For research use only. Not for therapeutic Use.
Epichlorohydrin β-Cyclodextrin(CAT: L027737) is a chemically modified β-cyclodextrin derivative widely utilized in pharmaceutical, biochemical, and material sciences. Formed through epichlorohydrin crosslinking, it retains the cyclic oligosaccharide structure of β-cyclodextrin while offering enhanced solubility, stability, and functionalization potential. This versatile compound is ideal for drug delivery systems, inclusion complex formation, and chromatography applications. Its unique structure allows encapsulation of hydrophobic molecules, improving solubility and bioavailability of active compounds. Epichlorohydrin β-Cyclodextrin supports advanced research in drug formulation, food technology, and environmental science, providing a reliable solution for molecular encapsulation and targeted delivery in industrial and academic settings.
Catalog Number | L027737 |
CAS Number | 25655-42-9 |
Molecular Formula | C45H75ClO36 |
Purity | ≥95% |
IUPAC Name | 2-(chloromethyl)oxirane;(1S,3R,5R,6S,8R,10R,11S,13R,15R,16S,18R,20R,21S,23R,25R,26S,28R,30R,31S,33R,35R,36R,37R,38R,39R,40R,41R,42R,43R,44R,45R,46R,47R,48R,49R)-5,10,15,20,25,30,35-heptakis(hydroxymethyl)-2,4,7,9,12,14,17,19,22,24,27,29,32,34-tetradecaoxaoctacyclo[31.2.2.23,6.28,11.213,16.218,21.223,26.228,31]nonatetracontane-36,37,38,39,40,41,42,43,44,45,46,47,48,49-tetradecol |
InChI | InChI=1S/C42H70O35.C3H5ClO/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;4-1-3-2-5-3/h8-63H,1-7H2;3H,1-2H2/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 | WKAAHQRZZAMMNX-ZQOBQRRWSA-N |
SMILES | C1C(O1)CCl.C([C@@H]1[C@@H]2[C@@H]([C@H]([C@H](O1)O[C@@H]3[C@H](O[C@@H]([C@@H]([C@H]3O)O)O[C@@H]4[C@H](O[C@@H]([C@@H]([C@H]4O)O)O[C@@H]5[C@H](O[C@@H]([C@@H]([C@H]5O)O)O[C@@H]6[C@H](O[C@@H]([C@@H]([C@H]6O)O)O[C@@H]7[C@H](O[C@@H]([C@@H]([C@H]7O)O)O[C@@H]8[C@H](O[C@H](O2)[C@@H]([C@H]8O)O)CO)CO)CO)CO)CO)CO)O)O)O |