TETRATHIAFULVALENE

Product Name: 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
Formula Weight: 204.34
MOL File: 31366-25-3.mol

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TETRATHIAFULVALENE Property

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)
EPA Substance Registry System: 1,3-Dithiole, 2-(1,3-dithiol-2-ylidene)- (31366-25-3)

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Safety

Hazard Codes: Xi
Risk Statements: 43-52/53
Safety Statements: 36/37-61-24/25
RIDADR: 3335
WGK Germany: 3
F: 10-23
TSCA: Yes
HS Code: 29309090

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Hazard and Precautionary Statements (GHS)

Symbol(GHS)

Signal word

Warning

Hazard statements

H317May cause an allergic skin reaction

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P321Specific treatment (see … on this label).

P333+P313IF SKIN irritation or rash occurs: Get medical advice/attention.

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N-Bromosuccinimide Price

Sigma-Aldrich

Product number: 183180
Product name: Tetrathiafulvalene
Purity: 97%
Packaging: 250mg
Price: $72.8
Updated: 2023/06/20

Sigma-Aldrich

Product number: 183180
Product name: Tetrathiafulvalene
Purity: 97%
Packaging: 1g
Price: $244
Updated: 2023/06/20

TCI Chemical

Product number: T0980
Product name: Tetrathiafulvalene
Purity: >98.0%(GC)
Packaging: 1g
Price: $160
Updated: 2024/03/01

TCI Chemical

Product number: T0980
Product name: Tetrathiafulvalene
Purity: >98.0%(GC)
Packaging: 5g
Price: $475
Updated: 2024/03/01

Alfa Aesar

Product number: L19229
Product name: Tetrathiafulvalene, 97%
Packaging: 250mg
Price: $56.65
Updated: 2024/03/01

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TETRATHIAFULVALENE Chemical Properties,Usage,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

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TETRATHIAFULVALENE Suppliers

Belgium 1 China 116 Germany 2 India 3 Japan 2 South Korea 1 Switzerland 1 United Kingdom 5 United States 14 Global 145

Mianyang Vandino Pharmaceutical Technology Co., Ltd.

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Energy Chemical

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Alfa Aesar

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TCI (Shanghai) Development Co., Ltd.

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Beijing HwrkChemical Technology Co., Ltd

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Energy Chemical

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ProdList: 44689
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View Lastest Price from TETRATHIAFULVALENE manufacturers

Career Henan Chemical Co

Product: TETRATHIAFULVALENE 31366-25-3
Price: US $3.00/KG
Min. Order: 1KG
Purity: 98%
Supply Ability: 200KG
Release date: 2020-01-07

31366-25-3, TETRATHIAFULVALENERelated Search:

TETRAKIS(OCTADECYLTHIO)TETRATHIAFULVALENE,Tetrakis(octadecylthio)tetrathiafulvalene [Organic Electronic Material] BIS(ETHYLENEDITHIO)TETRATHIAFULVALENE BIS(CARBONYLDITHIO)TETRATHIAFULVALENE 4,4',5-TRIMETHYLTETRATHIAFULVALENE Bis(methylenedithio)tetrathiafulvalene [Organic Electronic Material],BIS(METHYLENEDITHIO)TETRATHIAFULVALENE TETRATHIAFULVALENE TRIS(TETRATHIAFULVALENE) BIS(TETRAFLUOROBORATE) COMPLEX,TETRATHIAFULVALENE FLUOROBORATE 4,4'-DIMETHYLTETRATHIAFULVALENE TPT-TTF TETRAKIS(METHYLTHIO)TETRATHIAFULVALENE,Tetrakis(methylthio)tetrathiafulvalene [Organic Electronic Material] Bis-cyclohexyl-tetrathiafulvalene,BIS-TETRAMETHYLENE-TETRATHIAFULVALENE 4,4'-DIMETHYL-5,5'-DIPHENYLTETRATHIAFULVALENE 4,4'-DI-PHENYL-TETRATHIAFULVALENE 2H4-Tetrathiafulvalene,TETRATHIAFULVALENE-D4 2,3,6,7-TETRAKIS(BENZOYLTHIO)TETRATHIAFULVALENE BIS(ETHYLENEDIOXY)TETRATHIAFULVALENE 2,3,6,7-TETRAKIS(ETHYLTHIO)TETRATHIAFULVALENE BIS(ETHYLENEDITHIO)TETRATHIAFULVALENE-D8

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%

Tetrathiafulvalene, 98.5%

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

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