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Merck

33495

Supelco

Famoxadon -Lösung

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

Synonym(e):

3-Anilino-5-methyl-5-(4-phenoxyphenyl)-oxazolidin-2,4-dion

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About This Item

Empirische Formel (Hill-System):
C22H18N2O4
CAS-Nummer:
Molekulargewicht:
374.39
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
41116107
PubChem Substanz-ID:
NACRES:
NA.24

Qualität

analytical standard

Qualitätsniveau

Produktlinie

PESTANAL®

Haltbarkeit

limited shelf life, expiry date on the label

Konzentration

100 μg/mL in acetonitrile

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

Anwendung(en)

agriculture

Format

single component solution

Lagertemp.

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

InChIKey

PCCSBWNGDMYFCW-UHFFFAOYSA-N

Allgemeine Beschreibung

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

Anwendung

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.

Rechtliche Hinweise

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

Piktogramme

FlameExclamation mark

Signalwort

Danger

Gefahreneinstufungen

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

Lagerklassenschlüssel

3 - Flammable liquids

WGK

WGK 2

Flammpunkt (°F)

35.6 °F

Flammpunkt (°C)

2 °C

Persönliche Schutzausrüstung

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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Die Dokumentenbibliothek aufrufen

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
Bo Cheng et al.
Chemosphere, 247, 125870-125870 (2020-01-14)
As a new protective and therapeutic fungicide, studies on famoxadone-cymoxanil are rare, and its toxicity to aquatic organisms has not been reported. In the present study, zabrafish embryos were exposed to several concentrations of famoxadone-cymoxanil at 10 hpf. Then, the
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

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