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Medetomidine hydrochloride

Medetomidine hydrochloride Struktur
86347-15-1
CAS-Nr.
86347-15-1
Englisch Name:
Medetomidine hydrochloride
Synonyma:
MEDETOMIDINE HYDROCHLORIDE;(r)-4-[1-(2,3-dimethylphenyl)ethyl]-1h-imidazole hydrochloride;edetomidine;(R)-4-[1-(2;medeomidine hcl;Medetomidine HC;Metetomidine HCl;Medetomidine HCI;Medetomidine HCl Powder;Ethyl Acetate Impurity 85
CBNumber:
CB52130917
Summenformel:
C13H17ClN2
Molgewicht:
236.74
MOL-Datei:
86347-15-1.mol

Medetomidine hydrochloride Eigenschaften

Schmelzpunkt:
164-166°C
storage temp. 
Inert atmosphere,Store in freezer, under -20°C
L?slichkeit
Acetonitrile (Slightly), Methanol (Slightly), Water (Slightly)
Aggregatzustand
Solid
Farbe
White to Off-White
Biologische Quelle
synthetic
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
Sicherheit
  • Risiko- und Sicherheitserkl?rung
  • Gefahreninformationscode (GHS)
WGK Germany  WGK 3
Speicherklasse 6.1A - Combustible acute toxic Cat. 1 and 2
very toxic hazardous materials
Hazard Classifications Acute Tox. 2 Inhalation
Acute Tox. 2 Oral
Aquatic Acute 1
Aquatic Chronic 1
STOT RE 1
STOT SE 1
STOT SE 3
Bildanzeige (GHS) Exclamation Mark (GHS07)
Alarmwort Warnung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H317 Kann allergische Hautreaktionen verursachen. Sensibilisierung der Haut Kategorie 1A Warnung P261, P272, P280, P302+P352,P333+P313, P321, P363, P501
H319 Verursacht schwere Augenreizung. Schwere Augenreizung Kategorie 2 Warnung P264, P280, P305+P351+P338,P337+P313P
Sicherheit
P280 Schutzhandschuhe/Schutzkleidung/Augenschutz tragen.
P305+P351+P338 BEI KONTAKT MIT DEN AUGEN: Einige Minuten lang behutsam mit Wasser spülen. Eventuell vorhandene Kontaktlinsen nach M?glichkeit entfernen. Weiter spülen.

Medetomidine hydrochloride Chemische Eigenschaften,Einsatz,Produktion Methoden

Beschreibung

Medetomidine hydrochloride is a potent, highly selective α2-adrenoceptor agonist (Ki values are 1.08 and 1750 nM for α2- and α1-adrenoceptors respectively). It is an imidazole compound. Medetomidine hydrochloride shows greater selectivity over α1-adrenoceptors than clonidine and UK 14,304 (1620-, 220- and 300-fold respectively). In addition, it influences the adrenergic system by mimicking the action of adrenergic neurotransmitters.

Chemische Eigenschaften

White Solid

Indications

Medetomidine hydrochloride is an FDA-approved alpha2-adrenoceptor (α2-AR) agonist with analgesic, sedative and anxiolytic properties for use as a veterinary sedative. It has been approved for use in animals such as cats, sheep, and dogs (12 weeks of age and older.) In 1999, the FDA approved Medetomidine for human use in the sedation of intubated and mechanically ventilated intensive care unit (ICU) patients, including use as a pain reliever and for use in non-intubated patients prior to and during surgery and other procedures. In addition to its pharmaceutical uses, it is used as an antifouling agent in marine coatings.[1]

Pharmakokinetik

After intramuscular injection, medetomidine is rapidly and almost completely absorbed at the site of injection and its pharmacokinetics are very similar to that observed after intravenous injection. Maximum plasma concentrations are reached within 15 to 20 minutes. Estimated plasma half-life is 1.2 hours for dogs and 1.5 hours for cats. Medetomidine is mainly oxidised in the liver, while a small amount is methylated in the kidney. Metabolites are primarily excreted in urine.

Synthese

Medetomidine hydrochloride is synthesized using 2,3-Dimethylbromobenzene as the starting material through a series of Grignard reactions. This process yields tertiary alcohol 7, which is subsequently subjected to dehydration and hydrogenation. The overall yield achieved was 17 percent.[1] The reaction scheme is illustrated as follows:
Medetomidine hydrochloride synthesis
Additional synthetic processes encompass:
Selected Synthetic Routes for Medetomidine Hydrochloride

Medetomidine hydrochloride Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


Medetomidine hydrochloride Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

Global( 252)Lieferanten
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86347-15-1()Verwandte Suche:


  • 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
  • 3-Dimethylphenyl)ethyl]-1H-imidazole hydrochloride
  • Medetomidine (hydrochloride) cas86347-15-1
  • SIMS1031 Medetomidine HCl ---86347-15-1 25g
  • 2-amino-5-(2-ethoxyanilino)-4-hydroxy-1H-pyrimidin-6-one
  • Medetomidine Hcl Medetomidine Hydrochloride
  • (R)-4-[1-(2,3-Dimethylphenyl)ethyl]-1H-imidazole hydrochloride USP/EP/BP
  • Medetomidine Hydrochloride Impurities
  • Metoclopramide (metoclopramide)
  • medeomidine hcl
  • Medetomidine HCl (MPV-785)
  • MEDETOMIDINE HYDROCHLORIDE
  • Medetomidine hydrochloride,anxiolysis,inhibit,sedation,Medetomidine,α2-adrenoceptor,MPV-785,peripheral nervous system,analgesia,MPV 785,central nervous system,Inhibitor,muscle relaxation,Beta Receptor,Adrenergic Receptor
  • Medetomidine HCl Powder
  • Ethyl Acetate Impurity 85
  • Medetomidine hydrochloride, alpha2 adrenoceptor agonist (aqueous solution)
  • Medetomidine hydrochloride, alpha2 adrenoceptor agonist
  • Medetomidine hydrochloride, 10 mM in DMSO
  • Medetomidine HCI
  • Medetomidine HC
  • (r)-4-[1-(2,3-dimethylphenyl)ethyl]-1h-imidazole hydrochloride
  • 86347-15-1
  • Aromatics
  • Heterocycles
  • Intermediates & Fine Chemicals
  • Pharmaceuticals
  • Inhibitors
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