AnodyneWiki

Chlorobutanol

Chlorobutanol
Chlorobutanol
Salts
[]
Chlorobutanol hemihydrate
Generated by the Chemistry Development Kit (http://github.com/cdk)
Molecular structure via molpic based on CDK
Physical properties
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177.45 g/mol [1]
AppearanceNEEDLES (WATER+1) [1]
OdorCamphor odor [1]
TasteCamphor taste [1]
Melting point97 °C [1]
Boiling point167 °C [1]
DecompositionWhen heated to decomposition it emits toxic fumes of /hydrogen chloride/. [1]
SolubilityINSOL IN COLD WATER, SOL IN HOT WATER [1]
[1]
Structural Identifiers
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C4H7Cl3[1]
1,1,1-trichloro-2-methylpropan-2-ol [1]
CC(C)(C(Cl)(Cl)Cl)O [1]
InChI=1S/C4H7Cl3O/c1-3(2,8)4(5,6)7/h8H,1-2H3 [1]
InChIKeyOSASVXMJTNOKOY-UHFFFAOYSA-N [1]

Chlorobutanol (also known as Chlorbutol, 1,1,1-Trichloro-2-methyl-2-propanol, CHLORETONE, Chloreton, Acetone chloroform, Acetonchloroform, Acetochlorone, Clortran, Methaform or Sedaform)

Chemistry

Salts []

Chlorobutanol is typically found in the form of its hemihydrate salt.

 []

Chlorobutanol is a achiral mixture.

Pharmacology

In the () chlorobutanol acts

Metabolism

Subjective effects []

Experience reports []

There are currently 1 experience reports involving chlorobutanol on :

See also []

External links []

References []

  1. National Center for Biotechnology Information. PubChem Compound Summary for CID 5977, Chlorobutanol. Accessed May 5, 2026. https://pubchem.ncbi.nlm.nih.gov/compound/5977

  2. U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Chlorobutanol. UNII: HM4YQM8WRC. Global Substance Registration System. Accessed May 5, 2026. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/HM4YQM8WRC