57-15-8 Usage
Chemical Properties
Different sources of media describe the Chemical Properties of 57-15-8 differently. You can refer to the following data:
1. White or almost white, crystalline powder or colourless crystals, sublimes readily
2. Volatile, colorless or white crystals with a musty, camphoraceous
odor.
Originator
Chlorobutanol,Narchem
Uses
Different sources of media describe the Uses of 57-15-8 differently. You can refer to the following data:
1. Chlorobutanol is used as a preservative and sedative. It has also been shown to exhibit antibacterial properties.
2. Plasticizer for cellulose esters and ethers,
preservative for biological fluids and solutions,
antimicrobial agent, anesthetic in dentistry.
Production Methods
Chlorobutanol is prepared by condensing acetone and chloroform
in the presence of solid potassium hydroxide.
Manufacturing Process
33 g (0.59 mol) of powdered potassium hydroxide was added in small
amounts to a solution of 50 g (0.86 mol) of acetone in 100 g (0.84 mol) of
chloroform to form a reaction mixture containing approximately 0.7 mol of
KOH per mol of chloroform. The mixture was chilled to a temperature below
0°C, thoroughly agitated, and than allowed to stand at temperature of about
0°C for 24 hours. The mixture was then filtered and the filtrate was distilled.
The fraction boiling within the range of 165-175°C was poured into an equal
amount of water to precipitate the 1,1,1-trichloro-tert-butyl alcohol. The
precipitated 1,1,1-trichloro-tert-butyl alcohol was filtered and recrystallized
from an ethanol-water mixture and air dried. The yield of 1,1,1-trichloro-tertbutyl alcohol was 6 g, that is, somewhat less than 4% of the theoretical yield
based on chloroform charged. When calculated on the basis of chloroform
consumed the yield was about 15%.
Therapeutic Function
Hypnotic, Anesthetic, Antiseptic, Pharmaceutic aid,
Ophthalmologic
Synthesis Reference(s)
Journal of the American Chemical Society, 70, p. 1189, 1948 DOI: 10.1021/ja01183a092
Hazard
Action similar to chloral hydrate. Combustible.
Pharmaceutical Applications
Chlorobutanol 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 Profile
Poison 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.
Safety
Chlorobutanol 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
rare.
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
storage
Chlorobutanol 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℃.
Incompatibilities
Owing 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 Status
Included 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
Ingredients.
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.
Check Digit Verification of cas no
The CAS Registry Mumber 57-15-8 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 5 and 7 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 57-15:
(4*5)+(3*7)+(2*1)+(1*5)=48
48 % 10 = 8
So 57-15-8 is a valid CAS Registry Number.
InChI:InChI=1/C4H7Cl3O/c1-3(2,8)4(5,6)7/h8H,1-2H3
57-15-8Relevant articles and documents
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Seyferth,D. et al.
, p. 681 - 682 (1965)
-
METHOD FOR PRODUCING UNSATURATED ACID AND/OR UNSATURATED ACID ESTER
-
Paragraph 0072, (2015/07/02)
The present invention relates to a method for producing an unsaturated acid and/or an unsaturated acid ester, containing a process A of reacting a compound (1) represented by the following formula (1) at a temperature of 0° C. to 350° C. in the presence of a Br?nsted acid catalyst and/or a Lewis acid catalyst, to prepare a compound (2) represented by the following formula (2); in which each of R1, R2 and R4 independently represents a hydrogen atom, a deuterium atom or an alkyl group; each of R3 and R5 independently represents a hydrogen atom or a deuterium atom; R6 represents a hydrogen atom, a deuterium atom, or an alkyl group or an aryl group; and X represents a chlorine atom, a fluorine atom, a bromine atom, or an iodine atom.
Amidine-Promoted Addition of Chloroform to Carbonyl Compounds
Aggarwal, Varinder K.,Mereu, Andrea
, p. 7211 - 7212 (2007/10/03)
-
PRODUCTION OF 1,1,1-TRIHALOGENO-2-ALKANOLS AND SOME OF THEIR PROPERTIES
Bal'on, Ya. G.,Shul'man, M. D.,Vakulenko, L. I.
, p. 1231 - 1237 (2007/10/02)
The reaction of acyclic and carbocyclic carbonyl compounds with haloforms was studied in liquid ammonia and dimethylformamide in the presence of basic catalysts (t-BuOK, KOH).As a result of the reaction 1,1,1-trihalogeno-2-alkanols were obtained.They were used for the synthesis of 1,1,1-trihalogeno-2-methoxyalkanes, 1,1-dibromoalkenes, 1,1-dichloro-2-methoxyalkenes, and alkyl mono- and dichloromethyl ketones.
