793248
Polyhydroxylated fullerenes, water soluble
Synonym(s):
C60(OH)n, water soluble C60, Fullerenols, Polyhydroxy fullerenes
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About This Item
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form
solid
color
light yellow to yellow
solubility
water: soluble >50 mg/mL
DMSO: slightly soluble
methanol: slightly soluble
storage temp.
2-8°C
Related Categories
General description
Polyhydroxylated fullerenes, (water soluble)(PHF) is a functionalized fullerene that is also called fullerenol which can be used as a molecular anti-oxidant and a nanoparticle. It is a non-toxic fullerene which is attached with 12-42 hydroxyl groups per molecule that result in water solubility. Its structure and the position of the hydroxyl groups will depend on the existing pH of the media.
Application
PHF may be incorporated in titanium dioxide to form a nanocomposite which can be potentially used in the photocatalysis of semiconductors. Its photothermal and therapeutic properties may be used in non-invasive image based therapy of cancer.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin 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
Certificates of Analysis (COA)
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Enhancement of nano titanium dioxide photocatalysis in transparent coatings by polyhydroxy fullerene.
Applied Catalysis. B, Environmental, 125(1), 128-135 (2012)
Polyhydroxy fullerenes (fullerols or fullerenols): beneficial effects on growth and lifespan in diverse biological models.
PLoS ONE, 6(5), e19976-e19976 (2011)
Molecular and cellular biochemistry, 366(1-2), 191-200 (2012-04-03)
Reactive oxygen species has been suggested to be one of the key factors associated with the development of obesity. During spontaneous differentiation of mouse stromal preadipocytes OP9 into adipocytes, intracellular superoxide anion radicals (O (2) (-.) ) level markedly increases
Nanoscale, 11(24), 11933-11945 (2019-06-13)
Featuring small sizes, caged structures, low cytotoxicity and the capability to cross biological barriers, fullerene hydroxy derivatives named fullerenols have been explored as nanomedicinal candidates for amyloid inhibition. Understanding the surface chemistry effect of hydroxylation extents and the corresponding amyloid
Journal of photochemistry and photobiology. B, Biology, 102(1), 69-76 (2010-10-15)
Polyhydroxylated fullerenes (fullerenols: C(60)(OH)(n)) are known as the major water-soluble fullerene derivatives which possess particular significance as free radical scavengers or antioxidants in biological systems. Recently, the novel polyhydroxylated fullerene (C(60) (OH)(44)·8H(2)O: SHH-F) was successfully synthesized. In the present study
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