Determine the necessary mass, volume, or concentration for preparing a solution.
| Activity Type | Activity Value -log(M) | Mechanism of Action | Activity Reference | Publications (PubMed IDs) |
|---|
≥98%(T) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at 2-8°C,Protected from light Ships Wet ice 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 9 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
| Pubchem Sid | 488185658 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488185658 |
| Sonrisas canónicas | C(F)(F)(F)S(=O)(=O)N |
| IUPAC Name | trifluoromethanesulfonamide |
| InChIKey | KAKQVSNHTBLJCH-UHFFFAOYSA-N |
| INCHI | 1S/CH2F3NO2S/c2-1(3,4)8(5,6)7/h(H2,5,6,7) |
| Isómeros SMILES | C(F)(F)(F)S(=O)(=O)N |
| WGK Alemania | 3 |
| Peso molecular | 149.09 |
| Reaxy-Rn | 1812099 |
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 |
| Clase | Organic sulfonic acids and derivatives |
| Subclass | Organosulfonic acids and derivatives |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Organosulfonamides |
| Alternative Parents | Organic sulfonamides Aminosulfonyl compounds Trihalomethanes Organofluorides Organic oxides Organic nitrogen compounds Hydrocarbon derivatives Alkyl fluorides |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Organic sulfonic acid amide - Organosulfonic acid amide - Sulfonyl - Aminosulfonyl compound - Trihalomethane - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Organosulfur compound - Organofluoride - Organohalogen compound - Alkyl halide - Alkyl fluoride - Halomethane - Aliphatic acyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as organosulfonamides. These are compounds containing the sulfonamide functional group, an amide of sulfonic acid with the general structure R1S(=O)2N(R2)R3 (R1=alkyl, aryl; R2,R3=H, alkyl, aryl). |
| External Descriptors | Not available |
| Activity Type | Activity Value -log(M) | Mechanism of Action | Activity Reference | Publications (PubMed IDs) |
|---|
| Activity Type | Activity Value -log(M) | Mechanism of Action | Activity Reference | Publications (PubMed IDs) |
|---|
| Activity Type | Activity Value -log(M) | Mechanism of Action | Activity Reference | Publications (PubMed IDs) |
|---|
| Activity Type | Activity Value -log(M) | Mechanism of Action | Activity Reference | Publications (PubMed IDs) |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Fecha | Articulo |
|---|---|---|---|
| Certificate of Analysis | May 21, 2026 | T161647 | |
| Certificate of Analysis | May 21, 2026 | T161647 | |
| Certificate of Analysis | May 21, 2026 | T161647 | |
| Certificate of Analysis | May 21, 2026 | T161647 | |
| Certificate of Analysis | Aug 09, 2025 | T161647 | |
| Certificate of Analysis | Aug 09, 2025 | T161647 | |
| Certificate of Analysis | Aug 09, 2025 | T161647 | |
| Certificate of Analysis | Aug 09, 2025 | T161647 | |
| Certificate of Analysis | Apr 03, 2025 | T161647 | |
| Certificate of Analysis | Feb 14, 2025 | T161647 | |
| Certificate of Analysis | Feb 14, 2025 | T161647 | |
| Certificate of Analysis | Feb 14, 2025 | T161647 | |
| Certificate of Analysis | Feb 14, 2025 | T161647 | |
| Certificate of Analysis | Feb 14, 2025 | T161647 | |
| Certificate of Analysis | Nov 02, 2024 | T161647 | |
| Certificate of Analysis | Nov 02, 2024 | T161647 | |
| Certificate of Analysis | Nov 02, 2024 | T161647 | |
| Certificate of Analysis | Jun 28, 2024 | T161647 | |
| Certificate of Analysis | Jun 28, 2024 | T161647 | |
| Certificate of Analysis | Jun 28, 2024 | T161647 | |
| Certificate of Analysis | Jun 28, 2024 | T161647 | |
| Certificate of Analysis | Mar 12, 2024 | T161647 | |
| Certificate of Analysis | Mar 12, 2024 | T161647 | |
| Certificate of Analysis | Feb 14, 2023 | T161647 | |
| Certificate of Analysis | Feb 14, 2023 | T161647 | |
| Certificate of Analysis | Feb 14, 2023 | T161647 | |
| Certificate of Analysis | Feb 14, 2023 | T161647 | |
| Certificate of Analysis | Feb 14, 2023 | T161647 | |
| Certificate of Analysis | Feb 14, 2023 | T161647 | |
| Certificate of Analysis | Jan 27, 2022 | T161647 | |
| Certificate of Analysis | Dec 16, 2021 | T161647 | |
| Certificate of Analysis | Dec 16, 2021 | T161647 | |
| Certificate of Analysis | Dec 16, 2021 | T161647 |
| Solubilidad | Soluble in water. |
|---|---|
| Sensibilidad | Light sensitive |
| Punto de fusión (°C) | 118-124 °C |
| Peso molecular | 149.090 g/mol |
| XLogP3 | 0.100 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 6 |
| Rotatable Bond Count | 0 |
| Exact Mass | 148.976 Da |
| Monoisotopic Mass | 148.976 Da |
| Topological Polar Surface Area | 68.500 Ų |
| Heavy Atom Count | 8 |
| Formal Charge | 0 |
| Complexity | 161.000 |
| 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 | 1 |
| 1. Mengdi Wang, Qin Yao, Sanyin Qu, Yanling Chen, Hui Li, Lidong Chen. (2020) Preparation and Thermoelectric Properties of Semiconducting Single-Walled Carbon Nanotubes/Regioregular Poly(3-dodecylthiophene) Composite Films. Polymers, 12 (11): (2720). [PMID:33212899] [10.3390/polym12112720] |
| 2. Muhammad Mushtaq, Xianwei Guo, Yinzhong Wang, Liangwei Hao, Zhiyuan Lin, Haijun Yu. (2020) Composite Cathode Architecture with Improved Oxidation Kinetics in Polymer-Based Li–O2 Batteries. ACS Applied Materials & Interfaces, [PMID:32525303] [10.1021/acsami.0c01922] |
| 3. Hui Peng, Xin Fang, Wen Huang, Wei Liu, Yonggang Yang, Qun Zhou, Yi Li. (2024) Fabrication of Single-Ion Conductors Based on Liquid Crystal Polymer Network for Quasi-Solid-State Lithium Ion Batteries. ACS Applied Materials & Interfaces, [PMID:39145510] [10.1021/acsami.4c11500] |
| 4. Jiaqi Shuai, Shengqiu Zhao, Yucong Liao, Fanglin Wu, Rui Wang, Letian Wang, Chunhui Shen, Haolin Tang. (2024) Rationally designing anti-poisoning polymer electrolyte by electronegativity modulation: Towards efficient ammonia-cracked hydrogen fuel cells. JOURNAL OF MEMBRANE SCIENCE, [PMID:] [10.1016/j.memsci.2024.122528] |
| 5. Puyan Huang, Xiao Wang, Jian Guo, Yu Ding, Guorong Chen, Jifang Fu, Liyi Shi, Alena A. Nevar, Le Yu. (2025) Molecular design of cross-linked single-ion polymer electrolytes enabling robust LiF-rich solid electrolyte interface for stable lithium metal batteries. JOURNAL OF COLLOID AND INTERFACE SCIENCE, [PMID:40845446] [10.1016/j.jcis.2025.138708] |
| 6. Hui Peng, Tangqi Hu, Wen Huang, Wei Liu, Yonggang Yang, Yi Li. (2025) Control the single-ion conductivity by tuning smectic liquid crystal polymer network for quasi-solid-state electrolytes. COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS, [PMID:] [10.1016/j.colsurfa.2025.138396] |
| 7. Naijie Wang, Xiangqun Chen, Qiu Sun, Ying Song, Tiezhu Xin. (2023) Fast Li+ Transport Polyurethane-Based Single-Ion Conducting Polymer Electrolyte with Sulfonamide Side chains in the Hard Segment for Lithium Metal Batteries. ACS Applied Materials & Interfaces, [PMID:37552620] [10.1021/acsami.3c06956] |
| 8. Tangqi Hu, Wen Huang, Wei Liu, Yonggang Yang, Yi Li. (2026) Single-ionic conductive quasi-solid-state electrolyte membranes based on nematic liquid crystal polymer network. Journal of Energy Storage, [PMID:] [10.1016/j.est.2025.120272] |
| 9. Xinyuan Shan, Caiyun Wang, Zhaowei Song, Sijin Jin, Jia Tian, Lengwan Li, Xin Ma, Linming Bai, Hang Ding, Sheng Zhao, Wei Niu, Bingrui Li, Alexei P. Sokolov, Huabin Yang, Zhihong Nie, Peng-Fei Cao. (2026) Efficient Li+ Transport through a Single-Ion-Conducting Protective Layer for Stable Lithium–Metal Batteries. ACS Applied Materials & Interfaces, [PMID:] [10.1021/acsami.5c25202] |