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Supelco

Oxyfluorfen

PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C15H11ClF3NO4
CAS Number:
42874-03-3
Molecular Weight:
361.70
Beilstein:
2065259
EC Number:
255-983-0
MDL number:
MFCD00072435
UNSPSC Code:
41116107
PubChem Substance ID:
329755114
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

CCOc1cc(Oc2ccc(cc2Cl)C(F)(F)F)ccc1[N+]([O-])=O

InChI

1S/C15H11ClF3NO4/c1-2-23-14-8-10(4-5-12(14)20(21)22)24-13-6-3-9(7-11(13)16)15(17,18)19/h3-8H,2H2,1H3

InChI key

OQMBBFQZGJFLBU-UHFFFAOYSA-N

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General description

Oxyfluorfen is a diphenyl-ether herbicide, which can be commonly used in vineyards for weed control management. It can block the chlorophyll biosynthesis in plants by inhibiting protoporphyrinogen oxidase enzyme

Application

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

Environment
GHS09

Signal Word

Warning

Hazard Statements

H410

Precautionary Statements

P273 - P391 - P501

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
BCCH2937
BCBW2993
SZBD037XV
SZBB014XV
SZB7017XV

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Photochemical behaviour of oxyfluorfen: a diphenyl-ether herbicide
Scrano L, et al.
Journal of Photochemistry and Photobiology A: Chemistry, 129, 65-70 (1999)
Effect of oxyfluorfen and diuron alone and in mixture on antioxidative enzymes of Scenedesmus obliquus
Geoffroy L, et al.
Pesticide Biochemistry and Physiology, 72, 178-185 (2002)
Young Soo Keum et al.
Journal of agricultural and food chemistry, 56(19), 9146-9151 (2008-09-10)
Nitrodiphenyl ether herbicides, including chlomethoxyfen, nitrofen, and oxyfluorfen are potent herbicides. Some metabolites and parent compounds are considered as possible mutagens and endocrine disruptors. Both properties pose serious hygienic and environmental risks. Sphingomonas wittichii RW1 is a well-known degrader of
H J Lee et al.
Plant & cell physiology, 41(6), 743-749 (2000-08-17)
Protoporphyrinogen oxidase (Protox), the penultimate step enzyme of the branch point for the biosynthetic pathway of Chl and hemes, is the target site of action of diphenyl ether (DPE) herbicides. However, Bacillus subtilis Protox is known to be resistant to
Chloé Bonnineau et al.
Ecotoxicology (London, England), 21(4), 1208-1224 (2012-03-13)
In multiple stress situations, the co-occurrence of environmental and chemical factors can influence organisms' ability to cope with toxicity. In this context, the influence of light adaptation on the response of freshwater biofilms to sudden light changes or to herbicides
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