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45407

Supelco

Cyanazine

PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C9H13ClN6
CAS Number:
21725-46-2
Molecular Weight:
240.69
Beilstein:
615509
EC Number:
244-544-9
MDL number:
MFCD00055514
UNSPSC Code:
41116107
PubChem Substance ID:
329756707
NACRES:
NA.24

grade

analytical standard

Quality Level

100

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

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

application(s)

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)

InChI key

MZZBPDKVEFVLFF-UHFFFAOYSA-N

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General description

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

Application

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

Legal Information

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

Pictograms

Skull and crossbonesEnvironment
GHS06,GHS09

Signal Word

Danger

Hazard Statements

H301,H410

Hazard Classifications

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

Storage Class Code

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

WGK

WGK 3

Flash Point(F)

212.0 °F - closed cup

Flash Point(C)

100 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCG9629
BCBV4875

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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
Shannon M Lynch et al.
Environmental health perspectives, 114(8), 1248-1252 (2006-08-03)
Cyanazine is a common pesticide used frequently in the United States during the 1980s and 1990s. Animal and human studies have suggested that triazines may be carcinogenic, but results have been mixed. We evaluated cancer incidence in cyanazine-exposed pesticide applicators
Gaurav Saini et al.
Journal of chromatography. A, 1216(16), 3587-3593 (2009-01-03)
In spite of advances in solid-phase extraction (SPE) technology there are certain disadvantages to current SPE silica-based, column packings. The pH range over which extraction can occur is limited and each column is generally only used once. New diamond-based reversed
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