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1-Propyl-1H-imidazole

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CAS:35203-44-2
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1-Propyl-1H-imidazole manufacturers

  • 1-Propyl-1H-imidazole
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  • $100.00 / 1KG
  • 2025-09-25
  • CAS:35203-44-2
  • Min. Order: 1KG
  • Purity: 99%
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  • 1-Propylimidazole
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  • 2025-05-26
  • CAS:35203-44-2
  • Min. Order: 1KG
  • Purity: 99%
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1-Propyl-1H-imidazole Basic information
Product Name:1-Propyl-1H-imidazole
Synonyms:1-propyl-1H-imidazole;N-Propylimidazol;QuadraPure Bis(propyl-1H-imidazole);N-PROPYLIMIDAZOLE;1-PROPYLIMIDAZOLE;Clotrimazole Impurity 18;1-Propylimidazole>;1-Propyl-1H-imidazol
CAS:35203-44-2
MF:C6H10N2
MW:110.16
EINECS:252-431-0
Product Categories:pharmaceutical raw material;bc0001
Mol File:35203-44-2.mol
1-Propyl-1H-imidazole Structure
1-Propyl-1H-imidazole Chemical Properties
Boiling point 94°C/11mmHg(lit.)
density 0.95±0.1 g/cm3(Predicted)
refractive index 1.4810-1.4850
Fp 88°
storage temp. 2-8°C
pka7.09±0.10(Predicted)
form clear liquid
color Colorless to Yellow
InChIInChI=1S/C6H10N2/c1-2-4-8-5-3-7-6-8/h3,5-6H,2,4H2,1H3
InChIKeyIYVYLVCVXXCYRI-UHFFFAOYSA-N
SMILESC1N(CCC)C=CN=1
CAS DataBase Reference35203-44-2(CAS DataBase Reference)
Safety Information
HazardClass IRRITANT
HS Code 2933299090
MSDS Information
1-Propyl-1H-imidazole Usage And Synthesis
Uses 1-propyl-1H-imidazole (PrIm) could be selected as a ligand for a study on homoleptic Fe(II)-Imidazole complexes, allowing for a comparison between the two systems. Its extreme versatility as a ligand was unveiled as it gave rise to a new family of Fe(II) complexes with mono-, bi- and tetranuclear members[1].
1-Propyl-1H-imidazole
Synthesis
Imidazole

288-32-4

1-Bromopropane

106-94-5

1-Propyl-1H-imidazole

35203-44-2

Synthesis of 1-propyl-1H-imidazole: Sodium hydride (55%, 0.966 g, 22.1 mmol) was slowly added to a solution of tetrahydrofuran (50.0 mL) of imidazole (1.37 g, 20.1 mmol) at room temperature. The reaction mixture was stirred at room temperature for 1 hour. Subsequently, 1-bromopropane (5.48 mL, 60.3 mmol) was added dropwise at the same temperature and the reaction solution was continued to be stirred for 16 hours. Upon completion of the reaction, the reaction mixture was filtered through a diatomaceous earth pad and the filter cake was washed with tetrahydrofuran. The filtrate and washings were combined and concentrated under reduced pressure to remove the solvent. The resulting crude product was purified by fast column chromatography (silica gel as stationary phase and chloroform/methanol as eluent) to afford 1-propyl-1H-imidazole (2.07 g, 18.8 mmol, 93% yield) as a colorless oil.1H NMR (400 MHz, CDCl3) δ: 0.93 (3H, t, J = 7.2 Hz), 1.81 (2H, td, J = 7.2, 14.4 Hz), 3.90 (2H, t, J = 7.2 Hz), 6.91 (1H, s), 7.06 (1H, s), 7.46 (1H, s).

References[1] Willi Zeni. “A New Family of Fe(II) 1-Propyl-1H-Imidazole Complexes with Mono-, Bi-, and Tetra-Nuclear Members.” European Journal of Inorganic Chemistry 27 29 (2024).
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