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26670-16-6

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26670-16-6 Usage

Chemical compound

1,2-Bis-(5-tetrazolyl)-ethane

Molecular weight

242.2 g/mol

Type of compound

Zwitterionic buffer

pH stability

Maintains a stable pH in aqueous solutions

Applications

a. Biological buffer in biochemical and biological research
b. Manufacturing of pharmaceuticals
c. Component in diagnostic reagents

Solubility

Soluble in water

Melting point

192-195°C

Safety

Non-toxic and non-irritating

Check Digit Verification of cas no

The CAS Registry Mumber 26670-16-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,6,7 and 0 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 26670-16:
(7*2)+(6*6)+(5*6)+(4*7)+(3*0)+(2*1)+(1*6)=116
116 % 10 = 6
So 26670-16-6 is a valid CAS Registry Number.

26670-16-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-[2-(2H-tetrazol-5-yl)ethyl]-2H-tetrazole

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:26670-16-6 SDS

26670-16-6Upstream product

26670-16-6Relevant articles and documents

Polynuclear branched tetrazole systems. 3. Acidity of α,ω- ditetrazol-5-ylalkanes

Zubarev,Trifonov,Poborchii,Ostrovskii

, p. 469 - 474 (2006)

α,ω-Ditetrazol-5-ylalkanes with 1 to 5 methylene groups in the alkyl fragment display the properties of dibasic heterocyclic NH acids with pKa values lying in the range 3.4-6.1. The pKa values of these compounds are in a linear dependence on the values of the dielectric permeability of the medium, on the chemical shifts of the signals of the endocyclic carbon atom, and of the carbon atom of the α-methylene group in the 13C NMR spectra. 2006 Springer Science+Business Media, Inc.

Cocrystallization of photosensitive energetic copper(II) perchlorate complexes with the nitrogen-rich ligand 1,2-Di(1 H -tetrazol-5-yl)ethane

Evers, Jürgen,Gospodinov, Ivan,Joas, Manuel,Klap?tke, Thomas M.,Stierstorfer, J?rg

, p. 11749 - 11756 (2014)

Two recently introduced concepts in the design of new energetic materials, namely complexation and cocrystallization, have been applied in the synthesis and characterization of the energetic copper(II) compound [Cu(dt-5-e)2(H2O)](ClO4)2, which consists of two different complex cations and can be described as a model energetic ionic cocrystal. The presence of both the N-rich 1,2-di(1H-tetrazol-5-yl)ethane ligand and oxidizing perchlorate counterion results in a new type of energetic material. The ionic complex cocrystal consists of a mononuclear and a trinuclear complex unit. It can be obtained by precipitation from perchloric acid or by dehydration of the related mononuclear coordination compound [Cu(dt-5-e)2(H2O)2](ClO4)2·2H2O at 70 °C in the solid state. The transformation starting at 60 °C was monitored by X-ray powder diffraction and thermal analysis. The energetic ionic cocrystal was shown to be a new primary explosive suitable for laser ignition. The different coordination spheres within the ionic cocrystal (octahedral and square pyramidal) were shown by UV/vis/NIR spectroscopy to result in excellent light absorption.

Efficient transformation of inactive nitriles into 5-substituted 1 H-tetrazoles using microwave irradiation and their applications

Yoneyama, Hiroki,Usami, Yoshihide,Komeda, Seiji,Harusawa, Shinya

, p. 1051 - 1059 (2013/05/09)

Efficient transformations of inactive nitriles into 5-substituted 1H-tetrazoles in DMF in a microwave reactor are described. The present method is applied to the synthesis of tetrazolato-bridged dinuclear platinum(II) complex and tetrazole C1-ribonucleoside phosphoramidite. Georg Thieme Verlag Stuttgart, New York.

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