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F8639

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Famprofazone

analytical standard

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About This Item

Fórmula empírica (notación de Hill):
C24H31N3O
Número de CAS:
22881-35-2
Peso molecular:
377.52
Número CE:
245-284-9
Número MDL:
MFCD00079304
Código UNSPSC:
41116107
ID de la sustancia en PubChem:
329799771
NACRES:
NA.24

grado

analytical standard

Nivel de calidad

200

técnicas

HPLC: suitable
gas chromatography (GC): suitable

aplicaciones

forensics and toxicology
pharmaceutical (small molecule)
veterinary

Formato

neat

cadena SMILES

CC(C)C1=C(CN(C)C(C)Cc2ccccc2)N(C)N(c3ccccc3)C1=O

InChI

1S/C24H31N3O/c1-18(2)23-22(17-25(4)19(3)16-20-12-8-6-9-13-20)26(5)27(24(23)28)21-14-10-7-11-15-21/h6-15,18-19H,16-17H2,1-5H3

Clave InChI

GNUXVOXXWGNPIV-UHFFFAOYSA-N

Descripción general

Famprofazone is a pyrazole derivative[1] and belongs to the class of non-steroidal anti-inflammatory drugs.[2] It is widely used as an analgesic and antipyretic in medical applications.[3][4]

Aplicación

Famprofazone may be used as an analytical reference standard for the quantification of the analyte in biological samples using liquid chromatography coupled to tandem mass spectrometry.[5]
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Pictogramas

Exclamation mark
GHS07

Palabra de señalización

Warning

Frases de peligro

H302

Clasificaciones de peligro

Acute Tox. 4 Oral

Código de clase de almacenamiento

11 - Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 3

Equipo de protección personal

dust mask type N95 (US), Eyeshields, Gloves

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Certificados de análisis (COA)

Lot/Batch Number

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A rapid screening LC?MS/MS method based on conventional HPLC pumps for the analysis of low molecular weight xenobiotics: application to doping control analysis
Mazzarino M, et al.
Drug Testing and Analysis, 2(7), 311-322 (2010)
H S Shin et al.
Journal of chromatography. B, Biomedical applications, 661(2), 255-261 (1994-11-18)
Detection and identification of famprofazone and its metabolite, p-hydroxydesmethylfamprofazone, were described. The identity of the new metabolite was confirmed by comparing its mass spectrum and gas chromatographic retention time with that of the synthetic standard and its derivatives. Unchanged famprofazone
F Musshoff et al.
International journal of legal medicine, 111(6), 305-308 (1998-11-24)
After a traffic accident a 32-year-old man was suspected of having previously taken an illegal drug. An immunochemical screening procedure revealed positive results for amphetamines in both urine and blood samples. The preliminary test was confirmed by GC/MS and both
H S Shin
Chirality, 9(1), 52-58 (1997-01-01)
Following administration of famprofazone to humans, the stereoselective metabolism from the drug to its known metabolites (+,-)-ephedrine, (+,-)-pseudoephedrine, (+,-)-norephedrine, (+,-)-norpseudoephedrine, (+,-)-p-hyroxyamphetamine, (+,-)-p-hydroxymethamphetamine, and (+,-)-p-hydroxynorephedrine was studied. The enantiomers of the metabolites were derivatized with alpha-methoxy-alpha -(trifluoromethyl)-phenylacetyl chloride (MPTA.Cl) as the
Brandy Greenhill et al.
Journal of analytical toxicology, 27(7), 479-484 (2003-11-11)
There are a several drugs that lead to the production of methamphetamine and/or amphetamine in the body which are subsequently excreted in the urine. These drugs raise obvious concerns when interpreting positive amphetamine drug testing results. Famprofazone is an analgesic
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