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46289

Supelco

Furaltadone

VETRANAL®, analytical standard

Sinónimos:

5-Morpholinomethyl-3-(5-nitrofurfurylideneamino)-2-oxazolidinone

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About This Item

Fórmula empírica (notación de Hill):
C13H16N4O6
Número de CAS:
139-91-3
Peso molecular:
324.29
Beilstein:
8130725
Número CE:
205-384-5
Número MDL:
MFCD00057356
Código UNSPSC:
41116107
ID de la sustancia en PubChem:
329757123
NACRES:
NA.24

grado

analytical standard

Nivel de calidad

200

Línea del producto

VETRANAL®

caducidad

limited shelf life, expiry date on the label

técnicas

HPLC: suitable
gas chromatography (GC): suitable

aplicaciones

clinical testing

Formato

neat

temp. de almacenamiento

2-8°C

cadena 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+

Clave InChI

YVQVOQKFMFRVGR-VGOFMYFVSA-N

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Descripción general

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.

Aplicación

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.

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

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
BCCM3647
BCCD2702
BCCB0543

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Sigma-Aldrich

73340

5-Nitro-2-furaldehyde semicarbazone

Furazolidone

Sigma-Aldrich

F9505

Furazolidone

Chlortetracycline hydrochloride VETRANAL®, analytical standard

Supelco

46133

Chlortetracycline hydrochloride

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)
B Murugasu-Oei et al.
The Journal of antimicrobial chemotherapy, 46(6), 917-919 (2000-12-05)
Depletion of oxygen triggers the shift-down of Mycobacterium bovis BCG to a state of dormancy. Bacilli in their dormant state are resistant to standard anti-mycobacterials. The nitroimidazole metronidazole was the first compound identified to show bactericidal activity against dormant tubercle
Peng Jie Luo et al.
Biomedical and environmental sciences : BES, 25(4), 449-457 (2012-10-03)
To determine 3-amino-5-morpholinomethyl-2-oxazolidinone (AMOZ) residues released from protein bound AMOZ in animal tissues. Polyclonal and monoclonal antibodies were produced in this study. A rapid, sensitive, and specific competitive direct enzyme-linked immunosorbent assay (cdELISA) was developed. Rabbit polyclonal antibodies were used
A Stammati et al.
Cell biology and toxicology, 13(2), 125-130 (1997-02-01)
Nitrofuran drugs have been studied on cellular systems in order to develop in vitro tests for safety assessment of food contaminants. In the present study we have tested furaltadone on three cell lines (HEp-2, Caco-2 and V79), using the same
L P Jager et al.
European journal of pharmacology, 331(2-3), 325-331 (1997-07-23)
Changes in the biogenesis of corticosteroids caused by nitrofurans were studied. The three nitrofurans used: furazolidone, furaltadone and nitrofurantoin, altered the steroid production/release by porcine adrenocortical cells in vitro during 1 h incubations. With pregnenolone as a substrate the nitrofurans
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