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3133-01-5

3133-01-5

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3133-01-5 Usage

Chemical Properties

white shiny flakes or fine crystalline powder

Definition

ChEBI: 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 bulbs of Polianthes tuberosa, bran from the Italian bread wheat variety ital>Pegaso and its 11 near-isogenic lines, and from the aerial parts of f Centaurea austro-anatolica.

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

3133-01-5 Well-known Company Product Price

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  • Sigma

  • (T9524)  1-Tricosanol  

  • 3133-01-5

  • T9524-50MG

  • 782.73CNY

  • Detail

3133-01-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name tricosan-1-ol

1.2 Other means of identification

Product number -
Other names triconsanol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:3133-01-5 SDS

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.

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