2828447-14-7

Carboxymethyl-β-cyclodextrin sodium salt Chemical Structure
2828447-14-7

Chemical Structure

Carboxymethyl-β-cyclodextrin sodium salt

  • CAS 番号: 2828447-14-7
  • Formula:C56H84NaO49·xNa
  • Molecular Weight:1541.24 (Average)

SMILES: OC(COC[C@@H](O[C@@](O[C@](C1O)([H])[C@H](O[C@@](O[C@]([C@@H]2O)([H])[C@H](O[C@@](O[C@]([C@@H]([C@H]3O)O)([H])[C@H]4COCC(O)=O)([H])[C@@H]2O)COCC(O)=O)([H])[C@@H]1O)COCC(O)=O)([H])[C@@H]5O)[C@@](C5O)([H])O[C@@]([C@@H](C6O)O)([H])O[C@@H]([C@@]6([H])O[C@@]([C@@H](C7O)O)([H])O[C@@H]([C@@]7([H])O[C@@]([C@@H](C8O)O)([H])O[C@@H]([C@@]8([H])O[C@@]3([H])O4)COCC(O)=O)COCC(O)=O)COCC(O)=O)=O.[x].[Na]

Biological Activity: Carboxymethyl-β-cyclodextrin sodium salt is a negatively charged β-cyclodextrin derivative, as well as a metal ion chelator and solubilizing reagent. Carboxymethyl-β-cyclodextrin sodium salt forms stable aqueous complexes with Ba2+, Ca2+, Cd2+, Ni2+, Pb2+, Sr2+, and Zn2+ ions. Carboxymethyl-β-cyclodextrin sodium salt derived hydrogel carriers support oral insulin delivery via paracellular permeation across Caco-2 monolayers and produce sustained hypoglycemic effects in diabetic mice. Carboxymethyl-β-cyclodextrin sodium salt can be conjugated onto folate-modified BSA nanoparticles to boost folate receptor-mediated endocytosis, elevate intracellular anticancer drug uptake and trigger cell apoptosis. Carboxymethyl-β-cyclodextrin sodium salt can be utilized for chiral separation in capillary electrophoresis, development of nanoscale drug carriers and nucleic acid transfection research[1][2][3].

製品番号 製品名 純度 製品説明 Pricing
HY-W1113135
Carboxymethyl-β-cyclodextrin sodium salt 99.6% Carboxymethyl-β-cyclodextrin sodium salt is a negatively charged β-cyclodextrin derivative, as well as a metal ion chelator and solubilizing reagent. Carboxymethyl-β-cyclodextrin sodium salt forms stable aqueous complexes with Ba2+, Ca2+, Cd2+, Ni2+, Pb2+, Sr2+, and Zn2+ ions. Carboxymethyl-β-cyclodextrin sodium salt derived hydrogel carriers support oral insulin delivery via paracellular permeation across Caco-2 monolayers and produce sustained hypoglycemic effects in diabetic mice. Carboxymethyl-β-cyclodextrin sodium salt can be conjugated onto folate-modified BSA nanoparticles to boost folate receptor-mediated endocytosis, elevate intracellular anticancer drug uptake and trigger cell apoptosis. Carboxymethyl-β-cyclodextrin sodium salt can be utilized for chiral separation in capillary electrophoresis, development of nanoscale drug carriers and nucleic acid transfection research.
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HY-W1113135A
Carboxymethyl-β-cyclodextrin sodium salt, for capillary electrophoresis Carboxymethyl-β-cyclodextrin sodium salt, for capillary electrophoresis is a negatively charged β-cyclodextrin derivative, as well as a metal ion chelator and solubilizing reagent. Carboxymethyl-β-cyclodextrin sodium salt, for capillary electrophoresis forms stable aqueous complexes with Ba2+, Ca2+, Cd2+, Ni2+, Pb2+, Sr2+, and Zn2+ ions. Carboxymethyl-β-cyclodextrin sodium salt derived hydrogel carriers support oral insulin delivery via paracellular permeation across Caco-2 monolayers and produce sustained hypoglycemic effects in diabetic mice. Carboxymethyl-β-cyclodextrin sodium salt can be conjugated onto folate-modified BSA nanoparticles to boost folate receptor-mediated endocytosis, elevate intracellular anticancer drug uptake and trigger cell apoptosis. Carboxymethyl-β-cyclodextrin sodium salt can be utilized for chiral separation in capillary electrophoresis, development of nanoscale drug carriers and nucleic acid transfection research.
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  • /
loading...
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Stock Quantity Availability Operate
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In-stock
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(Estimated to ship TODAY)

Amount:

USD 0.00

This product is a controlled substance and not for sale in your territory.

This product is not for sale in your territory.

This compound is listed in the SVHC (Substances of Very High Concern) candidate list of ECHA (European Chemicals Agency).

Pricing 
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References