N-Benzylhydroxylamine hydrochloride

Names

[ Name ]:
N-Benzylhydroxylamine hydrochloride

[Synonym ]:
N-Benzylhydroxyamine hydrochloride
MFCD00043377
Benzenemethanamine, N-hydroxy-, hydrochloride (1:1)
BnNHOH*hydrochloride
benzyl hydroxylamine hydrochloride
N-Hydroxy-1-phenylmethanamine hydrochloride (1:1)
o-benzylhydroxyamine hydrochloride
N-benzyl-N-hydroxylamine hydrochloride
N-Benzylhydroxylamine HCl
N-Benzylhydroxylamine Hydrochloride
N-BenzylhydroxylamineHCl
benzyl-hydroxylamine monohydrochloride
O-benzylhydroxyamine HCl

Biological Activity

[Description]:

N-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

[In Vitro]

N-Benzylhydroxylamine 是一种潜在的药理学试剂，可预防和发展丙烯醛引起的视网膜色素上皮细胞损伤。

Chemical & Physical Properties

[ Boiling Point ]:
253.9ºC at 760 mmHg

[ Melting Point ]:
108-110ºC

[ Molecular Formula ]:
C₇H₁₀ClNO

[ Molecular Weight ]:
159.61

[ Flash Point ]:
135.2ºC

[ Exact Mass ]:
159.045090

[ PSA ]:
32.26000

[ LogP ]:
2.35830

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi:Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S37/39

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2928000090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

Customs

[ HS Code ]: 2928000090

[ Summary ]:
2928000090 other organic derivatives of hydrazine or of hydroxylamine VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:20.0%

Articles

Regio- and stereoselectivity of captodative olefins in 1,3-dipolar cycloadditions. A DFT/HSAB theory rationale for the observed regiochemistry of nitrones.

J. Org. Chem. 66 , 1252, (2001)

Captodative olefins 1-acetylvinyl carboxylates proved to be highly regioselective dipolarophiles in 1,3-dipolar cycloadditon to propionitrile oxide, arylphenylnitrile imines, diazoalkanes, and nitrone...

NBHA reduces acrolein-induced changes in ARPE-19 cells: possible involvement of TGFβ.

Curr. Eye Res. 36(4) , 370-8, (2011)

Acrolein, a toxic, reactive aldehyde formed metabolically and environmentally, has been implicated in the damage to and dysfunction of the retinal pigment epithelium (RPE) that accompanies age-related...

[1, 3]-Dipolar intramolecular nitrone olefin cycloaddition reaction of a sugar-derived a, ß-unsaturated ester: a new diastereo-and regioselective synthesis of an aminocyclopentitol. Jachak SM, et al.

Tetrahedron Lett. 42(29) , 4925-28, (2001)

Related Compounds

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