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EC number: 285-561-1 | CAS number: 85117-09-5 Mixtures of chemical substances produced by burning (below 1200°C) natural variants of limestone or chalk containing from 10 to 20%, or more, of clayey or siliceous materials which are predominantly SiO2, Al2O3 and iron oxide. Consist primarily of 2CaOsb.2, Ca(OH)2, CaO and 2CaOsb.2O3. 3CaO.2SiO2, 4CaOsb.2O3. Fe2O3, 2CaOsb.2O3sb.2, CaCO3 and SiO2 may also be included.
- 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
Basic toxicokinetics
Administrative data
- Endpoint:
- basic toxicokinetics in vivo
- Type of information:
- experimental study
- Adequacy of study:
- supporting study
- Study period:
- no data available
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- study well documented, meets generally accepted scientific principles, acceptable for assessment
Data source
Reference
- Reference Type:
- publication
- Title:
- Kinetics of calcium, strontium, barium, and radium in rats
- Author:
- Domanski, T.; et al.
- Year:
- 1 969
- Bibliographic source:
- In: Mays, C.F.; et al. (Eds.): Delayed Effects of Bone-Seeking Radionuclides, Univ. of Utah Press, 79-94
Materials and methods
- Objective of study:
- distribution
- excretion
- other: retention
Test guideline
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- The distribution, retention and excretion of different radionuclides administered in a single i.v. dose per test animal were determined.
- GLP compliance:
- no
Test material
- Reference substance name:
- Calcium
- EC Number:
- 231-179-5
- EC Name:
- Calcium
- Cas Number:
- 7440-70-2
- IUPAC Name:
- calcium
- Details on test material:
- - Name of test material (as cited in study report): Calcium ion (unspecified)
No further details are given.
Constituent 1
- Radiolabelling:
- yes
- Remarks:
- 45Ca radioisotopes
Test animals
- Species:
- rat
- Strain:
- Wistar
- Sex:
- male/female
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Age at study initiation: 8 months old
- Diet: For several weeks before and throughout the experiment, the rats were fed a diet containing 0.5 % Ca and 0.5 % P.
- Water: ad libitum
ENVIRONMENTAL CONDITIONS
No further details are given.
Administration / exposure
- Route of administration:
- intravenous
- Vehicle:
- other: acetate buffer solution of pH 4
- Details on exposure:
- no data
- Duration and frequency of treatment / exposure:
- single administration
Doses / concentrations
- Remarks:
- Doses / Concentrations:
Group I: 16 µCi of 45Ca and 5 µCi of 85Sr;
Group II: 0.8 µCi 85Sr and 1.7 µCi 133Ba;
Group III: 0.75 µCi 226Ra.
- No. of animals per sex per dose / concentration:
- 120 albino rats were used in total.
- Control animals:
- not specified
- Positive control reference chemical:
- No positive control substance was tested.
- Details on study design:
- - Dose selection rationale: no data
- Rationale for animal assignment (if not random): no data - Details on dosing and sampling:
- PHARMACOKINETIC STUDY (Absorption, distribution, excretion)
- Tissues and body fluids sampled: urine, faeces, blood, plasma and other tissues, bones
- Time and frequency of sampling: The animals were sacrificed serially in ether narcosis at 1, 2, 4, 6, 12, 18, 24, 48, 96 and 408 or 432 hours after administration of the isotopes. Blood was withdrawn at death, and the plasma was obtained by centrifugation in the presence of heparin.
From each animal at least one femur and one tibia were sampled for calcium assay and activity measurements.
Urine and faeces were collected quantitatively in metabolic cages in selected 20 hour periods from the first through the sixteenth day after injection of the radionuclides.
- Other: Plasma, bones, urine, faeces and in some cases whole carcasses were wet ashed with nitric acid and hydrogen peroxide, diluted to a constant volume, and appropriate aliquots analysed for stable calcium by the method of Bett and Fraser. The total and specific activity of 45Ca in the whole body was determined from beta-counting of the wet-ashed bones and the residual carcasses, corrected for self-absorption and radioactive decay.
METABOLITE CHARACTERISATION STUDIES
not examined - Statistics:
- no data
Results and discussion
- Preliminary studies:
- not performed
Toxicokinetic / pharmacokinetic studies
- Details on absorption:
- not examined
- Details on distribution in tissues:
- The calcium concentration in plasma was close to 100 µg/mL (mean value of 100.4 µg/mL for all groups). It appears that 24 hours after injection, the radioactivity per g Ca in the plasma fell off exponentially.
One day after injection, the retention of the 3 elements Ca, Ba, and Sr was almost identical; later, however, the strontium tracer disappeared from the body faster than did those of calcium and barium.
After 96 hours the highest retention in the bones was that for 133Ba with values for the other isotopes in the decreasing order 45Ca > 226Ra > 85Sr. At that time, levels in the tibiae were consistently lower than in the femora, by 10 to 35 % for all the elements studied. The relative retention for the different radionuclides in single bones is similar to that for whole-body retention.
- Details on excretion:
- The average urinary excretion of calcium over a 16 day period was 0.044, 0.062 and 0.058 mg/hour in group I, II and III, respectively.
The corresponding values for the total faecal calcium were 1.42, 1.02 and 1.47 mg/hour. The endogenous faecal calcium in group I was 0.05 mg/hour.
Metabolite characterisation studies
- Metabolites identified:
- not measured
- Details on metabolites:
- not examined
Applicant's summary and conclusion
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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