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1-Ethyl-1H-tetrazole, also known as ETZ, is a colorless, odorless, and water-soluble chemical compound with the molecular formula C3H6N4. It is commonly used as a high-energy additive in gas generating compositions and serves as a stabilizer in high explosives, propellants, and pyrotechnic compositions. Additionally, it has applications in pharmaceutical research, specifically in the synthesis of medicinal products. Despite its potential explosive and hazardous properties, 1-ETHYL-1H-TETRAZOLE is valued for its versatility and wide range of industrial uses.

25108-33-2

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25108-33-2 Usage

Uses

Used in Gas Generating Compositions:
1-Ethyl-1H-tetrazole is used as a high-energy additive for enhancing the performance of gas generating compositions, providing rapid gas release and increased energy output.
Used in High Explosives:
1-Ethyl-1H-tetrazole is used as a stabilizer in high explosives to improve their safety and reliability, reducing the risk of accidental detonation while maintaining high energy release upon intended activation.
Used in Propellants:
In propellants, 1-Ethyl-1H-tetrazole is used as a stabilizer to enhance the performance and safety of the propellant, ensuring consistent and controlled energy release during combustion.
Used in Pyrotechnic Compositions:
1-Ethyl-1H-tetrazole is used as a stabilizer in pyrotechnic compositions to improve their safety and reliability, providing consistent and controlled color and light output in various pyrotechnic applications.
Used in Pharmaceutical Research:
1-Ethyl-1H-tetrazole is used in pharmaceutical research as a key intermediate in the synthesis of medicinal products, contributing to the development of new drugs and therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 25108-33-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,1,0 and 8 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 25108-33:
(7*2)+(6*5)+(5*1)+(4*0)+(3*8)+(2*3)+(1*3)=82
82 % 10 = 2
So 25108-33-2 is a valid CAS Registry Number.

25108-33-2SDS

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 1-ethyltetrazole

1.2 Other means of identification

Product number -
Other names 1-Aethyl-1H-tetrazol

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:25108-33-2 SDS

25108-33-2Downstream Products

25108-33-2Relevant academic research and scientific papers

Comparison of 1-Ethyl-5H-tetrazole and 1-Azidoethyl-5H-tetrazole as Ligands in Energetic Transition Metal Complexes

Wurzenberger, Maximilian H. H.,Gruhne, Michael S.,Lommel, Marcus,Szimhardt, Norbert,Klap?tke, Thomas M.,Stierstorfer, J?rg

, p. 2018 - 2028 (2019)

Energetic coordination compounds (ECC) based on 3d or 4d transition metals show promising characteristics to be used as potential replacements for highly toxic lead-containing primary explosives. Herein we report the synthesis of 12 new ECC based on 1-azi

Polymer-Supported Fe-Phthalocyanine Derived Heterogeneous Photo-Catalyst for the Synthesis of Tetrazoles Under Visible Light Irradiation

Khajone, Vijay Baburao,Balinge, Kamlesh Rudreshwar,Bhagat, Pundlik Rambhau

, p. 1948 - 1960 (2020/11/23)

Abstract: Herein, a polymer supported Fe-Phthalocyanine entangled with carboxyl functionalized benzimidazolium moiety (PSFePcCFBM) explored as heterogenous photocatalyst, for regioselective synthesis of 1H-tetrazoles from sodium azide and other affordable

Microwave alkylation of lithium tetrazolate

Müller, Danny,Knoll, Christian,Weinberger, Peter

, p. 131 - 137 (2017/01/17)

Abstract: N1-substituted tetrazoles are interesting ligands in transition metal coordination chemistry, especially in the field of spin crossover. Their synthesis is performed in most cases according to the Franke-synthesis, using a primary amine as reagent introducing the substitution pattern. To enhance flexibility in means of substrate scope, we developed a new protocol based on alkylation of lithium tetrazolate with alkyl bromides. The N1–N2 isomerism of the tetrazole during the alkylation was successfully suppressed by use of highly pure lithium tetrazolate and 30?vol.% aqueous ethanol as solvent, leading to pure N1-substituted products. The feasibility of this reaction was demonstrated by a selection of different substrates. Graphical abstract: [Figure not available: see fulltext.]

REACTIONS OF TRIMETHYLSILYL AZIDE WITH ALDEHYDES: FACILE AND CONVENIENT SYNTHESES OF DIAZIDES, TETRAZOLES, AND NITRILES

Nishiyama, Kozaburo,Oba, Makoto,Watanabe, Akio

, p. 693 - 700 (2007/10/02)

The reactions of trimethylsilyl azide (TMSA) with various aldehydes were found to be versatile procedures for the synthesis of gem- and 1,3-diazides, tetrazoles, and nitriles, whose formation was varied by controlling the quantities of TMSA, catalyst, and the reaction conditions.

SYNTHESIS OF 1-SUBSTITUTED TETRAZOLES BY HETEROCYCLIZATION OF PRIMARY AMINES, ORTHOFORMIC ESTER, AND SODIUM AZIDE

Gaponik, P. N.,Karavai, V. P.,Grigor'ev, Yu. V.

, p. 1255 - 1258 (2007/10/02)

It has been shown that the reaction of heterocyclization of primary amines with orthoformic acid and sodium azide in acetic acid has a rather general character and is a convenient method for the synthesis of 1-substituted tetrazoles.On the basis of experimental data, a probable reaction mechanism is proposed.

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