Product name:1,10-DIIODODECANE
Synonymous: 1,10-diiodo-decan;DECAMETHYLENEDIIODIDE;1,10-DIIODODECANE;1,10-diiodododecane;1,10-Diiododecane,97%;1,10-DIIODODECANETECH;1,10-Diidodecane;1,10-DIIODODECANE1,10-DIIODODECANE1,10-DIIODODECANE1,10-DIIODODECANE
CAS No.:16355-92-3
Melocular formula:C10H20I2
Melocular weight:394.07
EINECS No.:240-415-6
Application: intermediate of Dequalinium chloride
*The following content is generated by AI and is for reference only.
1,10-Diiodododecane is a specialized organic halide featuring a twelve-carbon linear alkyl chain terminated by iodine atoms at both the first and tenth positions. Its molecular formula is C12H24I2, and it is uniquely identified by CAS Registry Number 1569-78-2. This compound belongs to the class of dihaloalkanes, where the presence of two heavy iodine atoms significantly influences its physical properties, including high density and distinct reactivity profiles compared to lighter halogenated analogs. The molecule exhibits a symmetrical structure that facilitates specific chemical transformations in synthetic laboratories.
In industrial and research applications, 1,10-Diiodododecane serves primarily as a versatile intermediate for advanced organic synthesis. Due to the high leaving group ability of the iodine moiety, it acts as an efficient electrophile in nucleophilic substitution reactions. Chemists frequently utilize this substrate to construct complex macrocycles or functionalized polymers through coupling strategies. It is particularly valuable in the development of self-assembled monolayers (SAMs) and surface modification techniques, where the long hydrophobic tail provides stability while the reactive ends allow for attachment to various substrates. Furthermore, its unique structure makes it suitable for investigating steric effects and conformational analysis in supramolecular chemistry.
The compound finds niche use in the pharmaceutical sector as a precursor for synthesizing bioactive molecules requiring specific alkyl spacer lengths. In materials science, it contributes to the formulation of specialized lubricants or additives designed for extreme pressure conditions, leveraging the protective properties of organo-iodine species. While handling requires standard safety precautions due to potential skin irritation and environmental toxicity associated with heavy halides, its utility in creating precise molecular architectures remains unmatched. Researchers continue to explore its potential in nanotechnology and drug delivery systems, capitalizing on the tunable solubility and reactivity inherent in this symmetric diiodoalkane. As a high-value specialty chemical, 1,10-Diiodododecane represents a critical tool for chemists pushing the boundaries of molecular design and material engineering.