Cookie Policy: This site uses cookies to improve your experience. You can find out more about our use of cookies in our Privacy Policy. By continuing to browse this site you agree to our use of cookies.
Chemodex
β-Cyclodextrin
54
CHF
CHF 54.00
In stock
CDX-C0261-G02525 gCHF 54.00
CDX-C0261-G100100 gCHF 162.00
CDX-C0261-G500500 gCHF 543.00
| Product Details | |
|---|---|
| Synonyms | β-Cyclodextrin; Caraway; Cycloheptaamylose; Cyclomaltoheptaose; Schardinger β-Dextrin |
| Product Type | Chemical |
| Properties | |
| Formula |
C42H70O35 |
| MW | 1134.98 |
| CAS | 7585-39-9 |
| Purity Chemicals | ≥97% |
| Appearance | White crystalline powder. |
| Solubility | Soluble in water (10mg/ml) or 1 M NH4OH (50mg/ml). |
| Declaration | Manufactured by Chemodex. |
| Other Product Data |
Click here for Original Manufacturer Product Datasheet |
| InChi Key | WHGYBXFWUBPSRW-FOUAGVGXSA-N |
| Smiles | O[C@H]([C@H]1O)[C@]2([H])O[C@@]3([H])O[C@H](CO)[C@@]([C@@H]([C@H]3O)O)([H])O[C@@]4([H])O[C@H](CO)[C@@]([C@@H]([C@H]4O)O)([H])O[C@@]5([H])O[C@H](CO)[C@@]([C@@H]([C@H]5O)O)([H])O[C@@]6([H])O[C@H](CO)[C@@]([C@@H]([C@H]6O)O)([H])O[C@@]7([H])O[C@H](CO)[C@@]([C@@H]([C@H]7O)O)([H])O[C@@]8([H])O[C@H](CO)[C@@]([C@@H]([C@H]8O)O)([H])O[C@@]1([H])O[C@@H]2CO |
| Shipping and Handling | |
| Shipping | AMBIENT |
| Short Term Storage | +20°C |
| Long Term Storage | +20°C |
| Handling Advice | Protect from light and moisture. |
| Use/Stability | Stable for at least 2 years after receipt when stored at +20°C. |
| Documents | |
| MSDS |
 Download PDF |
| Product Specification Sheet | |
| Datasheet |
Download PDF |
Description
Most commonly used as a complexing agent in food, pharmaceutical, drug delivery and chemical industries, as well as agriculture and environmental engineering. Forms complexes with hydrophobic compounds to enhance solubility and bioavailability (Drug Delivery System DDS). Commonly used to produce HPLC columns allowing chiral enantiomers separation. Used to remove large hydrophobic molecules like cholesterol. Reported to be useful for the selective precipitation of enantiomeric, positional or structural isomers. Cyclodextrins are cyclic oligosaccharides consisting of 6, 7, or 8 glucopyranose units with hydrophobic interiors, usually referred to as alpha-, beta- or gamma-cyclodextrins, respectively. Lipophilic drugs of a size compatible with the hydrophobic core of a cyclodextrin can form complexes, resulting in increased aqueous solubility of the drugs. Cyclodextrins are non-toxic in many species and do not denature proteins or interfere with enzymatic reactions.
Product References
(1) E.M. Martin Del Valle; Process Biochem. 39, 1033 (2004) (Review) | (2) G. Crini; Chem. Rev. 114, 10940 (2014) (Review)