E5264
2-Ethylidene-1,5-dimethyl-3,3-diphenylpyrrolidine perchlorate
analytical standard, for drug analysis
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Acerca de este artículo
Fórmula empírica (notación de Hill):
C20H23N · HClO4
Número CAS:
Peso molecular:
377.86
UNSPSC Code:
41116107
PubChem Substance ID:
MDL number:
Quality Level
drug control
regulated under CDSA - not available from Sigma-Aldrich Canada
technique(s)
HPLC: suitable, gas chromatography (GC): suitable
application(s)
forensics and toxicology
veterinary
format
neat
storage temp.
2-8°C
SMILES string
OCl(=O)(=O)=O.C\C=C1/N(C)C(C)CC1(c2ccccc2)c3ccccc3
InChI
1S/C20H23N.ClHO4/c1-4-19-20(15-16(2)21(19)3,17-11-7-5-8-12-17)18-13-9-6-10-14-18;2-1(3,4)5/h4-14,16H,15H2,1-3H3;(H,2,3,4,5)/b19-4-;
InChI key
CBNJWAYHGKHAFJ-YOJQKEKBSA-N
General description
2-Ethylidene-1,5-dimethyl-3,3-diphenylpyrrolidine perchlorate is a primary metabolite of methadone.
Application
A metabolite of methadone, useful as a marker in GC-MS analyses.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
2-Ethylidene-1,5-dimethyl-3,3-diphenylpyrrolidine perchlorate has been used as a standard in the quantitative determination of of methadone and metabolites in human meconium using liquid chromatography coupled with atmospheric pressure chemical ionization tandem mass spectrometry technique (LC–APCI–MS/MS).
Clase de almacenamiento
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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G I Kang et al.
Journal of chromatography, 231(2), 311-319 (1982-09-10)
The analysis of methadone and its metabolites in biological fluids by gas chromatography--mass spectrometry is described with deuterated methadone and metabolites as internal standards. The method allowed the determination of 20 ng methadone in 0.5 ml of plasma or saliva.
Determination of methadone, 2-ethylidene-1, 5-dimethyl-3, 3-diphenylpyrrolidine, 2-ethyl-5-methyl-3, 3-diphenylpyraline and methadol in meconium by liquid chromatography atmospheric pressure chemical ionization tandem mass spectrometry
Choo.ER, et al.
Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences, 814, 369-373 (2005)
Ana de Castro et al.
Clinical chemistry, 57(3), 449-458 (2011-01-20)
Few investigations have used placenta as an alternative matrix to detect in utero drug exposure, despite its availability at the time of birth and the large amount of sample. Methadone-maintained opioid-dependent pregnant women provide a unique opportunity to examine the