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32061

Supelco

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:
Molecular Weight:
335.28
Beilstein/REAXYS Number:
1893555
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

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

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

InChI key

ZSDSQXJSNMTJDA-UHFFFAOYSA-N

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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.

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.

Legal Information

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

signalword

Warning

Hazard Classifications

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

Storage Class

11 - Combustible Solids

wgk_germany

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


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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)
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)
I V Tanasienko et al.
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Method of biolistic transformation was used for genetic improvement of commercial barley cultivars (Oksamitoviy, Vodogray and Getman). The plasmid pHLFTuBA was used for particle bombardment that consists of the hLF gene under the control of the barley glutelin B-1 promoter
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Rising pesticide levels in streams draining intensively managed agricultural land have a detrimental effect on aquatic ecosystems and render water unfit for human consumption. The Soil and Water Assessment Tool (SWAT) was applied to simulate daily pesticide transfer at the

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