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B4932

Sigma-Aldrich

Butyl-γ-cyclodextrin

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About This Item

Numero MDL:
MFCD03452848
Codice UNSPSC:
12352201
ID PubChem:
329773246
NACRES:
NA.25

Stato

solid

Temperatura di conservazione

2-8°C

Stringa SMILE

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
GKKAPJLYIDRKJM-CEIOSFLZSA-N

Altre note

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

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

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)

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Certificati d'analisi (COA)

Lot/Batch Number
044K1617
113K1500
111K1195
017K1197
086K1628

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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
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
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
Gauti Jóhannesson et al.
Acta ophthalmologica, 92(6), 550-556 (2014-01-01)
We have developed nanoparticle γ-cyclodextrin dexamethasone (DexNP) and dorzolamide (DorzNP) eye drops that provide sustained high drug concentrations on the eye surface. To test these characteristics, we measured dexamethasone and dorzolamide levels in tear fluid in humans following eye drop
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