Registration Dossier
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EC number: 225-805-6 | CAS number: 5089-70-3
- 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
Link to relevant study record(s)
Description of key information
Key value for chemical safety assessment
Additional information
There are no in vivo data on the toxicokinetics of (3-chloropropyl)triethoxysilane. The following summary has therefore been prepared based on validated predictions of the physicochemical properties of the substance itself and its hydrolysis products. (3-chloropropyl)triethoxysilane is a moisture-sensitive, volatile liquid that hydrolyses slowly in contact with water (half-life 35 hours at pH 7), generating ethanol and 3-chloropropylsilanetriol. Human exposure can occur via the inhalation or dermal routes. Relevant inhalation and dermal exposure would be predominantly to the parent substance. The toxicokinetics of ethanol is discussed elsewhere and is not included in this summary.
Absorption
Oral: Significant oral exposure is not expected for this substance.
Dermal: Dermal exposure would be to the parent substance. The molecular weight of 3-chloropropyltriethoxysilane is not ideal for dermal absorption, but it would not preclude it. The predicted water solubility (33 mg/l) and predicted log Kow (3.4) of 3-chloropropyltriethoxysilane suggest that this parent substance has the potential to be absorbed quite effectively through the skin. There are no reliable repeated dose toxicity studies to check for signs of systemic availability. There were no signs of systemic toxicity in several skin irritation studies.
Inhalation: The water solubility and log Kow of 3-chloropropyltriethoxysilane suggest that it will be absorbed directly across the respiratory tract lining. There are no inhalation toxicity studies on 3-chloropropyltriethoxysilane to check for signs of systemic availability.
Distribution
The absorbed material is likely to be in the form of the parent substance. The log Kow of the parent substance means that it is likely to distribute into cells and the intracellular concentration might be higher than the extracellular concentration particularly in fatty tissues. The hydrolysis product is likely to be widely distributed in the blood, but with a log Kow of -1.1, uptake into organs and tissues will be limited by its diffusion across membranes. Reliable toxicity studies do not provide evidence for distribution to any particular organ or tissue.
Metabolism
There are no data on the metabolism of 3-chloropropyltriethoxysilane. However, it will hydrolyse gradually to form ethanol and 3-chloropropylsilanetriol once absorbed into the body. Genetic toxicity tests in vitro showed no observable differences in effects with and without metabolic activation.
Excretion
The water solubility and molecular weights of the parent and hydrolysis products (predicted water solubility of 1.0E+6 mg/l) mean that, once absorbed, they are likely to be excreted by the kidneys into urine.
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