Category: Triazoles

Authors Zhou, SR; Dong, Z; Yang, R; Wang, XY; Ye, ZW in WILEY-V C H VERLAG GMBH published article about in [Zhou, Shengren; Dong, Zhen; Yang, Rui; Wang, Xieyang; Ye, Zhiwen] Nanjing Univ Sci & Technol, Sch Chem Engn, Nanjing 210094, Peoples R China in 2021.0, Cited 24.0. Safety 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

Two energetic compounds, erythritol tetranitrocarbamate (ETNC) and pentaerythritol tetranitrocarbamate (PETNC), and their salts, were synthesized in three steps, characterized and compared. All synthesized compounds were characterized by IR, DSC and multinuclear NMR spectroscopy. Four compounds were further investigated by single crystal X-ray diffraction. All nonmetal salts show extremely low mechanical sensitivity (IS >= 30 J; FS >= 360 N). The heats of formation were calculated using Gaussian 09, and the detonation performances were calculated using EXPLO 5. Although these nonmetal salts are lower than the neutral compounds ETNC (D: 7960 m s(-1), P: 27.4 GPa) and PETNC (D: 7629 m s(-1), P: 24.3 GPa), they possess high detonation performances that are better than TNT. Erythritol-based and corresponding pentaerythritol-based energetic materials were compared in terms of their thermostability, detonation velocity and detonation pressure. They were also compared in their respective series. ETNC and PETNC and their salts have short preparation steps and are easy to isolate in high yields, and thus have promising potential applications as explosives.

Safety of 1H-1,2,4-Triazol-5-amine. Welcome to talk about 61-82-5, If you have any questions, you can contact Zhou, SR; Dong, Z; Yang, R; Wang, XY; Ye, ZW 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

An article Synthesis and properties of gem-dinitro energetic salts based on 1,2,4-oxadiazole with low impact sensitivity WOS:000609189100004 published article about HIGH-NITROGEN; DERIVATIVES; EXPLOSIVES in [Lu, Tian; He, Yuna; Song, Jia; Hou, Zhengwen; Yin, Hongquan; Chen, Fu-Xue] Beijing Inst Technol, Sch Chem Sc Chem Engn, Liangxiang Campus,8 Liangxiang East Rd, Beijing 102488, Peoples R China; [Fan, Guijuan] CAEP, Inst Chem Mat, Mianyang 621050, Sichuan, Peoples R China in 2021.0, Cited 37.0. 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: 1H-1,2,4-Triazol-5-amine

Eight energetic salts with a gem-dinitro group based on 1,2,4-oxadiazole were developed. All of the structures were confirmed by infrared (IR) spectroscopy, H-1 and C-13 nuclear magnetic resonance (NMR) spectroscopy, and high-resolution mass spectrometry (HRMS), and single-crystal X-ray diffraction was used to determine the structures of the pivotal intermediate 3-(chlorodinitromethyl)-5-methyl-1,2,4-oxadiazole (3), the potassium salt (4) and the hydrazinium salt (7). All of them are insensitive to impact (>40 J) and have higher energy levels than trinitrotoluene (TNT).

Recommanded Product: 1H-1,2,4-Triazol-5-amine. Welcome to talk about 61-82-5, If you have any questions, you can contact Lu, T; He, YN; Song, J; Hou, ZW; Yin, HQ; Fan, GJ; Chen, FX 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

In 2019.0 J SOLID STATE CHEM published article about METAL-ORGANIC FRAMEWORK; EFFICIENT; ACID; 5-AMINO-TETRAZOLATE; ANTIBIOTICS; SEPARATION; COMPLEXES; SERIES; MOFS 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 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. COA of Formula: C2H4N4

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

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.

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

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.

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.

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 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.

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 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.

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 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.

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

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 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.

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.

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 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.

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