5029-46-9 Usage
Description
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.
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.
5029-46-9Relevant articles and documents
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.
