beta-Cyclodextrin
| Code | Size | Price |
|---|
| CDX-C0261-G025 | 25 g | £59.00 |
Quantity:
| CDX-C0261-G100 | 100 g | £157.00 |
Quantity:
| CDX-C0261-G500 | 500 g | £499.00 |
Quantity:
Prices exclude any Taxes / VAT
Overview
Regulatory Status: RUO
Shipping:
Ambient
Storage:
Short Term: +20°C. Long Term: +20°C
Documents
Further Information
Alternate Names/Synonyms:
beta-Cyclodextrin; Caraway; Cycloheptaamylose; Cyclomaltoheptaose; Schardinger beta-Dextrin
Appearance:
White crystalline powder.
CAS:
7585-39-9
EClass:
32160000
Form (Short):
liquid
Handling Advice:
Protect from light and moisture.
InChi:
InChI=1S/C42H70O35/c43-1-8-29-15(50)22(57)36(64-8)72-30-9(2-44)66-38(24(59)17(30)52)74-32-11(4-46)68-40(26(61)19(32)54)76-34-13(6-48)70-42(28(63)21(34)56)77-35-14(7-49)69-41(27(62)20(35)55)75-33-12(5-47)67-39(25(60)18(33)53)73-31-10(3-45)65-37(71-29)23(58)16(31)51/h8-63H,1-7H2/t8-,9-,10-,11-,12-,13-,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-/m1/s1
InChiKey:
WHGYBXFWUBPSRW-FOUAGVGXSA-N
Long Description:
Chemical. CAS: 7585-39-9. Formula: C42H70O35. MW: 1134.98. Synthetic. 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.
MDL:
MFCD00078139
Molecular Formula:
C42H70O35
Molecular Weight:
1134.98
Package Type:
Vial
Product 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.
Purity:
>98%
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
Solubility Chemicals:
Soluble in water (10mg/ml) or 1 M NH4OH (50mg/ml).
Transportation:
Non-hazardous
UNSPSC Category:
Biochemical Reagents
UNSPSC Number:
12352200
Use & Stability:
Stable for at least 2 years after receipt when stored at +20°C.
References
(1) E.M. Martin Del Valle; Process Biochem. 39, 1033 (2004) (Review) | (2) G. Crini; Chem. Rev. 114, 10940 (2014) (Review)