BIS(ETHYLENEDITHIO)TETRATHIAFULVALENE Chemische Eigenschaften,Einsatz,Produktion Methoden

S-S?tze Betriebsanweisung:

S22:Staub nicht einatmen.
S24/25:Berührung mit den Augen und der Haut vermeiden.

Chemische Eigenschaften

RED LUSTROUS NEEDLES

Verwenden

It is used as a component for organic superconductors.

Allgemeine Beschreibung

Bis(ethylenedithio)tetrathiafulvalene (BEDT-TTF) is an organic superconducting polymer that is used as an electron donor with a superconducting transition temperature (Tc) of 10K.

BIS(ETHYLENEDITHIO)TETRATHIAFULVALENE Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte

BIS(ETHYLENEDITHIO)TETRATHIAFULVALENE Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

Firmenname	Telefon	E-Mail	Land	Produktkatalog	Edge Rate
Nanjing jinheyou Trading Co., Ltd.	15705188088	admin@jheyou.com	CHINA	1268	58
Jilin Chinese Academy of Sciences-yanshen Technology	+undefined18143011203	info@chemextension.com	China	42056	58
XIAMEN AMITY INDUSTRY AND TRADE CO., LTD.	+8618950047208	ellena@amitychem.com	China	30102	58
Mainchem Co., Ltd.	+86-0592-6210733	sale@mainchem.com	China	32343	55
J & K SCIENTIFIC LTD.	010-82848833 400-666-7788	jkinfo@jkchemical.com	China	96815	76
Meryer (Shanghai) Chemical Technology Co., Ltd.	021-61259108 18621169109	market03@meryer.com	China	40228	62
Alfa Aesar	400-6106006	saleschina@alfa-asia.com	China	30123	84
TCI (Shanghai) Development Co., Ltd.	021-67121386	Sales-CN@TCIchemicals.com	China	24529	81
Energy Chemical	021-021-58432009 400-005-6266	sales8178@energy-chemical.com	China	44688	61
TOKYO CHEMICAL INDUSTRY CO., LTD.	03-36680489	Sales-JP@TCIchemicals.com	Japan	28387	80

66946-48-3()Verwandte Suche:

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• BIS-ETHYLENDITHIO-TETRATHIAFULVALENE
• BI[5,6-DIHYDRO-1,3-DITHIOLO[4,5-B][1,4]-DITHIINE-2-YLIDENE]
• BIS(ETHYLENEDITHIO)TETRATHIAFULVALENE, 9 8%
• Bis(ethylenedithia)tetrathiafulvalene
• Bis(ethylenedithio)tetrathiafulvalene [Organic Electronic Material]
• BEDT-TTF, Bi[5,6-dihydro-1,3-dithiolo[4,5-b][1,4]-dithiine-2-ylidene]
• 2-(5,6-Dihydro-1,3-dithiolo[4,5-b][1,4]dithiin-2-ylidene)-5,6-dihydro-1,3-dithiolo[4,5-b][1,4]dithiin
• Bis(ethylendithiolo)tetrathiafulvalene
• BEDT-TIF
• Bis(ethylenedithio)tetrathiafluvalene
• Bis(ethylenedithiolo)tetrathiofulvalene
• 1,3-Dithiolo[4,5-b][1,4]dithiin, 2-(5,6-dihydro-1,3-dithiolo[4,5
• 1,3-Dithiolo[4,5-b][1,4]dithiin, 2-(5,6-dihydro-1,3-dithiolo[4,5-b][1,4]dithiin-2-ylidene)-5,6-dihydro-
• Bis(ethylenedithio)tetrathiafulvalene 
• RARECHEM AR PA 0052
• BEDT-TTF
• BIS(ETHYLENEDITHIOLO)TETRATHIAFULVALENE
• BIS(ETHYLENEDITHIO)TETRAHYDROFULVALENE
• BIS(ETHYLENEDITHIO)TETRATHIAFULVALENE
• Bis(ethylenedithio)tetrathiafulvalene 98%
• 5,5',6,6'-Tetrahydro-2,2'-bi[1,3]dithiolo[4,5-b][1,4]dithiinylidene
• 2-(5,6-dihydro-[1,3]dithiolo[4,5-b][1,4]dithiin-2-ylidene)-5,6-dihydro-[1,3]dithiolo[4,5-b][1,4]dithiine
• bis(ethylenedithio)tetrathiofulvalene
• 5,5',6,6'-Tetrahydro-2,2'-bi[1,3]dithiolo[4,5-b][1,4]dithiinylidene
• 66946-48-3
• C10H8S8
• Building Blocks
• TTF Derivatives
• Donors (Charge Transfer Complexes)
• Charge Transfer Complexes for Organic Metals
• Others
• S-Containing
• Heterocyclic Building Blocks
• Sulphur Derivatives
• Donors (Charge Transfer Complexes)
• TTF Derivatives
• Charge Transfer Complexes for Organic Metals
• Functional Materials