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5-Butyldecan-5-ol, also known as 5-butyl-5-decanol, is a colorless liquid with a molecular formula of C14H30O. It is an organic compound belonging to the class of alcohols, specifically a secondary alcohol. This chemical is characterized by a decanol backbone with a butyl group attached to the fifth carbon atom. It is insoluble in water but soluble in organic solvents. 5-Butyldecan-5-ol is used in the synthesis of various chemical compounds and can be found in some fragrances and flavorings due to its unique scent and taste properties. It is also used in the production of pharmaceuticals and as a chemical intermediate in the manufacturing of other organic compounds.

5340-34-1

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5340-34-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5340-34-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,4 and 0 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5340-34:
(6*5)+(5*3)+(4*4)+(3*0)+(2*3)+(1*4)=71
71 % 10 = 1
So 5340-34-1 is a valid CAS Registry Number.

5340-34-1SDS

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 5-butyldecan-5-ol

1.2 Other means of identification

Product number -
Other names 5-BUTYL-5-DECANOL

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:5340-34-1 SDS

5340-34-1Downstream Products

5340-34-1Relevant academic research and scientific papers

Cerium(III) chloride remarkably increases the rates of formation and yields of ketones in the reaction of lithium carboxylates with organolithiums

Ahn, Yoonmo,Cohen, Theodore

, p. 203 - 206 (2007/10/02)

The presence of CeCl3 greatly increases the yield of ketones in the reaction of organolithiums with lithium carboxylates. The CE(III) suppresses the enolization of the lithium carboxylate, previously unrecognized as a competing reaction except in special cases, and the formation of tertiary alcohols. One of the reasons for the latter effect is a surprising increase in the rate of addition of the organometallic to the lithium carboxylate in the presence of Ce(III).

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