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10578-34-4

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10578-34-4 Usage

General Description

Octadecyl benzoate is a chemical compound with the formula C24H38O2. It is a derivative of benzoic acid and is commonly used as an emollient and thickening agent in cosmetic and personal care products. Octadecyl benzoate has a variety of applications in the formulation of beauty and skincare products, such as lotions, creams, and sunscreen. It can also be used as a plasticizer in the manufacturing of films and coatings. Octadecyl benzoate is known for its ability to provide a smooth and silky feel to the skin, making it a popular ingredient in many beauty and skincare products.

Check Digit Verification of cas no

The CAS Registry Mumber 10578-34-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,5,7 and 8 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 10578-34:
(7*1)+(6*0)+(5*5)+(4*7)+(3*8)+(2*3)+(1*4)=94
94 % 10 = 4
So 10578-34-4 is a valid CAS Registry Number.
InChI:InChI=1/C25H42O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-20-23-27-25(26)24-21-18-17-19-22-24/h17-19,21-22H,2-16,20,23H2,1H3

10578-34-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name octadecyl benzoate

1.2 Other means of identification

Product number -
Other names Stearyl benzoate

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:10578-34-4 SDS

10578-34-4Relevant articles and documents

LiHMDS: Facile, highly efficient and metal-free transesterification under solvent-free condition

Gore, Kiran R.,Mittapelli, Lavanya L.

, (2021)

Transesterification is one of the important organic reactions employed in numerous industrial as well as laboratory applications for the synthesis of various esters. Herein, we report a rapid, highly efficient, and transition metal-free transesterification reaction in the presence of LiHMDS under solvent-free conditions. The transesterification reaction was carried out with three different benzoate esters and a wide range of primary and secondary alcohols (from C3-C18) in good to excellent yields (45 examples). By considering the commercial role of esters, this method will be promising for the facile synthesis of esters in industry-relevant applications.

INTEGRATED PROCESS FOR THE PRODUCTION OF BENZOATE PLASTICIZERS

-

, (2016/04/20)

The invention relates to a process that integrates the oxidation of toluene to benzoic acid with the production of benzoate plasticizers. Toluene is fed to an oxidation vessel in the presence of oxygen and an oxidation catalyst wherein benzoic acid serves as the solvent for the oxidation. The crude benzoic acid produced is not purified and is then reacted with an alcohol in the presence of an esterification catalyst to produce the crude benzoate ester. The oxidation catalyst, esterification catalyst, and other impurities can be mostly removed from the crude benzoate ester in subsequent washing and filtering steps. The benzoate esters produced through this method can be made in fewer steps with both yields and purities above 80%.

Potassium phosphate / benzyltriethylammonium chloride as efficient catalytic system for transesterification

Cepanec, Ivica,Zivkovic, Andreja,Bartolincic, Anamarija,Mikuldas, Hrvoje,Litvic, Mladen,Merkas, Sonja

experimental part, p. 519 - 523 (2010/01/07)

Potassium phosphate (K3PO4) in the presence of benzyltriethylammonium chloride have been found to catalyses the transesterifications of a wide variety of aliphatic and aromatic esters with primary and secondary alcohols affording the corresponding esters in good-to-excellent yields.

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