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Merck

32012

Supelco

Metalaxyl

PESTANAL®, analytical standard

Synonym(e):

N-(2,6-Dimethylphenyl)-N-(methoxyacetyl)-DL-alanin-methylester

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About This Item

Empirische Formel (Hill-System):
C15H21NO4
CAS-Nummer:
Molekulargewicht:
279.33
Beilstein:
2947777
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

Methode(n)

HPLC: suitable
NMR: suitable
gas chromatography (GC): suitable

mp (Schmelzpunkt)

69-73 °C

Eignung

passes test for identity (NMR)

Anwendung(en)

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

InChIKey

ZQEIXNIJLIKNTD-UHFFFAOYSA-N

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Verwandte Kategorien

Allgemeine Beschreibung

Metalaxyl, also known as Ridomil, is a phenylamide and systemic benzoic fungicide. It is generally used to control infection caused by Phytophthora infestans.

Anwendung

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.

Rechtliche Hinweise

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

Piktogramme

Exclamation mark

Signalwort

Warning

Gefahreneinstufungen

Acute Tox. 4 Oral - Aquatic Chronic 3 - Skin Sens. 1

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 2

Flammpunkt (°F)

212.0 °F - closed cup

Flammpunkt (°C)

100 °C - closed cup

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


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Analysenzertifikate (COA)

Lot/Batch Number

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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)
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)
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
P Sukul et al.
Reviews of environmental contamination and toxicology, 164, 1-26 (2003-02-18)
Metalaxyl is a systemic fungicide used to control plant diseases caused by Oomycete fungi. Its formulations include granules, wettable powders, dusts, and emulsifiable concentrates. Application may be by foliar or soil incorporation, surface spraying (broadcast or band), drenching, and seed
J Saab et al.
Chemosphere, 82(6), 929-934 (2010-11-26)
In this paper, we present the effect of inorganic cations such as Na+, K+, Ca2+, Mg2+ on the salting-out phenomenon of metalaxyl from pure water to aqueous salt solutions. Moreover the 1-octanol/water partition coefficient in pure water is presented. To

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