| Identification | Back Directory | [Name]
1-ETHYL-3-METHYLIMIDAZOLIUM ACETATE | [CAS]
143314-17-4 | [Synonyms]
EMIMAc
LM 1132
SKL1392
ium acetate
EMIM ACETATE
Basionics? BC 01
BASIONIC(TM) BC 01
BASIONIC(R) BC 01, EMIM Ac
1-ethyl-3-methylimidazole acetate
1-Ethyl-3-methylmidazolium acetic
1-Etyl-3-methylimidazolium acetate
1-ETHYL-3-METHYLIMIDAZOLIUM ACETATE
3-Ethyl-1-methylimidazolium acetate
1-Ethyl-3-methyl-3-imidazolium Acetate
1-ethyl-3-methylimidazol-3-ium,acetate
1-Ethyl-3-MethyliMidazoliuM acetate 97%
1-Ethyl-3-methylimidazolium Acetate >
3-Ethyl-1-methyl-1H-imidazol-3-ium acetate
1-Ethyl-3-MethyliMidazoliuM acetate
1-Ethyl-3-methylimidazolium acetate >=95.0% (HPLC)
1-Ethyl-3-MethyliMidazoliuM acetate produced by BASF
1-Ethyl-3-MethyliMidazoliuM acetate produced by BASF, >=90% | [EINECS(EC#)]
604-344-8 | [Molecular Formula]
C8H14N2O2 | [MDL Number]
MFCD06798186 | [MOL File]
143314-17-4.mol | [Molecular Weight]
170.21 |
| Chemical Properties | Back Directory | [Melting point ]
-20℃ | [density ]
1.027 g/cm 3 at 25 °C | [vapor pressure ]
0-0.001Pa at 20-50℃ | [refractive index ]
n20/D 1.502 | [Fp ]
164 °C | [storage temp. ]
Inert atmosphere,Room Temperature | [form ]
Liquid | [color ]
Light yellow to Amber to Dark green | [Water Solubility ]
Soluble in water, acetonitrile, acetone, dichloromethane. | [Sensitive ]
Moisture Sensitive | [InChI]
InChI=1S/C6H11N2.C2H4O2/c1-3-8-5-4-7(2)6-8;1-2(3)4/h4-6H,3H2,1-2H3;1H3,(H,3,4)/q+1;/p-1 | [InChIKey]
XIYUIMLQTKODPS-UHFFFAOYSA-M | [SMILES]
[N+]1(=CN(C=C1)CC)C.C(C)(=O)[O-] | [LogP]
-2.5--2 at 23℃ and pH6.4 | [EPA Substance Registry System]
1H-Imidazolium, 3-ethyl-1-methyl-, acetate (1:1) (143314-17-4) | [ECW]
3.2 V |
| Hazard Information | Back Directory | [Conductivity]
2.50 mS/cm | [Uses]
1-Ethyl-3-methylimidazolium Acetate is ionic liquid; used in method for efficiently extracting high purity gutta percha gum based on two-phase ionic liquid and organic solvent. | [General Description]
We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product has been enhanced for catalytic efficiency. Click here for more information. | [Synthesis]
General procedure for the synthesis of 1-ethyl-3-methylimidazole acetate from lead acetate trihydrate and 1-ethyl-3-methylimidazole bromide salt: First, 1-ethyl-3-methylimidazole bromide salt (0.2 mol) and lead (II) acetate trihydrate (0.1 mol) were dissolved in 30 mL and 70 mL of distilled water, respectively. After both were completely dissolved, the 1-ethyl-3-methylimidazole bromide salt solution was slowly added to the lead (II) acetate trihydrate solution under vigorous mechanical stirring. The reaction was stirred under nitrogen protection at a constant temperature of 35°C for 48 hours. Upon completion of the reaction, the reaction mixture was refrigerated at 3 °C for 12 h to promote the formation of a precipitate, which was subsequently removed by filtration. The filtrate was removed from water by distillation under reduced pressure to give the final 1-ethyl-3-methylimidazole acetate (EMIMAc), the product was a pale yellow viscous liquid with 0.02% moisture content and 0.004% bromide content in 93% yield. | [References]
[1] Carbohydrate Polymers, 2013, vol. 94, # 1, p. 505 - 510
[2] Journal of Molecular Structure, 2012, vol. 1015, p. 147 - 155
[3] Carbohydrate Polymers, 2012, vol. 89, # 1, p. 7 - 16
[4] Carbohydrate Polymers, 2012, vol. 90, # 2, p. 792 - 798 |
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