32805
双炔酰菌胺
PESTANAL®, analytical standard
别名:
2-(4-氯苯基)-N-[3-甲氧基-4-(2-丙炔基氧代)苯乙基]-2-(2-丙炔基氧代)乙酰胺
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关于此项目
经验公式（希尔记法）:
C23H22ClNO4
化学文摘社编号:
分子量:
411.88
UNSPSC Code:
41116107
NACRES:
NA.24
MDL number:
产品名称
双炔酰菌胺, PESTANAL®, analytical standard
InChI
1S/C23H22ClNO4/c1-4-14-28-20-11-6-17(16-21(20)27-3)12-13-25-23(26)22(29-15-5-2)18-7-9-19(24)10-8-18/h1-2,6-11,16,22H,12-15H2,3H3,(H,25,26)
SMILES string
ClC1=CC=C(C(OCC#C)C(NCCC2=CC=C(OCC#C)C(OC)=C2)=O)C=C1
InChI key
KWLVWJPJKJMCSH-UHFFFAOYSA-N
grade
analytical standard
product line
PESTANAL®
shelf life
limited shelf life, expiry date on the label
technique(s)
HPLC: suitable
gas chromatography (GC): suitable
application(s)
agriculture
environmental
format
neat
Quality Level
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Application
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
General description
Mandipropamid is a carboxylic acid amide, which belongs to the oomycete class of fungicides. It is found to be effective in controlling phytopathogens such as Plasmopara viticola on grapes and potato late blight caused by Phytophthora infestans.
Legal Information
PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
signalword
Warning
hcodes
pcodes
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
法规信息
农药列管产品
此项目有
Guofeng Xu et al.
Environmental science and pollution research international, 27(32), 40148-40155 (2020-07-15)
Enantioselective monitoring of chiral fungicide mandipropamid enantiomers were carried out in grapes and wine-making process. The enantiomers of mandipropamid were separated on a Lux Cellulose-2 column and determined by ultra-high-performance liquid chromatography coupled with tandem mass spectrometry (UHPLC-MS/MS). The processing
Mandipropamid targets the cellulose synthase?like PiCesA3 to inhibit cell wall biosynthesis in the oomycete plant pathogen, Phytophthora infestans.
Blum M, et al.
Molecular Plant Pathology, 11(2), 227-243 (2010)
Multicomponent reactions in fungicide research: The discovery of mandipropamid.
Lamberth C, et al.
Bioorganic & Medicinal Chemistry, 16(3), 1531-1545 (2008)
Vasileios Vangalis et al.
Journal of fungi (Basel, Switzerland), 6(4) (2020-12-11)
Woronin bodies are membrane-bound organelles of filamentous ascomycetes that mediate hyphal compartmentalization by plugging septal pores upon hyphal damage. Their major component is the peroxisomal protein Hex1, which has also been implicated in additional cellular processes in fungi. Here, we
Nikhilesh Dhar et al.
Plant disease, 104(1), 82-93 (2019-11-19)
The lettuce downy mildew pathogen, Bremia lactucae, is an obligate oomycete that causes extensive produce losses. Initial chlorotic symptoms that severely reduce the market value of the produce are followed by the appearance of white, downy sporulation on the abaxial
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