Product Details
| Product Name: Carboxymethyl-beta-Cyclodextrin | CAS No.: 218269-34-2 |
| Min. Order: 1g | Purity: 98%min |
| Supply Ability: 1000g | Release date: 2025/12/25 |
| Type: SZ01 |
Carboxymethyl-beta-Cyclodextrin Cas 218269-34-2
Specification
Items | Specifications | Results |
Appearance | White to light yellow powder,odorless | Conform |
Assay | ≥98.0% | 99.7% |
Betadex | ≤1.5% | 0.05% |
Loss and Drying | ≤10.0% | 7.9% |
Heavy Metal | ≤20ppm | <20ppm |
Packaging and storage | Preserve in well-closed containers. | |
Conclusion | Compliant to the enterprise standard. | |
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Carboxymethyl Beta Cyclodextrin (CM-β-CD) is a modified, water-soluble version of a naturally derived molecule called beta-cyclodextrin. It is widely used in pharmaceuticals, cosmetics, and food science to improve the solubility, stability, and bioavailability of poorly soluble compounds.
Detailed Explanation
1. The Base Molecule: Beta-Cyclodextrin (β-CD)
Structure: Beta-Cyclodextrin is a cyclic oligosaccharide (a ring-shaped sugar molecule) made of seven glucose units. Its key feature is a hydrophobic (water-repelling) inner cavity and a hydrophilic (water-attracting) outer surface.
Function: This structure allows it to act as a "host" molecule by forming inclusion complexes. It can encapsulate poorly soluble "guest" molecules (like drugs or flavors) inside its cavity, effectively shielding them from the aqueous environment.
Limitation: Native beta-cyclodextrin itself has relatively low water solubility and can be nephrotoxic (toxic to the kidneys) at higher doses.
2. The Modification: Carboxymethylation
To overcome these limitations, beta-cyclodextrin is chemically modified.
Process: Carboxymethyl groups (-CH₂-COOH) are attached to the hydroxyl (OH) groups on the outer rim of the cyclodextrin ring.
Resulting Benefits:
Greatly Enhanced Solubility: The introduction of the charged carboxymethyl groups makes CM-β-CD highly soluble in water, even over a wide pH range.
Reduced Toxicity: It is generally better tolerated and less toxic than the parent beta-cyclodextrin.
Retained Complexation Ability: It maintains the crucial ability to form inclusion complexes with hydrophobic molecules.
Primary Applications
CM-β-CD's main role is as a multi-functional solubilizing and stabilizing agent.
Pharmaceuticals (Drug Formulation): This is its most important application. It is used to:
Increase Solubility and Dissolution Rate: It allows poorly water-soluble drugs to be dissolved effectively, which is essential for them to be absorbed by the body.
Improve Bioavailability: By increasing solubility, it enhances the amount of drug that reaches the bloodstream.
Enhance Stability: It protects sensitive drugs from degradation by light, oxidation, or hydrolysis.
Mask Taste/Odor: It can encapsulate compounds with unpleasant tastes or smells.
Other Industries:
Cosmetics: Used to stabilize active ingredients in creams and lotions.
Food Science: Can be used to protect flavors, colors, or nutrients.
Analytical Chemistry: Used in techniques like capillary electrophoresis to separate complex mixtures.
Summary
| Feature | Description |
|---|---|
| Identity | A chemically modified, water-soluble derivative of beta-cyclodextrin. |
| Key Property | Forms inclusion complexes with hydrophobic molecules, dramatically improving their solubility in water. |
| Main Advantage | Higher solubility and lower toxicity compared to unmodified beta-cyclodextrin. |
| Primary Use | A key excipient in drug development to make insoluble drugs effective and stable. |
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Contact information
Spring Zhang
Email: export@fortunachem.com
Skype: Fortunachem201304
QQ:3169620873
Tel: +86-27-59207892
Website: www.fortunachem.com
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