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Diss Factsheets
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EC number: 200-756-3 | CAS number: 71-55-6
- 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
Acute Toxicity: other routes
Administrative data
- Endpoint:
- acute toxicity: other routes
- Type of information:
- experimental study
- Adequacy of study:
- supporting study
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: GLP study conducted by reputable laboratory
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 986
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- other: EEC 84/449/EEC, Annex 5, B1
- Deviations:
- no
- GLP compliance:
- yes
- Limit test:
- yes
Test material
- Reference substance name:
- 1,1,1-trichloroethane
- EC Number:
- 200-756-3
- EC Name:
- 1,1,1-trichloroethane
- Cas Number:
- 71-55-6
- Molecular formula:
- C2H3Cl3
- IUPAC Name:
- 1,1,1-trichloroethane
- Details on test material:
- -Name of test material (as cited in study report): BALTANW D (solvant du Foraperle 219). Stabilised 1,1,1-trichloroethane.
- Storage condition of test material: 4 0C
-No other details given:
Constituent 1
Test animals
- Species:
- rat
- Strain:
- Sprague-Dawley
- Sex:
- male/female
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source:Charles River, France
- Weight at study initiation: males 162 g and females 146 g
- Housing: 5 rats of the same sex per polycarbonate cage
– Diet: ad libitum A04C pelleted diet (U.A.R., 91360 Villemoisson sur Orge, France)
- Water : ad libitum drinking water filtered by a Millipore membrane (0.2µm)
- Acclimation period: > 5days
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 22+/-3°C
- Humidity (%): 30-70%. 12
- Photoperiod (hrs dark / hrs light): 12/12
IN-LIFE DATES: October 8th 1985
Administration / exposure
- Route of administration:
- intraperitoneal
- Vehicle:
- unchanged (no vehicle)
- Doses:
- 2.0 ml/kg
- No. of animals per sex per dose:
- 5
- Control animals:
- no
- Details on study design:
- - Duration of observation period following administration: 14 days
- Frequency of observations and weighing: clinical signs recorded once daily (with increase frequency in the first 3 hours after administration), animals weighed on days 1, 5, 8 and 15
- Necropsy of survivors performed: yes
Results and discussion
Effect levelsopen allclose all
- Sex:
- female
- Dose descriptor:
- LD50
- Effect level:
- > 2 000 mL/kg bw
- Remarks on result:
- other: no mortalities
- Sex:
- male
- Dose descriptor:
- LD50
- Effect level:
- < 2 000 mL/kg bw
- Remarks on result:
- other: 4/5 mortalities
- Mortality:
- Four male mortalities at the highest dose tested (2 ml/kg). On Days 1, 2 and 10
- Clinical signs:
- After dose administration all animals appeared sedated, had loss of balance and pilo-erection. 3 hours after administration females showed pilo-erection only and had recovered by Day 2.Surviving males had no clinical signs by Day 4.
- Body weight:
- All females showed continued weight gain during the 14 day observation period. One surviving male showed reduced weight gain on Days 5 and 8: this animal died on Day 10. The surviving male showed acceptable weight gain throughout the observation period
- Gross pathology:
- The male that died on Day 10 had haemorrhaging of the intestine. No other macroscopic findings were recorded at necropsy.
Applicant's summary and conclusion
- Conclusions:
- Under these experimental conditions, the oral LD50 of 1,1,1-trichloroethane is > 2 ml/kg for females and less than 2 ml/kg in males, following intra-peritoneal administration.
- Executive summary:
The Acute intra-peritoneal toxicity of 1,1,1-trichloroethane was evaluated in male and female rats in compliance with principles of Good Laboratory Practices. Animals were treated and then observed for 14 days for mortality, clinical signs and effect on body weight.
No female mortality was recorded in the 14 day-observation period, but 4/5 males had died by Day 10. Transient clinical signs (sedation, loss of balance, pilo-erection) were o served in both sexes. Females showed no effect on body weight.
Under these experimental conditions, the oral LD50 of 1,1,1-trichloroethane is > 2 ml/kg for females and less than 2 ml/kg in males, following intra-peritoneal administration.
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