5467-76-5 Usage
Properties
1. Chemical Name: 2,4,6-trinitro-N-(5H-tetrazol-5-ylidene)aniline
2. Common Name: Tetryl
3. Molecular Formula: C7H5N7O6
4. Physical State: Yellow crystalline solid
5. Solubility: Soluble in organic solvents
6. Explosive Nature: Highly explosive
7. Sensitivity: Susceptible to impact, friction, and heat
8. Usage: Primarily used as a military explosive
9. Performance Enhancement: Often used in combination with other high explosives to boost their effectiveness
10. Regulation: Strictly regulated; restricted to licensed professionals in controlled settings
11. Health Effects: Exposure can lead to adverse health effects
12. Handling: Proper handling and disposal procedures are essential
Chemical Structure
Molecular Formula: C7H5N7O6
Structure: 2,4,6-trinitro-N-(5H-tetrazol-5-ylidene)aniline
Physical Characteristics
Appearance: Yellow crystalline solid
Solubility: Soluble in organic solvents
Usage
Military Application: Commonly used as a military explosive
Performance Enhancement: Employed in combination with other high explosives to enhance their performance
Safety Concerns
Explosive Nature: Highly explosive compound
Sensitivity: Sensitive to impact, friction, and heat
Regulation: Strictly regulated substance, restricted to licensed professionals
Health Effects: Exposure can result in adverse health effects, requiring proper handling and disposal measures.
Check Digit Verification of cas no
The CAS Registry Mumber 5467-76-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,6 and 7 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5467-76:
(6*5)+(5*4)+(4*6)+(3*7)+(2*7)+(1*6)=115
115 % 10 = 5
So 5467-76-5 is a valid CAS Registry Number.
5467-76-5Relevant articles and documents
Thermal characterization and theoretical and experimental comparison of picryl chloride derivatives of heterocyclic energetic compounds
Yigiter, Aynur Ozler,Atakol, Melike Kundurac?,Levent Aksu,Atakol, Orhan
, p. 2199 - 2213 (2017/02/26)
There were 10 nitrogen-rich energetic compounds prepared by the reaction of 2,4,6-trinitrochlorobenzen (picryl chloride) with pyrazole, 1,2,4-triazole, imidazole, 3-aminopyrazole, 3-nitropyrazole, 3-amino-1,2,4-triazole, 3-nitro-1,2,4-triazole, 3,5-diamino-1,2,4-triazole and guanidine. These compounds were characterized with IR spectra, elemental analysis and 1H NMR and 13C NMR methods. They were also examined with thermogravimetry and differential thermal analyses. The heat generated after the explosion was measured by the use of differential scanning calorimetry. The formation enthalpies of some of the products synthesized were determined by the use of Gaussian 09 software, and probable products were estimated from the data reported in the literature. Finally, theoretical explosion energies of these compounds were calculated using the theoretical formation enthalpies and compared with experimental data.
A novel N-N bond cleavage in 1,5-diaminotetrazole: Synthesis and characterization of 5-picrylamino-1,2,3,4-tetrazole (PAT)
Tang, Yongxing,Yang, Hongwei,Ju, Xuehai,Huang, Hui,Lu, Chunxu,Cheng, Guangbin
, p. 4127 - 4131 (2014/03/21)
The reaction of 1,5-diaminotetrazole with picryl chloride (PiCl) forms 5-picrylamino-1,2,3,4-tetrazole (PAT) rather than the expected 1-picrylamino-5-amino-1,2,3,4-tetrazole or 5-picrylamino-1-amino-1,2,3,4- tetrazole. The structure of PAT was confirmed by single-crystal X-ray diffraction. Some of the energetic properties of the synthesized compound were also studied.
