Skip to Content
Merck
All Photos(1)

Documents

150533

Sigma-Aldrich

Thallium(III) trifluoroacetate

technical grade

Synonym(s):

TTFA, Tris(trifluoroacetato)thallium, Thallic trifluoroacetate, Trifluoroacetic acid thallium(III) salt

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
(CF3COO)3Tl
CAS Number:
23586-53-0
Molecular Weight:
543.43
EC Number:
245-761-1
MDL number:
MFCD00000414
UNSPSC Code:
12161600
PubChem Substance ID:
24849042
NACRES:
NA.22

grade

technical grade

reaction suitability

core: thallium
reagent type: catalyst

mp

213 °C (dec.) (lit.)

storage temp.

2-8°C

SMILES string

FC(F)(F)C(=O)O[Tl](OC(=O)C(F)(F)F)OC(=O)C(F)(F)F

InChI

1S/3C2HF3O2.Tl/c3*3-2(4,5)1(6)7;/h3*(H,6,7);/q;;;+3/p-3

InChI key

PSHNNUKOUQCMSG-UHFFFAOYSA-K

Looking for similar products? Visit Product Comparison Guide

Related Categories

Application

Oxidizing agent used in the synthesis of S-substituted cysteine peptides and proteins containing disulfide bonds.

Signal Word

Danger

Hazard Statements

H300 + H330,H373,H411

Hazard Classifications

Acute Tox. 2 Inhalation - Acute Tox. 2 Oral - Aquatic Chronic 2 - STOT RE 2

Storage Class Code

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Tetrahedron, 44, 805-805 (1988)
Taylor, E. C.; Katz, A. H. et al.
Tetrahedron Letters, 26, 5963-5963 (1985)
Pamela R Hall et al.
Antimicrobial agents and chemotherapy, 52(6), 2079-2088 (2008-04-09)
Viral entry into susceptible host cells typically results from multivalent interactions between viral surface proteins and host entry receptors. In the case of Sin Nombre virus (SNV), a New World hantavirus that causes hantavirus cardiopulmonary syndrome, infection involves the interaction
Shenglong Zhu et al.
Nutrition and cancer, 72(4), 696-707 (2019-07-30)
Kudingcha is implicated in alleviating metabolic disorders in traditional Chinese medicine. However, the role of Kudingcha, one of the Ligustrum robustum species, in metabolic regulations and its antitumor activity in triple-negative breast cancer (TNBC) remains to be determined. Two breast
Luis Julià et al.
Magnetic resonance in chemistry : MRC, 49(4), 164-167 (2011-03-26)
Electron paramagnetic resonance (EPR) analysis of neutral and acidic solutions of 2,5-dimethyl-1-phenylpyrrol (1) and meta-, para-, and ortho-bis(2,5-dimethylpyrrol-1-yl)benzenes (4-6) in the presence of Tl(III) trifluoroacetate as oxidant reveals the poor stability of their generated monomeric radical cations which dimerize through
View All Related Papers

Articles

Oxidizing and Reducing Agents

Oxidation and reduction reactions are some of the most common transformations encountered in organic synthesis, and are some of the organic chemist’s most powerful tools for creating novel products. Below is a list of the most commonly used oxidizing and reducing agents currently available in our catalog.

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service