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2420-55-5

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2420-55-5 Usage

Description

(9E,12Z)-octadeca-9,12-dienoic acid, also known as 9,12-octadecadienoic acid, is a long-chain polyunsaturated omega-6 fatty acid with 18 carbon atoms and two double bonds at the 9th and 12th positions in the carbon chain. It is essential for human health and must be obtained from the diet, as the body cannot produce it on its own. This fatty acid is commonly found in plant-based oils such as sunflower, safflower, and corn oil, as well as in certain nuts and seeds. It plays a vital role in various physiological processes, including lipid metabolism, inflammation, and the maintenance of healthy cell membranes. Studies have also explored its potential health benefits, particularly in reducing the risk of cardiovascular disease and improving overall well-being.

Uses

Used in the Food Industry:
(9E,12Z)-octadeca-9,12-dienoic acid is used as an essential nutrient for [application reason] because it is a crucial component of a healthy diet, contributing to the overall health and well-being of individuals.
Used in the Pharmaceutical Industry:
(9E,12Z)-octadeca-9,12-dienoic acid is used as a therapeutic agent for [application reason] due to its potential health benefits in reducing the risk of cardiovascular disease and its involvement in various physiological processes.
Used in the Nutritional Supplement Industry:
(9E,12Z)-octadeca-9,12-dienoic acid is used as an ingredient in nutritional supplements for [application reason] to ensure that individuals who may not be getting enough of this essential fatty acid through their diet can supplement their intake and maintain optimal health.
Used in the Cosmetics Industry:
(9E,12Z)-octadeca-9,12-dienoic acid is used as a component in skincare products for [application reason] because of its role in maintaining healthy cell membranes, which can contribute to the health and appearance of the skin.
Used in the Research and Development Industry:
(9E,12Z)-octadeca-9,12-dienoic acid is used as a subject of study for [application reason] to further explore its potential health benefits, mechanisms of action, and possible applications in various fields of medicine and healthcare.

Check Digit Verification of cas no

The CAS Registry Mumber 2420-55-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,2 and 0 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2420-55:
(6*2)+(5*4)+(4*2)+(3*0)+(2*5)+(1*5)=55
55 % 10 = 5
So 2420-55-5 is a valid CAS Registry Number.

2420-55-5SDS

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 (9E,12Z)-octadeca-9,12-dienoic acid

1.2 Other means of identification

Product number -
Other names 9E,12Z-octadecadienoic acid

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:2420-55-5 SDS

2420-55-5Relevant articles and documents

Fatty acid desaturation and elongation reactions of trichoderma sp. 1-OH-2-3

Ando, Akinori,Ogawa, Jun,Kishino, Shigenobu,Ito, Taiyo,Shirasaka, Norifumi,Sakuradani, Eiji,Yokozeki, Kenzo,Shimizu, Sakayu

experimental part, p. 227 - 233 (2010/06/16)

The fatty acid desaturation and elongation reactions catalyzed by Trichoderma sp. 1-OH-2-3 were investigated. This strain converted palmitic acid (16:0) mainly to stearic acid (18:0), and further to oleic acid (c9-18:1), linoleic acid (c9,c12-18:2), and α-linolenic acid (c9,c12,c15-18:3) through elongation, and Δ9, Δ12, and Δ15 desaturation reactions, respectively. Palmitoleic acid (c9-16:1) and cis-9,cis-12- hexadecadienoic acid were also produced from 16:0 by the strain. This strain converted n-tridecanoic acid (13:0) to cis-9-heptadecenoic acid and further to cis-9,cis-12-heptadecadienoic acid through elongation, and Δ9 and Δ12 desaturation reactions, respectively. trans-Vaccenic acid (t11-18:1) and trans-12-octadecenoic acid (t12-18:1) were desaturated by the strain through Δ9 desaturation. The products derived from t11-18:1 were identified as the conjugated linoleic acids (CLAs) of cis-9,trans-11-octadecadienoic acid and trans-9,trans-11-octadecadienoic acid. The product derived from t12-18:1 was identified as cis-9,trans-12-octadecadienoic acid. cis-6,cis-9-Octadecadienoic acid was desaturated to cis-6,cis-9,cis-12-octadecatrienoic acid by this strain through Δ12 desaturation. The broad substrate specificity of the elongation, and Δ9 and Δ12 desaturation reactions of the strain is useful for fatty acid biotransformation.

Photochimie et photoreacteurs solaires

Chevalier, J.-L.,Gaston-Bonhomme, Y.,Luciani, A.,Ucciani, E.,Cecchi, G.

, p. 1083 - 1087 (2007/10/02)

The simulation of a cylindrical photoreactor placed along the axis of a tronconic mirror directed to the sun shows that the fractional conversion is only function of a modified Damkoehler number and of the optical density.The conjugaison of dienic fatty acids with iodine as catalyst and the synthesis of cyclohexanone oxime are studied on a solar pilot plant.The simulation do not allow to consider all the parameters which interfere at the pilot scale.

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