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4-Chlorobenzhydrol

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4-Chlorobenzhydrol Basic information

Product Name:
4-Chlorobenzhydrol
Synonyms:
  • (4-Chlorophenyl)phenylmethanol
  • 4-chloro-alpha-phenyl-benzenemethano
  • 4-Chlorobenzohydrol
  • Benzhydrol, 4-chloro-
  • Benzhydrol, p-chloro-
  • Chlorobenzhydrol
  • AURORA KA-7061
  • P-CHLORO BENZHYDROL
CAS:
119-56-2
MF:
C13H11ClO
MW:
218.68
EINECS:
204-333-4
Product Categories:
  • Building Blocks
  • C11 to C30+
  • Pharmaceutical Intermediate
  • Chemical Synthesis
  • Organic Building Blocks
  • Oxygen Compounds
  • Benzhydrols, Benzyl & Special Alcohols
  • Alcohols
  • C9 to C30
  • Oxygen Compounds
Mol File:
119-56-2.mol
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4-Chlorobenzhydrol Chemical Properties

Melting point:
58-60 °C (lit.)
Boiling point:
150-151°C 2,6mm
Density 
1.1178 (rough estimate)
refractive index 
1.5260 (estimate)
Flash point:
150-151°C/2.6mm
storage temp. 
2-8°C
solubility 
insoluble
pka
13.34±0.20(Predicted)
color 
White to Off-White
Water Solubility 
insoluble
BRN 
2050235
CAS DataBase Reference
119-56-2(CAS DataBase Reference)
NIST Chemistry Reference
Benzenemethanol, 4-chloro-«alpha»-phenyl-(119-56-2)
EPA Substance Registry System
Benzenemethanol, 4-chloro-.alpha.-phenyl- (119-56-2)
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Safety Information

Hazard Codes 
Xn
Risk Statements 
20/21/22-36/37/38
Safety Statements 
24/25-36-26
WGK Germany 
3
TSCA 
Yes
HS Code 
29062990

MSDS

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4-Chlorobenzhydrol Usage And Synthesis

Chemical Properties

white crystalline powder

Uses

4-Chlorobenzhydrol was used as internal standard to measure the N-demethyl antipyrine metabolite in urine by gas chromatography-mass spectrometry. It was also used in the identification of the antihistamine cetirizine as a relevant cross-reactant for the carbamazepine-specific enzyme-linked immunosorbent assay .

Preparation

Preparation of 4-Chlorobenzhydrol(4-CB):
about 5.0g(0.023 mol) of 4-chloro benzophenone was dissolved in 15 mL of isopropyl alcohol (IPA) and heated to 50°C followed by the addition of 0.265g(0.007 mol) of sodium borohydride as a lot with the temperature maintained at 65°C for 2 h. The reaction mixture was distilled to expel isopropyl alcohol up to 90 %. The resulting solution was cooled and treated with dil HCl (5 mL of conc. HCl in 20 mL of water). Finally the reaction mass was extracted with 15 mL of toluene. The toluene extract was washed withwater to pH-7. The compound obtained in this step was taken to next step without isolation but aliquot sample was concentrated, isolated and checked for melting point (m.p. = 58-60°C).

Definition

ChEBI: P-Chlorobenzhydrol is a diarylmethane.

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