| Identification | Back Directory | [Name]
1,2-DIMETHYL-3-PROPYLIMIDAZOLIUM IODIDE | [CAS]
218151-78-1 | [Synonyms]
DMPII
PDMIMI
DMPImI
[PMMIm] I
1,2-DIMETHYL-3-PROPYLIMIDAZOLIUM
2,3-Dimethylpropylimidazolium iodide
1-propyl-2,3-methylimidazolium iodide
1,2-DIMETHYL-3-PROPYLIMIDAZOLIUM IODIDE
1-propenyl-2,3-MethyliMidazoliuM iodide
1-Propyl-2,3-dimethylimidazolium iodide
1,2-Dimethyl-3-propylimidazoliumIodide>
1,2-dimethyl-3-propylimidazol-1-ium,iodide
2,3-Dimethyl-1-propyl-1H-imidazolium, iodide
1,2-Dimethyl-3-propyl-1H-imidazol-3-ium iodide
N-Methyl-N'-n-propyl-2-methylimidazolium iodide
1,2-dimethyl-3-propylimidazolium Iodide (DMPII, [PMMIM]I) | [EINECS(EC#)]
200-145-6 | [Molecular Formula]
C8H15IN2 | [MDL Number]
MFCD15072160 | [MOL File]
218151-78-1.mol | [Molecular Weight]
266.123 |
| Chemical Properties | Back Directory | [density ]
1.45 g/cm3(Temp: 85 °C) | [storage temp. ]
Keep in dark place,Inert atmosphere,Room temperature | [Water Solubility ]
Soluble in water | [form ]
powder to crystal | [color ]
White to Orange to Green |
| Hazard Information | Back Directory | [Uses]
Solarpur? electrolyte components for DSSC applications meet the highest purity standards regarding water and other impurities required for this technology. | [Synthesis]
GENERAL STEPS: Synthesis of 1,2-dimethyl-3-propyl-1H-imidazol-3-ium iodide was carried out according to Scheme 1. A mixture of 1,2-dimethylimidazole (7.78 mL, 100 mmol) and 1-iodopropane (9.74 mL, 50 mmol) was heated and reacted at 120°C under microwave radiation conditions. Upon completion of the reaction, the solvent was removed from the reaction mixture by evaporation under reduced pressure, followed by washing the product with ether (5 x 20 mL) several times to remove excess 1-iodopropane. Afterwards, the solvent was removed and the product was dried under vacuum for 8 h. High purity 1,2-dimethyl-3-propyl-1H-imidazol-3-ium iodide was obtained as a light yellow liquid in 92% yield. | [References]
[1] Journal of Molecular Structure, 2017, vol. 1134, p. 582 - 590
[2] Journal of Heterocyclic Chemistry, 2012, vol. 49, # 2, p. 370 - 374 |
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