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4,4,4-Trinitrobutanoic acid, also known as TNBA, is a highly explosive chemical compound with the molecular formula C4H5N3O8. It is a derivative of butanoic acid with three nitro groups attached to the carbon backbone. TNBA is an extremely unstable and sensitive compound, making it a potentially hazardous and dangerous explosive material.

5029-46-9

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5029-46-9 Usage

Uses

Used in Military Applications:
4,4,4-Trinitrobutanoic acid is used as an explosive material for its high energy output and rapid detonation properties. Due to its extreme instability and sensitivity, it is primarily used in military and defense applications where precise control and handling can be ensured.
Used in Research and Development:
4,4,4-Trinitrobutanoic acid is used as a research compound for studying the properties and behavior of high explosives. Its unique characteristics and reactivity make it valuable for understanding the underlying mechanisms of detonation and developing new materials with improved safety and performance.
Note: Due to the high instability and potential for accidental detonation, 4,4,4-trinitrobutanoic acid is not commonly used or produced in large quantities. It is a controlled substance and is subject to strict regulations and handling procedures to prevent accidents and misuse.

Check Digit Verification of cas no

The CAS Registry Mumber 5029-46-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,2 and 9 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5029-46:
(6*5)+(5*0)+(4*2)+(3*9)+(2*4)+(1*6)=79
79 % 10 = 9
So 5029-46-9 is a valid CAS Registry Number.

5029-46-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,4,4-trinitrobutanoic acid

1.2 Other means of identification

Product number -
Other names Butyric acid,4,4,4-trinitro

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:5029-46-9 SDS

5029-46-9Relevant academic research and scientific papers

DESTRUCTIVE NITRATION OF POLYNITRO CARBONYL COMPOUNDS I. A NEW METHOD FOR THE PRODUCTION OF HEXANITROETHANE

Golod, E. L.,Bagal, L. I.

, p. 29 - 33 (2007/10/02)

The nitration of 1,1,1-trinitroalkyl ketones (NO2)3C(CH2)nCOR with a mixture of concentrated nitric and sulfuric acids leads to the formation of hexanitroethane with a yield of up to 80percent.The reaction is promoted by electron-donating substituents. 1,1-Dinitro-4-pentanone is nitrated in a similar way.Hexanitroethane is not formed in nitric acid alone.

ACTION OF NITRIC ACID ON 2,4,6-TRINITROPHENYL ARENE AND ALKANECARBOTHIOATES

Nurgatin, V. V.,Sharnin, G. P.,Savel'eva, L. A.,Nurgatina, R. B.

, p. 2167 - 2169 (2007/10/02)

For the case of the reaction of S,S'-bis(2,4,6-trinitrophenyl)dithiooxalate with concentrated nitric acid it was found that the sulfur-containing groups in the esters of thiocarboxylic acids are substituted by hydroxy and nitroso groups.The reaction, which is accompanied by copious release of nitrogen oxides and increase in temperature, leads to 2,4,6-trinitrophenol or 2,4,6-trinitronitrosobenzene.The structure of the latter was confirmed by IR and UV spectroscopy and by oxidation to 1,2,3,5-tetranitrobenzene. 2,4,6-Trinitrophenyl benzenecarbothioates give the nitroderivative only when the acids contain not more than one nitro group in the phenyl radical.The nitroso group in 2,4,6-trinitronitrosobenzene, like the halogen in picryl halides, is readily substituted by the action of nucleophilic reagents.

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