• 1. Fe(ii)-Assisted one-pot synthesis of ultra-small core–shell Au–Pt nanoparticles as superior catalysts towards the HER and ORR?
  Yi Cao,Yujiao Xiahou,Lixiang Xing,Xiang Zhang,Hong Li,ChenShou Wu,Haibing Xia Nanoscale, 2020,12, 20456-20466
• 2. Dissociation of large gaseous serine clusters produces abundant protonated serine octamer
  Jacob S. Jordan,Evan R. Williams Analyst, 2021,146, 2617-2625
• 3. Emulsifier-free, organotellurium-mediated living radical emulsion polymerization (emulsion TERP) of styrene: poly(dimethylaminoethyl methacrylate) macro-TERP agent?
  Yukiya Kitayama Polym. Chem., 2014,5, 2784-2792
• 4. EWOD-driven droplet microfluidic device integrated with optoelectronic tweezers as an automated platform for cellular isolation and analysis?
  Gaurav J. Shah,Eric P.-Y. Chiou,Ming C. Wu,Chang-Jin “CJ” Kim Lab Chip, 2009,9, 1732-1739
• 5. Embedding heteroatoms: an effective approach to create porphyrin-based functional materials
  Norihito Fukui,Keisuke Fujimoto,Hideki Yorimitsu,Atsuhiro Osuka Dalton Trans., 2017,46, 13322-13341

N-(8-Aminooctyl)-1,8-octanediamine: A Comprehensive Overview

N-(8-Aminooctyl)-1,8-octanediamine, identified by the CAS registry number 39202-36-3, is a versatile organic compound with significant applications in various fields of chemistry and materials science. This compound is characterized by its unique structure, which combines a long hydrocarbon chain with amino groups at both ends. The presence of these amino functionalities makes it highly reactive and suitable for a wide range of chemical reactions, including polymerization, cross-linking, and surface modification.

The synthesis of N-(8-Aminooctyl)-1,8-octanediamine typically involves multi-step chemical processes that ensure the precise placement of amino groups at the terminal positions of the octane chain. Recent advancements in synthetic methodologies have enabled the production of this compound with high purity and consistency, which is critical for its application in demanding industrial and research settings. Researchers have also explored alternative routes to enhance the efficiency of its synthesis, such as using catalytic systems or optimizing reaction conditions to minimize side reactions.

In terms of applications, N-(8-Aminooctyl)-1,8-octanediamine has found extensive use in the development of polymeric materials. Its ability to act as a diol or diamine component in polyurethane synthesis has made it a valuable ingredient in the production of high-performance elastomers and thermoplastics. Moreover, its role as a cross-linking agent has been pivotal in creating robust adhesives and coatings that exhibit excellent mechanical properties and durability under various environmental conditions.

Recent studies have highlighted the potential of N-(8-Aminooctyl)-1,8-octanediamine in biomedical applications. For instance, its use as a building block for hydrogels has shown promise in tissue engineering and drug delivery systems. The compound's ability to form networks with controlled porosity and biocompatibility makes it an attractive candidate for these applications. Additionally, researchers have investigated its role in creating stimuli-responsive materials that can adapt to changes in their environment, such as temperature or pH levels.

The structural properties of N-(8-Aminooctyl)-1,8-octanediamine also make it an ideal candidate for surface modification techniques. By reacting with functional groups on various substrates, this compound can impart desirable properties such as increased wettability, improved adhesion, or enhanced resistance to corrosion. These characteristics have led to its adoption in the development of advanced materials for aerospace, automotive, and electronic industries.

In conclusion, N-(8-Aminooctyl)-1,8-octanediamine (CAS No. 39202-36-3) is a multifaceted compound with a wide array of applications across diverse industries. Its unique chemical structure and reactivity continue to drive innovative research and development efforts, ensuring its relevance in both current and future technological advancements.

• 1120-49-6(Didecylamine)
• 143-16-8(Dihexylamine)
• 6835-13-8(N-(n-Octyl)-n-pentylamine)
• 26627-77-0(N-(n-Heptyl)-n-octylamine)
• 4835-11-4(N,N'-dibutyl-1,6-hexanediamine)
• 1120-48-5(Di-n-octylamine)
• 143-23-7(Bis(hexamethylene)triamine)
• 66793-76-8(N-Ethyl-1-heptanamine)
• 112-99-2(dioctadecylamine)
• 101012-97-9(Tridecanamine, N-tridecyl-, branched and linear)