Day: February 11, 2022

In 2021.0 CURR BIOL published article about OLFACTORY-BULB; LABELED LINES; INHIBITION; ORGANIZATION; REPRESENTATIONS; MECHANISMS; RECEPTORS; PATHWAYS; AMYGDALA; NEURONS in [Qiu, Qiang; Wu, Yunming; Ma, Limei; Yu, C. Ron] Stowers Inst Med Res, 1000 East 50th St, Kansas City, MO 64110 USA; [Yu, C. Ron] Univ Kansas, Med Ctr, Dept Anat & Cell Biol, 3901 Rainbow Blvd, Kansas City, KS 66160 USA; [Yu, C. Ron] Twitter YuLab19, Kansas City, KS 66160 USA in 2021.0, Cited 79.0. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5. Recommanded Product: 61-82-5

Odors carrying intrinsic values often trigger instinctive aversive or attractive responses. It is not known how innate valence is encoded. An intuitive model suggests that the information is conveyed through specific channels in hardwired circuits along the olfactory pathway, insulated from influences of other odors, to trigger innate responses. Here, we show that in mice, mixing innately aversive or attractive odors with a neutral odor and, surprisingly, mixing two odors with the same valence, abolish the innate behavioral responses. Recordings from the olfactory bulb indicate that odors are not masked at the level of peripheral activation and glomeruli independently encode components in the mixture. In contrast, crosstalk among the mitral and tufted (M/T) cells changes their patterns of activity such that those elicited by the mixtures can no longer be linearly decoded as separate components. The changes in behavioral and M/T cell responses are associated with reduced activation of brain areas linked to odor preferences. Thus, crosstalk among odor channels at the earliest processing stage in the olfactory pathway leads to re-coding of odor identity to abolish valence associated with the odors. These results are inconsistent with insulated labeled lines and support a model of a common mechanism of odor recognition for both innate and learned valence associations.

Recommanded Product: 61-82-5. Welcome to talk about 61-82-5, If you have any questions, you can contact Qiu, Q; Wu, YM; Ma, LM; Yu, CR 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

Authors Sweidan, NI; El-Abadelah, MM; Nazer, MZ; Voelter, W in WALTER DE GRUYTER GMBH published article about THIENOPYRIDINONE ANTIBACTERIALS; BIOLOGICAL EVALUATION; PART; DERIVATIVES; ACIDS in [Voelter, Wolfgang] Univ Tubingen, Interfak Inst Biochem, Hoppe Seyler Str 4, D-72076 Tubingen, Germany; [Sweidan, Nuha, I] Univ Petra, Fac Art & Sci, Dept Chem, Amman 961343, Jordan; [El-Abadelah, Mustafa M.; Nazer, Musa Z.] Univ Jordan, Fac Sci, Dept Chem, Amman 11942, Jordan in 2020.0, Cited 23.0. Category: Triazoles. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5

Interaction of methyl 3-ethoxy-2-(2,5-dichloro-3-thenoyl)acrylate (I) with 3-aminopyrazole and 3- amino-1,2,4-triazole generated the respective pyrazolo [1,5-alpha]pyrimidine (4) and triazolo[1,5-alpha]pyrimidine (7). The formation of 4 entails selective and consecutive displacement of the 3-ethoxy and methoxy (ester) anions in I by 3-NH2 and 1-NH of 3-aminopyrazole. On the other hand, the formation of 7 implies selective displacement of 3-ethoxy in I by the ring-NH followed by cyclocondensation involving the keto group in I and 3-NH2 of aminotriazole. This latter selective displacement sequence is also followed by 3-amino-5-hydroxypyrazole in its reaction with I. The structures of the new compounds are supported by microanalytical and spectral data.

Category: Triazoles. Welcome to talk about 61-82-5, If you have any questions, you can contact Sweidan, NI; El-Abadelah, MM; Nazer, MZ; Voelter, W 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

COA of Formula: C2H4N4. In 2021.0 J APPL POLYM SCI published article about MOLECULAR-STRUCTURE; HYDROGEN-BOND; POLYMERS; PERFORMANCE; SEPARATION; RUBBER; TOUGH in [Xiong, Chengtian; He, Hezhi; Xue, Bin; Wang, Yi; Li, Jiqian; Zhu, Zhiwen] South China Univ Technol, Sch Mech & Automot Engn, Natl Engn Res Ctr Novel Equipment Polymer Proc, Guangzhou 510640, Peoples R China; [Xiong, Chengtian; He, Hezhi; Xue, Bin; Wang, Yi; Li, Jiqian; Zhu, Zhiwen] South China Univ Technol, Sch Mech & Automot Engn, Key Lab Polymer Proc Engn, Minist Educ, Guangzhou, Peoples R China; [Xiong, Chengtian; He, Hezhi; Xue, Bin; Wang, Yi; Li, Jiqian; Zhu, Zhiwen] South China Univ Technol, Sch Mech & Automot Engn, Guangdong Prov Key Lab Tech & Equipment Macromol, Guangzhou, Peoples R China; [Li, Xiaoqing] Guangzhou Automobile Grp Component Co Ltd, Guangzhou, Peoples R China in 2021.0, Cited 34.0. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5.

Due to the disadvantages of lower tensile strength and fracture toughness, the widely application of Ethylene-propylene-diene-monomer rubber (EPDM) has been limited. In this study, a thermally reversible healing EPDM based elastomer with H-bonding and Zn-based-bonding dynamic cross-link network was prepared. The influence of mole ratio of ATA/MAH on tensile strength and fracture energy of mEPDM(0)-xATA was investigated. The results showed that increasing the content of ATA brings about a gradual improvement in tensile strength of the mEPDM(0)-xATA. Especially when the mole ratio of ATA/MAH is 1, the fracture energy of mEPDM(0)-ATA is dramatically enhanced to 33.9 MJ/m(3), which is best among the ratios studied in our research. After curing, the effect of ZnCl(2)content on tensile strength and fracture energy of mEPDM-ATA-nZn was also studied. Meanwhile, the uniaxial cyclic loading-unloading tensile test was used to study the viscous damping properties of mEPDM-ATA-0.4Zn, which showed reversible repair properties after heat treatment. The results of dynamic rheological measurement showed that the damping properties were improved.

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.. COA of 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

In 2019.0 ANAL CHEM published article about SERS DETECTION; NANOPARTICLES; POINT; PRECONCENTRATION; MOLECULES; FILMS in [Zhang, Qinmei; Li, Dan; Cao, Xiukai; Deng, Wei] Shanghai Inst Technol, Sch Chem & Environm Engn, 100 Haiquan Rd, Shanghai 201418, Peoples R China; [Gu, Haixin] Shanghai Fire Res Inst MEM, 918 Minjing Rd, Shanghai 200438, Peoples R China 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. HPLC of Formula: C2H4N4

Development of flexible surface-enhanced Raman spectroscopy (SERS) substrate with controllable hot spots has spurred increasing interest because of its unique structure and plasmonic properties. Here, charged poly(vinyl alcohol) microgels containing silver nanoparticles are developed by using microfluidic emulsification to produce a smart SERS sensor with charge screening and signals amplification. Importantly, this charged microgel enables the selective concentration of counter-charged molecules and induces the formation of assembled arrays at an immiscible liquid-liquid interface because of the electrostatic interaction. The SERS-active microgels arrays possess controllable structures and facilitate on-site determination of charged pesticides with an enhancement factor of 5.0 x 10(5). Such nanostructures present the ease of assembly, stability, and reproducibility which allow multiplex detection of analytes at aqueous and organic phases without any pretreatment of complex matrix samples. The interfacial sensing platform for on-site SERS analysis of charged pesticides will open vast possibilities for a wide range of in-field applications.

About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Zhang, QM; Li, D; Cao, XK; Gu, HX; Deng, W or concate me.. HPLC of 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

Sayed, GH; Azab, ME; Anwer, KE in [Sayed, Galal H.; Azab, Mohammad E.; Anwer, Kuris E.] Ain Shams Univ, Organ Chem Lab, Chem Dept, Fac Sci, Cairo 11566, Egypt published Conventional and Microwave-Assisted Synthesis and Biological Activity Study of Novel Heterocycles Containing Pyran Moiety in 2019.0, Cited 30.0. Quality Control of 1H-1,2,4-Triazol-5-amine. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5.

Under both conventional and microwave methods, 2-amino-4H-pyran-3-carbonitrile derivative 1 was synthesized and reacted with different reagents. Thus, 2-amino-4H-pyran-3-carbonitrile derivative was treated with chloroacetyl chloride, phenyl isocyanate, cyanoacetic acid, benzoyl chloride, triethyl orthoformate, acetic anhydride/H2SO4, arylidene malononitrile, urea, and/or p-aminosulphaguanidine producing chloroacetamide, 3-phenylurea, cyanoacetamide, N-benzoylpyran, ethylformimidate, pyranopyrimidin-4-one, pyranopyridine, pyranopyrimidin-2-one, and pyranopyrimidin-2-imine derivatives, respectively. Meanwhile, compound 1 was reacted with ethyl bromoacetate, phenacyl bromide, phthalic anhydride, different aromatic amines, and/or acetic acid/H2SO4 to produce 5-aminopyrano[2,3-b]pyrrole-6-carboxylate, dihydropyrano[2,3-b]pyrrole-6-yl-(phenyl)methanone, 1,3-dioxoisoindolinyl pyran, 1,4-dihydropyridine, and 2-hydroxy-1,4-dihydropyridine derivatives, respectively. On the other hand, when compound 1 was allowed to react with maleic anhydride and/or hydrazine hydrate, pyran-4-oxobut-2-enoic acid and 3-aminopyranopyrazole derivatives were obtained, respectively. Reaction of pyran-4-oxobut-2-enoic acid with malononitrile under different conditions gave 2-(furan-2-yl)-4H-pyran and 2-(4H-pyran-2-yl)-1H-pyrrole derivatives, while condensation of 3-aminopyranopyrazole with benzaldehyde gave 1,4-dihydropyrano[2,3-c]pyrazol-3-yl-1-phenylmethanimine derivative. The newly synthesized compounds were characterized by the spectroscopic tools IR, H-1-NMR, C-13-NMR, MS, and elemental analysis. Some of these compounds have been screened in vitro for antimicrobial activity against different strains of bacteria and fungi and also were tested against two cancer cell lines: mammary gland breast cancer (MCF-7) and colon cancer (HCT-118).

Quality Control of 1H-1,2,4-Triazol-5-amine. Welcome to talk about 61-82-5, If you have any questions, you can contact Sayed, GH; Azab, ME; Anwer, KE 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

Name: 1H-1,2,4-Triazol-5-amine. Authors Liu, XT; Xing, SS; Xu, YT; Chen, RQ; Lin, C; Guo, LQ in PERGAMON-ELSEVIER SCIENCE LTD published article about in [Liu, Xiaotao; Xing, Shanshan; Guo, Liangqia] Fuzhou Univ, Coll Chem, Fujian Prov Key Lab Anal & Detect Technol Food Sa, Minist Educ,Key Lab Analyt Sci Food Safety & Biol, Fuzhou 350116, Peoples R China; [Xu, Yuanteng; Lin, Chang] Fujian Med Univ, Affiliated Hosp 1, Dept Otorhinolaryngol, Fuzhou 350005, Peoples R China; [Chen, Ruiqing] Fujian Med Univ, Affiliated Hosp 1, Cent Lab, Fuzhou 350005, Peoples R China in 2021.0, Cited 40.0. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5

Graphitic carbon nitride (g-C3N4) has been shown as a promising visible-light photosensitizer for photodynamic therapy (PDT) application. Nevertheless, its therapeutic efficiency is limited by the low efficiency of visible-light utilization. To overcome this issue, 3-amino-1,2,4-triazole-derived graphitic carbon nitride nanosheets (g-C3N5 NSs) are prepared for PDT application. The addition of nitrogen-rich triazole group into the g-C3N4 motif significantly makes the light absorption of g-C3N5 NSs red-shift with the band gap down to 1.95 eV, corresponding to a absorption edge at a wavelength of 636 nm. g-C3N5 NSs generate superoxide anion radicals (O-2(center dot-)) and singlet oxygen (O-1(2)) under the irradiation of a low-intensity white light emitting diode. Owing to the high efficiency of visible-light utilization, g-C3N5 NSs show about 9.5 fold photocatalytic activity of g-C3N4 NSs. In vitro anticancer studies based on the results of CCK-8 assay, Calcein-AM/PI cell-survival assay and photo-induced intracellular ROS level analysis in living HeLa cells demonstrate the potential of g-C3N5 NSs as a low-toxic and biocompatible high-efficient photosensitizer for PDT. (C) 2020 Elsevier B.V. All rights reserved.

Welcome to talk about 61-82-5, If you have any questions, you can contact Liu, XT; Xing, SS; Xu, YT; Chen, RQ; Lin, C; Guo, LQ or send Email.. Name: 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

Application In Synthesis of 1H-1,2,4-Triazol-5-amine. I found the field of Chemistry very interesting. Saw the article A Stable Zn-Based Metal-Organic Framework as an Efficient Catalyst for Carbon Dioxide Cycloaddition and Alcoholysis at Mild Conditions published in 2020.0, Reprint Addresses Wang, J (corresponding author), Nanchang Univ, Minist Educ, Key Lab Poyang Environm & Resource Utilizat, Nanchang 330031, Jiangxi, Peoples R China.; Wang, J (corresponding author), Nanchang Univ, Sch Resource Environm & Chem Engn, Nanchang 330031, Jiangxi, Peoples R China.; Deng, SG (corresponding author), Arizona State Univ, Sch Engn Matter Transport & Energy, 551 E Tyler Mall, Tempe, AZ 85287 USA.. The CAS is 61-82-5. Through research, I have a further understanding and discovery of 1H-1,2,4-Triazol-5-amine.

Developing highly efficient heterogeneous catalysts for cycloaddition of CO2 and epoxides to produce cyclic carbonates is promising but challenging. In this work, a novel three-dimensional metal organic framework (MOF) with cylinder pore systems and unsaturated Zn sites has been demonstrated as potent candidate in CO2 fixation at mild and solvent-free conditions. The Zn(atz)(bdc)(0.5), where atz = aminotriazole and H(2)bdc = terephthalic, exhibits microporous nature that can regulate the catalytic interaction of active centers and substrates. The structure stability has been systematically investigated and proven to be sufficient for practical application. Furthermore, the cooperative effects of porosity, CO2 binding affinity, activation centers, and synergism with co-catalyst have been deeply investigated. Moreover, high propylene epoxide conversion (97%) and selectivity (> 99%) have been achieved at mild conditions (60 degrees C and 1 MPa) with excellent cycle stability. Owing to the well-defined pore system, an obvious substrates selectivity has been clearly observed. A possible catalytic mechanism has been proposed and verified by DFT calculations. Furthermore, the prepared Zn-MOF can also be used as an efficient heterogeneous catalyst for the reaction of epoxides with alcohols to produce beta-alkoxy alcohol. [GRAPHICS] .

Application In Synthesis of 1H-1,2,4-Triazol-5-amine. Welcome to talk about 61-82-5, If you have any questions, you can contact Luo, ZQ; Wang, J; He, YQ; Ao, Q; Deng, Q; Zeng, ZL; Wang, HM; Deng, SG 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

Application In Synthesis of 1H-1,2,4-Triazol-5-amine. Authors Ben Ali, A; El Bakri, Y; Lai, CH; Sebhaoui, J; El Ghayati, L; Essassi, E; Mague, JT in INT UNION CRYSTALLOGRAPHY published article about in [Ben Ali, Abdelkader] Mohammed V Univ Rabat, Fac Sci, Ctr Sci Mat, Lab Chim Appl Mat, Ave Ibn,BP 1014, Rabat, Morocco; [El Bakri, Youness; Sebhaoui, Jihad; El Ghayati, Lhoussaine; Essassi, El Mokhtar] Univ Mohammed 5, Fac Sci, Ctr Rech Sci Med, URAC 21,Pole Competence Pharmacochim, Av Ibn Battouta,BP 1014, Rabat, Morocco; [Lai, Chin-Hung] Chung Shan Med Univ, Dept Med Appl Chem, Taichung 40241, Taiwan; [Lai, Chin-Hung] Chung Shan Med Univ Hosp, Dept Med Educ, Taichung 40241, Taiwan; [Mague, Joel T.] Tulane Univ, Dept Chem, New Orleans, LA 70118 USA in 2019.0, Cited 38.0. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5

In the title molecule, C13H16N4O3, the mean planes of the phenyl and triazole rings are nearly perpendicular to one another as a result of the intramolecular C-H center dot center dot center dot O and C-H center dot center dot center dot pi(ring) interactions. In the crystal, layers parallel to (101) are generated by O-H center dot center dot center dot N, N-H center dot center dot center dot O and N-H center dot center dot center dot N hydrogen bonds. The layers are connected by inversion-related pairs of C-H center dot center dot center dot O hydrogen bonds. The experimental molecular structure is close to the gas-phase geometryoptimized structure calculated by DFT methods. Hirshfeld surface analysis indicates that the most important interaction involving hydrogen in the title compound is the H center dot center dot center dot H contact. The contribution of the H center dot center dot center dot O, H center dot center dot center dot N, and H center dot center dot center dot H contacts are 13.6, 16.1, and 54.6%, respectively.

Application In Synthesis of 1H-1,2,4-Triazol-5-amine. About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Ben Ali, A; El Bakri, Y; Lai, CH; Sebhaoui, J; El Ghayati, L; Essassi, E; Mague, JT or concate me.

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

Recently I am researching about HYDROGEN-PEROXIDE; INDUCED APOPTOSIS; OXIDATIVE STRESS; H2O2-INDUCED APOPTOSIS; SIGNAL-TRANSDUCTION; PC12 CELLS; DEATH; ACTIVATION; ACID; ACATALASEMIA, Saw an article supported by the JC Bose National fellowship [SB/SE/JCB-017/2015]. Published in SPRINGER/PLENUM PUBLISHERS in NEW YORK ,Authors: Nagarkoti, S; Dubey, M; Sadaf, S; Awasthi, D; Chandra, T; Jagavelu, K; Kumar, S; Dikshit, M. The CAS is 61-82-5. Through research, I have a further understanding and discovery of 1H-1,2,4-Triazol-5-amine. SDS of cas: 61-82-5

Neutrophil survival and oxidative stress during inflammatory conditions are linked to tissue damage. The present study explores less understood role of catalase, the enzyme catalysing hydrogen peroxide decomposition, in neutrophil survival/death. Importantly, inhibition of catalase activity following S-glutathionylation in the PMA, NO, or zymosan-activated neutrophils or treatment with catalase inhibitor led to neutrophil death. On the contrary, introducing reducing environment by TCEP rescued catalase activity and significantly improved neutrophil survival. Furthermore, augmentation in ROS generation by NOX-2 activation or induction of mitochondrial ROS by Antimycin-A induced catalase S-glutathionylation and cell death, which was prevented in the neutrophil cytosolic factor1 (NCF-1-/-) cells or was rescued by MitoTEMPO, a mitochondrial ROS scavenger, thus, suggesting a correlation between catalase S-glutathionylation/activity inhibition and reduced neutrophil survival. Altogether, enhanced NOX2 activation/mitochondrial dysfunction led to reduced survival of human and mice neutrophils, due to H2O2 accumulation, S-glutathionylation of catalase, and reduction in its enzymatic activity. The present study thus demonstrated mitigation of catalase activity under oxidative stress-impacted neutrophil survival.

Welcome to talk about 61-82-5, If you have any questions, you can contact Nagarkoti, S; Dubey, M; Sadaf, S; Awasthi, D; Chandra, T; Jagavelu, K; Kumar, S; Dikshit, M or send Email.. 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

An article A graphene oxide functionalized energetic coordination polymer possesses good thermostability, heat release and combustion catalytic performance for ammonium perchlorate WOS:000527532000023 published article about METAL-ORGANIC FRAMEWORKS; THERMAL-DECOMPOSITION; GRAPHITE; RDX; EXPLOSIVES; COMPLEXES; BEHAVIOR in [Yang, Desuo; Mo, Wenjiao; Zhang, Sheng; Hu, Dengwei] Baoji Univ Arts & Sci, Coll Chem & Chem Engn, Baoji 721013, Peoples R China; [Li, Bing] Ningxia Univ, Dept Chem & Chem Engn, Yinchuan 750021, Ningxia, Peoples R China; [Chen, Sanping] Northwest Univ, Coll Chem & Mat Sci, Key Lab Synthet & Nat Funct Mol Chem, Minis Educ, Xian 710069, Shaanxi, Peoples R China in 2020.0, Cited 45.0. Application In Synthesis of 1H-1,2,4-Triazol-5-amine. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5

A new energetic coordination polymer (ECP) composite, namely GO-Cu(II)-AmTZ, has been synthesized by 3-amino-1,2,4-triazole (AmTZ) and multifunctional graphene oxide (GO) coordination with Cu(II) successively. The ECP composite was further characterized through SEM, EDS and XPS analysis as well as FTIR and Raman spectroscopy. It shows high thermostability, high decomposition heat release and insensitivity to mechanical stimuli. What’s more, thermal analysis data for ammonium perchlorate (AP) have been obtained by mechanically mixing GO-Cu(II)-AmTZ and AP. The low-temperature decomposition (LTD, 335.3 degrees C) and high-temperature decomposition (HTD, 441.3 degrees C) peaks of AP were reduced to an exothermic peak at 298.4 degrees C at a heating rate of 10 degrees C min(-1). GO-Cu(II)-AmTZ exhibits outstanding catalytic performance by decreasing the activation energy from 168.7 kJ mol(-1) to 122.4 kJ mol(-1), indicating its promising application as a combustion catalyst for improving the thermal-catalytic decomposition performance of energetic materials largely. In addition, thermal analysis techniques including thermogravimetry coupled with mass spectrometry (TG/MS) and thermogravimetry coupled with infrared spectrometry (TG/IR) were employed to determine the decomposition mechanisms.

Application In Synthesis of 1H-1,2,4-Triazol-5-amine. About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Yang, DS; Mo, WJ; Zhang, S; Li, B; Hu, DW; Chen, SP or concate me.

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