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Merck
CN

B22984

O-Benzylhydroxylamine hydrochloride

99%

Synonym(s):

Benzyloxyamine hydrochloride

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About This Item

Linear Formula:
C6H5CH2ONH2 · HCl
CAS Number:
Molecular Weight:
159.61
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
220-249-0
Beilstein/REAXYS Number:
3687991
MDL number:
Assay:
99%
Form:
crystals
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Product Name

O-Benzylhydroxylamine hydrochloride, 99%

InChI key

HYDZPXNVHXJHBG-UHFFFAOYSA-N

InChI

1S/C7H9NO.ClH/c8-9-6-7-4-2-1-3-5-7;/h1-5H,6,8H2;1H

SMILES string

Cl.NOCc1ccccc1

assay

99%

form

crystals

mp

238 °C (subl.) (lit.)

Quality Level

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Application

Effective reagent used to prepare α-hydroxybenzylamines from α-hydroxyketones.

pictograms

CorrosionExclamation mark

signalword

Danger

Hazard Classifications

Eye Dam. 1 - Skin Irrit. 2 - Skin Sens. 1

Storage Class

11 - Combustible Solids

wgk

WGK 3

ppe

Eyeshields, Gloves, type N95 (US)


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S M Breckenridge et al.
Journal of chromatography. B, Biomedical sciences and applications, 694(2), 289-296 (1997-07-04)
Extraction and derivatization of carbonyls to benzyloximes, pentafluorobenzyloximes or 2,4-dinitrophenylhydrazones is simplified and reaction times are substantially reduced by simultaneous sorption and derivatization from aqueous solution onto a solid phase. In this reaction a macroreticular polystyrene-divinylbenzene resin acts as a
A A Purmal et al.
Mutation research, 364(3), 193-207 (1996-12-02)
Duplex oligonucleotides containing the base lesion analogs, O-methylhydroxylamine- and O-benzylhydroxylamine-modified abasic (AP) sites, were substrates for the DNA N-glycosylases endonuclease III, formamidopyrimidine DNA N-glycosylase and T4 endonuclease V. These N-glycosylases are known to have associated AP lyase activities. In contrast
D F Magin
Journal of chromatography, 202(2), 255-261 (1980-12-19)
A qualitative and semi-quantitative method was established for the investigation of low-molecular-weight volatile carbonyl compounds in cigarette whole smoke. The carbonyls were trapped on a silica gel "column" and eluted with water. The aqueous solution was then treated with benzyloxyamine
Tetrahedron Letters, 32, 711-711 (1991)
G Cardillo et al.
Organic letters, 3(8), 1165-1167 (2001-05-12)
[reaction: see text]. The 1,4-addition of O-benzylhydroxylamine to alpha,beta-unsaturated imide 1 in the presence of BF3.Et2O proceeds with the preferential attack of the nucleophile on the Cbeta-re face. To explain this unexpected reactivity 1H, 13C, and 11B NMR investigations have

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