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Supelco

Metalaxyl

PESTANAL®, analytical standard

Sinônimo(s):

N-(2,6-Dimethylphenyl)-N-(methoxyacetyl)-DL-alanine methyl ester

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About This Item

Fórmula empírica (Notação de Hill):
C15H21NO4
Número CAS:
Peso molecular:
279.33
Beilstein:
2947777
Número CE:
Número MDL:
Código UNSPSC:
41116107
ID de substância PubChem:
NACRES:
NA.24

grau

analytical standard

Nível de qualidade

linha de produto

PESTANAL®

prazo de validade

limited shelf life, expiry date on the label

técnica(s)

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

pf

69-73 °C

adequação

passes test for identity (NMR)

aplicação(ões)

agriculture
environmental

formato

neat

cadeia de caracteres SMILES

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

chave InChI

ZQEIXNIJLIKNTD-UHFFFAOYSA-N

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Descrição geral

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

Aplicação

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.

Informações legais

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

Pictogramas

Exclamation mark

Palavra indicadora

Warning

Frases de perigo

Classificações de perigo

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

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 2

Ponto de fulgor (°F)

212.0 °F - closed cup

Ponto de fulgor (°C)

100 °C - closed cup

Equipamento de proteção individual

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


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Certificados de análise (COA)

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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)
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
Alipio Bermudez-Couso et al.
Journal of agricultural and food chemistry, 59(13), 7286-7293 (2011-05-27)
Metalaxyl adsorption and desorption behavior in acid soils were evaluated via batch and stirred-flow chamber experiments. On the basis of batch experiments (adsorption curves of the Giles C-type), metalaxyl has a low affinity for acid soils. Also, as derived from
R Sowmya et al.
Marine biotechnology (New York, N.Y.), 13(5), 918-927 (2011-01-19)
Studies were carried out to utilize in situ proteases of shrimp heads to recover carotenoproteins possessing antioxidant activity. Highest protease activity of the buffer extract was found at pH 8.0 (9.85 ± 0.61 units). The protease activity increased with temperature up to

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