missing translation for 'onlineSavingsMsg'
Learn More
Learn More
Triisopropyl borate, 98+%
CAS: 5419-55-6 | C9H21BO3 | 188.074 g/mol
$106.66 - $905.56
Chemical Identifiers
| CAS | 5419-55-6 |
|---|---|
| Molecular Formula | C9H21BO3 |
| Molecular Weight (g/mol) | 188.074 |
| MDL Number | MFCD00008872 |
| InChI Key | NHDIQVFFNDKAQU-UHFFFAOYSA-N |
| Synonym | triisopropyl borate, isopropyl borate, triisopropoxyborane, triisopropoxyboron, boron isopropoxide, triisopropyl orthoborate, boric acid triisopropyl ester, triisopropoxy borane, boron triisopropoxide, boric acid h3bo3 , tris 1-methylethyl ester |
| PubChem CID | 21531 |
| IUPAC Name | tripropan-2-yl borate |
| SMILES | B(OC(C)C)(OC(C)C)OC(C)C |
| Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
|---|---|---|---|---|---|---|---|---|---|
| Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
|
AAA17592AE
|
Thermo Scientific Chemicals
A17592AE |
100 mL |
Each for $106.66
|
|
|||||
|
AAA17592AP
|
Thermo Scientific Chemicals
A17592AP |
500 mL |
Each for $246.97
|
|
|||||
|
AAA175920F
|
Thermo Scientific Chemicals
A175920F |
2500 mL |
Each for $905.56
|
|
|||||
Description
Triisopropyl borate is used as reagent in Pd-catalyzed coupling reaction with aryl halides such as Suzuki reaction. It is used as a reagent for the preparation of the boronic acids and esters; as a Lewis acid catalyst and involved in the ortho-borylation of 1-substituted naphthalenes. Furthermore, it plays an important role as a catalyst for the production of resins, waxes, paints and varnishes.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
ApplicationsTriisopropyl borate is used as reagent in Pd-catalyzed coupling reaction with aryl halides such as Suzuki reaction. It is used as a reagent for the preparation of the boronic acids and esters; as a Lewis acid catalyst and involved in the ortho-borylation of 1-substituted naphthalenes. Furthermore, it plays an important role as a catalyst for the production of resins, waxes, paints and varnishes.
Solubility
Miscible with ether, ethanol, isopropanol and benzene.
Notes
Moisture sensitive. Keep the container tightly closed in a dry and well-ventilated place. Incompatible with strong oxidizing agents. Decomposes in water.
Chemical Identifiers
| 5419-55-6 | |
| 188.074 | |
| NHDIQVFFNDKAQU-UHFFFAOYSA-N | |
| 21531 | |
| B(OC(C)C)(OC(C)C)OC(C)C |
| C9H21BO3 | |
| MFCD00008872 | |
| triisopropyl borate, isopropyl borate, triisopropoxyborane, triisopropoxyboron, boron isopropoxide, triisopropyl orthoborate, boric acid triisopropyl ester, triisopropoxy borane, boron triisopropoxide, boric acid h3bo3 , tris 1-methylethyl ester | |
| tripropan-2-yl borate |
Specifications
| 5419-55-6 | |
| 0.815 | |
| 17°C (62°F) | |
| C9H21BO3 | |
| [(CH3)2CHO]3B | |
| 100 mL | |
| 1701469 | |
| triisopropyl borate, isopropyl borate, triisopropoxyborane, triisopropoxyboron, boron isopropoxide, triisopropyl orthoborate, boric acid triisopropyl ester, triisopropoxy borane, boron triisopropoxide, boric acid h3bo3 , tris 1-methylethyl ester | |
| NHDIQVFFNDKAQU-UHFFFAOYSA-N | |
| tripropan-2-yl borate | |
| 21531 | |
| ≥98% |
| -59°C | |
| 139°C to 141°C | |
| Alcohol-like | |
| 1.376 | |
| MFCD00008872 | |
| UN2616 | |
| Moisture sensitive | |
| Miscible with ether,ethanol,isopropanol and benzene. | |
| B(OC(C)C)(OC(C)C)OC(C)C | |
| 188.074 | |
| 188.08 | |
| Triisopropyl borate |
Safety and Handling
GHS H Statement
H225
Highly flammable liquid and vapour.
P210-P233-P240-P241-P242-P243-P280-P303+P361+P353-P370+P378q-P501c
H225
DOTInformation : Transport Hazard Class: 3; Packing Group: II; Proper Shipping Name: TRIISOPROPYL BORATE
EINECSNumber : 226-529-9
RTECSNumber : ED5950000
TSCA : Yes
Recommended Storage : Ambient temperatures; Store under Argon
RUO – Research Use Only