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Furaltadone

Name: Furaltadone
Brand: SIGMA

Synonym(s):

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

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About This Item

Empirical Formula (Hill Notation):

C₁₃H₁₆N₄O₆

CAS Number:

139-91-3

Molecular Weight:

324.29

UNSPSC Code:

12352200

NACRES:

NA.77

PubChem Substance ID:

24894989

EC Number:

205-384-5

Beilstein/REAXYS Number:

8130725

MDL number:

MFCD00057356

Quality level:

200

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Properties

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

Description

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[1] and honey[2].

Biochem/physiol Actions

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

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1 of 1

This Item	46289	F9505	481984
Sigma-Aldrich F9130 Furaltadone	Supelco 46289 Furaltadone	Sigma-Aldrich F9505 Furazolidone	Sigma-Aldrich 481984 Nifuroxazide
Quality Level 200	Quality Level 200	Quality Level 200	Quality Level 100
storage temp. 2-8°C	storage temp. 2-8°C	storage temp. -	storage temp. 2-8°C

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pictograms

GHS07

signalword

Warning

hcodes

H302

pcodes

P264 - P270 - P301 + P312 - P501

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number

017H1158

035F0119

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Quantitation and Confirmation of Chloramphenicol, Florfenicol, and Nitrofuran Metabolites in Honey Using LC-MS/MS.

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)

[Evaluation of efficacy of oral quinolone against Streptococcus pneumoniae AND Haemophilus influenzae with the use of Monte Carlo simulation].

Hiroshige Mikamo et al.

The Japanese journal of antibiotics, 59(6), 468-473 (2007-03-06)

We investigated the efficacies of various administration methods for levofloxacin (LVFX) and tosufloxacin (TFLX) against 161 isolates of Streptococcus pneumoniae and 309 isolates of Haemophilus influenzae isolated in Gifu prefecture, using Monte Carlo simulation. The pharmacokinetic parameters of the fluoroquinolones

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Global Trade Item Number

SKU	GTIN
F9130-25G	04061833621363

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