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5,8,11,14-Eicosatetraenoic acid, also known as arachidonic acid, is a polyunsaturated omega-6 fatty acid with the chemical formula C20H32O2. It is an important component of cell membranes and plays a crucial role in various physiological processes, including inflammation, blood clotting, and immune function. Arachidonic acid is derived from dietary sources such as meat, eggs, and fish, and can also be synthesized in the body from linoleic acid. It serves as a precursor for the production of eicosanoids, which are hormone-like compounds involved in regulating various bodily functions. Due to its essential role in human health, arachidonic acid is a key component in the study of lipid metabolism and the development of treatments for various diseases.

7771-44-0

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7771-44-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7771-44-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,7 and 1 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7771-44:
(6*7)+(5*7)+(4*7)+(3*1)+(2*4)+(1*4)=120
120 % 10 = 0
So 7771-44-0 is a valid CAS Registry Number.
InChI:InChI=1/C20H32O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20(21)22/h6-7,9-10,12-13,15-16H,2-5,8,11,14,17-19H2,1H3,(H,21,22)/b7-6?,10-9+,13-12?,16-15?

7771-44-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name all-trans-arachidonic acid

1.2 Other means of identification

Product number -
Other names 5,8,11,14-EICOSATETRAENOIC 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:7771-44-0 SDS

7771-44-0Downstream Products

7771-44-0Relevant academic research and scientific papers

Synthesis of all-trans arachidonic acid and its effect on rabbit platelet aggregation

Anagnostopoulos, Dimitris,Chatgilialoglu, Chryssostomos,Ferreri, Carla,Samadi, Abdelouahid,Siafaka-Kapadai, Athanassia

, p. 2766 - 2770 (2007/10/03)

A simple and high-yielding method to convert natural all-cis PUFA derivatives to the corresponding all-trans geometrical isomers is described. The method is based on the thiyl radical-catalyzed cis-trans isomerization. The all-trans isomer of arachidonic acid was found to cause rabbit platelet aggregation at concentrations higher than 0.1 mM and inhibition of PAF-induced platelet aggregation in a concentration dependent manner with an IC50 in the micromolar range.

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