779008

α-Cyclodextrin

Produced by Wacker Chemie AG, Burghausen, Germany, Life Science, 98.0-101.0% cyclodextrin basis (HPLC)

• Sinónimos: Cavamax^® W6 Pharma, alpha-Cyclodextrin, α-Schardinger dextrin, Cyclohexaamylose, Cyclomaltohexaose
• Fórmula empírica (notación de Hill): C₃₆H₆₀O₃₀
• Número de CAS: 10016-20-3
• Peso molecular: 972.84
• Beilstein/REAXYS Number: 79627
• EC Number: 233-007-4
• MDL number: MFCD00078207
• UNSPSC Code: 12352005
• PubChem Substance ID: 329768007
• NACRES: NA.22

Propiedades

• grade: Produced by Wacker Chemie AG, Burghausen, Germany, Life Science
• assay: 98.0-101.0% cyclodextrin basis (HPLC)
• form: solid
• optical activity: [α]/D 147.0 to 152.0° in H₂O (USP)
• impurities: ≤0.20% reducing substances; ≤0.25% β- and γ-cyclodextrin (each); ≤0.5% related substances; ≤20 ppm residual solvents; ≤5 ppm heavy metals (USP)
• ign. residue: ≤0.10% (USP)
• loss: ≤10.0% loss on drying
• pH: 5.0-8.0 (1% in solution)
• mp: >278 °C (dec.) (lit.)
• absorption: ≤0.05 at 350-750 nm in solution at 1%; ≤0.10 at 230-250 nm in solution at 1%
• suitability: positive for identity (Ph Eur)
• functional group: ether; hydroxyl
• SMILES string: 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]1[C@H](O)[C@H]2O
• InChI: 1S/C36H60O30/c37-1-7-25-13(43)19(49)31(55-7)62-26-8(2-38)57-33(21(51)15(26)45)64-28-10(4-40)59-35(23(53)17(28)47)66-30-12(6-42)60-36(24(54)18(30)48)65-29-11(5-41)58-34(22(52)16(29)46)63-27-9(3-39)56-32(61-25)20(50)14(27)44/h7-54H,1-6H2/t7-,8-,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-/m1/s1
• InChI key: HFHDHCJBZVLPGP-RWMJIURBSA-N

Descripción

Application

α-Cyclodextrin can be used:

• As a ligand in the complexation of nonionic surfactants and polyethylene glycols. α-cyclodextrin shows strong interaction with the surfactants that contains no benzene group.
• To protect linoleic acid from oxidation.
• In the synthesis of binuclear copper(II) complexes with cyclodextrins, which can be further used as a template for the preparation of copper nanoparticles incorporated on mesoporous silica.

Legal Information

Cavasol is a registered trademark of Wacker Chemie AG

Información de seguridad

• Storage Class: 11 - Combustible Solids
• wgk_germany: WGK 1
• flash_point_f: Not applicable
• flash_point_c: Not applicable