Molecular Formula | C9H19BO3 |
Molar Mass | 186.06 |
Density | 0.912g/mLat 25°C(lit.) |
Boling Point | 73°C15mm Hg(lit.) |
Flash Point | 109°F |
Water Solubility | Soluble in water. |
Vapor Presure | 4.924mmHg at 25°C |
Appearance | Liquid |
Specific Gravity | 0.912 |
Color | Colorless |
BRN | 1906370 |
Storage Condition | Inert atmosphere,2-8°C |
Sensitive | Moisture Sensitive |
Refractive Index | n20/D 1.409(lit.) |
Hazard Symbols | Xi - Irritant |
Risk Codes | R10 - Flammable R36/37/38 - Irritating to eyes, respiratory system and skin. |
Safety Description | S16 - Keep away from sources of ignition. S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36 - Wear suitable protective clothing. |
UN IDs | UN 1993 3/PG 3 |
WGK Germany | 3 |
HS Code | 29209090 |
Hazard Class | 3 |
Packing Group | III |
introduction | isopropanol pinacol borate is an organic synthesis intermediate, used for aromatic ring coupling, and can be used in pharmaceutical research and development, photoelectric functional materials. After inadvertent contact with the eyes, immediately rinse with plenty of water and seek the doctor's advice. Wear appropriate protective clothing. |
application | isopropanol pinaol borate is an organic intermediate, which has been reported in the literature to be used to prepare corrugated paper high-strength adhesive, polymer absorbent and water-resistant antibacterial plastic masterbatch, etc. |
use | add triisopropyl borate (261.0g, 1.388 mol) and pinacol (142.5g, 1.207 mol) to a 20-liter four-neck bottle and heat it to ~ 90 ℃ for 12-16 hours. The standard for the completion of the reaction is through GC, pinacol <4.0%. After completion, the reaction is converted into distillation and the product fraction is collected (boiling at 174-178 degrees C). The title product was obtained in a colorless oil form in the 80-90% th yield range in six 20-liter batches in operation. GC records the purity of 87-96%, but 1H NMR shows that the product is very pure. Organic synthesis intermediates, used for aromatic ring coupling, can be used in pharmaceutical research and development, photoelectric functional materials. |