Trifluoromethanesulfonamide - ≥98%(T) , CAS No.421-85-2

CAS: 421-85-2 Cat. No.: T161647 Peso molecular: 149.09 Número EC: 431-270-1
Disponible para pedir
GRADE & PURITY ≥98%(T)
Synonyms
1,1,1-Trifluoromethanesulfonamide
Storage
Store at 2-8°C,Protected from light
Shipped In
Wet ice
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
1g
T161647-1g
5
11,90US$
5g
T161647-5g
≥10
29,90US$
10g
T161647-10g
2
53,90US$
25g
T161647-25g
5
129,90US$
100g
T161647-100g
1
369,90US$
500g
T161647-500g
1
1.465,90US$
Enter a quantity for the sizes you want to add.
🧪

Why this grade

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

🌡

Storage & shipping

Store at 2-8°C,Protected from light Ships Wet ice Check lot-specific COA for exact specifications.

📋

Quality documents

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

📚

Literature proof

Cited in 9 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Sinónimos
1, 1, 1-Trifluoromethanesulfonamide
Especificaciones y pureza
≥98%(T)
Condiciones de almacenamiento de almacenamiento
Store at 2-8°C, Protected from light
Enviado en
Wet ice
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Pureza
≥98%(T)
Nombres e identificadores
Pubchem Sid488185658
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488185658
Sonrisas canónicasC(F)(F)(F)S(=O)(=O)N
IUPAC Nametrifluoromethanesulfonamide
InChIKeyKAKQVSNHTBLJCH-UHFFFAOYSA-N
INCHI1S/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

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
ClaseOrganic sulfonic acids and derivatives
SubclassOrganosulfonic acids and derivatives
Intermediate Tree Nodes Not available
Direct ParentOrganosulfonamides
Alternative Parents Organic sulfonamides  Aminosulfonyl compounds  Trihalomethanes  Organofluorides  Organic oxides  Organic nitrogen compounds  Hydrocarbon derivatives  Alkyl fluorides  
Molecular FrameworkAliphatic 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
DescripciónThis 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
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
CA13 Tclin Carbonic anhydrase 13 (2 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
CA1 Tclin Carbonic anhydrase 1 (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
CA2 Tclin Carbonic anhydrase 2 (4 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
CA7 Tclin Carbonic anhydrase 7 (2 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
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
CA12 Tclin Carbonic anhydrase XII (6231 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
Ca7 Carbonic anhydrase VII (3 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Ca13 Carbonic anhydrase XIII (322 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
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.

33 results found

Lot NumberCertificate TypeFechaArticulo
F2605522Certificate of AnalysisMay 21, 2026 T161647
F2605521Certificate of AnalysisMay 21, 2026 T161647
F2605518Certificate of AnalysisMay 21, 2026 T161647
F2605490Certificate of AnalysisMay 21, 2026 T161647
K2511020Certificate of AnalysisAug 09, 2025 T161647
H2520692Certificate of AnalysisAug 09, 2025 T161647
H2520672Certificate of AnalysisAug 09, 2025 T161647
H2520651Certificate of AnalysisAug 09, 2025 T161647
G2113313Certificate of AnalysisApr 03, 2025 T161647
B2526382Certificate of AnalysisFeb 14, 2025 T161647
G2511047Certificate of AnalysisFeb 14, 2025 T161647
G2517087Certificate of AnalysisFeb 14, 2025 T161647
B2526380Certificate of AnalysisFeb 14, 2025 T161647
B2526385Certificate of AnalysisFeb 14, 2025 T161647
K2411480Certificate of AnalysisNov 02, 2024 T161647
K2411528Certificate of AnalysisNov 02, 2024 T161647
K2411529Certificate of AnalysisNov 02, 2024 T161647
G2409300Certificate of AnalysisJun 28, 2024 T161647
G2409301Certificate of AnalysisJun 28, 2024 T161647
G2409302Certificate of AnalysisJun 28, 2024 T161647
G2409303Certificate of AnalysisJun 28, 2024 T161647
C2429920Certificate of AnalysisMar 12, 2024 T161647
C2429919Certificate of AnalysisMar 12, 2024 T161647
B2427555Certificate of AnalysisFeb 14, 2023 T161647
C2306115Certificate of AnalysisFeb 14, 2023 T161647
G2315071Certificate of AnalysisFeb 14, 2023 T161647
C2306117Certificate of AnalysisFeb 14, 2023 T161647
C2306116Certificate of AnalysisFeb 14, 2023 T161647
C2306114Certificate of AnalysisFeb 14, 2023 T161647
C1809016Certificate of AnalysisJan 27, 2022 T161647
B2222431Certificate of AnalysisDec 16, 2021 T161647
B2222420Certificate of AnalysisDec 16, 2021 T161647
B2222418Certificate of AnalysisDec 16, 2021 T161647

Show more ⌵

Propiedades químicas y físicas
SolubilidadSoluble in water.
SensibilidadLight sensitive
Punto de fusión (°C)118-124 °C
Peso molecular149.090 g/mol
XLogP30.100
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count6
Rotatable Bond Count0
Exact Mass148.976 Da
Monoisotopic Mass148.976 Da
Topological Polar Surface Area68.500 Ų
Heavy Atom Count8
Formal Charge0
Complexity161.000
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 Count1
Citations of This Product
Referencias
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]
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