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Merck
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Documentos

19667

Supelco

Butylboronic acid

for GC derivatization, LiChropur™, ≥96.0% (T)

Sinônimo(s):

1-Butaneboronic acid

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About This Item

Fórmula linear:
CH3(CH2)3B(OH)2
Número CAS:
4426-47-5
Peso molecular:
101.94
Beilstein:
1733489
Número CE:
224-607-7
Número MDL:
MFCD00002106
Código UNSPSC:
41116105
ID de substância PubChem:
329751928
NACRES:
NA.22

grau

for GC derivatization

Nível de qualidade

100

Ensaio

≥96.0% (T)

qualidade

LiChropur™

adequação da reação

reagent type: derivatization reagent
reaction type: Alkylations

técnica(s)

gas chromatography (GC): suitable

pf

90-92 °C (lit.)
90-92 °C

cadeia de caracteres SMILES

CCCCB(O)O

InChI

1S/C4H11BO2/c1-2-3-4-5(6)7/h6-7H,2-4H2,1H3

chave InChI

QPKFVRWIISEVCW-UHFFFAOYSA-N

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Aplicação


  • Developing a reference measurement procedure for free glycerol in human serum by two-step gas chromatography-isotope dilution mass spectrometry.: This research employs butylboronic acid in a reference measurement procedure to quantify free glycerol in human serum. The method is significant for clinical diagnostics, providing accurate and reliable measurements for metabolic studies (Chen et al., 2015).

Outras notas

Derivatizing agent for gas chromatography
Reagent for butylboronate.
Suitable for the derivatization of proximal difunctional compounds (a- and ß-hydroxyacids; Ο-phenolic acids; enolizable a-oxo acids; 1,2- and 1,3-diols; enolizable 1,2- and 1,3-ketols; ß- and γ-hydroxyamines).

Informações legais

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

Eyeshields, Gloves, type N95 (US)

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Certificados de análise (COA)

Lot/Batch Number
0000217050
0000286382
0000201062
0000256879

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A. Darbre et al.
Handbook of Derivatives for Chromatography (1970)
D.R. Knapp
Handbook of Analytical Derivatization Reactions (1979)
Michał K Cyrański et al.
The Journal of chemical physics, 128(12), 124512-124512 (2008-04-02)
Boronic acids have emerged as one of the most useful class of organoboron molecules, with application in synthesis, catalysis, analytical chemistry, supramolecular chemistry, biology, and medicine. In this study, the structural and spectroscopic properties of n-butylboronic acid were investigated using
C C De Paola et al.
Biochemistry, 38(28), 9048-9053 (1999-07-22)
Hydrolases containing two metal ions connected by a bridging ligand catalyze reactions important in carcinogensis, tissue repair, post-translational modification, control and regulation of biochemical pathways, and protein degradation. The aminopeptidase from Aeromonas proteolytica serves as a paradigm for the study
Alicja J Copik et al.
Inorganic chemistry, 44(5), 1160-1162 (2005-03-01)
Metalloproteases utilize their active site divalent metal ions to generate a nucleophilic water/hydroxide. For methionine aminopeptidases (MetAPs), the exact location of this nucleophile, as well as of the substrate, with respect to the active site metal ion is unknown. In
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