ChemicalBook--->CAS DataBase List--->1216630-06-6

1216630-06-6

1216630-06-6 Structure

1216630-06-6 Structure
IdentificationBack Directory
[Name]

Medetomidine-13C,d3 Hydrochloride
[CAS]

1216630-06-6
[Synonyms]

Medetomidine-13C,d3 Hydrochloride
[13C,2H3]-Medetomidine Hydrochloride
4-[1-(2,3-DiMethylphenyl)ethyl-13C,d3]-1H-iMidazole
5-[2,2,2-trideuterio-1-(2,3-dimethylphenyl)(2^{13}C)ethyl]-1~{H}-imidazole
[Molecular Formula]

C13H16ClN2
[MOL File]

1216630-06-6.mol
[Molecular Weight]

235.733
Chemical PropertiesBack Directory
[Melting point ]

162-164°C
[storage temp. ]

-20°C Freezer, Under Inert Atmosphere
[solubility ]

Methanol (Slightly)
[form ]

Solid
[color ]

White to Pale Yellow
Safety DataBack Directory
[WGK Germany ]

WGK 2
[Storage Class]

3 - Flammable liquids
[Hazard Classifications]

Acute Tox. 3 Dermal
Acute Tox. 3 Inhalation
Acute Tox. 3 Oral
Flam. Liq. 2
STOT SE 1
Hazard InformationBack Directory
[Description]

Medetomidine-13C-d3 is intended for use as an internal standard for the quantification of medetomidine by GC- or LC-MS. Medetomidine is an imidazole compound that selectively binds to α2-adrenergic receptors (α2-ARs) over α1-ARs (Kis = 1.08 and 1,800 nM, respectively).
[Chemical Properties]

White Solid
[Uses]

Labelled α2-adrenergic agonist. Sedative; analgesic.
[in vivo]

Medetomidine (200 μg/kg, p.o. or i.m.) hydrochloride induces a sedation in cats[5].
Medetomidine (20 μg/kg, i.v.) hydrochloride shows sedative and analgesic effects in dogs[6].
Medetomidine (0.05-0.3 mg/kg, s.c.) hydrochloride protects against Diazinon-induced toxicosis in mice[7].

[References]

[1] O. VAINIO  T. V V. Reversal of medetomidine sedation by atipamezole in dogs[J]. Journal of veterinary pharmacology and therapeutics, 1990, 13 1: 15-22. DOI: 10.1111/j.1365-2885.1990.tb00742.x
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