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37729-18-3

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37729-18-3 Usage

General Description

Biphenyl-4-Ethanol, also known as 4-phenylphenol or p-phenylphenol, is a white crystalline solid that belongs to the family of aromatic alcohols. It is commonly used as a germicide and fungicide in various industrial and agricultural applications, as well as a preservative in food and personal care products. The compound has been shown to have antimicrobial properties, making it effective in preventing the growth and spread of bacteria and fungi. Biphenyl-4-Ethanol is also used in the synthesis of other organic compounds and as a corrosion inhibitor in the metalworking industry. Despite its widespread use, there is ongoing research into the potential health and environmental risks associated with exposure to this chemical.

Check Digit Verification of cas no

The CAS Registry Mumber 37729-18-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,7,2 and 9 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 37729-18:
(7*3)+(6*7)+(5*7)+(4*2)+(3*9)+(2*1)+(1*8)=143
143 % 10 = 3
So 37729-18-3 is a valid CAS Registry Number.

37729-18-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-phenylphenyl)ethanol

1.2 Other means of identification

Product number -
Other names 2-[1,1'-Biphenyl]-4-yl-1-ethanol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:37729-18-3 SDS

37729-18-3Upstream product

37729-18-3Relevant articles and documents

Enantioselective hydrosilylation of aromatic alkenes catalyzed by chiral bis(oxazolinyl)phenyl-rhodium acetate complexes

Naito, Tatsuo,Yoneda, Takuma,Ito, Jun-Ichi,Nishiyama, Hisao

, p. 2957 - 2960 (2013/02/22)

Highly efficient and enantioselective hydrosilylation of aromatic alkenes catalyzed by the chiral rhodium acetate complexes with the bis(oxazolinyl)phenyl ligands has been reported that afforded chiral silane derivatives with up to 99% ee. Georg Thieme Ve

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