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Key Documents

41062

Supelco

Sodium tetrapropylborate

for GC derivatization, LiChropur, ≥85.0% (T)

Synonyma:

NaBPr4

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About This Item

Číslo CAS:
Beilstein/REAXYS Number:
4007550
MDL number:
UNSPSC Code:
12352200
NACRES:
NA.22

grade

for GC derivatization

Quality Level

assay

≥85.0% (T)

form

solid

quality

LiChropur

reaction suitability

reagent type: catalyst
core: boron

reagent type: derivatization reagent
reaction type: Alkylations

technique(s)

gas chromatography (GC): suitable

SMILES string

CCC[B-](CCC)(CCC)CCC.[Na+]

General description

Sodium tetrapropylborate (NaBPr4) belongs to the class of tetraalkylborates, which are commonly used as derivatization agents to accomplish the multielement speciation of organometallic compounds on account of their ability to react with elements such as mercury, lead and tin. NaBPr4 is preferred because it eliminates the need for organic solvents as required in Grignard reactions, also resulting in reduced analysis time.

Application

Sodium tetrapropylborate may be used as a derivatization agent to enhance the sensitivity of methylmercury in fish, organolead compounds in water and road dust samples and mercury species in sea water samples prior to their determination using microwave digestion with gas chromatography-mass spectrometry (GC-MS), GC coupled to microwave-induced plasma atomic-emission spectrometry (MIP-AES) and GC with inductively coupled plasma (ICP) MS, respectively.

Recommended products

Discover LiChropur reagents ideal for HPLC or LC-MS analysis

Legal Information

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

related product

Č. produktu
Popis
Stanovení ceny

pictograms

Flame

signalword

Danger

hcodes

Hazard Classifications

Pyr. Sol. 1 - Water-react 2

Storage Class

4.2 - Pyrophoric and self-heating hazardous materials

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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Navštívit knihovnu dokumentů

In situ propylation using sodium tetrapropylborate as a fast and simplified sample preparation for the speciation analysis of organolead compounds using GC-MIP-AES
Heisterkamp M and Adams FC
Journal of Analytical Atomic Spectrometry, 14(9), 1307-1311 (1999)
Comparison of two derivatization reagents for the simultaneous determination of organolead and organomanganese compounds using solid-phase microextraction followed by gas chromatography with atomic emission detection
Pe?alver R, et al.
Talanta, 87(8), 268-275 (2011)
Mercury speciation analysis in sea water by solid phase microextraction-gas chromatography-inductively coupled plasma mass spectrometry using ethyl and propyl derivatization. Matrix effects evaluation
Bravo-Sanchez LR, et al.
Spectrochimica Acta. Part B: Atomic Spectroscopy, 59(1), 59-66 (2004)
Determination of methylmercury in fish using focused microwave digestion following by Cu2+ addition, sodium tetrapropylborate derivatization, n-heptane extraction, and gas chromatography-mass spectrometry
Chen SS, et al.
Journal of Chromatography A, 1024(1-2), 209-215 (2004)
A comparison of alkyl derivatization methods for speciation of mercury based on solid phase microextraction gas chromatography with furnace atomization plasma emission spectrometry detection.
Grinberg P, et al.
Journal of Analytical Atomic Spectrometry, 18(8), 902-909 (2003)

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