≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature,Argon charged 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 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Product Application:
Sodium tetraethylborate is used as a derivatizing agent for the detection of organotin, lead and mercury compounds by using gas chromatography coupled with various sensitive and selective detection methods, such as atomic absorption spectrometry (AAS), atomic emission spectrometry (AES), pulsed-flame photometric detection (PFPD), and mass spectrometry (MS). It is also used as an alkylating agent.
| Sonrisas canónicas | [B-](CC)(CC)(CC)CC.[Na+] |
|---|---|
| IUPAC Name | sodium;tetraethylboranuide |
| InChIKey | SZSBMTRYJRHYNI-UHFFFAOYSA-N |
| INCHI | 1S/C8H20B.Na/c1-5-9(6-2,7-3)8-4;/h5-8H2,1-4H3;/q-1;+1 |
| Isómeros SMILES | [B-](CC)(CC)(CC)CC.[Na+] |
| Número ONU | 3393 |
| Grupo de embalaje | I |
| Peso molecular | 150.05 |
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 |
| Clase | Organometalloid compounds |
| Subclass | Organoboron compounds |
| Intermediate Tree Nodes | Alkylboranes |
| Direct Parent | Trialkylboranes |
| Alternative Parents | Organic metalloid salts Organic sodium salts Hydrocarbon derivatives Organic cations |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Trialkylborane - Organic alkali metal salt - Organic metalloid salt - Hydrocarbon derivative - Organic sodium salt - Organic salt - Organic cation - Aliphatic acyclic compound |
| Descripción | 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 |
| Solubilidad | Dissolves in water with decomposition |
|---|---|
| Sensibilidad | Moisture Sensitive； Air Sensitive |
| Punto de fusión (°C) | 140-142 °C |
| Peso molecular | 150.050 g/mol |
| XLogP3 | |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 0 |
| Exact Mass | 150.156 Da |
| Monoisotopic Mass | 150.156 Da |
| Topological Polar Surface Area | 0.000 Ų |
| Heavy Atom Count | 10 |
| Formal Charge | 0 |
| Complexity | 52.100 |
| 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 |
| 1. Huang Yuanyuan, Yang Qingwei, Song Ling, Ran Hongjie, Jiang Hui, Sun Da. (2024) Efficient eradication of organotin utilizing K2FeO4 augmented by nZVI: revelations on influential factors, kinetic dynamics, and mechanistic insights. Frontiers in Environmental Science, [PMID:] [10.3389/fenvs.2024.1358297] |
H2512520