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Registration Dossier
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EC number: 201-201-8 | CAS number: 79-38-9
- 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

Endpoint summary
Administrative data
Key value for chemical safety assessment
Effects on fertility
Additional information
Short description of key information:
No toxicity concern was found for fertility in the existing repeated
dose toxicity studies and in a prenatal developmental toxicity test.
Therefore based on REACH, a two generation test does not need to be
conducted.
Effects on developmental toxicity
Description of key information
There was no evidence for developmental abnormalities at any level. Decreased body weight gain and food consumption was reported for the dams exposed to 90 and 180 ppm of CTFE. Decreased fetal weight and delayed ossification was seen in pups from dams exposed to 180 ppm. Based on these, the NOAEC for developmental toxicity was considered as 90 ppmV. However, even at the highest concentration 180 ppm, there was no evidence for developmental abnormalities.
Effect on developmental toxicity: via inhalation route
- Dose descriptor:
- NOAEC
- 428.72 mg/m³
Additional information
A prenatal toxicity test (Gary M. Hoffman, B.A. 2005) was conducted according to OECD test guideline 414, which was compliant with GLP. In the test, groups of 25 time-mated female rats were exposed once daily for 6 hours/day, 7 days/week during gestation days 6-19 and euthanized and necropsied on gestation day 20. Exposure levels were monitored using an on-line IR sampling procedure. Exposure at 180 ppm resulted in significant body weight loss in the dams. As a consequence, exposure to this group was terminated prior to the final scheduled exposure. However the rats were evaluated at the end of the gestation period along with the rats from the other groups. There was no evidence for developmental abnormalities at any level. Decreased body weight gain and food consumption was reported for the dams exposed to 90 and 180 ppm of CTFE. There was also slight reduction in the state of ossification of the fetal skeleton at the 180 ppm exposure level, but for the sporadic incidences of other fetal variants and abnormalities there was no indication of association with test substance exposure.
Based on above results, exposure at 30 ppm was considered as the no-observed-adverse-effect-level ((NOAEL) for maternal toxicity, exposure at 90 ppm as NOAEL for developmental toxicity, and 180 ppm as NOAEL for teratogenicity. The key value was selected as 90 ppm for developmental toxicity corresponding to 428.72 mg/m3in air at 25°C and 760 Torr..
.
Justification for classification or non-classification
There was no evidence for developmental abnormalities at any level set in the test. Furthermore no toxic concern for fertility was found in repeated dose toxicity test, neither in the prenatal toxicity test. Therefore CTFE dose not meet any criteria for reproductive toxicity classification under Regulation (EC) No 1272/2008.
Additional information
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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