• 1. Physicochemical and solution properties of quaternary-ammonium-salt-type amphiphilic trimeric ionic liquids
  Risa Kawai,Shiho Yada,Tomokazu Yoshimura Phys. Chem. Chem. Phys. 2019 21 25065
• 2. Synthesis, characterization and organic field effect transistor performance of a diketopyrrolopyrrole–fluorenone copolymer
  Prashant Sonar,Tae-Jun Ha,Ananth Dodabalapur Phys. Chem. Chem. Phys. 2013 15 7475
• 3. Synthesis, surface activities, and aggregation behavior of phenyl-containing carboxybetaine surfactants
  Shifeng Gao,Zhaozheng Song,Di Zhu,Fang Lan,Qingzhe Jiang RSC Adv. 2018 8 33256
• 4. High mobility isoindigo-based π-extended conjugated polymers bearing di(thienyl)ethylene in thin-film transistors
  Jicheol Shin,Hyun Ah Um,Dae Hee Lee,Tae Wan Lee,Min Ju Cho,Dong Hoon Choi Polym. Chem. 2013 4 5688
• 5. A fluorenone based low band gap solution processable copolymer for air stable and high mobility organic field effect transistors
  Prashant Sonar,Tae-Jun Ha,Ananth Dodabalapur Chem. Commun. 2013 49 1588

• Solvents and Organic Chemicals Organic Compounds Organic Halides
• Solvents and Organic Chemicals Organic Compounds Hydrocarbons

Comprehensive Guide to 1-Bromotetradecane (CAS No. 112-71-0): Properties, Applications, and Industry Insights

1-Bromotetradecane (CAS No. 112-71-0), also known as tetradecyl bromide, is a significant organic compound widely utilized in synthetic chemistry and industrial applications. This long-chain alkyl bromide is characterized by its molecular formula C14H29Br and serves as a versatile intermediate in the production of surfactants, lubricants, and specialty chemicals. Its unique properties, including a high boiling point (typically above 300°C) and hydrophobic nature, make it indispensable in formulations requiring controlled reactivity and stability.

The growing demand for 1-Bromotetradecane is driven by its role in synthesizing quaternary ammonium compounds (quats), which are pivotal in fabric softeners, disinfectants, and phase-transfer catalysts. Recent trends highlight its relevance in green chemistry, where researchers explore its potential in biodegradable surfactants and low-toxicity formulations. A frequently searched question—"What are the alternatives to 1-Bromotetradecane in sustainable chemistry?"—reflects industry shifts toward eco-friendly substitutes without compromising performance.

From a structural perspective, 1-Bromotetradecane features a 14-carbon alkyl chain terminated by a bromine atom, enabling nucleophilic substitution reactions. This reactivity is exploited in organic synthesis to create longer-chain derivatives or modify surface properties in coatings. Analytical techniques like GC-MS and NMR spectroscopy are commonly employed to verify its purity, a critical factor given its use in precision-dependent applications such as pharmaceutical intermediates.

In the context of market dynamics, the compound’s supply chain resilience has been a topic of interest, especially post-pandemic. Searches for "1-Bromotetradecane price fluctuations 2023" or "reliable suppliers of CAS 112-71-0" underscore its commercial importance. Manufacturers emphasize adherence to ISO standards and REACH compliance to meet global regulatory requirements, ensuring safe handling and transportation.

Emerging applications of 1-Bromotetradecane include nanotechnology, where it acts as a stabilizing agent for nanoparticles, and advanced material science, contributing to self-assembling monolayers (SAMs). These innovations align with searches like "nanomaterial synthesis using alkyl bromides" or "1-Bromotetradecane in smart coatings." Such interdisciplinary uses highlight its adaptability beyond traditional roles.

To address common queries, storage recommendations for 1-Bromotetradecane typically advise inert atmospheres and moisture-free conditions to prevent degradation. Meanwhile, its biodegradation pathways are under study to align with circular economy principles—a response to queries like "Is 1-Bromotetradecane environmentally persistent?" This dual focus on utility and sustainability positions it as a compound of enduring relevance.

• 2159-17-3(1-Bromohexane-2,2,3,3,4,4,5,5,6,6,6-d11)
• 347840-09-9(1-Bromotetradecane-14,14,14-d3)
• 347841-80-9(1-Bromotetradecane-d29)
• 349553-91-9(1-Bromotridecane-d27)
• 350818-70-1(1-Bromohexane-6,6,6-d3)
• 349553-92-0(1-Bromoundecane-d23)
• 26746-34-9(Octane, bromo-)
• 31772-06-2(Octadecane,1,18-dibromo-)
• 2159-25-3(Dodecane-1,1-d2,1-bromo- (7CI,9CI))
• 25495-91-4(Hexane, bromo-)