Determine the necessary mass, volume, or concentration for preparing a solution.
≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Protected from light,Room temperature,Argon charged Ships Normal Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 7 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
| Canonical Smiles | C(F)(F)(F)S(=O)(=O)[O-].C(F)(F)(F)S(=O)(=O)[O-].C(F)(F)(F)S(=O)(=O)[O-].[In+3] |
|---|---|
| IUPAC Name | indium(3+);trifluoromethanesulfonate |
| InChIKey | UCYRAEIHXSVXPV-UHFFFAOYSA-K |
| INCHI | 1S/3CHF3O3S.In/c3*2-1(3,4)8(5,6)7;/h3*(H,5,6,7);/q;;;+3/p-3 |
| Isomeric SMILES | C(F)(F)(F)S(=O)(=O)[O-].C(F)(F)(F)S(=O)(=O)[O-].C(F)(F)(F)S(=O)(=O)[O-].[In+3] |
| WGK Germany | 3 |
| PubChem CID | 2734680 |
| UN Number | 3261 |
| Molecular Weight | 562.03 |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic acids and derivatives |
| Class | Organic sulfonic acids and derivatives |
| Subclass | Organosulfonic acids and derivatives |
| Intermediate Tree Nodes | Alkanesulfonic acids and derivatives - Alkanesulfonic acids |
| Direct Parent | Trifluoromethanesulfonates |
| Alternative Parents | Sulfonyls Organosulfonic acids Methanesulfonates Trihalomethanes Organic metal halides Organofluorides Organic oxides Hydrocarbon derivatives Alkyl fluorides |
| Molecular Framework | Not available |
| Substituents | Trifluoromethanesulfonate - Methanesulfonate - Organosulfonic acid - Sulfonyl - Trihalomethane - Organic metal halide - Halomethane - Hydrocarbon derivative - Organic salt - Organic oxide - Organosulfur compound - Organofluoride - Organohalogen compound - Organic oxygen compound - Alkyl halide - Alkyl fluoride - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as trifluoromethanesulfonates. These are alkanesulfonic acids, that contain a sulfonate group that is substituted with a trifluoromethyl group. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
| Certificate of Analysis | Feb 13, 2025 | I113623 | |
| Certificate of Analysis | Feb 13, 2025 | I113623 | |
| Certificate of Analysis | Feb 13, 2025 | I113623 | |
| Certificate of Analysis | Feb 13, 2025 | I113623 | |
| Certificate of Analysis | Feb 13, 2025 | I113623 | |
| Certificate of Analysis | Feb 13, 2025 | I113623 | |
| Certificate of Analysis | Feb 13, 2025 | I113623 | |
| Certificate of Analysis | Feb 13, 2025 | I113623 | |
| Certificate of Analysis | Feb 13, 2025 | I113623 | |
| Certificate of Analysis | Feb 13, 2025 | I113623 | |
| Certificate of Analysis | Jul 13, 2024 | I113623 | |
| Certificate of Analysis | Jul 13, 2024 | I113623 | |
| Certificate of Analysis | Jul 13, 2024 | I113623 | |
| Certificate of Analysis | Dec 23, 2021 | I113623 | |
| Certificate of Analysis | Dec 23, 2021 | I113623 | |
| Certificate of Analysis | Dec 23, 2021 | I113623 | |
| Certificate of Analysis | Dec 23, 2021 | I113623 | |
| Certificate of Analysis | Dec 23, 2021 | I113623 | |
| Certificate of Analysis | Dec 23, 2021 | I113623 |
| Solubility | Slightly soluble in hydrocarbons and diethyl ether. Insoluble in water |
|---|---|
| Sensitivity | Moisture sensitive. |
| Molecular Weight | 562.000 g/mol |
| XLogP3 | |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 18 |
| Rotatable Bond Count | 0 |
| Exact Mass | 561.76 Da |
| Monoisotopic Mass | 561.76 Da |
| Topological Polar Surface Area | 197.000 Ų |
| Heavy Atom Count | 25 |
| Formal Charge | 0 |
| Complexity | 145.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 4 |
| 1. Weidong Zhang, Zeyu Shen, Siyuan Li, Lei Fan, Xinyang Wang, Fang Chen, Xiaoxian Zang, Tian Wu, Fuyuan Ma, Yingying Lu. (2020) Engineering Wavy-Nanostructured Anode Interphases with Fast Ion Transfer Kinetics: Toward Practical Li-Metal Full Batteries. ADVANCED FUNCTIONAL MATERIALS, 30 (39): (2003800). [PMID:] [10.1002/adfm.202003800] |
| 2. Huang Zhongliang, Hu Shengnan, Sun Mingzi, Xu Yong, Liu Shangheng, Ren Renjie, Zhuang Lin, Chan Ting-Shan, Hu Zhiwei, Ding Tianyi, Zhou Jing, Liu Liangbin, Wang Mingmin, Huang Yu-Cheng, Tian Na, Bu Lingzheng, Huang Bolong, Huang Xiaoqing. (2024) Implanting oxophilic metal in PtRu nanowires for hydrogen oxidation catalysis. Nature Communications, 15 (1): (1-11). [PMID:38321034] [10.1038/s41467-024-45369-x] |
| 3. Fukun Li, Lin Shuai, Yuan Tian, Zheng Tian, QingYa Cao, Jinhang Dai, Song Wang, Haifeng Gong, Junjun Shi. (2025) Microwave-assisted catalytic upgrading of 2,5-hexanedione to 2,5-dimethyltetrahydrofuran over metal triflate under H2-free conditions. INDUSTRIAL CROPS AND PRODUCTS, [PMID:] [10.1016/j.indcrop.2025.120741] |
| 4. Zilong Rao, Yu Zhang, Shuailong Zhao, Huai Liu, Rui Zhang, Wenlong Jia, Junhua Zhang, Yong Sun, Lincai Peng. (2025) Rational Improvement for the Catalytic Alcoholysis of Straw Biomass by Understanding the Role of Inorganic Components. ACS Sustainable Chemistry & Engineering, [PMID:] [10.1021/acssuschemeng.5c00690] |
| 5. Mingjie Wu, Xing Li, Yingmeng Zhang, Xuecui Mei, Fengli Shen, Chaoyue Zheng, Jin-Peng Xue, Lei Zhou. (2025) In-Situ Polymerization of 1,3-Dioxane Driven by a Bifunctional Initiator as Polymer Electrolytes for High Performance Solid-State Lithium Metal Batteries. ACS Applied Energy Materials, [PMID:] [10.1021/acsaem.5c01965] |
| 6. Haoyu Deng, Xueting Yang, Hanghang Chen, Dezhan Ye, Xiancai Jiang, Yazhou Chen, Chenyi Wang. (2024) Superior initiator reactivity and electrochemical properties of In(OTf)3 over Sn(OTf)2 for 1,3-dioxolane based solid polymer electrolyte. Journal of Energy Storage, [PMID:] [10.1016/j.est.2024.113693] |
| 7. Ruijie Guo, Zhenxi Li, Yiming Guo, Shilun Gao, Chao-Peng Wang, Huabin Yang, Peng-Fei Cao. (2026) Surpassing the conductivity-conversion trade-off in plasticizer-rich poly(1,3-dioxolane) electrolytes via an efficient initiator. Journal of Energy Chemistry, [PMID:] [10.1016/j.jechem.2026.02.019] |