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1-Palmitoyl-2-palmitoyl-3-acetylglycerol is a complex lipid molecule consisting of a glycerol backbone with two palmitoyl groups attached to the first and second carbon atoms, and an acetyl group attached to the third carbon atom. 1-palmitoyl-2-palmitoyl-3-acetylglycerol is a type of triacylglycerol, which is a major component of fats and oils. The palmitoyl groups are fatty acid chains derived from palmitic acid, a saturated fatty acid with 16 carbon atoms. The acetyl group is a two-carbon fragment derived from acetic acid. This specific arrangement of fatty acids and the acetyl group gives the molecule unique properties, such as its melting point and solubility, which can be important in various biological and industrial applications.

87553-94-4

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87553-94-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87553-94-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,5,5 and 3 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 87553-94:
(7*8)+(6*7)+(5*5)+(4*5)+(3*3)+(2*9)+(1*4)=174
174 % 10 = 4
So 87553-94-4 is a valid CAS Registry Number.

87553-94-4Downstream Products

87553-94-4Relevant academic research and scientific papers

Chemical synthesis method for 1,2-fatty diglyceride with customizable structure

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Paragraph 0012, (2018/03/01)

The invention discloses a chemical synthesis method for 1,2-fatty diglyceride with a customizable structure. The method is characterized by comprising the following steps: (a) weighing a certain amount of 3-glycerol-chlorohydrin and sodium acetate and adding into a reactor with a reflux condensation apparatus so as to obtain gylcerol monoacetate; (b) selecting fatty acid methyl ester types of biodiesel according to customization needs in presence of a base catalyst, and heating and refluxing the gylcerol monoacetate with the biodiesel in an organic solvent so as to obtain triglyceride; and (c) dissolving the triglyceride obtained in the previous step in a proper amount of methanol, adding potassium carbonate to react at room temperature, extracting with an organic solvent, and recrystallizing, thereby obtaining the high-purity (more than 90%) 1,2-fatty diglyceride. The method disclosed by the invention is simple and convenient in synthetic route, simple in after-treatment and high in total yield (more than 75%), and the 1,2-fatty diglyceride can be effectively synthesized.

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