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Diss Factsheets
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EC number: 206-190-3 | CAS number: 306-83-2
- 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
Key value for chemical safety assessment
Additional information
HCFC 123 has a low acute toxicity following oral, dermal and inhalatory exposure. However, signs of CNS depression and sublethal toxic changes in the liver were observed in acute toxicity experiments.
Oral exposure
An approximate lethal concentration of 9000 mg/kg in male rats administered via gavage was reported by Haskell (1975).
Inhalation
Studies in rats, hamsters and guinea pigs are available. 4 -h exposure in rats (ECETOC, 2005) and hamsters (Allied Signal, 1981) gave consistent results with LC50 of 32000 and 28400 ppm, respectively. CNS depression was observed to occur during the exposure period in those studies, with full recovery of the surviving animals shortly after the cessation of the exposure.
No lethality was observed in guinea pigs exposed up to 30000 ppm for 4 hours, but hepatoxicity was observed at 1000 ppm and above (Marit et al., 1994).
Dermal exposure
Acute dermal toxicity was studied in rats (Haskell, 1988a) and rabbits (Haskell, 1988b). In both studies, no lethality was observed up to the highest tested dose of 2000 mg/kg. No clinical signs were noted in the rabbit study, whereas red nasal and ocular discharges were noted in 2 rats exposed to 2000 mg/kg. No signs of skin irritation were recorded. A slight bodyweight loss was also observed at the end of the 14 -day recovery period.
Justification for classification or non-classification
HCFC 123 does not meet the criteria for acute toxicity classification in accordance with EU Directive 67/548/EEC and EU Classification, Labeling and Packaging of Substances and Mixtures (CLP) Regulation (EC) No. 1272/2008.
In accordance with Directive 67/548/EEC, HCFC 123 is classified as Harmful - possible risk of irreversible effects (Xn R68/20) in view of the significant hepatotoxicity observed in guinea pigs and to the reported data in humans (see Section 7.10.5)
In accordance with Regulation EC 1272/2008 HCFC 123 is classifiable as STOT-SE Category 2 (H371) in view of the weight of evidence (significant hepatotoxicity observed in guinea pigs and reported human data).
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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