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Butylboronic acid

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

Synonym(s):

1-Butaneboronic acid

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About This Item

Linear Formula:
CH3(CH2)3B(OH)2
CAS Number:
Molecular Weight:
101.94
Beilstein:
1733489
EC Number:
MDL number:
UNSPSC Code:
41116105
PubChem Substance ID:
NACRES:
NA.22

grade

for GC derivatization

Quality Level

Assay

≥96.0% (T)

quality

LiChropur

reaction suitability

reagent type: derivatization reagent
reaction type: Alkylations

technique(s)

gas chromatography (GC): suitable

mp

90-92 °C (lit.)
90-92 °C

SMILES string

CCCCB(O)O

InChI

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

InChI key

QPKFVRWIISEVCW-UHFFFAOYSA-N

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Application


  • 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).

Other Notes

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).

Legal Information

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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D.R. Knapp
Handbook of Analytical Derivatization Reactions (1979)
A. Darbre et al.
Handbook of Derivatives for Chromatography (1970)
[Gas chromatographic separation of the diastereomers of labetalol as n-butylboronate].
T Goromaru et al.
Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan, 103(9), 974-978 (1983-09-01)
J O Baker et al.
Biochemical and biophysical research communications, 130(3), 1154-1160 (1985-08-15)
The transition-state-analog inhibitor, 1-butaneboronic acid, markedly enhances the uptake of one g-atom of Zn2+ ions from a metal ion buffer system by Zn-depleted Aeromonas aminopeptidase. In contrast, a substrate-analog inhibitor, n-valeramide, does not perturb the equilibrium between Zn2+ ions and
M Inouye et al.
Japanese journal of medicine, 27(1), 29-33 (1988-02-01)
A highly sensitive and specific quantitative assay for inositol in serum has been developed. Uremic serum, to which hexahydroxybenzene as an internal standard was added, was deproteined with trichloroacetate. The supernatant aqueous phase was taken after lipids in serum were

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