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Diss Factsheets
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EC number: 231-298-2 | CAS number: 7487-88-9
- 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
Key value for chemical safety assessment
Additional information
No Ames or chromosome aberration study with magensium sulphate is present.
However, an in vitro Ames test performed according to OECD test guideline 471 with potassium sulphate showed no mutagenicity with or without metabolic activation in 4 strains of Salmonella typhimurium (TA98, TA100, TA1535 and TA1537) and in E. coli bacteria (WP2 uvr A). The substance was tested up to the maximum concentration. In a second in vitro study according to OECD test guideline 473, CHO cells were exposed to 217.5, 435, 870, and 1,740 μg/mL with and without metabolic activation. No chromosome abberrations were found.
An in vitro TK assay in L5178Y mouse lymphoma cells with magnesium sulphate performed according to OECD 476 was present, showing no genotoxicity. Cells were exposed to a maximum of 2 µg/mL without metabolic activation and to a maximum of 17 μg/mL with metabolic activation and treated for 3 or 24 hours. Test concentrations were based upon cytotoxicity found in the screening study at
at dose levels of 1 or 3 µg/mL in the absence of metabolic activation for 24 or 3 hours treatment, respectively and at dose levels of 33 µg/mL in the presence of metabolic actvation.
In addition, ammonium sulphate also showed no mutagenicity in several in vitro tests, such as the Ames test and a chromosome aberration study.
Short description of key information:
Only in vitro studies are present for sulphate salts. Potassium and ammonium sulphate were not mutagenic in Ames and chromosome aberration studies. Magensium sulphate itself was negative in a TK assay in mouse lymphoma cells.
Endpoint Conclusion: No adverse effect observed (negative)
Justification for classification or non-classification
The available data indicate that no classification is required with regard to mutagenicity for magnesium sulphate according to Directive 67/548/EC and the CLP directive.
Information on Registered Substances comes from registration dossiers which have been assigned a registration number. The assignment of a registration number does however not guarantee that the information in the dossier is correct or that the dossier is compliant with Regulation (EC) No 1907/2006 (the REACH Regulation). This information has not been reviewed or verified by the Agency or any other authority. The content is subject to change without prior notice.
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