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45414

Supelco

Cyromazin

PESTANAL®, analytical standard

Synonym(s):

N-Cyclopropyl-1,3,5-triazin-2,4,6-triamine, Cyromazin

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About This Item

Empirical Formula (Hill Notation):
C6H10N6
CAS Number:
Molecular Weight:
166.18
Beilstein:
882879
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

mp

223-227 °C (lit.)

application(s)

agriculture
environmental

format

neat

SMILES string

Nc1nc(N)nc(NC2CC2)n1

InChI

1S/C6H10N6/c7-4-10-5(8)12-6(11-4)9-3-1-2-3/h3H,1-2H2,(H5,7,8,9,10,11,12)

InChI key

LVQDKIWDGQRHTE-UHFFFAOYSA-N

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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

Environment

Hazard Statements

Precautionary Statements

Hazard Classifications

Aquatic Chronic 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

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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Hongyuan Yan et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 908, 137-142 (2012-10-09)
A simple, convenient and high selective molecularly imprinted matrix solid-phase dispersion (MI-MSPD) using water-compatible cyromazine-imprinted polymer as adsorbent was proposed for the rapid screening of melamine from bovine milk coupled with liquid chromatography-ultraviolet detection. The molecularly imprinted polymers (MIPs) synthesized
Mu Li et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 878(25), 2333-2338 (2010-08-03)
Molecularly-imprinted polymers in the form of microspheres were synthesized using the dispersion polymerization protocol; cyromazine was used as dummy template, while methacrylic acid, ethylene glycol dimethacrylate and acetonitrile (MeCN) were used as functional monomer, cross-linker, and porogen, respectively. When compared
Howard A Bell et al.
Pest management science, 66(7), 693-695 (2010-06-10)
House fly control in livestock-rearing facilities is heavily reliant on the use of the larvicide cyromazine. While extensive use of this compound has led to the development of resistance in several countries, no elevated tolerance has so far been reported
Xinle Zhu et al.
Journal of agricultural and food chemistry, 57(23), 11075-11080 (2009-11-11)
A gas chromatography-mass spectrometric (GC-MS) method was established for the determination of cyromazine and its metabolite, melamine, in animal-derived food. Chicken and tilapia muscle samples were spiked with (15)N(3)-melamine, extracted with an acidic acetonitrile/water solution, and defatted with dichloromethane. Egg
Huan Yu et al.
Analytica chimica acta, 682(1-2), 48-58 (2010-11-09)
Simple and sensitive methods have been developed for simultaneous detection of cyromazine, melamine and their metabolites (ammeline, ammelide and cyanuric acid) in samples of animal origins. These include a high performance liquid chromatography (HPLC) method and a liquid chromatography-tandem mass

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