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Diss Factsheets
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EC number: 202-446-3 | CAS number: 95-74-9
- 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: other routes
Administrative data
- Endpoint:
- acute toxicity: other routes
- Type of information:
- experimental study
- Adequacy of study:
- other information
Data source
Reference
- Reference Type:
- publication
- Title:
- 3-Chloro-p-Toluidine: Effects of Lethal Doses in Rats and Cats
- Author:
- Borison HL, Snow SR, Longnecker DS, Smith RP
- Year:
- 1 975
- Bibliographic source:
- Toxicol Appl Pharmacol 31, 403-412 (1975)
Materials and methods
- Principles of method if other than guideline:
- Effects of lethal doses in rats and cats.
- GLP compliance:
- no
Results and discussion
Applicant's summary and conclusion
- Executive summary:
Chloro-p-toluidine (3-CPT) given systemically to rats or into the cerebroventricular system of cats produced death in respiratory arrest. Respiratory depression in cats can also be induced by the
rapid systemic infusion of 3-CPT, but methemoglobin formation and hemolysis are complications of the iv route in cats. The respiratory effects of 3-CPT in cats mimic those of surgical vagotomy, e.g., alterations in pattern, slowing of rate, and abolition of the Hering-Breuer reflex. Despite these drastic changes, the CO2-tidal volume response relationship was not altered.
Incidental effects observed after ip injection in rats, which may at least in part be secondary to hypoxia, include metabolic acidosis (lactic acidemia), hyperkalemia, hemoconcentration, loss of plasma proteins, and ascitic fluid in the abdomen. Rats also exhibited an early and transient skeletal muscle paralysis which is probably of central origin. A transient fall in blood pressure prior to the final state of collapse may be due to direct capillary vasodilation. In the late stages of collapse the peripheral vasodilation may be replaced by an increase in capillary permeability. 3-Chloro-ptoluidine appears to be directly cytotoxic, and on serosal surfaces it produced superficial necrosis l-6 cell layers deep after only 3-8 hr of contact.
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