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EC number: 211-479-2 | CAS number: 650-51-1
- 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
Skin sensitisation
Administrative data
- Endpoint:
- skin sensitisation: in vivo (non-LLNA)
- Type of information:
- experimental study
- Adequacy of study:
- weight of evidence
- Study period:
- From 09.02.2004 to 12.03.2004
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Test method according to OECD guideline 406, but no data on GLP. No data on positive control.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 004
- Report date:
- 2004
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 406 (Skin Sensitisation)
- Deviations:
- no
- GLP compliance:
- not specified
- Type of study:
- Buehler test
Test material
- Reference substance name:
- TCA
- EC Number:
- 211-479-2
- EC Name:
- TCA
- Cas Number:
- 650-51-1
- Molecular formula:
- C2HCl3O2.Na
- IUPAC Name:
- trichloroacetic acid
- Details on test material:
- - Name of test material (as cited in study report): Tricloroacetato de sodio
- Analytical purity: 99 % (w/w)
Constituent 1
In vivo test system
Test animals
- Species:
- guinea pig
- Strain:
- not specified
- Sex:
- male/female
- Details on test animals and environmental conditions:
- TEST ANIMALS
- Age at study initiation: Young adult animals
- Housing: Animals were housed in cages groups of 5.
- Diet (e.g. ad libitum): Ad libitum
- Water (e.g. ad libitum): Ad libitum
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 20 ºC
- Humidity (%): 60 %
- Photoperiod: 12 hrs dark / 12 hrs light
IN-LIFE DATES: From 09.02.2004 to 12.03.2004
Study design: in vivo (non-LLNA)
Inductionopen allclose all
- Route:
- epicutaneous, occlusive
- Vehicle:
- petrolatum
- Concentration / amount:
- 0.5 g test substance
Challengeopen allclose all
- Route:
- epicutaneous, occlusive
- Vehicle:
- petrolatum
- Concentration / amount:
- 0.5 g test substance
- No. of animals per dose:
- 20 guinea pigs (10 male and 10 females)
- Details on study design:
- MAIN STUDY
A. INDUCTION EXPOSURE
- No. of exposures: 3
- Exposure period: 6 hours
- Test groups: 0.5 g test substance
- Control group: 0.5 mL vehicle
- Frequency of applications: one each 7 days
- Duration: Three weeks period
B. CHALLENGE EXPOSURE
- No. of exposures: 1
- Day(s) of challenge: On day 28
- Exposure period: 6 hours
- Test groups: 0.5 g test substance
- Control group: 0.5 mL vehicle
- Evaluation (hr after challenge): 30 and 45 hours
Classification system for effects: Described by Magnusson Kligman - Positive control substance(s):
- not specified
Results and discussion
In vivo (non-LLNA)
Resultsopen allclose all
- Hours after challenge:
- 30
- Group:
- test chemical
- Dose level:
- 0.5 g
- No. with + reactions:
- 0
- Total no. in group:
- 20
- Remarks on result:
- other: . Hours after challenge: 30.0. Group: test group. Dose level: 0.5 g. No with. + reactions: 0.0. Total no. in groups: 20.0.
- Hours after challenge:
- 54
- Group:
- test chemical
- Dose level:
- 0.5 g
- No. with + reactions:
- 0
- Total no. in group:
- 20
- Remarks on result:
- other: . Hours after challenge: 54.0. Group: test group. Dose level: 0.5 g. No with. + reactions: 0.0. Total no. in groups: 20.0.
- Hours after challenge:
- 30
- Group:
- negative control
- No. with + reactions:
- 0
- Total no. in group:
- 10
- Remarks on result:
- other: . Hours after challenge: 30.0. Group: negative control. No with. + reactions: 0.0. Total no. in groups: 10.0.
- Hours after challenge:
- 54
- Group:
- negative control
- No. with + reactions:
- 0
- Total no. in group:
- 10
- Remarks on result:
- other: . Hours after challenge: 54.0. Group: negative control. No with. + reactions: 0.0. Total no. in groups: 10.0.
Any other information on results incl. tables
The results of this study show that sodium trichloroacetate does not cause skin sensitization.
Applicant's summary and conclusion
- Interpretation of results:
- not sensitising
- Remarks:
- Migrated information
- Conclusions:
- The results of this study show that sodium trichloroacetate does not cause skin sensitization.
- Executive summary:
This study has been carried out with the aim of evaluating the possible sensitizer effects of the product sodium trichloroacetate on the skin of white guinea pigs (Cavia porcellus). The method of the assay has been developed according to the OECD Protocol No. 406, 1992. After initial exposure to the product being tested, animals are exposed in order to prove whether a state of hypersensitivity to the product has been induced. A group of twenty adult guinea pigs (ten female and ten males) is initially exposed (induction exposure), to three inductive applications, one every 7 days. After a three weeks period (Induction period), during which the immune response has developed, animals are exposed to a single application aimed at proving the sensitization to the product (challenge exposure). The range and degree of skin reaction after the challenge exposure are assessed by comparing this group of animals with the witness group, not treated, after their exposure to the challenge. During the assay period, environmental conditions were kept constant (Temperature: 20°C, Humidity: 60 % and Photoperiod: twelve hours light and twelve hours darkness). The results of this study show that sodium trichloroacetate does not cause skin sensitization.
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