추천 제품
Grade
derivatization grade ((HPLC))
Quality Level
분석
≥99.0% (GC)
양식
crystals
품질
LiChropur™
기술
HPLC: suitable
무기 잔류물
≤0.05% (as SO4)
bp
202-205 °C/105 mmHg (lit.)
mp
71-74 °C (lit.)
71-74 °C
SMILES string
[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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일반 설명
4-Nitrobenzoyl chloride is a derivatization reagent. It reacts with L-glutamic acid undergoing methylation using formaldehyde, synthesizing N-(4-methylaminobenzoyl)glutaminic acid.
애플리케이션
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.
기타 정보
Derivatization of hydroxy groups for HPLC
법적 정보
LiChropur is a trademark of Merck KGaA, Darmstadt, Germany
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Eye Dam. 1 - Met. Corr. 1 - Skin Corr. 1B
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 1
Flash Point (°F)
215.6 °F - closed cup
Flash Point (°C)
102 °C - closed cup
개인 보호 장비
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
이미 열람한 고객
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)
Synthesis of cellulose benzoates under homogeneous conditions in an ionic liquid.
Zhang, Jinming, et al.
Cellulose, 16, 299-308 (2009)
Ruben Vardanyan, Victor Hruby
Synthesis of Essential Drugs, 391-391 (2006)
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
Journal of Chromatography A, 136, 279-279 (1977)
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