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| SKU | Size | Availability |
Price | Qty |
|---|---|---|---|---|
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S302996-250mg
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250mg |
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
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$39.90
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S302996-1g
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1g |
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
|
$95.90
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| Synonyms | Sodium tetraethylborate | 15523-24-7 | sodium;tetraethylboranuide | Borate(1-), tetraethyl-, sodium | MFCD00061547 | Sodium tetraethylborate, 97% | DTXSID90165859 | BCP23723 | BORATE(1-),TETRAETHYL-, SODIUM (1:1) |
|---|---|
| Specifications & Purity | ≥98% |
| Storage Temp | Room temperature,Argon charged |
| Shipped In | Normal |
| Product Description |
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. |
Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organometallic compounds |
| Class | 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 |
| Description | 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 |
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| IUPAC Name | sodium;tetraethylboranuide |
|---|---|
| INCHI | InChI=1S/C8H20B.Na/c1-5-9(6-2,7-3)8-4;/h5-8H2,1-4H3;/q-1;+1 |
| InChIKey | SZSBMTRYJRHYNI-UHFFFAOYSA-N |
| Smiles | [B-](CC)(CC)(CC)CC.[Na+] |
| Isomeric SMILES | [B-](CC)(CC)(CC)CC.[Na+] |
| PubChem CID | 23681030 |
| Molecular Weight | 150.05 |
| Solubility | Dissolves in water with decomposition |
|---|---|
| Sensitivity | Moisture Sensitive; Air Sensitive |
| Melt Point(°C) | 140-142 °C |
| Molecular Weight | 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, 12 |