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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:
131807-57-3
Molecular Weight:
374.39
EC Number:
200-835-2
MDL number:
MFCD03427409
UNSPSC Code:
41116107
PubChem Substance ID:
329754563
NACRES:
NA.24

grade

analytical standard

Quality Level

100

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
GHS02,GHS07

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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Certificates of Analysis (COA)

Lot/Batch Number
BCCL4647
BCCG7182
BCCB2876
BCBR9481V
SZBE066XV

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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
Marcin Sarewicz et al.
Biochemistry, 52(37), 6388-6395 (2013-08-15)
Efficient energy conversion often requires stabilization of one-electron intermediates within catalytic sites of redox enzymes. While quinol oxidoreductases are known to stabilize semiquinones, one of the famous exceptions includes the quinol oxidation site of cytochrome bc1 (Qo), for which detection
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
Meng Wang et al.
Environmental science and pollution research international, 28(13), 15947-15953 (2020-11-28)
The chiral pesticide famoxadone is mainly applied to control fungal diseases on fruiting vegetables. The fungicidal activity, ecotoxicological effects, and degradation behavior of famoxadone enantiomers are less well known. In this study, a systemic assessment of the stereoselectivity of famoxadone
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