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1,2-Benzenediol, 4-(3-hydroxybutyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61152-58-7

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61152-58-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61152-58-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,1,5 and 2 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 61152-58:
(7*6)+(6*1)+(5*1)+(4*5)+(3*2)+(2*5)+(1*8)=97
97 % 10 = 7
So 61152-58-7 is a valid CAS Registry Number.

61152-58-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(3-hydroxybutyl)benzene-1,2-diol

1.2 Other means of identification

Product number -
Other names -

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:61152-58-7 SDS

61152-58-7Relevant academic research and scientific papers

Very long-chain phenylpropyl and phenylbutyl esters from Taxus baccata needle cuticular waxes

Jetter, Reinhard,Klinger, Adelheid,Sch?ffer, Stefanie

, p. 579 - 587 (2007/10/03)

The cuticular wax of Taxus baccata L. needles was found to contain four different classes of long-chain esters that were identified by various chemical transformations with product assignment employing GC-MS. Homologous series of (1) 3-(4′-hydroxyphenyl)-propyl esters of C20-C36 fatty acids, (2) 4-(4′-hydroxyphenyl)-2-butyl esters of C18-C28 fatty acids, (3) 3-(3′,4′-dihydroxyphenyl)-propyl esters of C20-C32 fatty acids, and (4) 4-(3′,4′-dihydroxyphenyl)-2-butyl esters of C18-C28 fatty acids were identified. The four compound classes amounted to 0.1-3.6 μg/cm2 of needle surface area, corresponding to 0.2-7.6% of the wax mixture, respectively. While both phenylpropyl ester series had a maximum for the homolog containing tetracosanoic acid, in the phenylbutyl esters homologs containing eicosanoic and docosanoic acids predominated.

Hair dyeing composition containing an aryldiamine and a substituted catechol

-

, (2008/06/13)

A composition for use in the dyeing of keratinous fibre such as hair includes an aqueous anaerobic solution of an aryldiamine and a substituted catechol. Optionally, an aromatic coupling agent can also be incorporated in the composition to modify the shade of color produced. Anaerobic storage conditions can, for example, be maintained by packing the composition in an aerosol container with a halocarbon propellant.

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