90795

Tributyl borate

≥99.0% (T)

• Sinónimos: Boric acid tributylester, Tributoxyborane
• Fórmula lineal: [CH₃(CH₂)₃O]₃B
• Número de CAS: 688-74-4
• Peso molecular: 230.15
• Beilstein/REAXYS Number: 1703865
• EC Number: 211-706-5
• MDL number: MFCD00009434
• UNSPSC Code: 12352103
• PubChem Substance ID: 57653407
• NACRES: NA.22

Propiedades

• vapor density: 7.95 (vs air)
• assay: ≥99.0% (T)
• form: liquid
• refractive index: n20/D 1.409 (lit.); n20/D 1.409
• bp: 114-115 °C/12 mmHg (lit.); 230-235 °C (lit.)
• mp: −70 °C (lit.)
• density: 0.853 g/mL at 25 °C (lit.)
• SMILES string: CCCCOB(OCCCC)OCCCC
• InChI: 1S/C12H27BO3/c1-4-7-10-14-13(15-11-8-5-2)16-12-9-6-3/h4-12H2,1-3H3
• InChI key: LGQXXHMEBUOXRP-UHFFFAOYSA-N

Descripción

General description

Tributyl borate is an organoboron compound, that is often used as a reagent in organic synthesis for the preparation of various boronic acid derivatives, which are widely used in Suzuki coupling reactions in the synthesis of biaryls and other organic molecules. It is also used as a catalyst in a range of organic reactions, including the transesterification of esters and Biginelli reactions.

Application

Tributyl borate can be used as:    

• A catalyst in the synthesis of dihydropyrimidinone derivatives via the Biginelli reaction.   
• A boron oxide source to prepare carbon nanotube-B₂O₃ nanocomposite by solvothermal method.

Información de seguridad

• pictograms: GHS07
• signalword: Warning
• hcodes: H315,H319,H335
• pcodes: P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338
• Hazard Classifications: Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
• target_organs: Respiratory system
• Storage Class: 10 - Combustible liquids
• wgk_germany: WGK 3
• flash_point_f: 158.0 °F - closed cup
• flash_point_c: 70 °C - closed cup
• ppe: Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter