N-Benzylhydroxylamine hydrochloride
Suppliers
Names
[ CAS No. ]:
29601-98-7
[ 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
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
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
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
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...
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)