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Merck
CN

46068

Cyproconazol

PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C15H18ClN3O
CAS Number:
94361-06-5
Molecular Weight:
291.78
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329756594
MDL number:
MFCD01678672
Beilstein/REAXYS Number:
8396421

Key Documents

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Product Name

Cyproconazol, PESTANAL®, analytical standard

InChI

1S/C15H18ClN3O/c1-11(12-2-3-12)15(20,8-19-10-17-9-18-19)13-4-6-14(16)7-5-13/h4-7,9-12,20H,2-3,8H2,1H3

SMILES string

CC(C1CC1)C(O)(Cn2cncn2)c3ccc(Cl)cc3

InChI key

UFNOUKDBUJZYDE-UHFFFAOYSA-N

grade

analytical standard

description

mixture of diastereomers

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

100

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Application

Cyproconazol may be used as an analytical reference standard for the quantification of the analyte in processed fruits and vegetables using capillary gas chromatography after gel permeation chromatography.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

General description

Cyproconazol is an azole compound fungicide, commonly used as a wood preservative and as a biocide for protecting fruits and vegetable crops.

Legal Information

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

signalword

Danger

Hazard Classifications

Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Repr. 1B - STOT RE 2

target_organs

Liver

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type P3 (EN 143) respirator cartridges

Regulatory Information

农药列管产品
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Certificates of Analysis (COA)

Lot/Batch Number
BCCN8088
BCCM9934
BCCM8883
BCCD4066
BCBT9296

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Paul M White et al.
The Science of the total environment, 408(6), 1393-1402 (2009-12-18)
Pesticides are typically applied as mixtures and or sequentially to soil and plants during crop production. A common scenario is herbicide application at planting followed by sequential fungicide applications post-emergence. Fungicides depending on their spectrum of activity may alter and
Ioannis Stergiopoulos et al.
Pest management science, 59(12), 1333-1343 (2003-12-12)
Molecular mechanisms that account for variation in base-line sensitivity to azole fungicides were examined in a collection of twenty field isolates, collected in France and Germany, of the wheat pathogen Mycosphaerella graminicola (Fuckel) Schroeter. The isolates tested represent the wide
Developmental toxicity of cyproconazole, an inhibitor of fungal ergosterol biosynthesis, in the rat.
K Machera
Bulletin of environmental contamination and toxicology, 54(3), 363-369 (1995-03-01)
Richard C Peffer et al.
Toxicological sciences : an official journal of the Society of Toxicology, 99(1), 315-325 (2007-06-15)
Cyproconazole, a triazole fungicide, causes hepatocellular adenomas and carcinomas in CD-1 mice at dose levels of 100 and 200 ppm. The constitutive androstane receptor (CAR) has been shown to play a significant role in the overall mode of action for
Jane Muncke et al.
Environmental toxicology, 22(2), 185-193 (2007-03-17)
The MolDarT is a novel short-term assay for testing mechanism-based molecular effects in developing zebrafish embryos. The objective of this study was to evaluate the inducibility of vitellogenin1 mRNA (Vtg1) by the estrogenically active compounds 17beta-Estradiol (E2), 17alpha-Ethinylestradiol (EE2), Nonylphenol
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