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Merck
CN

379654

[5,6]-Fullerene-C70

95%

Synonym(s):

Buckminsterfullerene C70, Fullerene-C70

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About This Item

Empirical Formula (Hill Notation):
C70
CAS Number:
115383-22-7
Molecular Weight:
840.75
UNSPSC Code:
12352103
PubChem Substance ID:
24863677
MDL number:
MFCD00146976

Key Documents

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InChI

1S/C70/c1-2-22-5-6-24-13-14-26-11-9-23-4-3(21(1)51-52(22)54(24)55(26)53(23)51)33-31(1)61-35-7-8-27-15-16-29-19-20-30-18-17-28-12-10(25(7)56-57(27)59(29)60(30)58(28)56)37(35)63(33)65-36(4)40(9)67(44(17)42(12)65)69-46(11)47(14)70(50(20)49(18)69)68-43(13)39(6)66(45(16)48(19)68)64-34(5)32(2)62(61)38(8)41(15)64

SMILES string

C1CC2C3CCC4C5C3C6C2C7C1CC8CC9CC%10CC%11C%12CC%13CC4C%13%14C%12C%15C%11C%16C%10C9C%17C8C7C%18C%17C%16C%15C(C6%18)C5%14

InChI key

ATLMFJTZZPOKLC-UHFFFAOYSA-N

assay

95%

form

crystalline

mp

>280 °C (lit.)

orbital energy

HOMO 6.2 eV , LUMO 4.6 eV 

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Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
11809JH
11401HD
01810LC
16402TF
03316CN

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Annealing effect in the sexithiophene:C70 small molecule bulk heterojunction organic photovoltaic cells
Sakai, J.; Taima, T.; Yamanari, T.; et al.
Solar Energy Materials and Solar Cells, 93, 1149-1153 (2009)
Ratul Mitra et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 89, 284-293 (2012-01-27)
The present article reports for the first time on supramolecular interaction between fullerenes (C60 and C70) and a designed monoporphyrin in solution, e.g., 5,10,15,20-tetrakis(4-methoxyphenyl)-21H,23H-porphine (1), in absence and presence of silver nanoparticles (AgNp) having varying diameter of range between 3
Troy M Benn et al.
Environmental pollution (Barking, Essex : 1987), 159(5), 1334-1342 (2011-02-09)
Detection methods are necessary to quantify fullerenes in commercial applications to provide potential exposure levels for future risk assessments of fullerene technologies. The fullerene concentrations of five cosmetic products were evaluated using liquid chromatography with mass spectrometry to separate and
Sibayan Mukherjee et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 79(5), 1952-1958 (2011-06-28)
The present paper reports the synthesis of a designed bisporphyrin (1), and its supramolecular complexes with C60, C70 and their derivatives, namely, tert-butyl-(1,2-methanofullerene)-61-carboxylate (2) and [6,6]-phenyl C70 butyric acid methyl ester (3) in toluene medium. C60, C70 and their derivatives
Sarah K Norton et al.
The Journal of allergy and clinical immunology, 130(3), 761-769 (2012-06-06)
Fullerenes are molecules being investigated for a wide range of therapeutic applications. We have shown previously that certain fullerene derivatives (FDs) inhibit mast cell (MC) function in vitro, and here we examine their in vivo therapeutic effect on asthma, a disease in
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