What is the Medetomidine hydrochloride?

Medetomidine hydrochloride is , while it's Molecular Formula is C13H17ClN2. a2-Adrenergic aginist. Sedative; analgesic

What is the CAS number for Medetomidine hydrochloride?

The CAS number of Medetomidine hydrochloride is 106807-72-1.

What is Medetomidine hydrochloride (106807-72-1) used for?

Medetomidine hydrochloride is a potent and selective a2-adrenergic agonist, characterized as a white to off-white crystalline solid. It is known for its sedative and analgesic properties, making it a valuable compound in various medical and veterinary applications.InChI:InChI=1/C13H16N2.ClH/c1-9-5-4-6-12(10(9)2)11(3)13-7-14-8-15-13;/h4-8,11H,1-3H3,(H,14,15);1H

What is the Medetomidine hydrochloride?

Medetomidine hydrochloride is , while it's Molecular Formula is C13H17ClN2. a2-Adrenergic aginist. Sedative; analgesic

What is the CAS number for Medetomidine hydrochloride?

The CAS number of Medetomidine hydrochloride is 106807-72-1.

What is Medetomidine hydrochloride (106807-72-1) used for?

Medetomidine hydrochloride is a potent and selective a2-adrenergic agonist, characterized as a white to off-white crystalline solid. It is known for its sedative and analgesic properties, making it a valuable compound in various medical and veterinary applications.InChI:InChI=1/C13H16N2.ClH/c1-9-5-4-6-12(10(9)2)11(3)13-7-14-8-15-13;/h4-8,11H,1-3H3,(H,14,15);1H

Factory Sells Best Quality (r)-4-[1-(2,3-dimethylphenyl)ethyl]-1h-imidazole hydrochloride 106807-72-1 with USP

Product Details

Quick Details

CasNo： 106807-72-1
Molecular Formula： C13H17ClN2
Purity： 99%

Factory Sells Best Quality (r)-4-[1-(2,3-dimethylphenyl)ethyl]-1h-imidazole hydrochloride 106807-72-1 with USP

Molecular Formula:C13H17ClN2
Molecular Weight:236.7405
Vapor Pressure:1.08E-05mmHg at 25°C
Boiling Point:381.9°C at 760 mmHg
Flash Point:191.3°C
PSA：28.68000
LogP:3.98030

Medetomidine hydrochloride(Cas 106807-72-1) Usage

Biological Activity

Potent, highly selective α 2 -adrenoceptor agonist (K i values are 1.08 and 1750 nM for α 2 - and α 1 -adrenoceptors respectively). Displays greater selectivity over α 1 -adrenoceptors than clonidine and UK 14,304 (1620-, 220- and 300-fold respectively). Inhibits twitch response in electrically stimulated mouse vas deferens (pD 2 = 9.0). Active in vivo ; displays hypotensive, bradycardic, sedative, anxiolytic, hypothermic and analgesic effects.

InChI:InChI=1/C13H16N2.ClH/c1-9-5-4-6-12(10(9)2)11(3)13-7-14-8-15-13;/h4-8,11H,1-3H3,(H,14,15);1H

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