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Merck
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重要文件

32061

Supelco

氟乐灵

PESTANAL®, analytical standard

同義詞:

2,6-二硝基-N,N-二丙基-4-三氟甲基苯胺

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About This Item

經驗公式(希爾表示法):
C13H16F3N3O4
CAS號碼:
分子量::
335.28
Beilstein:
1893555
EC號碼:
MDL號碼:
分類程式碼代碼:
41116107
PubChem物質ID:
NACRES:
NA.24

等級

analytical standard

品質等級

產品線

PESTANAL®

儲存期限

limited shelf life, expiry date on the label

技術

HPLC: suitable
gas chromatography (GC): suitable

應用

agriculture
environmental

形式

neat

SMILES 字串

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 密鑰

ZSDSQXJSNMTJDA-UHFFFAOYSA-N

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一般說明

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

應用

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.

法律資訊

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

訊號詞

Warning

危險分類

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

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 2

閃點(°F)

212.0 °F - closed cup

閃點(°C)

100.00 °C - closed cup

個人防護裝備

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


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分析證明 (COA)

Lot/Batch Number

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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)
R A Cardoso et al.
Genetics and molecular research : GMR, 9(1), 231-238 (2010-03-04)
Some herbicides are suspected of promoting teratogenic, carcinogenic and mutagenic events. Detection of induced mitotic crossing-over has proven to be an indirect way of testing the carcinogenic properties of suspicious substances, because mitotic crossing-over is involved in the multistep process
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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