73200
O-(4-Nitrobenzyl)hydroxylamine hydrochloride
≥98.5% (AT)
Synonym(s):
4-Nitrobenzyloxyamine hydrochloride
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About This Item
Linear Formula:
O2NC6H4CH2ONH2 · HCl
CAS Number:
Molecular Weight:
204.61
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
218-228-6
Beilstein/REAXYS Number:
3709565
MDL number:
Assay:
≥98.5% (AT)
Form:
crystals
Product Name
O-(4-Nitrobenzyl)hydroxylamine hydrochloride, ≥98.5% (AT)
Quality Level
InChI key
LKCAFSOYOMFQSL-UHFFFAOYSA-N
InChI
1S/C7H8N2O3.ClH/c8-12-5-6-1-3-7(4-2-6)9(10)11;/h1-4H,5,8H2;1H
SMILES string
Cl.NOCc1ccc(cc1)[N+]([O-])=O
assay
≥98.5% (AT)
form
crystals
mp
215 °C (dec.) (lit.)
functional group
nitro
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Other Notes
Reagent for the preparation of N-(4-nitrobenzyloxy)-amino acids as substrates for an unambiguous N-hydroxypeptide synthesis
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Regulatory Information
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Journal of chromatography, 272(1), 9-20 (1983-01-14)
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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2-Deoxy-scyllo-inosose (DOI) has been a valuable starting natural product for the manufacture of pharmaceuticals or chemical engineering resources such as pyranose catechol. DOI synthase, which uses glucose-6-phosphate (Glc6P) as a substrate for DOI biosynthesis, is indispensably involved in the initial
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Mutation research, 273(3), 253-261 (1992-05-01)
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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