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Merck
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Documenti fondamentali

31713

Supelco

Fenhexamid

PESTANAL®, analytical standard

Sinonimo/i:

N-(2,3-Dichloro-4-hydroxyphenyl)-1-methylcyclohexanecarboxamide

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About This Item

Formula empirica (notazione di Hill):
C14H17Cl2NO2
Numero CAS:
Peso molecolare:
302.20
Beilstein:
8996658
Numero CE:
Numero MDL:
Codice UNSPSC:
41116107
ID PubChem:
NACRES:
NA.24

Grado

analytical standard

Livello qualitativo

Nome Commerciale

PESTANAL®

Durata

limited shelf life, expiry date on the label

tecniche

HPLC: suitable
gas chromatography (GC): suitable

applicazioni

agriculture
environmental

Formato

neat

Stringa SMILE

CC1(CCCCC1)C(=O)Nc2ccc(O)c(Cl)c2Cl

InChI

1S/C14H17Cl2NO2/c1-14(7-3-2-4-8-14)13(19)17-9-5-6-10(18)12(16)11(9)15/h5-6,18H,2-4,7-8H2,1H3,(H,17,19)
VDLGAVXLJYLFDH-UHFFFAOYSA-N

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Descrizione generale

Fenhexamid is an anti-botrytis fungicide widely used against a broad spectrum of fungi in agricultural crops. Its mode of action involves the inhibition of sterol biosynthesis.

Applicazioni

Fenhexamid may be used as a standard in the determination of fenhexamid in:
  • Fruits using enzyme-linked immunosorbent assay (ELISA).
  • Tomatoes, grape and wine samples using high-performance liquid chromatography coupled with ultraviolet detector and gas chromatography (GC) coupled with detectors such as nitrogen–phosphorus detector (NPD), electron capture detector (ECD) and ion trap mass spectrometry (ITMS).

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

Note legali

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

Pittogrammi

Environment

Indicazioni di pericolo

Consigli di prudenza

Classi di pericolo

Aquatic Chronic 2

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves


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Certificati d'analisi (COA)

Lot/Batch Number

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Matthias Kretschmer et al.
PLoS pathogens, 5(12), e1000696-e1000696 (2009-12-19)
The grey mould fungus Botrytis cinerea causes losses of commercially important fruits, vegetables and ornamentals worldwide. Fungicide treatments are effective for disease control, but bear the risk of resistance development. The major resistance mechanism in fungi is target protein modification
Determination of fenhexamid residues in grape must, kiwifruit, and strawberry samples by enzyme-linked immunosorbent assay
Esteve-Turrillas.AF, et al.
Food Chemistry, 124(4), 1727-1733 (2011)
Genetic analysis of fenhexamid-resistant field isolates of the phytopathogenic fungus Botrytis cinerea
Fillinger S, et al.
Antimicrobial Agents and Chemotherapy, 52(11), 3933-3940 (2008)
The hydroxyanilide fenhexamid, a new sterol biosynthesis inhibitor fungicide efficient against the plant pathogenic fungus Botryotinia fuckeliana (Botrytis cinerea)
Debieu D, et al.
Pest Management Science, 57(11), 1060-1067 (2001)
Facundo Rivera-Becerril et al.
The Science of the total environment, 577, 84-93 (2016-11-08)
Pesticide contamination of the environment can result from agricultural practices. Persistence of pesticide residues is a threat to the soil biota including plant roots and beneficial microorganisms, which support an important number of soil ecosystem services. Arbuscular mycorrhizal fungi (AMF)

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