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About This Item
Empirical Formula (Hill Notation):
C14H17Cl2NO2
CAS Number:
Molecular Weight:
302.20
Beilstein:
8996658
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
technique(s)
HPLC: suitable
gas chromatography (GC): suitable
application(s)
agriculture
environmental
format
neat
SMILES string
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)
InChI key
VDLGAVXLJYLFDH-UHFFFAOYSA-N
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General description
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.
Application
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.
Legal Information
PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
Hazard Statements
Precautionary Statements
Hazard Classifications
Aquatic Chronic 2
Storage Class Code
11 - Combustible Solids
WGK
WGK 2
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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)
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
Kim Christopher Cohrs et al.
Fungal genetics and biology : FG & B, 100, 42-51 (2017-02-12)
The gray mold fungus Botrytis cinerea features a wide host range and causes severe economic losses, making it an important object for molecular research. Thus far, genetic modification of the fungus mainly is relied on two selection systems (nourseothricin and
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)
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