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31697

Supelco

Azoxystrobin

PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C22H17N3O5
CAS Number:
131860-33-8
Molecular Weight:
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

Signal Word

Danger

Hazard Statements

H331,H410

Hazard Classifications

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

Storage Class Code

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

WGK

WGK 2

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
BCCF6593
BCBT1118V
SZBF054XV
SZBB130XV
SZB8163XV

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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
Yingnan Han et al.
Ecotoxicology and environmental safety, 107, 214-219 (2014-07-11)
Azoxystrobin has been widely used in recent years. The present study investigated the oxidative stress and DNA damage effects of azoxystrobin on earthworms (Eisenia fetida). Earthworms were exposed to different azoxystrobin concentrations in an artificial soil (0, 0.1, 1, and
Yongkang Liu et al.
Applied microbiology and biotechnology, 102(2), 539-551 (2017-11-28)
Camelid single-domain antibodies (sdAbs, VHHs, or Nanobodies®) are types of antibody fragments that are composed of the heavy-chain variable domain only. These VHHs possess unique structural and functional features, as they are small in size and exhibit thermal stability and
Zhiwen Wang et al.
Pesticide biochemistry and physiology, 147, 83-89 (2018-06-24)
SYP-14288 is a novel fungicide developed by the Shenyang Research Institute of Chemical Industry in China. Although preliminary studies indicate that SYP-14288 is highly effective against 32 important plant pathogens belonging to a range of taxonomic groups, its mode of
Fangjie Cao et al.
Environmental pollution (Barking, Essex : 1987), 219, 1109-1121 (2016-09-13)
In the past few decades, extensive application of azoxystrobin has led to great concern regarding its adverse effects on aquatic organisms. The objective of the present study was to evaluate the reproductive toxicity of azoxystrobin to zebrafish. After adult zebrafish
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