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CAS RN: 31366-25-3 | Product Number: T0980
Tetrathiafulvalene
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Purity: >98.0%(GC)
Synonyms:
- TTF
Product Documents:
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| Product Number | T0980 |
Purity / Analysis Method 
|
>98.0%(GC) |
| Molecular Formula / Molecular Weight | C__6H__4S__4 = 204.34 |
| Physical State (20 deg.C) | Solid |
| Storage Temperature
|
Room Temperature (Recommended in a cool and dark place, <15°C) |
| Store Under Inert Gas | Store under inert gas |
| Condition to Avoid | Light Sensitive,Air Sensitive |
| Packaging and Container
|
1G-Glass Bottle with Plastic Insert (View image) |
| CAS RN | 31366-25-3 |
| Reaxys Registry Number | 1282106 |
| PubChem Substance ID | 87576791 |
| SDBS (AIST Spectral DB) | 13743 |
| Merck Index (14) | 9242 |
| MDL Number | MFCD00005492 |
Specifications
| Appearance | Orange to Brown powder to crystal |
| Purity(GC) | min. 98.0 % |
| Melting point | 118.0 to 123.0 °C |
Properties (reference)
| Melting Point | 120 °C |
| Maximum Absorption Wavelength | 369 nm (CHCl__3) |
GHS
Related Laws:
Transport Information:
| H.S.code* | 2934.99-000 |
Application
An Organic Electron Donor
Tetrathiafulvalene (TTF) was first synthesized by Wudl et al.1, 2) It works as an organic electron donor, and used for radical reactions by Murphy et al.3)
References
- 1)Bis-1,3-dithiolium chloride: an unusually stable organic radical cation
- 2)Electrical conductivity by the bis(1,3-dithiole)-bis(1,3-dithiolium) system
- 3)Tetrathiafulvalene as a catalyst for radical–polar crossover reactions
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Related Products
Tetrathiafulvalene (purified by sublimation)
| Product # | T3380 |
| CAS RN | 31366-25-3 |
| Purity / Analysis Method: | >99.0%(GC) |