Registration Dossier
Registration Dossier
Diss Factsheets
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EC number: 203-459-7 | CAS number: 107-07-3
- 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
See discussion section.
Key value for chemical safety assessment
Additional information
In NTP TR 275 a summary is given of avaialable literature on acute toxicity (page 16 -17):
"2-Chloroethanol is toxic when administered to laboratory animals at the concentrations and by the routes shown in Table 1. 2-Chloroethanol is
highly irritating to mucous membranes but produces little if any reaction upon contact with rabbit skin. It is not a sensitizer in the guinea pig test. Toxic amounts can be absorbed through the skin without causing dermal irritation (Gleason et al., 1969). Toxic reactions in humans exposed to 2-chloroethanol dermally or by inhalation were first reported by Koelsch (1927). Human fatalities have resulted from ingestion, inhalation, or dermal contact with 2 - chloroethanol (Goldblatt and Chiesman, 1944; Bush et al., 1949; Ballotta et al., 1963; Saitanov and Konanova, 1976). In all cams, neurotoxic symptoms were described. Death was attributed to cardiac and respiratory collapee. Guess (1970), in a study of the response of rabbit
tissues, showed that mucosal tissue was more sensitive to 2-chloroethanol than to ethanol; edema and erythema were produced by both. Of
particular interest in this study were tissues that might come in contact with ethylene oxide sterilized plastic devices used in medical or surgical procedures, devices that might contain residues of 2-chloroethanol. On intracutaneous administration, 2-chloroethanol was more toxic than ethanol; a 1: 10 dilution caused hemorrhagic reactions within 15 minutes, and affected areas became necrotic within 24 hours. Histologic examination showed localized edema, cellular destruction, and infiltration by polymorphonuclear leukocytes and lymphocytes.
Kronevi et al. (1979) studied the effects of several industrial solvents on the skin of guinea pigs. Exposure of guinea pig skin to 2-chloroethanol
produced pyknosis of the basal cell nuclei; severity progressively increased and all epidermal layers were affected. Perinuclear edema was progressive, and cytoplasmic vacuolization occurred after 16 hours' exposure. The livers of animals administered 2-chloroethanol showed centrilobular hydropic changes characterized by large, clear spaces in the cytoplasm. Similar but less severe skin changes were induced
by carbon tetrachloride, hexane, or toluene."
Justification for classification or non-classification
2 -chloroethanol is classified as " R26/27/28 Very toxic by inhalation, in contact with skin and if swallowed" according to Directive 67/548/EEC Annex I. This will be replaced by the classification according to Regulation (EC) 1272/2008 (CLP) Annex VI.
"Acute Tox. 2, H330 Fatal if inhaled"
"Acute Tox. 1, H310 Fatal in contact with skin" "Acute Tox. 2, H300 Fatal if swallowed"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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