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ChemicalBook > Product Catalogue >Biochemical Engineering >Inhibitors >Neuronal Signaling >Adrenergic Receptor agonists >Medetomidine hydrochloride

Medetomidine hydrochloride

Medetomidine hydrochloride Structure
  • ₹0
  • Product name: Medetomidine hydrochloride
  • CAS: 86347-15-1
  • MF: C13H17ClN2
  • MW: 236.74
  • EINECS:645-306-0
  • MDL Number:
  • Synonyms:(r)-4-[1-(2,3-dimethylphenyl)ethyl]-1h-imidazole hydrochloride;1H-Imidazole, 5-[1-(2,3-dimethylphenyl)ethyl]-, hydrochloride (1:1);5-[1-(2,3-diMethylphenyl)ethyl]-1H-IMidazole hydrochloride;edetomidine;Medetomidine hydrochloride (R)-4-[1-(2,3-Dimethylphenyl)ethyl]-1H-imidazole hydrochloride;5-[1-(2,3-dimethylphenyl)ethyl]-1H-imidazole monohydrochloride;Metetomidine HCl;(R)-4-[1-(2
Manufacturer Product number Product description Packaging Price Updated Buy

Properties

Melting point :164-166°C
storage temp. :Inert atmosphere,Store in freezer, under -20°C
solubility :Acetonitrile (Slightly), Methanol (Slightly), Water (Slightly)
form :Solid
color :White to Off-White
InChI :InChI=1S/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
InChIKey :VPNGEIHDPSLNMU-UHFFFAOYSA-N
SMILES :C(C1N=CNC=1)(C1C=CC=C(C)C=1C)C.Cl

Safety Information

Symbol(GHS): GHS hazard pictograms
Signal word: Warning
Hazard statements:
Code Hazard statements Hazard class Category Signal word Pictogram P-Codes
H317 May cause an allergic skin reaction Sensitisation, Skin Category 1 Warning GHS hazard pictograms P261, P272, P280, P302+P352,P333+P313, P321, P363, P501
H319 Causes serious eye irritation Serious eye damage/eye irritation Category 2A Warning GHS hazard pictograms P264, P280, P305+P351+P338,P337+P313P
Precautionary statements:
P280 Wear protective gloves/protective clothing/eye protection/face protection.
P305+P351+P338 IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

Description

Medetomidine is an imidazole derivative that acts as a selective agonist of α2-adrenoceptors (Ki = 1.08 nM vs. 1750 nM for α1-adrenoceptors). Medetomidine is a mixture of D and L isomers, with the D form, known as dexmedetomidine , described as the active form. Through its effect on α2-adrenoceptors, medetomidine has sedative, antinociceptive, analgesic, and hypothermic actions. Its effects on pain are additive or synergistic with fentanyl-type opioids. The effects of medetomidine are effectively countered by α2-adrenoceptor antagonists, like atipamezole. Selective α2-adrenoceptor agonists, including medetomidine, have anesthetic sparing properties, greatly reducing the dose of anesthetic required following premedication with the α2-adrenoceptor agonist.

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