Day: November 9, 2021

An article Double network anion exchange membrane with excellent flexibility and stability WOS:000473579800005 published article about POLY(ARYLENE ETHER SULFONE)S; QUATERNARY AMMONIUM GROUPS; FUEL-CELL APPLICATIONS; SIDE-CHAINS; CROSS-LINKING; KETONE); BLOCK; CONDUCTIVITY; ELECTROLYTE; CATIONS in [Du, Xinming; Wang, Zhe; Zhang, Hongyu; Liu, Wenchang; Chen, Zhaoyu; Xu, Jingmei] Changchun Univ Technol, Coll Chem Engn, Changchun 130012, Jilin, Peoples R China; [Du, Xinming; Wang, Zhe; Xu, Jingmei] Changchun Univ Technol, Adv Inst Mat Sci, Changchun 130012, Jilin, Peoples R China in 2019.0, Cited 48.0. Product Details of 61-82-5. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5

A double-network anion exchange membrane (TA/AT-PEK/PVA-x) was prepared by Br-PEK and PVA, 3-amino-1,2,4 triazole forms a cross-linking structure with PVA under the action of 1,4-phthalaldehyde and then triazole can be linked with Br-PEK. The structure of membranes was verified by FT-IR. The composite membrane is uniform and smooth can be seen from the scanning electron microscope (SEM) and exhibit good hydrophilic/hydrophobic micro-phase separation structure proved by Transmission electron micrograph (TEM). The ionic conductivity of TA/AT-PEK/PVA-0.15 is 0.062 S/cm at 80 degrees C. With the addition of PVA within a certain range, the water uptake, swelling ratio hydroxide conductivity and alkaline stability are increase. The membranes are more flexible. After immersing in 4M NaOH solutions for 240 h at 80 degrees C, it remains at least 65% of its initial hydroxide ion conductivity of TA/AT-PEK/PVA-0.3 membrane. With the increasing number of water molecules solvating the hydroxide, its nucleophilicity and basicity were hindered, which enhance alkaline stability of anion exchange membranes.

Product Details of 61-82-5. Bye, fridends, I hope you can learn more about C2H4N4, If you have any questions, you can browse other blog as well. See you lster.

Reference:
Article; Safari, Niloufar; Shirini, Farhad; Tajik, Hassan; Journal of Molecular Structure; vol. 1201; (2020);,
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics

Computed Properties of C2H4N4. Authors Xu, XQ; Wu, P; Li, CY; Zhao, KY; Wang, CR; Deng, RP; Zhang, JL in AMER CHEMICAL SOC published article about in [Xu, Xiaoqing; Zhao, Keyong; Wang, Chiran; Deng, Renpan; Zhang, Jinli] Shihezi Univ, Key Lab Green Proc Chem Engn Xinjiang Bingtuan, Sch Chem & Chem Engn, Shihezi 832003, Peoples R China; [Wu, Peng] Soochow Univ, Sch Chem & Environm Engn, Suzhou 215123, Jiangsu, Peoples R China; [Li, Changyong] Univ Bremen, Ctr Appl Space Technol & Micrograv ZARM, D-28359 Bremen, Germany in 2021.0, Cited 59.0. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5

In this work, amine-functionalized ZIF8 (i.e., ZIF8-A) was dispersed in n-heptanol (ZIF8-A/n-heptanol) to remove SO2. The effects of ZIF8-A proportion, SO2 concentration, and absorption and desorption temperatures on the removal of SO2 were systematically investigated. The experimental results showed that the activity of ZIF8-A on SO2 removal was enhanced after being dispersed in n-heptanol. The SO2 saturation capacity increased with increasing proportion of ZIF8-A and SO(2)concentration. The optimal temperatures for SO2 absorption and desorption were found to be 25 and 120 degrees C, respectively. Under the optimal experimental conditions (25 degrees C and 4% SO2), the SO2 saturation capacity was 589 mg/g. Five continuous absorption-desorption cycles suggested a good regeneration performance. Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, ultraviolet analyses, and computational simulation indicated that SO2 mainly interacted with ZIF8-A via hydrogen bonds besides physical absorption. The simulation results further indicated that the enhanced SO2 adsorption performance of ZIF8-A when dispersed in n-heptanol was due to the lower self-diffusion coefficient and higher isosteric heat of SO2 molecules in ZIF8-A/nheptanol.

Welcome to talk about 61-82-5, If you have any questions, you can contact Xu, XQ; Wu, P; Li, CY; Zhao, KY; Wang, CR; Deng, RP; Zhang, JL or send Email.. Computed Properties of C2H4N4

Reference:
Article; Safari, Niloufar; Shirini, Farhad; Tajik, Hassan; Journal of Molecular Structure; vol. 1201; (2020);,
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics

Product Details of 61-82-5. I found the field of Chemistry very interesting. Saw the article Divalent manganese, cobalt, copper and cadmium complexes of (Z)-N-benzoyl-N ‘-(1H-1,2,4-triazol-3-yl)carbamimidothioic acid: Preparation, characterization, computational and biological studies published in 2021.0, Reprint Addresses Abu El-Reash, GM (corresponding author), Mansoura Univ, Dept Chem, Fac Sci, POB 70, Mansoura, Egypt.. The CAS is 61-82-5. Through research, I have a further understanding and discovery of 1H-1,2,4-Triazol-5-amine.

In this work, (Z)-N-benzoyl-N ‘-(1H-1,2,4-triazol-3-yl)carbamimidothioic acid and its Mn(II), Co(II), Cu(II) and Cd(II) complexes were introduced for the first time. This carbonyl thiourea ligand was prepared by the reaction of 1H-1,2,4-triazol-3-amine with benzoyl isothiocyanate. The structural elucidation of these compounds was performed using elemental analysis and spectral and magnetic measurements. Octahedral structures of all complexes, except Cd(II) complex with a tetrahedral geometry, were confirmed by applying DFT structural optimization. The thermal decomposition behaviour of metal complexes of carbonyl thiourea ligand is discussed. The calculation of kinetic parameters for prepared complexes (E-a, A, Delta H*, Delta S* and Delta G*) of all thermal degradation stages has been evaluated using two comparable approaches. Antimicrobial and ABTS-antioxidant studies indicated potent activity of Cd(II) complex compared with the other investigated compounds. The cytotoxic activity of the prepared compounds was investigated in vitro. The results indicated potent activity of Mn(II) complex against both HePG2 (liver carcinoma) and MCF-7 (breast carcinoma) cancer cells.

Bye, fridends, I hope you can learn more about C2H4N4, If you have any questions, you can browse other blog as well. See you lster.. Product Details of 61-82-5

Reference:
Article; Safari, Niloufar; Shirini, Farhad; Tajik, Hassan; Journal of Molecular Structure; vol. 1201; (2020);,
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics

In 2021.0 ACS APPL MATER INTER published article about CHEMICAL-MODIFICATIONS; EFFLUX PUMPS; NANOPARTICLES; RESISTANCE; MODE; GENERATION; BACTERIA; DELIVERY; MICRO in [Si, Zhangyong; Hou, Zheng; Vikhe, Yogesh Shankar; Thappeta, Kishore Reddy Venkata; Chan-Park, Mary B.] Nanyang Technol Univ NTU, Sch Chem & Biomed Engn, Singapore 637459, Singapore; [Si, Zhangyong; Hou, Zheng; Vikhe, Yogesh Shankar; Thappeta, Kishore Reddy Venkata; Chan-Park, Mary B.] Nanyang Technol Univ, Ctr Antimicrobial Bioengn, Singapore 637459, Singapore; [Thappeta, Kishore Reddy Venkata] Nanyang Technol Univ, Singapore Ctr Environm & Life Sci SCELSE, Singapore 637551, Singapore; [Marimuthu, Kalisvar; Ng, Oon Tek] Tan Tock Seng Hosp, Dept Infect Dis, Singapore 308442, Singapore; [Marimuthu, Kalisvar; Ng, Oon Tek] Natl Ctr Infect Dis, Singapore 637459, Singapore; [De, Partha Pratim] Tan Tock Seng Hosp, Dept Lab Med, Singapore 308433, Singapore; [Ng, Oon Tek; Pethe, Kevin] Nanyang Technol Univ, Lee Kong Chian Sch Med, Singapore 636921, Singapore; [Li, Peng] Northwestern Polytech Univ, Inst Flexible Elect, Xian 710072, Peoples R China; [Zhu, Yabin] Ningbo Univ, Med Sch, Ningbo 315211, Zhejiang, Peoples R China; [Pethe, Kevin] Nanyang Technol Univ, Sch Biol Sci, Singapore 636921, Singapore; [Chan-Park, Mary B.] Nanyang Technol Univ, Lee Kong Chian Sch Med, Singapore 637459, Singapore; [Chan-Park, Mary B.] Nanyang Technol Univ, Sch Phys & Math Sci, Singapore 637459, Singapore in 2021.0, Cited 49.0. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5. Application In Synthesis of 1H-1,2,4-Triazol-5-amine

Cationic polymers are promising antibacterial agents because bacteria have a low propensity to develop resistance against them, but they usually have low biocompatibility because of their hydrophobic moieties. Herein, we report a new biodegradable and biocompatible chitosan-derived cationic antibacterial polymer, 2,6-diamino chitosan (2,6-DAC). 2,6-DAC shows excellent broad-spectrum antimicrobial activity with minimum inhibitory concentrations (MICs) of 8-32 mu g/mL against clinically relevant and multidrug-resistant (MDR) bacteria including Listeria monocytogenes, Staphylococcus aureus, Escherichia coli, Klebsiella pneumoniae, Pseudomonas aeruginosa, and Acinetobacter baumannii. Furthermore, 2,6-DAC shows an excellent synergistic effect with various clinically relevant antibiotics proved by decreasing the MICs of the ntibiotics against MDR A. baumannii and methicillin-resistant Staphylococcus aureus to <1 mu g/mL. In vivo biocompatibility of 2,6-DAC is proved by a dosage of 100 mg/kg compound via oral administration and 25 mg/kg compound via intraperitoneal injection to mice; 2,6-DAC does not cause any weight loss and any significant change in liver and kidney biomarkers or the important blood electrolytes. The combinations of 2,6-DAC together with novobiocin and rifampicin show >2.4 log(10) reduction of A. baumannii in murine intraperitoneal and lung infection models. The novel chitosan derivative, 2,6-DAC, can be utilized as a biocompatible broad-spectrum cationic antimicrobial agent alone or in synergistic combination with various antibiotics.

Welcome to talk about 61-82-5, If you have any questions, you can contact Si, ZY; Hou, Z; Vikhe, YS; Thappeta, KRV; Marimuthu, K; De, PP; Ng, OT; Li, P; Zhu, YB; Pethe, K; Chan-Park, MB or send Email.. Application In Synthesis of 1H-1,2,4-Triazol-5-amine

Reference:
Article; Safari, Niloufar; Shirini, Farhad; Tajik, Hassan; Journal of Molecular Structure; vol. 1201; (2020);,
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics

An article Facile Regioselective On-Water Synthesis of 4,7-Dihydropyrazolo[1,5-a]Pyrimidines and 4,7-Dihydro[1,2,4]Triazolo[1,5-a]Pyrimidines WOS:000467059700011 published article about DESIGN; INHIBITOR; POTENT; 5-AMINOPYRAZOLE; ANAGLIPTIN; DINACICLIB; ESSRAMYCIN; PYRAZOLE in [Gol, Ravindra M.; Barot, Vijaykumar M.] Smt SM Panchal Sci Coll, Dept Chem, Talod 383215, Gujarat, India; [Khatri, Taslimahemad T.] Govt Sci Coll, Dept Chem, Chikhli 396521, Gujarat, India in 2019.0, Cited 50.0. Formula: C2H4N4. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5

Efficient and regioselective on-water synthesis of variously substituted 5-amino-4,7-dihydropyrazolo[1,5-a]pyrimidine-6-carbonitriles and 5-amino-4,7-dihydro[1,2,4]triazolo[1,5-a]pyrimidine-6-carbonitriles using 1,8-diazabicyclo[5.4.0]undec-7-ene as catalyst has been demonstrated. The reaction of 2-benzylidenemalononitriles and 3-aryl-1H-pyrazol-5-amines or 1H-1,2,4-triazol-5-amine allows to obtain the respective pyrazolo[1,5-a]pyrimidines and [1,2,4]triazolo[1,5-a]pyrimidines in high yields up to 93%. Main advantages of the developed synthetic protocol are application of water as environmentally friendly solvent, short reaction times, simple workup procedure that often does not require further purification of products, and broad substrate scope.

Bye, fridends, I hope you can learn more about C2H4N4, If you have any questions, you can browse other blog as well. See you lster.. Formula: C2H4N4

Reference:
Article; Safari, Niloufar; Shirini, Farhad; Tajik, Hassan; Journal of Molecular Structure; vol. 1201; (2020);,
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics

Authors Salimi, P; Norouzi, O; Pourhoseini, SEM; Bartocci, P; Tavasoli, A; Di Maria, F; Pirbazari, SM; Bidini, G; Fantozzi, F in PERGAMON-ELSEVIER SCIENCE LTD published article about CLADOPHORA-GLOMERATA MACROALGAE; BIO-OIL PRODUCTION; HYDROGEN-RICH GAS; ELECTROCHEMICAL PERFORMANCE; MARINE BIOMASS; FURAN COMPOUNDS; ENERGY-STORAGE; POROUS CARBON; ELECTROLYTE; NANOSHEETS in [Salimi, Pejman] Tarbiat Modares Univ, Fac Sci, Dept Phys Chem, POB 14115-175, Tehran, Iran; [Norouzi, Omid; Pourhoseini, S. E. M.; Tavasoli, Ahmad; Pirbazari, S. M.] Univ Tehran, Sch Chem, Coll Sci, Tehran, Iran; [Norouzi, Omid; Bartocci, Pietro; Bidini, Gianni; Fantozzi, Francesco] Univ Perugia, Dept Engn, Via G Duranti 67, I-06125 Perugia, Italy; [Norouzi, Omid; Di Maria, Francesco] Univ Perugia, Dipartimento Ingn, LAR5 Lab, Via G Duranti 93, I-06125 Perugia, Italy in 2019.0, Cited 67.0. SDS of cas: 61-82-5. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5

In this work, Cladophora glomerata, a harmful seaweed, is converted into an olive-shaped magnetic biochar by a slow pyrolysis process catalyzed by iron. The resultant magnetic biochar has a high surface area of 296.4 m(2) g(-1) with a carbon-rich structure that makes it suitable to be used as an electrode in Li ion batteries. The catalytic pyrolysis process showed significant effect on steam reforming, ketonization and deoxygenation and/or denitrogenation reactions. The overall quality of the pyrolysis products increases: the gas contains a higher percentage of hydrogen (up to 22%), while the oil is enriched in furans (with a selectivity of about 14%). The electrochemistry behavior of magnetic biochar has been also evaluated, using galvanostatic charge discharge, cyclic voltammetry (CV), and electrochemical impedance spectroscopy (EIS) analyses. The electrochemical results indicated a higher initial specific discharge capacity (740 mAh g(-1)) and great cyclic stability for magnetic electrode as compared to the biochar electrode. (C) 2019 Elsevier Ltd. All rights reserved.

Bye, fridends, I hope you can learn more about C2H4N4, If you have any questions, you can browse other blog as well. See you lster.. SDS of cas: 61-82-5

Reference:
Article; Safari, Niloufar; Shirini, Farhad; Tajik, Hassan; Journal of Molecular Structure; vol. 1201; (2020);,
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics

COA of Formula: C2H4N4. Zhang, SY; Liu, B; Zhang, SH; Yue, KF; Huang, ZQ in [Zhang, Shu-Yu; Liu, Bei; Zhang, Shi-Hui; Yue, Ke-Fen; Huang, Zhen-Qi] Northwest Univ, Natl Demonstrat Ctr Expt Chem Educ, Shaanxi Key Lab Physicoinorgan Chem, Minist Educ,Coll Chem & Mat Sci,Key Lab Synthet &, Xian 710122, Shaanxi, Peoples R China published Crystal structures and thermal decomposition kinetics of three new Zn(II) coordination polymers based on 3-amino-1,2,4-triazole in 2019.0, Cited 36.0. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5.

Solvothermal reactions of Zn(NO3)(2)center dot 6H(2)O, 3-amino-1,2,4-triazole as well as three different carboxylate ligands afforded three novel coordination polymers: [Zn-2 (azdc) (atz) (OH) (H2O)](n) (1), {[Zn-1.5 (btc)(0.5) (atz)]center dot 1.5H(2)O}(n) (2), and {[Zn-4 (nipa)(2) (atz)(3)(OH) (H2O)]center dot 2H(2)O}(n) (3) (H(2)azdc = 4,4′-azobenzoic acid, H(4)btc = 1,2,4,5-benzenetetracarboxylic acid, 5-H(2)nipa = 5-nitroisophthalic acid, Hatz = 3-amino-1,2,4-triazole). Moreover, the three coordination polymers have been characterized by IR spectroscopy, elemental analysis, single-crystal X-ray diffraction, and powder X-ray diffraction techniques. Complex 1 reveals a 2D layer structure, which is further connected through pi-pi stacking interactions forming a 3D supramolecular network. Complex 2 exhibits a 3D porous framework with 1D open channels. Complex 3 shows a 3D pillared-layer framework. Notably, the thermal decomposition processes of 1-3 were investigated by simultaneous TG-DSC techniques. The TG curves reveal that complexes 1-3 possess pretty good thermostability up to 321 degrees C, 416 degrees C and 418 degrees C, respectively. The apparent activation energy E (E-1 = 194.975 kJ mol(-1), E-2 = 220.360 kJ mol(-1), E-3 = 223.600 kJ mol(-1)) and the pre exponential factor A of skeleton collapse for the complexes 1-3 were calculated by the integral Kissinger’s method and Ozawa-Doyle’s method. The structural stability could be illustrated from the point of thermal decomposition kinetics.

COA of Formula: C2H4N4. Welcome to talk about 61-82-5, If you have any questions, you can contact Zhang, SY; Liu, B; Zhang, SH; Yue, KF; Huang, ZQ or send Email.

Reference:
Article; Safari, Niloufar; Shirini, Farhad; Tajik, Hassan; Journal of Molecular Structure; vol. 1201; (2020);,
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics

I found the field of Science & Technology – Other Topics very interesting. Saw the article Correlation between the structure and skin permeability of compounds published in 2021. HPLC of Formula: C2H4N4, Reprint Addresses Deng, JY; Yu, XL (corresponding author), Hunan Inst Engn, Hunan Prov Key Lab Environm Catalysis & Waste Reg, Coll Mat & Chem Engn, Xiangtan 411104, Hunan, Peoples R China.. The CAS is 61-82-5. Through research, I have a further understanding and discovery of 1H-1,2,4-Triazol-5-amine

A three-descriptor quantitative structure-activity/toxicity relationship (QSAR/QSTR) model was developed for the skin permeability of a sufficiently large data set consisting of 274 compounds, by applying support vector machine (SVM) together with genetic algorithm. The optimal SVM model possesses the coefficient of determination R-2 of 0.946 and root mean square (rms) error of 0.253 for the training set of 139 compounds; and a R-2 of 0.872 and rms of 0.302 for the test set of 135 compounds. Compared with other models reported in the literature, our SVM model shows better statistical performance in a model that deals with more samples in the test set. Therefore, applying a SVM algorithm to develop a nonlinear QSAR model for skin permeability was achieved.

HPLC of Formula: C2H4N4. Bye, fridends, I hope you can learn more about C2H4N4, If you have any questions, you can browse other blog as well. See you lster.

Reference:
Article; Safari, Niloufar; Shirini, Farhad; Tajik, Hassan; Journal of Molecular Structure; vol. 1201; (2020);,
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics

An article Synthesis and Characterization of Novel Azole Functionalized Poly(glycidyl methacrylate)s for Antibacterial and Anticandidal Activity WOS:000504668300004 published article about ANTIMICROBIAL ACTIVITY; QUATERNARY AMMONIUM; CHITOSAN; AMINE; MODE in [Rehman, Suriya; Alsalem, Zainab H.] Imam Abdulrahman Bin Faisal Univ, IRMC, Epidem Dis Res Dept, POB 1982, Dammam 31441, Saudi Arabia; [Gunday, Seyda T.; Bozkurt, Ayhan] Imam Abdulrahman Bin Faisal Univ, IRMC, Dept Biophys, POB 1982, Dammam 31441, Saudi Arabia in 2019.0, Cited 35.0. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5. Application In Synthesis of 1H-1,2,4-Triazol-5-amine

Background: Presently, rise in the infectious diseases and subsequent development of drug resistance, is a global threat to human health. However, much efforts are being made by scientists, to develop novel antimicrobials, and also to improve the efficacy of available drugs, in order to combat the life-threatening infections. Objective: Synthesis and characterization of azole functional polymer systems for antimicrobial applications. Materials and Methods: Poly(glycidyl methacrylate) (PGMA), was produced by free radical polymerization of the monomer, glycidyl methacrylate (GMA). Different azole functional PGMAs were produced, through chemical modification with imidazole (Im), 1H-1,2,4-triazole (Tri) and 3-amino-1,2,4-triazole (ATri), to get PGMA-Imi, PGMA-Tri and PGMA-ATri, respectively. The structure was confirmed by Fourier transform infrared spectroscopy (FT-IR), thermal properties were investigated by Thermogravimetric Analysis (TGA), and surface morphology was studied by scanning electron microscopy (SEM). Newly synthesized derivatives were further explored, for their antibacterial and anticandidal activities. Results: All the three synthesized and characterized derivatives, displayed a significant activity against the tested microorganisms. The minimum inhibitory concentration (MIC) and minimum bactericidal/fungicidal concentration (MBC/MFC), recorded against Staphylococcus aureus (S. aureus), was 0.5 &1mg/ml for PGMA-Imi, followed by PGMA-ATri & PGMA-Tri, respectively, followed by E. coli with, 1 & 2 mg/ml, 4 & 8 mg/ml, 4& 8 mg/ml, respectively, whereas the maximum MIC & MFC was recorded against C. albicans i.e., 8 & 16 mg/ml, 4 & 8 mg/ml ,4 & 8 mg/ml for PGMA-ATri, PGMA-Tri, PGMA-Imi, respectively. Conclusion: In the present work, we report on the state-of-the-art, azole functional polymer systems for antimicrobial applications. These findings suggest that the synthesized azole functional polymer films have antimicrobial properties, which could be potential candidates for coating applications in the biomedical and wastewater treatment field.

Application In Synthesis of 1H-1,2,4-Triazol-5-amine. Bye, fridends, I hope you can learn more about C2H4N4, If you have any questions, you can browse other blog as well. See you lster.

Reference:
Article; Safari, Niloufar; Shirini, Farhad; Tajik, Hassan; Journal of Molecular Structure; vol. 1201; (2020);,
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics

Recommanded Product: 1H-1,2,4-Triazol-5-amine. Recently I am researching about DISSOLVED ORGANIC-MATTER; MOLECULAR-OXYGEN; PHOTOLYSIS; DEGRADATION; PESTICIDES; MECHANISM; ATRAZINE; STATE, Saw an article supported by the Russian Foundation for Basic ResearchRussian Foundation for Basic Research (RFBR) [18-53-00002_BEL, 17-03-00252]; Belarusian Republican Foundation for Fundamental Research [N~ F18R-140]. Published in PERGAMON-ELSEVIER SCIENCE LTD in OXFORD ,Authors: Pozdnyakov, IP; Parkhats, MV. The CAS is 61-82-5. Through research, I have a further understanding and discovery of 1H-1,2,4-Triazol-5-amine

Reactivity of the singlet oxygen (SO), which is assumed to be one of the important oxidizers in natural waters, towards to a set of persistent herbicides, was measured for the first time using time resolved luminescence technique. It was observed that rate constants of SO reactions with the majority of studied herbicides are less than 10(6) M(-1)s(-1) allowing to conclude about negligible participation of SO in oxidation of the compounds in natural waters. (C) 2020 Elsevier Ltd. All rights reserved.

Bye, fridends, I hope you can learn more about C2H4N4, If you have any questions, you can browse other blog as well. See you lster.. Recommanded Product: 1H-1,2,4-Triazol-5-amine

Reference:
Article; Safari, Niloufar; Shirini, Farhad; Tajik, Hassan; Journal of Molecular Structure; vol. 1201; (2020);,
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics