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6178-32-1

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6178-32-1 Usage

Uses

Glycidyl 4-nonylphenyl ether may be employed for the preparation of patterned template for the surface patterning of Escherichia coli (a gram negative bacterium) and Bacillus subtilis (a gram positive bacterium).

Check Digit Verification of cas no

The CAS Registry Mumber 6178-32-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,7 and 8 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6178-32:
(6*6)+(5*1)+(4*7)+(3*8)+(2*3)+(1*2)=101
101 % 10 = 1
So 6178-32-1 is a valid CAS Registry Number.
InChI:InChI=1/C18H28O2/c1-2-3-4-5-6-7-8-9-16-10-12-17(13-11-16)19-14-18-15-20-18/h10-13,18H,2-9,14-15H2,1H3

6178-32-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(4-nonylphenoxy)methyl]oxirane

1.2 Other means of identification

Product number -
Other names EINECS 228-224-6

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:6178-32-1 SDS

6178-32-1Downstream Products

6178-32-1Relevant articles and documents

Epoxy-acrylic macromolecular compounds on the basis of phenol and para-alkyl substituted phenol

Ca?caval, Constantin N.,Ro?u, Dan

, p. 731 - 737 (2007/10/03)

Some phenolic glycidyl ethers and suitable acrylic monomers on the basis of phenol and para-alkyl [-CH3, -C(CH3)3, -C9H19] substituted phenols were synthesized and characterized. The monomers were thermally polymerized in the presence of benzoyl peroxide. The polymerization reaction was studied by viscometry, as well as by curing process. The synthesized polymers degrade statistically by a radical mechanism. The apparent thermal stability is higher for para-tert-butylphenol epoxy-acrylic polymer and lower for phenol epoxy-acrylic polymer.

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