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Sodium tetraethylborate - 98%, high purity , CAS No.15523-24-7

    Grade & Purity:
  • ≥98%
In stock
Item Number
S302996
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Availability
Price Qty
S302996-250mg
250mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$39.90
S302996-1g
1g
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Production requires sourcing of materials. We appreciate your patience and understanding.
$95.90
View related series
Inorganic catalysts (170)

Basic Description

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.

Taxonomic Classification

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

Names and Identifiers

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

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Chemical and Physical Properties

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

Citations of This Product

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   

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