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45407

Supelco

Cyanazine

PESTANAL®, analytical standard

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About This Item

Formula empirica (notazione di Hill):
C9H13ClN6
Numero CAS:
21725-46-2
Peso molecolare:
240.69
Beilstein:
615509
Numero CE:
244-544-9
Numero MDL:
MFCD00055514
Codice UNSPSC:
41116107
ID PubChem:
329756707
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
solid phase extraction (SPE): suitable

applicazioni

agriculture
environmental

Formato

neat

Stringa SMILE

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)
MZZBPDKVEFVLFF-UHFFFAOYSA-N

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Descrizione generale

Standard for Supelco MIP SPE cartridges. For more information request Supelco Literature T407075, T706023

Applicazioni

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

Note legali

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

Pittogrammi

Skull and crossbonesEnvironment
GHS06,GHS09

Avvertenze

Danger

Indicazioni di pericolo

H301,H410

Classi di pericolo

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

Codice della classe di stoccaggio

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

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

212.0 °F - closed cup

Punto d’infiammabilità (°C)

100 °C - closed cup

Dispositivi di protezione individuale

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

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Certificati d'analisi (COA)

Lot/Batch Number
BCCG9629
BCBV4875
SZBD275XV
SZBB264XV
SZB7036XV

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Atrazine PESTANAL®, analytical standard

Supelco

45330

Atrazine

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

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