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64118-39-4

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64118-39-4 Usage

Uses

Dodecanoic-2,2-d2 Acid (CAS# 64118-39-4) is a useful isotopically labeled research compound.

Check Digit Verification of cas no

The CAS Registry Mumber 64118-39-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,1,1 and 8 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 64118-39:
(7*6)+(6*4)+(5*1)+(4*1)+(3*8)+(2*3)+(1*9)=114
114 % 10 = 4
So 64118-39-4 is a valid CAS Registry Number.

64118-39-4SDS

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 2,2-dideuteriododecanoic acid

1.2 Other means of identification

Product number -
Other names 2,2-dideuterio-dodecanoic 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:64118-39-4 SDS

64118-39-4Relevant articles and documents

Investigation into the Mechanism for Generation of the Helical Axis in Cholesteric Lyotropic Liquid Crystals

Tracey, Alan S.,Zhang, Xin

, p. 3889 - 3894 (2007/10/02)

The molecular based process responsible for the generation of the helical axis in the cholesteric mesophase of potassium N-dodecanoyl-L-alaninate, decanol, electrolyte, and water has been investigated.The headgroup dipolar couplings have been correlated with deuterium quadrupole splittings from the aliphatic chain as a function of amphiphile concentration.The results show that the change in the pitch of the helical axis with concentration is reflected by a change in preferred conformation of the amphiphile.This change in conformation is centered about the amide bonds where the aliphatic chain is joined to the alaninate headgroups.The effect presumably results from destabilization of the normally preferred rotamer in favor to others and will have its source in selective interactions between the chiral centers of adjacent amphiphiles.Studies similar to those discussed show that the variation in pitch caused by temperature changes is not correlated with similar selective changes in headgroup orientation.

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