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TETRATHIAFULVALENE

CAS No.
31366-25-3
Chemical Name:
TETRATHIAFULVALENE
Synonyms
TTF;ARHH;RHOH;NSC 222862;etrathiafulvalene;TETRATHIAFULVALENE;Tetrathiafulvalene 97%;Tetrathiafulvalene,98%;Tetrathiafulvalene,97%;ω-2,2’-Bi-1,3-dithiole
CBNumber:
CB6359496
Molecular Formula:
C6H4S4
Molecular Weight:
204.34
MDL Number:
MFCD00005492
MOL File:
31366-25-3.mol
MSDS File:
SDS
Last updated:2023-05-04 17:34:37

TETRATHIAFULVALENE Properties

Melting point 116-119 °C (lit.)
Boiling point 90℃ (1 Torr)
Density 1.448 (estimate)
refractive index 1.6000 (estimate)
storage temp. 2-8°C
form Crystals or Crystalline Powder
color Orange to brownish
Water Solubility It is insoluble in water. Soluble in organic solvents.
Sensitive Air & Light Sensitive
λmax 369nm(CHCl3)(lit.)
Merck 14,9242
BRN 1617956
InChIKey FHCPAXDKURNIOZ-UHFFFAOYSA-N
CAS DataBase Reference 31366-25-3(CAS DataBase Reference)
FDA UNII HY1EN16W9T
EPA Substance Registry System 1,3-Dithiole, 2-(1,3-dithiol-2-ylidene)- (31366-25-3)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H317
Precautionary statements  P261-P280g-P302+P352a-P321-P333+P313-P501a
Hazard Codes  Xi
Risk Statements  43-52/53
Safety Statements  36/37-61-24/25
RIDADR  3335
WGK Germany  3
10-23
TSCA  Yes
HS Code  29309090
NFPA 704
1
0 0

TETRATHIAFULVALENE price More Price(25)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 183180 Tetrathiafulvalene 97% 31366-25-3 250mg $72.8 2023-06-20 Buy
Sigma-Aldrich 183180 Tetrathiafulvalene 97% 31366-25-3 1g $244 2023-06-20 Buy
TCI Chemical T0980 Tetrathiafulvalene >98.0%(GC) 31366-25-3 1g $160 2024-03-01 Buy
TCI Chemical T0980 Tetrathiafulvalene >98.0%(GC) 31366-25-3 5g $475 2024-03-01 Buy
Alfa Aesar L19229 Tetrathiafulvalene, 97% 31366-25-3 250mg $56.65 2024-03-01 Buy
Product number Packaging Price Buy
183180 250mg $72.8 Buy
183180 1g $244 Buy
T0980 1g $160 Buy
T0980 5g $475 Buy
L19229 250mg $56.65 Buy

TETRATHIAFULVALENE Chemical Properties,Uses,Production

Chemical Properties

ORANGE TO BROWNISH CRYSTALS OR CRYSTALLINE POWDER

Uses

Electron donor for supramolecular synthesis,1 charge-transfer complex synthesis2 with 7,7,8,8-tetracyanoquinodimethane (cat. no. 157635), and for electron transfer to diazonium salts.3

Uses

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.

Uses

Molecular sensors; radical catalyst.

Definition

ChEBI: Tetrathiafulvalene is a member of the class of fulvalenes that is ethene substituted by 1,3-dithiol-2-ylidene groups at positions 1 and 2. It is an organosulfur heterocyclic compound and a member of fulvalenes.

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.

Purification Methods

Recrystallise it from cyclohexane/hexane under an argon atmosphere [Kauzlarich et al. J Am Chem Soc 109 4561 1987]. [Beilstein 19/11 V 380.]

TETRATHIAFULVALENE Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 145)Suppliers
Supplier Tel Email Country ProdList Advantage
Suzhou Origin Specialty Chemicals Co., Ltd.
+86-512-68662322 +86-17312436797 hanqun@origsc.com China 730 58
Capot Chemical Co.,Ltd.
571-85586718 +8613336195806 sales@capotchem.com China 29797 60
Jilin Chinese Academy of Sciences - Yanshen Technology Co., Ltd.
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Accela ChemBio Inc.
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career henan chemical co
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Fuxin Pharmaceutical
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Antai Fine Chemical Technology Co.,Limited
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Shanghai Daeyeon Chemicals Co., Ltd
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Hefei TNJ Chemical Industry Co.,Ltd.
0551-65418671 sales@tnjchem.com China 34572 58
ANHUI WITOP BIOTECH CO., LTD
+8615255079626 eric@witopchemical.com China 23556 58

View Lastest Price from TETRATHIAFULVALENE manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
TETRATHIAFULVALENE pictures 2020-01-08 TETRATHIAFULVALENE
31366-25-3
US $3.00 / KG 1KG 98% 200KG Career Henan Chemical Co
1,3-Dithiole, 2-(1,3-dithiol-2-ylidene)- 1,4,5,8-Tetrathiafulvalen 1,4,5,8-Tetrathiafulvalene 2-(1,3-dithiol-2-ylidene)-1,3-dithiol Δ2,2μ-Bi-1,3-dithiole, TTF Delta2,2'-bi-1,3-dithiol [2,2']-Bi[1,3]-dithioylidene Tetrathiafulvalene, 99+% 1GR Tetrathiafulvalene, 99+% 250MG Anti-RHOH, C-Terminal antibody produced in rabbit ARHH GTP-binding protein TTF RHOH Rho-related GTP-binding protein RhoH Tetrathiafulvalene (purified by sublimation) NSC 222862 Tetrathiafulvalene 97% 2,2'-bi(1,3-dithiolylidene) DELTA2,2'-BI-1,3-DITHIOLE DELTA^2^,^2^-Bi-1,3-dithiole~TTF delta-2:2-bis(1,3-dithiazole) TetrathiafulvaleneTTForangextl Tetrathiafulvalene,98% Tetrathiafulvalene,97% Tetrathiafulvalene, 99+% 2-(1,3-Dithiol-2-ylidene)-1,3-dithiole 2-(1,3-dithiol-2-ylidene)-3-dithiole ω-2,2’-Bi-1,3-dithiole Tetrathiafulvalene,98+%TTF TETRATHIAFULVALENE TTF TETRATHIAFULVALENE TTF Tetrathiafulvalene, 98.5% etrathiafulvalene tetrathiafulvalene dication 2,2'-Bi(1,3-dithiolylidene) 31366-25-3 C6H4S4 Heterocyclic Building Blocks Others S-Containing Building Blocks Donors (Charge Transfer Complexes) TTF Derivatives Charge Transfer Complexes for Organic Metals Functional Materials TTF Derivatives Building Blocks Chemical Synthesis Heterocyclic Building Blocks Materials Science Organic and Printed Electronics Organic Field Effect Transistor (OFET) Materials Others p-Type Organic Semiconductors p-Type Small Molecules S-Containing Charge Transfer Complexes for Organic Metals