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Bromine azide (BrN3) is a chemical compound that exists in the form of crystals or a red liquid. It is characterized by its strong oxidizing properties and is highly reactive, making it prone to explosion when subjected to shock or heat.

13973-87-0

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13973-87-0 Usage

Uses

Used in Explosive Industry:
Bromine azide is used as a strong oxidizing agent for the production of detonators and other explosive devices. Its high reactivity and explosive nature make it a crucial component in the creation of these devices, ensuring their effectiveness and reliability in various applications.

Hazard

Explosive when heated or shocked. Will ignite combustible materials on contact.

Safety Profile

A poison. Can explode spontaneously. The solid, liquid and vapor are shock-sensitive explosives. Concentrated solutions in organic solvents may explode. Moderate fire hazard in the form of vapor by chemical reaction. A powerful oxidant. Moderately explosive when exposed to heat. The liquid explodes on contact with arsenic, sodium, silver foil, or phosphorus. Incompatible with Sb, ethyl ether, Ag, metals. When heated to decomposition it emits highly toxic fumes of Brand explodes. See also BROMINE and AZIDES.

Check Digit Verification of cas no

The CAS Registry Mumber 13973-87-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,9,7 and 3 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 13973-87:
(7*1)+(6*3)+(5*9)+(4*7)+(3*3)+(2*8)+(1*7)=130
130 % 10 = 0
So 13973-87-0 is a valid CAS Registry Number.
InChI:InChI=1/BrN3/c1-3-4-2

13973-87-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Bromine azide

1.2 Other means of identification

Product number -
Other names Azidobromide

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:13973-87-0 SDS

13973-87-0Relevant articles and documents

Solid-state structure of bromine azide

Lyhs, Benjamin,Blaeser, Dieter,Woelper, Christoph,Schulz, Stephan,Jansen, Georg

, p. 1970 - 1974 (2012)

A new twist: The single-crystal structural analysis of BrN3 is described. In contrast to IN3, which forms chains, BrN3 forms a helical structure in the solid state (see picture). Such a structural feature has not been previously observed in covalent p-block azide chemistry.

Low viscosity azide-containing mono and dicationic ionic liquids with unsaturated side chain

Fareghi-Alamdari, Reza,Hatefipour, Razieh

, p. 793 - 799 (2016/12/30)

A new class of azide-functionalized monocationic and unsymmetrical dicationic ionic liquids (ILs) with low viscosity and high liquid range was synthesized. All of the synthesized ILs, were characterized by FT-IR, 1HNMR, 13CNMR spectroscopies and elemental analysis. Some thermophysical properties including melting point, density, shear viscosity, decomposition temperature and heat capacity of the unsymmetrical dicationic azide functionalized IL with dicyanamide (DCA) were measured. To find the unique and general features of this dicationic IL, its properties were compared with the ones of the similar monocationic ILs. The results showed that the shear viscosity, density, thermal stability and heat capacity of the unsymmetrical dicationic IL are higher than monocationic analogues. In addition we found that the shear viscosity for the synthesized unsymmetrical dicationic IL containing azide group and DCA anion is 83.9?cP whereas the shear viscosities for other dicationic ILs reported in the literature are higher than 240?cP.

Antineoplastic heteronapthoquinones

-

, (2008/06/13)

This invention relates to a naphthoquinone derivatives, to processes and to intermediates for preparing these derivatives, to pharmaceutical composition and to the use of these derivatives as antitumor agents in mammals.

Processes antineoplastic heteronaphthoquinones

-

, (2008/06/13)

This invention relates to a naphthoquinone derivatives, to processes and to intermediates for preparing these derivatives, to pharmaceutical composition and to the use of these derivatives as antitumor agents in mammals.

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