δ-2:2'-Bis(1,3-dithiazol)

TETRATHIAFULVALENE Struktur
31366-25-3
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
Wasserlöslichkeit
It is insoluble in water. Soluble in organic solvents.
Sensitive 
Air & Light Sensitive
maximale Wellenlänge (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 Sicherheitserklärung
  • Gefahreninformationscode (GHS)
Kennzeichnung gefährlicher Xi
R-Sätze: 43-52/53
S-Sätze: 36/37-61-24/25
RIDADR  3335
WGK Germany  3
10-23
TSCA  Yes
HS Code  29309090
Bildanzeige (GHS) GHS hazard pictograms
Alarmwort Warnung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H317 Kann allergische Hautreaktionen verursachen. Sensibilisierung der Haut Kategorie 1A Warnung GHS hazard pictogramssrc="/GHS07.jpg" width="20" height="20" /> 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: Ärztlichen Rat einholen/ärztliche Hilfe hinzuziehen.

δ-2:2'-Bis(1,3-dithiazol) Chemische Eigenschaften,Einsatz,Produktion Methoden

R-Sätze Betriebsanweisung:

R43:Sensibilisierung durch Hautkontakt möglich.

S-Sätze 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.

läuterung 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 Händler.

Global( 144)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
Capot Chemical Co.,Ltd.
571-85586718 +8613336195806
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0431-80514535 13634302652
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daeyeon001@vip.163.com China 2062 58
Hefei TNJ Chemical Industry Co.,Ltd.
0551-65418671
sales@tnjchem.com China 34571 58
ANHUI WITOP BIOTECH CO., LTD
+8615255079626
eric@witopchemical.com China 23556 58
Hefei Hirisun Pharmatech Co., Ltd
+8615056975894
shawn@hirisunpharm.com CHINA 9923 58

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
  • 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
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