Dexmedetomidine hydrochloride

(HB2686)
Technical documents: CoA Datasheet

Product overview

Name Dexmedetomidine hydrochloride
Alternative names d-Medetomidine hydrochloride
Purity >99%
Description

Potent, highly selective α2 adrenoceptor agonist.

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Biological Data

Biological description

Potent, highly selective α2 adrenoceptor agonist (Ki values are 1.08 and 1750 nM at α2 and α1 receptors, respectively). Active isomer of medetomidine. Shows greater selectivity for α1-adrenoceptors than clonidine and UK14304. Shows various actions such as hypotensive, bradycardic, anxiolytic, hypothermic, sedative and analgesic properties.

Solubility & Handling

Storage instructions -20°C
Solubility overview

Soluble in water (100 mM), and in DMSO (100 mM)

Important This product is for RESEARCH USE ONLY and is not intended for therapeutic or diagnostic use. Not for human or veterinary use

Calculators

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Dilution

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Chemical Data

Purity >99%
Chemical name 4-[(1S)-1-(2,3-Dimethylphenyl)ethyl]-1H-imidazole hydrochloride
Molecular Weight 236.74
Chemical structure Dexmedetomidine hydrochloride [145108-58-3] Chemical Structure
Molecular Formula C13H16N2.HCl
CAS Number 145108-58-3
PubChem identifier 6918081
SMILES CC1=C(C(=CC=C1)[C@H](C)C2=CN=CN2)C.Cl
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/t11-;/m0./s1
InChiKey VPNGEIHDPSLNMU-MERQFXBCSA-N
Appearance White solid