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Organic iodides are organic compounds containing a carbon-iodine (C-I) bond. The carbon-iodine bond is weaker than other carbon-halogen bonds due to the poor electronegative nature of the iodine atom. In general, organic iodides are light-sensitive and turn yellow during storage, owing to the formation of iodine. Organic iodides can be alkyl, alkenyl, or alkynyl, and all of them are very reactive toward with many kinds of nucleophiles.

Alkyl iodides react at a faster rate than alkyl fluorides due to the weak C-I bond. Iodo alkanes participate in a variety of organic synthesis reactions, which include the Simmons–Smith reaction (cyclopropanation using iodomethane), Williamson ether synthesis, Wittig reaction, Grignard reaction, alkyl coupling reactions, and Wurtz reaction.

Organic iodides are used in veterinary products (Organic Iodide Powder) as a nutritional source of iodine. In the chemical industry, alkyl iodides serve as excellent alkylating agents and, specifically, methyl iodide is used as a methylating agent in the synthesis of various pharmaceutical drugs. Oceanic alkyl iodides are believed to be the principal source of atmospheric iodine.

  • 11-Chloro-1,1'-di-n-propyl-3,3,3',3'-tetramethyl-10,12-trimethyleneindatricarbocyanine iodide, 95%
  • 1,1'-Diethyl-2,2'-carbocyanine iodide, 96%
  • 1,1'-Diethyl-2,2'-cyanine iodide, 97%
  • 1,1'-Diethyl-4,4'-carbocyanine iodide, 96%
  • 1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide methiodide, 98%
  • 1-Aminopyridinium iodide, 97%
  • 1-Ethyl-2-methylquinolinium iodide, 97%
  • 1-Ethyl-3-methylimidazolium iodide, 97%
  • 1-Ethylquinolinium iodide, 98%
  • 1-Methyl-3-n-propylimidazolium iodide, 98%
  • 1-n-Hexyl-3-methylimidazolium iodide, 98%
  • 2-[4-(Dimethylamino)styryl]-1-ethylpyridinium iodide, 99+%
  • 2-Chloro-1-methylpyridinium iodide, 97%
  • 3,3'-Diethyl-9-methylthiacarbocyanine iodide, 98%
  • 3,3'-Diethyloxacarbocyanine iodide, 98%
  • 3,3'-Diethyloxadicarbocyanine iodide, 96%
  • 3,3'-Diethylthiacarbocyanine iodide, 96%
  • 3,3'-Diethylthiadicarbocyanine iodide
  • 3,3'-Diethylthiatricarbocyanine iodide, 96%
  • 3,3'-Di-n-heptyloxacarbocyanine iodide, 97%
  • 3,3'-Di-n-hexyloxacarbocyanine iodide, 98%
  • 3,3'-Di-n-pentyloxadicarbocyanine iodide, 96%
  • 3,3'-Di-n-pentylthiacarbocyanine iodide, 96%
  • 3,3'-Di-n-pentylthiadicarbocyanine iodide, 96%
  • 3,3'-Di-n-propylthiacarbocyanine iodide, 96%
  • 3,3'-Di-n-propylthiadicarbocyanine iodide, 96%
  • 3-Ethyl-2-methylbenzoxazolium iodide, 95%
  • 3-Methylbenzothiazolium iodide, 98+%
  • Benzoylcholine iodide, 98+%
  • Benzyltriethylammonium dichloroiodate, 97%
  • Benzyltrimethylammonium dichloroiodate, 95%
  • Benzyltrimethylammonium iodide, 98%
  • Choline iodide, 98%
  • Diphenyliodonium iodide, 98%
  • Phenyltrimethylammonium iodide, 99%
  • S-Acetylthiocholine iodide, 98%
  • Tetraethylammonium iodide, 98+%
  • Tetramethylammonium iodide, 99%
  • Tetra-n-dodecylammonium iodide, 98%
  • Tetra-n-pentylammonium iodide, 98%
  • Triethylsulfonium iodide, 97%
  • Trimethylsulfonium iodide, 99%
  • Trimethylsulfoxonium iodide, 98+%
  • Vinyl iodide, tech. 85%

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