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Supelco

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
Beilstein:
7813601
MDL number:
MFCD01632330
UNSPSC Code:
41116107
PubChem Substance ID:
329754975
NACRES:
NA.24

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

SMILES string

Cc1cc(nc(Nc2ccccc2)n1)C3CC3

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)

InChI key

HAORKNGNJCEJBX-UHFFFAOYSA-N

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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

Signal Word

Warning

Hazard Statements

H317,H410

Hazard Classifications

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

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCD6496
BCCD3560
BCBW7596
SZBE092XV
SZBB103XV

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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
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
Francesc A Esteve-Turrillas et al.
Journal of agricultural and food chemistry, 60(19), 4803-4811 (2012-04-17)
Cyprodinil is an anilinopyrimidine fungicide applied worldwide for the prevention and treatment of highly destructive plant diseases in a large variety of crops, including cereals, fruits, and vegetables. This paper describes the development of the first reported immunoassays for cyprodinil.
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