Hazard assessment of 2,4,6-trinitrotoluene TNT - GUPEA

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IARC Monogr Eval Carcinog Risks Hum. 1996;65:449-75. 2,4,6-Trinitrotoluene. [No authors listed] PMID: 9097116 [PubMed - indexed for MEDLINE] 2,4,6-Trinitrotoluene. Molecular Formula C 7 H 5 N 3 O 6; Average mass 227.131 Da; Monoisotopic mass 227.017838 Da; ChemSpider ID 8073 Title: Microsoft Word - 2,4,6-Trinitrotoluene.rtf Author: bailey_ezra Created Date: 7/3/2001 11:00:08 AM 2,4,6 Trinitrotoluene (TNT): In identification and characterisation of high explosives thermoptometry with or without DSC plays an important role. High explosives may be organic, inorganic or mixtures of the two. McCrone [38] showed that inorganic compounds can be identified by microchemical tests. 1-METHYL-2,4,6-TRINITROBENZENE;TNT.

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However most of the material absorbed is strongly bound and desorption from sediment is slow(1).

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2021-03-26 2,4,6-TRINITROTOLUENE: ICSC: 0967: PHYSICAL & CHEMICAL INFORMATION; Physical State; Appearance COLOURLESS-TO-YELLOW CRYSTALS. Physical dangers Chemical dangers May decompose explosively on shock, friction or concussion. May explode on heating above 240°C. Upon heating, toxic fumes are formed.

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The synthesis of 2,4,6-trinitrotoluene (TNT) has gained a lot of scientific and industrial interest since it was the first high explosive that was able to fulfil the expectations of producers and the military. It was first synthesized in the 1860s and was later produced in … 2,4,6-Trinitrotoluene (TNT) is a yellow, odourless, unstable solid. TNT does not occur naturally in the environment. TNT is an explosive used in military shells, bombs, and grenades; in industrial uses; and in underwater blasting. 1-METHYL-2,4,6-TRINITROBENZENE;TNT. 2,4,6-TRINITROTOLUENE;92-050.

ERT-022S. 1000 μg/mL in acetonitrile, ampule of 1.2 mL, certified reference material, Cerilliant ®. Supelco.
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This paper describes the nitration of 2,4-dinitrotoluene (DNT) and its conversion to 2,4,6-trinitrotoluene (TNT) at a gram scale with the use of a fully automated flow chemistry system. The conversion of DNT to TNT traditionally requires the use of highly hazardous reagents like fuming sulfuric acid (oleum), fuming nitric acid (90-100%), and elevated temperatures. The synthesis of 2,4,6-trinitrotoluene (TNT) has gained a lot of scientific and industrial interest since it was the first high explosive that was able to fulfil the expectations of producers and the military.
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Name, Name: 2,4,6-trinitrotoluene / Synonyms: TNT. Wikipedia, Wikipedia - TNT: 2,4,6-Trinitrotoluene (TNT). 10 mg/mL in Acetonitrile |. Certified Reference Material 2,4,6-trinitrotoluene is prepared by nitrating 2,4-dinitrotoluene with the nitrating mixture containing 83% of concentrated sulfuric acid and 14.5% of fuming nitric Quantifying Trace 2,4,6-Trinitrotoluene (TNT) in Polymer Microspheres. Published. October 16, 2015. Author(s). Timothy M. Brewer, Robert A. Fletcher, Matthew 2,4,6-TNT.

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Timothy M. Brewer, Robert A. Fletcher, Matthew 2,4,6-TNT. TNT sym-trinitrotoluene tritol triton trotyl tolite.

2,4,6-Trinitrotoluene (TNT) November 2017. Introduction . This fact sheet, developed by the U.S. Environmental Protection Agency (EPA) Federal Facilities Restoration and Reuse Office (FFRRO), provides a summary of 2,4,6-trinitrotoluene (TNT), including its physical and chemical properties; environmental and health impacts; existing 2,4,6-Trinitrotoluene is an explosive used in military shells, bombs, and grenades, in industrial uses, and in underwater blasting. Exposure may results from drinking contaminated water that has migrated from chemical waste disposal sites, breathing contaminated air, eating contaminated foods such as fruits and vegetables, and/or eating contaminated soil. Have questions?