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Fusarsäure

for HPLC derivatization, ≥99.0% (HPLC)

Synonym(e):

5-Butyl-picolinsäure, 5-Butyl-pyridin-2-carbonsäure

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About This Item

Empirische Formel (Hill-System):
C10H13NO2
CAS-Nummer:
536-69-6
Molekulargewicht:
179.22
Beilstein:
125804
EG-Nummer:
208-643-0
MDL-Nummer:
MFCD00006298
UNSPSC-Code:
12352204
NACRES:
NA.22

Qualität

for HPLC derivatization

Qualitätsniveau

100

Assay

≥99.0% (HPLC)

Methode(n)

HPLC: suitable

SMILES String

CCCCc1ccc(nc1)C(O)=O

InChI

1S/C10H13NO2/c1-2-3-4-8-5-6-9(10(12)13)11-7-8/h5-7H,2-4H2,1H3,(H,12,13)

InChIKey

DGMPVYSXXIOGJY-UHFFFAOYSA-N

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Allgemeine Beschreibung

Fusaric acid is a novel proton-affinitive derivatizing agent, having an ionization moiety and a hydrophobic moiety. It is commonly used for the derivatization of alcohols and phenols, by liquid chromatography coupled with electrospray ionization tandem mass spectrometry (LC/ESI-MS/MS).

Anwendung

Fusaric acid may be used as a derivatizing reagent for the quantification of hydroxysteroids and dehydroepiandrosterone (DHEA) and sulfated DHEA in biological samples using liquid chromatography electrospray-ionization-tandem mass spectrometry (LC/ESI-MS/MS) technique.

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Piktogramme

Exclamation mark
GHS07

Signalwort

Warning

H-Sätze

H302

Gefahreneinstufungen

Acute Tox. 4 Oral

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

Lot/Batch Number
BCCK7071
BCBT2161

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Die Dokumentenbibliothek aufrufen

Sevcan Mamur et al.
Drug and chemical toxicology, 43(2), 149-157 (2018-09-12)
Fusaric acid (FA) is produced by several Fusarium species and is commonly found in grains. This investigation was performed to evaluate the cytotoxic and genotoxic effects of FA either in human cervix carcinoma (HeLa) cell line using 3-(4,5-dimethylthiazolyl-2)-2,5 diphenyltetrazolium bromide
Chemical derivatization to enhance ionization of anabolic steroids in LC-MS for doping-control analysis
I. Athanasiadou et all.
TrAC, Trends in Analytical Chemistry, 42, 137-156 (2013)
Kouwa Yamashita et al.
Journal of the American Society for Mass Spectrometry, 21(2), 249-253 (2009-11-17)
A highly sensitive derivatization method for liquid chromatography (LC)-electrospray ionization (ESI) tandem mass spectrometry of dehydroepiandrosterone (DHEA), testosterone (T), pregnenolone (P5), and 17alpha-OH-pregnenolone (17-OHP5) was developed based on the use of fusaric acid as a reagent. DHEA, P5, and 17-OHP5
Yasuhiro Shibata et al.
The Journal of steroid biochemistry and molecular biology, 145, 193-199 (2014-05-06)
A reliable and sensitive method for analyzing steroids using liquid chromatography tandem mass spectrometry (LC-MS/MS) is required for research concerning dehydroepiandrosterone (DHEA), which plays a central role in steroid hormone biosynthesis and metabolism. Furthermore, after the first proposal of the
T Santa
Drug discoveries & therapeutics, 7(1), 9-17 (2013-03-26)
Liquid chromatography coupled with electrospray ionization tandem mass spectrometry (LC/ESI-MS/MS) has been frequently utilized for the sensitive and selective determination of the trace level compounds in biological samples. In LC/ESI-MS/MS, chemical derivatization is sometimes used to enhance the detection sensitivity

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