• 1. Fc microparticles can modulate the physical extent and magnitude of complement activity?
  David White,Sean R. Stowell Biomater. Sci., 2017,5, 463-474
• 2. Fatty acid positional distribution in colostrum and mature milk of women living in Inner Mongolia, North Jiangsu and Guangxi of China?
  Long Deng,Qian Zou,Biao Liu,Wenhui Ye,Chengfei Zhuo,Li Chen,Ze-Yuan Deng,Ya-Wei Fan,Jing Li Food Funct., 2018,9, 4234-4245
• 3. Emergence of cationic polyamine dendrimersomes: design, stimuli sensitivity and potential biomedical applications
  Partha Laskar,Christine Dufès Nanoscale Adv., 2021,3, 6007-6026
• 4. Estimates of hydride ion stability in condensed systems: energy of formation and solvation in aqueous and polar-organic solvents
  Craig A. Kelly,David R. Rosseinsky Phys. Chem. Chem. Phys., 2001,3, 2086-2090
• 5. Fast synthesis of red Li3BaSrLn3(WO4)8:Eu3+ phosphors for white LEDs under near-UV excitation by a microwave-assisted solid state reaction method and photoluminescence studies
  Bo Wei,Zhenyu Liu,Chen Xie,Shu Yang,Wentao Tang,Aiwei Gu,Wing-Tak Wong,Ka-Leung Wong J. Mater. Chem. C, 2015,3, 12322-12327

Comprehensive Overview of Sodium Naphthalene-1-sulfinate (CAS No. 64326-13-2): Properties, Applications, and Industry Insights

Sodium Naphthalene-1-sulfinate (CAS No. 64326-13-2) is a specialized organic compound widely recognized for its role in synthetic chemistry and industrial processes. This sodium salt derivative of naphthalene-1-sulfinic acid exhibits unique reactivity, making it valuable for applications ranging from pharmaceuticals to advanced material synthesis. With the growing demand for high-performance chemical intermediates, this compound has garnered significant attention in research and commercial sectors.

The molecular structure of Sodium Naphthalene-1-sulfinate features a sulfinate group (-SO₂Na) attached to the naphthalene ring, which enhances its solubility in polar solvents and reactivity in nucleophilic reactions. Recent studies highlight its utility as a sulfonation agent in polymer modification and as a precursor for photoinitiators in UV-curable coatings—a trending topic aligned with sustainable manufacturing practices. Researchers are particularly interested in its potential for green chemistry applications, where milder reaction conditions are prioritized.

In the pharmaceutical industry, CAS 64326-13-2 serves as a building block for sulfone-containing drugs, addressing the rising demand for novel therapeutic agents. Its compatibility with cross-coupling reactions (e.g., Suzuki-Miyaura reactions) makes it indispensable in modern drug discovery pipelines. A 2023 market analysis revealed increased searches for "sulfinate derivatives in drug synthesis," reflecting industry interest in optimizing synthetic routes using this compound.

From an environmental perspective, Sodium Naphthalene-1-sulfinate aligns with the circular economy paradigm due to its recyclability in certain catalytic systems. Laboratories focusing on waste reduction strategies have explored its use in metal recovery processes, a hot topic in ESG (Environmental, Social, and Governance) discussions. The compound's stability under ambient conditions also makes it preferable for safe handling protocols, a frequently searched term in chemical safety databases.

Technological advancements have expanded its applications in electronic materials, particularly in the synthesis of conductive polymers for flexible electronics. With the global push toward Internet of Things (IoT) devices, material scientists are investigating its role in creating solution-processable electrodes. Patent filings related to "naphthalene sulfinates in organic electronics" saw a 40% increase from 2020–2023, per WIPO data.

Quality control of Sodium Naphthalene-1-sulfinate involves rigorous HPLC analysis and spectroscopic characterization (FTIR, NMR), topics frequently queried in academic forums. The compound typically appears as a white to off-white crystalline powder with ≥98% purity in commercial grades. Storage recommendations emphasize protection from moisture—addressing common user questions about "chemical shelf life optimization."

Emerging research explores its derivatives for battery electrolyte additives, capitalizing on the sulfinate group's ability to stabilize electrode interfaces. This connects with trending searches around "next-generation energy storage" solutions. Meanwhile, its biodegradation pathways are under study to meet evolving REACH compliance standards in the European market.

In conclusion, Sodium Naphthalene-1-sulfinate (CAS No. 64326-13-2) represents a versatile compound bridging traditional chemistry and cutting-edge applications. Its evolving role in sustainable technologies and alignment with industry 4.0 trends ensure continued relevance across scientific and industrial domains.

• 130-14-3(Sodium naphthalene-1-sulfonate)
• 1655-29-4(Sodium 1,5-Naphthalenedisulfonate)
• 1655-43-2(disodium naphthalene-1,6-disulfonate)
• 873-55-2(Benzenesulfinic acid, sodium salt)
• 64586-62-5(Copper(II) benzenesulfinate hydrate)
• 24308-84-7(Benzenesulfinic acid;zinc)
• 1321-69-3(Sodium 1-naphthalenesulfonate)
• 618-41-7(Benzenesulfinic acid)
• 25932-11-0(Sodiumbenzenesulfinatedihydrate)
• 104432-57-7(1,6-Naphthalenedisulfonicacid, sodium salt (1:?))