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Benzyloxyamine hydrochloride structure, CAS 2687-43-6

Benzyloxyamine hydrochloride

CAS Number2687-43-6

Synonymsphenylmethoxyamine hydrochloride; Benzylhydroxylamine HCl; [(aminooxy)methyl]benzolhydrochlorid; [(Aminooxy)methyl]benzene hydrochloride; 2-BenzylhydroxylamineHcl; O-benzylhydroxylamine hydrochloride; MFCD00012952; O-BENZYLHYDROXYLAMINE HCL; [(Aminooxy)methyl]benzene hydrochloride (1:1); BENZYLOXYAMINE; Benzyloxyammonium Chloride; O-benzylhydroxylammonium chloride; EINECS 220-249-0; BENZYLOXYAMINE HCL; Hydroxylamine, O- (phenylmethyl)-, hydrochloride; Benzene, [(aminooxy)methyl]-, hydrochloride (1:1)

Molecular FormulaC6H5CH2ONH2 · HCl

Molecular Weight159.61

Purity99%

Density

Boiling Point237.5ºC at 760 mmHg

Melting Point238 °C (subl.) (lit.)

Flash Point

Appearancecrystals

EINECS220-249-0

MSDSChineseEnglish

SymbolTransport

Signal WordWarning

Cat. No.: 2A-9007212 Purity: 99%
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Quality Control of [ 2687-43-6 ] Purity: 99% SDS Specification MoL

Chemical & Physical Properties
CAS Number2687-43-6
Catalog No.2A-9007212
Chinese Name苄氧基胺盐酸盐
Synonymsphenylmethoxyamine hydrochloride; Benzylhydroxylamine HCl; [(aminooxy)methyl]benzolhydrochlorid; [(Aminooxy)methyl]benzene hydrochloride; 2-BenzylhydroxylamineHcl; O-benzylhydroxylamine hydrochloride; MFCD00012952; O-BENZYLHYDROXYLAMINE HCL; [(Aminooxy)methyl]benzene hydrochloride (1:1); BENZYLOXYAMINE; Benzyloxyammonium Chloride; O-benzylhydroxylammonium chloride; EINECS 220-249-0; BENZYLOXYAMINE HCL; Hydroxylamine, O- (phenylmethyl)-, hydrochloride; Benzene, [(aminooxy)methyl]-, hydrochloride (1:1)
Molecular FormulaC6H5CH2ONH2 · HCl
Molecular Weight159.61
Purity99
Boiling Point237.5ºC at 760 mmHg
Melting Point238 °C (subl.) (lit.)
Appearancecrystals
Water SolubilityWater solubility: soluble
Storage ConditionThis product should be kept sealed.
ApplicationO-Benzylhydroxylamine hydrochloride is a biochemical reagent that can be used as a biological material or organic compound for life science-related research.
EINECS220-249-0
HTC2928000090
PubChem ID24891644
MDL NumberMFCD00012952
SMILESCl.NOCc1ccccc1
InChI1S/C7H9NO.ClH/c8-9-6-7-4-2-1-3-5-7;/h1-5H,6,8H2;1H
InChI KeyHYDZPXNVHXJHBG-UHFFFAOYSA-N
Beilstein/REAXYS3687991
NACRES CodeNA.22
UNSPSC12352100
Hazard SymbolsTransport
Safety DescriptionS22;S24/25
MSDSmsds/7212_1_2687_43_6.pdf
BioactivityO-Benzylhydroxylamine hydrochloride is a biochemical reagent that can be used as a biological material or organic compound for life science related research. Related Catalog Research Areas >> Others Signaling Pathways >> Others >> Others In Vitro O-Benzylhydroxylamine is a basic ingredient. It has been used in the synthesis of β-lactam inhibitor precursors and fluoroquinolone derivatives with antibiotic activity. References [1]. Bellettini, JR, and Miller, MJA short synthesis of an important precursor to a new class of bicyclic β-lactamase inhibitorsTetrahedron Lett.38(2)167-168(1997) [2]. Asadipour, A., Moshafi, MH, Khosravani, L., et al.N-substituted piperazinyl sarafloxacin derivatives: synthesis and in in vitro antibacterial evaluationDaru.26(2)199-207(2018) Chemical & Physical Properties Boiling Point 237.5ºC at 760 mmHg Melting Point 238 °C (subl.)(lit.) Molecular Formula C7H10ClNO Molecular Weight 159.61 Flash Point 113.1ºC Exact Mass 159.045090 PSA 35.25000 LogP 2.57920 Vapor Pressure 0.00923mmHg at 25°C InChIKey HYDZPXNVHXJHBG-UHFFFAOYSA-N SMILES Cl.NOCc1ccccc1 Storage condition Store at RT.
Use ofO-Benzylhydroxylamine hydrochloride is a biochemical reagent that can be used as a biological material or organic compound for life science related research. Properties Articles14 Name Benzylhydroxylamine hydrochloride Synonym More Synonyms O-Benzylhydroxylamine hydrochloride Biological Activity Description O-Benzylhydroxylamine hydrochloride is a biochemical reagent that can be used as a biological material or organic compound for life science related research. Related Catalog Research Areas >> Others Signaling Pathways >> Others >> Others In Vitro O-Benzylhydroxylamine is an essential ingredient. It has been used in the synthesis of β-lactam inhibitor precursors and fluoroquinolone derivatives with antibiotic activity. References [1]. Bellettini, JR, and Miller, MJA short synthesis of an important precursor to a new class of bicyclic β-lactamase inhibitorsTetrahedron Lett.38(2)167-168(1997) [2]. Asadipour, A., Moshafi, MH, Khosravani, L., et al.N-substituted piperazinyl sarafloxacin derivatives: synthesis and in in vitro antibacterial evaluationDaru.26(2)199-207(2018) Chemical & Physical Properties Exact Mass 159.045090 PSA 35.25000 LogP 2.57920 InChIKey HYDZPXNVHXJHBG-UHFFFAOYSA-N Storage condition Store at RT.
Tax Rebate13.0%
SupervisionNone. MFN tariff: 6.5%. Ordinary tariff: 30.0%
Transport InfoShipping Name: UN
MSDS Transport InfoModule 14. Shipping information 14.1 UN dangerous goods number European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.2 United Nations shipping name European Land Transport Dangerous Regulations: Non-dangerous goods IMDG Code: Non-dangerous goods International air transport dangerous goods regulations: non-dangerous goods 14.3 Transport hazard categories European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.4 Package group European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.5 Environmental hazards European Land Transport Danger Regulations: No International Maritime Danger Regulations International Air Transport Danger Regulations: No Marine pollutants (yes/no): No 14.6 Special reminder to users No data available
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