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About This Item
Empirical Formula (Hill Notation):
C15H21NO4
CAS Number:
Molecular Weight:
279.33
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
260-979-7
Beilstein/REAXYS Number:
2947777
MDL number:
grade
analytical standard
Quality Level
product line
PESTANAL®
shelf life
limited shelf life, expiry date on the label
technique(s)
HPLC: suitable, NMR: suitable, gas chromatography (GC): suitable
mp
69-73 °C
suitability
passes test for identity (NMR)
application(s)
agriculture
environmental
format
neat
SMILES string
COCC(=O)N(C(C)C(=O)OC)c1c(C)cccc1C
InChI
1S/C15H21NO4/c1-10-7-6-8-11(2)14(10)16(13(17)9-19-4)12(3)15(18)20-5/h6-8,12H,9H2,1-5H3
InChI key
ZQEIXNIJLIKNTD-UHFFFAOYSA-N
General description
Metalaxyl, also known as Ridomil, is a phenylamide and systemic benzoic fungicide. It is generally used to control infection caused by Phytophthora infestans.
Application
Metalaxyl has been used as reference standard in Fourier transform infrared (FTIR) spectrometric method for determination of metalaxyl in pesticide formulations.
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
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signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 3 - Skin Sens. 1
Storage Class
11 - Combustible Solids
wgk
WGK 2
flash_point_f
212.0 °F - closed cup
flash_point_c
100 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
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Widespread distribution and probable origin of resistance to metalaxyl in clonal genotypes of Phytophthora infestans in the United States and Western Canada.
Goodwin, Stephen B., Ludwik S. Sujkowski, and William E. Fry.
Phytopathology, 86, 793-800 (1996)
Simultaneous determination of Folpet and Metalaxyl in pesticide formulations by flow injection Fourier transform infrared spectrometry.
Quintas, Guillermo, et al.
Analytica Chimica Acta, 480.1, 11-21 (2003)
R Celis et al.
The Science of the total environment, 444, 288-297 (2013-01-02)
Improving the existing knowledge on the enantioselectivity of processes affecting chiral pesticide enantiomers in the environment is necessary to maximize the efficacy and minimize the environmental impact caused by the use of pesticides with chiral properties. In this work, the
