N,N-DIMETHYLHYDROXYLAMINE HYDROCHLORIDE

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Names

[ Name ]:
N,N-DIMETHYLHYDROXYLAMINE HYDROCHLORIDE

[Synonym ]:
N,N-Dimethylhydroxylamine hydrochloride
dimethyl hydroxylamine hydrochloride
dimethyl hydroxyamine hydrochloride
HCl.HN(Ome)Me
EINECS 240-691-8
MFCD00012600
N-methyl-O-methylhydroxyamine hydrochloride

Chemical & Physical Properties

[ Boiling Point ]:
64.2ºC at 760mmHg

[ Melting Point ]:
107-109ºC(lit.)

[ Molecular Formula ]:
C₂H₈ClNO

[ Molecular Weight ]:
97.54400

[ Flash Point ]:
16.5ºC

[ Exact Mass ]:
97.02940

[ PSA ]:
23.47000

[ LogP ]:
0.73920

[ Vapour Pressure ]:
138mmHg at 25°C

[ Index of Refraction ]:
1.414

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319

[ Precautionary Statements ]:
P305 + P351 + P338

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

[ Hazard Codes ]:
Xi: Irritant;

[ Risk Phrases ]:
R36/38

[ Safety Phrases ]:
26-36

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2928000090

Precursor & DownStream

Precursor

DownStream

N6,N6-Dimethyl-2',3',5'-tri-O-acetyladenosine
2',3',5'-Tri-O-acetylinosine
2-Chloro-N-methoxy-N-methylnicotinamide
Methanesulfonamide,N,N-dimethyl-
Hydroxylamine,N,N-dimethyl-O-[(p-nitrophenyl)carbamoyl]- (8CI)
6-(dimethylaminooxy)-2-N,2-N,4-N,4-N-tetramethyl-1,3,5-triazine-2,4-diamine
5-Bromo-2-chloro-N-methoxy-N-methylbenzamide

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

In vitro haematotoxic effects of three methylated hydroxylamines.

Arch. Toxicol. 71(5) , 299-305, (1997)

Hydroxylamine (HYAM, HONH2) and some of its derivatives are known to cause erythrotoxic effects both in vitro and in vivo. Previous studies have shown that the primary in vitro effect of HYAM and O-et...

Free radical intermediates in the oxidation of N-methylhydroxylamine and N,N-dimethylhydroxylamine by oxyhemoglobin.

Free Radic. Res. Commun. 8(2) , 123-31, (1990)

Nitroxide radicals have been detected in the methemoglobin formation reaction between oxyhemoglobin and the substituted hydroxylamine compounds, N-methylhydroxylamine and N,N-dimethylhydroxylamine, by...

Two mechanisms for toxic effects of hydroxylamines in human erythrocytes: involvement of free radicals and risk of potentiation.

Blood Cells Mol. Dis. 24(3) , 280-95, (1998)

The toxic potency of three industrially used hydroxylamines was studied in human blood cells in vitro. The parent compound hydroxylamine and the O-ethyl derivative gave very similar results. Both comp...

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