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Chlorobutanol

CAS No.
57-15-8
Chemical Name:
Chlorobutanol
Synonyms
HCP;Chlorbutanol;CHLORETONE;1,1,1-TRICHLORO-2-METHYL-2-PROPANOL;Methaform;Chloreton;2-Propanol, 1,1,1-trichloro-2-methyl-;HRC;HCPH;PTN6
CBNumber:
CB8715683
Molecular Formula:
C4H7Cl3O
Molecular Weight:
177.46
MDL Number:
MFCD00004461
MOL File:
57-15-8.mol
MSDS File:
SDS
Last updated:2026-04-16 17:44:27
Product description Number Pack Size Price
Chlorobutanol European Pharmacopoeia (EP) Reference Standard Y0002037 50 mg $166
SHP-1 Active human recombinant, expressed in E. coli, ≥90% (SDS-PAGE) SRP0216 50 μg $514
PTPN6, active, GST tagged human recombinant, expressed in E. coli, ≥70% (SDS-PAGE), buffered aqueous glycerol solution SRP5076 10 μg $431
SHP-1 Active human recombinant, expressed in E. coli, ≥90% (SDS-PAGE) SRP0216 20 μg $531
SHP-1 Active human recombinant, expressed in E. coli, ≥90% (SDS-PAGE) SRP0216 1 unit $480
More product size

Chlorobutanol Properties

Melting point ~78 °C
Boiling point 173 °C
Density 1.3170 (estimate)
Flash point >110°C
storage temp. Sealed in dry,Room Temperature
solubility Slightly soluble in water, very soluble in ethanol (96 per cent), soluble in glycerol (85 per cent).
form Solid
pka 12.87±0.29(Predicted)
color Hydrated crystals
Odor camphor odor
biological source rabbit
Water Solubility 8g/L(20 ºC)
Specific Activity 820-1110nmol/min·mg
Stability Stable. Generates toxic fumes on combustion.
Cosmetics Ingredients Functions PRESERVATIVE
InChI 1S/C4H7Cl3O/c1-3(2,8)4(5,6)7/h8H,1-2H3
InChIKey OSASVXMJTNOKOY-UHFFFAOYSA-N
SMILES ClC(Cl)(Cl)C(O)(C)C
LogP 2.030
CAS DataBase Reference 57-15-8(CAS DataBase Reference)
FDA UNII HM4YQM8WRC
NCI Dictionary of Cancer Terms HCP
NIST Chemistry Reference 2-(Trichloromethyl)-2-propanol(57-15-8)
EPA Substance Registry System 1,1,1-Trichloro-2-methyl-2-propanol (57-15-8)
UNSPSC Code 41116107
NACRES NA.41

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P280-P301+P312-P302+P352-P305+P351+P338
Hazard Codes  Xn
Risk Statements  22-36/37/38
Safety Statements  26-36/37/39
WGK Germany  3
TSCA  TSCA listed
Storage Class 11 - Combustible Solids
Hazard Classifications Acute Tox. 4 Oral
Hazardous Substances Data 57-15-8(Hazardous Substances Data)
Toxicity MLD orally in dogs, rabbits (mg/kg): 238, 213 (Impens)

Chlorobutanol price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich Y0002037 Chlorobutanol European Pharmacopoeia (EP) Reference Standard 57-15-8 50 mg $166 2026-03-19 Buy
Sigma-Aldrich SRP0216 SHP-1 Active human recombinant, expressed in E. coli, ≥90% (SDS-PAGE) 50 μg $514 2026-03-19 Buy
Sigma-Aldrich SRP5076 PTPN6, active, GST tagged human recombinant, expressed in E. coli, ≥70% (SDS-PAGE), buffered aqueous glycerol solution 10 μg $431 2026-03-19 Buy
Sigma-Aldrich SRP0216 SHP-1 Active human recombinant, expressed in E. coli, ≥90% (SDS-PAGE) 20 μg $531 2026-03-19 Buy
Sigma-Aldrich SRP0216 SHP-1 Active human recombinant, expressed in E. coli, ≥90% (SDS-PAGE) 1 unit $480 2025-07-31 Buy
Product number Packaging Price Buy
Y0002037 50 mg $166 Buy
SRP0216 50 μg $514 Buy
SRP5076 10 μg $431 Buy
SRP0216 20 μg $531 Buy
SRP0216 1 unit $480 Buy

Chlorobutanol Chemical Properties,Uses,Production

Chemical Properties

White or almost white, crystalline powder or colourless crystals, sublimes readily

Chemical Properties

Volatile, colorless or white crystals with a musty, camphoraceous odor.

Originator

Chlorobutanol,Narchem

Uses

Chlorobutanol is used as a preservative and sedative. It has also been shown to exhibit antibacterial properties.

Uses

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.

Definition

ChEBI: Chlorobutanol is a tertiary alcohol.

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.

Biological Activity

In mammary epithelial cells, protein tyrosine phosphatase, non-receptor type 6 (PTPN6) controls EGFR (epidermal growth factor receptor) signaling. It participates in the JAK/ST at (janus kinase/signal transducers and activators of transcription) signaling pathway. PTPN6 regulates cytokine receptors like interleukin- 3 (IL-3) and erythropoietin.

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.

Toxics Screening Level

The ITSL for chlorobutanol has been changed from 0.04 μg/m3 to 0.1 μg/m3 based on an annual averaging time.

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.

67-66-3
67-64-1
57-15-8
Synthesis of Chlorobutanol from Chloroform and Acetone
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View Lastest Price from Chlorobutanol manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Chlorobutanol pictures 2026-04-16 Chlorobutanol
57-15-8
US $0.00 / kg 1kg 98% Customise Hefei Lbao Physical & Chemical Science Co.,Ltd
Chlorobutanol pictures 2026-04-16 Chlorobutanol
57-15-8
US $43.00 / mL 99.51% 10g TargetMol Chemicals Inc.
Chlorobutanol pictures 2026-04-16 Chlorobutanol
57-15-8
US $43.00 / mL 99.51% 10g TargetMol Chemicals Inc.
  • Chlorobutanol pictures
  • Chlorobutanol
    57-15-8
  • US $0.00 / kg
  • 98%
  • Hefei Lbao Physical & Chemical Science Co.,Ltd
  • Chlorobutanol pictures
  • Chlorobutanol
    57-15-8
  • US $43.00 / mL
  • 99.51%
  • TargetMol Chemicals Inc.
  • Chlorobutanol pictures
  • Chlorobutanol
    57-15-8
  • US $43.00 / mL
  • 99.51%
  • TargetMol Chemicals Inc.
1,1,1-TRICHLORO-2-METHYL-2-PROPANOL 2-TRICHLOROMETHYL-2-PROPANOL 2-METHYL-1,1,1-TRICHLORO-2-PROPANOL CHLORETONE BETA,BETA,BETA-TRICHLORO-TERT-BUTYL ALCOHOL ACETONE CHLOROFORM 2-Trichhloromethyl-2-propanol Acetone chloroform~Chloretone~Chlorobutanol~1-Methyl-1-(trichloromethyl)ethanol~1,1,1-Trichloro-2-methyl-2-propanol ACETONE CHLOROFORM HEMIHYDRATE DAB, PH. EUR., B.P., N. F., PH. FRANC. CHLORBUTOLANHYDROUS CHLOROBUTANOL,ANHYDROUS,NF β, β, β-Trichloro-tert-butanol hemihydrate 1,1,1-Trichlor-2-methyl-2-propanol 1,1,1-Trichloro-2-methylpropanol-2 Chlorobutanol 1,1,1-Trichloro-2-methyl-2-propanol hemihydrate,β,β,β-Trichloro-tert-butyl alcohol hemihydrate, ‘Acetone chloroform’, ‘Chlorobutanol’ HPTP1C PTPN6, active, GST tagged human SH-PTP1 Hematopoietic cell phosphatase ,,-Trichloro-tert-butylalcohol .beta.,.beta.,.beta.,-Trichloro-tert.-butanol 1,1,1-trichloro-2-methyl-2-propano 1,1,1-Trichloro-tert-butyl alcohol 1,1,1-trichloro-tert-butylalcohol PTP-1C PTPN6 SHP-1 Active human SHP-1L ANTI-HRC (CENTER) antibody produced in rabbit HRC Sarcoplasmic reticulum histidine-rich calcium-binding protein 70Z-SHP Anti-SHP-1, C-Terminal antibody produced in rabbit HCPH Hematopoietic cell protein-tyrosine phosphatase PTN6 2-(Trichloromethyl)propan-2-ol 2,2,2-Trichloro-1,1-dimethylethanol 2-methyl-1,1,1-trichloro-2-propano 2-Propanol, 1,1,1-trichloro-2-methyl- 2-Propanol, 2-methyl-1,1,1-trichloro- Acetochlorone Acetonchloroform anhydrouschlorobutanol Chlorbutanol chlorobutanol,anhydrous Chlortran Clortran Coliquifilm Dentalone Khloreton Methaform Sedaform tert-Trichlorobutyl alcohol Trichlorobutanol Trichloro-t-butyl alcohol trichloro-t-butylalcohol