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
Other names: RDX; Cyclonite; s-Triazine, hexahydro-1,3,5-trinitro-; Cyclonit; Cyclotrimethylenenitramine; Cyclotrimethylenetrinitramine; Geksogen; Hexahydro-1,3,5-trinitro-s-triazine; Hexahydro-1,3,5-trinitro-1,3,5-triazine; Hexogen; Hexogen 5W; PBX(AF) 108; Trimethylenetrinitramine; T4; 1,3,5-Triaza-1,3,5-Trinitrocyclohexane; 1,3,5-Trinitro-1,3,5-triazacyclohexane; 1,3,5-Trinitrohexahydro-s-triazine; 1,3,5-Trinitrohexahydro-1,3,5-triazine; 1,3,5-Trinitroperhydro-1,3,5-triazine; sym-Trimethylenetrinitramine; Esaidro-1,3,5-trinitro-1,3,5-triazina; Heksogen; Hexahydro-1,3,5-trinitro-1,3,5-triazin; Hexogeen; Hexogen (explosive); Hexolite; Trimethyleentrinitramine; Trinitrocyclotrimethylene triamine; Cyklonit; PBXW 108(E); UN 0072; 1,3,5-Triazacyclohexane 1,3,5-trinitro-; CX 84A; NSC 312447; PE 4; perhydro-1,3,5-trinitro-1,3,5-triazine ...
Triazine is the chemical species of six-membered heterocyclic ring compound with three nitrogens replacing carbon-hydrogen units in the benzene ring structure. The names of the three isomers indicate which of the carbon-hydrogen units on the benzene ring position of the molecule have been replaced by nitrogens, called 1,2,3-triazine, 1,2,4-triazine, and 1,3,5-triazine respectively. Symmetrical 1,3,5-triazine is the common. Triazines are prepared from 2-azidocyclopropene through thermal rearrangement (1,2,3-triazine), from 1,2-dicarbonyl compound with amidrazone by condensation reaction (1,2,4-triazine) and from cyanic acid amide by trimerization (1,3,5-triazine). Pyridine is the aromatic nitrogen heterocycle compound having only one nitrogen, and diazines are with 2 nitrogen atoms and tetrazines are with 4 nitrogen atoms on the benzene ring system. Triazines are weak base. Triazines have much weaker resonance energy than benzene, so nucleophilic substitution is preferred than electrophilic ...
292607865 - EP 1087948 A1 2001-04-04 - 2,4-DIAMINO-1,3,5-TRIAZINE, METHOD FOR THE PRODUCTION AND USE OF THE SAME AS HERBICIDES AND PLANT GROWTH REGULATORS - [origin: DE19925329A1] 2-Amino-1,3,5-triazine derivatives (I) are new. 2-Amino-1,3,5-triazine derivatives of formula (I) and their salts are new: R1 = optionally substituted aryl, 3-9C cycloalkyl or heterocyclyl; or 1-6C alkyl, 2-6C alkenyl or 2-6C alkynyl optionally substituted by halogen, OH, CN, NO2, SCN, 1-4C alkoxy, 1-4C haloalkoxy, 2-4C alkenyloxy, 2-4C haloalkenyloxy, 1-4C alkylthio, 1-4C alkylsulfinyl, 1-4C alkylsulfonyl, 1-4C haloalkylsulfinyl, 1-4C haloalkylsulfonyl, optionally substituted 3-9C cycloalkyl, optionally substituted phenyl, optionally substituted heterocyclyl, C(Z )R , ZC(Z )R , C(Z )ZR , C(Z )NR R, OC(Z )ZR , ZC(Z )NR R, N(R)C(Z )ZR and/or N(R )C(Z )NR R; R , R, R = optionally substituted 1-6C alkyl, aryl, aryl(1-6C)alkyl, 3-9C cycloalkyl or (3-9C)cycloalkyl(1-6C)alkyl; Z, Z = O or S; R2 = optionally substituted 3
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VALLEY COTTAGE, N.Y. - Introduction: Cyanuric Chloride Market Commercially, cyanuric chloride is a well-known organic compound having the chemical formula (NCCl)3 and also referred to as a trimer of cyanogen chloride. Cyanuric chloride is one of the derivatives of 1,3,5,-triazine. On the commercial scale, cyanuric c...
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The 5,7-diamino[1,2,4]triazolo[1,5-a][1,3,5]triazines were synthesized by cyclocondensation of 3(5)-amino-1,2,4-triazoles with cyanoguanidine. The substituted 3(5)-amino-1,2,4-triazoles were prepared from corresponding hydrazides and S-methylisothiourea via ring closure of the intermediate acylaminoguanidines. The 3,5-diamino-1,2,4-triazoles were prepared using partial aminolysis of dimethyl N-cyanodithiocarbonimidate followed by cyclization of the obtained N-substituted N-cyano-S-methylisothioureas with hydrazine. The structures of the prepared compound were confirmed using NMR spectral data.. ...
303403968 - EP 0453405 B1 2000-07-12 - Compounds containing o-hydroxyphenyl-1,3,5-triazines and sterile inhibited amines - [origin: CA2040774A1] Compounds which comprise at least one group of the formula I or II (see formula I or II) and at least one polyalkylpiperidine group of the formula III (III), in which R and R1 to R6 have the meaning indicated in claim 1, are effective stabilisers for organic materials against damage by light, oxygen and heat.[origin: CA2040774A1] A-l8042/A Compounds formed from o-hydroxyphenyl-1,3,5-triazines and sterically hindered amines Compounds which comprise at least one group of the formula I or II (I) or (II) and at least one polyalkylpiperidine group of the formula III (III), in which R and R1 to R6 have the meaning indicated in claim 1, are effective stabilisers for organic materials against damage by light, oxygen and heat.[origin: CA2040774A1] Compounds which comprise at least one group of the formula I or II (see formula I or II) and at least one
The report generally describes 2,4-dichloro-6-morpholino-1,3,5-triazine, examines its uses, production methods, patents. 2,4-Dichloro-6-morpholino-1,3,5-triazine
Hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX) is a serious environmental pollutant on military land. This compound is the most widely used explosive and pollution has arisen primarily as the result of military training, along with munition manufacturing and disassembly processes. This toxic explosive is recalcitrant to degradation in the environment and leaches rapidly into groundwater, where accumulation in aquifers is threatening drinking water supplies (Clausen, et al., 2004). While plants have only limited degradative activity towards RDX, microorganisms, including Rhodococcus rhodochrous 11Y, have been isolated from contaminated land. Despite the presence of microbial RDX-metabolising activity in contaminated soils, the persistence of RDX in leachate from contaminated soil indicates that this activity or biomass is insufficient, limiting its use to remediate polluted soils. Bacterial activity in the rhizosphere is of magnitudes greater than in the surrounding soil, and the roots of grass ...
Biotransformation of hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX) catalyzed by a NAD(P)H: nitrate oxidoreductase from Aspergillus niger
Global Cyanuric Chloride Market Report gives latest insights that includes market sales, share and growth in key regions for their top manufacturers with forecast research for the Cyanuric Chloride Industry.
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A number of reactive dichlorotriazine dyes specifically and irreversibly inactivate pig heart lactate dehydrogenase, yeast glucose 6-phosphate dehydrogenase and yeast hexokinase at sites competitive with NAD+, NADP+, and ATP respectively. Monochlorotriazine dyes, including Cibacron Blue F3G-A, do not inactivate lactate dehydrogenase but display high affinity and thus inhibit the inactivation by dichlorotriazine dyes. These data are interpreted in terms of the ability of nucleotide-binding enzymes to bind polysulphonated aromatic chromophores.. ...
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The nitramines are the most recently introduced class of organic nitrate explosives. The most prominent member of this class is RDX (research department explosive; hexahydro-1,3,5-trinitro-1,3,5 triazine, which is also known as cyclonite); HMX (high melting explosive; octahydro-1,3,5,7-tetranitro-1,3,5,7 tetrazocine), nitroguanidine, and tetryl are also significant nitramines
94279-01-3 - CHPWHRVLSQHJNK-UHFFFAOYSA-N - Hexahydro-1,3,5-trioctyl-1,3,5-triazine - Similar structures search, synonyms, formulas, resource links, and other chemical information.
Nitramine propellants absent a pressure exponent shift in the burning rate curves are prepared by matching the burning rate of a selected nitramine or combination of nitramines within 10% of burning rate of a plasticized active binder so as to smooth out the break point appearance in the burning rate curve.
Clinical studies have shown that lamotrigine has some beneficial antidepressant effects in major depressive episodes (Normann et al., 2002; Barbosa et al., 2003; Barbee et al., 2011), whereas currently there are no clinical studies for the use of carisbamate in mood disorders. However, carisbamate and lamotrigine present some similarities in that their main mechanism of action is at VGSCs, and they both have antidepressant-like effects in the FST model of depression; hence their comparison may allow a better understanding of their preclinical and clinical effects.. Carisbamate and lamotrigine administration for both 2 and 14 days resulted in a decrease in DRN 5-HT neuronal firing activity. The latter result may not be due to an acute increase in 5-HT, as it was reported that lamotrigine (20 mg/kg), when administered systemically, dose-dependently decreases the extracellular 5-HT levels in the DRN (Tanahashi et al., 2012). Alternatively, previous in vitro evidence indicates that ionotropic ...
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Design, synthesis, and structure-activity relationship of imidazolidin-2-one-1,3,5-triazine conjugates as Enterovirus 71 and Coxsackievirus A16 Inhibitor, Wen-li Gao, Jing-xiu Li
3-(Isobutyrylhydrazino)-5-phenyl-1,2,4-triazine, hydrochloride | C13H16ClN5O | CID 51099 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety/hazards/toxicity information, supplier lists, and more.
2-chloro-4,6-diethoxy-1,3,5-triazine | C7H10ClN3O2 | CID 35649 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety/hazards/toxicity information, supplier lists, and more.
The reactions of 2,4,6-tri(2-pyridyl)-1,3,5-triazine (tpt) with copper(I) halides under solvothermal or traditional conditions yielded two polymeric Cu(I) complexes [Cu2I2(tpt)]n (1) and [Cu3I3(tpt)]n (2), one mixed-valence Cu(I)−Cu(II) complex [Cu4Cl2I4(tpt)2] (3), and two Cu(II) complexes [CuBr(bpca)] (4) and [CuI(bpca)] (5) (bpca = bis(2-pyridylcarbonyl)amine). Complex 1 is a zigzag chain with tpt in a bis-bipyridine-like coordination mode, whereas complex 2 with tpt chelating three Cu(I) cations is a ladderlike coordination polymer. Complex 3 is mixed-valence, with Cu(I) in a distorted tetrahedral geometry and Cu(II) in a distorted square pyramidal geometry, forming a ladderlike supramolecular chain. Complexes 4 and 5 are the products of in situ hydrolysis of tpt involving the oxidation of Cu(I). The synthesis and characterization of complex 1, 2, and 5 indicated that Cu(I) cannot promote the hydrolysis of tpt. The theoretical study shows that the main effect for hydrolysis of tpt is the ...
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2547-66-2 - VWVZIRPJPFJGFE-UHFFFAOYSA-N - 1,3,5-Tribenzylhexahydro-1,3,5-triazine - Similar structures search, synonyms, formulas, resource links, and other chemical information.
Learn more about 2-2-5-methylfuran-2-yl-vinyl-4-6-bis-trichloromethyl-1-3-5-triazine. We enable science by offering product choice, services, process excellence and our people make it happen.
You are viewing an interactive 3D depiction of the molecule naphtho[1,2-e]tetrazolo[1,5-b]1,2,4-triazine (C11H7N6+) from the PQR.
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4-methyl-2H-1,2,3-benzotriazine-1-carbaldehyde - chemical structural formula, chemical names, chemical properties, synthesis references
5,7-dimethylpyrimido[5,4-d][1,2,3]triazine-6,8(5H,7H)-dione 3-oxide - C7H7N5O3, synthesis, structure, density, melting point, boiling point
This page contains information on the chemical 1,3,5-Triazine-1,3,5(2h,4h,6h)-Triethanol (9ci) including: 2 synonyms/identifiers.
The invention relates to new 6,7-dihydropyrazole-[1,5-a][1,3,5]triazine-2-sulphonamides of general formula I ##STR1## in which Ar, R.sub.6, R.sub.7, R.sub.8, R.sub.9 and X have the meanings given in t
Learn more about n-2-methoxy-5-methylphenyl-1-3-5-triazine-2-4-diamine. We enable science by offering product choice, services, process excellence and our people make it happen.
[65 Pages Report] Check for Discount on tris(2-ethylhexyl)-4,4,4-(1,3,5-triazine-2,4,6-triyltriimino)tribenzoate Global Market and Forecast Research report by ChemReport. DescriptionWe provide independent and unbiased information on manufacturers, prices, production...
Two strains belonging to the genus Shewanella, HAW-EB2T and HAW-EB5T, were isolated previously from marine sediment sampled from the Atlantic Ocean, near Halifax harbour in Canada, for their potential to degrade explosive hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX). In the present study, strains HAW-EB2T and HAW-EB5T were found to display high 16S rRNA gene sequence similarity (90-99.5 %) to species of Shewanella, but their gyrB sequences were significantly different from each other and from species of Shewanella (79-87.6 %). Furthermore, DNA-DNA hybridization showed that the genomic DNA of the two strains was only 22 % related and showed less than 41 % relatedness to closely related species of Shewanella. In comparison to other species of Shewanella, strains HAW-EB2T and HAW-EB5T were also unique in some phenotypic properties such as activities of β-galactosidase and tyrosine arylamidase and the ability to metabolize certain organic acids and sugars. Both strains HAW-EB2T and HAW-EB5T utilize malate
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One study of lamotrigine (Lamictal, a popular, well tolerated anti-seizure medication with mood-stabilizing side effects) involved just 14 people. Another involved 31 patients. A study with 40 patients found "Adjunctive treatment with lamotrigine did not result in a significant difference in HAM-D total score at the endpoint of the study when compared with paroxetine alone." Another study, with just 20 patients (and no placebo arm), found "there was no significant difference between treatment groups." Another (a lamotrigine monotherapy study) looked at depression-score improvements in 32 epilepsy patients (and 38 controls); this was, at least, a randomized, double-blind, placebo controlled study. And it did find significantly better improvement on Beck Depression Inventory scores, after 12 weeks, for the lamotrigine group (8.9 point drop) versus the placebo group (1.7 point drop), but two things need to be noted about this otherwise-good study. First, the patients (with an average Beck score of ...
One study of lamotrigine (Lamictal, a popular, well tolerated anti-seizure medication with mood-stabilizing side effects) involved just 14 people. Another involved 31 patients. A study with 40 patients found "Adjunctive treatment with lamotrigine did not result in a significant difference in HAM-D total score at the endpoint of the study when compared with paroxetine alone." Another study, with just 20 patients (and no placebo arm), found "there was no significant difference between treatment groups." Another (a lamotrigine monotherapy study) looked at depression-score improvements in 32 epilepsy patients (and 38 controls); this was, at least, a randomized, double-blind, placebo controlled study. And it did find significantly better improvement on Beck Depression Inventory scores, after 12 weeks, for the lamotrigine group (8.9 point drop) versus the placebo group (1.7 point drop), but two things need to be noted about this otherwise-good study. First, the patients (with an average Beck score of ...
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