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EC number: 201-161-1 | CAS number: 78-95-5
- 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
Toxicological Summary
- Administrative data
- Workers - Hazard via inhalation route
- Workers - Hazard via dermal route
- Workers - Hazard for the eyes
- Additional information - workers
- General Population - Hazard via inhalation route
- General Population - Hazard via dermal route
- General Population - Hazard via oral route
- General Population - Hazard for the eyes
- Additional information - General Population
Administrative data
Workers - Hazard via inhalation route
Systemic effects
Acute/short term exposure
DNEL related information
Local effects
Acute/short term exposure
DNEL related information
Workers - Hazard via dermal route
Systemic effects
Acute/short term exposure
DNEL related information
Workers - Hazard for the eyes
Additional information - workers
Source: Beratergremium für umweltrelevante Altstoffe (BUA) Vol:226 (2001) 71 p Abstract:
Toxicological Aspect. Data on the metabolism are missing. Investigations on rat hepatocytes have shown that monochloroacetone reacts directly with a biologically relevant macromolecule containing sulfhydryl groups and with glutathione. After splitting off the chloride ion, the compound may act as an alkylating agent. Monochloroacetone is a potent tear gas. In humans, monochloroacetone causes irritation of the eyes and upper respiratory tract. Skin contact causes painful blistering. In animal experiments, lung edema and hydrothorax were observed after inhalation exposure. Male rats are more sensitive to acute toxicity through inhalation than females. After oral and i.p. administration to the mouse and rat and dermal application to the rabbit, the compound shows comparable, very high acute toxicity. Repeated oral administration to rats causes necrosis of the liver, spleen, adrenal gland, and testis, as well as ulceration and perforation in the gastric area. Repeated inhalation exposure to the rat causes congestion of blood in the liver and lung, higher exposure rates causing blood congestion in the heart, kidney, and spleen, as well. Repeated spreading onto the skin causes inflammations in guinea pigs, and additionally causes necroses in rabbits. In an inadequately documented experiment in guinea pigs, no sensitizing effect was demonstrated. The available genotoxicity studies on bacteria, drosophila, and newts, none of which meets present methodical requirements, gave contradictory results and do not permit unequivocal conclusions. In the studies at hand, no tumor-initiating effect was shown. Carcinogenicity studies are not available.
General Population - Hazard via inhalation route
Systemic effects
Acute/short term exposure
DNEL related information
Local effects
Acute/short term exposure
DNEL related information
General Population - Hazard via dermal route
Systemic effects
Acute/short term exposure
DNEL related information
General Population - Hazard via oral route
Systemic effects
Acute/short term exposure
DNEL related information
General Population - Hazard for the eyes
Additional information - General Population
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