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572500

Sigma-Aldrich

Fullerene-C60

greener alternative

sublimed, 99.9%

Synonym(s):

Buckminsterfullerene

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About This Item

Empirical Formula (Hill Notation):
C60
CAS Number:
Molecular Weight:
720.64
Beilstein:
5901022
MDL number:
UNSPSC Code:
12352103
NACRES:
NA.23

Quality Level

Assay

99.9%

form

sublimed

greener alternative product characteristics

Design for Energy Efficiency
Learn more about the Principles of Green Chemistry.

sustainability

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mp

>280 °C (lit.)

solubility

organic solvents: soluble
organic solvents: soluble

Orbital energy

HOMO 6.1 eV 
LUMO 4.5 eV 

OLED Device Performance

ITO/CuPc/NPD/Alq3/C60/Mg:Ag

  • Color: green
  • Max. Luminance: 17200 Cd/m2

ITO/NPD/Alq3/C60/LiF:Al:Ag
  • Color: green
  • Max. Luminance: 7000 Cd/m2
  • Turn-On Voltage: <5 V

ITO/TPD/Alq3/C60/LiF/Al/Ag
  • Color: green
  • Max. Luminance: 4000 Cd/m2
  • Turn-On Voltage: <5 V

greener alternative category

SMILES string

c12c3c4c5c1c6c7c8c2c9c%10c3c%11c%12c4c%13c%14c5c%15c6c%16c7c%17c%18c8c9c%19c%20c%10c%11c%21c%22c%12c%13c%23c%24c%14c%15c%25c%16c%26c%17c%27c%18c%19c%28c%20c%21c%29c%22c%23c%30c%24c%25c%26c%31c%27c%28c%29c%30%31

InChI

1S/C60/c1-2-5-6-3(1)8-12-10-4(1)9-11-7(2)17-21-13(5)23-24-14(6)22-18(8)28-20(12)30-26-16(10)15(9)25-29-19(11)27(17)37-41-31(21)33(23)43-44-34(24)32(22)42-38(28)48-40(30)46-36(26)35(25)45-39(29)47(37)55-49(41)51(43)57-52(44)50(42)56(48)59-54(46)53(45)58(55)60(57)59

InChI key

XMWRBQBLMFGWIX-UHFFFAOYSA-N

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General description

C60 is an n-channel organic semiconductor. High reactivity of fullerenes is attributed to its characteristic pyramidalization of the sp2 carbons. C60 is purified by column chromatography in toluene, then heat-treated under vacuum to remove solvent residue. Highly crystalline sublimed material with low solvent and metal content was recovered.
Fullerene-C60 (C60) has a closed-cage structure that is icosachedrally shaped with 60 sp2 hybridized carbon. It is majorly utilized in the development of novel materials for a wide range of energy based applications.
We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product has been enhanced for energy efficiency. Find details here.

Application

An n-channel organic semiconductor. Water suspension of C60 was studied for its effect on the growth, cell viability and membrane integrity of Escherichia coli B23.
C60 can be used for a wide range of applications, such as anode materials for lithium (Li)-ion batteries, and pentacene-C60 based solar cells with high quantum efficiency. It can be incorporated in (1,4-phenylene vinylene) (PPV) matrix for applications in photovoltaics.
Fullerene-C60 (sublimed, 99.9%) belongs to the class of carbonaceous materials. It can be used for a variety of alternative energy applications, which include lithium-ion batteries, organic photovoltaic cells (OPV), heterojunction solar cells, polymeric photodetectors, photodiodes, and photocatalysis.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Nicklas Raun Jacobsen et al.
Particle and fibre toxicology, 6, 2-2 (2009-01-14)
The toxic and inflammatory potential of 5 different types of nanoparticles were studied in a sensitive model for pulmonary effects in apolipoprotein E knockout mice (ApoE-/-). We studied the effects instillation or inhalation Printex 90 of carbon black (CB) and
A Silicon--Singlet Fission Tandem Solar Cell Exceeding 100% External Quantum Efficiency with High Spectral Stability
Pazos-Outo?n LM, et al.
ACS Energy Letters, 2(2) (2017)
Genotoxicity, cytotoxicity, and reactive oxygen species induced by single-walled carbon nanotubes and C60 fullerenes in the FE1-Muta?Mouse lung epithelial cells.
Jacobsen NR, et al.
Environmental and Molecular Mutagenesis, 49(6), 476-487 (2008)
Silylethyne-Substituted Pentacenes
Anthony JE, et al.
Material Matters, 4(3), 58-58 null
Synthesis and photophysical properties of a charm-bracelet type C60-grafted PPV derivative
Che Y, et al.
Polymer, 46(23), 9803-9809 (2005)

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