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Merck
CN

73120

Supelco

4-硝基苯甲酰氯

derivatization grade (HPLC), LiChropur, ≥99.0% (GC)

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线性分子式:
O2NC6H4COCl
化学文摘社编号:
分子量:
185.56
Beilstein:
473192
EC 号:
MDL编号:
UNSPSC代码:
23151817
PubChem化学物质编号:
NACRES:
NA.22
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等级

derivatization grade (HPLC)

质量水平

方案

≥99.0% (GC)

表单

crystals

质量

LiChropur

技术

HPLC: suitable

灼烧残渣

≤0.05% (as SO4)

沸点

202-205 °C/105 mmHg (lit.)

mp

71-74 °C (lit.)
71-74 °C

SMILES字符串

[O-][N+](=O)c1ccc(cc1)C(Cl)=O

InChI

1S/C7H4ClNO3/c8-7(10)5-1-3-6(4-2-5)9(11)12/h1-4H

InChI key

SKDHHIUENRGTHK-UHFFFAOYSA-N

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一般描述

4-Nitrobenzoyl chloride is a derivatization reagent. It reacts with L-glutamic acid undergoing methylation using formaldehyde, synthesizing N-(4-methylaminobenzoyl)glutaminic acid.

应用

4-Nitrobenzoyl chloride was used in separating polyhydric alcohols using HPLC. It was used in snythesizing cellulose benzotates by adding to cellulose/1-allyl-3-methylimidazolium chloride followed by characterization using FT-IF, 1H-NMR and 13C-NMR spectroscopy. It may be used in synthesizing 1-aryloxyacetyl-4-(4-nitrobenzoyl)-thiosemicarbazides under phase transfer catalysis and microwave irradiation with ammonium thiocyanate and aryloxyacetic acid hydrazides.

其他说明

HPLC 羟基衍生化
Discover LiChropur reagents ideal for HPLC or LC-MS analysis

法律信息

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

象形图

Corrosion

警示用语:

Danger

危险声明

危险分类

Eye Dam. 1 - Met. Corr. 1 - Skin Corr. 1B

储存分类代码

8A - Combustible corrosive hazardous materials

WGK

WGK 1

闪点(°F)

215.6 °F - closed cup

闪点(°C)

102 °C - closed cup

个人防护装备

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

法规信息

危险化学品
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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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The synthesis of silica-immobilized 1, 2-naphthoquinone thiosemicarbazone with 3-aminopropyltriethoxy silane and 4-nitrobenzoyl chloride.
Audu, Aramani A.
Reactive Polymers, 10, 3-9 (1989)
F Nachtmann et al.
Journal of chromatography, 122, 293-303 (1976-07-07)
The separation and quantitative determination of digitalis glycosides by high performance liquid chromatography following derivatization with 4-nitrobenzoylchloride (4-NBC1) is described. The compounds of primary interest were the digitalis glycosides and aglycones of the pharmaceutically important A, B and C series
Ruben Vardanyan, Victor Hruby
Synthesis of Essential Drugs, 391-391 (2006)
Synthesis of cellulose benzoates under homogeneous conditions in an ionic liquid.
Zhang, Jinming, et al.
Cellulose, 16, 299-308 (2009)
Separation of some polyhydric alcohols by high-performance liquid chromatography.
Schwarzenbach, Rolf.
Journal of Chromatography A, 140, 304-309 (1977)

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