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Tetrathiafulvalene, 97%
CAS: 31366-25-3 | C6H4S4 | 204.338 g/mol
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Catalog number L19229.03
also known as L19229-03
Price (USD)
188.00
Each
Quantity:
1 g
Price (USD)
188.00
Each
Chemical Identifiers
CAS31366-25-3
IUPAC Name2-(2H-1,3-dithiol-2-ylidene)-2H-1,3-dithiole
Molecular FormulaC6H4S4
InChI KeyFHCPAXDKURNIOZ-UHFFFAOYSA-N
SMILESS1C=CSC1=C1SC=CS1
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Specifications
Specification Sheet
Specification SheetMelting Point (clear melt)115.0-124.0?C
Appearance (Color)Orange to brown
Assay (GC)≥96.0%
FormCrystals or powder or crystalline powder
Identification (FTIR)Conforms
Tetrathiafulvalene, holds wide application in HPLC, NMR. This heterocyclic compound contributed to the development of molecular electronics. They are used as a organic super conductors.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
Tetrathiafulvalene, holds wide application in HPLC, NMR. This heterocyclic compound contributed to the development of molecular electronics. They are used as a organic super conductors.
Solubility
It is insoluble in water. Soluble in organic solvents.
Notes
Air & Light Sensitive. Keep container tightly closed in a dry and well-ventilated place. Keep away from oxidizing agents. Stable under recommended storage conditions.
Tetrathiafulvalene, holds wide application in HPLC, NMR. This heterocyclic compound contributed to the development of molecular electronics. They are used as a organic super conductors.
Solubility
It is insoluble in water. Soluble in organic solvents.
Notes
Air & Light Sensitive. Keep container tightly closed in a dry and well-ventilated place. Keep away from oxidizing agents. Stable under recommended storage conditions.
RUO – Research Use Only
General References:
- JB Torrance.; A Girlando.; JJ Mayerle.; JI Crowley. Anomalous nature of neutral-to-ionic phase transition in tetrathiafulvalene-chloranil. Physical Review Letters. 198147 (24), 1747-1751.
- N Svenstrup.; KM Rasmussen.; TK Hansen.; J Beche. The chemistry of TTFTT. I: New efficient synthesis and reactions of tetrathiafulvalene-2, 3, 6, 7-tetrathiolate (TTFTT): an important building block in TTF-syntheses. Synthesis. 19946 (1), 809-812.