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Undecanoic acid, 11-[4-[(1E)-(4-hexylphenyl)azo]phenoxy]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

169205-16-7

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169205-16-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 169205-16-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,9,2,0 and 5 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 169205-16:
(8*1)+(7*6)+(6*9)+(5*2)+(4*0)+(3*5)+(2*1)+(1*6)=137
137 % 10 = 7
So 169205-16-7 is a valid CAS Registry Number.

169205-16-7SDS

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 trans-11-{4-[(4-hexylphenyl)azo]phenoxy}undecanoic acid

1.2 Other means of identification

Product number -
Other names 11-[4-((4-hexylphenyl)azo)phenoxy]undecanoic acid

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:169205-16-7 SDS

169205-16-7Downstream Products

169205-16-7Relevant academic research and scientific papers

Langmuir monolayers of azobenzene derivative with a urea head group

Seki, Takahiro

, p. 2807 - 2816 (2007/10/03)

An azobenzene (Az) containing amphiphile having a urea head group [N- (10-{4-[(4-hexylphenyl)azo]phenoxy})decylurea (6Az10-Urea)] was synthesized for the first time, and the spreading behavior, morphology, absorption spectral features, and photoreactivity of this amphiphile at the air-water interface was examined. The features of this monolayer were argued in comparison with those of a carboxylic acid derivative of the homologous structure. Polymer-like stable stable monolayers were formed form 6Az10-Urea both in the trans and cis forms of the Az unit, possibly indicating the formation of intermolecular bifurcated NH...O=C hydrogen bonds of urea heads. Unlike monolayers of simple long alkylureas, the present monolayer did not show a thermal phase transition within the temperature region examined (10 - 35 °C). In the trans-6Az10-Urea monolayer, the Az unit formed tilted aggregates. In this aggregation state, the trans-tocis photoisomerization in the 6Az10-Urea monolayer was completely hindered despite the fact that the monolayer was more expanded than that of a corresponding carboxylic acid derivative in which the photoisomerization proceeded.

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