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21668-90-6

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21668-90-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 21668-90-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,6,6 and 8 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 21668-90:
(7*2)+(6*1)+(5*6)+(4*6)+(3*8)+(2*9)+(1*0)=116
116 % 10 = 6
So 21668-90-6 is a valid CAS Registry Number.

21668-90-6SDS

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 dideuterio 2,2,3,3-tetradeuteriobutanedioate

1.2 Other means of identification

Product number -
Other names Butanedioic acid-d6

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:21668-90-6 SDS

21668-90-6Downstream Products

21668-90-6Relevant articles and documents

Long-distance inter-hydrogen bond coupling effects in the polarized IR spectra of succinic acid crystals

Flakus, Henryk T.,Hachu?a, Barbara,Ho?aj-Krzak, Jakub T.

, p. 126 - 134 (2015)

The spectral properties of four different crystalline succinic acid (HOOC-(CH2)2-COOH) (SAC) isotopomer systems, h6, d2, d4 and d6, were examined by means of the IR spectroscopy in polarized light aided by numerical simulations of the νO-H and νO-D band contour shapes on utilizing the "strong-coupling" model. The abnormal IR spectral properties of SAC crystals in relation to the corresponding properties of glutaric, pimelic and adipic acid crystals were ascribed to the hyperconjugation electronic effects in the acid associated molecules. A vibronic coupling mechanism involving the proton stretching vibrations in the (COOH)2 cycles and the electronic motions in the molecular skeletons, the isotopic "H/D self-organization" mechanisms and a long-distance vibrational exciton coupling between the adjacent (COOH)2 cycles in the molecular chains are mainly responsible for the generation of the temperature effects in the crystalline IR spectra.

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