551295
N-Cyclopropyl-2,4,6-triamino-1,3,5-triazine
97%
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:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
97%
mp
223-227 °C (lit.)
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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General description
N-Cyclopropyl-2,4,6-triamino-1,3,5-triazine, also known as cyromazine, is an insect growth regulator(IGR) that is commonly used as an insecticide. It undergoes metabolism in plants and animals to form melamine. Surface-enhanced Raman scattering (SERS) spectroscopic study indicates that it interacts with the surface of silver colloid through the lone pair on nitrogen.
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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Raman and surface-enhanced Raman study of insecticide cyromazine.
Mukherjee K, et al.
Vibrational Spectroscopy, 25(1), 91-99 (2001)
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
Hanwen Sun et al.
Electrophoresis, 31(13), 2236-2241 (2010-07-02)
A novel and simple method was, for the first time, developed for effective separation and sensitive detection of cyromazine (CM) and its metabolite melamine (MM) by CZE with DAD (CZE-DAD). Among different solvents, ACN containing 20% NH(4)OH was found to
Yulin Gao et al.
PloS one, 7(5), e36622-e36622 (2012-06-05)
Closely related invasive species may often displace one another, but it is often difficult to determine mechanisms because of the historical nature of these events. The leafmining flies Liriomyza sativae and Liriomyza trifolii have become serious invasive agricultural pests throughout
Yulin Gao et al.
Journal of economic entomology, 104(6), 1771-1773 (2012-02-04)
Under field conditions, species displacements have occurred in different directions between the same invasive species of leafminers (Diptera: Agromyzidae). Liriomyza sativae (Blanchard) was displaced by L. trifolii (Burgess) in the western United States, with evidence suggesting that lower insecticide susceptibility
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