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Merck

34364

Norflurazon

PESTANAL®, analytical standard

Synonym(s):

4-Chloro-5-(methylamino)-2-(α,α,α-trifluoro-m-tolyl)-3(2H)-pyridazinone

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About This Item

Empirical Formula (Hill Notation):
C12H9ClF3N3O
CAS Number:
27314-13-2
Molecular Weight:
303.67
NACRES:
NA.24
PubChem Substance ID:
329754964
UNSPSC Code:
41116107
EC Number:
248-397-1
MDL number:
MFCD00128055

Key Documents

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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

CNC1=C(Cl)C(=O)N(N=C1)c2cccc(c2)C(F)(F)F

InChI

1S/C12H9ClF3N3O/c1-17-9-6-18-19(11(20)10(9)13)8-4-2-3-7(5-8)12(14,15)16/h2-6,17H,1H3

InChI key

NVGOPFQZYCNLDU-UHFFFAOYSA-N

Related Categories

General description

Norflurazon is a weed controlling agent which acts by inhibiting carotenoid biosynthesis.

Application

Norflurazon may be used as an analytical reference standard for the determination of the analyte in plant tissue, food stuffs and ground water samples by various chromatography techniques.
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

signalword

Warning

hcodes

H400

Hazard Classifications

Aquatic Acute 1

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCN9191
BCCG7106
BCCC2415
BCBT4076

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1O2-mediated and EXECUTER-dependent retrograde plastid-to-nucleus signaling in norflurazon-treated seedlings of Arabidopsis thaliana.
Kim C and Apel K
Molecular plant, 6(5), 1580-1591 (2013)
Determination of National Survey of Pesticides analytes in groundwater by liquid chromatography with postcolumn reaction detection.
Miles CJ
Journal of Chromatography A, 592(1-2), 283-290 (1992)
Megan E Andriankaja et al.
Plant molecular biology, 85(3), 233-245 (2014-02-20)
The establishment of the photosynthetic apparatus during chloroplast development creates a high demand for iron as a redox metal. However, iron in too high quantities becomes toxic to the plant, thus plants have evolved a complex network of iron uptake
Determination of pesticide residues in foods by fluorine-19 Fourier transform nuclear magnetic resonance spectrscopy.
Mazzola EP, et al.
Journal of Agricultural and Food Chemistry, 32(5) (1984)
Holger Nestler et al.
Journal of proteomics, 75(17), 5370-5385 (2012-07-04)
Exposure to a toxicant causes proteome alterations in an organism. In ecotoxicology, analysis of these changes may allow linking them to physiological and biochemical endpoints, providing insights into subcellular exposure effects and responses and, ultimately mechanisms of action. Based on
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