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517-25-9

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517-25-9 Usage

Description

Trinitromethane, also known as nitroform, is a powerful explosive compound with the chemical formula CHN3O6. It is a white crystalline solid that is highly sensitive to shock and heat. Trinitromethane is known for its high heat of combustion and its ability to dissolve in water.

Uses

Used in Propellant and Explosive Manufacturing:
Trinitromethane is used as a key component in the production of propellants and explosives due to its high heat of combustion and explosive properties. Its sensitivity to shock and heat makes it a valuable addition to the manufacturing process, enhancing the overall performance and effectiveness of the end products.
The provided materials indicate that trinitromethane is used in the manufacture of propellants and explosives, highlighting its chemical properties such as being white crystals, decomposing above 25°C, and having a heat of combustion of 746 cal/g. Its solubility in water also plays a role in its various applications.

Hazard

Explodes on heating, concentrations above 50% in air may explode.

Safety Profile

Poison by ingestion and intraperitoneal routes. Moderately toxic by inhalation. Irritating to skin, eyes, and mucous membranes. Inhalation can cause headache and nausea. Causes mild narcosis. A very dangerous explosion hazard; explodes when heated rapidly. Dissolution is exothermic and solutions of more than 50% can explode. mxtures of 90% trinitromethane + 10% isopropyl alcohol in polyethylene bottles have exploded. Frozen mixtures with 2-propanol(lO%) explode when thawed. Can explode during distillation. Mixtures with divinyl ketone can explode at 4℃. When heated to decomposition it emits toxic fumes of NOx. See also NITRO COMPOUNDS.

Check Digit Verification of cas no

The CAS Registry Mumber 517-25-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,1 and 7 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 517-25:
(5*5)+(4*1)+(3*7)+(2*2)+(1*5)=59
59 % 10 = 9
So 517-25-9 is a valid CAS Registry Number.
InChI:InChI=1/CHN3O6/c5-2(6)1(3(7)8)4(9)10/h1H

517-25-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name trinitromethane

1.2 Other means of identification

Product number -
Other names Trinitromethane [Forbidden]

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:517-25-9 SDS

517-25-9Relevant articles and documents

Reaction of the carbanionic aldolase-substrate intermediate with tetranitromethane. Identification of the products, hydroxypyruvaldehyde phosphate and D-5-ketofructose 1,6-diphosphate.

Healy,Christen

, p. 7911 - 7916 (1972)

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Trinitromethane

Schoedel, Holger,Dienelt, Ruediger,Bock, Hans

, p. 1790 - 1792 (1994)

The structure of cubic trinitromethane, CHN3O6, has been determined at 200 K.Warning: a severe explosion has been reported during the preparation of a sodium trinitromethanide salt.

THE MECHANISM OF AROMATIC NITRATION BY TETRANITROMETHANE

Isaacs, Neil S.,Abed, Obaid Hassan

, p. 2799 - 2802 (1982)

Aromatic nitrations by tetranitromethane are shown to be photochemically initiated and are believed to proceed via trinitromethyl nitrite.

Kokorekina et al.

, (1972)

Synthesis of Neutral and Charged Trinitromethyl Borohydrides and Their Complexes

Shitov,Tartakovskii,Ioffe

, p. 1647 - 1657 (2015/02/05)

We propose several simple and effective methods for the synthesis of previously unknown trinitromethyl borohydrides and their complexes with simple cyclic ethers and aromatic nitrogen- containing heterocycles, whereas acyclic ethers did not form such complexes. The data from physicochemical investigations showed that these unique compounds contain directly linked oxidizing and reducing fragments. Some transformations of trinitromethylborane complexes were demonstrated, which can occur by cleavage of all types of bonds formed by boron atom in the starting compounds.

Reaction of nitrosolic acid salts with dinitrogen tetraoxide

Sheremetev,Aleksandrova,Tukhbatshin,Penzin,Belyakov

scheme or table, p. 487 - 488 (2010/07/09)

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