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Final Thoughts on Chemistry for C2H4N4

SDS of cas: 61-82-5. About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Zhang, DY; Gao, T; Xu, RJ; Sun, L; Zhang, CF; Bai, L; Chen, W; Liu, KY; Zhou, Y; Jiao, X; Zhang, GH; Guo, RL; Li, JX; Gao, Y; Jiao, WJ; Tian, H or concate me.

Zhang, DY; Gao, T; Xu, RJ; Sun, L; Zhang, CF; Bai, L; Chen, W; Liu, KY; Zhou, Y; Jiao, X; Zhang, GH; Guo, RL; Li, JX; Gao, Y; Jiao, WJ; Tian, H in [Zhang, Dong-Yang; Xu, Rong-Jian; Jiao, Wen-Jie] Qingdao Univ, Affiliated Hosp, Dept Thorac Surg, Qingdao 266000, Peoples R China; [Zhang, Dong-Yang; Gao, Tong; Sun, Lu; Zhang, Chun-Feng; Bai, Long; Chen, Wei; Liu, Kai-Yu; Zhou, Yang; Jiao, Xuan; Zhang, Gui-Huan; Tian, Hai] Harbin Med Univ, Affiliated Hosp 2, Future Med Lab, Harbin, Peoples R China; [Gao, Tong; Sun, Lu; Zhang, Chun-Feng; Bai, Long; Chen, Wei; Liu, Kai-Yu; Zhou, Yang; Jiao, Xuan; Zhang, Gui-Huan; Tian, Hai] Harbin Med Univ, Affiliated Hosp 2, Dept Cardiovasc Surg, Harbin 150086, Peoples R China; [Guo, Rui-Lin; Li, Jing-Xuan; Gao, Ying] Harbin Med Univ, Clin Coll 2, Harbin, Peoples R China published SIRT3 Transfection of Aged Human Bone Marrow-Derived Mesenchymal Stem Cells Improves Cell Therapy-Mediated Myocardial Repair in 2020.0, Cited 37.0. 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.

Sirtuin 3 (SIRT3) is a deacetylase important for antioxidant protection, cell longevity, and aging. We hypothesized that SIRT3 improve oxidative resistance of aged cells and improve cell therapy in aged patients. In vitro, the proliferation and oxidative resistance of human mesenchymal stem cells (hMSCs) significantly declined with age. The expression and activity of antioxidant enzymes, including catalase (CAT) and manganese superoxide dismutase (MnSOD), increased after transfection of SIRT3 in hMSCs from older donors (O-hMSCs). The protein level of Forkhead box O3a (FOXO3a) in nucleus increased after SIRT3 overexpression. The antioxidant capacity of O-hMSCs increased after SIRT3 overexpression. 3-Amino-1,2,4-triazole (3-AT, CAT inhibitor) or diethyldithiocarbamate (DETC, SOD inhibitor) that was used to inhibit CAT or SOD activity significantly blocked the antioxidant function of SIRT3. When two inhibitors were used together, the antioxidant function of SIRT3 almost disappeared. Following myocardial infarction and intramyocardial injections of O-hMSCs in rats in vivo, the survival rate of O-hMSCs increased by SIRT3 transfection. The cardiac function of rats was improved after SIRT3-overexpressed O-hMSC transplantation. The infarct size, collagen content, and expression levels of matrix metalloproteinase 2 (MMP2) and MMP9 decreased. Besides, the protein level of vascular endothelial growth factor A and vascular density increased after cell transplantation with SIRT3-modified O-hMSCs. These results indicate that damage resistance of hMSCs decline with age and SIRT3 might protect O-hMSCs against oxidative damage by activating CAT and MnSOD through transferring FOXO3a into nucleus. Meanwhile, the therapeutic effect of aged hMSC transplantation can be improved by SIRT3 overexpression.

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

Archives for Chemistry Experiments of 61-82-5

About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Wang, S; Shen, DD; Zhao, LJ; Yuan, XH; Cheng, JL; Yu, B; Zheng, YC; Liu, HM or concate me.. Quality Control of 1H-1,2,4-Triazol-5-amine

Quality Control of 1H-1,2,4-Triazol-5-amine. Wang, S; Shen, DD; Zhao, LJ; Yuan, XH; Cheng, JL; Yu, B; Zheng, YC; Liu, HM in [Yu, Bin; Zheng, Yichao; Liu, Hongmin] Zhengzhou Univ, Key Lab Technol Drug Preparat, Minist Educ China, Zhengzhou 450001, Peoples R China; Zhengzhou Univ, Sch Pharmaceut Sci, Zhengzhou 450001, Peoples R China published Discovery of [1,2,4]triazolo[1,5-a]pyrimidine derivatives as new bromodomain-containing protein 4 (BRD4) inhibitors in 2020, Cited 47. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5.

Targeting bromodomain-containing protein 4 (BRD4) has been proved to be an effective strategy for cancer therapy. To date, numerous BRD4 inhibitors and degraders have been identified, some of which have advanced into clinical trials. In this work, a focused library of new [1,2,4]triazolo[1,5-a]pyrimidine derivatives were discovered to be able to inhibit BRD4. WS-722 inactivated BRD4 (BD1/BD2), BRD2 (BD1 BD2) and BRD3 (BD1/BD2) broadly with the IC50 values less than 5 mu mol/L. Besides, WS-722 inhibited growth of THP-1 cells with an IC50 value of 3.86 mu mol/L. Like (+)-JQ1, WS-722 inhibited BRD4 in a reversible manner and enhanced protein stability. Docking studies showed that WS-722 occupied the central acetyl-lysine (Kac) binding cavity and formed a hydrogen bond with Asn140. In THP-1 cells, WS-722 showed target engagement to BRD4. Cellular effects of WS-722 on THP-1 cells were also examined, showing that WS-722 could block c-MYC expression, induce G0/G1 phase arrest and p21 up-regulation, and promote differentiation of THP-1 cells. BRD4 inhibition by WS-722 resulted in cell apoptosis and up-regulated expression of cleaved caspased-3/7 and PARP in THP-1 cell lines. The [1,2,4]triazolo[1,5-a] pyrimidine is a new template for the development of new BRD4 inhibitors. (C) 2019 Chinese Chemical Society and Institute of Materia Medica, Chinese Academy of Medical Sciences. Published by Elsevier B.V. All rights reserved.

Final Thoughts on Chemistry for 1H-1,2,4-Triazol-5-amine

Product Details of 61-82-5. About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Wang, S; Shen, DD; Zhao, LJ; Yuan, XH; Cheng, JL; Yu, B; Zheng, YC; Liu, HM or concate me.

Wang, S; Shen, DD; Zhao, LJ; Yuan, XH; Cheng, JL; Yu, B; Zheng, YC; Liu, HM in [Yu, Bin; Zheng, Yichao; Liu, Hongmin] Zhengzhou Univ, Key Lab Technol Drug Preparat, Minist Educ China, Zhengzhou 450001, Peoples R China; Zhengzhou Univ, Sch Pharmaceut Sci, Zhengzhou 450001, Peoples R China published Discovery of [1,2,4]triazolo[1,5-a]pyrimidine derivatives as new bromodomain-containing protein 4 (BRD4) inhibitors in 2020, Cited 47. 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.

Product Details of 61-82-5. About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Wang, S; Shen, DD; Zhao, LJ; Yuan, XH; Cheng, JL; Yu, B; Zheng, YC; Liu, HM or concate me.

How did you first get involved in researching C2H4N4

Category: Triazoles. About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Tang, YZ; Huang, HL; Peng, B; Chang, YJ; Li, Y; Zhong, CL or concate me.

An article A thiadiazole-based covalent triazine framework nanosheet for highly selective and sensitive primary aromatic amine detection among various amines WOS:000561168500038 published article about METAL-ORGANIC FRAMEWORK; FLUORESCENT-PROBE; IONIC LIQUIDS; ANILINE; LUMINESCENT; BENZOTHIADIAZOLE; ADSORPTION; MOLECULES; REMOVAL; CAPTURE in [Tang, Yuanzhe; Huang, Hongliang; Peng, Ben; Chang, Yanjiao; Li, Yang; Zhong, Chongli] Tiangong Univ, State Key Lab Separat Membranes & Membrane Proc, Tianjin 300387, Peoples R China; [Tang, Yuanzhe; Huang, Hongliang; Peng, Ben; Chang, Yanjiao; Li, Yang; Zhong, Chongli] Tiangong Univ, Sch Chem & Chem Engn, Tianjin 300387, Peoples R China; [Zhong, Chongli] Beijing Univ Chem Technol, Coll Chem Engn, Beijing 100029, Peoples R China in 2020.0, Cited 53.0. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5. Category: Triazoles

Primary aromatic amines (PAAs), as a class of persistent and highly toxic organic pollutants, have been posing a great threat to human health and the environment. Therefore, the design and preparation of a highly sensitive and selective luminescent probe to detect PAAs among various amines are important but challenging. In this work, by introducing electron-deficient monomer 4,4 ‘-(benzo[c][1,2,5]thiadiazole-4,7-diyl)dibenzaldehyde (BTDD) with an aggregation-caused quenching behavior into the 2D framework, fluorescent ultrathin covalent triazine framework (F-CTF) nanosheets were constructed. Compared with the aggregated BTDD monomer, the obtained F-CTF-3 nanosheet shows much higher fluorescence quantum yield due to the BTDD fragment being well dispersed in the 2D framework. The F-CTF-3 nanosheet exhibits high stability, high porosity, and high fluorescence performance and has a rich electron-deficient unit in the pore channel, making it an ideal platform for sensing electron-rich PAA molecules. In fact, the F-CTF-3 nanosheet shows high sensitivity and selectivity for PAA detection by fluorescence quenching, among various amines, covering some classic aliphatic amines, heterocyclic amines, secondary aromatic amines and tertiary aromatic amines. To the best of our knowledge, it is the first reported fluorescent sensor for selective sensing of PAAs among various amines. Moreover, F-CTF-3 exhibits unprecedented low detection limits of 11.7 and 1.47 nM toward phenylamine (PA) andp-phenylenediamine (PDA), respectively, surpassing all the reported fluorescent sensors. The combination of experimental analysis and density functional theory (DFT) calculations demonstrates that the unique PAA detection performance of F-CTF-3 can be attributed to the static quenching process, which is confirmed by the formation of a ground-state fluorescence-quenched complex on account of the hydrogen bonding interactions between F-CTF-3 and PAAs. This work not only provides a thiadiazole-based 2D fluorescent organic framework nanosheet, but also an excellent fluorescent sensor with unexpected sensitivity and selectivity for PAA detection.

Category: Triazoles. About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Tang, YZ; Huang, HL; Peng, B; Chang, YJ; Li, Y; Zhong, CL or concate me.

Let`s talk about compound :61-82-5

Computed Properties of C2H4N4. About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Zacarias, NVO; van Veldhoven, JPD; den Hollander, LS; Dogan, B; Openy, J; Hsiao, YY; Lenselink, EB; Heitman, LH; IJzerman, AP or concate me.

Authors Zacarias, NVO; van Veldhoven, JPD; den Hollander, LS; Dogan, B; Openy, J; Hsiao, YY; Lenselink, EB; Heitman, LH; IJzerman, AP in AMER CHEMICAL SOC published article about BINDING-SITE; SMALL-MOLECULE; POTENT; DRUGS in [Zacarias, Natalia V. Ortiz; van Veldhoven, Jacobus P. D.; den Hollander, Lisa S.; Dogan, Burak; Openy, Joseph; Hsiao, Ya-Yun; Lenselink, Eelke B.; Heitman, Laura H.; IJzerman, Adriaan P.] Leiden Univ, Div Drug Discovery & Safety, Leiden Acad Ctr Drug Res, POB 9502, NL-2300 RA Leiden, Netherlands in 2019.0, Cited 60.0. Computed Properties of C2H4N4. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5

CC chemokine receptors 2 (CCR2) and 5 (CCR5) are involved in many inflammatory diseases; however, most CCR2 and CCR5 clinical candidates have been unsuccessful. (Pre)clinical evidence suggests that dual CCR2/CCR5 inhibition might be more effective in the treatment of such multifactorial diseases. In this regard, the highly conserved intracellular binding site in chemokine receptors provides a new avenue for the design of multitarget ligands. In this study, we synthesized and evaluated the biological activity of a series of triazolopyrimidinone derivatives in CCR2 and CCR5. Radioligand binding assays first showed that they bind to the intracellular site of CCR2, and in combination with functional assays on CCR5, we explored structure-affinity/activity relationships in both receptors. Although most compounds were CCR2-selective, 39 and 43 inhibited beta-arrestin recruitment in CCR5 with high potency. Moreover, these compounds displayed an insurmountable mechanism of inhibition in both receptors, which holds promise for improved efficacy in inflammatory diseases.

Brief introduction of 1H-1,2,4-Triazol-5-amine

About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Vadivel, S; Hariganesh, S; Paul, B; Rajendran, S; Habibi-Yangjeh, A; Maruthamani, D; Kumaravel, M or concate me.. Product Details of 61-82-5

An article Synthesis of novel AgCl loaded g-C3N5 with ultrahigh activity as visible light photocatalyst for pollutants degradation WOS:000501784200050 published article about FABRICATION; CATALYSTS in [Vadivel, S.; Hariganesh, S.; Maruthamani, D.; Kumaravel, M.] PSG Coll Technol, Dept Chem, Coimbatore 641004, Tamil Nadu, India; [Paul, Bappi] Natl Inst Technol Silchar, Dept Chem, Silchar 788010, Assam, India; [Rajendran, Saravanan] Univ Tarapaca, Dept Mech Engn, Fac Engn, Avda Gen Velasquez, Arica 1775, Chile; [Habibi-Yangjeh, Aziz] Univ Mohaghegh, Dept Chem, Fac Sci, POB 179, Ardebil, Iran in 2020.0, Cited 22.0. 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

We report the photocatalytic property of a novel AgCl loaded carbon nitride (AgCl/g-C3N5) composite was prepared by a simple precipitation route. The brown colored g-C3N5 was synthesized by a nano-hard templating method using 3-amino-1,2,4-triazole precursor. The morphology, crystallinity and optical properties of the AgCl/g-C3N5 composite were characterized using the X-ray diffraction analysis (XRD), transmission electron microscopy (TEM), and diffuse reflectance spectroscopy (UV-DRS) spectroscopy. The rhodamine B (RhB) removal efficiency was reached 96% within 30 min, which could be attributed to the effective formation of a heterojunction and excellent visible light absorption of AgCl by g-C3N5 incorporation.

Chemical Properties and Facts of 61-82-5

Recommanded Product: 61-82-5. About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Mabkhot, YN; Kaal, NA; Alterary, S; Mubarak, MS; Alsayari, A; Bin Muhsinah, A or concate me.

An article New Thiophene Derivatives as Antimicrobial Agents WOS:000492694300015 published article about ANTIOXIDANT ACTIVITIES; ESSENTIAL OIL in [Mabkhot, Yahia Nasser] King Khalid Univ, Coll Pharm, Dept Pharmaceut Chem, Abha, Saudi Arabia; [Kaal, Nahed Ahmed; Alterary, Seham] King Saud Univ, Coll Sci, Dept Chem, POB 2455, Riyadh 11451, Saudi Arabia; [Mubarak, Mohammad S.] Univ Jordan, Dept Chem, Amman 11942, Jordan; [Alsayari, Abdulrhman; Bin Muhsinah, Abdullatif] King Khalid Univ, Coll Pharm, Dept Pharmacognosy, Abha, Saudi Arabia in 2019.0, Cited 25.0. 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

Phenacylbromide derivatives constitute a multilateral group of precursors for the synthesis of numerous heterocycles of organic compounds. Briefly, 5-(2-bromo-acetyl)-substituted-thiophene derivative has been used as a synthon for synthesis of new thiophene-containing compounds through the reaction with nucleophilic nitrogen compounds and thioamides. The suggested structures of the newly synthesized thiophene compounds were confirmed and assured with different spectroscopic tools and with CHN elemental analysis. Additionally, the antimicrobial activity of these thiophene compounds was recorded to investigate their potency against various types of bacteria and fungi. Results showed that these compounds exhibit significant inhibitory activity against the growth of tested bacterial and fungal strains and that some derivatives were more potent than the employed reference drugs.

Recommanded Product: 61-82-5. About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Mabkhot, YN; Kaal, NA; Alterary, S; Mubarak, MS; Alsayari, A; Bin Muhsinah, A or concate me.

Chemical Properties and Facts of C2H4N4

Safety of 1H-1,2,4-Triazol-5-amine. About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Zhu, TY; Yu, X; Yi, M; Wang, Y or concate me.

In 2020.0 ACS SUSTAIN CHEM ENG published article about COMPOSITE MEMBRANES; WATER-ADSORPTION; HYBRID MEMBRANES; PDMS MEMBRANE; PERVAPORATION; RECOVERY; MIXTURES; ALCOHOL; SOLVENT; PERMEABILITY in [Zhu, Tengyang; Yu, Xi; Yi, Ming; Wang, Yan] Huazhong Univ Sci & Technol, Sch Chem & Chem Engn, Minist Educ, Key Lab Mat Chem Energy Convers & Storage, Wuhan 430074, Peoples R China; [Zhu, Tengyang; Yu, Xi; Yi, Ming; Wang, Yan] Huazhong Univ Sci & Technol, Sch Chem & Chem Engn, Hubei Key Lab Mat Chem & Serv Failure, Wuhan 430074, Peoples R China in 2020.0, Cited 64.0. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5. Safety of 1H-1,2,4-Triazol-5-amine

The interfacial design is critical in preparing high-performance mixed matrix membranes (MMMs), especially for the separation of larger sized components from mixtures. Herein, a facile and novel strategy was employed to design covalently linked zeolitic imidazolate framework-8-polydimethylsiloxane (ZIF-8@PDMS) MMMs without interfacial defects by a onestep synthesis route for ethanol recovery from ethanol aqueous solution. In this strategy, 3-glycidyloxypropyltrimethoxysilane (GOPTS) worked as the covalent linker of PDMS and amine-functionalized ZIF-8 nanoparticles (AZIF-8) simultaneously. The chemical structures and morphologies of AZIF-8 and AZIF-8@PDMS MMMs were demonstrated by various characterization techniques. The results exhibited that AZIF-8 and the MMMs were successfully prepared and AZIF-8 as the filler displayed better dispersion in the PDMS matrix and compatibility with the PDMS matrix as compared to ZIF-8 or GOPTS-modified ZIF-8 (GZIF-8). Therefore, AZIF-8@PDMS MMMs showed more excellent separation performance than ZIF-8 or GZIF-8-filled MMMs. In particular, AZIF-8@PDMS MMM with 7 wt % AZIF-8 loading exhibited the highest separation factor of 17.7 and a comparable total flux of 585.6 g/m(2) h at 40 degrees C with 5 wt % ethanol aqueous solution, which were improved by 176.6 and 34.5%, respectively, in comparison with the pristine PDMS membrane, breaking the trade-off effect between the flux and separation factor. This study might provide some new insights into the fabrication of high-performance MMMs for pervaporation recovery of various organic systems.

Safety of 1H-1,2,4-Triazol-5-amine. About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Zhu, TY; Yu, X; Yi, M; Wang, Y or concate me.

What Kind of Chemistry Facts Are We Going to Learn About C2H4N4

HPLC of Formula: C2H4N4. About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Wang, FG; Liu, YY; Shi, YQ; Han, DL; Wu, YY; Ye, WX; Yang, HL; Li, GW; Cui, F; Wan, SB; Lai, JB; Yang, CW or concate me.

HPLC of Formula: C2H4N4. In 2020.0 PLANT PHYSIOL published article about ABIOTIC STRESS; ARABIDOPSIS; SUMO; PROTEINS; DROUGHT; CONJUGATION; BINDING; TOLERANCE; PATHWAYS; IDENTIFY in [Wang, Feige; Shi, Yaqiao; Han, Danlu; Wu, Yuanyuan; Ye, Weixian; Yang, Huanling; Lai, Jianbin; Yang, Chengwei] South China Normal Univ, Sch Life Sci, Guangdong Prov Key Lab Biotechnol Plant Dev, Guangzhou 510631, Peoples R China; [Liu, Yiyang; Li, Guowei; Cui, Feng; Wan, Shubo] Shandong Acad Agr Sci, Biotechnol Res Ctr, Jinan 250100, Peoples R China; [Liu, Yiyang; Li, Guowei; Cui, Feng; Wan, Shubo] Shandong Prov Key Lab Crop Genet Improvement Ecol, Jinan 250100, Peoples R China in 2020.0, 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.

Heat stress (HS) has serious effects on plant development, resulting in heavy agricultural losses. A critical transcription factor network is involved in plant adaptation to high temperature. DEHYDRATION RESPONSIVE ELEMENT-BINDING PROTEIN2A (DREB2A) is a key transcription factor that functions in plant thermotolerance. The DREB2A protein is unstable under normal temperature and is degraded by the 26S proteasome; however, the mechanism by which DREB2A protein stability dramatically increases in response to HS remains poorly understood. In this study, we found that the DREB2A protein of Arabidopsis (Arabidopsis thaliana) is stabilized under high temperature by the posttranslational modification SUMOylation. Biochemical data indicated that DREB2A is SUMOylated at K163, a conserved residue adjacent to the negative regulatory domain during HS. SUMOylation of DREB2A suppresses its interaction with BPM2, a ubiquitin ligase component, consequently increasing DREB2A protein stability under high temperature. In addition, analysis of plant heat tolerance and marker gene expression indicated that DREB2A SUMOylation is essential for its function in the HS response. Collectively, our data reveal a role for SUMOylation in the maintenance of DREB2A stability under high temperature, thus improving our understanding of the regulatory mechanisms underlying HS response in plant cells. SUMOylation increases the protein stability of DREB2A, a key transcription factor in the response to heat stress in plant cells.

Simple exploration of 1H-1,2,4-Triazol-5-amine

Product Details of 61-82-5. About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Li, Z; Lu, Y; Zhang, S; Sun, XW; Dang, TY; Zhang, Z; Tian, HR; Liu, SX or concate me.

Product Details of 61-82-5. Recently I am researching about METAL-ORGANIC FRAMEWORKS, Saw an article supported by the National Natural Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [21872021, 21671033]. Published in WILEY-V C H VERLAG GMBH in WEINHEIM ,Authors: Li, Z; Lu, Y; Zhang, S; Sun, XW; Dang, TY; Zhang, Z; Tian, HR; Liu, SX. The CAS is 61-82-5. Through research, I have a further understanding and discovery of 1H-1,2,4-Triazol-5-amine

Nowadays, the research of proton conductive materials has been extended from traditional sulfonated polymers to novel crystalline solid materials. It is important but still challenging to develop high-performance proton-conducting materials suitable for proton exchange membrane fuel cells (PEMFCs). Considering the features of molybdenum oxide and triazole in the construction of proton-conducting material, two triazole-modified molybdenum oxides, [MoO3(trz)(0.5)]1and [H(atrz)(4)[(atrz)(2)(gamma-Mo8O26)] . 2H(2)O2(trz=1,2,4-triazole, atrz=3-amino-1,2,4-triazole), were re-synthesized under optimized synthetic conditions, and their proton-conducting performances were investigated.1and2show high proton conductivities of 1.94×10(-2) S cm(-1)(85 degrees C, 95 % RH) and 1.3×10(-3) S cm(-1)(65 degrees C, 95 % RH), respectively.

Product Details of 61-82-5. About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Li, Z; Lu, Y; Zhang, S; Sun, XW; Dang, TY; Zhang, Z; Tian, HR; Liu, SX or concate me.