| Identification | Back Directory | [Name]
FULLERENE | [CAS]
99685-96-8 | [Synonyms]
C60
FULLERENE
CARBON 60
BUCKYBALL
CARBON C60
follene-60
FOOTBALLENE
Fullerene-C
C60FULLERENE
Fulleren C60
soccerballene
SOOCERBALLENE
FULLERENE C60
[60]Fullerene
icosahedralC60
Fullerene powder
FULLERENE, FILMS
Fullerene ,99.5%
Fullerene-C60 98%
FULLERENE EXTRACT
CARBON CLUSTER C60
[5,6]FULLERENE-C60
Fullerene C60
5,6Fullerene-C60-Ih
Fullerene C60 (pure)
BUCKMINSTERFULLERENE
Fullerene C60, 99.9+%
Fullerene C60, 99.90%
FULLERENE EXTRACT, C60
BUCKMINSTERFULLERENE C60
FULLERENE, WATER-SOLUBLE
Fullerene, C_6_0, 99.5+%
Fullerenepowder,99.5%C60
Fullerene powder, 97% C70
BUCKMINSTERFULLERENE, 99.5%
Fullerene powder, C60, 99.5%
Fullerene powder, C60, 99.9%
Fullerene powder, 99% C{6}{0}
Fullerene-C60 subliMed, 99.9%
FULLERENE-C6O, SUBLIMED, 99.9%
FULLERENE, ISOTOPICALLY ENRICHED
FULLERENE, EXTRACT MIXED (FULLERITE)
Fullerene powder, hydrogenated, C6Hx
Fullerene powder, sublimed, C60, 99.9%
Buckminsterfullerene C60
C60
Carbon C60
Fullerene powder, sublimed, 99.92+% C60
Fullerene powder, mixed, 88% C6, 12% C7
Fullerene powder, sublimed, 99.95+% C60
FULLERENE, POWDER HYDROXYLATED C60(OH)N
Fullerene powder, mixed, 98% C60 and 2% C70
FULLERENE, C60 99.9+% (BUCKMINSTERFULLERENE,)
FULLERENE, C60 99.5+% (BUCKMINSTERFULLERENE,)
Fullerene-C60,min.99.9%(Buckminsterfullerene)
FULLERENE, C60 99.95+% (BUCKMINSTERFULLERENE,)
Fullerene powder, 99.5% C60
Fullerene powder, 99.9+% C60
FULLERENE, HIGHER ORDER MIXTURES (C76 THROUGH C96)
FULLERENE, POWDER HYDROGENATED C60HX (FULLERENE, HYDRIDES)
Fullerene powder, sublimed, 99.9+% C60
FULLERENE, POWDER MIXED HYDROGENATED, TYPICALLY 77% C60HX, 22% C70HY
FULLERENE, POWDER MIXED REFINED, TYPICALLY 77% C60, 22% C70, <2% HIGHER
Fullerene, carbon nanotube, multi-walled, ≤8 nm OD, 2-5 nm ID, 0.5-2 micron long
Fullerene powder, mixed, typically 98% C60, 2% C70
Fullerene powder, mixed refined, typically 73% C60, 22% C70, higher 5%
Fullerene powder, mixed refined, typically 77% C60, 22% C70, <2% higher | [EINECS(EC#)]
205-105-7 | [Molecular Formula]
C60 | [MDL Number]
MFCD00151408 | [MOL File]
99685-96-8.mol | [Molecular Weight]
720.64 |
| Chemical Properties | Back Directory | [Appearance]
black to brown crystalline powder | [Melting point ]
>280 °C(lit.)
| [Boiling point ]
500-600℃ subl. | [density ]
5.568 | [RTECS ]
LS9252500 | [Fp ]
94 °C | [storage temp. ]
Dark Room | [solubility ]
organic solvents: soluble
| [form ]
sublimed
| [color ]
Dark brown to black | [Stability:]
Stable. Highly flammable. Incompatible with strong oxidizing agents. | [Water Solubility ]
Soluble in toluene. Insoluble in water. | [Specific Heat Capacity]
Cp(crystal):0.721581J/(g·K);Cp(gas):0.71048J/(g·K),at 25℃ | [Merck ]
1462 | [BRN ]
5901022 | [Cosmetics Ingredients Functions]
SKIN CONDITIONING - MISCELLANEOUS
ANTIMICROBIAL | [InChIKey]
XMWRBQBLMFGWIX-UHFFFAOYSA-N | [LogP]
5.800 (est) | [EPA Substance Registry System]
[5,6]Fullerene-C60-Ih (99685-96-8) |
| Hazard Information | Back Directory | [Chemical Properties]
black to brown crystalline powder | [Definition]
ChEBI: Fullerene C60(99685-96-8) is a fullerene. It has a role as a geroprotector. It is a polyhedral CARBON structure composed of around 60-80 carbon atoms in pentagon and hexagon configuration. They are named after Buckminster Fuller because of structural resemblance to geodesic domes. Fullerenes can be made in high temperature such as arc discharge in an inert atmosphere. | [General Description]
Fullerene C60(99685-96-8) is a molecule with prominent electron acceptor property composed of 60 carbons in the shape of a hollow football with 20 hexagons and 12 pentagons. Fullerene is unsaturated, each carbon connecting to 3 other carbons instead of 4 with fused 5 and 6 membered rings. |
| Questions And Answer | Back Directory | [Description]
Fullerenes are molecules that composed entirely of carbon. They are similar in structure to graphite, which is composed of a sheet of linked hexagonal and pentagonal rings that prevent the sheet from being planar. Each carbon atom on the surface of fullerenes is bonded to three carbon neighbors, therefore, is sp2 hybridized. Fullerenes are in the form of a hollow sphere, ellipsoid, tube, and many other shapes. Spherical fullerenes C60, the first fullerene molecule manufactured in 1985, is named as buckminsterfullerene, resembles the balls used in football. Cylindrical fullerenes are known as carbon nanotubes (CNTs). As the discovery of fullerenes came after buckminsterfullerene, the shortened name “fullerene” is used to refer to the family of fullerenes, of which each carbon atom is covalently bonded to three others.
The most specific feature of fullerenes is that they are excellent electron acceptors (n-type semiconductors), which are suitable for organic electronic materials with electron carriers. Fullerenes can be used to fabricate polymer/fullerene blend for organic photovoltaics, in which fullerene acts as the n-type semiconductor. Fullerenes are powerful antioxidants, which react readily and at a high rate with free radicals. These free radicals usually lead to cell damage or death. Therefore, fullerenes show great promise in health and personal care applications, in which the prevention of oxidative cell damage or death is desirable. Fullerenes are also used in non-physiological applications, where oxidation and radical processes are destructive (food spoilage, plastics deterioration, metal corrosion). Research interests on fullerenes include also the use of fullerenes to control the neurological damage of diseases such as Alzheimer’s disease and Lou Gehrig’s disease. Fullerenes are used as additives for polymers to create copolymers or composites with specific physical and mechanical properties. Fullerenes can be doped with rubidium and cesium to fabricate superconductors with electron carriers, of which the superconducting transitions occur at more than 30 K. | [Uses]
High purity carbon 60 fullerenes for use in thermal evaporation systems as either electron acceptors, n-type semiconductors or interface layers.
| [References]
[1] K. Tanigaki, T. W. Ebbesen, S. Saito, J. Mizuki, J. S. Tsai, Kubo & S. Kuroshima (1991) Superconductivity at 33 K in CsxRbyC60, Nature, 352, 222-223
[2] https://en.wikipedia.org/wiki/Fullerene
[3] B. C. Yadav, Ritesh Kumar (2008) Structure, properties and applications of fullerenes, International Journal of Nanotechnology and Applications, 2, 15-24
[4] XU J, WANG H, HU Y, et al. Inhibition of CaMKIIα Activity Enhances Antitumor Effect of Fullerene C60 Nanocrystals by Suppression of Autophagic Degradation[J]. Advanced Science, 2019, 6. DOI:10.1002/advs.201801233.
[5] FRANSKEVYCH D, PALYVODA K O, PETUKHOV D M, et al. Fullerene C60 Penetration into Leukemic Cells and Its Photoinduced Cytotoxic Effects[J]. Nanoscale Research Letters, 2017, 12. DOI:10.1186/s11671-016-1819-5. |
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Energy Chemical
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