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Azoxystrobin

PESTANAL®, analytical standard

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About This Item

Fórmula empírica (notación de Hill):
C22H17N3O5
Número de CAS:
131860-33-8
Peso molecular:
403.39
Colour Index Number:
23860
MDL number:
MFCD08277047
UNSPSC Code:
41116107
PubChem Substance ID:
329753888
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

CO\C=C(\C(=O)OC)c1ccccc1Oc2cc(Oc3ccccc3C#N)ncn2

InChI

1S/C22H17N3O5/c1-27-13-17(22(26)28-2)16-8-4-6-10-19(16)30-21-11-20(24-14-25-21)29-18-9-5-3-7-15(18)12-23/h3-11,13-14H,1-2H3/b17-13+

InChI key

WFDXOXNFNRHQEC-GHRIWEEISA-N

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General description

Azoxystrobin belongs to strobilurin class of fungicides which is based on lead molecule strobilurin A. Its target site is mitochondrial respiration of fungi.

Application

Azoxystrobin has been used as reference for determination of azoxystrobin residue from different aquatic tox mediums using HPLC.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Legal Information

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

Pictograms

Skull and crossbonesEnvironment
GHS06,GHS09

signalword

Danger

hcodes

H331,H410

Hazard Classifications

Acute Tox. 3 Inhalation - Aquatic Acute 1 - Aquatic Chronic 1

Storage Class

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

wgk_germany

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges

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Certificados de análisis (COA)

Lot/Batch Number
BCCF6593
BCBT1118V
SZBF054XV
SZBB130XV
SZB8163XV

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Elsa Teresa Rodrigues et al.
Environment international, 53, 18-28 (2013-01-15)
The use of pesticides for crop protection may result in the presence of toxic residues in environmental matrices. In the aquatic environment, pesticides might freely dissolve in the water or bind to suspended matter and to the sediments, and might
Majid Ali Khan et al.
The Science of the total environment, 573, 1573-1579 (2016-09-20)
Studies with small soil columns (2cm i.d.×5.4cm depth) compared leaching of four pesticides added either as technical material or as commercial formulations. Pesticides were selected to give a gradient of solubility in water between 7 and 93mgL-1, comprising azoxystrobin (emulsifiable
Xin Guo et al.
Electrophoresis, 38(16), 2004-2010 (2017-05-13)
A nonaqueous micellar electrokinetic capillary chromatography method with indirect LIF was developed for the determination of strobilurin fungicide residues in fruits and vegetables. Hydrophobic CdTe quantum dots (QDs) synthesized in aqueous phase were used as background fluorescent substance. The BGE
Christopher C Howell et al.
Chemosphere, 112, 194-202 (2014-07-23)
The application of plant protection products has the potential to significantly affect soil microbial community structure and function. However, the extent to which soil microbial communities from different trophic levels exhibit resistance and resilience to such compounds remains poorly understood.
Xin-Yu Huo et al.
Molecules (Basel, Switzerland), 23(6) (2018-06-06)
The copper catalytic azide and terminal alkyne cycloaddition reaction, namely "click chemistry", gives a new and convenient way to create l,4-disubstitutd-l,2,3-triazoles. In this work, 2-pyrrolecarbaldiminato⁻Cu(II) complexes were established as efficient catalysts for the three-component 1,3-dipolar cycloaddition reaction of arylboronic acid
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