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Merck
CN

32061

Trifluralin

PESTANAL®, analytical standard

Synonym(s):

2,6-Dinitro-N,N-dipropyl-4-trifluoromethylaniline

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About This Item

Empirical Formula (Hill Notation):
C13H16F3N3O4
CAS Number:
1582-09-8
Molecular Weight:
335.28
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329753721
EC Number:
216-428-8
Beilstein/REAXYS Number:
1893555
MDL number:
MFCD00055241

Key Documents

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Product Name

Trifluralin, PESTANAL®, analytical standard

InChI key

ZSDSQXJSNMTJDA-UHFFFAOYSA-N

InChI

1S/C13H16F3N3O4/c1-3-5-17(6-4-2)12-10(18(20)21)7-9(13(14,15)16)8-11(12)19(22)23/h7-8H,3-6H2,1-2H3

SMILES string

CCCN(CCC)c1c(cc(cc1[N+]([O-])=O)C(F)(F)F)[N+]([O-])=O

grade

analytical standard

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

Quality Level

100

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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.
Trifluralin may have been used as standard in mass spectrometry employing negative chemical
ionization (GC-MS-NCI) technique for qualitative and quantitative analysis of trifluralin from soil extract samples.

General description

Trifluralin is a dinitroaniline herbicide used mostly as antiparasitic agent. It is used in controlling weeds and is characterized as microtubule-depolymerizing chemical.

Legal Information

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

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Warning

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2 - Skin Sens. 1

Storage Class

11 - Combustible Solids

wgk

WGK 2

flash_point_f

212.0 °F - closed cup

flash_point_c

100.00 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

Regulatory Information

农药列管产品
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Certificates of Analysis (COA)

Lot/Batch Number
BCCM9416
BCCM4245
BCCH1781
BCBV7369

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Mechanism of micronuclei formation in polyploidizated cells of Allium cepa exposed to trifluralin herbicide.
Fernandes, Thais CC, Dania Elisa C. Mazzeo, and Maria A. Marin-Morales.
Pesticide Biochemistry and Physiology, 88.3, 252-259 (2007)
Inhibition of leishmanias but not host macrophages by the antitubulin herbicide trifluralin.
Chan, Marion Man-Ying, and Dunne Fong.
Science, 249.4971, 924-924 (1990)
Quantitative confirmation of ethalfluralin and trifluralin in soil extracts by negative chemical ionization mass spectrometry.
Moyer, James R., and James L. Elder.
Journal of Agricultural and Food Chemistry, 32.4, 866-868 (1984)
Subir K Nag et al.
Chemosphere, 84(11), 1572-1577 (2011-06-24)
We evaluated wheat straw biochar produced at 450°C for its ability to influence bioavailability and persistence of two commonly used herbicides (atrazine and trifluralin) with different modes of action (photosynthesis versus root tip mitosis inhibitors) in two contrasting soils. The
Sedat Bozari et al.
Drug and chemical toxicology, 36(2), 163-169 (2012-03-15)
Trifluralin is a widely used dinitroaniline herbicide throughout the world. However, limited efforts have been made to study its genotoxic effects on different plants. The present study aimed to evaluate the herbicide's genotoxic potential on maize (Zea mays) by using
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