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45506

Supelco

Fluorodifen

PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C13H7F3N2O5
CAS Number:
15457-05-3
Molecular Weight:
328.20
Beilstein:
2018474
EC Number:
239-474-0
MDL number:
MFCD00055532
UNSPSC Code:
41116107
PubChem Substance ID:
329756796
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

[O-][N+](=O)c1ccc(Oc2ccc(cc2[N+]([O-])=O)C(F)(F)F)cc1

InChI

1S/C13H7F3N2O5/c14-13(15,16)8-1-6-12(11(7-8)18(21)22)23-10-4-2-9(3-5-10)17(19)20/h1-7H

InChI key

HHMCAJWVGYGUEF-UHFFFAOYSA-N

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Application

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 markEnvironment
GHS07,GHS09

Signal Word

Warning

Hazard Statements

H319,H332,H400

Hazard Classifications

Acute Tox. 4 Inhalation - Aquatic Acute 1 - Eye Irrit. 2

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
BCCG4630
BCBT4616
SZBC061XV
SZB7166XV
SZE7166X

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Daniele Del Buono et al.
Journal of agricultural and food chemistry, 59(4), 1324-1329 (2011-02-04)
Many varieties of Italian ryegrass (Lolium multiflorum) show resistance to herbicides; while this ability was frequently attributed to alterations in the target sites of the herbicide's action of the plant or to an efficient oxidative metabolism, little attention has been
S Pflugmacher et al.
Phytochemistry, 54(3), 267-273 (2000-06-28)
Soluble and microsomal glutathione S-transferase activities for five model xenobiotics (nitrobenzene derivatives), two pesticidal xenobiotics (atrazine and fluorodifen), and a natural substrate (cinnamic acid), were determined in 59 different plant species and four plant cell suspension cultures. These enzyme activities
Daniele Del Buono et al.
Journal of agricultural and food chemistry, 59(22), 12109-12115 (2011-10-18)
A study was carried out to compare the effects of treating wheat (Triticum aestivum) and Italian ryegrass (Lolium multiflorum) with atrazine and fluorodifen. The herbicides interfered with photosynthesis and dark respiration, depending on the species. Atrazine decreased photosynthesis in both
Daniele Del Buono et al.
Journal of agricultural and food chemistry, 57(17), 7924-7930 (2009-08-08)
The effect of treatments with four herbicides and a safener on the activity of triosephosphate isomerase (TPI) extracted from shoots of Italian ryegrass was investigated. It was found that atrazine and fluorodifen, herbicides which interfere with photosynthesis, caused a decrease
David P Dixon et al.
The Journal of biological chemistry, 278(26), 23930-23935 (2003-04-15)
Plant Tau class glutathione transferases (GSTUs) detoxify diphenylether herbicides such as fluorodifen, determining their selectivity in crops and weeds. Using reconstructive PCR, a series of mutant GSTUs were generated from in vitro recombination and mutagenesis of the maize sequences ZmGSTU1
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