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Tributylbismuthine, also known as tri-n-butylbismuth, is an organobismuth compound with the chemical formula (C4H9)3Bi. It is a colorless, oily liquid that is soluble in organic solvents and has a molecular weight of 446.2 g/mol. TRIBUTYLBISMUTHINE is primarily used as a catalyst in various chemical reactions, particularly in the production of polyurethane foams and as a flame retardant additive. Due to its potential toxicity and environmental concerns, tributylbismuthine is subject to strict regulations and is being phased out in some applications. It is important to handle this chemical with care, as it can pose health risks if not managed properly.

3692-81-7

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3692-81-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3692-81-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,9 and 2 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3692-81:
(6*3)+(5*6)+(4*9)+(3*2)+(2*8)+(1*1)=107
107 % 10 = 7
So 3692-81-7 is a valid CAS Registry Number.

3692-81-7SDS

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 tributylbismuthane

1.2 Other means of identification

Product number -
Other names Tributylbismuth

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:3692-81-7 SDS

3692-81-7Relevant academic research and scientific papers

Preparation and properties of dibismuthines

Ashe III, Arthur J.,Ludwig Jr., Edward G.,Oleksyszyn, Josef

, p. 1859 - 1866 (2008/10/08)

Tetramethyldibismuthine, 1, tetraisopropenyldibismuthine, 15, 1,1′-bibismolane, 16, and tetrakis(2-methyl-1-propenyl)dibismuthine, 17, have been prepared from the reaction of the corresponding tertiary bismuthines with sodium in liquid ammonia followed by treatment with 1,2-dichloroethane. Tetraphenyldibismuthine, 4, was prepared by an analogous route from diphenylbismuth chloride. While all the dibismuthines are red in solution, 1, 15, and 16 freeze to blue solids. Compounds 4 and 17 form red solids. The Raman, UV, and mass spectra of the dibismuthines are discussed. The dibismuthines thermally decompose to form bismuth metal and corresponding tertiary bismuthine. The reactions of tetramethyldibismuthine with iodine, bromotrichloromethane, benzyl bromide, hydrochloric acid, and butyllithium have been explored. The reactions afford products in which the Bi-Bi bond has been cleaved.

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