3133-01-5 Usage
Description
1-Tricosanol is a long-chain primary fatty alcohol that is tricosane in which a hydrogen attached to one of the terminal carbons is replaced by a hydroxy group. It has been isolated from various sources, including the bulbs of Polianthes tuberosa, bran from the Italian bread wheat variety Pegaso and its 11 near-isogenic lines, and from the aerial parts of Centaurea austro-anatolica. It is characterized by its white shiny flakes or fine crystalline powder appearance.
Uses
1. Used in Pharmaceutical Industry:
1-Tricosanol is used as an active pharmaceutical ingredient for its potential health benefits. It has been found to have cholesterol-lowering properties and is being studied for its effects on high-density lipoprotein (HDL) levels, which can help reduce the risk of cardiovascular diseases.
2. Used in Cosmetics Industry:
1-Tricosanol is used as an ingredient in cosmetics for its moisturizing and skin-conditioning properties. It can be found in various skincare products, such as creams, lotions, and balms, to provide hydration and improve the overall texture of the skin.
3. Used in Food Industry:
1-Tricosanol can be used as an additive in the food industry due to its fatty alcohol nature. It may be utilized as an emulsifier, stabilizer, or thickening agent in the production of various food products.
4. Used in Chemical Industry:
1-Tricosanol, in its white shiny flakes or fine crystalline powder form, can be used as a raw material in the chemical industry for the synthesis of various compounds and materials, such as surfactants, lubricants, and plasticizers.
Check Digit Verification of cas no
The CAS Registry Mumber 3133-01-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,3 and 3 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3133-01:
(6*3)+(5*1)+(4*3)+(3*3)+(2*0)+(1*1)=45
45 % 10 = 5
So 3133-01-5 is a valid CAS Registry Number.
InChI:InChI=1/C23H48O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24/h24H,2-23H2,1H3
3133-01-5Relevant articles and documents
Synthesis of the enantiomers of some methyl-branched cuticular hydrocarbons of the ant, Diacamma sp.
Marukawa, Kaoru,Takikawa, Hirosato,Mori, Kenji
, p. 305 - 314 (2007/10/03)
The enantiomers of 3-methylpentacosane, 3-methylheptacosane, 3-methylnonacosane, 13-methylheptacosane, and 5-methylheptacosane were synthesized by starting from the enantiomers of 2-methylbutyl bromide or citronellol. These methyl-branched alkanes are the characteristic components of the cuticular hydrocarbons of queen of the ant, Diacamma sp.
A New Synthesis of Long Chain Acid Esters and Carbinols
Rao, S. Jagadishwar,Bhalerao, U. T.,Tilak, B. D.
, p. 208 - 211 (2007/10/02)
A versatile synthesis of difficulty accessible long chain acid esters and carbinols is described.The synthesis involves acylations at 2- and 5-positions of thiophene.Thioketalation of the resulting ketoesters followed by Raney nickel desulfurization yield acid esters which on LAH reduction give the corresponding carbinols.