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EC number: 244-344-1 | CAS number: 21351-79-1
- 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:
- supporting study
- Study period:
- 1972
- Reliability:
- 4 (not assignable)
- Rationale for reliability incl. deficiencies:
- other: Non GLP and non guideline study, but sufficient for hazard assessment together with read-across to other Cs-salts.
Cross-reference
- Reason / purpose for cross-reference:
- reference to other study
Data source
Referenceopen allclose all
- Reference Type:
- publication
- Title:
- Acute toxicity of cesium and rubidium compounds
- Author:
- Johnson, G.T.; Lewis, R.T. and Wagner, W.D.
- Year:
- 1 975
- Bibliographic source:
- Toxicology and applied pharmacology 32, 239-245 (1975)
- Reference Type:
- publication
- Title:
- Unnamed
- Year:
- 1 972
Materials and methods
Test guidelineopen allclose all
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 406 (Skin Sensitisation)
- Deviations:
- not specified
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- EU Method B.6 (Skin Sensitisation)
- Deviations:
- not specified
- GLP compliance:
- no
- Type of study:
- other: similar to Landsteiner and Jacobs (1935)
Test material
- Reference substance name:
- Caesium hydroxide
- EC Number:
- 244-344-1
- EC Name:
- Caesium hydroxide
- Cas Number:
- 21351-79-1
- Molecular formula:
- CsHO
- IUPAC Name:
- caesium hydroxide
- Reference substance name:
- Cesium hydroxide
- IUPAC Name:
- Cesium hydroxide
- Test material form:
- solid: crystalline
Constituent 1
Constituent 2
In vivo test system
Test animals
- Species:
- guinea pig
- Strain:
- other: albino
- Sex:
- male
- Details on test animals and environmental conditions:
- TEST ANIMALS
- Age at study initiation: young adult
- Weight at study initiation: 300 - 400 g
Study design: in vivo (non-LLNA)
Inductionopen allclose all
- Route:
- intradermal and epicutaneous
- Vehicle:
- water
- Concentration / amount:
- 0.1 % induction and challenge
Challengeopen allclose all
- Route:
- intradermal
- Vehicle:
- water
- Concentration / amount:
- 0.1 % induction and challenge
- No. of animals per dose:
- control: 5 males
test group 10 males - Details on study design:
- MAIN STUDY
A. INDUCTION EXPOSURE
- No. of exposures: The test material was injected three times weekly for a total of nine treatments.
- Exposure period: three weeks
- Test groups: treatment with test material (0.1%)
- Control group: treatment with test material (0.1%)
- Site: back of the animal (clipped free of hair)
B. CHALLENGE EXPOSURE
- No. of exposures: one single treatment
- Day of challenge: 2 weeks after last induction
- Test groups: treatment with test material (0.1%)
- Control group: treatment with vehicle (water)
- Site: back of the animal (clipped free of hair)
- Evaluation (hr after challenge): 24, 48 and 72
EVALUATION CRITERIA:
If the response to the challenge injection is greater in terms of intensity or local inflammatory response than to the sensitizing doses, or the number of animals responding is substantially greater, then the material is considered to be a skin sensitizer. - Positive control substance(s):
- no
Results and discussion
Any other information on results incl. tables
There was no evidence of erythema, swelling or dicolorartion of the test sites after each of the nine sensitizing cutaneous injections or after the challenge dose. These results indicate that cesium hydroxide did not induce cutaneous sensitisation in guinea pigs in any of the 10 test animals.
Applicant's summary and conclusion
- Interpretation of results:
- not sensitising
- Remarks:
- Migrated information Criteria used for interpretation of results: EU
- Conclusions:
- Cesium hydroxide did not induce cutaneous sensitisation in guinea pigs.
- Executive summary:
In a dermal sensitization study with cesium hydroxide (0.1 %) in water, young adult male albino guinea pigs (in total 15 animals) were tested using the method of Landsteiner and Jacobs (1935). The test compound was administered intradermally three times a week, for a total of nine treatments. Following a two-week period with no further injections a challenge of 0.1% was administered the same way. There was no evidence of erythema, swelling or dicolorartion of the test sites after each of the nine sensitizing cutaneous injections or after the challenge dose. These results indicate that cesium hydroxide did not induce cutaneous sensitisation in guinea pigs.
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