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Butralin

PESTANAL®, analytical standard

Synonyme(s) :

N-sec-Butyl-4-tert-butyl-2,6-dinitroaniline

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About This Item

Formule empirique (notation de Hill):
C14H21N3O4
Numéro CAS:
Poids moléculaire :
295.33
Numéro Beilstein :
2947948
Numéro CE :
Numéro MDL:
Code UNSPSC :
41116107
ID de substance PubChem :

Qualité

analytical standard

Niveau de qualité

Gamme de produits

PESTANAL®

Durée de conservation

limited shelf life, expiry date on the label

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Application(s)

agriculture
environmental

Format

neat

Chaîne SMILES 

CCC(C)Nc1c(cc(cc1[N+]([O-])=O)C(C)(C)C)[N+]([O-])=O

InChI

1S/C14H21N3O4/c1-6-9(2)15-13-11(16(18)19)7-10(14(3,4)5)8-12(13)17(20)21/h7-9,15H,6H2,1-5H3

Clé InChI

SPNQRCTZKIBOAX-UHFFFAOYSA-N

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Description générale

Butralin is a selective preemergence herbicide, which is widely used for the control of annual grasses and broadleaf weeds in fruit trees, vegetables, nuts and green crops.

Application

Butralin may be used as an analytical reference standard for the quantification of the analyte in tobacco and juice samplesusing various chromatographic techniques.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Informations légales

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

Pictogrammes

Health hazardExclamation markEnvironment

Mention d'avertissement

Warning

Mentions de danger

Classification des risques

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Repr. 2

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges


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Certificats d'analyse (COA)

Lot/Batch Number

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Consulter la Bibliothèque de documents

Multiresidue determination of pesticides in juice by solid-phase extraction and gas chromatography--mass spectrometry
Albero B, et al.
Talanta, 66(4), 917-924 (2005)
E Yamamoto et al.
The Plant cell, 10(2), 297-308 (1998-04-29)
Dinitroaniline herbicides are antimicrotubule drugs that bind to tubulins and inhibit polymerization. As a result of repeated application of dinitroaniline herbicides, highly resistant and intermediately resistant biotypes of goosegrass (Eleusine indica) developed in previously wild-type populations. Three alpha-tubulin cDNA classes
K C Wang et al.
Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica, 25(4), 210-213 (2003-01-07)
To select low-residue herbicide for cultivation of Bupleurum falcatum. Probing the effect of various kinds of herbicide on the budding, growth and yield of B. falcatum both in laboratory and in the fields. Haloxyfop acts slightly on the growth of
Hongxia Liu et al.
Journal of agricultural and food chemistry, 52(23), 6912-6915 (2004-11-13)
A simultaneous residue analysis of pendimethalin, isopropalin, and butralin in tobacco was developed with high-performance liquid chromatography with ultraviolet monitoring and electrospray ionization mass spectrometry (HPLC-UV-ESI/MS). The herbicide residues of pendimethalin, isopropalin, and butralin in tobaccos were extracted by ultrasonication
T R Edgerton et al.
Journal of analytical toxicology, 9(1), 15-19 (1985-01-01)
A method is presented for the analysis of trace amounts of dinitroaniline herbicides in tissue and excreta. The method employs extraction of the tissue or excreta with organic solvent, clean up by liquid/liquid partitioning or silica gel chromatography, and ultimate

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