Product Added to Cart!
$318.00

FREE
SHIPPING

100% MONEY
BACK GUARANTEE

ONLINE
SUPPORT 24/7

Available on backorder. Please allow 2-3 weeks for production.
Sku SC09-7170_250_G
US-Strem
Get Bulk Quote

Product Information

Product Name
Trifluoracetic anhydride, min. 98%
Brand Name
US-Strem
Product Number
09-7170
CAS
407-25-0
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
9845
IUPAC Name
(2,2,2-trifluoroacetyl) 2,2,2-trifluoroacetate
InChI Key
QAEDZJGFFMLHHQ-UHFFFAOYSA-N
SMILES
C(=O)(C(F)(F)F)OC(=O)C(F)(F)F

Description

Trifluoroacetic anhydride is widely utilized in research focused on:

Synthesis of Fluorinated Compounds: It serves as a powerful reagent for the synthesis of various fluorinated organic compounds, which are essential in pharmaceuticals and agrochemicals.

Peptide Coupling Reactions: This chemical is commonly used in peptide synthesis, facilitating the formation of peptide bonds, which is crucial in developing new drugs and biopharmaceuticals.

Modification of Polymers: It can modify polymer properties, enhancing their performance in industries such as coatings and adhesives, leading to improved durability and chemical resistance.

Analytical Chemistry: Trifluoroacetic anhydride is employed in derivatization processes for gas chromatography and mass spectrometry, improving the detection and analysis of various compounds.

Environmental Applications: It is used in the synthesis of fluorinated surfactants, which can aid in pollution control and remediation efforts, showcasing its versatility in addressing environmental challenges.

References Data Source From Pubchem

Use of nitrogen as an alternative to helium in gas chromatography/mass spectrometry for forensic toxicological analysis

Publication Name: Forensic Toxicology
Publication Date: 2026-02-25
DOI: 10.1007/s11419-025-00744-1

Synthesis and Properties of 4-Amino-5-oxoproline Derivatives (A Review)

Publication Name: Russian Journal of General Chemistry
Publication Date: 2026-02-24
DOI: 10.1134/s1070363225606003

Collective asymmetric synthesis of the Strychnos alkaloids via thiophene S,S-dioxide cycloadditions

Publication Name: Nature Chemistry
Publication Date: 2026-01-23
DOI: 10.1038/s41557-025-02041-1

Multilayer metabolomic integration reveals bioenergetic disruption in Long COVID

Publication Name: Journal of Translational Medicine
Publication Date: 2026-01-20
DOI: 10.1186/s12967-026-07684-3

Customized cycloparaphenylene skeletons prepared via the intramolecular coupling of extended biphen[n]arenes

Publication Name: Nature Synthesis
Publication Date: 2026-01-06
DOI: 10.1038/s44160-025-00965-7