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Diss Factsheets
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EC number: 201-132-3 | CAS number: 78-67-1
- 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
Endpoint summary
Administrative data
Description of key information
The oral LD50 value was 100 mg/kg for rats. General anesthetic, somnolence, and ataxia was observed.
However, in the dissemination view on the ECHA website of the full registration dossier a GLP-compliant Guideline study, conducted in 2010, comprised an acute oral LD50 value between 300 and 2000 mg/kg bw in rats.
In an inhalation study, no mortality was observed at a concentration of 12 g/m³ for 4 hours. Exciting behavior, conjunctive irritation, and weight loss or decreased weight gain were observed.
Key value for chemical safety assessment
Acute toxicity: via oral route
Link to relevant study records
- Endpoint:
- acute toxicity: oral
- Type of information:
- experimental study
- Adequacy of study:
- other information
- Reliability:
- 4 (not assignable)
- Rationale for reliability incl. deficiencies:
- secondary literature
- GLP compliance:
- no
- Sex:
- not specified
- Dose descriptor:
- LD50
- Effect level:
- 100 mg/kg bw
Reference
Endpoint conclusion
- Endpoint conclusion:
- adverse effect observed
- Dose descriptor:
- LD50
- Value:
- 100 mg/kg bw
Acute toxicity: via inhalation route
Link to relevant study records
- Endpoint:
- acute toxicity: inhalation
- Type of information:
- experimental study
- Adequacy of study:
- other information
- Study period:
- 1989
- Reliability:
- 4 (not assignable)
- Rationale for reliability incl. deficiencies:
- secondary literature
- GLP compliance:
- no
- Species:
- rat
- Duration of exposure:
- 4 h
- Dose descriptor:
- LCLo
- Effect level:
- > 12 mg/L air
- Clinical signs:
- other: Exciting behavior, conjunctive irritation
- Body weight:
- weight loss or decreased weight gain
Reference
Endpoint conclusion
- Endpoint conclusion:
- adverse effect observed
- Dose descriptor:
- discriminating conc.
- Value:
- 12 000 mg/m³ air
Acute toxicity: via dermal route
Endpoint conclusion
- Endpoint conclusion:
- no study available
Additional information
Acute oral toxicity
In a study on acute oral toxicity, the oral LD50 value was 100 mg/kg for rats. General anesthetic, somnolence, and ataxia was observed. (NTIS, 1989)
However, in the dissemination view on the ECHA website of the full registration dossier a GLP-compliant Guideline study, conducted in 2010, comprised an acute oral LD50 value between 300 and 2000 mg/kg bw in rats. (ECHA Dissemination View, accessed on 2018-09-27)
Rusin et al. determined an oral LD50 value of 700 mg/kg bw (1958). Additionally, the Toxic Substances Control Act provides several literature data on acute oral toxicity. LD50 values for rat of 50.0 - 400.0 mg/kg bw (1992) and 100.0 - 200.0 mg/kg bw (1984) and for mice of 200.0 - 400.0 mg/kg bw (1984) are reported. In another literature source, an approximately lethal dose (ALD) of 450.0 mg/kg bw for female rats and of 670.0 mg/kg bw for male rats was determined (1962).
Acute inhalation toxicity
In an inhalation study, no mortality was observed at a concentration of 12 g/m³ for 4 hours during a 14 days observation period. Exciting behavior, conjunctive irritation, and weight loss or decreased weight gain were observed. (NTIS, 1989)
IGW Elberfeld examined the acute inhalation toxicity with an aerosol of the substance in different species. After an exposure duration of 8 h, all mice died within a few days after single or repeated (2 - 3 times) exposure. No deaths occurred among rats, rabbits and cats.
Rusin et al. determined an inhalative LC50 of 0.7 g/kg for mice that were exposed to an aerosol of the substance (1958).
Additionally, the Toxic Substances Control Act provides several literature data on acute inhalative toxicity. An approximately lethal concentration (ALC) of 950 mg/m³ for rats after an exposure of 4 h was determined (1992).
Justification for classification or non-classification
Classification, Labelling, and Packaging Regulation (EC) No. 1272/2008
The available experimental test data are reliable and suitable for classification purposes under Regulation 1272/2008. The oral LD50 was 100 mg/kg for rats. However, in the dissemination view on the ECHA website of the full registration dossier a GLP-compliant Guideline study, conducted in 2010, comprised an acute oral LD50 value between 300 and 2000 mg/kg bw in rats.
No mortality but exciting behavior, conjunctive irritation, and weight loss or decreased weight gain were observed in an inhalation study at a concentration of 12 g/m³. As a result and according to Annex VI (index number 608-019-00-1) the substance is considered to be classified for acute oral toxicity Category 4 and acute inhalation toxicity Category 4 under Regulation (EC) No. 1272/2ßß8, as amended for the tenth time in Regulation (EC) No. 2017/776.
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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