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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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Teruhisa Miyauchi et al.
Journal of chromatography. A, 1063(1-2), 137-141 (2005-02-11)
Solid-phase extraction (SPE) procedures were developed to avoid interference during the quantitative determination of cyproconazole and tebuconazole co-existing in wood extractives. Five species of wood were used, Japanese cedar (Cryptomeria japonica), Japanese larch (Larix leptolepis), Yezo spruce (Picea jezoensis), Sakhalin
Ramin Roohparvar et al.
Applied and environmental microbiology, 73(15), 5011-5019 (2007-06-05)
Medical drugs known to modulate the activity of human ATP-binding cassette (ABC) transporter proteins (modulators) were tested for the ability to potentiate the activity of the azole fungicide cyproconazole against in vitro growth of Mycosphaerella graminicola and to control disease
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
Lute-Harm Zwiers et al.
Antimicrobial agents and chemotherapy, 46(12), 3900-3906 (2002-11-19)
Laboratory strains of Mycosphaerella graminicola with decreased susceptibilities to the azole antifungal agent cyproconazole showed a multidrug resistance phenotype by exhibiting cross-resistance to an unrelated chemical, cycloheximide or rhodamine 6G, or both. Decreased azole susceptibility was found to be associated
J Zhan et al.
International journal for parasitology, 37(8-9), 861-870 (2007-04-25)
Most eukaryotes use sexual reproduction to transmit genetic information from generation to generation despite the advantages offered by asexual reproduction. One theory to explain the origin and maintenance of sexual reproduction hypothesises that sexual recombination generates genetic variation that allows
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