45414
Cyromazin
PESTANAL®, analytical standard
Sinónimos:
N-Cyclopropyl-1,3,5-triazin-2,4,6-triamine
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Acerca de este artículo
Fórmula empírica (notación de Hill):
C6H10N6
Número CAS:
Peso molecular:
166.18
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
266-257-8
Beilstein/REAXYS Number:
882879
MDL number:
Servicio técnico
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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
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
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hcodes
pcodes
Hazard Classifications
Aquatic Chronic 2
Clase de almacenamiento
11 - Combustible Solids
wgk
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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D B Taylor et al.
Journal of economic entomology, 105(2), 726-731 (2012-05-23)
Hay mixed with manure and urine residues at sites where hay has been provided as supplemental winter feed for cattle provide an excellent substrate for the development of immature stable flies, Stomoxys calcitrans (L.). Such sites are primary sources of
G W Levot
Australian veterinary journal, 91(1-2), 61-64 (2013-01-30)
To determine the significance of cyromazine resistance in blowfly larvae from a region where resistance has been previously confirmed and to measure susceptibility of the cyromazine-resistant blowflies to ivermectin and spinosad. Blowfly larvae from five properties located within 5 km
Xianhua Wang et al.
Analytical and bioanalytical chemistry, 404(5), 1555-1564 (2012-07-24)
A magnetic molecularly imprinted polymer (M-MIP) for cyromazine and melamine was prepared by simple suspension polymerization using a pseudo template, 2-(4,6-diamino-1,3,5-triazin-2-ylamino)ethanethiol disulfide. The M-MIP was characterized by scanning electron microscopy, Fourier-transform infrared spectroscopy, and vibrating sample magnetometry. Molecular recognition properties