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Bipicryl, also known as HNBP (2,2-Bis(4-nitrophenyl)acetonitrile), is a chemical compound characterized by its yellow crystalline appearance and high sensitivity to heat, shock, and friction. It is recognized for its potent explosive properties, which necessitate stringent safety measures during handling. Due to its hazardous nature, Bipicryl is regulated and restricted to authorized use by specific individuals and organizations.

4433-16-3

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4433-16-3 Usage

Uses

Used in Color Photography:
Bipicryl, HNBP is used as a sensitizer in color photography for enhancing the sensitivity of photographic materials to light, allowing for the capture of images under various lighting conditions.
Used in Military and Commercial Applications:
Bipicryl, HNBP is used as an explosive ingredient in military and commercial applications for its powerful detonation capabilities. Its high sensitivity to heat, shock, and friction makes it a potent explosive material, but also requires careful handling and strict safety protocols to prevent accidental detonation.
Due to the inherent risks associated with Bipicryl's explosive properties, its use is strictly limited and controlled in many countries, ensuring that only authorized individuals and organizations have access to this highly sensitive compound.

Check Digit Verification of cas no

The CAS Registry Mumber 4433-16-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,3 and 3 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4433-16:
(6*4)+(5*4)+(4*3)+(3*3)+(2*1)+(1*6)=73
73 % 10 = 3
So 4433-16-3 is a valid CAS Registry Number.

4433-16-3SDS

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 1,3,5-trinitro-2-(2,4,6-trinitrophenyl)benzene

1.2 Other means of identification

Product number -
Other names Biphenyl,2,2',4,4',6,6'-hexanitro-(6CI,7CI,8CI)

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:4433-16-3 SDS

4433-16-3Downstream Products

4433-16-3Relevant articles and documents

Ullmann reaction of picryl bromide in the presence of ultrasound

Nelson,Adolph

, p. 293 - 305 (2007/10/02)

Ultrasonic irradiation was found to promote the Ullman coupling of picryl bromide at or below room temperature. In the presence of excess copper, a long-lived intermediate is formed that is quenched upon work-up affording variable mixtures of trinitrobenzene and picric acid.

Synthesis of Polynitro-Substituted 2'-Nitrobiphenyl-2-amines, Analogues of Polynitro Benzocinnoline Oxide Derivatives

Bell, Anthony J.,Read, Roger W.

, p. 1813 - 1829 (2007/10/02)

2',3,4',5- and 2',3,5,6'-Tetranitrobiphenyl-2-amines, and 2',3,4',5,6'- and 2',4,4',6,6'-pentanitrobiphenyl-2-amines, have been synthesized for the first time, along with the known 2,4,8- and 2,4,10-trinitrobenzocinnoline 6-oxides and 1,3,7,9-tetranitrobenzocinnoline 5-oxide.The benzocinnoline oxide derivatives were found to have higher densities and thermal stability than those of the corresponding biphenylamines.These observations are discussed in terms of structure.

SYNTHESIS OF POLYNITRO-SUBSTITUTED 2-CARBOXYBIPHENYLS

Adrievskii, A. M.,Poplavskii, A. N.,Dyumaev, K. M.

, p. 1195 - 1198 (2007/10/02)

Methods were developed for the synthesis of polynitro-substituted 2-carboxybiphenyls.During the nitration of 2-carboxybiphenyl under rigorous conditions or during the heating of nitro-substituted 2-carboxybiphenyls in concentrated sulfuric acid or high-strength oleum decarboxylation and cyclization occur with the formation of nitro-substituted biphenyls and fluorenone.

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