Basic information Safety Supplier Related

4,4'-Dichlorobenzhydrol

Basic information Safety Supplier Related

4,4'-Dichlorobenzhydrol Basic information

Product Name:
4,4'-Dichlorobenzhydrol
Synonyms:
  • DBH (Bis-(4-chlorophenyl)carbinol)
  • Benzenemethanol, 4-chloro-alpha-(4-chlorophenyl)-
  • Bis(4-chlorophenyl)methanol
  • 4,4'-DICHLOROBENZHYDROL
  • 4,4'-dichlorbenzhydrol
  • 4,4'-dichlorodiphenylmethanol
  • 4,4''-DICHLOROBENZHYDROL 98%
  • 4,4''Dichlorobenzhyolrol
CAS:
90-97-1
MF:
C13H10Cl2O
MW:
253.12
EINECS:
202-029-6
Product Categories:
  • Benzhydrols, Benzyl & Special Alcohols
  • Alcohols
  • C9 to C30
  • Oxygen Compounds
Mol File:
90-97-1.mol
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4,4'-Dichlorobenzhydrol Chemical Properties

Melting point:
91-95 °C
Boiling point:
386.1±32.0 °C(Predicted)
Density 
1.2806 (estimate)
storage temp. 
Sealed in dry,Room Temperature
solubility 
Chloroform (Slightly), Methanol (Slightly)
form 
Solid
pka
13.14±0.20(Predicted)
color 
White to Off-White
Water Solubility 
Insoluble in water.
BRN 
1878717
CAS DataBase Reference
90-97-1(CAS DataBase Reference)
NIST Chemistry Reference
Methanol, bis-(p-chlorophenyl)-(90-97-1)
EPA Substance Registry System
p,p'-Dichlorobenzhydrol (90-97-1)
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Safety Information

Hazard Codes 
Xn,Xi
Risk Statements 
36/37/38-22
Safety Statements 
37/39-26-36
HS Code 
2906290090

MSDS

  • Language:English Provider:ACROS
  • Language:English Provider:ALFA
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4,4'-Dichlorobenzhydrol Usage And Synthesis

Chemical Properties

cream to light brown granular powder

Uses

4,4'-Dichlorobenzhydrol is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuff fields.

Definition

ChEBI: 4,4'-dichlorobenzhydrol is a secondary alcohol that is diphenylmethanol which carries chloro groups at positions 4 and 4'. It is a metabolite of the insecticide DDT. It has a role as a bacterial xenobiotic metabolite. It is a secondary alcohol, a member of benzyl alcohols and a member of monochlorobenzenes. It is functionally related to a diphenylmethanol.

Synthesis Reference(s)

The Journal of Organic Chemistry, 15, p. 1108, 1950 DOI: 10.1021/jo01151a030

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