10361-12-3 | 3,4,5-Trihydroxybenzoic acid stearyl ester

Packsize	Purity	Availability	Price	Discounted Price
5g	98%	in stock	$13.00	$9.00
25g	98%	in stock	$37.00	$26.00
100g	98%	in stock	$99.00	$69.00
500g	98%	in stock	$273.00	$191.00

Description

• Catalog Number: AB46802
• Chemical Name: 3,4,5-Trihydroxybenzoic acid stearyl ester
• CAS Number: 10361-12-3
• Molecular Formula: C25H42O5
• Molecular Weight: 422.5980
• MDL Number: MFCD01753118
• SMILES: CCCCCCCCCCCCCCCCCCOC(=O)c1cc(O)c(c(c1)O)O

Computed Properties

• Complexity: 402
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 30
• Hydrogen Bond Acceptor Count: 5
• Hydrogen Bond Donor Count: 3
• Rotatable Bond Count: 19
• XLogP3: 9.1

Upstream Synthesis Route

Octadecyl Gallate is a versatile compound widely used in chemical synthesis for its unique properties and applications. As an antioxidant, Octadecyl Gallate plays a crucial role in protecting various organic materials from oxidation and degradation by scavenging free radicals and inhibiting oxidative processes. In chemical synthesis, Octadecyl Gallate can be utilized as a stabilizer in the production of polymers, plastics, and elastomers to prevent deterioration caused by exposure to heat, light, or oxygen. Its ability to inhibit oxidation reactions makes it an essential ingredient in the formulation of cosmetics, pharmaceuticals, and food products. Additionally, Octadecyl Gallate is employed as a reagent in organic synthesis to introduce specific functional groups or modify chemical structures, contributing to the development of novel compounds and materials in diverse fields of research and industry.

Literature

• Effects of alkyl chain length of gallate on self-association and membrane binding.

  Journal of biochemistry 20110801

• Relation between lipophilicity of alkyl gallates and antifungal activity against yeasts and filamentous fungi.

  Bioorganic & medicinal chemistry letters 20090315

• Antiproliferative and apoptosis-inducing activities of alkyl gallate and gallamide derivatives related to (-)-epigallocatechin gallate.

  Bioorganic & medicinal chemistry 20080901

• Anti-HSV-1 and anti-HIV-1 activity of gallic acid and pentyl gallate.

  Memorias do Instituto Oswaldo Cruz 20080801

• Inhibition of human immunodeficiency viral replication by tannins and related compounds.

  Antiviral research 19920501