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Merck

34348

Supelco

Hexaconazol

PESTANAL®, analytical standard

Synonym(e):

(±)-2-(2,4-Dichlorphenyl)-1-(1H-1,2,4-triazol-1-yl)-hexan-2-ol

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About This Item

Empirische Formel (Hill-System):
C14H17Cl2N3O
CAS-Nummer:
Molekulargewicht:
314.21
Beilstein:
8328399
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
41116107
PubChem Substanz-ID:
NACRES:
NA.24

Qualität

analytical standard

Qualitätsniveau

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

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

InChIKey

STMIIPIFODONDC-UHFFFAOYSA-N

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Allgemeine Beschreibung

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

Anwendung

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.

Rechtliche Hinweise

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

Piktogramme

Exclamation markEnvironment

Signalwort

Warning

Gefahreneinstufungen

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

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 2

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

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


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Analysenzertifikate (COA)

Lot/Batch Number

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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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