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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:
1582-09-8
Molecular Weight:
335.28
Beilstein:
1893555
EC Number:
216-428-8
MDL number:
MFCD00055241
UNSPSC Code:
41116107
PubChem Substance ID:
329753721
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

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

Signal Word

Warning

Hazard Statements

H302,H317,H351,H410

Hazard Classifications

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

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

212.0 °F - closed cup

Flash Point(C)

100.00 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCCM4245
BCCH1781
BCBV7369
SZBD106XV
SZB8210XV

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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)
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)
V K Shormanov et al.
Sudebno-meditsinskaia ekspertiza, 53(5), 31-33 (2011-01-27)
Results of extraction of trifluralin from an aqueous acetonitrile solution using various organic solvents are presented. The degree of extraction was shown to depend on the nature of extractant and the water/acetonitrile ratio. An optimal electrolyte and the degree of
Perihan Binnur Kurt-Karakus et al.
Environmental toxicology and chemistry, 30(7), 1539-1548 (2011-04-08)
Concentrations of current-use pesticides (CUPs) in water, zooplankton, precipitation, and air samples as well as stereoisomer fractions (SF; herbicidally active/total stereoisomers) of metolachlor were determined in water samples collected from 10 remote inland lakes in Ontario, Canada, between 2003 and
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