• 1. Emerging investigator series: bacteriophages as nano engineering tools for quality monitoring and pathogen detection in water and wastewater
  Fereshteh Bayat Environ. Sci.: Nano, 2021,8, 367-389
• 2. Essential effect of the electrolyte on the mechanical and chemical degradation of LiNi0.8Co0.15Al0.05O2 cathodes upon long-term cycling??
  Xiaoming Liu,Zachary D. Hood,Wangda Li,Donovan N. Leonard,Arumugam Manthiram,Miaofang Chi J. Mater. Chem. A, 2021,9, 2111-2119
• 3. Esterase-responsive polymeric prodrug-based tumor targeting nanoparticles for improved anti-tumor performance against colon cancer?
  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
• 4. Emergence of cationic polyamine dendrimersomes: design, stimuli sensitivity and potential biomedical applications
  Partha Laskar,Christine Dufès Nanoscale Adv., 2021,3, 6007-6026
• 5. Fate of nitrogen-15 in the subsequent growing season of greenhouse tomato plants (Lycopersicon esculentum Mill) as influenced by alternate partial root-zone irrigation
  Maomao Hou,Fenglin Zhong,Qiu Jin,Enjiang Liu,Jie Feng,Tengyun Wang,Yue Gao RSC Adv., 2017,7, 34392-34400

• Solvents and Organic Chemicals Organic Compounds Organic nitrogen compounds Organonitrogen compounds Amines Secondary amines

Professional Introduction to (5-Aminopentyl)(ethyl)amine (CAS No. 258818-11-0)

(5-Aminopentyl)(ethyl)amine, identified by the Chemical Abstracts Service Number (CAS No.) 258818-11-0, is a significant compound in the field of chemical and pharmaceutical research. This introduction provides a comprehensive overview of its chemical properties, applications, and recent advancements in its utilization within the pharmaceutical and biotechnology sectors.

The compound (5-Aminopentyl)(ethyl)amine is an organic amine with a molecular structure that includes both primary and secondary amine functional groups. Its molecular formula is C?H??N?, reflecting a chain of eight carbon atoms with ethyl and amine substituents. The presence of multiple amine groups makes it a versatile intermediate in organic synthesis, particularly in the development of pharmaceuticals and specialty chemicals.

In recent years, there has been growing interest in (5-Aminopentyl)(ethyl)amine due to its role as a building block in the synthesis of more complex molecules. Its structural features allow for modifications that can enhance binding affinity and selectivity, making it valuable in drug design. For instance, derivatives of this compound have been explored as potential ligands for enzyme inhibition and receptor modulation.

One of the most notable applications of (5-Aminopentyl)(ethyl)amine is in the development of peptide mimetics and peptidomimetics. These molecules mimic the structure and function of natural peptides but with improved stability and pharmacokinetic properties. The compound's ability to form stable hydrogen bonds and interact with biological targets makes it an ideal candidate for such applications. Recent studies have demonstrated its use in creating novel compounds that exhibit potent activity against various therapeutic targets.

The pharmaceutical industry has also leveraged (5-Aminopentyl)(ethyl)amine in the synthesis of small-molecule drugs. Its incorporation into drug candidates has led to the discovery of several promising compounds that are currently undergoing preclinical evaluation. These include molecules targeting neurological disorders, infectious diseases, and cancer. The versatility of this compound allows chemists to fine-tune its properties, optimizing it for specific biological interactions.

Advances in synthetic chemistry have further expanded the utility of (5-Aminopentyl)(ethyl)amine. Modern techniques such as flow chemistry and catalytic processes have enabled more efficient and scalable production methods. These innovations not only reduce costs but also improve the purity and yield of the final product. As a result, researchers can now access larger quantities of this compound for their studies, accelerating the pace of discovery.

In addition to its pharmaceutical applications, (5-Aminopentyl)(ethyl)amine has found utility in materials science and biotechnology. Its ability to form stable complexes with metal ions makes it valuable in the development of metal-organic frameworks (MOFs) and other functional materials. These materials have potential applications in gas storage, catalysis, and sensing technologies.

The biotechnology sector has also explored the use of (5-Aminopentyl)(ethyl)amine in protein engineering and molecular biology research. Its incorporation into peptides and proteins can alter their conformational properties, influencing their function and stability. This has opened up new avenues for developing biotherapeutics with enhanced efficacy and durability.

Recent research has highlighted the importance of understanding the stereochemistry of (5-Aminopentyl)(ethyl)amine. Studies have shown that enantiomeric purity can significantly impact the biological activity of derived compounds. Advances in chiral synthesis techniques have enabled researchers to produce enantiomerically pure forms of this compound, which are crucial for developing drugs with minimal side effects.

The environmental impact of synthesizing and using (5-Aminopentyl)(ethyl)amine is another area of growing interest. Researchers are actively exploring green chemistry approaches to minimize waste and reduce energy consumption during production. These efforts align with broader sustainability goals within the chemical industry, ensuring that compounds like this one can be produced responsibly.

In conclusion, (5-Aminopentyl)(ethyl)amine (CAS No. 258818-11-0) is a multifaceted compound with significant applications across multiple industries. Its role as an intermediate in pharmaceutical synthesis, its utility in materials science, and its contributions to biotechnology underscore its importance in modern research. As scientific understanding continues to evolve, it is likely that new applications for this compound will emerge, further solidifying its place as a cornerstone molecule in chemical innovation.

• 2098070-20-1(2-(3-(Pyridin-3-yl)-1H-pyrazol-1-yl)acetimidamide)
• 2680771-01-9(4-cyclopentyl-3-{(prop-2-en-1-yloxy)carbonylamino}butanoic acid)
• 1444113-98-7(N-(3-cyanothiolan-3-yl)-2-[(2,2,2-trifluoroethyl)sulfanyl]pyridine-4-carboxamide)
• 332062-08-5(Fmoc-S-3-amino-4,4-diphenyl-butyric acid)
• 1270529-38-8(1,2,3,4,5,6-Hexahydro-[2,3]bipyridinyl-6-ol)
• 941977-17-9(N'-(3-chloro-2-methylphenyl)-N-2-(dimethylamino)-2-(naphthalen-1-yl)ethylethanediamide)
• 2138166-62-6(2,2-Difluoro-3-[methyl(2-methylbutyl)amino]propanoic acid)
• 89640-58-4(2-Iodo-4-nitrophenylhydrazine)
• 1449132-38-0(3-Fluoro-5-(2-fluoro-5-methylbenzylcarbamoyl)benzeneboronic acid)
• 2034271-14-0(2-(1H-indol-3-yl)-N-{[6-(thiophen-2-yl)-[1,2,4]triazolo[4,3-b]pyridazin-3-yl]methyl}acetamide)