506-45-6 Usage
Description
22-Hydroxydocosanoic acid is a hydroxylated fatty acid that has been identified in the suberin component of various plant sources, including the silver birch (Betula pendula) outer bark and the leaves, roots, and wood of Quercus ilex from Cala Violina and Colognole, Italy. It is a lipophilic extract from Acacia dealbata and is characterized by its ability to enhance the hydrophobicity of suberin fatty acids.
Uses
Used in Pharmaceutical Industry:
22-Hydroxydocosanoic acid is used as an active pharmaceutical ingredient for its potential therapeutic applications. The expression is: 22-hydroxydocosanoic acid is used as a therapeutic agent for its lipophilic properties and potential medicinal uses.
Used in Cosmetics Industry:
In the cosmetics industry, 22-hydroxydocosanoic acid is used as an ingredient in various skincare and hair care products for its hydrophobic properties, which can help improve the texture and appearance of the skin and hair. The expression is: 22-hydroxydocosanoic acid is used as a hydrophobic agent for enhancing the texture and appearance of skincare and hair care products.
Used in Chemical Industry:
22-Hydroxydocosanoic acid can be utilized in the chemical industry as a building block for the synthesis of various compounds, such as surfactants, lubricants, and other specialty chemicals. The expression is: 22-hydroxydocosanoic acid is used as a building block for the synthesis of various compounds in the chemical industry.
Used in Agriculture:
In agriculture, 22-hydroxydocosanoic acid may be employed as a component in the development of bio-based pesticides or as a natural additive to enhance the hydrophobicity of plant surfaces, potentially improving their resistance to water and certain pathogens. The expression is: 22-hydroxydocosanoic acid is used as a natural additive for enhancing the hydrophobicity and resistance of plant surfaces in agriculture.
Check Digit Verification of cas no
The CAS Registry Mumber 506-45-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,0 and 6 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 506-45:
(5*5)+(4*0)+(3*6)+(2*4)+(1*5)=56
56 % 10 = 6
So 506-45-6 is a valid CAS Registry Number.
506-45-6Relevant articles and documents
Macrolactonization Reactions Driven by a Pentafluorobenzoyl Group**
Ciofini, Ilaria,Force, Guillaume,Leb?uf, David,Mayer, Robert J.,Perfetto, Anna
supporting information, p. 19843 - 19851 (2021/08/13)
Macrolactones constitute a privileged class of natural and synthetic products with a broad range of applications in the fine chemicals and pharmaceutical industry. Despite all the progress made towards their synthesis, notably from seco-acids, a macrolactonization promoter system that is effective, selective, flexible, readily available, and, insofar as possible, compatible with manifold functional groups is still lacking. Herein, we describe a strategy that relies on the formation of a mixed anhydride incorporating a pentafluorophenyl group which, due to its high electronic activation enables a convenient access to macrolactones, macrodiolides and esters with a broad versatility. Kinetic studies and DFT computations were performed to rationalize the reactivity of the pentafluorophenyl group in macrolactonization reactions.
DEPOLYMERIZATION EXTRACTION OF COMPOUNDS FROM BIRCH BARK
-
Page/Page column 37; 44, (2008/06/13)
The invention provides improved processes for the extraction of betulin, lupeol, betulinic acid, suberinic acids, and/or other organic compounds and compositions from birch bark.
Syntheis of the linoleic acid esters of some unsaturated long-chain ω-hydroxy fatty acids
Heslinga, L.,Pabon, H. J. J.
, p. 348 - 351 (2007/10/02)
The (Z)-32-hydroxy-23-Dotriacontenoic acid ester of linoleic acid (19), a compound implicated in skin metabolism, and related compounds have been synthesized in a nine-steps scheme, starting from 10-undecynoic acid.Overall yield amounted to 5.2percent.
