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1,2-Benzenediol,4-heptyl-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

2628-64-0

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2628-64-0 Usage

Synonyms

p-heptylhydroquinone

Parent compound

Hydroquinone

Appearance

White to off-white crystalline solid

Solubility

Insoluble in water, soluble in organic solvents

Uses

Production of hair dyes and other cosmetic products

Structural feature

Heptyl group attached to the benzene ring

Property

Longer and more hydrophobic than hydroquinone

Environmental and health concerns

Not extensively studied, caution advised in use

Chemical classification

Aromatic organic compound

Check Digit Verification of cas no

The CAS Registry Mumber 2628-64-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,2 and 8 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2628-64:
(6*2)+(5*6)+(4*2)+(3*8)+(2*6)+(1*4)=90
90 % 10 = 0
So 2628-64-0 is a valid CAS Registry Number.

2628-64-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-heptyl-pyrocatechol

1.2 Other means of identification

Product number -
Other names 4-Heptyl-brenzcatechin

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:2628-64-0 SDS

2628-64-0Downstream Products

2628-64-0Relevant academic research and scientific papers

Conception, characterization and correlation of new marine odorants

Kraft, Philip,Eichenberger, Walter

, p. 3735 - 3743 (2007/10/03)

Via a synthetic sequence consisting of PPA-mediated Friedel-Crafts acylation of veratrol (8), Clemmensen reduction, demethylation with TMSI, Williamson ether synthesis employing 3-chloro-2-(chloromethyl)prop-1-ene and in-situ ruthenium tetroxide oxidation, numerous substituted benzo[b][1,4]dioxepinones 15-27 and 2,3-dihydro-1H-5,9-di-oxacyclohepta[f]indenones 7, 13 and 14 were prepared to study their odor-structure correlation. In the course of these studies, we discovered the extremely powerful new marine odorant 7-(3′ -methylbutyl)benzo[b][1,4]dioxepin-3-one (16). On the basis of the measured odor threshold data, an olfactophore model was constructed that rationalizes the observed odor intensities, and indicates an aliphatic hydrophobe at a distance of 6.3 A from the centre of the aromatic-ring binding site. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003.

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