Registration Dossier
Registration Dossier
Data platform availability banner - registered substances factsheets
Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.
The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.
Diss Factsheets
Use of this information is subject to copyright laws and may require the permission of the owner of the information, as described in the ECHA Legal Notice.
EC number: 253-425-0 | CAS number: 37247-91-9
- 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
Developmental toxicity / teratogenicity
Administrative data
- Endpoint:
- developmental toxicity
- Type of information:
- migrated information: read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- key study
- Study period:
- no data available
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: see 'Remark'
- Remarks:
- The Japanese paper with an abstract and presentation of results in English is considered as a reasonably well-documented publication. The study allows the derivation of a NOAEL value for developmental toxicity of Mg. Under physiological conditions, the hydroxyl-ions released from lime following oral adminstration have been neutralised in the GI tract and are therefore not relevant for consideration of systemic toxicity. Therefore for assessment of any systemic effects (including develpmental toxicity) of lime following administration via the oral route, the magnesium ion Mg2+ is the chemical species of interest. In the current study, magnesium was administered in the form of magnesium chloride, the chloride ion being an ubiquitous component of mammalian mineral supply via the diet, omnipresent in body fluids and involved in osmoregulation, and therefore of limited toxicologically relevance at the tested doses. The objective of the study was the evaluation of any effects of magnesium. In view of the the limited relevance of the anionic counter-ions discussed here, magnesium released both from calcium magnesium oxide and magnesium chloride can be considered as structurally equivalent, and the results of the study can be used by read-across.
Data source
Reference
- Reference Type:
- publication
- Title:
- Teratogenicity study of magnesium chloride hexahydrate in rats
- Author:
- Usami, M.; et al.
- Year:
- 1 996
- Bibliographic source:
- Bull. Natl. Inst. Health Sci. 114, 16-20
Materials and methods
Test guideline
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- Teratogenicity test, not performed according to OECD 414, but fulfilling basic scientific principles for evaluating this endpoint.
- GLP compliance:
- no
- Limit test:
- no
Test material
- Reference substance name:
- 7791-18-6
- EC Number:
- 616-575-1
- Cas Number:
- 7791-18-6
- IUPAC Name:
- 7791-18-6
- Reference substance name:
- Magnesium chloride hexahydrate
- IUPAC Name:
- Magnesium chloride hexahydrate
- Details on test material:
- - Name of test material (as cited in study report): Magnesium chloride hexahydrate
- Physical state: solid
No further details are given.
Constituent 1
Constituent 2
Test animals
- Species:
- rat
- Strain:
- other: No details could be extracted from the Japanese publication.
- Details on test animals or test system and environmental conditions:
- No details could be extracted from the Japanese publication.
Administration / exposure
- Route of administration:
- oral: gavage
- Vehicle:
- water
- Details on exposure:
- PREPARATION OF DOSING SOLUTIONS: MgCl2 x 6 H2O dissolved in distilled water was given to pregnant Wistar rats by gavage.
No further details could be drawn from the text, since the publication is written in Japanese. - Analytical verification of doses or concentrations:
- not specified
- Details on analytical verification of doses or concentrations:
- No details available.
- Details on mating procedure:
- No details could be drawn from the Japanese publication.
- Duration of treatment / exposure:
- MgCl2 was given to rats from day 6-15 of pregnancy.
- Frequency of treatment:
- Once daily.
- Duration of test:
- The rats were killed on day 20 of gestation.
Doses / concentrationsopen allclose all
- Remarks:
- Doses / Concentrations:
0 mg/kg bw/day
Basis:
nominal in water
- Remarks:
- Doses / Concentrations:
200 mg/kg bw/day
Basis:
nominal in water
- Remarks:
- Doses / Concentrations:
400 mg/kg bw/day
Basis:
nominal in water
- Remarks:
- Doses / Concentrations:
800 mg/kg bw/day
Basis:
nominal in water
- No. of animals per sex per dose:
- 4 rats
- Control animals:
- yes
- Details on study design:
- No further details are given.
Examinations
- Maternal examinations:
- DETAILED CLINICAL OBSERVATIONS: Yes
BODY WEIGHT: Yes
- Time schedule for examinations: Body weights were recorded on days 0, 1, 2, 3, 6, 9, 12, 15, 17 and 20.
FOOD CONSUMPTION AND COMPOUND INTAKE: Yes
- Time schedule: Food consumption was recorded on days 1, 3, 6, 9, 12, 15, 17 and 20.
No further details could be extracted from the Japanese publication. - Ovaries and uterine content:
- The ovaries and uterine content was examined after termination: Yes
Examinations included:
- Gravid uterus weight: No data
- Number of corpora lutea: Yes
- Number of implantations: Yes
- Number of early resorptions: No data
- Number of late resorptions: No data
- Other: sex ratio (male/female): Yes
No further details could be extracted from the Japanese publication. - Fetal examinations:
- The pregnant rats were killed on day 20 of gestation and their foetuses were examined for malformations.
- External examinations: Yes: foetal weight
- Soft tissue examinations: Yes
- Skeletal examinations: Yes
No further details could be drawn from the Japanese publication. - Statistics:
- No details could be extracted from the Japanese publication.
- Indices:
- No details could be extracted from the Japanese publication.
- Historical control data:
- No data available.
Results and discussion
Results: maternal animals
Maternal developmental toxicity
- Details on maternal toxic effects:
- Maternal toxic effects:no effects
Details on maternal toxic effects:
No toxic signs were observed in the dams.
Effect levels (maternal animals)
- Dose descriptor:
- NOAEL
- Effect level:
- > 800 mg/kg bw/day
- Basis for effect level:
- other: maternal toxicity
Results (fetuses)
- Details on embryotoxic / teratogenic effects:
- Embryotoxic / teratogenic effects:no effects
Details on embryotoxic / teratogenic effects:
MgCl2 x 6 H2O caused no increased incidences of gross malformations and of visceral and skeletal variations in foetuses.
No toxic signs were observed in the foetuses.
Effect levels (fetuses)
- Dose descriptor:
- NOAEL
- Effect level:
- > 800 mg/kg bw/day
- Basis for effect level:
- other: teratogenicity
Fetal abnormalities
- Abnormalities:
- not specified
Overall developmental toxicity
- Developmental effects observed:
- not specified
Applicant's summary and conclusion
- Conclusions:
- It was concluded that MgCl2 x 6 H2O is not teratogenic in this study. The NOAEL was estimated to be higher than 800 mg/kg bw/d for both the pregnant rats and rat foetuses. This dose level corresponds to a Mg dose of 95.7 mg/kg bw/d.
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.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.