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Chlorobutanol CAS#57-15-8

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Chemical Name：Chlorobutanol

CAS No.: 57-15-8

Molecular Formula：C4H7Cl3O

Molecular weight:177.46

Sample: Available

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Product Details

Products Description of Chlorobutanol CAS#57-15-8

Colorless crystals. There are two types of crystals: containing half molecular crystal water and anhydrous. The melting point of the containing half molecular crystal water type is 78℃, slightly soluble in water (1:250), easily soluble in ethanol (1:1), glycerol (1:10), ether, chloroform and volatile oil. The melting point of the anhydrous type is 97℃, the boiling point is 167℃, and the 135℃ (32.7kPa). It is easily soluble in hot water, 1g can be dissolved in 1ml ethanol or 10ml glycerol, soluble in ether, petroleum ether, acetone, chloroform, glacial acetic acid, and oils. It is easy to sublime when heated and can evaporate with water vapor. It smells like camphor.

Chlorobutanol Chemical Properties

Melting point	~78 °C
Boiling point	173 °C
density	1.3170 (estimate)
Fp	>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
Water Solubility	8g/L(20 ºC)
Stability:	Stable. Generates toxic fumes on combustion.
LogP	2.030
CAS DataBase Reference	57-15-8(CAS DataBase Reference)
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)

Safety Information

Hazard Codes	Xn
Risk Statements	22-36/37/38
Safety Statements	26-36/37/39
WGK Germany	3
Hazardous Substances Data	57-15-8(Hazardous Substances Data)
Toxicity	MLD orally in dogs, rabbits (mg/kg): 238, 213 (Impens)

Product Application of Chlorobutanol CAS#57-15-8

Chlorobutanol is mainly used as a pharmaceutical raw material to make antiseptics, antiemetics, and local analgesics. Its 1% aqueous solution or 5%-10% ointment can be used for disinfection and sterilization. It can also be used in organic synthesis.

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