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Merck
CN

19667

Supelco

丁基硼酸

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

别名:

1-丁烷硼酸

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About This Item

线性分子式:
CH3(CH2)3B(OH)2
CAS号:
分子量:
101.94
Beilstein:
1733489
EC 号:
MDL编号:
UNSPSC代码:
41116105
PubChem化学物质编号:
NACRES:
NA.22

等级

for GC derivatization

质量水平

方案

≥96.0% (T)

质量

LiChropur

反应适用性

reagent type: derivatization reagent
reaction type: Alkylations

技术

gas chromatography (GC): suitable

mp

90-92 °C (lit.)
90-92 °C

SMILES字符串

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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应用


  • 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).

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)


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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)
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
F Ramos et al.
Journal of chromatography. B, Biomedical sciences and applications, 716(1-2), 366-370 (1998-11-21)
A derivatization procedure for confirmatory residue analysis of beta2-agonists is described. Methyl (MBA) and butyl (BBA) boronic acids are simultaneously used for the derivatization of tulobuterol, mabuterol, mapenterol, salbutamol, clenproperol, clenbuterol, clenpenterol and bromobuterol by GC-MS determination. A temperature of

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