Guanidines
Guanidines are a class of organic compounds characterized by the presence of one or more guanidine groups, which consist of two amino groups linked to a nitrogen atom. These molecules exhibit unique properties and are widely used in various applications due to their amphoteric nature and strong basicity. Common guanidine derivatives include L-lysine di-guanide, ethylene-diamino-tetra-acetic acid (EDTA), and melamine. In pharmaceuticals, guanidines are employed as antimicrobial agents, antifungal drugs, and in the treatment of HIV. Additionally, they find applications in agriculture as insecticides and herbicides. Guanidines also play a significant role in the manufacturing of dyes, plastics, and polymers due to their ability to form hydrogen bonds with other molecules, enhancing solubility and stability.
| Structure | Chemical Name | CAS | MF |
|---|---|---|---|
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Guanidine,N-[3-[[4-[(aminoiminomethyl)amino]butyl]amino]propyl]- | 2465-97-6 | C9H23N7 |
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1,3-Dimethylguanidine | 3324-71-8 | C3H9N3 |
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3-carbamimidoyl-1-ethylthiourea | 44830-57-1 | C4H10N4S |
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N-methylguanidine | 471-29-4 | C2H7N3 |
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Guanidine,N-cyano-N',N''-bis(hydroxymethyl)- | 40074-04-2 | C4H8N4O2 |
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Synthalin | 111-23-9 | C12H28N6 |
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Radam | 115044-19-4 | C18H41N7 |
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Guancydine | 1113-10-6 | C7H14N4 |
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Guanidine-15N3 Hydrochloride | 121616-39-5 | CH6ClN3 |
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Guanidine,N,N'''-(dithiodi-2,1-ethanediyl)bis- | 1072-13-5 | C6H16N6S2 |
Related Literature
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Xinhuan Wang,Shuangfei Cai,Cui Qi Analyst, 2017,142, 2500-2506
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Yaling Zhang,Chunhui Dai,Shiwei Zhou,Bin Liu Chem. Commun., 2018,54, 10092-10095
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Gang Pan,Yi-jie Bao,Jie Xu,Tao Liu,Cheng Liu,Yan-yan Qiu,Xiao-jing Shi,Hui Yu,Ting-ting Jia,Xia Yuan,Ze-ting Yuan,Yi-jun Cao RSC Adv., 2016,6, 42109-42119
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Jason Wan Lab Chip, 2020,20, 4528-4538
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Yukiya Kitayama Polym. Chem., 2014,5, 2784-2792
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