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Trinitrofluoranthene is a chemical compound that is a derivative of fluoranthene, consisting of three nitro groups attached to the benzene ring. It is known for its high explosiveness and sensitivity to heat, shock, and friction. Its high reactivity and volatility make it a compound of interest in the explosives industry.

102493-22-1

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102493-22-1 Usage

Uses

Used in Explosives Industry:
Trinitrofluoranthene is used as an explosive ingredient for its powerful detonation properties. It is incorporated into munitions, fireworks, and pyrotechnics to enhance their explosive capabilities.
Used in Munitions:
Trinitrofluoranthene is used as a component in the manufacturing of munitions, where its high explosiveness is crucial for the effectiveness of the ordnance.
Used in Fireworks and Pyrotechnics:
In the entertainment industry, trinitrofluoranthene is used in fireworks and pyrotechnics to create visually impressive and powerful explosions for various events and celebrations.
Note: Due to the hazardous nature and potential toxicity of trinitrofluoranthene, it requires careful handling, storage, and disposal to prevent accidents and environmental contamination.

Check Digit Verification of cas no

The CAS Registry Mumber 102493-22-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,4,9 and 3 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 102493-22:
(8*1)+(7*0)+(6*2)+(5*4)+(4*9)+(3*3)+(2*2)+(1*2)=91
91 % 10 = 1
So 102493-22-1 is a valid CAS Registry Number.
InChI:InChI=1/C16H7N3O6/c20-17(21)9-5-8-6-13(18(22)23)16(19(24)25)15-11-4-2-1-3-10(11)12(7-9)14(8)15/h1-7H

102493-22-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,5-trinitrofluoranthene

1.2 Other means of identification

Product number -
Other names 1,2,5-Trinitro-fluoranthene

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:102493-22-1 SDS

102493-22-1Downstream Products

102493-22-1Relevant academic research and scientific papers

Reaction of Dinitrogen Pentoxide with Fluoranthene

Zielinska, Barbara,Arey, Janet,Atkinson, Roger,Ramdahl, Thomas,Winer, Arthur M.,Pitts, James N. Jr.

, p. 4126 - 4132 (2007/10/02)

The products and mechanisms of the reactions of dinitrogen pentoxide (N2O5) with fluoranthene (FL) in aprotic solvents have been investigated.The influence of solvent polarity and temperature and the effects of addition of HNO3 on the resulting nitrofluoranthene (NFL) isomer distributions have been studied.These data compared with the NFL isomer distributions resulting from the reactions of FL with N2O5 and other nitrating agents in the gas and absorbed phases.In the gas phase and in CCl4 solution at ambient temperature, 2-NFL is the only mononitro isomer formed from the reaction of FL with N2O5.However, in more polar solvents (CH3CN and CH3NO2) and in CCl4 at subambient remperature (-15 grad C), as well as with FL in the adsorbed state, reaction with N2O5 produces only the 3-, 8-, 7-, and 1-NFL isomers.A homolyticmechanism for the formation of the 2-NFL isomer is postulated.

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