Dexmedetomidine hydrochloride

Suppliers

Names

[ Name ]:
Dexmedetomidine hydrochloride

[Synonym ]:
4-[(a-Methyl)-2,3-dimethylbenzyl]imidazole Monohydrochloride
4-[1-(2,3-Dimethylphenyl)ethyl]-1H-imidazole hydrochloride (1:1)
Dexdor
1H-imidazole, 4-[(1S)-1-(2,3-dimethylphenyl)ethyl]-, monohydrochloride
5-[(1S)-1-(2,3-dimethylphenyl)ethyl]-1H-imidazole,hydrochloride
MFCD07772269
1H-Imidazole, 4-[(1S)-1-(2,3-dimethylphenyl)ethyl]-, hydrochloride (1:1)
UNII:BH210P244U
UNII-1018WH7F9I
4-[1-(2,3-Dimethylphenyl)ethyl]-1H-imidazole Monohydrochloride
5-[(1S)-1-(2,3-dimethylphenyl)ethyl]-1H-imidazole hydrochloride
Precedex
(S)-4-(1-(2,3-Dimethylphenyl)ethyl)-1H-imidazole Monohydrochloride
1H-Imidazole, 4-[1-(2,3-dimethylphenyl)ethyl]-, hydrochloride (1:1)
Dexmedetomidine HCL
4-[(1S)-1-(2,3-Dimethylphenyl)ethyl]-1H-imidazole hydrochloride (1:1)
4-((S)-a,2,3-Trimethylbenzyl)imidazole Monohydrochloride
(±)-4-(a,2,3-Trimethylbenzyl)imidazole Monohydrochloride
Dexmedetomidine Hydrochloride
4-[(1S)-1-(2,3-Dimethylphenyl)ethyl]-1H-imidazolhydrochlorid
4-[(1S)-1-(2,3-diméthylphényl)éthyl]-1H-imidazole chlorhydrate
Dexmedetomidine HCl
4-(S)-[1-(2,3-DIMETHYLPHENYL)ETHYL]-1 H-IMIDAZOLE MONOHY DROCHLORIDE (DEXMEDETOMIDINE HYDROCHLORIDE)
Dexmedetomidine (hydrochloride)

Chemical & Physical Properties

[ Boiling Point ]:
381.9ºC at 760 mmHg

[ Melting Point ]:
153 - 158ºC

[ Molecular Formula ]:
C₁₃H₁₇ClN₂

[ Molecular Weight ]:
236.740

[ Exact Mass ]:
236.108032

[ PSA ]:
28.68000

[ LogP ]:
3.98030

[ Vapour Pressure ]:
1.08E-05mmHg at 25°C

[ Storage condition ]:
Desiccate at RT

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H302-H315-H319-H335

[ Precautionary Statements ]:
P301 + P312 + P330-P305 + P351 + P338

[ Hazard Codes ]:
Xn

[ Risk Phrases ]:
22-36/37/38

[ Safety Phrases ]:
26-36/37/39

[ RIDADR ]:
NONH for all modes of transport

[ RTECS ]:
NI5156750

Articles

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Optimized on-line enantioselective capillary electrophoretic method for kinetic and inhibition studies of drug metabolism mediated by cytochrome P450 enzymes.

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Pharmacokinetic and pharmacodynamic properties of a chiral drug can significantly differ between application of the racemate and single enantiomers. During drug development, the characteristics of can...