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693-38-9

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693-38-9 Usage

General Description

Palmitic Acid Vinyl Ester is a compound derived from palmitic acid, which is a saturated long-chain fatty acid found in many animal and plant fats. The vinyl ester of palmitic acid is used in a variety of industrial and commercial applications, including as a chemical intermediate in the production of surfactants, lubricants, and additives for coatings and adhesives. It is also used as a raw material in the production of polymers and resins. Palmitic Acid Vinyl Ester is known for its stable chemical properties and resistance to oxidation, making it a valuable component in the manufacturing of various products.

Check Digit Verification of cas no

The CAS Registry Mumber 693-38-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,9 and 3 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 693-38:
(5*6)+(4*9)+(3*3)+(2*3)+(1*8)=89
89 % 10 = 9
So 693-38-9 is a valid CAS Registry Number.

693-38-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name ethenyl hexadecanoate

1.2 Other means of identification

Product number -
Other names Vinyl palmitate

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:693-38-9 SDS

693-38-9Relevant articles and documents

The selective O-acylation of enolates providing a simple entry to O-enesters

Limat, Dominique,Schlosser, Manfred

, p. 5799 - 5806 (1995)

In the presence of catalytic amounts of a fluoride source, O-trimethylsilyl enethers undergo condensation with acyl fluorides to afford O-enesters with high yields. The intermediates and final products are pure (Z) isomers if only one double bond is in conjugation with the oxygen atom whereas (E) isomers prevail if silyl dienethers or trienethers and O-trienesters are formed.

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