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Merck
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B4932

Sigma-Aldrich

Butyl-γ-cyclodextrin

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About This Item

MDL號碼:
MFCD03452848
分類程式碼代碼:
12352201
PubChem物質ID:
329773246
NACRES:
NA.25

形狀

solid

儲存溫度

2-8°C

SMILES 字串

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

InChI 密鑰

GKKAPJLYIDRKJM-CEIOSFLZSA-N

其他說明

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

儲存類別代碼

11 - Combustible Solids

水污染物質分類（WGK）

WGK 3

閃點（°F）

Not applicable

閃點（°C）

Not applicable

個人防護裝備

Eyeshields, Gloves, type N95 (US)

历史批次信息供参考:

分析证书(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
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
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