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34045

Supelco

Azaconazole

PESTANAL®, analytical standard

Synonym(s):

1-[2-(2,4-Dichlorophenyl)-1,3-dioxolan-2-ylmethyl]-1H-1,2,4-triazole

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About This Item

Empirical Formula (Hill Notation):
C12H11Cl2N3O2
CAS Number:
60207-31-0
Molecular Weight:
300.14
EC Number:
262-102-3
MDL number:
MFCD00865600
UNSPSC Code:
41116107
PubChem Substance ID:
329754779
NACRES:
NA.24

grade

analytical standard

Quality Level

100

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

Clc1ccc(c(Cl)c1)C3(Cn2cncn2)OCCO3

InChI

1S/C12H11Cl2N3O2/c13-9-1-2-10(11(14)5-9)12(18-3-4-19-12)6-17-8-15-7-16-17/h1-2,5,7-8H,3-4,6H2

InChI key

AKNQMEBLVAMSNZ-UHFFFAOYSA-N

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General description

Azaconazole has been used as an internal standard in the determination of propiconazole, a fungistatic agent in white spruce, using gas chromatography/mass spectrometry (GC/MS).

Application

Azaconazole, is an agricultural fungicide, which shows activity against wood destroying fungi and sapstain fungi. It can also play the role of a disinfectant in mushroom cultivation and in the storage of fruits and vegetables.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

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Legal Information

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

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302

Precautionary Statements

P264 - P270 - P301 + P312 - P501

Hazard Classifications

Acute Tox. 4 Oral

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

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
BCCK2245
BCCJ3750
BCBX0196
SZBD156XV
SZBA125XV

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G O Rankin et al.
Toxicology, 34(1), 1-11 (1985-01-01)
Azaconazole is an experimental agricultural fungicide which has shown promise for use in controlling powdery mildew on crops and bean rust. This study examined the nephrotoxic potential of a single intraperitoneal azaconazole injection (0.4 or 0.6 mmol/kg) or daily azaconazole
Interaction of azole derivatives with cytochrome P-450 isozymes in yeast, fungi, plants and mammalian cells.
Bossche VH, et al.
Pest Management Science, 21.4, 289-306 (1987)
Raman microscopy for the quantitation of propiconazole in white spruce
Kurti E, et al.
Wood Science and Technology, 39.8, 618-629 (2005)
Roberts RT and Hutson HD
Metabolic Pathways of Agrochemicals: Herbicides and plant growth regulators; (1998)
Bryce E Mansfield et al.
PLoS pathogens, 6(9), e1001126-e1001126 (2010-10-14)
Despite the wealth of knowledge regarding the mechanisms of action and the mechanisms of resistance to azole antifungals, very little is known about how the azoles are imported into pathogenic fungal cells. Here the in-vitro accumulation and import of Fluconazole

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