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Merck
CN

46297

Supelco

呋喃唑酮

VETRANAL®, analytical standard

别名:

3-(5-硝基呋喃甲叉氨基)-2-噁唑烷酮

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About This Item

经验公式(希尔记法):
C8H7N3O5
CAS号:
分子量:
225.16
Beilstein:
8317414
EC 号:
MDL编号:
UNSPSC代码:
41116107
PubChem化学物质编号:
NACRES:
NA.24

等级

analytical standard

质量水平

产品线

VETRANAL®

保质期

limited shelf life, expiry date on the label

技术

HPLC: suitable
gas chromatography (GC): suitable

抗生素抗菌谱

Gram-positive bacteria
parasites

应用

cleaning products
clinical
cosmetics
food and beverages
forensics and toxicology
personal care
pharmaceutical (small molecule)

格式

neat

作用机制

enzyme | inhibits

SMILES字符串

[O-][N+](=O)c1ccc(\C=N\N2CCOC2=O)o1

InChI

1S/C8H7N3O5/c12-8-10(3-4-15-8)9-5-6-1-2-7(16-6)11(13)14/h1-2,5H,3-4H2/b9-5+

InChI key

PLHJDBGFXBMTGZ-WEVVVXLNSA-N

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一般描述

Furazolidone is an effective antiprotozoal and antibacterial agent.

应用

Furazolidone may be used as a reference standard:
  • For the determination of the analyte in pharmaceutical formulations by second-derivative spectrophotometry.
  • For the determination of the analyte in animal feeds using liquid chromatography with ultraviolet and thermospray mass spectrometric detection.

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

法律信息

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

相关产品

产品编号
说明
价格

象形图

Health hazard

警示用语:

Warning

危险声明

危险分类

Repr. 2

WGK

WGK 3

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves


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分析证书(COA)

Lot/Batch Number

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Determination of furazolidone in animal feeds using liquid chromatography with UV and thermospray mass spectrometric detection.
McCracken RJ and Kennedy DG
Journal of Chromatography A, 771(1-2), 349- 354 (1997)
Formulation and advantages of furazolidone in liposomal drug delivery systems.
Alam MI, et al.
European Journal of Pharmaceutical Sciences, 84, 139- 145 (2016)
C V Prasad et al.
Journal of pharmaceutical and biomedical analysis, 21(5), 961-968 (2000-03-07)
A second-derivative spectrophotometric procedure has been developed for the simultaneous determination of tinidazole (TD), furazolidone (FD) and diloxanide furoate (DF) in a commercial preparation. The method consists of the utilization of second-derivative absorption spectra of tablet extract in distilled water
B H Ali
Veterinary research communications, 6(1), 1-11 (1983-01-01)
The pharmacological and toxicological properties of furazolidone have been briefly reviewed. Among the most important pharmacological actions of furazolidone is the inhibition of mono- and diamine oxidase activities, which seem to depend, at least in some species, on the presence
In vivo and in vitro metabolic studies of furazolidone: a risk evaluation.
L H Vroomen et al.
Drug metabolism reviews, 22(6-8), 663-676 (1990-01-01)

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