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33495

Supelco

Famoxadone solution

100 μg/mL in acetonitrile, PESTANAL®, analytical standard

Synonym(s):

3-Anilino-5-methyl-5-(4-phenoxyphenyl)oxazolidine-2,4-dione

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About This Item

Empirical Formula (Hill Notation):
C22H18N2O4
CAS Number:
Molecular Weight:
374.39
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

concentration

100 μg/mL in acetonitrile

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture

format

single component solution

storage temp.

2-8°C

SMILES string

O=C1OC(C(C=C2)=CC=C2OC3=CC=CC=C3)(C)C(N1NC4=CC=CC=C4)=O

InChI

1S/C22H18N2O4/c1-22(16-12-14-19(15-13-16)27-18-10-6-3-7-11-18)20(25)24(21(26)28-22)23-17-8-4-2-5-9-17/h2-15,23H,1H3

InChI key

PCCSBWNGDMYFCW-UHFFFAOYSA-N

General description

Famoxadone belongs to the oxazolidinedione class of fungicides used to control broad spectrum of fungal diseases in agricultural crops.

Application

Famoxadone may be used as a reference standard for the determination of the analyte in wine and grape samples using gas chromatography (GC) coupled to electron capture (EC) and mass spectrometric (MS) methods of detection respectively.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Legal Information

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

Pictograms

FlameExclamation mark

Signal Word

Danger

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 2

Storage Class Code

3 - Flammable liquids

WGK

WGK 2

Flash Point(F)

35.6 °F

Flash Point(C)

2 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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A comparison of a gas chromatographic with electron-capture detection and a gas chromatographic with mass spectrometric detection screening methods for the analysis of famoxadone in grapes and wines.
Abreu MDS, et al.
Journal of Chromatography A, 1103(2), 362-367 (2006)
Yongbo Cui et al.
PloS one, 12(7), e0181075-e0181075 (2017-07-13)
The aim of this study was to elucidate the molecular mechanisms by which food-derived casein glycomacropeptide (CGMP) maintains internal homeostasis in the intestinal mucosa and to investigate the effects of CGMP on the intestinal mucosal immunological barrier and related signal
Guofeng Xu et al.
Journal of separation science, 41(20), 3871-3880 (2018-08-24)
Famoxadone is a widely used chiral fungicide on tomato, apple, and grape. But it is still being employed as a racemic mixture without distinguishing the difference between enantiomers, which often leads to its inaccurate risk assessment. In this study, a
Guofeng Xu et al.
Chirality, 33(3), 134-142 (2021-01-19)
Famoxadone enantiomers were separated on Lux Amylose-1 chiral column and determined by ultra-performance liquid chromatography coupled with tandem mass spectrometry (UPLC-MS/MS). The half-lives of R-(-)-famoxadone and S-(+)-famoxadone were 69.3 and 86.6 h in apple cider, 231.0 and 346.5 h in
Mohd Aamir et al.
Frontiers in pharmacology, 9, 1038-1038 (2018-11-09)
Vascular wilt of tomato caused by Fusarium oxysporum f.sp. lycopersici (FOL) is one of the most devastating diseases, that delimits the tomato production worldwide. Fungal short-chain dehydrogenases/reductases (SDRs) are NADP(H) dependent oxidoreductases, having shared motifs and common functional mechanism, have

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