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Diss Factsheets
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EC number: 233-140-8 | CAS number: 10043-52-4
- 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
Endpoint summary
Administrative data
Description of key information
The combined oral LD50 for male and female rats, determined in a GLP-compliant guideline study, was 2301 mg/kg bw. The dermal LD50 for rabbits was above 5000 mg/kg bw. No reliable animal data on acute inhalation toxicity are available; however, human data suggest that calcium chloride is not acutely toxic by inhalation. A non-reliable acute toxicity study with rats reported signs of respiratory tract irritation at 40 and 160 mg/m3.
Key value for chemical safety assessment
Acute toxicity: via oral route
Endpoint conclusion
- Dose descriptor:
- LD50
- Value:
- 2 301 mg/kg bw
Acute toxicity: via dermal route
Endpoint conclusion
- Dose descriptor:
- LD50
- Value:
- 5 000 mg/kg bw
Additional information
The acute toxicity of calcium chloride is low. The combined oral LD50 value in the GLP-compliant study with rat was 2301 mg/kg bw (Toxicological Laboratories Limited, 1987). The dermal LD50 value in the study with rabbits was above 2000 mg/kg bw (Carreon et al., 1981a). No reliable animal data are available on the acute inhalation toxicity; however, in accordance with Column 2 of REACH Annex VIII, the study does not need to be conducted, as sufficient data are available on two other routes of exposure, oral and dermal. In the acute inhalation toxicity study with rats of low reliability, signs of irritation of the respiratory tract were described at both exposure levels (40 and 160 mg/m3), suggesting that inhalation of calcium chloride can cause an irritation of the respiratory tract. As no deaths were observed, LC50 was established to exceed 160 mg/m3.
In addition, Vinnikov et al. (1962) reported treating tuberculosis patients with aerosol inhalations of 2 -5% aqueous calcium chloride.The number of inhalations varied from below 10 (24 patients), till over 30 (2 patients). Several patients reported irritation of mucos membranes of pharinx and throat and unpleasant sensation in mouth already after the first inhalations. However, the frequency of such cases was described as minor by the authors. Overall calcium chloride inhalations were said to have beneficiary effects on disease symptoms (improved quality of spatum, decreased amounts of spatum, improved ease of spatum expellance, decreased frequency of coughing). These data are considered to prove that calcium chloride is not acutely toxic by inhalation.
Justification for classification or non-classification
The combined oral LD50 value in the GLP-compliant study with rat was 2301 mg/kg bw. The dermal LD50 value in the study with rabbits was above 5000 mg/kg bw. These values are above the cut-off limit of 2000 mg/kg bw, established by the CLP Regulation (EC) No. 1272/2008. Therefore classification for acute toxicity is not warranted.
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