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34348

Supelco

Hexaconazol

PESTANAL®, analytical standard

Sinonimo/i:

(±)-2-(2,4-Dichlorophenyl)-1-(1H-1,2,4-triazol-1-yl)-2-hexanol

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About This Item

Formula empirica (notazione di Hill):
C14H17Cl2N3O
Numero CAS:
79983-71-4
Peso molecolare:
314.21
Beilstein:
8328399
Numero CE:
413-050-7
Numero MDL:
MFCD00144441
Codice UNSPSC:
41116107
ID PubChem:
329754959
NACRES:
NA.24

Grado

analytical standard

Livello qualitativo

100

Nome Commerciale

PESTANAL®

Durata

limited shelf life, expiry date on the label

tecniche

HPLC: suitable
gas chromatography (GC): suitable

applicazioni

agriculture
environmental

Formato

neat

Stringa SMILE

CCCCC(O)(Cn1cncn1)c2ccc(Cl)cc2Cl

InChI

1S/C14H17Cl2N3O/c1-2-3-6-14(20,8-19-10-17-9-18-19)12-5-4-11(15)7-13(12)16/h4-5,7,9-10,20H,2-3,6,8H2,1H3
STMIIPIFODONDC-UHFFFAOYSA-N

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Descrizione generale

Hexaconazol is a triazole systemic fungicide effective against Ascomycetes and Basidiomycetes.

Applicazioni

Hexaconazol may be used as an analytical reference standard for the determination of the analyte in honey, surface water samples, black tea, and fruits/vegetables by various chromatography techniques.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Note legali

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

Pittogrammi

Exclamation markEnvironment
GHS07,GHS09

Avvertenze

Warning

Indicazioni di pericolo

H302,H317,H411

Classi di pericolo

Acute Tox. 4 Oral - Aquatic Chronic 2 - Skin Sens. 1

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

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Certificati d'analisi (COA)

Lot/Batch Number
BCBV8439

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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(2), 1229-1238 (1999)
Thermodynamic properties of diniconazole and hexaconazole.
Yan B, et al.
The Journal of Chemical Thermodynamics, 99, 82-85 (2016)
Xinquan Wang et al.
Journal of agricultural and food chemistry, 60(9), 2212-2218 (2012-02-09)
In this study, the enantioselective dissipation behavior of hexaconazole was investigated in cucumber fruit, head cabbage, and two different types of agricultural soils. The dissipation kinetics was determined by reverse-phase liquid chromatography-tandem mass spectrometry on a cellulose tris (3-chloro-4-methylphenylcarbamate) chiral
S Yilmaz et al.
Genetika, 44(3), 323-328 (2008-07-31)
The genotoxic effects of fungicide Conan 5FL (containing 50 g/L hexaconazole) in mouse bone-marrow cells and human lymphocytes have been evaluated. Three different concentrations of Conan 5FL (17.50, 35.00 and 70.00 microg/mL for human lymphocytes and 17.50, 35.00 and 70.00
Halimah Muhamad et al.
Drug testing and analysis, 4 Suppl 1, 112-117 (2012-08-08)
In oil palm plantations, the fungicide hexaconazole is used to control Ganoderma infection that threatens to destroy or compromisethe palm. The application of hexaconazole is usually through soil drenching, trunk injection, or a combination of these two methods. It is
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