Sodium trifluoromethanesulfonate - ≥98% , CAS No.2926-30-9

CAS: 2926-30-9 Cat. No.: S102743 Molecular Weight: 172.06 Beilstein Registry Number: 3728797 EC Number: 629-418-7 PubChem CID: 23676748
AVAILABLE TO ORDER
GRADE & PURITY ≥98%
Synonyms
Methanesulfonic acid, trifluoro-, sodium salt | Sodium triflate | AKOS005063791 | MFCD00061607 | Methanesulfonic acid, 1,1,1-trifluoro-, sodium salt (1:1) | Trifluoromethanesulfonic acid sodium salt | Sodium trifluoromethanesulfonate, Trace metals grade,
Storage
Argon charged,Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
5g
S102743-5g
2
$9.90
10g
S102743-10g
2
$10.90
25g
S102743-25g
2
$17.90
100g
S102743-100g
3
$49.90
500g
S102743-500g
1
$199.90
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Why this grade

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

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Storage & shipping

Argon charged,Room temperature 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.

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Literature proof

Cited in 27 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

Product Introduction

Sodium trifluoromethanesulfonate (Sodium triflate or NaOTf) is an efficient catalyst as well as a reagent in many organic reactions. The prominent application includes catalytic asymmetric Mannich-type reactions, Mannich-type reactions in water, and Diels-Alder reactions.


Application

Sodium trifluoromethanesulfonate can be employed as a reagent for the preparation of:

• Aryl fluorides via silver-catalyzed fluorination of arylstannanes.

• Ionic liquids such as N, N -dialkylpyrrolidinium triflate, N,N-dialkylimidazolium triflate, and N-alkylpyridinium triflate.

It can be also used as supporting electrolyte in electrochemical O-glycosylation of primary alcohols with O-protected thioglycosides.

Specifications

Synonyms
Methanesulfonic acid, trifluoro-, sodium salt | Sodium triflate | AKOS005063791 | MFCD00061607 | Methanesulfonic acid, 1, 1, 1-trifluoro-, sodium salt (1:1) | Trifluoromethanesulfonic acid sodium salt | Sodium trifluoromethanesulfonate, Trace metals grade,
Specifications & Purity
≥98%
Storage
Argon charged, Room temperature
Shipped In
Normal
Purity
≥98%
Names and Identifiers
Pubchem Sid488200493
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488200493
Canonical SmilesC(F)(F)(F)S(=O)(=O)[O-].[Na+]
IUPAC Namesodium;trifluoromethanesulfonate
InChIKeyXGPOMXSYOKFBHS-UHFFFAOYSA-M
INCHI1S/CHF3O3S.Na/c2-1(3,4)8(5,6)7;/h(H,5,6,7);/q;+1/p-1
Isomeric SMILES C(F)(F)(F)S(=O)(=O)[O-].[Na+]
WGK Germany 3
PubChem CID 23676748
Molecular Weight 172.06
Beilstein 3728797
Reaxy-Rn 3728797

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
SuperclassOrganic acids and derivatives
ClassOrganic sulfonic acids and derivatives
SubclassOrganosulfonic acids and derivatives
Intermediate Tree Nodes Alkanesulfonic acids and derivatives - Alkanesulfonic acids
Direct ParentTrifluoromethanesulfonates
Alternative Parents Sulfonyls  Organosulfonic acids  Methanesulfonates  Trihalomethanes  Organic metal halides  Organofluorides  Organic sodium salts  Organic oxides  Hydrocarbon derivatives  Alkyl fluorides  Organic cations  
Molecular FrameworkAliphatic acyclic compounds
Substituents Trifluoromethanesulfonate - Methanesulfonate - Organosulfonic acid - Sulfonyl - Trihalomethane - Organic metal halide - Organic alkali metal salt - Alkyl fluoride - Alkyl halide - Hydrocarbon derivative - Organic sodium salt - Organic salt - Halomethane - Organic oxide - Organosulfur compound - Organofluoride - Organohalogen compound - Organic oxygen compound - Organic cation - Aliphatic acyclic compound
DescriptionThis 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
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
CA2 Tclin Carbonic anhydrase II (17698 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA1 Tclin Carbonic anhydrase I (13240 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
Carbonic anhydrase (69 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mechanisms of Action
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.

45 results found

Lot NumberCertificate TypeDateItem
L2502648Certificate of AnalysisOct 20, 2025 S102743
J2531626Certificate of AnalysisOct 20, 2025 S102743
J2531627Certificate of AnalysisOct 20, 2025 S102743
J2531628Certificate of AnalysisOct 20, 2025 S102743
J2531629Certificate of AnalysisOct 20, 2025 S102743
J2531630Certificate of AnalysisOct 20, 2025 S102743
C2606082Certificate of AnalysisOct 20, 2025 S102743
L2502616Certificate of AnalysisOct 20, 2025 S102743
L2502617Certificate of AnalysisOct 20, 2025 S102743
L2502646Certificate of AnalysisOct 20, 2025 S102743
L2502647Certificate of AnalysisOct 20, 2025 S102743
E2526459Certificate of AnalysisApr 26, 2025 S102743
E2526460Certificate of AnalysisApr 26, 2025 S102743
E2526462Certificate of AnalysisApr 26, 2025 S102743
E2526471Certificate of AnalysisApr 26, 2025 S102743
E2526472Certificate of AnalysisApr 26, 2025 S102743
L2413726Certificate of AnalysisNov 29, 2024 S102743
L2413718Certificate of AnalysisNov 29, 2024 S102743
L2413732Certificate of AnalysisNov 29, 2024 S102743
I2413248Certificate of AnalysisAug 31, 2024 S102743
I2413252Certificate of AnalysisAug 31, 2024 S102743
I2413251Certificate of AnalysisAug 31, 2024 S102743
I2413250Certificate of AnalysisAug 31, 2024 S102743
I2413249Certificate of AnalysisAug 31, 2024 S102743
K2418410Certificate of AnalysisJun 19, 2024 S102743
K2418409Certificate of AnalysisJun 19, 2024 S102743
K2418408Certificate of AnalysisJun 19, 2024 S102743
I2312635Certificate of AnalysisAug 14, 2023 S102743
I2312634Certificate of AnalysisAug 14, 2023 S102743
I2312633Certificate of AnalysisAug 14, 2023 S102743
E2414047Certificate of AnalysisAug 14, 2023 S102743
B2303965Certificate of AnalysisFeb 15, 2023 S102743
B2303964Certificate of AnalysisFeb 15, 2023 S102743
E23291166Certificate of AnalysisFeb 09, 2023 S102743
G2315034Certificate of AnalysisFeb 09, 2023 S102743
I2311063Certificate of AnalysisFeb 09, 2023 S102743
C23021180Certificate of AnalysisFeb 09, 2023 S102743
C23021179Certificate of AnalysisFeb 09, 2023 S102743
C23021178Certificate of AnalysisFeb 09, 2023 S102743
C23021174Certificate of AnalysisFeb 09, 2023 S102743
C23021173Certificate of AnalysisFeb 09, 2023 S102743
C23021172Certificate of AnalysisFeb 09, 2023 S102743
C23021171Certificate of AnalysisFeb 09, 2023 S102743
K2217240Certificate of AnalysisNov 09, 2021 S102743
K2217241Certificate of AnalysisNov 09, 2021 S102743

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Chemical and Physical Properties
SolubilitySoluble in water (1000g/L).
SensitivityHygroscopic.
Melt Point(°C)253-255°C
Molecular Weight172.060 g/mol
XLogP3
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count6
Rotatable Bond Count0
Exact Mass171.942 Da
Monoisotopic Mass171.942 Da
Topological Polar Surface Area65.600 Ų
Heavy Atom Count9
Formal Charge0
Complexity162.000
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. Guoqing Wang, Miao Jiang, Zhao Sun, Leilei Qian, Guangjun Ji, Lei Ma, Cunyao Li, Hong Du, Li Yan, Yunjie Ding.  (2023)  Tandem Conversion of Fructose to Bio-diketones Using a Multifunctional Pd-POPs-CF3SO3H Catalyst.  ChemCatChem,  15  (20): (e202300793).  [PMID:] [10.1002/cctc.202300793]
2. Depeng Li, Qingqing Guan, Xiaoyun Hu, Yuhong Su, Zhen Su.  (2023)  Reversible and irreversible stimuli-responsive chromism of a square-planar platinum(II) salt.  RSC Advances,  13  (36): (24878-24886).  [PMID:37614796] [10.1039/D3RA03554A]
3. Dengfeng Yu, Bo Yang, Huimin Liang, Gongyuan Zhao, Hong Zhang, Yuanlin Wang, Ye Sun, Miao Yu.  (2022)  Fabrication of Co0.85Se@CN double-walled hollow cages to address the volume expansion of anode and enhance ion diffusion for sodium-ion storage.  ELECTROCHIMICA ACTA,      [PMID:] [10.1016/j.electacta.2022.140839]
4. Jianghe Liu, Zijian Ye, Xingcheng Hu, Sultan Ahmed, Shenhua Song.  (2021)  High-Performance Na-Ion Conducting Polymer Gel Membrane for Supercapacitor Applications.  ACS Applied Polymer Materials,      [PMID:] [10.1021/acsapm.1c01267]
5. Huang Zhaodong, Hou Yue, Wang Tairan, Zhao Yuwei, Liang Guojin, Li Xinliang, Guo Ying, Yang Qi, Chen Ze, Li Qing, Ma Longtao, Fan Jun, Zhi Chunyi.  (2021)  Manipulating anion intercalation enables a high-voltage aqueous dual ion battery.  Nature Communications,  12  (1): (1-11).  [PMID:34035250] [10.1038/s41467-021-23369-5]
6. Zhen Su, Yushu Li, Jiguang Li, Xincun Dou.  (2021)  Ultrasensitive luminescent turn-on detection of perchlorate particulates by triggering supramolecular self-assembly of platinum(II) complex in hydrogel matrix.  SENSORS AND ACTUATORS B-CHEMICAL,      [PMID:] [10.1016/j.snb.2021.129728]
7. Yajun Zhao, Tao Sun, Qing Yin, Jian Zhang, Shuoxiao Zhang, Jianeng Luo, Hong Yan, Lirong Zheng, Jingbin Han, Min Wei.  (2019)  Discovery of a new intercalation-type anode for high-performance sodium ion batteries.  Journal of Materials Chemistry A,  (25): (15371-15377).  [PMID:] [10.1039/C9TA03753E]
8. Haibin Wang, Shaodong Liu, Tingting Sun, Zhanao Lv, Zhen Zhan, Guochuan Yin, Zhuqi Chen.  (2019)  Lewis acid promoted double bond migration in O-allyl to Z-products by Ru-H complexes.  Molecular Catalysis,      [PMID:] [10.1016/j.mcat.2019.02.007]
9. Bingcheng Ge, Yangyang Wang, Yong Sun, Yunping Li, Jianyu Huang, Qiuming Peng.  (2019)  A proof-of-concept of Na-N2 rechargeable battery.  Energy Storage Materials,      [PMID:] [10.1016/j.ensm.2019.02.018]
10. Suli Chen, Fan Feng, Yimei Yin, Haiying Che, Xiao-Zhen Liao, Zi-Feng Ma.  (2018)  A solid polymer electrolyte based on star-like hyperbranched β-cyclodextrin for all-solid-state sodium batteries.  JOURNAL OF POWER SOURCES,      [PMID:] [10.1016/j.jpowsour.2018.07.096]
11. Jianguang Qi, Yufeng Hu, Weiting Ma, Haiyan Wang, Siqi Jiang, Liuyi Yin, Xianming Zhang, Zhenyu Yang, Yichuan Wang.  (2017)  The reactions that determine the yield and selectivity of 1,3,5-trioxane.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2017.08.101]
12. Zhanao Lv, Zhuqi Chen, Yue Hu, Wenrui Zheng, Haibin Wang, Wanling Mo, Guochuan Yin.  (2017)  A General Strategy for Open-Flask Alkene Isomerization by Ruthenium Hydride Complexes with Non-Redox Metal Salts.  ChemCatChem,  (20): (3849-3859).  [PMID:] [10.1002/cctc.201700687]
13. Zhanao Lv, Haibin Wang, Zhuqi Chen, Shuhua Zou, Shuaishuai Zhu, Chenlin Lou, Guochuan Yin.  (2017)  Non-redox metal ions promoted dehydrogenation of saturated C–C bond by a ruthenium catalyst with dioxygen activation.  Molecular Catalysis,      [PMID:] [10.1016/j.mcat.2016.12.027]
14. Na Li, Dan Xu, Di Bao, Jinling Ma, Xinbo Zhang.  (2016)  A binder-free, flexible cathode for rechargeable Na-O2 batteries.  CHINESE JOURNAL OF CATALYSIS,      [PMID:] [10.1016/S1872-2067(15)61089-0]
15. Shuhao Qin, Lei Dong, Zhuqi Chen, Sicheng Zhang, Guochuan Yin.  (2015)  Non-redox metal ions can promote Wacker-type oxidations even better than copper(II): a new opportunity in catalyst design.  DALTON TRANSACTIONS,  44  (40): (17508-17515).  [PMID:26390300] [10.1039/C5DT02612A]
16. Jun Yang, Zan Hua, Tao Wang, Bo Wu, Guangming Liu, Guangzhao Zhang.  (2015)  Counterion-Specific Protein Adsorption on Polyelectrolyte Brushes.  LANGMUIR,      [PMID:25985929] [10.1021/acs.langmuir.5b01145]
17. Lei Dong, Yujuan Wang, Yanzong Lv, Zhuqi Chen, Fuming Mei, Hui Xiong, Guochuan Yin.  (2013)  Lewis-Acid-Promoted Stoichiometric and Catalytic Oxidations by Manganese Complexes Having Cross-Bridged Cyclam Ligand: A Comprehensive Study.  INORGANIC CHEMISTRY,      [PMID:23600453] [10.1021/ic400361s]
18. Wei Song, Shan Yang, Jiaxiang An, Lixin Zhang, Ruina Shi, Niping Chen, Guisheng Qi, Luchao Yue.  (2024)  Atomic-level modulation of electron density in iron sulfides for enhancing sodium storage kinetics.  JOURNAL OF COLLOID AND INTERFACE SCIENCE,      [PMID:38936085] [10.1016/j.jcis.2024.05.154]
19. Dong Yangtao, Murugesan Balaji, Lin Weidi, Wang Chao, Dai Junjie, Li Wenwen, Ma Quangui, Yang Xiaogang, Cai Yurong.  (2024)  Construction of a novel heterostructure of Bi2S3/Sb2S3 nanorod with improved sodium storage performances.  IONICS,      [PMID:] [10.1007/s11581-024-05550-0]
20. Junjie Li, Liang Li, Jing Zhang, Chun Yang, Jun Ma.  (2024)  Efficient defluorination of PFOA by vacuum ultraviolet coupling with sulfite and iodide.  Journal of Water Process Engineering,      [PMID:] [10.1016/j.jwpe.2024.106079]
21. Jiabao Li, Jingjing Hao, Quan Yuan, Ruoxing Wang, Frederick Marlton, Tianyi Wang, Chengyin Wang, Xin Guo, Guoxiu Wang.  (2024)  The effect of salt anion in ether-based electrolyte for electrochemical performance of sodium-ion batteries: A case study of hard carbon.  Carbon Energy,      [PMID:] [10.1002/cey2.518]
22. Shengnan Zhong, Lina Tian, Lixin Yi, Yifan Liu, Weiguo Cheng, Yibo Wang, Yunong Li.  (2023)  Phosphine-based ionic liquids for CO2 chemical fixation: Improving stability and activity by asymmetric flexible steric hindrance.  Journal of Environmental Chemical Engineering,      [PMID:] [10.1016/j.jece.2023.109883]
23. Yanmei Li, Qiaonan Zhu, Liwei Cheng, Shuai Dong, Lianbo Ma, Jiawei Wang, Jing Zhou, Mirtemir Kurbanov, Hua Wang.  (2025)  A high-energy-density aqueous dual-ion anode-free Zn battery under cryogenic conditions.  Energy Storage Materials,      [PMID:] [10.1016/j.ensm.2025.104159]
24. Jisheng Zhang, Yujuan Wang, Nengchao Luo, Zhuqi Chen, Kangbing Wu, Guochuan Yin.  (2015)  Redox inactive metal ion triggered N-dealkylation by an iron catalyst with dioxygen activation: a lesson from lipoxygenases.  DALTON TRANSACTIONS,  44  (21): (9847-9859).  [PMID:25939391] [10.1039/C5DT00804B]
25. Zhongfei Shang, Meimei Wang, Jiguang Li, Zhenzhen Cai, Luyan Yang, Xincun Dou, Baiyi Zu.  (2025)  Exactly Matching the FRET Energy of the Functionalized Upconversion Nanoprobe to Boost the Sensing Performance toward Perchlorate.  ANALYTICAL CHEMISTRY,      [PMID:40525890] [10.1021/acs.analchem.5c01167]
26. Lyuchao Zhuang, Qi Wei, Ren Hui, Duanzijing Liu, Wei Gao, Yiming He.  (2026)  Multi-Site Anchoring for Tilted Octahedral Structure Stability Toward Efficient Blue Perovskite LEDs.  Laser & Photonics Reviews,      [PMID:] [10.1002/lpor.202502898]
27. Yingxuan Zhao, Chenyang Shen, Qing Liu, Siyuan Zhao, Ruiyao Zhao, Xiangke Guo, Nianhua Xue, Luming Peng, Xuefeng Guo, Yan Zhu, Weiping Ding.  (2026)  Electrocatalytic oxidation or amidation of olefins by asymmetric electrolytes steering carbocation pathways.  GREEN CHEMISTRY,      [PMID:] [10.1039/D5GC07050C]
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