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Merck

45407

Supelco

Cyanazin

PESTANAL®, analytical standard

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About This Item

Empirische Formel (Hill-System):
C9H13ClN6
CAS-Nummer:
Molekulargewicht:
240.69
Beilstein:
615509
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
41116107
PubChem Substanz-ID:
NACRES:
NA.24

Qualität

analytical standard

Qualitätsniveau

Produktlinie

PESTANAL®

Haltbarkeit

limited shelf life, expiry date on the label

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable
solid phase extraction (SPE): suitable

Anwendung(en)

agriculture
environmental

Format

neat

SMILES String

CCNc1nc(Cl)nc(NC(C)(C)C#N)n1

InChI

1S/C9H13ClN6/c1-4-12-7-13-6(10)14-8(15-7)16-9(2,3)5-11/h4H2,1-3H3,(H2,12,13,14,15,16)

InChIKey

MZZBPDKVEFVLFF-UHFFFAOYSA-N

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Allgemeine Beschreibung

Standard für die Supelco MIP SPE-Kartuschen. Bitte fordern Sie für weiterführende Informationen die Supelco-Literatur T407075 und T706023 an.

Anwendung

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Rechtliche Hinweise

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

Piktogramme

Skull and crossbonesEnvironment

Signalwort

Danger

H-Sätze

Gefahreneinstufungen

Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1

Lagerklassenschlüssel

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flammpunkt (°F)

212.0 °F - closed cup

Flammpunkt (°C)

100 °C - closed cup

Persönliche Schutzausrüstung

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


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Analysenzertifikate (COA)

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Atrazin PESTANAL®, analytical standard

Supelco

45330

Atrazin

Sabine Beulke et al.
Journal of environmental quality, 34(6), 1933-1943 (2005-10-14)
There is evidence that degradation of pesticides in simple laboratory systems may differ from that in the field, but it is not clear which of the simplifications inherent in laboratory studies present serious shortcomings. Laboratory experiments evaluated several simplifying assumptions
D W Kolpin et al.
Environmental science & technology, 35(6), 1217-1222 (2001-05-12)
A recently developed analytical method using liquid chromatography/mass spectrometry was used to investigate the occurrence of cyanazine and its degradates cyanazine acid (CAC), cyanazine amide (CAM), deethylcyanazine (DEC), and deethylcyanazine acid (DCAC) in groundwater. This research represents some of the
Ji-Guang Gu et al.
Chemosphere, 52(9), 1515-1521 (2003-07-18)
Persistence and degradation of the herbicides Atrazine, Cyanazine and Dicamba were measured in laboratory microcosms incubated under methanogenic condition using three soils of China. Results showed that Atrazine was more resistant to degradation than Cyanazine and Dicamba for the 300
Guowen Zhang et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 78(1), 238-242 (2010-10-27)
A spectrophotometric method for the simultaneous determination of two herbicides, atrazine and cyanazine, is described for the first time based on their reaction with p-aminoacetophenone in the presence of pyridine in hydrochloric acid medium. The absorption spectra were measured in
Mohammad Bagher Gholivand et al.
Analytica chimica acta, 713, 36-44 (2011-12-28)
A computational approach was used for screening functional monomers and polymerization solvent in the rational design of molecularly imprinted polymers (MIPs). It was based on the comparison of the binding energy of the complexes between the template and functional monomers.

Protokolle

HPLC Analysis of Urea, Carbamate, Triazine, Aniline Pesticides on Discovery® C18

Separation of Atrazine-desethyl; Metoxuron; Hexazinone; Simazine; Cyanazine; Methabenzthiazuron; Atrazine; Monolinuron; Diuron; Isoproturon; Metobromuron; Metazachlor; Sebuthylazin; Linuron; Metolachlor

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