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2,4,6-trinitrophenol - 1-methyl-1H-imidazole (1:1) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

6314-33-6

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6314-33-6 Usage

Appearance

Yellow crystalline powder.

Explosive properties

The compound has explosive characteristics and can be used in the production of explosives.

Reactivity

Highly reactive, requiring proper handling and storage to prevent accidents.

Uses

Commonly used in the production of explosives, dyes, and pharmaceuticals.

Hazards

Potential risks of explosion and toxicity if not handled properly.

Safety precautions

Typically used in industrial and research settings with strict safety measures in place.

2,4,6-trinitrophenol (picric acid)

An explosive compound with three nitro groups (-NO2) attached to a phenol ring.

1-methyl-1H-imidazole

An organic compound with a five-membered imidazole ring and a methyl group (-CH3) attached to it.

Check Digit Verification of cas no

The CAS Registry Mumber 6314-33-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,1 and 4 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6314-33:
(6*6)+(5*3)+(4*1)+(3*4)+(2*3)+(1*3)=76
76 % 10 = 6
So 6314-33-6 is a valid CAS Registry Number.

6314-33-6SDS

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 1-methylimidazole,2,4,6-trinitrophenol

1.2 Other means of identification

Product number -
Other names 1-Methyl-1H-imidazol,Picrat

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:6314-33-6 SDS

6314-33-6Downstream Products

6314-33-6Relevant academic research and scientific papers

Synthesis, limitations, and thermal properties of energetically- substituted, protonated imidazolium picrate and nitrate salts and further comparison with their methylated analogs

Smiglak, Marcin,Hines, C. Corey,Reichert, W. Matthew,Vincek, Adam S.,Katritzky, Alan R.,Thrasher, Joseph S.,Sun, Luyi,McCrary, Parker D.,Beasley, Preston A.,Kelley, Steven P.,Rogers, Robin D.

experimental part, p. 702 - 722 (2012/05/04)

The possibility of forming simple energetic ionic liquids via the straightforward protonation of heterocyclic amines with nitric or picric acid was explored with 1-alkylimidazoles, 1-alkyl-2-methylimidazoles, and nitro, dinitro, and dicyano-substituted derivatives. The melting points of most of the prepared salts were lower than expected and of the 30 compounds prepared, more than half were found to melt below 100 °C. Limitations in the approach were found as a result of the use of energetic electron withdrawing substituents, such as nitro or cyano, which results in a reduction in nucleophilicity of the heterocycle and an inability to form salts with the acids studied. Interesting thermal behavior was observed with several of the new salts including supercooling and crystallization on heating. Comparison of the simple protonated imidazolium nitrate and picrate salts with their methylated analogs indicated that the protonated ionic liquids do not differ substantially in their melting points from the methylated analogs. However, the thermal stabilities of protonated imidazolium salts are much lower than their alkylated derivatives. Nitrate salts with alkylated cations tend to be more thermally stable than the corresponding picrate salts, but with protonated cations, the picrate salts tend to be approximately 70-80 °C more stable than the nitrate salts. Moreover, accelerating rate calorimetry (ARC) revealed that alkylated salts decompose much less exothermically (in some cases endothermically) than the protonated analogs, and that among all the analyzed salts, the most energetic materials found were protonated 1-methylimidazolium nitrate and 1,2-dimethylimidazolium picrate. The Royal Society of Chemistry and the Centre National de la Recherche Scientifique 2012.

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