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4-Hydroxyoctadecanoic acid methyl ester, also known as methyl 4-hydroxyoctadecanoate, is a chemical compound with the molecular formula C19H38O3. It is a derivative of 4-hydroxyoctadecanoic acid, where the carboxylic acid group has been esterified with methanol. This results in a molecule that is a fatty acid ester, specifically a monoester of a hydroxy fatty acid. The compound is characterized by a long hydrocarbon chain with 18 carbon atoms and a hydroxyl group at the 4th position, with a methyl group attached to the carboxylic acid function. It is found in various natural sources, such as plants and animal fats, and is used in the synthesis of certain pharmaceuticals, cosmetics, and other industrial applications due to its unique properties.

2420-38-4

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2420-38-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2420-38-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,2 and 0 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2420-38:
(6*2)+(5*4)+(4*2)+(3*0)+(2*3)+(1*8)=54
54 % 10 = 4
So 2420-38-4 is a valid CAS Registry Number.

2420-38-4Relevant academic research and scientific papers

A new family of polymerizable lyotropic liquid crystals: Control of feature size in cross-linked inverted hexagonal assemblies via monomer structure

Reppy,Gray,Pindzola,Smithers,Gin

, p. 363 - 371 (2007/10/03)

An efficient and versatile synthesis of a series of polymerizable amphiphilic mesogens that affords control over tail length and position of the polymerizable group is described. The synthesis employs a novel and facile method of preparing styrene ethers. The monomers are sodium salts of styrene ether-modified fatty acids that can be used to form cross-linkable inverted hexagonal (HII) lyotropic liquid crystal (LLC) phases at ambient temperature with controllable nanometer-scale dimensions. Examination of a series of regioisomers with the same alkyl chain length but with the styrene ether group at different locations along the chain revealed that the position of the styrene ether has a profound effect on the dimensions of the resulting HII phase at a fixed temperature and composition. Increasing overall monomer tail length also has a significant, although smaller, effect on the unit cell dimensions of the LLC phase. By controlling the structure of the LLC monomer in this manner, cross-linked HII phases with interchannel distances (ICD) ranging from 29 to 54 A can be obtained. Furthermore, changing the counterion from Na+ to tetraalkylammonium ions leads to further expansion of the HII unit cell to a maximum ICD of 65 A, as well as to the production of a lamellar phase. Use of these monomers affords a new and unparalleled degree of control over phase structure and dimensions for the production of nanostructured organic materials.

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