73200
O-(4-Nitrobenzyl)-hydroxylamin -hydrochlorid
≥98.5% (AT)
Synonym(e):
4-Nitrobenzyloxyamin -hydrochlorid
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About This Item
Empfohlene Produkte
Qualitätsniveau
Assay
≥98.5% (AT)
Form
crystals
mp (Schmelzpunkt)
215 °C (dec.) (lit.)
Funktionelle Gruppe
nitro
SMILES String
Cl.NOCc1ccc(cc1)[N+]([O-])=O
InChI
1S/C7H8N2O3.ClH/c8-12-5-6-1-3-7(4-2-6)9(10)11;/h1-4H,5,8H2;1H
InChIKey
LKCAFSOYOMFQSL-UHFFFAOYSA-N
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Verwandte Kategorien
Sonstige Hinweise
Reagent for the preparation of N-(4-nitrobenzyloxy)-amino acids as substrates for an unambiguous N-hydroxypeptide synthesis
Lagerklassenschlüssel
11 - Combustible Solids
WGK
WGK 3
Flammpunkt (°F)
Not applicable
Flammpunkt (°C)
Not applicable
Persönliche Schutzausrüstung
Eyeshields, Gloves, type N95 (US)
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The abasic site is one of the most frequent changes occurring in DNA and has been shown to be lethal and mutagenic. An abasic site in DNA can be tagged by reaction with O-4-nitrobenzylhydroxylamine (NBHA), resulting in the formation of
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An improved procedure has been developed for the rapid derivatization of oligosaccharides with UV-detectable p-nitrobenzylhydroxylamine (PNB). The improved conditions used result in quantitative derivatization of neutral oligosaccharides. Sialylated oligosaccharides can also be quantitatively PNB-derivatized without detectable desialylation. Of the oligosaccharides
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A new quantitative procedure for the high-performance liquid chromatographic (HPLC) resolution of human brain gangliosides employing reversed-phase chromatography is described. To provide a derivative which can be determined by UV absorption techniques, p-nitrobenzyloxyamine was coupled to the gangliosides. Derivatization involves
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