for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships 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.
Description
Reactant for:Preparation of modifiable bidentate systems via nitrogen-carbon rearrangementPreparation of bioactive boranophosphonic acidsPreparation of precursors for synthesis of boronated oligonucleotide sequencesSynthesis of dithymidine boranophosphate via the oxathiaphospholane approachPreparation of adenosine boranothiotriphosphate ribonucleoside and thymidine boranothiotriphosphate deoxyribonucleosidePreparation of borane-amine complexes
| Sourires canoniques | [B].CCN(C(C)C)C(C)C |
|---|---|
| InChIKey | BYKCUMSOQIPHSR-UHFFFAOYSA-N |
| INCHI | 1S/C8H19N.B/c1-6-9(7(2)3)8(4)5;/h7-8H,6H2,1-5H3; |
| Isomères SMILES | [B].CCN(C(C)C)C(C)C |
| WGK Allemagne | 3 |
| Poids moléculaire | 143.08 |
| Reaxy-Rn | 62255983 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=62255983&ln= |
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 | Organic nitrogen compounds |
| Classe | Organonitrogen compounds |
| Subclass | Amines |
| Intermediate Tree Nodes | Tertiary amines |
| Direct Parent | Trialkylamines |
| Alternative Parents | Organic metalloid salts Hydrocarbon derivatives |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Tertiary aliphatic amine - Organic metalloid salt - Hydrocarbon derivative - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as trialkylamines. These are organic compounds containing a trialkylamine group, characterized by exactly three alkyl groups bonded to the amino nitrogen. |
| External Descriptors | Not available |
| Indice de réfraction | 1.46 |
|---|---|
| Point d'éclair (°F) | 104 °F |
| Point d'éclair (°C) | 40 °C |
| Point de fusion (°C) | 15-17 °C |
| Poids moléculaire | 140.060 g/mol |
| XLogP3 | |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 3 |
| Exact Mass | 140.161 Da |
| Monoisotopic Mass | 140.161 Da |
| Topological Polar Surface Area | 3.200 Ų |
| Heavy Atom Count | 10 |
| Formal Charge | 0 |
| Complexity | 59.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 2 |
