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EC number: 215-628-2 | CAS number: 1335-30-4
- 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
Oral:
LD50: > 2000 mg/kg bw for rats
Inhalation:
LC50: > 2.07 mg/L , 4 hours, limit test, rats (RA calcined Kaolin)
Dermal:
LD50: > 5000 mg/kg bw for rabbit after 2 observation days (RA Silicic acid, aluminium sodium salt)
Key value for chemical safety assessment
Additional information
Oral
The acute oral toxicity of Silicic acid, aluminium salt was tested according to OECD guideline 423 (Colas, 2010, RL1). The test substance was administered by gavage to six female rats at a fixed dose of 2000 mg/kg bw. During the observation period of 14 days, no mortality occured and no signs of toxicity were recorded. Thus, the oral LD50 is > 2000 mg/kg bw. In accordance with OECD guideline 423, the LD50 cut-off of the test item may be considered higher than 5000 mg/kg bw for the oral route in the rat.
Inhalation
No experimental data are available for silicic acid, aluminium salt regarding acute inhalation toxicity, but there is an acute inhalation study performed with aerosolized powder of the structurally related compound M-97-009 kaolin, calcined (Engelhard Corp., 1997, RL2). Five male and five female Sprague-Dawley rats were exposed to 2.07 mg/L kaolin, calcined in the air of whole body exposure chambers for 4 hours. The mass median aerodynamic diameter was estimated to be 2.5 microns. No mortality occurred during the study. Clinical signs were ocular and nasal discharge, irregular respiration, hunched posture and hypoactivity during the exposure time. All rats recovered from these symptoms within 17 hours after exposure. Gross necropsy findings at terminal sacrifice revealed red foci on the surface of the lungs of one female. Apart from red lung discoloration consistent with CO2 inhalation (the euthanasia procedure), all other tissues and organs appeared normal. The LC50 is > 2.07 mg/l air.
Dermal
No data were located for silicic acid, aluminium salt regarding acute dermal toxicity. But there are data available for structurally related compounds for this endpoint.
After acute dermal application of 2000, 3000, 4000 and 5000 mg/kg bw of Zeolex 23A as aqueous paste to the intact skin of 4 rabbits per dose for 24 hours under occlusive conditions, no signs of systemic or organ toxicity were recorded and no deaths occured. Dermal reactions were limited to slight erythema and edema which were fully reversible at the latest within 4 days (Woltjen and Calkins, 1978, RL2). The dermal LD50 is > 5000 mg/kg bw.
After acute dermal application of 2000 mg/kg bw of Syloid 244 as powder to the intact skin of rabbits for 24 hours under occlusive conditions, no signs of systemic or organ toxicity were recorded and no deaths occured. Not even erythemas or edemas were observed 24 and 48 hours after exposition (Calkins, 1976, RL2). The dermal LD50 is > 2000 mg/kg bw.
Other routes
Following intratracheal inoculation of 0 or 5 mg of the read across substance Indian Kaolin in 0.1 mL NaCl the pulmonary fibrogenic response of the test substance was investigated in mice over a period of 210 days. The test substance incited acute inflammatory reaction at early periods followed by macrophage reaction, proliferation of fibroblasts and formation of focal fibrotic areas comprised of thick dense reticulination (grade II). However, the fibrotic lesions in mice at 210 days were quite different to that of nodular or diffuse interstitial fibrotic lesions described in Kaolin workers (Sahu et al., 1978, RL2).Justification for classification or non-classification
Based on the results obtained, silicic acid, aluminium salt does not fulfill the criteria to be classified for acute toxicity according to DSD (67/548/EEC) or CLP (1272/2008/EC).
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