Skip to Content
Merck
CN

88150

Tetrathiafulvalene

purum, ≥98.0% (HPLC)

Synonym(s):

Δ2,2′-Bi-1,3-dithiole, TTF

Sign In to View Organizational & Contract Pricing.

Select a Size

Change View

About This Item

Empirical Formula (Hill Notation):
C6H4S4
CAS Number:
Molecular Weight:
204.36
EC Number:
250-593-7
UNSPSC Code:
12352103
MDL number:
Beilstein/REAXYS Number:
1617956
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

grade

purum

assay

≥98.0% (HPLC)

mp

116-119 °C

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

Regulatory Information

新产品

This item has


Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

It looks like we've run into a problem, but you can still download Certificates of Analysis from our Documents section.

If you need assistance, please contact Customer Support

Already Own This Product?

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

Visit the Document Library

Yang Wang et al.
The journal of physical chemistry. A, 115(45), 13080-13087 (2011-10-01)
Formation of self-assembled chains of tetrathiafulvalene (TTF) on the Cu(100) surface has been investigated by scanning tunneling microscopy and density functional theory calculations that include semiempirical van der Waals (vdW) interaction corrections. The calculations show that the chain structures observed
Hongpeng Jia et al.
Chemphyschem : a European journal of chemical physics and physical chemistry, 13(14), 3370-3382 (2012-07-04)
A tetrathiafulvalene (TTF) donor is annulated to porphyrins (P) via quinoxaline linkers to form novel symmetric P-TTF-P triads 1 a-c and asymmetric P-TTF dyads 2 a,b in good yields. These planar and extended π-conjugated molecules absorb light over a wide region of
Fabrice Pointillart et al.
Inorganic chemistry, 52(3), 1610-1620 (2013-01-18)
The reaction between the tetrakis(2-pyridyl-N-oxidemethylthio)tetrathiafulvalene ligand (L) and Ln(hfac)(3)·2H(2)O precursors (where hfac(-) = 1,1,1,5,5,5-hexafluoroacetylacetonate anion and Ln = Tb(III) (1), Dy(III) (2), Er(III) (3), and Yb(III) (4) and (4b)) leads to the formation of five tetranuclear complexes of formula [Ln(4)(hfac)(12)(L)(2)](n)·xCHCl(3)·yC(6)H(14)
Fei Sun et al.
Chemistry, an Asian journal, 7(1), 183-189 (2011-10-06)
A new calix[4]arene 1 with tetrathiafulvalene (TTF), quinone, and crown ether units in the lower rim was designed and synthesized with the aim to investigate the possibility to tune the metal-ion promoted electron transfer by coordination of the crown ether
Qi Li et al.
Inorganic chemistry, 51(23), 12929-12937 (2012-11-14)
The charge-transfer material TTF-SV(IV)Mo(11)O(40) (TTF = tetrathiafulvalene) was prepared by a spontaneous redox reaction between TTF and the vanadium-substituted polyoxometalate (n-Bu(4)N)(3)[SV(V)Mo(11)O(40)] in both solution and solid state phases. Single crystal X-ray diffraction gave the stoichiometry TTF(4)[SVMo(11)O(40)]·2H(2)O·2CH(2)Cl(2), with the single V

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