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Merck

87472

Supelco

Hydrogen chloride solution

~3 M in 1-butanol, for GC derivatization, LiChropur

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About This Item

CAS号:
Beilstein:
1098214
MDL编号:
UNSPSC代码:
12352301
PubChem化学物质编号:
NACRES:
NA.22
价格与库存信息目前不能提供

产品名称

氯化氢 - 1-丁醇 溶液, ~3 M in 1-butanol, for GC derivatization, LiChropur

等级

derivatization grade ((GC derivatization))
for GC derivatization

质量水平

表单

solution

质量

LiChropur

反应适用性

reagent type: derivatization reagent
reaction type: Acylations

浓度

~3 M in 1-butanol

技术

gas chromatography (GC): suitable

密度

0.87 g/mL at 20 °C

储存温度

2-8°C

SMILES字符串

Cl

InChI

1S/ClH/h1H

InChI key

VEXZGXHMUGYJMC-UHFFFAOYSA-N

一般描述

Acylation, an alternative to silylation, is the conversion of compounds that contain active hydrogens (-OH, -SH and -NH) into esters, thioesters, and amides through the action of a carboxylic acid or derivative. The presence of a carbonyl group adjacent to the halogenated carbons enhances electron capture detector (ECD) response. Acylation has many benefits:
  • It improves the stability of compounds by protecting unstable groups.
  • It may confer volatility on substances such as carbohydrates or amino acids, which have so many polar groups that they are non-volatile and normally decompose on heating.
  • It assists in separations not possible with underivatized compounds.
  • Compounds are detectable at very low levels with an ECD.

Hydrogen chloride-1-butanol is a reagent utilized to form fragmentation-directing derivatives for GC/MS analysis.

应用

Hydrogen chloride - 1-butanol solution has been used for butylation of amino acids during blood sample analysis for determination of ethylenediaminetetraacetic acid using mass spectrometry.

其他说明

Reagent for the esterification of amino acids and carnites for GC-MS analysiscitation
GC-MS 分析氨基酸和肉碱的酯化试剂[1]

法律信息

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

警示用语:

Danger

危险分类

Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 3 - Met. Corr. 1 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

储存分类代码

3 - Flammable liquids

WGK

WGK 1

个人防护装备

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter


历史批次信息供参考:

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M S Rashed et al.
Clinical chemistry, 43(7), 1129-1141 (1997-07-01)
Metabolic profiling of amino acids and acylcarnitines from blood spots by automated electrospray tandem mass spectrometry (ESI-MS/MS) is a powerful diagnostic tool for inborn errors of metabolism. New approaches to sample preparation and data interpretation have helped establish the methodology
Q Miao et al.
Physical review letters, 109(23), 233905-233905 (2013-02-02)
X-ray lasing is predicted to ensue when molecules are pumped into dissociative core-excited states by a free-electron-laser pulse. The lasing is due to the population inversion created in the neutral dissociation product, and the process features self-trapping of the x-ray
J Marwaha et al.
Experimental parasitology, 134(1), 12-17 (2013-02-16)
Intestinal cestodes with complex life cycles have to pass through the acid stomach lumen of their vertebrate host(s) in order to reach their preferred site of development. The cestode's tegument is the only organ in constant contact with this hostile
Elena N Makarova et al.
Carbohydrate polymers, 92(2), 1817-1826 (2013-02-13)
The pectic polysaccharide named abienan AS-A was isolated from the wood greenery of Abies sibirica using dilute hydrochloric acid (pH 4.0) at 70°C. The structure of abienan AS-A was elucidated using sugar composition analysis, ion-exchange chromatography and partial acid hydrolysis
Takashi Kondo et al.
American journal of physiology. Gastrointestinal and liver physiology, 304(6), G568-G573 (2013-02-02)
Prostaglandin E(2) (PGE(2)) plays a major role in pain processing and hypersensitivity. This study investigated whether PGE(2) levels are increased in the esophageal mucosa after acid infusion and whether increases in PGE(2) are associated with heartburn. Furthermore, expression of the

商品

In this article we provide a complete workflow of quantification and identification of acylcarnitines in dried blood spots (DBS) using stable isotope-labeled (SIL) acylcarnitines CRMs by FIA-MS/MS.

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