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46289

Supelco

Furaltadone

VETRANAL®, analytical standard

Synonyme(s) :

5-morpholinométhyl-3-(5-nitrofurfurylidèneamino)-2-oxazolidinone

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About This Item

Formule empirique (notation de Hill):
C13H16N4O6
Numéro CAS:
139-91-3
Poids moléculaire :
324.29
Numéro Beilstein :
8130725
Numéro CE :
205-384-5
Numéro MDL:
MFCD00057356
Code UNSPSC :
41116107
ID de substance PubChem :
329757123
Nomenclature NACRES :
NA.24

Qualité

analytical standard

Niveau de qualité

200

Gamme de produits

VETRANAL®

Durée de conservation

limited shelf life, expiry date on the label

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Application(s)

clinical testing

Format

neat

Température de stockage

2-8°C

Chaîne SMILES 

[O-][N+](=O)c1ccc(\C=N\N2CC(CN3CCOCC3)OC2=O)o1

InChI

1S/C13H16N4O6/c18-13-16(14-7-10-1-2-12(22-10)17(19)20)9-11(23-13)8-15-3-5-21-6-4-15/h1-2,7,11H,3-6,8-9H2/b14-7+

Clé InChI

YVQVOQKFMFRVGR-VGOFMYFVSA-N

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Description générale

Furaltadone is a nitrofuran drug, with broad-spectrum antimicrobial activity. It is widely used in veterinary medicine for intensive animal production, especially in pigs, poultry, fish and to provide resistance against infections caused by Escherichia coli and Salmonella.

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support. Furaltadone may be used as an analytical reference standard for the quantification of the analyte in milk samples and poultry eggs using different chromatography techniques.

Produits recommandés

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.

Informations légales

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

Pictogrammes

Exclamation mark
GHS07

Mention d'avertissement

Warning

Mentions de danger

H302

Classification des risques

Acute Tox. 4 Oral

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Équipement de protection individuelle

dust mask type N95 (US), Eyeshields, Gloves

Faites votre choix parmi les versions les plus récentes :

Certificats d'analyse (COA)

Lot/Batch Number
BCCD2702
BCCB0543
SZBF119XV
SZBB193XV
SZB7303XV

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Si vous avez besoin d'une version particulière, vous pouvez rechercher un certificat spécifique par le numéro de lot.

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Sigma-Aldrich

73340

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Sigma-Aldrich

F9505

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Determination of nitrofurantoin, furazolidone and furaltadone in milk by high-performance liquid chromatography with electrochemical detection
Diaz G.T, et al.
Analytical Methods : Advancing Methods and Applications, 764(2), 243-248 (1997)
R J McCracken et al.
Food additives and contaminants, 24(1), 26-33 (2006-12-14)
Nitrofuran antibiotics have been banned for use in food-producing animals in many countries, including the European Union, owing to the threat they pose to human health. Research continues into the accumulation of these drugs in animal tissues and into the
Sara Leston et al.
Chemosphere, 82(7), 1010-1016 (2010-11-27)
The use of pharmaceuticals in the food production industry as prophylatic and therapeutic agents is necessary to promote animal health, but may entail significant consequences to natural ecosystems, especially in the cases of overdosing and use of banned pharmaceuticals. The
Zhen-Lin Xu et al.
Talanta, 103, 306-313 (2012-12-04)
A heterologous competitive indirect enzyme-linked immunosorbent assay (ciELISA) for the determination of the furaltadone metabolite 3-amino-5-morpholinomethyl-2-oxazolidinone (AMOZ) was developed. AMOZ was derivatised with 2-(4-formylphenoxy) acetic acid or 2-(3-formylphenoxy) acetic acid to obtain two novel immunizing haptens. The ability of these
M C Mahedero et al.
Journal of pharmaceutical and biomedical analysis, 29(3), 477-485 (2002-06-14)
An UV spectroscopic method is proposed to analyze mixtures of the nitrofuran derivatives, nitrofurantoin, furaltadone and furazolidone, used in veterinary. The change of absorption spectra due to photo-decomposition is used. A 20% dimethylformamide/water, basic medium of pH 9.4 (ammonium chloride/ammonia)
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