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(7Z,10Z,13Z)-hexadeca-7,10,13-trienoic acid, commonly known as 16:3(n-3), is a long-chain polyunsaturated omega-3 fatty acid with 16 carbon atoms and three double bonds in a cis configuration. It is found in small quantities in certain plant oils and algae and has been recognized for its potential health benefits, particularly in anti-inflammatory and cardiovascular protection. This fatty acid also serves as a precursor to essential signaling molecules in the body, such as eicosanoids, which are involved in immune response and the regulation of inflammation.

7561-64-0

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7561-64-0 Usage

Uses

Used in Pharmaceutical Applications:
(7Z,10Z,13Z)-hexadeca-7,10,13-trienoic acid is used as a therapeutic agent for its anti-inflammatory properties, which can help in reducing inflammation and related symptoms in various conditions. Its role in cardiovascular protection also makes it a potential candidate for the development of treatments for heart-related diseases.
Used in Nutritional Supplements:
As a source of omega-3 fatty acids, (7Z,10Z,13Z)-hexadeca-7,10,13-trienoic acid is used in the formulation of nutritional supplements designed to support general health and well-being. These supplements can be particularly beneficial for individuals seeking to improve their heart health and reduce inflammation.
Used in Research and Development:
(7Z,10Z,13Z)-hexadeca-7,10,13-trienoic acid is utilized in the scientific research and development of new drugs and therapies, particularly those targeting inflammation and cardiovascular health. Its role as a precursor to eicosanoids makes it an important compound for studying the complex interactions within the immune system and inflammation regulation.
Used in the Food Industry:
(7Z,10Z,13Z)-hexadeca-7,10,13-trienoic acid can be incorporated into the food industry as an additive or ingredient in products aimed at promoting heart health and reducing inflammation. Its presence in plant oils and algae makes it a suitable candidate for use in the development of health-conscious food products.
Used in Cosmetics:
Due to its anti-inflammatory properties, (7Z,10Z,13Z)-hexadeca-7,10,13-trienoic acid may also find applications in the cosmetics industry, particularly in products designed to soothe and protect the skin from inflammation and other irritations.

Check Digit Verification of cas no

The CAS Registry Mumber 7561-64-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,6 and 1 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7561-64:
(6*7)+(5*5)+(4*6)+(3*1)+(2*6)+(1*4)=110
110 % 10 = 0
So 7561-64-0 is a valid CAS Registry Number.

7561-64-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (7Z,10Z,13Z)-hexadeca-7,10,13-trienoic acid

1.2 Other means of identification

Product number -
Other names 7,10,13-hexadecatrienoic 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:7561-64-0 SDS

7561-64-0Upstream product

7561-64-0Relevant academic research and scientific papers

Verification of the versatility of the in vitro enzymatic reaction giving (+)-cis-12-Oxo-phytodienoic acid

Ito, Yusuke,Sasaki, Kento,Ogihara, Tsuyoshi,Kitaoka, Naoki,Takahahi, Kosaku,Matsuura, Hideyuki

supporting information, (2021/08/03)

Jasmonic acid (JA) is a plant hormone involved in the defense response against insects and fungi. JA is synthesized from α-linolenic acid (LA) by the octadecanoid pathway in plants. 12-oxo-Phytodienoic acid (OPDA) is one of the biosynthetic intermediates in this pathway. The reported stereo selective total synthesis of cis-(+)-OPDA is not very efficient due to the many steps involved in the reaction as well as the use of water sensitive reactions. Therefore, we developed an enzymatic method for the synthesis of OPDA using acetone powder of flax seed and allene oxide cyclase (PpAOC2) from Physcomitrella patens. From this method, natural cis-(+)-OPDA can be synthesized in the high yield of approximately 40%. In this study, we investigated the substrate specificity of the enzymatic synthesis of other OPDA analogs with successions to afford OPDA amino acid conjugates, dinor-OPDA (dn-OPDA), and OPDA monoglyceride, and it was suggested that the biosynthetic pathway of arabidopsides could occur via MGDG.

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