• 1. An integrated chip for immunofluorescence and its application to analyze lysosomal storage disorders
  Jie Shen,Ying Zhou,Tu Lu,Junya Peng,Zhixiang Lin,Yuhong Pang,Li Yu Lab Chip, 2012,12, 317-324
• 2. An all-solid-state imprinted polymer-based potentiometric sensor for determination of bisphenol S?
  Rongning Liang,Tanji Yin,Ruiqing Yao,Wei Qin RSC Adv., 2016,6, 73308-73312
• 3. An automatic determination of thoria in thoria-urania mixtures
  Analyst, 1966,91, 208-210
• 4. An atom efficient route to N-aryl and N-alkyl pyrrolines by transition metal catalysis?
  Supaporn Sawadjoon,Joseph S. M. Samec Org. Biomol. Chem., 2011,9, 2548-2554
• 5. An insight into the hybridization mechanism of hairpin DNA physically immobilized on chemically modified graphenes
  Adeline Huiling Loo,Alessandra Bonanni,Martin Pumera Analyst, 2013,138, 467-471

• Solvents and Organic Chemicals Organic Compounds Organohalogen compounds Alkyl halides Perfluoroalkyl carboxylic acid and derivatives
• Solvents and Organic Chemicals Organic Compounds Organohalogen compounds Alkyl halides Alkyl fluorides Perfluoroalkyl carboxylic acid and derivatives
• Solvents and Organic Chemicals Organic Compounds Acids/Esters

Professional Introduction to Ethyl Perfluorononanoate (CAS No. 30377-52-7)

Ethyl Perfluorononanoate, a compound with the chemical formula C₉H₁FO₂, is a perfluorinated ester that has garnered significant attention in the field of chemical and pharmaceutical research. This compound, identified by its unique CAS number 30377-52-7, is characterized by its nonpolar and chemically stable properties, making it a valuable candidate for various applications in industry and academia.

The structure of Ethyl Perfluorononanoate consists of a nonanoic acid backbone with all hydrogen atoms replaced by fluorine atoms, resulting in a highly fluorinated molecule. This perfluorinated moiety imparts exceptional thermal stability and resistance to hydrolysis, which are critical attributes for its use in demanding environments. The ethyl ester group at one end of the molecule enhances its solubility in organic solvents, facilitating its integration into diverse chemical processes.

In recent years, Ethyl Perfluorononanoate has been extensively studied for its potential applications in pharmaceutical formulations. Its unique chemical properties make it an ideal candidate for use as an intermediate in the synthesis of active pharmaceutical ingredients (APIs). The compound's stability under extreme conditions ensures that it can be used in multi-step synthetic pathways without degradation, thereby improving the overall yield and efficiency of drug production.

One of the most compelling aspects of Ethyl Perfluorononanoate is its role in developing advanced materials. Researchers have explored its use as a precursor for high-performance polymers and coatings that exhibit exceptional durability and resistance to environmental factors. These materials are particularly valuable in industries where exposure to harsh chemicals or extreme temperatures is common. The perfluorinated nature of the compound contributes to the formation of a robust molecular network, enhancing the mechanical strength and chemical resistance of the final products.

The pharmaceutical industry has also shown interest in Ethyl Perfluorononanoate for its potential as a drug delivery system. Its ability to form stable complexes with various bioactive molecules has been leveraged to develop novel formulations that improve drug solubility and bioavailability. This has significant implications for therapies targeting recalcitrant diseases, where conventional drug delivery methods often fall short. The compound's biocompatibility and lack of toxicity make it a promising candidate for clinical applications.

Recent advancements in analytical chemistry have highlighted the utility of Ethyl Perfluorononanoate as a reference standard for high-resolution mass spectrometry (HRMS). Its well-defined molecular structure and high purity make it an invaluable tool for identifying and quantifying complex mixtures in pharmaceutical samples. This application underscores the compound's importance not only as a synthetic intermediate but also as a diagnostic tool in modern medicine.

The environmental impact of Ethyl Perfluorononanoate has also been a subject of thorough investigation. Despite its synthetic complexity, studies indicate that it exhibits low toxicity and environmental persistence when compared to other fluorinated compounds. This makes it an attractive option for industries seeking sustainable alternatives without compromising performance. Efforts are ongoing to optimize its synthesis pathways further to minimize any potential ecological footprint.

In conclusion, Ethyl Perfluorononanoate (CAS No. 30377-52-7) is a multifaceted compound with broad applications across multiple sectors. Its unique chemical properties, coupled with recent advancements in synthetic and analytical techniques, position it as a cornerstone material in both pharmaceuticals and advanced materials science. As research continues to uncover new possibilities, Ethyl Perfluorononanoate is poised to play an increasingly pivotal role in shaping the future of chemical innovation.

• 623171-63-1(OCTANOIC ACID, PENTADECAFLUORO-, EICOSYL ESTER)
• 73155-66-5(DECANOIC ACID, NONADECAFLUORO-, PROPYL ESTER)
• 134638-96-3(Hexanoic acid, undecafluoro-, butyl ester)
• 110408-04-3(Heptanoic acid, tridecafluoro-, dodecyl ester)
• 89014-13-1(Pentanoic acid, nonafluoro-, 2,2,3,3-tetrafluoropropyl ester)
• 134638-93-0(Propyl perfluorohexanoate)
• 647-50-7(HEXANOIC ACID, UNDECAFLUORO-, ETHYL ESTER)
• 187675-83-8(HEPTADECANOIC ACID, TRITRIACONTAFLUORO-, EICOSYL ESTER)
• 134638-94-1(Propyl perfluoroheptanoate)
• 400-57-7(Octadecyl 2,2,3,3,4,4,4-heptafluorobutanoate)