Tetrathiafulvalene TCI T0980

Chemical Identity

CAS No.: 31366-25-3
PubChem: CID 99451·SID 87576791
Formula: C6H4S4
Molecular weight: 204.4 g/mol
Purity: >98.0%(GC)
Reference databases: ChEBI·ChemSpider·ECHA·Wikipedia

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 2-(1,3-dithiol-2-ylidene)-1,3-dithiole
SMILES: C1=CSC(=C2SC=CS2)S1
InChIKey: FHCPAXDKURNIOZ-UHFFFAOYSA-N

Rp 3.578.400,00

~~Rp 2.517.900,00~~ Rp 3.578.400,00

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Tetrathiafulvalene (TTA), with the CAS number 31366-25-3, is an organic chemical compound featuring a heterocyclic structure composed of two sulfur atoms and two carbon atoms. This compound is widely used in chemical reactions as a building block due to its unique electronic properties. In the laboratory, TTA plays a crucial role in the synthesis of complex molecules that require specific reactivity and stability. Its ability to participate in redox reactions makes it a valuable tool for organic chemists.

TTA is known for its reactive nature and stable structure, which allows it to serve as an electron donor in various synthetic reactions. It is particularly effective in reactions such as the Diels-Alder and substitution reactions, where its electronic properties are essential. These characteristics make TTA a preferred choice for researchers seeking to develop new materials and compounds. Its versatility and reactivity contribute to its popularity in both academic and industrial research settings.

In Indonesian laboratories, TTA is commonly used in scientific research, especially in the fields of organic chemistry and material science. Its unique electronic properties and reactivity make it an essential component in the development of new materials and compounds. Researchers in Indonesia rely on TTA for its ability to contribute to the synthesis of complex structures, supporting advancements in chemical and material research.

Advantages (TCI brochure)

TTF derivatives function as donor molecules with a hole carrier

TCI brochures (PDF)

Molecular Conductors 2025-11-13 · p. 4

Related TCI products

Organic synthesis applications benefit from TTA’s ability to act as an electron donor, enabling the formation of complex molecular structures.
Material science research utilizes TTA due to its conductive properties, making it suitable for electronic material development.
Redox reaction studies rely on TTA’s reactivity, allowing for the investigation of electron transfer mechanisms in various chemical systems.
Synthetic pathway optimization uses TTA as a building block, enhancing the efficiency and selectivity of chemical reactions.
Electrochemical studies incorporate TTA for its unique electronic behavior, aiding in the exploration of conductive materials and devices.

From the TCI brochure

Donor molecule for molecular conductors

Brand	TCI
CAS number	31366-25-3
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Heterocyclic Building Blocks
Pack sizes	Available in various quantities as per supplier specifications
Physical form	Solid, typically in powder or crystalline form
Storage	Store in a cool, dry place away from moisture and light

Tetrathiafulvalene should be stored in a cool, dry environment to maintain its stability and reactivity. It is recommended to keep it in a sealed container to prevent exposure to moisture and air, which can affect its chemical properties. Due to its reactive nature, TTA should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. It is advisable to store TTA in a well-ventilated area to minimize the risk of inhalation. Proper labeling and storage conditions are essential to ensure the safety of laboratory personnel and the integrity of the compound. Always follow standard laboratory safety protocols when working with reactive chemicals like TTA.

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