| Weight | 230.157 g/mol |
|---|---|
| Formula | C12H27BO3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 12 |
TRIBUTYL BORATE (688-74-4)
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- Sigma-Aldrich - TRIBUTYL BORATE77.80 - 167.50 USD
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- TCI - TRIBUTYL BORATE19.00 - 103.00 USD
- Esterification of carboxylic acids by tributyl borate under solvent- and catalyst-free conditions (Green Chemistry, 2005)
- Solvothermal synthesis of carbon nanotube-B2O3 nanocomposite using tributyl borate as boron oxide source (Inorganic Chemistry Communications, 2008)
- Tributyl Borate Mediated Biginelli Reaction : A Facile Microwave-Assisted Green Synthetic Strategy toward Dihydropyrimidinones (Bulletin of the Chemical Society of Japan, 2010)
- Normal tributyl borate (1928)
- Results of turbojet engine operation tests using a 50-50 mixture of JP-4 and tributyl borate as the fuel (1957)
- Reactions of cyclodimethylsilazanes with butyl alcohol and tributyl borate (Russian Chemical Bulletin, 1965)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESB(OCCCC)(OCCCC)OCCCC
-
InChIKeyLGQXXHMEBUOXRP-UHFFFAOYSA-N
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(102-70-5)
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(143-27-1, 68037-95-6)
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(122-51-0, 108055-42-1)
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(1838-19-3, 112-90-3)
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TRIBUTYL BORATE
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