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2,3,4,5-Tetranitro-1H-pyrrole, commonly referred to as TNPy, is a high-energy, highly explosive chemical compound characterized by its molecular formula C4N6O8. It is a nitro derivative of the pyrrole ring, featuring four nitro groups attached at the 2, 3, 4, and 5 positions. With a high nitrogen content, TNPy is recognized for its potent explosive capabilities, making it a significant material in the field of military applications. Its sensitivity to heat, shock, and friction necessitates meticulous handling and storage under stringent safety protocols.

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  • 146779-41-1 Structure
  • Basic information

    1. Product Name: 2,3,4,5-Tetranitro-1H-pyrrole
    2. Synonyms: 2,3,4,5-Tetranitro-1H-pyrrole
    3. CAS NO:146779-41-1
    4. Molecular Formula: C4HN5O8
    5. Molecular Weight: 247.07944
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 146779-41-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 556.819°C at 760 mmHg
    3. Flash Point: 290.554°C
    4. Appearance: /
    5. Density: 2.146g/cm3
    6. Vapor Pressure: 0mmHg at 25°C
    7. Refractive Index: 1.749
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 2,3,4,5-Tetranitro-1H-pyrrole(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2,3,4,5-Tetranitro-1H-pyrrole(146779-41-1)
    12. EPA Substance Registry System: 2,3,4,5-Tetranitro-1H-pyrrole(146779-41-1)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 146779-41-1(Hazardous Substances Data)

146779-41-1 Usage

Uses

Used in Military Applications:
2,3,4,5-Tetranitro-1H-pyrrole is used as a high-energy explosive material for its powerful detonation properties, suitable for various military applications where high explosive power is required.
Used in Explosive Production:
TNPy is utilized as a key ingredient in the production of various types of explosives and propellants, leveraging its high energy output and explosive characteristics to enhance the performance of these products.
Used in Research and Development of Energetic Materials:
In the scientific community, 2,3,4,5-Tetranitro-1H-pyrrole serves as a subject of research and development for the advancement of energetic materials, focusing on improving their efficiency, safety, and potential applications in different fields.
Due to the hazardous nature of 2,3,4,5-Tetranitro-1H-pyrrole, its use is strictly regulated, and special handling and storage measures are mandatory to ensure safety and prevent accidental detonations.

Check Digit Verification of cas no

The CAS Registry Mumber 146779-41-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,6,7,7 and 9 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 146779-41:
(8*1)+(7*4)+(6*6)+(5*7)+(4*7)+(3*9)+(2*4)+(1*1)=171
171 % 10 = 1
So 146779-41-1 is a valid CAS Registry Number.
InChI:InChI=1/C4HN5O8/c10-6(11)1-2(7(12)13)4(9(16)17)5-3(1)8(14)15/h5H

146779-41-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3,4,5-Tetranitro-1H-pyrrole

1.2 Other means of identification

Product number -
Other names -

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:146779-41-1 SDS

146779-41-1Downstream Products

146779-41-1Relevant articles and documents

Synthesis of 2,3,4,5-Tetranitropyrrole

Hinshaw, Jerald C.,Edwards, W. Wayne,George, Clifford,Gilardi, Richard

, p. 1721 - 1724 (2007/10/02)

Dealkylation of 1-tert-butyl-2,3,4-trinitropyrrole in boiling trifluoroacetic acid gave 2,3,4-trinitropyrrole, the structure of which was confirmed by X-ray crystallography.Treatment of this trinitropyrrole with nitric acid/oleum briefly at 60 deg gave 2,3,4,5-tetranitropyrrole.

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