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183180

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:
31366-25-3
Molecular Weight:
204.36
Beilstein:
1617956
EC Number:
250-593-7
MDL number:
MFCD00005492
UNSPSC Code:
12352103
PubChem Substance ID:
24851038
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 Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

183180-100MG:
183180-VAR:
183180-1G:
183180-250MG:
183180-BULK:

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’.

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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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