106920-29-0

Basic information

• Product Name: TPT-TTF
• Synonyms: TETRAKIS(N-PENTYLTHIO)TETRATHIAFULVALENE;TETRAKIS(PENTYLTHIO)TETRATHIAFULVALENE;TETRAKIS(AMYLTHIO)TETRATHIAFULVALENE;TPT-TTF;Tetrakis(pentylthio)tetrathiafulvalene [Organic Electronic Material];4,4',5,5'-Tetra(pentylthio)-Δ2,2'-bi(1,3-dithiole);TPT-TTF Tetrakis(amylthio)tetrathiafulvalene;Tetrakis(pentylthio)tetrathiafulvalene
• CAS NO: 106920-29-0
• Molecular Formula: C26H44S8
• Molecular Weight: 613.15
• Product Categories: Charge Transfer Complexes for Organic Metals;Donors (Charge Transfer Complexes);Functional Materials;TTF Derivatives
• Mol File: 106920-29-0.mol
• Article Data: 1

Chemical Properties

• Melting Point: 32 °C
• Boiling Point: 594.551°C at 760 mmHg
• Flash Point: 292.989°C
• Appearance: /
• Density: 1.211g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.633
• Storage Temp.: Refrigerator
• CAS DataBase Reference: TPT-TTF(CAS DataBase Reference)
• NIST Chemistry Reference: TPT-TTF(106920-29-0)
• EPA Substance Registry System: TPT-TTF(106920-29-0)

Safety Data

• Hazardous Substances Data: 106920-29-0(Hazardous Substances Data)

Usage

Description

TPT-TTF, also known as Tetrakis(pentylthio)tetrathiafulvalene, is an electron-rich compound with high conductivity. It is known for its ability to form metallic charge-transfer salts, making it a promising candidate for various applications in different industries.

Uses

Used in Electronics Industry:
TPT-TTF is used as a conductive material for its high conductivity and ability to form metallic charge-transfer salts, which can be beneficial in the development of electronic devices and components.
Used in Chemical Industry:
TPT-TTF is used as a precursor in the synthesis of various organic and metallic nanoparticles, which can be employed as carriers for drug delivery systems. This application aims to improve the delivery, bioavailability, and therapeutic outcomes of certain pharmaceuticals.
Used in Pharmaceutical Industry:
TPT-TTF can be used in the development of drug delivery systems, particularly for anticancer applications. Its ability to form metallic charge-transfer salts can enhance the chemo-sensitivity and efficacy of conventional chemotherapeutic drugs, making it a valuable component in the fight against cancer.

InChI:InChI=1/C26H44S8/c1-5-9-13-17-27-21-22(28-18-14-10-6-2)32-25(31-21)26-33-23(29-19-15-11-7-3)24(34-26)30-20-16-12-8-4/h5-20H2,1-4H3

Upstream product

• 64394-47-4 5-(5-Oxo<1,3>dithiolo<4,5-d>-1,3-dithiol-2-yliden)<1,3>dithiolo<4,5-d>-1,3-dithiol-2-on 

Relevant articles and documents

UNCAPPED ALKYLTHIO SUBSTITUTED TETRATHIAFULVALENES (TTCn-TTF) AND THEIR CHARGE TRANSFER COMPLEXES

A series of tetraalkylthio substituted tetrathiafulvalenes (TTCn-TTF) was prepared.The syntheses, molecular and crystal structures, and physical properties of TTCn-TTF reveal marked differences from those of BEDT-TTF.The conformational change of TTC1-TTF molecule on the formation of charge transfer complexes and the mode of the S..S contacts are described in connection with those of BEDT-TTF compounds.