ChemicalBook > Product Catalog > API > Digestive system drugs > Emetics and antiemetics > Chlorobutanol
Chlorobutanol Chemical Properties
- Melting point:~78 °C
- Boiling point:173 °C
- Density 1.3170 (estimate)
- Flash point:>110°C
- storage temp. -20°C
- solubility Slightly soluble in water, very soluble in ethanol (96 per cent), soluble in glycerol (85 per cent).
- color Hydrated crystals
- Odorcamphor odor
- Water Solubility 8g/L(20 ºC)
- Stability:Stable. Generates toxic fumes on combustion.
- CAS DataBase Reference57-15-8(CAS DataBase Reference)
- NIST Chemistry Reference2-(Trichloromethyl)-2-propanol(57-15-8)
- EPA Substance Registry System1,1,1-Trichloro-2-methyl-2-propanol (57-15-8)
Chlorobutanol Usage And Synthesis
- Chemical PropertiesWhite or almost white, crystalline powder or colourless crystals, sublimes readily
- Chemical PropertiesVolatile, colorless or white crystals with a musty, camphoraceous odor.
- UsesPlasticizer for cellulose esters and ethers, preservative for biological fluids and solutions, antimicrobial agent, anesthetic in dentistry.
- Production MethodsChlorobutanol is prepared by condensing acetone and chloroform in the presence of solid potassium hydroxide.
- HazardAction similar to chloral hydrate. Combustible.
- Pharmaceutical ApplicationsChlorobutanol is primarily used in ophthalmic or parenteral dosage forms as an antimicrobial preservative at concentrations up to 0.5% w/v. It is commonly used as an antibacterial agent for epinephrine solutions, posterior pituitary extract solutions, and ophthalmic preparations intended for the treatment of miosis. It is especially useful as an antibacterial agent in nonaqueous formulations. Chlorobutanol is also used as a preservative in cosmetics ; as a plasticizer for cellulose esters and ethers; and has been used therapeutically as a mild sedative and local analgesic in dentistry.
- Safety ProfilePoison by ingestion. A narcotic. A skin and eye irritant. Mutation data reported. See also CHLORAL HYDRATE, whch acts similarly. Dangerous; can react with oxidizing materials. Combustible when exposed to heat or flame. When heated to decomposition it emits toxic fumes of Cl-. See also PHOSGENE.
- SafetyChlorobutanol is widely used as a preservative in a number of
pharmaceutical formulations, particularly ophthalmic preparations.
Although animal studies have suggested that chlorobutanol
may be harmful to the eye, in practice the widespread use of
chlorobutanol as a preservative in ophthalmic preparations has
been associated with few reports of adverse reactions. A study of the
irritation potential of a local anesthetic on the murine cornea
indicated significant corneal surface damage in the presence of
0.5% w/v chlorobutanol, which may be related to the preservative’s
effective concentration. Reported adverse reactions to chlorobutanol
include: cardiovascular effects following intravenous
administration of heparin sodium injection preserved with chlorobutanol; neurological effects following administration of a
large dose of morphine infusion preserved with chlorobutanol;
and hypersensitivity reactions, although these are regarded as
The lethal human dose of chlorobutanol is estimated to be 50–500 mg/kg.
LD50 (dog, oral): 0.24 g/kg
LD50 (mouse, oral): 0.99 g/kg
LD50 (rabbit, oral): 0.21 g/kg
- storageChlorobutanol is volatile and readily sublimes. In aqueous solution,
degradation to carbon monoxide, acetone and chloride ion is
catalyzed by hydroxide ions. Stability is good at pH 3 but becomes
progressively worse with increasing pH. The half-life at pH 7.5
for a chlorobutanol solution stored at 258℃ was determined to be
approximately 3 months. In a 0.5% w/v aqueous chlorobutanol
solution at room temperature, chlorobutanol is almost saturated
and may crystallize out of solution if the temperature is reduced.
Losses of chlorobutanol also occur owing to its volatility, with appreciable amounts being lost during autoclaving; at pH 5 about 30% of chlorobutanol is lost. Porous containers result in losses from solutions, and polyethylene containers result in rapid loss. Losses of chlorobutanol during autoclaving in polyethylene containers may be reduced by pre-autoclaving the containers in a solution of chlorobutanol; the containers should then be used immediately. There is also appreciable loss of chlorobutanol through stoppers in parenteral vials.
The bulk material should be stored in an airtight container at a temperature of 8–158℃.
- IncompatibilitiesOwing to problems associated with sorption, chlorobutanol is incompatible with plastic vials, rubber stoppers, bentonite, magnesium trisilicate, polyethylene, and polyhydroxyethylmethacrylate, which has been used in soft contact lenses. To a lesser extent, carboxymethylcellulose and polysorbate 80 reduce antimicrobial activity by sorption or complex formation.
- Regulatory StatusIncluded in the FDA Inactive Ingredients Database (IM, IV, and SC
injection; inhalations; nasal, otic, ophthalmic, and topical preparations).
Labeling must state ‘contains chlorobutanol up to 0.5%.’
Included in nonparenteral and parenteral medicines licensed in the
UK. Included in the Canadian List of Acceptable Non-medicinal
In the UK, the maximum concentration of chlorobutanol permitted for use in cosmetics, other than foams, is 0.5%. It is not suitable for use in aerosols.
- BIS(2,2,2-TRICHLORO-1,1-DIMETHYLETHYL) PHOSPHOROCHLORIDATE Chlorobutanol Chlorobutanol Bensulfuron methyl Chloroform Kresoxim-methyl Parathion-methyl Methylparaben Sucralose 2-Methyl-1-propanol Methyl acrylate 1-Propanol Sodium tert-butoxide Thiophanate-methyl tert-Butanol Potassium tert-butoxide Methyltrichlorosilane Isopropyl alcohol
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