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Key Documents

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32581

Supelco

Bixafen

PESTANAL®, analytical standard

Sinônimo(s):

N-(3′,4′-Dichloro-5-fluorobiphenyl-2-yl)-3-(difluoromethyl)-1-methylpyrazole-4-carboxamide

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About This Item

Fórmula empírica (Notação de Hill):
C18H12Cl2F3N3O
Número CAS:
581809-46-3
Peso molecular:
414.21
Número MDL:
MFCD16652583
Código UNSPSC:
41116107
ID de substância PubChem:
329754038
NACRES:
NA.24

grau

analytical standard

Nível de qualidade

100

linha de produto

PESTANAL®

prazo de validade

limited shelf life, expiry date on the label

técnica(s)

HPLC: suitable
gas chromatography (GC): suitable

aplicação(ões)

agriculture
environmental

formato

neat

cadeia de caracteres SMILES

Cn1cc(C(=O)Nc2ccc(F)cc2-c3ccc(Cl)c(Cl)c3)c(n1)C(F)F

InChI

1S/C18H12Cl2F3N3O/c1-26-8-12(16(25-26)17(22)23)18(27)24-15-5-3-10(21)7-11(15)9-2-4-13(19)14(20)6-9/h2-8,17H,1H3,(H,24,27)

chave InChI

LDLMOOXUCMHBMZ-UHFFFAOYSA-N

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Descrição geral

Bixafen is a succinate dehydrogenase, which belongs to the pyrazole group of fungicides. It finds applications as a broad spectrum fungicide in controlling pathogens in cereal plantations.

Aplicação

Bixafen may be used as a reference standard in the determination of bixafen in agricultural food products using liquid chromatography coupled with tandem mass spectrometry (LC-MS-MS).
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Produtos recomendados

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Informações legais

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

Pictogramas

Environment
GHS09

Palavra indicadora

Warning

Frases de perigo

H400

Declarações de precaução

P273 - P391 - P501

Classificações de perigo

Aquatic Acute 1

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 2

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Escolha uma das versões mais recentes:

Certificados de análise (COA)

Lot/Batch Number
BCCF5281
BCBS9732V
SZBF118XV
SZBD210XV
SZBA018XV

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Se precisar de uma versão específica, você pode procurar um certificado específico pelo número do lote ou da remessa.

Pesquise por COA

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Supelco

45642

Propiconazole

Sodium bicarbonate-13C 98 atom % 13C, 99% (CP)

Sigma-Aldrich

372382

Sodium bicarbonate-13C

Ramla Sahli et al.
Environmental science and pollution research international, 25(30), 29775-29783 (2017-05-10)
Zymoseptoria tritici, responsible for Septoria tritici blotch, is the most important pathogen of wheat. The control of this parasite relies mainly on synthetic fungicides, but their use is increasingly controversial and searching for alternative management strategies is encouraged. In this
Simultaneous determination of five pyrazole fungicides in cereals, vegetables and fruits using liquid chromatography/tandem mass spectrometry.
Dong F, et al.
Journal of Chromatography A, 1262, 98-106 (2012)
Effect of bixafen on senescence and yield formation of wheat.
Berdugo AC, et al.
Pesticide Biochemistry and Physiology, 104(3), 171-177 (2012)
Ignaz J Buerge et al.
Journal of agricultural and food chemistry, 64(26), 5301-5309 (2016-06-02)
Metabolism of chiral pesticides in crops is typically studied using achiral analytical methods and, consequently, the stereoisomer composition of residues is unknown. In this study, we developed an enantioselective GC-MS/MS method to quantify residues of the fungicides fenpropidin, fenpropimorph, and
Kang Yu et al.
Frontiers in plant science, 9, 1195-1195 (2018-09-04)
Producing quantitative and reliable measures of crop disease is essential for resistance breeding, but is challenging and time consuming using traditional phenotyping methods. Hyperspectral remote sensing has shown potential for the detection of plant diseases, but its utility for phenotyping
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