779105

βß-Ciclodextrina

Wacker Chemie AG, ≥95.0% (HPLC)

• Sinônimo(s): β-Dextrina de Schardinger, Caraway, Cicloheptaamilose, Ciclomaltoheptaose
• Fórmula empírica (Notação de Hill): C₄₂H₇₀O₃₅
• Número CAS: 7585-39-9
• Peso molecular: 1134.98
• Beilstein: 78623
• Número CE: 231-493-2
• Número MDL: MFCD00078139
• Código UNSPSC: 12352005
• ID de substância PubChem: 329768012
• NACRES: NA.22

Propriedades

• Ensaio: ≥95.0% (HPLC)
• Formulário: powder
• atividade óptica: [α]20/D +162±3°, c = 1.5% in H₂O
• fabricante/nome comercial: Wacker Chemie AG
• perda: ≤14.0% loss on drying
• pf: 290-300 °C (dec.) (lit.)
• grupo funcional: ether; hydroxyl
• cadeia de caracteres SMILES: OC[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]1[C@H](O)[C@H]2O
• 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
• chave InChI: WHGYBXFWUBPSRW-FOUAGVGXSA-N

Descrição

Aplicação

β-Cyclodextrin, a water-soluble cyclic oligosaccharide consisting of seven α-(1,4)-linked glucopyranose subunits,[1][2] is used in the preparation of:

• Linear cationic β-cyclodextrin-based polymers (β-CDPs) and polycationic β-cyclodextrin ‘click clusters′ for gene delivery applications.[3][4]
• Multiresponsive supramolecular nanogated ensemble by grafting onto mesoporous silica for controlled release of trapped molecules.[5]
• EDTA-cross-linked β-cyclodextrin (EDTA-β-CD) bifunctional adsorbent for simultaneous adsorption of metals and dyes.[6]
• β-Cyclodextrin derived siRNA delivery vector for gene silencing.[7]
• β-CD chiral stationary phase (CCNCSP) for the enantioseparation of chiral drugs by high-performance liquid chromatography (HPLC).[8]

Informações legais

Cavasol is a registered trademark of Wacker Chemie AG

Informações de segurança

• Código de classe de armazenamento: 11 - Combustible Solids
• Classe de risco de água (WGK): WGK 1
• Ponto de fulgor (°F): Not applicable
• Ponto de fulgor (°C): Not applicable