• 1. Excellent humidity sensor based on ultrathin HKUST-1 nanosheets?
  Qiaoe Wang,Meiling Lian,Xiaowen Zhu,Xu Chen RSC Adv., 2021,11, 192-197
• 2. Dissociation of aryl sulfonyl phthalimide radical anions: relevance to the biological activity of arylsulfonyl amides?
  Abdelaziz Houmam,Emad M. Hamed Chem. Commun., 2012,48, 11328-11330
• 3. Emulsion technologies for multicellular tumour spheroid radiation assays?
  Kay S. McMillan,Anthony G. McCluskey,Annette Sorensen,Marie Boyd,Michele Zagnoni Analyst, 2016,141, 100-110
• 4. Establishing new scaling relations on two-dimensional MXenes for CO2 electroreduction?
  Albertus D. Handoko,Khoong Hong Khoo,Teck Leong Tan,Hongmei Jin,Zhi Wei Seh J. Mater. Chem. A, 2018,6, 21885-21890
• 5. Emerging investigator series: bacteriophages as nano engineering tools for quality monitoring and pathogen detection in water and wastewater
  Fereshteh Bayat Environ. Sci.: Nano, 2021,8, 367-389

• Solvents and Organic Chemicals Organic Compounds Hydrocarbons

Comprehensive Analysis of cis-5-Decene (CAS No. 7433-78-5): Properties, Applications, and Industry Trends

cis-5-Decene (CAS No. 7433-78-5) is a high-value unsaturated hydrocarbon belonging to the alkene family. As a cis-configuration isomer, it exhibits unique chemical reactivity and physical properties, making it indispensable in organic synthesis, fragrance formulation, and specialty polymer production. With growing interest in sustainable chemicals and bio-based intermediates, cis-5-Decene has garnered attention for its versatility in green chemistry applications.

The molecular structure of cis-5-Decene features a double bond at the fifth carbon position with cis-orientation, resulting in a distinct dipole moment compared to its trans-isomer counterpart. This structural nuance contributes to its lower melting point (-89°C) and higher boiling point (170°C), which are critical parameters for industrial purification processes. Recent studies highlight its role as a precursor for flavor & fragrance compounds, particularly in synthesizing citrus-like aroma molecules demanded by the cosmetics industry.

In material science, cis-5-Decene serves as a building block for functionalized polyolefins with tailored elasticity. Its controlled polymerization yields low-crystallinity polymers used in adhesives and sealants – a sector experiencing 6.2% annual growth (2023 market data). The compound's compatibility with metathesis catalysts also enables efficient production of C10-C20 olefin derivatives, addressing the pharmaceutical industry's need for chiral intermediates.

Environmental considerations have propelled research into catalytic dehydrogenation of decane as a production method for cis-5-Decene, reducing reliance on petrochemical cracking. Advanced molecular sieve technologies now achieve 92% isomer selectivity in pilot plants, aligning with carbon footprint reduction initiatives. Analytical techniques like GC-MS quantification and FTIR spectroscopy ensure product purity exceeding 99.5%, meeting stringent REACH compliance standards.

The global market for mid-chain alkenes including cis-5-Decene is projected to reach $780 million by 2027, driven by demand for non-phthalate plasticizers and low-VOC formulations. Emerging applications in agrochemical adjuvants and electronic-grade solvents further expand its commercial potential. Storage recommendations emphasize nitrogen blanketing to prevent peroxide formation, while transportation follows ADR/RID Class 3 guidelines for flammable liquids.

Cutting-edge research explores enzyme-mediated synthesis of cis-5-Decene using engineered fatty acid desaturases, potentially revolutionizing production economics. Patent analysis reveals 23% annual growth in olefin functionalization technologies since 2020, with particular focus on stereoselective hydrogenation processes. These developments position cis-5-Decene as a strategic compound in the transition toward circular hydrocarbon economies.

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