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EC number: 203-051-9 | CAS number: 102-76-1
- 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
Additional information
Studies investigating the terrestrial toxicity of triacetin (CAS 102-76-1) are not available. Due to the properties of triacetin a hazard to soil organisms is assumed to be low.
Acute and chronic study results proved that triacetin has only a low toxicity in mammals and aquatic organisms. For humans Fatty Acid Glycerides like triacetin constitute a large part of the fat content within the diet. They participate in normal physiological processes and are thus inherently harmless. The common metabolic fate of triacetin involves stepwise hydrolysis to acetic acid and free glycerol (Barry et al. 1966). Acetic acid and glycerol feed into physiological pathways like the citric acid cycle, sugar synthesis and lipid synthesis. Furthermore glycerol is a part of membrane lipids and thus present in all living organism.
Natural occurring triglycerides, like triacetin, are energy source for all living organisms. They are synthesised by plants and stored in the fatty tissue of organisms. Also in microorganisms inclusion of fat droplets is common. Fungi, for example, store triglycerides in vacuoles. Thus, as triglycerides like triacetin are constituents of terrestrial macro and micro-organisms, and naturally produced by plants, toxic effects caused by triacetin are implausible. Moreover, as Triacetin is readily biodegradable and has a log Kow < 3 (0.25), an indirect exposure of soil organisms through sludge application can be ruled out.
Hence, considering the lack of indirect exposure via sludge and the most likely harmlessness of triacetin for terrestrial organisms, no soil toxicity data have to be generated.
References:
Barry, R.J.C. et al. (1966). Handling of glycerides of acetic acid by rat small intestine in vitro. J. Physiol., 185: 667-683.
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