• 1. Fe3O4/PEG-SO3H as a heterogeneous and magnetically-recyclable nanocatalyst for the oxidation of sulfides to sulfones or sulfoxides
  Saeideh Mirfakhraei,Malak Hekmati,Fereshteh Hosseini Eshbala,Hojat Veisi New J. Chem., 2018,42, 1757-1761
• 2. Dissolution of cork biopolymers in biocompatible ionic liquids
  Helga Garcia,Rui Ferreira,Marija Petkovic,Jamie L. Ferguson,Maria C. Leit?o,H. Q. Nimal Gunaratne,Luís Paulo N. Rebelo Green Chem., 2010,12, 367-369
• 3. Fe3O4@PANI: a magnetic polyaniline nanomaterial for highly efficient and handy enrichment of intact N-glycopeptides??
  Zhizhen Lai,Mo Zhang,Jinyu Zhou,Tianjing Chen,Dan Li,Xuejing Shen,Jia Liu,Jiang Zhou,Zhili Li Analyst, 2021,146, 4261-4267
• 4. Establishment and implications of a characterization method for magnetic nanoparticle using cell tracking velocimetry and magnetic susceptibility modified solutions
  Huading Zhang,Lee R. Moore,Maciej Zborowski,P. Stephen Williams,Shlomo Margel,Jeffrey J. Chalmers Analyst, 2005,130, 514-527
• 5. Fe3O4 nanosphere@microporous organic networks: enhanced anode performances in lithium ion batteries through carbonization?
  Byungho Lim,Jaewon Jin,Jin Yoo,Seung Yong Han,Kyeongyeol Kim,Sungah Kang,Nojin Park,Sang Moon Lee,Hae Jin Kim,Seung Uk Son Chem. Commun., 2014,50, 7723-7726

Comprehensive Overview of 1-Butylcyclopentan-1-amine (CAS No. 68288-41-5): Properties, Applications, and Industry Insights

1-Butylcyclopentan-1-amine (CAS No. 68288-41-5) is a specialized organic compound belonging to the class of cycloalkylamines. Its molecular structure features a cyclopentane ring substituted with a butyl group and an amine functional group at the 1-position, making it a versatile intermediate in synthetic chemistry. The compound's unique structural characteristics contribute to its reactivity profile, enabling applications in pharmaceuticals, agrochemicals, and material science. Recent studies highlight its potential as a chiral building block in asymmetric synthesis, aligning with the growing demand for enantioselective catalysts in green chemistry initiatives.

In the context of sustainable chemistry trends, researchers are increasingly exploring 1-butylcyclopentan-1-amine derivatives for bio-based polymer modifications. The compound's lipophilic nature and amine functionality make it suitable for designing self-healing materials—a hot topic in materials science forums. Analytical techniques like GC-MS and NMR spectroscopy confirm its high purity (>98%), a critical parameter for industries requiring stringent quality control, such as electronic-grade chemicals production.

The synthetic pathways for CAS No. 68288-41-5 often involve reductive amination of 1-butylcyclopentanone or nucleophilic substitution reactions. Optimized protocols now incorporate microwave-assisted synthesis—a technique frequently searched in academic databases—to reduce reaction times by 60% compared to conventional methods. Environmental considerations have also spurred interest in catalytic hydrogenation approaches using Pd/C catalysts, reflecting the industry's shift toward atom-efficient processes.

Market analytics reveal rising queries for "1-butylcyclopentan-1-amine suppliers" and "CAS 68288-41-5 technical data sheets," particularly from Asia-Pacific regions. This correlates with expanding applications in flexible electronics and OLED materials, where the compound serves as a precursor for charge-transport layers. Regulatory-compliant storage recommendations (dry, inert atmosphere at 2-8°C) are another frequently searched aspect, emphasizing the need for proper chemical handling protocols.

Innovative research directions include investigating 1-butylcyclopentan-1-amine's role in CO2 capture technologies. Its secondary amine group shows promising carbamate formation kinetics, a subject gaining traction in climate change mitigation discussions. Furthermore, computational chemistry studies utilizing DFT calculations predict its potential as a corrosion inhibitor—addressing a common industrial challenge documented in recent patent filings.

Quality assurance protocols for CAS No. 68288-41-5 now integrate HPLC-UV and LC-MS for impurity profiling, responding to pharmaceutical industry demands for ICH Q3D compliance. The compound's logP value (experimentally determined as 2.8) makes it a candidate for blood-brain barrier penetration studies, connecting to trending neuroscientific research. These multifaceted applications position 1-butylcyclopentan-1-amine as a compound of significant interdisciplinary interest.

• 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)