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Merck

34389

Cyprodinil

PESTANAL®, analytical standard

Synonym(s):

4-Cyclopropyl-6-methyl-N-phenylpyrimidin-2-amine

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About This Item

Empirical Formula (Hill Notation):
C14H15N3
CAS Number:
121552-61-2
Molecular Weight:
225.29
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329754975
MDL number:
MFCD01632330
Beilstein/REAXYS Number:
7813601

Product Name

Cyprodinil, PESTANAL®, analytical standard

InChI

1S/C14H15N3/c1-10-9-13(11-7-8-11)17-14(15-10)16-12-5-3-2-4-6-12/h2-6,9,11H,7-8H2,1H3,(H,15,16,17)

SMILES string

Cc1cc(nc(Nc2ccccc2)n1)C3CC3

InChI key

HAORKNGNJCEJBX-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

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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.

Legal Information

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

pictograms

Exclamation markEnvironment
GHS07,GHS09

signalword

Warning

hcodes

H317,H410

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Skin Sens. 1

Storage Class

11 - Combustible Solids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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

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Certificates of Analysis (COA)

Lot/Batch Number
BCCN3445
BCCM5346
BCCD6496
BCCD3560
BCBW7596

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Coraline Mattei et al.
Chemosphere, 228, 75-82 (2019-04-26)
A fraction of the atmospheric pesticides can be adsorbed on particles surface according to their physicochemical properties. After adsorption, pesticides can undergo heterogeneous reactivity with atmospheric oxidants such as ozone, but the influence of the pesticide surface coating (i.e., the
G A Bardas et al.
Phytopathology, 98(4), 443-450 (2008-10-24)
The fitness of anilinopyrimidine-resistant isolates of Botrytis cinerea compared with that of sensitive isolates, collected from vegetable crops in Greece during 2005, was investigated. Stability of resistance to anilinopyrimidine fungicides was determined after consecutive transfers of the fungal isolates on
Arnaud Auber et al.
Ecotoxicology (London, England), 20(8), 2042-2055 (2011-07-28)
The impacts of current and alternative wheat crop protection programs were compared in outdoor pond mesocosms in a 10-month long study. Realistic exposure scenarios were built based upon the results of modelling of drift, drainage and runoff of pesticides successively
H Basa Cesnik et al.
Food additives & contaminants. Part A, Chemistry, analysis, control, exposure & risk assessment, 25(4), 438-443 (2008-03-19)
Although the list of pesticides used in integrated pest management (IPM) in grape growing and their annual application rates are limited, we are still confronted with the problem of pesticide residues in grapes. This paper presents the results of pesticide
Gustavo Cordero-Bueso et al.
Frontiers in microbiology, 8, 2025-2025 (2017-11-23)
The increasing level of hazardous residues in the environment and food chains has led the European Union to restrict the use of chemical fungicides. Thus, exploiting new natural antagonistic microorganisms against fungal diseases could serve the agricultural production to reduce
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