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464-10-8

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464-10-8 Usage

General Description

Prismatic crystals or oily colorless or clear dark amber liquid.

Air & Water Reactions

May be sensitive to prolonged exposure to air and light. Insoluble in water.

Reactivity Profile

tribromonitromethane decomposes with explosive violence if heated rapidly. Incompatible with oxidizing agents.

Fire Hazard

Flash point data for tribromonitromethane are not available. tribromonitromethane is probably flammable.

Safety Profile

Poison by intraperitoneal route. In vapor form it is highly toxic by ingestion and inhalation and on contact with skin, eyes, and mucous membranes. An explosive. When heated to decomposition it emits very toxic fumes of Brand NOx. See also NITRO COMPOUNDS and BROMIDES.

Purification Methods

Steam distil it, dry it with anhydrous Na2SO4 and distil it again in a vacuum. HIGHLY TOXIC. [Beilstein 1 H 77, 1 I 21, 1 II 43, 1 III 115, 1 IV 106.]

Check Digit Verification of cas no

The CAS Registry Mumber 464-10-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,6 and 4 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 464-10:
(5*4)+(4*6)+(3*4)+(2*1)+(1*0)=58
58 % 10 = 8
So 464-10-8 is a valid CAS Registry Number.
InChI:InChI=1/CBr3NO2/c2-1(3,4)5(6)7

464-10-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name tribromo(nitro)methane

1.2 Other means of identification

Product number -
Other names Bromopicrin

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:464-10-8 SDS

464-10-8Relevant articles and documents

A PROCESS FOR THE PREPARATION OF BRONOPOL

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Page/Page column 19, (2009/10/21)

The invention provides a process for preparing bronopol, which process comprises charging a reaction vessel with water, bromopicrin, nitromethane and paraformaldehyde, gradually feeding a base into said reaction vessel under stirring, bringing the reaction to completion and separating bronopol from the aqueous reaction mixture.

PROCESS OF PREPARING BROMOPICRIN

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Page/Page column 51-54; 57-59, (2008/06/13)

Process of preparing high purity bromopicrin, and high purity bromopicrin produced therefrom. Providing a mixture of nitromethane and bromine, and preferably water, and absent of organic solvent. Adding an aqueous solution of an alkaline substance to the mixture, thereby providing a reaction mixture containing bromopicrin, the adding performed such that no excess of the alkaline substance occurs in the reaction mixture during the adding. Collecting the organic phase (containing the bromopicrin) from the reaction mixture. No need for subjecting the organic phase of the reaction mixture to distillation or extraction, for obtaining near quantitative yield of bromopicrin having purity of at least equal to or greater than 96 weight percent. Process parameters controlling selectivity of reaction forming bromopicrin are molar ratio of bromine and nitromethane in the mixture; reaction temperature while bromopicrin is formed; concentration of the alkaline substance in the aqueous solution; and reaction time.

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