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793248

Sigma-Aldrich

Polyhydroxylated fullerenes, water soluble

Sinonimo/i:

C60(OH)n, water soluble C60, Fullerenols, Polyhydroxy fullerenes

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About This Item

Formula empirica (notazione di Hill):
C60(OH)n · mH2O (n>40, m>8)
Codice UNSPSC:
12352103
NACRES:
NA.23

Forma fisica

solid

Colore

light yellow to yellow

Solubilità

water: soluble >50 mg/mL
DMSO: slightly soluble
methanol: slightly soluble

Temperatura di conservazione

2-8°C

Descrizione generale

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.

Applicazioni

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.

Pittogrammi

Exclamation mark

Avvertenze

Warning

Indicazioni di pericolo

Classi di pericolo

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Organi bersaglio

Respiratory system

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable


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Synthesis and Biological Activity of Fullerenols with Various Contents of Hydroxyl Groups
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Pharmaceutical Chemistry Journal, 47(2), 87-91 (2013)
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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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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
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