δ-2:2'-Bis(1,3-dithiazol)
CAS-Nr.
31366-25-3
Bezeichnung:
δ-2:2'-Bis(1,3-dithiazol)
Englisch Name:
TETRATHIAFULVALENE
Synonyma:
TTF;ARHH;RHOH;NSC 222862;etrathiafulvalene;TETRATHIAFULVALENE;Tetrathiafulvalene 97%;Tetrathiafulvalene,98%;Tetrathiafulvalene,97%;ω-2,2’-Bi-1,3-dithiole
CBNumber:
CB6359496
Summenformel:
C6H4S4
Molgewicht:
204.34
MOL-Datei:
31366-25-3.mol
δ-2:2'-Bis(1,3-dithiazol) Eigenschaften
Schmelzpunkt:
116-119 °C (lit.)
Siedepunkt:
90℃ (1 Torr)
Dichte
1.448 (estimate)
Brechungsindex
1.6000 (estimate)
storage temp.
2-8°C
Aggregatzustand
Crystals or Crystalline Powder
Farbe
Orange to brownish
Wasserl?slichkeit
It is insoluble in water. Soluble in organic solvents.
Sensitive
Air & Light Sensitive
maximale Wellenl?nge (λmax)
369nm(CHCl3)(lit.)
Merck
14,9242
BRN
1617956
InChIKey
FHCPAXDKURNIOZ-UHFFFAOYSA-N
CAS Datenbank
31366-25-3(CAS DataBase Reference)
EPA chemische Informationen
1,3-Dithiole, 2-(1,3-dithiol-2-ylidene)- (31366-25-3)
Sicherheit
Risiko- und Sicherheitserkl?rung
Gefahreninformationscode (GHS)
Bildanzeige (GHS)
Alarmwort
Warnung
Gefahrenhinweise
Code
Gefahrenhinweise
Gefahrenklasse
Abteilung
Alarmwort
Symbol
P-Code
H317
Kann allergische Hautreaktionen verursachen.
Sensibilisierung der Haut
Kategorie 1A
Warnung
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P261, P272, P280, P302+P352,P333+P313, P321, P363, P501
Sicherheit
P261
Einatmen von Staub vermeiden.
P321
Besondere Behandlung
P333+P313
Bei Hautreizung oder -ausschlag: ?rztlichen Rat einholen/?rztliche Hilfe hinzuziehen.
δ-2:2'-Bis(1,3-dithiazol) Chemische Eigenschaften,Einsatz,Produktion Methoden
R-S?tze Betriebsanweisung:
R43:Sensibilisierung durch Hautkontakt m?glich.
S-S?tze Betriebsanweisung:
S36/37:Bei der Arbeit geeignete Schutzhandschuhe und Schutzkleidung tragen.
Chemische Eigenschaften
ORANGE TO BROWNISH CRYSTALS OR CRYSTALLINE POWDER
Verwenden
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.
Allgemeine Beschreibung
Tetrathiafulvalene (TTF) is an electron-donor which consists of oligomers, dendrimers and polymers which can be used in the formation of redox macromolecules.
l?uterung methode
Recrystallise it from cyclohexane/hexane under an argon atmosphere [Kauzlarich et al. J Am Chem Soc 109 4561 1987]. [Beilstein 19/11 V 380.]
δ-2:2'-Bis(1,3-dithiazol) Upstream-Materialien And Downstream Produkte
Upstream-Materialien
Downstream Produkte
δ-2:2'-Bis(1,3-dithiazol) Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.
Global( 166)Lieferanten
Belgium 1
China 137
Germany 2
India 3
Japan 2
South Korea 1
Switzerland 1
United Kingdom 5
United States 14
Global 166
31366-25-3(δ-2:2'-Bis(1,3-dithiazol))Verwandte Suche:
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
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
Donors (Charge Transfer Complexes)