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Merck
CN

73200

O-(4-硝基苄基)羟胺 盐酸盐

≥98.5% (AT)

别名:

4-硝基苄基羟胺 盐酸盐

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关于此项目

线性分子式:
O2NC6H4CH2ONH2 · HCl
化学文摘社编号:
分子量:
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
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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

Other Notes

用于制备 N-(4-硝基苄氧基)-氨基酸的试剂,N-(4-硝基苄氧基)-氨基酸可作为N-羟基肽精确合成的底物

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

法规信息

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T D Traylor et al.
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
Joo Hyun Lim et al.
Frontiers in microbiology, 9, 2333-2333 (2018-10-16)
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M Pauly et al.
Carbohydrate research, 282(1), 1-12 (1996-02-28)
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
M Pauly et al.
Planta, 212(5-6), 842-850 (2001-05-12)
Xyloglucans were isolated by sequential extraction of the cell walls of pea (Pisum sativum L. cv. Alaska) with a xyloglucan-specific endoglucanase and KOH. The xyloglucan content and xyloglucan-oligosaccharide composition were determined for fractions obtained from the elongating and non-elongating segments
Kenneth P Roberts et al.
Chemical research in toxicology, 19(2), 300-309 (2006-02-21)
A new method has been developed to accurately measure apurinic and apyrimidinic (AP) DNA damage sites, which are lesions in DNA formed by loss of a nucleobase from oxidative stress or carcinogen adducts. If AP sites are left unrepaired (or

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