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1,3-diferuloyl-sn-glycerol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

83008-46-2

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83008-46-2 Usage

Natural chemical compound

1,3-diferuloyl-sn-glycerol is a naturally occurring compound found in some plants, particularly in the seeds of certain species.

Group of compounds

It belongs to a group of compounds known as phenolic lipids, which are bioactive molecules with potential health benefits.

Antioxidant and anti-inflammatory properties

1,3-diferuloyl-sn-glycerol has been studied for its antioxidant and anti-inflammatory properties, which can help protect the body from damage caused by free radicals and reduce inflammation.

Treatment and prevention of diseases

It has shown potential in the treatment and prevention of various diseases, including cardiovascular disease, cancer, and inflammatory conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 83008-46-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,0,0 and 8 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 83008-46:
(7*8)+(6*3)+(5*0)+(4*0)+(3*8)+(2*4)+(1*6)=112
112 % 10 = 2
So 83008-46-2 is a valid CAS Registry Number.

83008-46-2Downstream Products

83008-46-2Relevant academic research and scientific papers

Comparative Study of Soybean Oil and the Mixed Fatty Acids as Acyl Donors for Enzymatic Preparation of Feruloylated Acylglycerols in Ionic Liquids

Sun, Shangde,Hu, Bingxue,Qin, Fei,Bi, Yanlan

, p. 7261 - 7269 (2015/09/01)

Feruloylated acylglycerols (FAGs) are the lipophilic derivatives of ferulic acid. In this work, soybean oil (SBO) and the mixed fatty acids (MFA) were selected as fatty acyl donors, and reacted with glyceryl monoferulate (GMF) to prepare FAGs in ionic liquids (ILs). Effect of various reaction parameters (time, temperature, enzyme concentration, and substrate ratio) and ILs on the GMF conversion and the reaction selectivity for FAGs formation were investigated. Response surface methodology (RSM) based on a 3-level-4-factor Box-Behnken experimental design was employed to evaluate the inactive effect of reaction parameters. For the esterification of GMF with MFA, the maximum GMF conversion (98.9 ± 0.9%) and FAG yield (88.9 ± 0.6%) were achieved in [C10mim]PF6. However, for the transesterification of GMF with SBO, the maximum GMF conversion (94.3 ± 0.7%) and FAG yield (83.8 ± 1.0%) were obtained in [C12mim]PF6. High FAG selectivities (~0.90) were also obtained using SBO or MFA as acyl donors.

Identification and quantification of feruloylated mono-, Di-, and triacylglycerols from vegetable oils

Compton, David L.,Laszlo, Joseph A.,Berhow, Mark A.

, p. 753 - 758 (2007/10/03)

The use of HPLC-MS to separate and identify the feruloylated acylglycerols formed during the transesterification of ethyl ferulate with TAG was examined. Novozym 435 (Candida antarctica lipase B)-catalyzed transesterifications of ethyl ferulate and soybea

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