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104-07-4

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104-07-4 Usage

General Description

Cyclohexyl octadecanoate consists of a long-chain fatty acid, octadecanoic acid (also known as stearic acid), attached to a cyclohexyl group. It falls into the category of esters, which are commonly used as ingredients in various industrial and consumer products.

Check Digit Verification of cas no

The CAS Registry Mumber 104-07-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,0 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 104-07:
(5*1)+(4*0)+(3*4)+(2*0)+(1*7)=24
24 % 10 = 4
So 104-07-4 is a valid CAS Registry Number.
InChI:InChI=1/C24H46O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-19-22-24(25)26-23-20-17-16-18-21-23/h23H,2-22H2,1H3

104-07-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name cyclohexyl octadecanoate

1.2 Other means of identification

Product number -
Other names EINECS 203-171-1

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:104-07-4 SDS

104-07-4Downstream Products

104-07-4Relevant articles and documents

Esterifications of carboxylic acids and alcohols catalyzed by Al 2(SO4)3 · 18H2O under solvent-free condition

Gang, Li,Wenhui, Pang

experimental part, p. 559 - 565 (2011/01/07)

Esterifications of equimolar mixture of carboxylic acids and alcohols can be effectively catalyzed by Al2(SO4)3 · 18H2O under solvent-free condition. The esterification catalyzed by Al2(SO4)3 · 18H2O is a promising green method thanks to no need of organic solvent, no pollution, no causticity and ease to handle after reaction. This catalyst is of a low toxicity (usually it is used as purifying agent for drinking water), low-cost compound and is easily separated from the reaction mixture by simple filtration. Moreover, the catalyst can be recycled for the further esterification and the conversion does not evidently decrease.

The synthesis of esters under microwave irradiation using dry-media conditions

Loupy, Andre,Petit, Alain,Ramdani, Mohamed,Yvanaeff, Celine,Majdoub, Mustapha,et al.

, p. 90 - 95 (2007/10/02)

Practical and simple techniques are described for using nonmodified domestic microwave ovens as safe and convenient laboratory devices to obtain numerous esters.High pressures are avoided by conducting reactions with reactants impregnated on solid mineral supports in "dry media" or by phase transfer catalysis (PTC) in the absence of organic solvents.Two kinds of microwave effects are involved: (1) displacement of the equilibrium by evaporation of volatile polar molecules (water or alcohols) in esterfications and transesterfications; (2) acceleration of ionic reactions in carboxylate alkylations.As solvents are avoided, there is no need for sealed vessels and water separators.

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