32492
Florfenicol amine
VETRANAL®, analytical standard
Sinónimos:
(αR)-α-[(1S)-1-Amino-2-fluoroethyl]-4-(methylsulfonyl)benzenemethanol, D-(−)-threo-2-Amino-3-fluoro-1-[4-(methylsulfonyl)phenyl]-1-propanol
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About This Item
Fórmula empírica (notación de Hill):
C10H14FNO3S
Número de CAS:
Peso molecular:
247.29
Número MDL:
Código UNSPSC:
41116107
ID de la sustancia en PubChem:
NACRES:
NA.24
Productos recomendados
grado
analytical standard
Nivel de calidad
Línea del producto
VETRANAL®
caducidad
limited shelf life, expiry date on the label
técnicas
HPLC: suitable
gas chromatography (GC): suitable
aplicaciones
forensics and toxicology
pharmaceutical (small molecule)
Formato
neat
cadena SMILES
CS(=O)(=O)c1ccc(cc1)[C@@H](O)[C@H](N)CF
InChI
1S/C10H14FNO3S/c1-16(14,15)8-4-2-7(3-5-8)10(13)9(12)6-11/h2-5,9-10,13H,6,12H2,1H3/t9-,10-/m1/s1
Clave InChI
XLSYLQDVLAXIKK-NXEZZACHSA-N
Categorías relacionadas
Descripción general
Florfenicol amine is a polar metabolite of florfenicol.
Aplicación
Florfenicol amine may be used as an analytical reference standard for the determination of the analyte in:
- Poultry and porcine muscle and liver by gas chromatography-negative chemical ionization mass spectrometry (GC-NCI/MS) with selected ion monitoring (SIM) detection.
- Food samples by ultra-high performance liquid chromatography-electrospray ionization-tandem mass spectrometry (UHPLC-ESI-MS/MS) operating in selected reaction monitoring (SRM) detection mode.
- Chicken muscle by LC-ESI-MS/MS with multiple reaction monitoring (MRM) detection.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Productos recomendados
Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.
Información legal
VETRANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
Código de clase de almacenamiento
11 - Combustible Solids
Clase de riesgo para el agua (WGK)
WGK 3
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Los clientes también vieron
A P Pfenning et al.
Journal of AOAC International, 83(1), 26-30 (2000-02-29)
A gas chromatographic (GC) method is presented for determining residues of chloramphenicol (CAP), florfenicol (FF), florfenicol amine (FFa), and thiamphenicol (TAP) in shrimp tissues, with meta-nitrochloramphenicol (mCAP) as the internal standard. The composited shrimp is extracted with basic ethyl acetate
B-K Park et al.
Journal of veterinary pharmacology and therapeutics, 29(1), 37-40 (2006-01-20)
The pharmacokinetics of florfenicol and its metabolite, florfenicol amine, was investigated after its intravenous (i.v.) and oral (p.o.) administration of 20 mg/kg of body weight in Korean catfish (Silurus asotus). After i.v. florfenicol injection (as a bolus), the terminal half-life
Jin-E Wu et al.
Journal of agricultural and food chemistry, 56(18), 8261-8267 (2008-08-20)
Florfenicol (FF) is a broad-spectrum antibiotic used increasingly in aquaculture, livestock, and poultry to treat diseases. To avoid using labor-intensive instrumental methods to detect residues of FF in food and food products, a simple and convenient indirect competitive enzyme-linked immunosorbent
Suxia Zhang et al.
Journal of AOAC International, 89(5), 1437-1441 (2006-10-18)
A rapid and sensitive gas chromatography method was developed for the simultaneous determination of florfenicol (FF) and its metabolite florfenicol amine (FFA) in fish, shrimp, and swine muscle. The extracted samples were defatted with hexane and cleaned up by solid-phase
Jeffery M van de Riet et al.
Journal of AOAC International, 86(3), 510-514 (2003-07-11)
A liquid chromatographic (LC)/mass spectrometric (MS) method was developed for determining the residues of chloramphenicol, thiamphenicol, florfenicol, and florfenicol amine in a number of aquatic species. The phenicols are extracted with acetone, the extracts are partitioned with dichloromethane, the aqueous
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