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1,4,5-trimethyl-1H-tetrazol-4-ium is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

36739-73-8

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36739-73-8 Usage

Type of compound

Tetrazolium salt

Physical state

Solid

Color

Colorless

Solubility

Water-soluble

Applications

a. Detection of reducing agents
b. Measurement of enzyme activity
c. Cell viability assays
d. Indicator in chemical reactions

Toxicity

Non-toxic

Environmental impact

Low

Popularity

Widely used in laboratory and industrial applications

Check Digit Verification of cas no

The CAS Registry Mumber 36739-73-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,7,3 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 36739-73:
(7*3)+(6*6)+(5*7)+(4*3)+(3*9)+(2*7)+(1*3)=148
148 % 10 = 8
So 36739-73-8 is a valid CAS Registry Number.

36739-73-8SDS

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 1,4,5-trimethyltetrazol-1-ium

1.2 Other means of identification

Product number -
Other names 1,4,5-Trimethylpyrrol-2-carbonitril

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:36739-73-8 SDS

36739-73-8Downstream Products

36739-73-8Relevant academic research and scientific papers

QUATERNIZATION OF TETRAZOLES UNDER HIGH PRESSURE AND ESTABLISHMENT OF THE STRUCTURES OF QUATERNARY TETRAZOLIUM SALTS BY 13C NMR SPECTROSCOPY

Semenov, V. V.,Bogdanov, V. S.,El'yanov, B. S.,Mel'nikova, L. G.,Shevelev, S. A.,et al.

, p. 859 - 864 (1982)

The quaternization of 1- and 2-acetonyl-5-R-tetrazoles, as well as dimethyltetrazole, was accomplished under high pressure conditions (5000-14,000 kgf/cm2) by means of bromoacetone and methyl iodide and at atmospheric pressure and room temperature under the influence of methyl fluorosulfate.The structure of the salts were ascertained by 13C NMR spectroscopy, and the principles of the change in the chemical shifts and the spin-spin coupling constants during quaternization and protonation of the tetrazoles were studied.

Energetic salts of substituted 1,2,4-triazolium and tetrazolium 3,5-dinitro-l,2,4-triazolates

Xue, Hong,Twamley, Brendan,Shreeve, Jean'ne M.

, p. 3459 - 3465 (2007/10/03)

Energetic salts comprised of substituted 1,2,4-triazolium and tetrazolium cations and 3,5-dinitro-1,2,4-triazolate anion were synthesized and characterized. The structure of 4,5-dimethyl-1-aminotetrazolium 3,5-dinitro-1,2,4-triazolate (16) was confirmed by X-ray analysis. Based on experimentally obtained heats of combustion, these materials have calculated heats of formation ranging from ΔHf° = 118 (2) to 778 kJ mol-1 (10) with densities >1.5 g cm-3. Salts, 2, 4, 7, 9 and 10, fall into the ionic liquid class (mp 100 °C). The Royal Society of Chemistry 2005.

Energetic salts of azotetrazolate, iminobis(5-tetrazolate) and 5, 5′-bis(tetrazolate)

Ye, Chengfeng,Xiao, Ji-Chang,Twamley, Brendan,Shreeve, Jean'ne M.

, p. 2750 - 2752 (2007/10/03)

Energetic ionic salts of azotetrazolate (AT), iminobis(5-tetrazolate) (IBT) and 5, 5′-bis(tetrazole) (BT) were synthesized; 1-methyl-4- aminotriazolium azotetrazolate has a layered structure and exhibits a heat of formation of 44360 kJ kg-1. The Royal Society of Chemistry 2005.

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