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30595-49-4

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30595-49-4 Usage

Appearance

Yellow crystalline solid

Molecular Weight

265.14 g/mol

Primary Use

Explosives and propellants

Sensitivity

Highly sensitive

Power

Powerful

Reactivity

Highly reactive

Explosive Nature

Yes

Nitrogen Content

High

Potential Energy

Similar to cyclotetramethylene-tetranitramine (HMX)

Safety Precautions

Handle with extreme caution, store properly to prevent accidental detonation.

Check Digit Verification of cas no

The CAS Registry Mumber 30595-49-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,5,9 and 5 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 30595-49:
(7*3)+(6*0)+(5*5)+(4*9)+(3*5)+(2*4)+(1*9)=114
114 % 10 = 4
So 30595-49-4 is a valid CAS Registry Number.

30595-49-4SDS

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-(2,4-dinitrophenyl)-4-nitrotriazole

1.2 Other means of identification

Product number -
Other names 2-(2,4-dinitro-phenyl)-4-nitro-2H-[1,2,3]triazole

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:30595-49-4 SDS

30595-49-4Relevant articles and documents

Sensitive Energetics from the N-Amination of 4-Nitro-1,2,3-Triazole

Wozniak, Dominique R.,Salfer, Benjamin,Zeller, Matthias,Byrd, Edward F. C.,Piercey, Davin G.

, p. 806 - 811 (2020/05/25)

Energetic N-amino-C-nitro compounds 1-amino-4-nitro-1,2,3-triazole and 2-amino-4-nitro-1,2,3-triazole are characterized for the first time as energetic materials. These compounds were characterized chemically by nuclear magnetic resonance (NMR), Infrared

Nitration of 4-Substituted 2-Phenyl-1,2,3-triazoles

Meshcheryakov,Mikiya,Kirillova,Shul'gina,Vereshchagin

, p. 1641 - 1644 (2007/10/03)

Substituent in position 4 of the heteroring influences the nitration of 2-phenyl-1,2,3-triazoles. Electron-donor substituents favor nitration at the heteroring.

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