Contents

Chloroacetone

Chloroacetone

Names
Preferred IUPAC name 1-Chloropropan-2-one
Other names Acetonyl chloride, chloropropanone, 1-chloro-2-propanone, monochloroacetone, 1-chloro-2-ketopropane, 1-chloro-2-oxypropane UN 1695
Identifiers
CAS Number	78-95-5 Y
3D model (JSmol)	Interactive image
Beilstein Reference	605369
ChEBI	CHEBI:47220 Y
ChemSpider	6323 Y
ECHA InfoCard	100.001.056
EC Number	201-161-1
PubChem CID	6571
RTECS number	UC0700000
UNII	60ZTR74268 Y
CompTox Dashboard (EPA)	DTXSID0021547
InChI InChI=1S/C3H5ClO/c1-3(5)2-4/h2H2,1H3 Y Key: BULLHNJGPPOUOX-UHFFFAOYSA-N Y Key: BULLHNJGPPOUOX-UHFFFAOYAY
SMILES ClCC(=O)C
Properties
Chemical formula	C3H5ClO
Molar mass	92.52 g·mol−1
Appearance	Colorless liquid, oxidizes to amber
Density	1.123 g/cm3
Melting point	−44.5 °C (−48.1 °F; 228.7 K)
Boiling point	119 °C (246 °F; 392 K)
Solubility in water	10 g/100 mL at 20 °C
Solubility	miscible with alcohol, ether, chloroform
Vapor pressure	1.5 kPa
Magnetic susceptibility (χ)	-50.9·10−6cm3/mol
Dipole moment	2.36
Hazards
Flash point	35 °C (95 °F; 308 K)
Autoignition temperature	610 °C (1,130 °F; 883 K)
Explosive limits	3.4% - ?[1]
Lethal dose or concentration (LD, LC):
LD50 (median dose)	100 mg/kg (rats, oral)[2]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Y verify (what is YN ?) Infobox references

Chemical compound

Chloroacetone is a chemical compound with the formula CH₃COCH₂Cl. At STP it is a colorless liquid with a pungent odor.^[3] On exposure to light, it turns to a dark yellow-amber color.^[4] It was used as a tear gasinWorld War I.^[5]

Synthesis[edit]

Chloroacetone may be synthesized from the reaction between chlorine and diketene, or by the chlorination of acetone.

Applications[edit]

Chloroacetone is used to make dye couplers for colour photography, and is an intermediate in chemical manufacturing.^[2] It is also used in the Feist-Benary synthesisoffurans.^[6]

• Reaction of phenoxide with chloroacetone gives phenoxyacetone,^[7] which is used to make a wide variety of different pharmaceuticals. A catalytic amount of potassium iodide is also necessary to facilitate a Finkelstein reaction.

Purification[edit]

Chloroacetone purchased from commercial suppliers contains 5% impurities including mesityl oxide, which is not removed by distillation. Mesityl oxide can be oxidized using acidified KMnO₄ to form a diol (followed by separation with ether), which is removed on subsequent distillation.^[8]

Transportation regulations[edit]

Transportation of unstabilized chloroacetone has been banned in the United States by the US Department of Transportation. Stabilized chloroacetone is in hazard class 6.1 (Poison Inhalation Hazard). Its UN number is 1695.

See also[edit]

• Bromoacetone
• Dichloroacetone
• Fluoroacetone
• Hexachloroacetone
• Use of poison gas in World War I

References[edit]

External links[edit]

• The Halogenation of Carbonyls