B22984
O-Benzylhydroxylamine hydrochloride
99%
Synonym(s):
Benzyloxyamine hydrochloride
Sign Into View Organizational & Contract Pricing
All Photos(2)
About This Item
Linear Formula:
C6H5CH2ONH2 · HCl
CAS Number:
Molecular Weight:
159.61
Beilstein:
3687991
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Quality Level
Assay
99%
form
crystals
mp
238 °C (subl.) (lit.)
SMILES string
Cl.NOCc1ccccc1
InChI
1S/C7H9NO.ClH/c8-9-6-7-4-2-1-3-5-7;/h1-5H,6,8H2;1H
InChI key
HYDZPXNVHXJHBG-UHFFFAOYSA-N
Looking for similar products? Visit Product Comparison Guide
Application
Effective reagent used to prepare α-hydroxybenzylamines from α-hydroxyketones.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Dam. 1 - Skin Irrit. 2 - Skin Sens. 1
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Customers Also Viewed
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
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
G Stampf et al.
Die Pharmazie, 35(1), 43-44 (1980-01-01)
The study of the blood levels and tissue concentrations in mice to which 14C-benzyloxyamine hydrochloride was applied in the form of a spray and of a suspensoid aerosol evidenced the good abosrption of this pharmacon. Maximum blood levels were observed
[Thermographic analysis of precipitates formed by the interaction of active ingredients and additives].
G Stampf et al.
Acta pharmaceutica Hungarica, 53(6), 268-272 (1983-11-01)
Yin Luo et al.
ChemMedChem, 7(9), 1587-1593 (2012-07-20)
Forty-three oxime derivatives were synthesized by allowing O-benzylhydroxylamines to react with primary benzaldehydes or salicylaldehydes; these products were gauged as potential inhibitors of β-ketoacyl-(acyl-carrier-protein) synthase III (FabH). Among the 43 compounds, 38 are reported herein for the first time. These
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service