Copper trifluoromethanesulfonate - ≥98% , CAS No.34946-82-2

CAS: 34946-82-2 Cat. No.: C100681 Molecular Weight: 361.68 Beilstein Registry Number: 4028198 EC Number: 252-300-8
AVAILABLE TO ORDER
GRADE & PURITY ≥98%
Synonyms
Copper(II) trifluoromethanesulphonate | Copper (II) trifluoromethanesulfonate | Cu(OTf)2 | Copper(II) triflate | Copper(II) trifluoromethanesulfonate | copper(ii)trifluoromethanesulfonate
Storage
Room temperature,Argon charged
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
1g
C100681-1g
2
$9.90
5g
C100681-5g
3
$10.90
10g
C100681-10g
1
$11.90
25g
C100681-25g
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$14.90

$16.90
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100g
C100681-100g
5

$49.90

$59.90
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500g
C100681-500g
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$174.90

$287.90
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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 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 10 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

Usually used as catalyst for Mannich condensation,Annulative amination,Friedel-Crafts reaction,Henry reaction, Hypervalent iodine reagent-mediated preparation of carbazoles,Intramolecular oxidative C-N bond formation for the synthesis of carbazoles,the efficient addition of trimethylsilyl cyanide to carbonyl compounds.

Specifications

Synonyms
Copper(II) trifluoromethanesulphonate | Copper (II) trifluoromethanesulfonate | Cu(OTf)2 | Copper(II) triflate | Copper(II) trifluoromethanesulfonate | copper(ii)trifluoromethanesulfonate
Specifications & Purity
≥98%
Storage
Room temperature, Argon charged
Shipped In
Normal
Purity
≥98%
Names and Identifiers
Pubchem Sid504761235
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504761235
Canonical SmilesC(F)(F)(F)S(=O)(=O)[O-].C(F)(F)(F)S(=O)(=O)[O-].[Cu+2]
IUPAC Namecopper;trifluoromethanesulfonate
InChIKeySBTSVTLGWRLWOD-UHFFFAOYSA-L
INCHI1S/2CHF3O3S.Cu/c2*2-1(3,4)8(5,6)7;/h2*(H,5,6,7);/q;;+2/p-2
Isomeric SMILES C(F)(F)(F)S(=O)(=O)[O-].C(F)(F)(F)S(=O)(=O)[O-].[Cu+2]
WGK Germany 3
UN Number 3261
Molecular Weight 361.68
Beilstein 4028198
Reaxy-Rn 4028198
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=4028198&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
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 oxides  Organic copper salts  Hydrocarbon derivatives  Alkyl fluorides  
Molecular FrameworkNot available
Substituents Trifluoromethanesulfonate - Methanesulfonate - Organosulfonic acid - Sulfonyl - Trihalomethane - Organic metal halide - Organic transition metal salt - Alkyl fluoride - Organic copper salt - Hydrocarbon derivative - Organic salt - Halomethane - Organic oxide - Organosulfur compound - Organofluoride - Organohalogen compound - Organic oxygen compound - Alkyl halide - 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





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.

31 results found

Lot NumberCertificate TypeDateItem
C2605319Certificate of AnalysisJan 24, 2026 C100681
C2605321Certificate of AnalysisJan 24, 2026 C100681
C2605322Certificate of AnalysisJan 24, 2026 C100681
F2611173Certificate of AnalysisJan 24, 2026 C100681
L2511091Certificate of AnalysisJun 28, 2025 C100681
A2612026Certificate of AnalysisJun 28, 2025 C100681
A2612029Certificate of AnalysisJun 28, 2025 C100681
G2511189Certificate of AnalysisJun 28, 2025 C100681
G2511188Certificate of AnalysisJun 28, 2025 C100681
G2511182Certificate of AnalysisJun 28, 2025 C100681
G2511181Certificate of AnalysisJun 28, 2025 C100681
I2510096Certificate of AnalysisJun 28, 2025 C100681
H2111370Certificate of AnalysisMay 13, 2025 C100681
D2525065Certificate of AnalysisNov 04, 2024 C100681
K2414622Certificate of AnalysisNov 04, 2024 C100681
K2414621Certificate of AnalysisNov 04, 2024 C100681
K2414623Certificate of AnalysisNov 04, 2024 C100681
D2418554Certificate of AnalysisApr 01, 2024 C100681
J2418161Certificate of AnalysisApr 01, 2024 C100681
D2418553Certificate of AnalysisApr 01, 2024 C100681
D2418552Certificate of AnalysisApr 01, 2024 C100681
D2410246Certificate of AnalysisMar 20, 2024 C100681
D2410245Certificate of AnalysisMar 20, 2024 C100681
A2403201Certificate of AnalysisDec 18, 2023 C100681
B2401012Certificate of AnalysisDec 18, 2023 C100681
A2403200Certificate of AnalysisDec 18, 2023 C100681
H2308256Certificate of AnalysisMar 21, 2022 C100681
G2307578Certificate of AnalysisMar 21, 2022 C100681
G2307575Certificate of AnalysisMar 21, 2022 C100681
F2214386Certificate of AnalysisMar 21, 2022 C100681
F2214385Certificate of AnalysisMar 21, 2022 C100681

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Chemical and Physical Properties
SolubilitySoluble in water.
SensitivityHygroscopic
Melt Point(°C)≥300°C
Molecular Weight361.700 g/mol
XLogP3
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count12
Rotatable Bond Count0
Exact Mass360.834 Da
Monoisotopic Mass360.834 Da
Topological Polar Surface Area131.000 Ų
Heavy Atom Count17
Formal Charge0
Complexity145.000
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 Count3
Documents & Articles
Citations of This Product
References
1. Fukun Li, Ronghe Yang, Zheng Tian, Ziting Du, Jinhang Dai, Xingmin Wang, Ning Li, Jie Zhang.  (2023)  Microwave-Assisted One Pot Cascade Conversion of Furfural to γ-Valerolactone over Sc(OTf)3.  CHEMISTRY-A EUROPEAN JOURNAL,  29  (52): (e202300950).  [PMID:37392150] [10.1002/chem.202300950]
2. Minmin Gou, Weifang Zhu, Yanyong Sun, Ruili Guo.  (2020)  Introducing two-dimensional metal-organic frameworks with axial coordination anion into Pebax for CO2/CH4 separation.  SEPARATION AND PURIFICATION TECHNOLOGY,      [PMID:] [10.1016/j.seppur.2020.118107]
3. Mei-Yuan Shi, Ming Xu, Zhi-Yuan Gu.  (2019)  Copper-based two-dimensional metal-organic framework nanosheets as horseradish peroxidase mimics for glucose fluorescence sensing.  ANALYTICA CHIMICA ACTA,      [PMID:31387707] [10.1016/j.aca.2019.06.042]
4. Lijing Nan, Jiao Li, Wanjun Jin, Ming Wei, Mengjun Tang, Chengjian Wang, Guiping Gong, Linjuan Huang, Ying Zhang, Zhongfu Wang.  (2019)  Comprehensive quali-quantitative profiling of neutral and sialylated O-glycome by mass spectrometry based on oligosaccharide metabolic engineering and isotopic labeling.  RSC Advances,  (28): (15694-15702).  [PMID:35521403] [10.1039/C9RA01114E]
5. Yan Li, Tao Li, Long-Qiang Xiao, Yue-Fei Zhang.  (2018)  Novel Synthesis of Down-/Up-Conversion Fluorescent Oligo(2-pyrazoline)s.  INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH,      [PMID:] [10.1021/acs.iecr.8b02709]
6. 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]
7. Shaohuan Lv, Zhanhong Yuan, Juanjuan Zheng, Zirong Liu, Jiawang Ye, Jiefang Li, Shanshan Xu, Feng Xie, Dongdong Ye, Bin Li.  (2024)  Preparation of reusable copper-based biomass-carbon aerogel catalysts and their application in highly selective reduction of maleimides to succinimides with hydrosilane as a hydrogen source.  GREEN CHEMISTRY,  26  (5): (2592-2598).  [PMID:] [10.1039/D3GC04697D]
8. 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]
9. Irfan Ijaz, Aysha Bukhari, Ammara Nazir, Ezaz Gilani, Hina Zain, Attia Shaheen, Mohammed Rafi Shaik, Mujeeb Khan, Jilani P. Shaik.  (2025)  Simultaneous adsorption of sulfamethoxazole and neodymium from wastewater by a MXene-, α-aminophosphonate-, and sulfated fucan-based ternary composite based on anion-synergistic interactions.  RSC Advances,  15  (7): (5042-5059).  [PMID:39963457] [10.1039/D4RA08766F]
10. Debin Wang, Hongyan Liu, Aochen Yang, Huijuan Zhang.  (2025)  Dual-Coordination Synergy in Polyurethane Hot-Melt Adhesives: Integrating Ultrahigh Strength, Self-Healing, and Extreme Environmental Tolerance.  ACS Applied Polymer Materials,      [PMID:] [10.1021/acsapm.5c03198]
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