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623-55-2

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623-55-2 Usage

General Description

5-Methyl-3-hexanol, also known as isoamyl alcohol, is a colorless liquid with a strong, fruity odor. It is a primary alcohol with the chemical formula C7H16O, and it is commonly used as a solvent and flavoring agent in the production of food and beverages. It is also used in the manufacturing of perfumes and cosmetics, as well as in the synthesis of other chemicals. Additionally, 5-Methyl-3-hexanol has antimicrobial properties and can be used as an antiseptic. However, it is flammable and should be handled with care.

Check Digit Verification of cas no

The CAS Registry Mumber 623-55-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,2 and 3 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 623-55:
(5*6)+(4*2)+(3*3)+(2*5)+(1*5)=62
62 % 10 = 2
So 623-55-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H16O/c1-4-7(8)5-6(2)3/h6-8H,4-5H2,1-3H3

623-55-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-METHYL-3-HEXANOL

1.2 Other means of identification

Product number -
Other names Aethyl-isobutyl-carbinol

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:623-55-2 SDS

623-55-2Relevant articles and documents

Facile deoxygenation of dicarbonyl compounds using a samarium diiodide-additive system

Kamochi, Yasuko,Kudo, Tadahiro,Masuda, Toshinobu,Takadate, Akira

, p. 1017 - 1020 (2007/10/03)

The reduction of α- and β-dicarbonyl compounds was investigated with samarium diiodide in the presence of additive. Diketones and ketocarboxylic acids were easily reduced at room temperature to give the mono-alcohols in good to excellent yield, and ketoester afforded the saturated ester as the major product in moderate yield. These reductions containing the reductive deoxygenation can be rapidly performed under the facile and mild conditions by this method.

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