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Documentos Principais

B4932

Sigma-Aldrich

Butyl-γ-cyclodextrin

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About This Item

Número MDL:
Código UNSPSC:
12352201
ID de substância PubChem:
NACRES:
NA.25

Formulário

solid

temperatura de armazenamento

2-8°C

cadeia de caracteres SMILES

CCCCOC[C@H]1O[C@@H]2O[C@H]3[C@H](O)[C@@H](O)[C@H](O[C@@H]3CO)O[C@H]4[C@H](O)[C@@H](O)[C@H](O[C@@H]4CO)O[C@H]5[C@H](O)[C@@H](O)[C@H](O[C@@H]5CO)O[C@H]6[C@H](O)[C@@H](O)[C@H](O[C@@H]6CO)O[C@H]7[C@H](O)[C@@H](O)[C@H](O[C@@H]7CO)O[C@H]8[C@H](O)[C@@H](O)[C@H](O[C@@H]8CO)O[C@H]9[C@H](O)[C@@H](O)[C@H](O[C@@H]9CO)O[C@H]1[C@H](O)[C@H]2O

InChI

1S/C52H88O40/c1-2-3-4-76-12-20-44-28(67)36(75)52(84-20)91-43-19(11-59)82-50(34(73)26(43)65)89-41-17(9-57)80-48(32(71)24(41)63)87-39-15(7-55)78-46(30(69)22(39)61)85-37-13(5-53)77-45(29(68)21(37)60)86-38-14(6-54)79-47(31(70)23(38)62)88-40-16(8-56)81-49(33(72)25(40)64)90-42-18(10-58)83-51(92-44)35(74)27(42)66/h13-75H,2-12H2,1H3/t13-,14-,15-,16-,17-,18-,19-,20-,21-,22-,23-,24-,25-,26-,27-,28-,29-,30-,31-,32-,33-,34-,35-,36-,37-,38-,39-,40-,41-,42-,43-,44-,45-,46-,47-,48-,49-,50-,51-,52-/m1/s1

chave InChI

GKKAPJLYIDRKJM-CEIOSFLZSA-N

Outras notas

To gain a comprehensive understanding of our extensive range of Oligosaccharides for your research, we encourage you to visit our Carbohydrates Category page.

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

Eyeshields, Gloves, type N95 (US)


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Visite a Biblioteca de Documentos

J Hu et al.
Methods and findings in experimental and clinical pharmacology, 31(7), 449-456 (2009-11-13)
Owing to their bioadaptability and multifunctional characteristics, cyclodextrins have been shown to be useful in drug delivery systems. This article presents the unique structure and properties and the current application of natural and chemically modified cyclodextrins in transdermal drug delivery
Kaneto Uekama
Chemical & pharmaceutical bulletin, 52(8), 900-915 (2004-08-12)
The pharmaceutically useful cyclodextrins (CyDs) are classified into hydrophilic, hydrophobic, and ionic derivatives. Because of the multi-functional characteristics and bioadaptability, these CyDs are capable of alleviating the undesirable properties of drug molecules through the formation of inclusion complexes or the
Birna S Gudmundsdottir et al.
Journal of ocular pharmacology and therapeutics : the official journal of the Association for Ocular Pharmacology and Therapeutics, 30(1), 35-41 (2013-11-12)
To test a new drug delivery platform with dorzolamide γ-cyclodextrin (γCD) nanoparticle eye drops for intraocular pressure (IOP) control and safety and compare with Trusopt.(®) Self-aggregating γCD nanoparticle eye drops containing 3% dorzolamide were given once a day (QD) and
Prosenjit Bhattacharya et al.
Journal of fluorescence, 24(3), 719-725 (2013-12-18)
This paper reports the double confinement of 4,4-diaminodiphenyl sulfone (Dapsone) inside γ-cyclodextrin (CD) in presence of surfactants (cationic, anionic and nonionic) using steady-state and time-resolved fluorescence spectroscopy. Interpretation of fluorescence spectra, fluorescence anisotropy and time resolved fluorescence decay of the
Feng Zhao et al.
Biomaterials, 35(3), 1050-1062 (2013-11-06)
For developing a multifunctional bioreducible targeted and synergistic co-delivery system for anticancer drug paclitaxel (PTX) and p53 gene for potential cancer therapy, supramolecular self-assembled inclusion complex was prepared from PTX and star-shaped cationic polymer containing γ-cyclodextrin (γ-CD) and multiple oligoethylenimine

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