a Fullerene, C60 and its derivatives have been fully investigated and commercialized. The importance of the large carbon cage-based fullerenes for the biomedical applications were gradually recognized due to their fantastic biological effects. In nanotoxicology, the key detection technique was able to retain the intrinsic structure and properties of nanomatrials in biological background. However, it was a puzzled question how to get facilely the detectable fullerene nanomaterials and their formation process. In this study, 13 C-enriched fullerenes of large carbon cage, C70, were synthesized in a large scale from 13 C-enriched raw carbon material by arc-discharge method. The stable isotopes 13 C were directly incorporated into the skeleton of the fullerenes cages without destroying their intrinsic structures. The isotopic effects of 13 C-labeled C70 were investigated in detail. The 13 C labeled amounts of C70 was about 7 % higher than that of natural abundance, which greatly improved the 13 C detection signal in isotope ratio mass spectrometry and apparent 8-fold carbon nuclear magnetic resonance signal enhancement of fullerenes. The 13 C-enriched fullerenes showed significant isotopic effects, such as the strongest peak position shift up (m/z>840) and the Poisson distribution of isotopic peaks in the mass spectra, the migration or splitting of infrared and Raman characteristic peaks. Comparison of the 13 C labeled amounts and isotopic effects of 13 C-enriched C70 and those of 13 C-enriched C60, the formation dynamics of fullerenes were different with the changes of carbon cage, lower carbon cage fullerenes were easily generated in the process of arc-discharge, the 13 C stable isotopic effects in high carbon fullerenes were also slight weak. Moreover, these important isotopic effects of 13 C-enriched fullerene will facilitate the development of new analytical methods for carbon nanomaterials in vivo.