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Merck
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Key Documents

Altri documenti

F9130

Sigma-Aldrich

Furaltadone

Sinonimo/i:

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

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About This Item

Formula empirica (notazione di Hill):
C13H16N4O6
Numero CAS:
139-91-3
Peso molecolare:
324.29
Beilstein:
8130725
Numero CE:
205-384-5
Numero MDL:
MFCD00057356
Codice UNSPSC:
12352200
ID PubChem:
24894989
NACRES:
NA.77

Livello qualitativo

200

Temperatura di conservazione

2-8°C

Stringa SMILE

[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+
YVQVOQKFMFRVGR-VGOFMYFVSA-N

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Descrizione generale

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

Applicazioni

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

Azioni biochim/fisiol

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

Pittogrammi

Exclamation mark
GHS07

Avvertenze

Warning

Indicazioni di pericolo

H302

Classi di pericolo

Acute Tox. 4 Oral

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

Certificati d'analisi (COA)

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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
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
Jorge Barbosa et al.
Journal of agricultural and food chemistry, 60(17), 4227-4234 (2012-04-11)
The use of nitrofurans as veterinary drugs has been banned from intensive animal production in the European Union (EU) since 1993. The objective of the present study was to evaluate the accumulation and depletion of furaltadone and nifursol and their
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
Eric Verdon et al.
Analytica chimica acta, 586(1-2), 336-347 (2007-03-28)
Following the ban of four nitrofurans in the mid-90s (furazolidone, furaltadone, nitrofurantoine, nitrofurazone), the nifursol, a veterinary drug from the nitrofuran class of antibacterials which has been used prophylactically as feed additive for treating turkeys against histomoniasis (blackhead disease) was
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