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Diss Factsheets
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EC number: 200-877-1 | CAS number: 75-54-7
- 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 key oral LD50 value (0.28 mg/kg based on density of 1.105) is derived from a gavage study (BRRC, 1981) in Wistar rats comparable to the now deleted OECD 401. Sluggishness was the main clinical sign of toxicty, but there were also some instances of dyspnea, unsteady gait and prostration. Gross necropsy mainly revealed discoloured, fluid-filled and/or enlarged organs (liver, spleen, intestines, stomach, kidneys). The key inhalation LD50 value is derived from a whole body one-hour vapour inhalation study (DCC, 2001) in Fischer 344 rats comparable to OECD 403. The principal clinical signs were indicative of respiratory and ocular effects: labored breathing, gasping and rales, ocular opacity that progressed to more severe ocular damage well into the observation period, salivation, green staining of various body surfaces, dried material around the eyes nose and/or mouth, lacrimation, hypoactivity, red and swollen paws and nasal discharge. The most common necropsy finding in this study was ocular damage. There are no acute dermal data.
Key value for chemical safety assessment
Acute toxicity: via oral route
Endpoint conclusion
- Dose descriptor:
- LD50
- Value:
- 280 mg/kg bw
Acute toxicity: via inhalation route
Endpoint conclusion
- Dose descriptor:
- LC50
- Value:
- 8 397.9 mg/m³ air
Additional information
In the case of the inhalation route, there are two reliability score 1 studies; the most recent of these was selected as the key study. The second study supports the LD50 obtained in the key study.
Justification for classification or non-classification
This substance is labelled as 'R22 Harmful if swallowed' according to Directive 67/548/EEC, and the proposed hazard class under Regulation 1272/2008 is 'Acute toxic 3 (oral)' based on an acute oral LD50 of 280 mg/kg (0.25 ml/kg).
In the case of dermal toxicity, there are no existing classification, and there is no evidence to suggest that dichloro(methyl)silane should be classified for acute systemic toxicity.
Labelling for the inhalation route is 'R20 Harmful by inhalation' according to Directive 67/548/EEC, and the proposed hazard class under Regulation 1272/2008 is 'Acute toxic 3 (vapour)', as the LD50 is in the range 2.0 to 10.0 mg/l.
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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