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Supelco

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
Beilstein:
8396421
MDL number:
MFCD01678672
UNSPSC Code:
41116107
PubChem Substance ID:
329756594
NACRES:
NA.24

grade

analytical standard

Quality Level

100

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

SMILES string

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

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

InChI key

UFNOUKDBUJZYDE-UHFFFAOYSA-N

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General description

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

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.

Legal Information

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

Signal Word

Danger

Hazard Statements

H301,H360D,H373,H410

Hazard Classifications

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

Target Organs

Liver

Storage Class Code

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

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCD4066
BCBT9296
SZBC170XV
SZBC048XV
SZB7283XV

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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
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
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
Wan Aini Wan Ibrahim et al.
Electrophoresis, 30(11), 1976-1982 (2009-06-12)
An efficient method for the simultaneous enantioseparation of cyproconazole, bromuconazole, and diniconazole enantiomers was developed by CD-modified MEKC using a dual mixture of neutral CDs as chiral selector. Three neutral CDs namely hydroxypropyl-beta-CD, hydroxypropyl-gamma-CD, and gamma-CD were tested as chiral
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