7359-98-0

Basic information

• Product Name: 2,4,6-Tributylboroxin
• Synonyms: 2,4,6-Tributylboroxin;Tributylboroxin
• CAS NO: 7359-98-0
• Molecular Formula: C₁₂H₂₇B₃O₃
• Molecular Weight: 251.774
• Mol File: 7359-98-0.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 271.2°Cat760mmHg
• Flash Point: 117.8°C
• Appearance: /
• Density: 0.86g/cm³
• Vapor Pressure: 0.0109mmHg at 25°C
• Refractive Index: 1.401
• CAS DataBase Reference: 2,4,6-Tributylboroxin(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4,6-Tributylboroxin(7359-98-0)
• EPA Substance Registry System: 2,4,6-Tributylboroxin(7359-98-0)

Safety Data

• Hazardous Substances Data: 7359-98-0(Hazardous Substances Data)

Usage

General Description

2,4,6-Tributylboroxin is a chemical compound with the molecular formula C15H33BO3. It is a boron-based compound that is commonly used as a catalyst in organic synthesis reactions. This chemical is known for its ability to facilitate various chemical reactions, including the formation of carbon-carbon bonds and the conversion of organic compounds into different forms. 2,4,6-Tributylboroxin is also used as a reagent in organic reactions and has been studied for its potential applications in medicinal chemistry and materials science. It is a colorless, odorless liquid with a relatively low melting point and boiling point, making it easy to handle and store in laboratory settings.

InChI:InChI=1/C12H27B3O3/c1-4-7-10-13-16-14(11-8-5-2)18-15(17-13)12-9-6-3/h4-12H2,1-3H3

Upstream product

• 45085-78-7 (n-C₄H₉)2BNHCOCH₃ 
• 111-66-0 oct-1-ene 
• 13292-87-0 dimethylsulfide borane complex 
• 122-56-5 tributyl borane 
• 80937-33-3 oxygen 

Downstream Products

• 14090-22-3 butyl-dichloro-borane 
• 106-97-8 n-butane 
• 4426-47-5 butylboronic acid 
• 11113-50-1 boric acid 
• 129145-37-5 (R)-(+)-2-butyl-CBS-oxazaborolidine 
• 7647-01-0 hydrogenchloride 
• 10294-34-5 boron trichloride 
• 32429-86-0 Dibutan-1-borinsaeure-ethylester 
• 101-36-0 tri-n-butoxyboroxin 
• 129145-37-5 (S)-tetrahydro-1-butyl-3,3-diphenyl-1H,3H-pyrrolo{2,1-c}{1,3,2}oxazaborole 
• 122-56-5 tributyl borane 

Relevant articles and documents

Low-Temperature Hypergolic Ignition of 1-Octene with Low Ignition Delay Time

The attainment of the efficient ignition of traditional liquid hydrocarbons of scramjet combustors at low flight Mach numbers is a challenging task. In this study, a novel chemical strategy to improve the reliable ignition and efficient combustion of hydrocarbon fuels was proposed. A directional hydroboration reaction was used to convert hydrocarbon fuel into highly active alkylborane, thereby leading to changes in the combustion reaction pathway of hydrocarbon fuel. A directional reaction to achieve the hypergolic ignition of 1-octene was designed and developed by using Gaussian simulation. Borane dimethyl sulfide (BDMS), a high-energy additive, was allowed to react spontaneously with 1-octene to achieve the hypergolic ignition of liquid hydrocarbon fuel at -15 °C. Compared with the ignition delay time of pure 1-octene (565 °C), the ignition delay time of 1-octene/BDMS (9:1.2) decreased by 3850% at 50 °C. Fourier transform infrared spectroscopy and gas chromatography-mass spectrometry confirmed the directional reaction of the hypergolic ignition reaction pathway of 1-octene and BDMS. Moreover, optical measurements showed the development trend of hydroxyl radicals (OH·) in the lower temperature hypergolic ignition and combustion of 1-octene. Finally, this study indicates that the enhancement of the low-temperature ignition performance of 1-octene by hydroboration in the presence of BDMS is feasible and promising for jet propellant design with tremendous future applications.