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45414

Supelco

Cyromazin

PESTANAL®, analytical standard

Sinónimos:

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

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About This Item

Fórmula empírica (notación de Hill):
C6H10N6
Número de CAS:
66215-27-8
Peso molecular:
166.18
Beilstein/REAXYS Number:
882879
EC Number:
266-257-8
MDL number:
MFCD00078650
UNSPSC Code:
41116107
PubChem Substance ID:
329756712
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

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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Categorías relacionadas

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
GHS09

hcodes

H411

Hazard Classifications

Aquatic Chronic 2

Storage Class

11 - Combustible Solids

wgk_germany

WGK 2

flash_point_f

212.0 °F - closed cup

flash_point_c

100 °C - closed cup

ppe

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

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Certificados de análisis (COA)

Lot/Batch Number
BCCH9793
BCCF1581
BCBW6886
BCBS3656V
SZBD302XV

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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
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
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
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
G W Levot
Australian veterinary journal, 90(11), 433-437 (2012-10-31)
To investigate the cause of cyromazine failure to protect lambs from flystrike. Lucilia cuprina larvae from a Nimmitabel (New South Wales) population associated with failure of a cyromazine spray-on to protect lambs from flystrike were compared with larvae from a
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