N,N'-Diethyl-N''-isopropyl-1,3,5-triazine-2,4,6-triamine - CAS 30360-19-1
Category:
Main Product
Product Name:
N,N'-Diethyl-N''-isopropyl-1,3,5-triazine-2,4,6-triamine
Catalog Number:
B-0001-105664
Synonyms:
4-N,6-N-diethyl-2-N-propan-2-yl-1,3,5-triazine-2,4,6-triamine; 30360-19-1; N,N'-Diethyl-N''-isopropyl-1,3,5-triazine-2,4,6-triamine; 2,4-Bis(ethylamino)-6-isoproylamino-1,3,5-triazine; EINECS 250-146-6; 2-Ethylaminoatrazine; 2-(Ethylamino)atrazine; AC1L1SY9; SCHEMBL11452149; ZINC2011064; Melamine, N2,N4-diethyl-N6-isopropyl-; HE048494; N2,N4-DIETHYL-N6-ISOPROPYLMELAMINE; 3B1-004129; 4-N,6-N-diethyl-2-N-propan-2-yl-1,3,5-triazine-2,4,6-triamine; N N'-DIETHYL-N''-ISOPROPYL-1 3 5-TRIAZINE-2 4 6-TRIAMINE; N2,N4-diethyl-N6-(propan-2-yl)-1,3,5-triazine-2,4,6-triamine
CAS Number:
30360-19-1
Description:
N,N'-Diethyl-N''-isopropyl-1,3,5-triazine-2,4,6-triamine, also called 2-Ethylaminoatrazine, under the IUPAC name 2-Ethylaminoatrazine, can be used as insecticide and herbicide.
Molecular Weight:
224.31
Molecular Formula:
C10H20N6
Quantity:
Grams-Kilos
Quality Standard:
In-house Standard
COA:
Certificate of Analysis-N,N'-Diethyl-N''-isopropyl-1,3,5-triazine-2,4,6-triamine 30360-19-1 B16WW06281  
MSDS:
Inquire
Canonical SMILES:
CCNC1=NC(=NC(=N1)NC(C)C)NCC
InChI:
1S/C10H20N6/c1-5-11-8-14-9(12-6-2)16-10(15-8)13-7(3)4/h7H,5-6H2,1-4H3,(H3,11,12,13,14,15,16)
InChIKey:
ANCXQLFAWHZRLK-UHFFFAOYSA-N
Size Price Stock Quantity
1 g $698 In stock
5 g $998 In stock
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Chemical Structure
CAS 30360-19-1 N,N'-Diethyl-N''-isopropyl-1,3,5-triazine-2,4,6-triamine

Reference Reading


1.sym-Trisubstituted 1,3,5-Triazine Derivatives as Promising Organic Corrosion Inhibitors for Steel in Acidic Solution.
El-Faham A1,, Dahlous KA, Al Othman ZA, Al-Lohedan HA, El-Mahdy GA. Molecules. 2016 Mar 31;21(4). pii: E436. doi: 10.3390/molecules21040436.
Triazine derivatives, namely, 2,4,6-tris(quinolin-8-yloxy)-1,3,5-triazine (T3Q), N²,N⁴,N⁶-tris(pyridin-2-ylmethyl)-1,3,5-triazine-2,4,6-triamine (T3AMPy) and 2,2',2''-[(1,3,5-triazine-2,4,6-triyl)tris(azanediyl)] tris(ethan-1-ol) (T3EA) were synthesized and their inhibition of steel corrosion in hydrochloric acid solution was investigated using electrochemical techniques. The corrosion protection of the prepared compounds increased with increasing concentration and reached up to 98% at 250 ppm. The adsorption of T3Q, T3AMPy, and T3EA on the steel surface was in accordance with the Langmuir adsorption isotherm. The electrochemical results revealed that T3Q, T3AMPy and T3EA act as excellent organic inhibitors and can labeled as mixed type inhibitors. The efficiencies of the tested compounds were affected by the nature of the side chain present in the triazine ring, where T3EA gave the least inhibition while T3Q and T3AMPy gave higher and almost the same inhibition effects. The inhibition efficiencies obtained from the different electrochemical techniques were in good agreement.
CO2-Induced Reversible Dispersion of Graphene by a Melamine Derivative.
Yin H, Liu H, Wang W, Feng Y. Langmuir. 2015 Nov 10;31(44):12260-7. doi: 10.1021/acs.langmuir.5b02831. Epub 2015 Oct 28.
Smart graphene with stimuli-responsive dispersity has great potential for applications in medical and biochemical fields. Nevertheless, reversible dispersion/aggregation of graphene in water with biocompatible and removable trigger still represents a crucial challenge. Here, we report CO2-induced reversible graphene dispersion by noncovalent functionalization of reduced graphene oxide with N(2),N(4),N(6)-tris(3-(dimethylamino)propyl)-1,3,5-triazine-2,4,6-triamine (MET). It was demonstrated that MET can be strongly adsorbed on graphene surface through van der Waals interaction to facilitate dispersing graphene in water. Moreover, reversible aggregation/dispersion of graphene can be achieved simply by alternately bubbling CO2 and N2 to control the desorption/adsorption of MET on graphene surface.
3.Multifunctional uranyl hybrid materials: structural diversities as a function of pH, luminescence with potential nitrobenzene sensing, and photoelectric behavior as p-type semiconductors.
Song J, Gao X, Wang ZN, Li CR, Xu Q, Bai FY, Shi ZF1, Xing YH. Inorg Chem. 2015 Sep 21;54(18):9046-59. doi: 10.1021/acs.inorgchem.5b01364. Epub 2015 Sep 2.
A series of uranyl-organic frameworks (UOFs), {[(UO2)2(H2TTHA)(H2O)]·4,4'-bipy·2H2O}n (1), {[(UO2)3(TTHA)(H2O)3]}n (2), and {[(UO2)5(TTHA) (HTTHA)(H2O)3]·H3O}n (3), have been obtained by the hydrothermal reaction of uranyl acetate with a flexible hexapodal ligand (1,3,5-triazine-2,4,6-triamine hexaacetic acid, H6TTHA). These compounds exhibited three distinct 3D self-assembly architectures as a function of pH by single-crystal structural analysis, although the used ligand was the same in each reaction. Surprisingly, all of the coordination modes of the H6TTHA ligand in this work are first discovered. Furthermore, the photoluminescent results showed that these compounds displayed high-sensitivity luminescent sensing functions for nitrobenzene. Additionally, the surface photovoltage spectroscopy and electric-field-induced surface photovoltage spectroscopy showed that compounds 1-3 could behave as p-type semiconductors.
4.Monodispersed N-doped carbon nanospheres for supercapacitor application.
Lee WH, Moon JH. ACS Appl Mater Interfaces. 2014 Aug 27;6(16):13968-76. doi: 10.1021/am5033378. Epub 2014 Jul 30.
Highly monodispersed nitrogen-doped carbon nanospheres are prepared by the pyrolytic carbonization of emulsion-polymerized polystyrene-based colloidal spheres in the presence of a nitrogen-enriched molecule, melamine (1,3,5-triazine-2,4,6-triamine). The nitrogen-doped carbon spheres are successfully tested for use as electrode materials in supercapacitors. The nitrogen content incorporated into the carbon sphere is controlled by changing the weight ratio of melamine to the polymer spheres. The nitrogen doping concentration is proportional to the mixing weight ratio. The nitrogen doping produces relatively abundant pyridinic and pyrrolic configurations, and these configurations are observed to be more abundant for carbon spheres with high nitrogen doping. The nitrogen doping enhances the pseudocapacitance and the electrical conductivity of carbon, thereby enhancing the specific capacitance. We obtain a specific capacitance of up to 191.9 F g(-1) with 20% nitrogen doped carbon nanospheres, which is 14 times higher than that of the undoped carbon nanospheres. Moreover, the capacitance retention remains up to 10,000 cycles, which clearly displays a good cycling stability the nitrogen-doped carbon nanospheres as the supercapacitve electrode materials.