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Merck
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Documentos

F9130

Sigma-Aldrich

Furaltadone

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/REAXYS Number:
8130725
EC Number:
205-384-5
MDL number:
MFCD00057356
UNSPSC Code:
12352200
PubChem Substance ID:
24894989
NACRES:
NA.77

Quality Level

200

storage temp.

2-8°C

SMILES string

[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+

InChI key

YVQVOQKFMFRVGR-VGOFMYFVSA-N

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General description

Furaltadone is a nitrofuran containing a 5-nitrofuran ring and is a member of synthetic antibiotics.

Application

Furaltadone has been used as a reference standard in liquid chromatography-mass spectrometry (LC-MS/MS) quantifying nitrofuran metabolites in aquaculture matrixes and honey.

Biochem/physiol Actions

Nitrofurans are commercially used as feed additives to promote growth in various fields such as aquaculture, bee colonies, and livestock.

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H302

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Brian T Veach et al.
Journal of AOAC International, 101(3), 897-904 (2017-12-01)
This paper describes a rapid and robust method utilizing a single liquid-liquid extraction for the quantitation and confirmation of chloramphenicol, florfenicol, and nitrofuran metabolites in honey. This methodology combines two previous extraction methods into a single extraction procedure and utilizes
Nitrofuran antibiotics: a review on the application, prohibition and residual analysis
Vass M, et al.
Veterinary medicine (Auckland, N.Z.), 53(9), 469-469 (2008)
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
Sara Leston et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 879(32), 3832-3836 (2011-11-23)
Presently, the rise of new contaminants in the environment has widened the scope of pharmaceutical analyses as to face the demanding new challenges. An increasing tendency for the interconnection and overlap of research fields, such as ecology and biochemistry, is
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
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