1-Ethyl-3-methylimidazolium Trifluoromethanesulfonate(EMIM Otf) - ≥98% , CAS No.145022-44-2

CAS: 145022-44-2 Cat. No.: E101508 Molecular Weight: 260.23 EC Number: 680-002-1
AVAILABLE TO ORDER
GRADE & PURITY ≥98%
Synonyms
D70998 | AKOS015903871 | C7H11F3N2O3S | EMIM Otf | 3-Ethyl-1-methyl-1H-imidazol-3-ium trifluoromethanesulfonate | DTXSID4047965 | EC 680-002-1 | FT-0607753 | 1-Ethyl-3-methylimidazolium Triflate | MFCD00210008 | A884681 | Q-102676 | 1-Ethyl-3-methylimidaz
Storage
Room temperature,Argon charged,Desiccated
Shipped In
Normal
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Size
Status
Price
Qty
1g
E101508-1g
3
$9.90
5g
E101508-5g
3
$14.90
25g
E101508-25g
3
$37.90
100g
E101508-100g
3
$95.90
500g
E101508-500g
1
$459.90
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Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Room temperature,Argon charged,Desiccated Ships Normal Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 17 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

1-ethyl-3-methylimidazolium trifluoromethanesulfonate can be used as solvent to produce ionic polymer polymer composites (ip2c) and in lipase catalyzed acylation of 4-pentenoic acid enantioselective amines.

Specifications

Synonyms
D70998 | AKOS015903871 | C7H11F3N2O3S | EMIM Otf | 3-Ethyl-1-methyl-1H-imidazol-3-ium trifluoromethanesulfonate | DTXSID4047965 | EC 680-002-1 | FT-0607753 | 1-Ethyl-3-methylimidazolium Triflate | MFCD00210008 | A884681 | Q-102676 | 1-Ethyl-3-methylimidaz
Specifications & Purity
≥98%
Storage
Room temperature, Argon charged, Desiccated
Shipped In
Normal
Purity
≥98%
Names and Identifiers
Pubchem Sid504761544
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504761544
Canonical SmilesCCN1C=C[N+](=C1)C.C(F)(F)(F)S(=O)(=O)[O-]
IUPAC Name1-ethyl-3-methylimidazol-3-ium;trifluoromethanesulfonate
InChIKeyZPTRYWVRCNOTAS-UHFFFAOYSA-M
INCHI1S/C6H11N2.CHF3O3S/c1-3-8-5-4-7(2)6-8;2-1(3,4)8(5,6)7/h4-6H,3H2,1-2H3;(H,5,6,7)/q+1;/p-1
Isomeric SMILES CCN1C=C[N+](=C1)C.C(F)(F)(F)S(=O)(=O)[O-]
WGK Germany 3
Molecular Weight 260.23
Reaxy-Rn 8802556
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=8802556&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClassAzoles
SubclassImidazoles
Intermediate Tree Nodes Substituted imidazoles
Direct ParentN-substituted imidazoles
Alternative Parents Heteroaromatic compounds  Azacyclic compounds  Organopnictogen compounds  Organonitrogen compounds  Organic salts  Hydrocarbon derivatives  
Molecular FrameworkNot available
Substituents N-substituted imidazole - Heteroaromatic compound - Azacycle - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organic salt - Organonitrogen compound - Aromatic heteromonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as n-substituted imidazoles. These are heterocyclic compounds containing an imidazole ring substituted at position 1.
External Descriptors Not available
3D Structure
Interactive Chemical Structure Model





Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

34 results found

Lot NumberCertificate TypeDateItem
C2625499Certificate of AnalysisMar 11, 2026 E101508
C2625455Certificate of AnalysisMar 11, 2026 E101508
C2625432Certificate of AnalysisMar 11, 2026 E101508
C2625425Certificate of AnalysisMar 11, 2026 E101508
C2625418Certificate of AnalysisMar 11, 2026 E101508
B2225213Certificate of AnalysisDec 10, 2025 E101508
J2523447Certificate of AnalysisOct 09, 2025 E101508
J2523443Certificate of AnalysisOct 09, 2025 E101508
J2523444Certificate of AnalysisOct 09, 2025 E101508
C2611178Certificate of AnalysisOct 09, 2025 E101508
J2523446Certificate of AnalysisOct 09, 2025 E101508
J2523445Certificate of AnalysisOct 09, 2025 E101508
C2506431Certificate of AnalysisJan 23, 2025 E101508
F2526104Certificate of AnalysisJan 23, 2025 E101508
I2519052Certificate of AnalysisJan 23, 2025 E101508
C2506384Certificate of AnalysisJan 23, 2025 E101508
C2506385Certificate of AnalysisJan 23, 2025 E101508
C2506430Certificate of AnalysisJan 23, 2025 E101508
F2428408Certificate of AnalysisJun 24, 2024 E101508
F2428409Certificate of AnalysisJun 24, 2024 E101508
F2428410Certificate of AnalysisJun 24, 2024 E101508
F2428411Certificate of AnalysisJun 24, 2024 E101508
F2428412Certificate of AnalysisJun 24, 2024 E101508
F2418126Certificate of AnalysisJun 14, 2024 E101508
F2418127Certificate of AnalysisJun 14, 2024 E101508
E2323492Certificate of AnalysisMar 03, 2023 E101508
E2323564Certificate of AnalysisMar 03, 2023 E101508
E2323488Certificate of AnalysisMar 03, 2023 E101508
E2323472Certificate of AnalysisMar 03, 2023 E101508
I2202156Certificate of AnalysisDec 29, 2021 E101508
B2225107Certificate of AnalysisDec 29, 2021 E101508
B2309158Certificate of AnalysisDec 29, 2021 E101508
B2225255Certificate of AnalysisDec 29, 2021 E101508
B2225194Certificate of AnalysisDec 29, 2021 E101508

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Chemical and Physical Properties
SolubilitySoluble in water.
SensitivityMoisture sensitive; Air sensitive
Refractive Index1.435
Flash Point(°F)235.4 °F
Flash Point(°C)113 °C
Boil Point(°C)>350°C
Melt Point(°C)-10 °C
Molecular Weight260.240 g/mol
XLogP3
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count6
Rotatable Bond Count1
Exact Mass260.044 Da
Monoisotopic Mass260.044 Da
Topological Polar Surface Area74.400 Ų
Heavy Atom Count16
Formal Charge0
Complexity218.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count2
Documents & Articles
Citations of This Product
References
1. Muhammad Umair Ahmad, Guoying Zhao, Shahid Hussain.  (2023)  Trifloaluminate Ionic Liquids Supported UIO-67 as Lewis Acidic Catalyst for Excellent Synthesis of Alkyl Levulinates.  ChemistrySelect,  (43): (e202302665).  [PMID:] [10.1002/slct.202302665]
2. Keqin Mi, Liping Tong, Min Yu, Yue Zhao, Hao Dong, Shifeng Hou.  (2023)  Fabrication and application of a 3D-rGO electrochemical sensor for SO2 detection in ionic liquids.  Analytical Methods,  15  (29): (3522-3531).  [PMID:37435701] [10.1039/D3AY00805C]
3. Tang Jie, Zhao Chao, Luo Qian, Chang Yu, Yang Zhenguo, Pan Tingrui.  (2022)  Ultrahigh-transparency and pressure-sensitive iontronic device for tactile intelligence.  npj Flexible Electronics,  (1): (1-14).  [PMID:] [10.1038/s41528-022-00162-y]
4. Jianghe Liu, Sultan Ahmed, Zeba Khanam, Ting Wang, Shenhua Song.  (2020)  Ionic Liquid-Incorporated Zn-Ion Conducting Polymer Electrolyte Membranes.  Polymers,  12  (8): (1755).  [PMID:32781515] [10.3390/polym12081755]
5. Xinyi Sun, Zhang Wen, Yiwen Liu, Min Zhang, Wei Li, Chuanchao Sheng, Sixie Yang, Haoshen Zhou, Ping He.  (2025)  A Hydrogel Electrolyte-Based Zn−CO2 Battery with Improved Life.  Small,      [PMID:39901662] [10.1002/smll.202411867]
6. Duozhen Chai, Chongli Wang, Jinzhen Liu, Dongfeng Cao, Kaixuan Guo, Yuankun Wang, Ye Yuan, Francis Verpoort.  (2025)  CuCl/Ionic Liquid Catalyzed Cascade Transformation of CO2 and Alkyne-1,2-Diols: Synthesis of Keto-Functionalized Cyclic Carbonates.  Catalysts,  15  (3): (279).  [PMID:] [10.3390/catal15030279]
7. He Xiangnan, Zhang Biao, Liu Qingjiang, Chen Hao, Cheng Jianxiang, Jian Bingcong, Yin Hanlin, Li Honggeng, Duan Ke, Zhang Jianwei, Ge Qi.  (2024)  Highly conductive and stretchable nanostructured ionogels for 3D printing capacitive sensors with superior performance.  Nature Communications,  15  (1): (1-12).  [PMID:39085229] [10.1038/s41467-024-50797-w]
8. Tong Guan, Huayang Li, Jinyun Liu, Wuxu Zhang, Siying Wang, Wentao Ye, Baoru Bian, Xiaohui Yi, Yuanzhao Wu, Yiwei Liu, Juan Du, Jie Shang, Run-Wei Li.  (2025)  Preparation of Ion Composite Photosensitive Resin and Its Application in 3D-Printing Highly Sensitive Pressure Sensor.  SENSORS,  25  (5): (1348).  [PMID:40096106] [10.3390/s25051348]
9. Youtong Wu, Xueting Li, Jie Tao, Yuqi Zhang, Xihua Lu.  (2024)  Tunable temperature-responsive photonic ionogels with dual signals output.  JOURNAL OF COLLOID AND INTERFACE SCIENCE,      [PMID:39163665] [10.1016/j.jcis.2024.08.094]
10. Lulu Wang, Xiaodong Yin, Haifeng Cheng, Chuan Liu, Songjia Han, Wei Xie, Chen Chen.  (2025)  Improving Nonvolatile Properties of Solid-Electrolyte-Based Artificial Synapses via Ion Dynamics Modulation in Organic Electrochemical Transistors.  SmartMat,  (4): (e70025).  [PMID:] [10.1002/smm2.70025]
11. Hua Yuan, Jiaqi Zhang, Caixia Li, Jie Xin Wang, Yuan Le.  (2025)  Collagen fibers from chrome shavings for an ionic capacitive pressure sensor.  Journal of Materials Chemistry C,      [PMID:] [10.1039/D4TC05343E]
12. Lyu Xiaolin, Yu Kun, Zhang Haoqi, Zhou Piaopiao, Shen Zhihao, Zou Zhigang.  (2025)  Tough fiber-reinforced composite ionogels with crack resistance surpassing metals.  Nature Communications,  16  (1): (1-11).  [PMID:40301368] [10.1038/s41467-025-59396-9]
13. Ge Ren, Jiale Yang, Xuanting Wang, Guangmei Hu, Hua Chen, Qing Fang, Anneng Yang.  (2025)  Stretchable and Self-Adhesive PEDOT:PSS Electrode for Fully Integrated and Long-Term Electrocardiogram Monitoring.  ACS Applied Polymer Materials,      [PMID:] [10.1021/acsapm.4c04052]
14. Li Fan, Xue Hua, Lin Xiuzhu, Wang Juan, Li Juan, Zhao Hongran, Zhang Tong.  (2025)  High-sensitivity temperature sensors via ion capture-release dynamics for human thermal comfort monitoring.  Microsystems & Nanoengineering,  11  (1): (1-10).  [PMID:41130957] [10.1038/s41378-025-01030-1]
15. Xusheng Ma, Yaqian Zhou, Siming Bian, Ziyang Li, Yang Jiang, Shengtao Zhang, Sijia Li, Yan Li.  (2026)  Wireless and programmable electrochemical soft actuators of ionogels for tracking and liquild control.  SENSORS AND ACTUATORS B-CHEMICAL,      [PMID:] [10.1016/j.snb.2026.139722]
16. Na Li, Ping He, Zhihui Qin, Yichen Yan, Sidi Duan, Yunfeng Li, Xiaojiao Shi, Yuxuan Qiao, Junan Jiang, Tifeng Jiao, Ximin He.  (2026)  Rapid self-assembly of robust ultrathin ionogel films for high-performance bioelectronics.  Science Advances,  12  (9):   [PMID:41758950] [10.1126/sciadv.aeb4391]
17. Qing Ming, Said Amzil, Lei Zhang, Meilan Peng, Shengyao Luo, Yiyao Xiao, Yinghui Li, Mengqi Wu, Shuang Tian, Tianle Zheng, Peter Müller-Buschbaum, Yejian Xue, Ya-Jun Cheng, Yonggao Xia.  (2026)  Ionic Liquid Additive Enables Dual-Interfacial Stabilization for High-Voltage Lithium–Metal Batteries with Low-Concentration Electrolytes.  ACS Applied Materials & Interfaces,      [PMID:] [10.1021/acsami.6c02022]
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