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Propanenitrile, 3,3'-[1,4-phenylenebis(oxy)]bis-, also known as Bisphenol A diglycidyl ether (BADGE), is a chemical compound with the molecular formula C21H24O4. It is a colorless, viscous liquid that is soluble in most organic solvents. BADGE is primarily used as a monomer in the production of epoxy resins, which are widely employed in various industries, including coatings, adhesives, and composite materials. The compound is synthesized by reacting bisphenol A with epichlorohydrin in the presence of a base catalyst. Due to its potential health and environmental concerns, there has been ongoing research and debate regarding the safety of BADGE and its derivatives, particularly in relation to their use in food packaging and consumer products.

3055-91-2

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3055-91-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3055-91-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,5 and 5 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3055-91:
(6*3)+(5*0)+(4*5)+(3*5)+(2*9)+(1*1)=72
72 % 10 = 2
So 3055-91-2 is a valid CAS Registry Number.

3055-91-2SDS

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 3-[4-(2-cyanoethoxy)phenoxy]propanenitrile

1.2 Other means of identification

Product number -
Other names 3,3'-p-Phenylendioxy-di-propionitril

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:3055-91-2 SDS

3055-91-2Relevant academic research and scientific papers

Araliphatic diisocyanates

-

, (2008/06/13)

Novel araliphatic diisocyanates having the formula are disclosed wherein X is oxygen or a single bond and Ar is an arylene radical. The araliphatic diisocyanates are prepared from well known and readily obtainable starting materials. When X represents a single bond, the starting material is a monohydric phenol wherein a C-alkylation reaction followed by an O-alkylation reaction with acrylonitrile provides an intermediate dipropionitrile which is converted to the diisocyanate via phosgenation of the corresponding diamine. When X represents oxygen, the starting material is a dihydric phenol wherein O-alkylation with acrylonitrile provides the dipropionitrile which in turn is converted to the diisocyanate via the phosgenation of the corresponding diamine. The diisocyanates find particular utility in the preparation of color and light stable polyurethane products.

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