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32805

Mandipropamid

PESTANAL®, analytical standard

Synonym(s):

2-(4-Chlorophenyl)-N-[3-methoxy-4-(2-propynyloxy)phenethyl]-2-(2-propynyloxy)acetamide

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About This Item

Empirical Formula (Hill Notation):
C23H22ClNO4
CAS Number:
374726-62-2
Molecular Weight:
411.88
UNSPSC Code:
41116107
NACRES:
NA.24
MDL number:
MFCD09751510
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grade

analytical standard

Quality Segment

100

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

SMILES string

ClC1=CC=C(C(OCC#C)C(NCCC2=CC=C(OCC#C)C(OC)=C2)=O)C=C1

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)

InChI key

KWLVWJPJKJMCSH-UHFFFAOYSA-N

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.

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Legal Information

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

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pictograms

Environment
GHS09

signalword

Warning

hcodes

H410

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Information

农药列管产品

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Certificates of Analysis (COA)

Lot/Batch Number
BCCN9580
BCCF9297
BCBW8925
BCBT4049

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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)
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
Multicomponent reactions in fungicide research: The discovery of mandipropamid.
Lamberth C, et al.
Bioorganic & Medicinal Chemistry, 16(3), 1531-1545 (2008)
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Global Trade Item Number

SKUGTIN
32805-100MG04061826717165