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Supelco

Trifluralin

PESTANAL®, analytical standard

Sinonimo/i:

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

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About This Item

Formula empirica (notazione di Hill):
C13H16F3N3O4
Numero CAS:
1582-09-8
Peso molecolare:
335.28
Beilstein:
1893555
Numero CE:
216-428-8
Numero MDL:
MFCD00055241
Codice UNSPSC:
41116107
ID PubChem:
329753721
NACRES:
NA.24

Grado

analytical standard

Livello qualitativo

100

Nome Commerciale

PESTANAL®

Durata

limited shelf life, expiry date on the label

tecniche

HPLC: suitable
gas chromatography (GC): suitable

applicazioni

agriculture
environmental

Formato

neat

Stringa SMILE

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
ZSDSQXJSNMTJDA-UHFFFAOYSA-N

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Categorie correlate

Descrizione generale

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

Applicazioni

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.

Note legali

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

Avvertenze

Warning

Indicazioni di pericolo

H302,H317,H351,H410

Classi di pericolo

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

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

212.0 °F - closed cup

Punto d’infiammabilità (°C)

100.00 °C - closed cup

Dispositivi di protezione individuale

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

Choose from one of the most recent versions:

Certificati d'analisi (COA)

Lot/Batch Number
BCCH1781
BCBV7369
SZBD106XV
SZB8210XV
SZE8210X

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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)
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)
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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