compliance:
- no
- Test type:
- other: Acute inhalation toxicity in rats
- Limit test:
- yes
Test material
- Reference substance name:
- p-cymene
- EC Number:
- 202-796-7
- EC Name:
- p-cymene
- Cas Number:
- 99-87-6
- Molecular formula:
- C10H14
- IUPAC Name:
- 1-isopropyl-4-methylbenzene
Constituent 1
Test animals
- Species:
- rat
- Sex:
- not specified
- Details on test animals or test system and environmental conditions:
- not specifed
Administration / exposure
- Route of administration:
- inhalation
- Type of inhalation exposure:
- not specified
- Vehicle:
- air
- Details on inhalation exposure:
- not specifed
- Analytical verification of test atmosphere concentrations:
- not specified
- Duration of exposure:
- ca. 5 h
- Concentrations:
- Rats were exposed to atmospheres saturated with 9.7 mg /L of p-cymene for a period of 5 hours.
- No. of animals per sex per dose:
- 3
- Control animals:
- not specified
- Details on study design:
- - Duration of observation period following administration: 30 min, 45 min and 1 day
- Frequency of observations and weighing: not specified
- Necropsy of survivors performed: no
- Other examinations performed: clinical signs - Statistics:
- A "lethal concentration time value (LCt)" was calculated based on the "shortest period of exposure causing death", where the concentration was expressed as mg/l and time as minutes
Results and discussion
- Preliminary study:
- not applicable
Effect levels
- Key result
- Sex:
- not specified
- Dose descriptor:
- other: lethal concentration time value (LCt)
- Effect level:
- > 9.7 mg/L air
- Based on:
- test mat.
- Exp. duration:
- 5 h
- Remarks on result:
- other: no deaths
- Mortality:
- No deaths were reported
- Clinical signs:
- other: other:
- Body weight:
- not specified
- Gross pathology:
- not specified
Applicant's summary and conclusion
- Interpretation of results:
- study cannot be used for classification
- Conclusions:
- A "lethal concentration time value (LCt)" of >9.7 mg/L was calculated based on the "shortest period of exposure causing death", where the concentration was expressed as mg/l and time as minutes. No deaths were observed during the exposure period. The morning after exposure, the rats appeared fully recovered from the clinical signes observed during the exposure period.
- Executive summary:
In this study, rats were exposed to atmospheres saturated with 9.7 mg /L of p-Cymene for a period of 5 hours. Clinical signs and mortality were recorded. Surviving animals were removed from the exposure chamber and observed for an additional week.
Signs reported during the first 30 minutes were those typical of irritation: excitement, pawing at the eyes and nose, increased blinking, squinting, and eye closure. After 45 minutes, equilibrium loss and increased salivation were noted. One-half hour later, fine tremors began and increased to quivering after another 15 minutes. Clonic convulsions were reported after another 15 minutes and the rats staggered about aimlessly until the end of the exposure. The morning after exposure, the rats appeared fully recovered.
A "lethal concentration time value (LCt)" of >9.7 mg/Lwas calculated based on the "shortest period of exposure causing death", where the concentration was expressed as mg/l and time as minutes.
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