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10403-71-1

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10403-71-1 Usage

Chemical structure

A compound consisting of two ethenyloxy functional groups attached to an octadecane backbone.

Common uses

Surfactant or emulsifier in industrial and commercial applications
Production of cosmetics and personal care products
Lubricants

Amphiphilic properties

Hydrophilic (water-attracting) component
Hydrophobic (water-repelling) component

Effectiveness

Stabilizes oil-in-water or water-in-oil emulsions
Enhances the bonding of different materials

Additional applications

Coating or adhesion promoter in polymer and adhesive products

Versatility

Diverse applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 10403-71-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,4,0 and 3 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 10403-71:
(7*1)+(6*0)+(5*4)+(4*0)+(3*3)+(2*7)+(1*1)=51
51 % 10 = 1
So 10403-71-1 is a valid CAS Registry Number.

10403-71-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,12-bis(ethenoxy)octadecane

1.2 Other means of identification

Product number -
Other names 1,12-bis-vinyloxy-octadecane

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:10403-71-1 SDS

10403-71-1Downstream Products

10403-71-1Relevant articles and documents

METHOD FOR PRODUCING DIVINYL ETHER COMPOUND HAVING ALKYLENE SKELETON

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Paragraph 0106-0109, (2022/02/11)

A method of purifying a divinyl ether compound having an alkylene skeleton may take place with low energy and in a simplified manner. Such a method for producing a divinyl ether compound may include: reacting a compound of formula (1) wherein R1 is an alkylene group having 4 to 20 carbon atoms, with acetylene by using an alkali metal catalyst; and purifying the divinyl ether compound of formula (2) which is obtained in the reacting, without an extraction.

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