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![3,9-Bis(2,4-dicumylphenoxy)-2,4,8,10-tetraoxa-3,9-diphosphaspiro[5.5]undecane](/deepweb/assets/sigmaaldrich/product/structures/163/089/23367906-df78-4721-b2a6-690cd4c2a9a9/640/23367906-df78-4721-b2a6-690cd4c2a9a9.png)
グレード
analytical standard
品質水準
製品種目
PESTANAL®
シェルフライフ
limited shelf life, expiry date on the label
テクニック
HPLC: suitable
gas chromatography (GC): suitable
アプリケーション
agriculture
environmental
フォーマット
neat
SMILES記法
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)
InChI Key
LDLMOOXUCMHBMZ-UHFFFAOYSA-N
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詳細
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.
アプリケーション
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.
おすすめ製品
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.
法的情報
PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
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シグナルワード
Warning
危険有害性情報
危険有害性の分類
Aquatic Acute 1
保管分類コード
11 - Combustible Solids
WGK
WGK 2
引火点(°F)
Not applicable
引火点(℃)
Not applicable
適用法令
試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。
Jan Code
32581-VAR:
32581-100MG:
32581-BULK:
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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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