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214751-20-9

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214751-20-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 214751-20-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,4,7,5 and 1 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 214751-20:
(8*2)+(7*1)+(6*4)+(5*7)+(4*5)+(3*1)+(2*2)+(1*0)=109
109 % 10 = 9
So 214751-20-9 is a valid CAS Registry Number.

214751-20-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 11-[4-(10-carboxydecoxy)phenoxy]undecanoic acid

1.2 Other means of identification

Product number -
Other names -

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:214751-20-9 SDS

214751-20-9Downstream Products

214751-20-9Relevant articles and documents

Synthesis and vesicle formation from hybrid bolaphile/ amphiphile ion-pairs. Evidence of membrane property modulation by molecular design

Bhattacharya, Santanu,De Soma,Subramanian

, p. 7640 - 7651 (2007/10/03)

Four new hybrid (bolaphile/amphiphile) ion-pairs were synthesized. Electron microscopy indicated that each of these forms bilayer membranes upon dispersion in aqueous media. Membrane properties have also been examined by differential scanning calorimetry, microcalorimetry, temperature-dependent fluorescence anisotropy measurements, and UV-vis spectroscopy. The Tm values for the vesicular 1,2,3,4, and 5 were 38,12,85,31.3, and 41.6 °C, respectively. Interestingly the Tm values for 1 and 3 were found to depend on their concentration. The entrapment of small solute and the release capability have also been examined to demonstrate that these bilayers form enclosed vesicles. X-ray diffraction of the cast films has been performed to understand the nature and the thickness of these membrane organizations. The membrane widths ranged from 33 to 47 A. Finally, the above observations have been analyzed in light of the results obtained from molecular modeling studies. Thus we have demonstrated that membrane properties can be modulated by simple structural changes at the amphiphile level. It was shown that by judicious incorporation of central, isomeric, disubstituted aromatic units as structural anchors into different bolaphiles, one can modulate the properties of the resulting vesicles.

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