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Sigma-Aldrich

Tetrathiafulvalene

97%

Synonym(s):

Δ2,2′-Bi-1,3-dithiole, TTF

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About This Item

Empirical Formula (Hill Notation):
C6H4S4
CAS Number:
Molecular Weight:
204.36
Beilstein/REAXYS Number:
1617956
EC Number:
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.23

assay

97%

form

solid

mp

116-119 °C (lit.)

SMILES string

S1C=CS\C1=C2/SC=CS2

InChI

1S/C6H4S4/c1-2-8-5(7-1)6-9-3-4-10-6/h1-4H

InChI key

FHCPAXDKURNIOZ-UHFFFAOYSA-N

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General description

Tetrathiafulvalene (TTF) is an electron-donor which consists of oligomers, dendrimers and polymers which can be used in the formation of redox macromolecules.

Application

TTF may be linked with lithium chloride (LiCl) to form a precipitated layer on the lithium oxide (Li2O2) for the fabrication of high performance Li-O2 batteries. Bio-sourced carbon nanodots can be surface modified by TTF which can be potentially used for electrochemical applications.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves


Certificates of Analysis (COA)

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Chemical Society Reviews, 23, 41-41 (1994)
Laurence Albiges et al.
European journal of cancer (Oxford, England : 1990), 51(17), 2580-2586 (2015-09-09)
Monoclonal antibodies that target the programmed death-1 (PD-1)/programmed death-ligand 1(PD-L1) pathway have shown antitumour activity in metastatic renal cell carcinoma (mRCC) and are currently being developed in first-line (in combination) and in previously treated patients. The efficacy targeted therapy (TT)
Tetrahedron Letters, 35, 8675-8675 (1994)
Exploring Tetrathiafulvalene-Carbon Nanodot Conjugates in Charge Transfer Reactions.
Ferrer-Ruiz A, et al.
Angewandte Chemie (International Edition in English), 57(4), 1001-1005 (2018)
Surface-nhanced near-infrared fourier transform Raman scattering of tetrathiafulvalene adsorbed on silver powder
Nie, S., & Yu, N. T.
Journal of Raman Spectroscopy, 22(9), 489-495 (1991)

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