1.0 M in THF for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships Normal Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Catalyst for: · Allylic alkylations for synthesis of unsaturated aldehydes and alcohols. · Cis-addition of carbon-hydrogen bonds of pyrroles and thiophenes to alkynes. · Borane-induced radical reduction of alkenyl and alkynyliodanes. · Initiating polymerization for synthesis of polymethylenes and ethylene-propylene. · Asymmetric synthesis of vinylglycidols. · Asymmetric addition of alcohols to vinyl epoxides.
| Pubchem Sid | 504756526 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504756526 |
| Sorrisi canonici | B(C(C)CC)(C(C)CC)C(C)CC |
| IUPAC Name | tri(butan-2-yl)borane |
| InChIKey | YUPAWYWJNZDARM-UHFFFAOYSA-N |
| INCHI | 1S/C12H27B/c1-7-10(4)13(11(5)8-2)12(6)9-3/h10-12H,7-9H2,1-6H3 |
| Isomeri SMILES | B(C(C)CC)(C(C)CC)C(C)CC |
| WGK Germania | 1 |
| PubChem CID | 102559 |
| Numero UN | 2056 |
| Gruppo di imballaggio | II |
| Peso molecolare | 182.15 |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organometallic compounds |
| Classe | Organometalloid compounds |
| Subclass | Organoboron compounds |
| Intermediate Tree Nodes | Alkylboranes |
| Direct Parent | Trialkylboranes |
| Alternative Parents | Hydrocarbon derivatives |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Trialkylborane - Hydrocarbon derivative - Aliphatic acyclic compound |
| Descrizione | This compound belongs to the class of organic compounds known as trialkylboranes. These are organoboron compounds where the boron atom is substituted by only three alkyl groups. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Data | Oggetto |
|---|---|---|---|
 F2202255 | Certificate of Analysis | Dec 10, 2025 | T140660 |
| F2202256 | Certificate of Analysis | Dec 10, 2025 | T140660 |
| K2113104 | Certificate of Analysis | May 09, 2025 | T140660 |
| K2222386 | Certificate of Analysis | Aug 22, 2024 | T140660 |
| L2010126 | Certificate of Analysis | Jun 19, 2024 | T140660 |
| Peso molecolare | 182.160 g/mol |
|---|---|
| XLogP3 | |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 0 |
| Rotatable Bond Count | 6 |
| Exact Mass | 182.221 Da |
| Monoisotopic Mass | 182.221 Da |
| Topological Polar Surface Area | 0.000 Ų |
| Heavy Atom Count | 13 |
| Formal Charge | 0 |
| Complexity | 98.500 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 3 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
