Registration Dossier
Registration Dossier
Data platform availability banner - registered substances factsheets
Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.
The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.
Diss Factsheets
Use of this information is subject to copyright laws and may require the permission of the owner of the information, as described in the ECHA Legal Notice.
EC number: 206-564-6 | CAS number: 354-58-5
- 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
Repeated dose toxicity: oral
Administrative data
- Endpoint:
- short-term repeated dose toxicity: oral
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 1992-01 - 1992-03
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Study well documented and performed under GLP compliance; although not performed according to a guideline, generally accepted scientific principles were met.
Cross-reference
- Reason / purpose for cross-reference:
- reference to same study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 996
- Report date:
- 1996
Materials and methods
Test guideline
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- Adult male Fischer 344/N rats received the test item 1,1,1-trichloro-2,2,2-trifluoroethane by gavage daily over a test period of 21 days. Subsequently, the liver and kidney of these rats were evaluated histopathologically. Urinalysis was also performed.
- GLP compliance:
- yes
- Limit test:
- no
Test material
- Reference substance name:
- Trichlorotrifluoroethane
- EC Number:
- 206-564-6
- EC Name:
- Trichlorotrifluoroethane
- Cas Number:
- 354-58-5
- Molecular formula:
- C2Cl3F3
- IUPAC Name:
- 1,1,1-trichloro-2,2,2-trifluoroethane
- Details on test material:
- - Name of test material (as cited in study report): 1,1,1-Trichloro-2,2,2-trifluoroethane & 1,1,1TriC-2,2,2-TFE
- Physical state: liquid
- Color: colorless
- Analytical purity: 99%
- Impurities: 0.8% 1,1,2-trichloro-1,2,2-trifluoroethane (measured with gas chromatography)
- Lot/batch No.: 0730191-2
- Supplier: Columbia Organic Chemical Company, Inc., Camden SC
- Stability under test conditions: The test item showed losses in concentration when stored either at room temperature or at 5°C which wewre attributed to the volatility of the compound.
- Storage condition of test material: at room temperature in the dark
Constituent 1
Test animals
- Species:
- rat
- Strain:
- Fischer 344
- Sex:
- male
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: Taconic Farms, Germantown NY
- Age at study initiation: 15 weeks
- Weight at study initiation: 286-288 g
- Housing: 5 per cage
- Diet (e.g. ad libitum): ad libitum
- Water (e.g. ad libitum): ad libitum
- Acclimation period: 15 d
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 20.6-23.9 °C
- Humidity (%): 35-65 %
- Air changes (per hr): 10
- Photoperiod (hrs dark / hrs light): 12/12
IN-LIFE DATES: From: 1992-02-07 (first dosing) To: 1992-02-28
Administration / exposure
- Route of administration:
- oral: gavage
- Vehicle:
- corn oil
- Details on oral exposure:
- PREPARATION OF DOSING SOLUTIONS:
Dose formulations were prepared by mixing the test item with corn oil and magnetical stirring. Due to concentration losses of the test item during storage, a second set of ftest item formulations was prepared for the last week of dosing.
VEHICLE
- Vehicle: Corn oil
- Amount of vehicle (if gavage): 5 mL/kg bw
Doses:
vehicle control
116.2 mg/kg bw/day (in report given as: 0.62 mmol/kg bw/day)
232.3 mg/kg bw/day (in report given as: 1.24 mmol/kg bw/day) - Analytical verification of doses or concentrations:
- no
- Duration of treatment / exposure:
- 21 days on 7 d/week
- Frequency of treatment:
- once daily
Doses / concentrationsopen allclose all
- Dose / conc.:
- 116.2 mg/kg bw/day (nominal)
- Dose / conc.:
- 232.3 mg/kg bw/day (nominal)
- No. of animals per sex per dose:
- 5 male rats per dose group
- Control animals:
- yes, concurrent vehicle
- Details on study design:
- - Dose selection rationale: Based on the results of a 2-year study performed with pentachloroethane (NTP Technical Report Series No. 232, NIH Publication No. 83-1788)
- Rationale for animal assignment: random distribution into groups of approximately equal initial mean body weight
The dose levels were set to 0.62 and 1.24 mmol/kg bw/day, which corresponds for 1,1,1-trichloro-2,2,2-trifluoroethane (187.376 g/mol) to 116.2 mg/kg bw/day and 232.3 mg/kg bw/day, respectively.
Examinations
- Observations and examinations performed and frequency:
- CAGE SIDE OBSERVATIONS: Yes
- Time schedule: twice daily
DETAILED CLINICAL OBSERVATIONS: Yes
- Time schedule: weekly
BODY WEIGHT: Yes
- Time schedule for examinations: weekly
OPHTHALMOSCOPIC EXAMINATION: No
HAEMATOLOGY: No
CLINICAL CHEMISTRY:No
URINALYSIS: Yes
- Time schedule for collection of urine: 4 days before end of the study
- Metabolism cages used for collection of urine: Yes
- Animals fasted: Yes
- Parameters checked in table 1 were examined.
NEUROBEHAVIOURAL EXAMINATION: No
OTHER: - Sacrifice and pathology:
- GROSS PATHOLOGY: Yes (see table 2)
HISTOPATHOLOGY: Yes (see table 2) - Statistics:
- Organ and body weight data: Dunnett-test
Urinalysis data: Dunn-test
Significance of dose-response trends: Jonckheere-test
Outlier test: according to Dixon and Massey
Results and discussion
Results of examinations
- Clinical signs:
- no effects observed
- Mortality:
- no mortality observed
- Body weight and weight changes:
- no effects observed
- Urinalysis findings:
- no effects observed
- Organ weight findings including organ / body weight ratios:
- no effects observed
- Gross pathological findings:
- no effects observed
- Histopathological findings: non-neoplastic:
- no effects observed
- Details on results:
- CLINICAL SIGNS AND MORTALITY
All rats administered 1,1,1-Tirchloro-2,2,2-trifluoroethane survived until the end of the study. No clinical signs of toxicity were observed.
BODY WEIGHT AND WEIGHT GAIN
The final mean body weights and mean body weight gains of dosed animals were not distinguishable to those of the control animals (Table 3).
URINALYSIS
There were no significant differences in urinalysis parameters between dosed and control males (Table 6).
ORGAN WEIGHTS
There were no significant differences in organ weights between dosed and control males (Table 5).
HISTOPATHOLOGY
No microscopic effects were present in either the kidney or the liver at either dose level (Table 4).
Effect levels
- Remarks on result:
- not determinable due to absence of adverse toxic effects
Target system / organ toxicity
- Critical effects observed:
- not specified
Any other information on results incl. tables
Table 3: Survival and Body Weights of F344/N Rats in the 3-Week Gavage Study of 1,1,1-Trichloro-2,2,2-trifluoroethane
Dose [mg/kg bw/day] |
Survival |
Mean body weight [g] |
Final weight relative to controls [%] |
||
Initial |
Final |
Change |
|||
Vehicle control |
5/5 |
291 |
323 |
33 |
|
116.2 |
5/5 |
288 |
328 |
40 |
102 |
232.3 |
5/5 |
286 |
320 |
34 |
99 |
Table 4: Kidney Effects in Male F344/N Rats in the 3-Week Gavage Study of 1,1,1-Trichloro-2,2,2-trifluoroethane
Dose [mg/kg bw/day] |
Hyaline droplet nephropathy |
Tubule regeneration |
Granular casts |
116.2 |
0 |
0/5 |
0/5 |
232.3 |
0 |
0/5 |
0/5 |
Table 5: Body and organ weights in Male F344/N Rats in the 3-Week Gavage Study of 1,1,1-Trichloro-2,2,2-trifluoroethane
Organ |
Vehicle control |
1,1,1-Trichloro-2,2,2-trifluoroethane [mg/kg bw/day] |
|
116.25 |
232.50 |
||
Necropsy bw [g] |
323±3 |
328±6 |
320±7 |
Right kidney absolute [g] relative [mg/g bw] |
1.031±0.024 3.19±0.05 |
1.048±0.023 3.19±0.05 |
1.028±0.040 3.21±0.10 |
Liver absolute [g] relative [mg/g bw] |
11.611±0.103 35.92±0.46 |
11.920±0.284 36.33±0.52 |
11.720±0.524 36.61±1.21 |
Right testis absolute [g] relative [mg/g bw] |
1.435±0.038 4.44±0.11 |
1.472±0.025 4.49±0.10 |
1.354±0.080 4.24±0.27 |
Table 6: Urinalysis results of Male F344/N Rats in the 3-Week Gavage Study of 1,1,1-Trichloro-2,2,2-trifluoroethane
Endpoint |
Vehicle control |
1,1,1-Trichloro-2,2,2-trifluoroethane [mg/kg bw/day] |
|
116.25 |
232.50 |
||
Creatinine [mg/dL] |
97.46±9.43 |
72.58±8.61 |
85.14±16.11 |
Glucose [µg/mg creatinine] |
160±6 |
205±11 |
161±12 |
Protein [µg/mg creatinine] |
1.227±78 |
1.461±102 |
1.396±75 |
Aspartate aminotransferase [mU/mg creatinine] |
8±1 |
16±4 |
13±1 |
g-Glutamyltransferase [mU/mg creatinine] |
1.384±78 |
1.533±57 |
1.684±64 |
N-Acetyl-b-D-glucoseaminidase [mU/mg creatinine] |
11±1 |
17±4 |
12±1 |
Volume [mL/16 h] |
7.4±0.9 |
7.8±1.0 |
8.3±2.1 |
Specific gravity |
1.023±0.002 |
1.020±0.002 |
1.021±0.003 |
Applicant's summary and conclusion
- Conclusions:
- No apparent toxicity was observed after 21 oral application of 1,1,1-trichloro-2,2,2-trifluoroethane to male F344/N rats.
- Executive summary:
Repeated dose oral toxicity of 1,1,1-trichloro-2,2,2-trifluoroethane was assessed in a sub-acute 21 day study on male F344/N rats. The study was performed under GLP but no guideline was indicated.
Male rats were administered to the test item in corn oil (nominal concentrations 116.2 and 232.3 mg/kg bw/day) by gavage daily for 21 days. Clinical signs of toxicity and body weights were determined weekly. Cages were checked for dead animals twice a day. Necropsies were performed on all survivors. The right kidney, liver, and right testis were weighed. Organs and tissues were observed for gross lesions. Histopathologic examinations of the right kidney, liver (left lobe), and grossly visible lesions were performed. Urin was collected from all animals using metabolism cages and volume, specific gravity, creatinine, glucose, total protein, aspartate aminotransferase, g-glutamyl transpeptidase, and N-acetyl-D-glucosaminidase were determined.
No apparent signs of toxicity could be observed during or after 21 days of treatment. All animals survived until end of the study without showing clinical signs of toxicity. Body weights, weight gains, organ weights, and urinalysis parameters were similar to those of the controls. No microscopic effects were present in either kidney or liver.
Taken together, sub-acute oral administration of 1,1,1-trichloro-2,2,2-trifluoroethane in concentrations up to 232.3 mg/kg bw/day was not toxic to rats.
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.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.