Merck
CN

19667

Supelco

丁基硼酸

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

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别名:
1-丁烷硼酸
线性分子式:
CH3(CH2)3B(OH)2
CAS号:
分子量:
101.94
Beilstein:
1733489
EC 号:
MDL编号:
PubChem化学物质编号:
NACRES:
NA.22

等级

for GC derivatization

质量水平

检测方案

≥96.0% (T)

质量

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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其他说明

气相色谱的衍生化试剂
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).

法律信息

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)


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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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