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EC number: 241-234-5 | CAS number: 17194-00-2
- 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

Toxicity to other above-ground organisms
Administrative data
- Endpoint:
- toxicity to other above-ground organisms
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: No guideline study, but study was conducted in a scientifically correct way, and data are useful for the evaluation of Ba-toxicity via oral exposure
Cross-reference
- Reason / purpose for cross-reference:
- reference to same study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 994
Materials and methods
Test guideline
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- Original report not available: mice and rats were fed barium via drinking water for 13wk and 2y.
- GLP compliance:
- not specified
Test material
- Reference substance name:
- barium(2+) dichloride dihydrate
- EC Number:
- 600-412-6
- Cas Number:
- 10326-27-9
- IUPAC Name:
- barium(2+) dichloride dihydrate
Constituent 1
Sampling and analysis
- Analytical monitoring:
- not specified
- Details on sampling:
- not reported in Dallas and Williams, 2001
Test organisms
- Test organisms (species):
- other: rats and mice
- Details on test organisms:
- not reported in Dallas and Williams, 2001
Study design
- Study type:
- laboratory study
- Limit test:
- no
- Total exposure duration:
- 104 wk
Test conditions
- Test temperature:
- not reported in Dallas and Williams, 2001
- Details on test conditions:
- not reported in Dallas and Williams, 2001
- Nominal and measured concentrations:
- not reported in Dallas and Williams, 2001
Results and discussion
Effect concentrationsopen allclose all
- Duration:
- 13 wk
- Dose descriptor:
- other: NOAEL
- Effect conc.:
- 2 000 other: ppm barium chloride dihydrate
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- behaviour
- Remarks on result:
- other: data for rats and mice
- Duration:
- 104 wk
- Dose descriptor:
- other: NOAEL
- Effect conc.:
- 60 other: mg/kg/d
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- other: neoplasms or nonneoplastic lesions
- Remarks on result:
- other: male rat
- Duration:
- 104 wk
- Dose descriptor:
- other: NOAEL
- Effect conc.:
- 75 other: mg/kg/d
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- other: neoplasms or nonneoplastic lesions
- Remarks on result:
- other: female rat
- Duration:
- 104 wk
- Dose descriptor:
- other: NOAEL
- Effect conc.:
- 75 other: mg/kg/d
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- other: kidneys, nephropathy, renal tubule regeneration, lymphoid depletions
- Remarks on result:
- other: male mice
- Duration:
- 104 wk
- Dose descriptor:
- other: NOAEL
- Effect conc.:
- 90 other: mg/kg/d
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- other: kidneys, nephropathy, renal tubule regeneration, lymphoid depletions
- Remarks on result:
- other: female mice
- Details on results:
- The main findings of the long-term exposures (13 wk, 2 yr) are summarized hereunder:
- I3 wk study: It was concluded from the neurobehavioural data that there were no consistent effects on behaviour produced by Ba exposure. The No-observed-adverse-effect-level (NOAEL) for this subchronic study was considered to be 2000 ppm Ba chloride dihydrate; this corresponds to 110 mg Ba/kg/d for male rats, 115 mg Ba/kg/d for female rats, 205 mg Ba/kg/d for male mice, and 200 mg Ba/kg/d for female mice. These data were also reported by Dietz et al (1992).
- 13 wk study: Death in mice in the highest dose groups (450 mg Ba/kg/d for males and 495 mg Ba/kg/d for females) were associated with renal toxicity. Renal lesions in rats were much less severe at the highest dose level (200 mg Ba/kg/d for males and 180 mg Ba/kg/d for females).
- In the 2yr study, the evaluated endpoints were hematology values and increases in neoplasms; the conclusion was “no increased incidences of neoplasms or nonneoplastic lesions that could be attributed to BaCl2 dihydrate” for rats receiving average dose rates of 60 (male) and 75 (female) mg/kg/d.
- For mice (endpoints were kidneys, nephropathy, renal tubule regeneration, lymphoid depletions) the identified NOAEL was 75 mg Ba/kg/d for males, and 90 mg Ba/kg/d for females.
Applicant's summary and conclusion
- Conclusions:
- Data can be used in a weight of evidence approach for the derivation of a PNECoral (secondary poisoning)
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