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46068

Supelco

Cyproconazol

PESTANAL®, analytical standard

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About This Item

Empirische Formel (Hill-System):
C15H18ClN3O
CAS-Nummer:
94361-06-5
Molekulargewicht:
291.78
Beilstein:
8396421
MDL-Nummer:
MFCD01678672
UNSPSC-Code:
41116107
PubChem Substanz-ID:
329756594
NACRES:
NA.24

Qualität

analytical standard

Qualitätsniveau

100

Beschreibung

mixture of diastereomers

Produktlinie

PESTANAL®

Haltbarkeit

limited shelf life, expiry date on the label

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

Anwendung(en)

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

InChIKey

UFNOUKDBUJZYDE-UHFFFAOYSA-N

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Allgemeine Beschreibung

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

Anwendung

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.

Rechtliche Hinweise

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

Signalwort

Danger

Gefahreneinstufungen

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

Zielorgane

Liver

Lagerklassenschlüssel

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

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

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

Choose from one of the most recent versions:

Analysenzertifikate (COA)

Lot/Batch Number
BCCD4066
BCBT9296
SZBC170XV
SZBC048XV
SZB7283XV

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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
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
Fangjie Cao et al.
Environmental science and pollution research international, 26(5), 4913-4923 (2018-12-21)
Cyproconazole is a triazole fungicide used to protect a diverse range of fruits, vegetables, and grain crops. As such, it has the potential to enter aquatic environments and affect non-target organisms. The objective of this study was to assess the
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)
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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