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Supelco

Oxadiazon

PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C15H18Cl2N2O3
CAS Number:
Molecular Weight:
345.22
Beilstein:
558070
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

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

CC(C)Oc1cc(N2N=C(OC2=O)C(C)(C)C)c(Cl)cc1Cl

InChI

1S/C15H18Cl2N2O3/c1-8(2)21-12-7-11(9(16)6-10(12)17)19-14(20)22-13(18-19)15(3,4)5/h6-8H,1-5H3

InChI key

CHNUNORXWHYHNE-UHFFFAOYSA-N

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General description

Oxadiazon is a herbicide, which is used for weed control management of obnoxious grasses and broad leaved weeds in a variety of crop plantations.

Application

Oxadiazon may be used as a reference standard in the determination of oxadiazon in soil, water and urine samples using gas chromatography coupled with mass spectrometry (GC-MS).
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

Environment

Signal Word

Warning

Hazard Statements

Precautionary Statements

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1

Storage Class Code

11 - Combustible Solids

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

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Determination of tebufenpyrad and oxadiazon by solid-phase microextraction and gas chromatography-mass spectrometry.
Navalon A, et al.
Chromatographia, 54(5-6), 377-382 (2001)
Pesticide Chemistry (1989)
The degradation of oxadiazon and oxyfluorfen by photolysis.
Ying G-G and Williams B
Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes, 34(4), 549-567 (1999)
Yang Zuo et al.
Bioorganic & medicinal chemistry, 20(1), 296-304 (2011-12-02)
Protoporphyrinogen oxidase (Protox, EC 1.3.3.4) has attracted great interest during the last decades due to its unique biochemical characteristics and biomedical significance. As a continuation of our research work on the development of new PPO inhibitors, 23 new 1,3,4-thiadiazol-2(3H)-ones bearing
R Varsano et al.
FEBS letters, 272(1-2), 106-108 (1990-10-15)
The specific binding of the herbicide acifluorfen 5-[2-chloro-4-(trifluoromethyl)phenoxy]-2-nitrobenzoic acid to corn etioplast membranes is competitively inhibited by protoporphyrinogen IX, the substrate of protoporphyrinogen oxidase. Three other peroxidizing molecules, oxadiazon [5-terbutyl-3-(2,4-dichloro-5-isopropoxyphenyl)-1,3,4-oxadiazol -2-one], LS 82556 [(S)3-N-(methylbenzyl)carbamoyl-5-propionyl-2,6-lutidine], and M&B 39279 [5-amino-4-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)pyrazol], also compete

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