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Detomidine hydrochloride monohydrate

VETRANAL®, analytical standard

Synonym(s):

5-[(2,3-Dimethylphenyl)methyl]-1H-imidazole hydrochloride monohydrate

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About This Item

Empirical Formula (Hill Notation):
C12H14N2 · HCl · H2O
CAS Number:
Molecular Weight:
240.73
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

product line

VETRANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

forensics and toxicology
pharmaceutical (small molecule)

format

neat

SMILES string

O.Cl.Cc1cccc(Cc2cnc[nH]2)c1C

InChI

1S/C12H14N2.ClH.H2O/c1-9-4-3-5-11(10(9)2)6-12-7-13-8-14-12;;/h3-5,7-8H,6H2,1-2H3,(H,13,14);1H;1H2

InChI key

IQBSKEIWIRTMOT-UHFFFAOYSA-N

General description

Detomidine hydrochlorides belong to the class of α2-adrenergic agonists that are majorly used for the sedation of horses.[1]

Application

Detomidine hydrochloride monohydrate may be used as a precursor for the preparation of detomidine that can be employed as an analytical reference standard for the determination of the analyte in equine liver samples by enantioselective capillary electrophoresis.[2]
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

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Legal Information

VETRANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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Effect of the ?2-receptor agonists medetomidine, detomidine, xylazine, and romifidine on the ketamine metabolism in equines assessed with enantioselective capillary electrophoresis.
Sandbaumhuter FA, et al.
Electrophoresis, 38(15), 1895-1904 (2017)
K Veldre et al.
European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences, 44(3), 273-280 (2011-08-30)
The thermodynamic stability of detomidine hydrochloride monohydrate has been evaluated on the basis of phase transition kinetics in solid state. A method free of empirical models was used for the treatment of kinetic data, and compared to several known solid

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