| Identification | More | [Name]
4-Chlorobenzhydrol | [CAS]
119-56-2 | [Synonyms]
4-CHLORO-ALPHA-PHENYL-BENZENEMETHANOL
4-CHLORO-(ALPHA-PHENYL) BENZYL ALCOHOL
4-CHLOROBENZHYDROL
4-Chlorobenzhydryl alcohol
4-CHLORODIPHENYLCARBINOL
4-CHLORODIPHENYLMETHANOL
4-CHLORO-O-PHENYLBENZYL ALCOHOL
4-CHLOROPHENYL PHENYL CARBINOL
AURORA KA-7061
P-CHLORO BENZHYDROL
(4-Chlorophenyl)phenylmethanol
4-chloro-alpha-phenyl-benzenemethano
4-Chlorobenzohydrol
Benzhydrol, 4-chloro-
Benzhydrol, p-chloro-
Chlorobenzhydrol
4-Chlorodiphenylmethanol~4-Chlororphenyl phenyl carbinol
Benzenemethanol, 4-chloro-.alpha.-phenyl-
4-CHLOROBENZHYDROL 98+%
4-Chloro-a-phenyl-benzenemethanol | [EINECS(EC#)]
204-333-4 | [Molecular Formula]
C13H11ClO | [MDL Number]
MFCD00004491 | [Molecular Weight]
218.68 | [MOL File]
119-56-2.mol |
| Safety Data | Back Directory | [Hazard Codes ]
Xn | [Risk Statements ]
R20/21/22:Harmful by inhalation, in contact with skin and if swallowed .
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S24/25:Avoid contact with skin and eyes .
S36:Wear suitable protective clothing .
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . | [WGK Germany ]
3
| [TSCA ]
Yes | [HS Code ]
29062990 |
| Hazard Information | Back Directory | [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 . | [Definition]
ChEBI: P-Chlorobenzhydrol is a diarylmethane. | [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). |
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