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Gamma-linolenyl mesylate (GLM) is a chemical compound derived from gamma-linolenic acid (GLA), an essential omega-6 fatty acid. It is a methyl ester of GLA, which is obtained through a chemical reaction involving the esterification of GLA with methanesulfonic acid. GLM is used as an intermediate in the synthesis of various pharmaceuticals and nutraceuticals, particularly those targeting inflammatory conditions and skin health. It is also known for its potential role in hormone regulation and the management of certain medical conditions, such as atopic eczema and rheumatoid arthritis. Due to its bioactive properties, GLM is considered a valuable component in the development of health supplements and therapeutic agents.

60187-52-2

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60187-52-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60187-52-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,1,8 and 7 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 60187-52:
(7*6)+(6*0)+(5*1)+(4*8)+(3*7)+(2*5)+(1*2)=112
112 % 10 = 2
So 60187-52-2 is a valid CAS Registry Number.

60187-52-2Relevant academic research and scientific papers

PROCESS FOR PREPARING AND PURIFYING FATTY ACIDS

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Page/Page column 16-17, (2011/08/21)

There is provided a process for purifying a fatty acid, which process comprises reacting a fatty acid with a lithium salt in a first solution and under conditions to allow formation of a precipitate of a lithium salt of the fatty acid; isolating the precipitate; dissolving the precipitate in a second solution followed by separation of the organic and aqueous layers so formed; and evaporating the organic layer to isolate the purified fatty acid. There is also provided a process for increasing the length of a fatty acid, and the use of a lithium salt to purify a fatty acid.

Optimization of synthetic conditions for the preparation of dihomo-γ-linolenic acid from γ-linolenic acid

Xue, Gang,Liu, Fengxia,Wang, Ying,Huang, Kaixun

experimental part, p. 77 - 82 (2010/03/31)

Orthogonal experiments were employed to optimize the correlated parameters of reduction, sulfonation, substitution and hydrolysis. These reactions were used to convert γ-linolenic acids into dihomo-γ-linolenic acids (DGLA). For the reduction, the best rea

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