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19926-63-7

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19926-63-7 Usage

General Description

(Z,Z,E)-3,6,8-Dodecatrien-1-ol is a chemical compound that is classified as a volatile organic compound. Its structure consists of a chain of 12 carbon atoms with a hydroxyl (alcohol) group at one end. The chemical has three double bonds positioned at the third, sixth, and eighth carbon atoms. This triene compound is used in various industries, predominantly in the fragrance industry due to its scent that is similar to natural sebaceous secretions. It is also used as a flavoring agent in food and beverages, as well as in personal care and cleaning products.

Check Digit Verification of cas no

The CAS Registry Mumber 19926-63-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,9,2 and 6 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 19926-63:
(7*1)+(6*9)+(5*9)+(4*2)+(3*6)+(2*6)+(1*3)=147
147 % 10 = 7
So 19926-63-7 is a valid CAS Registry Number.

19926-63-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name dodeca-3,6,8-trien-1-ol

1.2 Other means of identification

Product number -
Other names 3,6,8-Dodecatrien-1-ol,(Z,Z,Z)

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:19926-63-7 SDS

19926-63-7Downstream Products

19926-63-7Relevant articles and documents

Syntheses and NMR analyses of the eight geometric isomers of 3,6,8-dodecatrien-1-ol, subterranean termite trail pheromone

Eya, Bryan K.,Otsuka, Toshikazu,Kubo, Isao,Wood, David L.

, p. 2695 - 2706 (2007/10/02)

Eight geometric isomers of 3,6,8-dodecatrien-1-ol 1, the trail-following pheromone of subterranean termites (Reticulitermes sp. Banks), were synthesized via a Wittig olefination reaction. The convergent syntheses of 1 consisted of a combination of two fragments, each containing an olefin with a fixed configuration, by formation of a third double bond to give a mixture of two geometric isomers. The mixtures of 1 were resolved by recycle high-performance liquid chromatography methods. 1H and 13C NMR peak assignments of the individual isomers were accomplished by homonuclear COSY, and one-bond CH correlation spectroscopy.

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