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Cyproconazol

PESTANAL®, analytical standard

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About This Item

Formule empirique (notation de Hill):
C15H18ClN3O
Numéro CAS:
94361-06-5
Poids moléculaire :
291.78
Numéro Beilstein :
8396421
Numéro MDL:
MFCD01678672
Code UNSPSC :
41116107
ID de substance PubChem :
329756594
Nomenclature NACRES :
NA.24

Qualité

analytical standard

Niveau de qualité

100

Description

mixture of diastereomers

Gamme de produits

PESTANAL®

Durée de conservation

limited shelf life, expiry date on the label

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Application(s)

agriculture
environmental

Format

neat

Chaîne SMILES 

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

Clé InChI

UFNOUKDBUJZYDE-UHFFFAOYSA-N

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Catégories apparentées

Description générale

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.

Informations légales

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

Pictogrammes

Skull and crossbonesHealth hazardEnvironment
GHS06,GHS08,GHS09

Mention d'avertissement

Danger

Mentions de danger

H301,H360D,H373,H410

Classification des risques

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

Organes cibles

Liver

Code de la classe de stockage

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

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

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

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Certificats d'analyse (COA)

Lot/Batch Number
BCCD4066
BCBT9296
SZBC170XV
SZBC048XV
SZB7283XV

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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
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)
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
Multiresidue determination of 19 fungicides in processed fruits and vegetables by capillary gas chromatography after gel permeation chromatography
Sannino A, et al.
Journal of AOAC (Association of Official Analytical Chemists) International, 82, 1229-1238 (1999)
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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