55268-58-1 Usage
Description
9-[(Z)-2-[(1Z,3Z)-3-Hexenylidene]cyclopropylidene]nonanoic acid 2-hydroxy-1-(hydroxymethyl)ethyl ester, also known as a 2-monoglyceride, is a compound where the acyl group is (9Z,12Z,15Z)-octadecatrienoyl (alpha-linolenoyl). It is derived from the combination of a glycerol molecule with a specific fatty acid, resulting in a versatile and functional molecule with potential applications in various industries.
Uses
Used in Pharmaceutical Applications:
9-[(Z)-2-[(1Z,3Z)-3-Hexenylidene]cyclopropylidene]nonanoic acid 2-hydroxy-1-(hydroxymethyl)ethyl ester is used as an active pharmaceutical ingredient for its potential therapeutic properties. 9-[(Z)-2-[(1Z,3Z)-3-Hexenylidene]cyclopropylidene]nonanoic acid 2-hydroxy-1-(hydroxymethyl)ethyl ester's unique structure allows it to interact with various biological targets, making it a promising candidate for the development of new drugs.
Used in Cosmetic Applications:
In the cosmetic industry, 9-[(Z)-2-[(1Z,3Z)-3-Hexenylidene]cyclopropylidene]nonanoic acid 2-hydroxy-1-(hydroxymethyl)ethyl ester is used as an ingredient in various skincare and hair care products. Its emollient and moisturizing properties help improve the texture and appearance of the skin and hair, providing a smooth and healthy look.
Used in Food Industry:
9-[(Z)-2-[(1Z,3Z)-3-Hexenylidene]cyclopropylidene]nonanoic acid 2-hydroxy-1-(hydroxymethyl)ethyl ester is used as an additive in the food industry, particularly in the formulation of edible oils and spreads. Its ability to improve the stability and texture of these products makes it a valuable component in the production of various food items.
Used in Research Applications:
In the field of scientific research, 9-[(Z)-2-[(1Z,3Z)-3-Hexenylidene]cyclopropylidene]nonanoic acid 2-hydroxy-1-(hydroxymethyl)ethyl ester serves as a valuable tool for studying the properties and interactions of various biological systems. Its unique structure allows researchers to gain insights into the mechanisms of action of different molecules and their potential applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 55268-58-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,2,6 and 8 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 55268-58:
(7*5)+(6*5)+(5*2)+(4*6)+(3*8)+(2*5)+(1*8)=141
141 % 10 = 1
So 55268-58-1 is a valid CAS Registry Number.
55268-58-1Relevant articles and documents
Influence of fatty acid desaturation on spontaneous acyl migration in 2-monoacylglycerols
Compton, David L.,Laszlo, Joseph A.,Appell, Michael,Vermillion, Karl E.,Evans, Kervin O.
, p. 2259 - 2267 (2013/01/15)
The effect of desaturation from the C9 to the C15 carbon of 2-monoacylglycerol (2-MAG) fatty acids on spontaneous acyl migration is described. Three 2-MAG species, 2-monooleoylglycerol (C18:1 cis-Δ9), 2-monolinoleoylglycerol (C18:2 cis-Δ9,12), and 2-monolinolenoylglycerol (C18:3 cis-Δ9,12,15) were synthesized by lipase-catalyzed ethanolysis of their respective triacylglycerols and isolated in >60 % yield and at 2-MAG purities of >95 % relative to 1-monoacylglycerol (1-MAG). 1H-NMR spectroscopy was used to monitor the spontaneous acyl migration of the 2-MAG species over a temperature range from 20 to 80 °C. The relative energies of activation calculated from the Arrhenius relationships of the 2-MAG acyl migration rate constants were 73.3, 68.0, and 72.9 kJ mol-1 for the three 2-MAG species, respectively. Density functional calculations performed using the B3LYP functional at the 6-31+G* basis set on the three ketal ring intermediate of the three 2-MAG species followed a similar trend with a lack of relative energetic preference associated with the degree of desaturation. The kinetically determined relative activation energies were approximately twofold higher than the theoretical relative Gibbs free energies of the intermediates, suggesting that other factors influence acyl migration. In general, increasing desaturation after the C9 carbon of 2-MAG fatty acids had no appreciable effect on acyl migration rates. AOCS (outside the USA) 2012.
Biologically active lipids binding membrane receptors
-
, (2008/06/13)
Neutral lipids are provided characterized by binding to phorboid and ingenoid receptors. These lipids are found in a wide variety of cellular sources as well as milk and may be isolated by specific extraction and chromatographic procedures. Depending upon the source, the glycerides may be mono- or di-glycerides, wherein the total number of carbon atoms of the fatty acids is in the range of 18 to 26, so that the monoglyceride has a fatty acid of at least 18 carbon atoms, while the di-glyceride has a fatty acid of at least 14 carbon atoms.