12008-19-4

Basic information

• Product Name: Hexaborane(12)
• Synonyms: Boronhydride (B6H12); Dodecahydrohexaborane; arachno-Hexaborane(12)
• CAS NO: 12008-19-4
• Molecular Formula: B6H12
• Molecular Weight: 76.9613
• Mol File: 12008-19-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Hexaborane(12)(CAS DataBase Reference)
• NIST Chemistry Reference: Hexaborane(12)(12008-19-4)
• EPA Substance Registry System: Hexaborane(12)(12008-19-4)

Safety Data

• Hazardous Substances Data: 12008-19-4(Hazardous Substances Data)

Usage

General Description

Hexaborane(12) is a chemical compound with the chemical formula B6H12. It is a highly reactive and air-sensitive compound that is mainly used in the synthesis of boron-based materials. Hexaborane(12) is a colorless liquid at room temperature and is highly flammable. It has a strong, unpleasant odor and is toxic if inhaled or ingested. The compound is also used as a chemical intermediate in the production of boron-containing polymers and as a high-energy fuel for rockets and missiles. Due to its highly reactive nature, Hexaborane(12) must be handled with extreme caution and stored in a cool, dry, and well-ventilated area.

Upstream product

• 19287-45-7 diborane 

Downstream Products

• 19624-22-7 pentaborane⁽⁹⁾ 
• 19287-45-7 diborane 

Relevant articles and documents

Kinetic studies of reactions of hexaborane(10) with other binary boranes in the gas phase

Cothermolysis reactions of B6H10 with the binary boranes B2H6, B4H10, B5H9, and B5H11 have been studied by a quantitative mass-spectrometric technique to gain insight into the role of B6H10 in borane interconversion reactions. Except in the B6H10-B5H9 system the initial rate of consumption of B6H10 was found to be considerably more rapid than in the thermolysis of B6H10 alone, indicating that interactions were occuring. Detailed kinetic studies of the B6H10-B2H6 and B6H10-B4H10 reactions showed that the rate of consumption of B6H10 was governed in each case by the rate-determining step in the decomposition of the co-reactant, the orders being 3/2 with respect to B2H6 and 1 with respect to B4H10; a considerable increase in the conversion of B6H10 to B10H14 at the expense of polymeric solids was also observed. Added hydrogen was found to have very little effect on the reaction rates and product distributions in the cothermolysis reactions, in marked contrast to its effect on the reactions of B2H6 and B4H10 alone. The kinetic results are entirely consistent with earlier suggestion, based on qualitative observations, that the reactive intermediates {B3H7} and {B4H8} are scavenged by reactions with B6H10, and suggest strongly that this borane, unlike B6H12, plays a pivotal role in the build-up to B10H14 and other higher boranes.