Online Database of Chemicals from Around the World

3-Amino-5-mercapto-1,2,4-triazole
[CAS# 16691-43-3]

List of Suppliers
Simagchem Corporation China Inquire  
+86 13806087780
sale@simagchem.com
Chemical manufacturer since 2002
chemBlink standard supplier since 2008
Hefei TNJ Chemical Industry Co., Ltd. China Inquire  
+86 (551) 6541-8684
sales@tnjchem.com
Chemical manufacturer since 2001
chemBlink standard supplier since 2010
SL Drugs and Pharmaceuticals Pvt. Ltd. India Inquire  
+91 (40) 6661-1133
enquiry@sldrugs.com
Chemical distributor since 1999
chemBlink standard supplier since 2010
BOC Sciences USA Inquire  
+1 (631) 485-4226
info@bocsci.com
Chemical manufacturer
chemBlink standard supplier since 2010
LOBA Feinchemie AG Austria Inquire  
+43 (223) 277-391
sales@loba.co.at
Chemical distributor
chemBlink standard supplier since 2012
PTG Advanced Catalyst Co. Limited China Inquire  
+86 (10) 6073-9051
market@ptgchem.com
Chemical distributor since 2013
chemBlink standard supplier since 2014
Leap Chem Co., Ltd. China Inquire  
+86 (852) 3060-6658
market19@leapchem.com
QQ chat
Chemical manufacturer since 2006
chemBlink standard supplier since 2015
Shanghai Yuanye Bio-Technology Co., Ltd. China Inquire  
+86 (21) 6184-5781
+86 13585604150
shyysw053@163.com
QQ chat
Chemical manufacturer since 2009
chemBlink standard supplier since 2016
Complete supplier list of 3-Amino-5-mercapto-1,2,4-triazole
Identification
Classification Pharmaceutical intermediate >> Heterocyclic compound intermediate >> Pyrimidine compound >> Amine
Name 3-Amino-5-mercapto-1,2,4-triazole
Synonyms 3-Amino-1,2,4-triazole-5-thiol; 5-Amino-4H-1,2,4-triazole-3-thiol
Molecular Structure CAS # 16691-43-3, 3-Amino-5-mercapto-1,2,4-triazole, 3-Amino-1,2,4-triazole-5-thiol, 5-Amino-4H-1,2,4-triazole-3-thiol
Molecular Formula C2H4N4S
Molecular Weight 116.14
CAS Registry Number 16691-43-3
EC Number 240-735-6
SMILES C1(=NC(=S)NN1)N
Properties
Solubility Soluble (hot water) (Expl.)
Density 1.7±0.1 g/cm3, Calc.*
Melting point 300 ºC (Expl.)
Index of Refraction 1.791, Calc.*
Boiling Point 389.1±25.0 ºC (760 mmHg), Calc.*
Flash Point 189.1±23.2 ºC, Calc.*
* Calculated using Advanced Chemistry Development (ACD/Labs) Software.
Safety Data
Hazard Symbols symbol   GHS07 Warning    Details
Hazard Statements H315-H319-H335    Details
Precautionary Statements P261-P264-P264+P265-P271-P280-P302+P352-P304+P340-P305+P351+P338-P319-P321-P332+P317-P337+P317-P362+P364-P403+P233-P405-P501    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Skin irritationSkin Irrit.2H315
Specific target organ toxicity - single exposureSTOT SE3H335
Eye irritationEye Irrit.2H319
Acute toxicityAcute Tox.4H302
Eye irritationEye Irrit.2AH319
Acute toxicityAcute Tox.4H332
Acute toxicityAcute Tox.4H312
SDS Available
up Discovory and Applicatios
3-Amino-5-mercapto-1,2,4-triazole is a chemical compound with a triazole ring structure that contains both amino and mercapto groups. This compound is of interest in various fields of chemistry due to its diverse reactivity and potential for applications in medicinal chemistry, material science, and agricultural chemistry. The discovery of 3-amino-5-mercapto-1,2,4-triazole can be traced back to research focused on the synthesis of heterocyclic compounds with biologically active properties. Triazoles, in general, have attracted significant attention because of their ability to interact with biological systems, making them promising candidates for drug development and other industrial applications.

The discovery of 3-amino-5-mercapto-1,2,4-triazole is part of a broader effort to explore the reactivity of heterocyclic compounds that combine nitrogen, sulfur, and carbon in their structures. The presence of the amino group provides opportunities for the compound to engage in various chemical reactions, including nucleophilic substitution and condensation reactions. The mercapto group, on the other hand, is known for its ability to form strong interactions with metals, which is particularly useful in coordinating compounds and catalysis.

In medicinal chemistry, 3-amino-5-mercapto-1,2,4-triazole has shown potential for use in the development of drugs aimed at treating conditions related to fungal infections, cancer, and other diseases. Its structure is similar to certain antifungal agents, and research has suggested that it may possess antifungal properties. Moreover, its ability to form metal complexes has raised interest in its potential use in anticancer therapies, where metal-based drugs are known for their effectiveness in targeting and killing cancer cells. The thiol group in particular is of interest for its ability to interact with proteins and enzymes, making 3-amino-5-mercapto-1,2,4-triazole a potential candidate for enzyme inhibition studies and other therapeutic applications.

Beyond medicinal chemistry, 3-amino-5-mercapto-1,2,4-triazole has found applications in the field of agriculture, specifically in the development of new fungicides and pest control agents. The compound's structural features, including the mercapto and amino groups, enable it to interact with various biological targets in plants and microorganisms. As agricultural research focuses on finding new ways to protect crops from fungal diseases and pests, compounds like 3-amino-5-mercapto-1,2,4-triazole offer a promising option due to their bioactivity and potential for modifying existing chemical agents to enhance their efficacy and reduce environmental impact.

Additionally, the compound has been studied for its role in materials science, particularly in the development of novel catalysts and polymerization agents. The ability of 3-amino-5-mercapto-1,2,4-triazole to form coordination complexes with metal ions makes it a potential candidate for use in catalysis, where it could aid in accelerating chemical reactions under mild conditions. Its application in polymer chemistry has also been explored, with a focus on improving the synthesis of various polymers with desirable properties.

Despite its promising applications, the use of 3-amino-5-mercapto-1,2,4-triazole is still an area of ongoing research. Challenges remain in fully understanding its toxicity, stability, and the range of its reactivity under different conditions. Further studies are required to optimize its synthesis, improve its biological activity, and explore its full potential in industrial applications.

In conclusion, 3-amino-5-mercapto-1,2,4-triazole is a compound with significant promise in fields ranging from medicinal chemistry to materials science and agriculture. Its unique structural features allow for a wide range of applications, and its potential for the development of new therapeutic agents and industrial products makes it a compound of continued interest for research and development.
Market Analysis Reports
List of Reports Available for 3-Amino-5-mercapto-1,2,4-triazole
Related Products
N-[4-[[(2R)-2-Amino-3-mercapto-1-oxopropyl]amino]benzoyl]-L-methionine  2-Amino-3-mercapto-1-propanol  N-[[5-[[(2R)-2-Amino-3-mercaptopropyl]amino][1,1'-biphenyl]-2-yl]carbonyl]-L-methionine methyl ester monohydrochloride  N-[(2S)-((2R)-2-Amino-3-mercaptopropylamino)-3-methylbutyl]-L-phenylalanyl-L-methionine  3-Amino-4-mercaptopyridine  4-Amino-3-mercaptopyridine  4-Amino-2-mercaptopyrimidine-5-carbonitrile  3-Amino-4-mercaptoquinoline  5-Amino-2-mercaptothiazole  5-Amino-2-mercapto-4-thiazolecarboxamide  Aminomercuric chloride  Aminomethanesulfonic acid  4-Amino-1-methanesulfonylpiperidine  Aminomethanetrispropionic acid  3'-Amino-4'-methoxyacetanilide  2-Amino-4'-methoxyacetophenone  2'-Amino-4'-methoxyacetophenone  2-Amino-4'-methoxyacetophenone hydrochloride  4-Amino-3-methoxyazobenzene-3'-sulfonic acid sodium salt  2-Amino-4-methoxybenzaldehyde