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
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
新产品
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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
M Pauly et al.
Carbohydrate research, 282(1), 1-12 (1996-02-28)
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B X Chen et al.
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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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