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Carboxymethylcellulose Calcium (CMC-Ca) Superdisintegrant | High Swelling Capacity for Fast Tablet Disintegration | USP/EP/ChP Compliant

Our Carboxymethylcellulose Calcium (Carmellose Calcium, CMC-Ca) is a high-purity pharmaceutical excipient that functions as an effective disintegrant, binder, and diluent for oral solid dosage forms . It is the calcium salt of carboxymethylcellulose, appearing as a white to off-white hygroscopic powder that is practically insoluble in water but rapidly swells to several times its original volume upon contact with aqueous media . This unique swelling mechanism ensures rapid tablet disintegration and enhanced drug dissolution. Key advantages include: no sodium content (suitable for cardiovascular and sodium-restricted patients) , excellent compressibility, and compatibility with both direct compression and wet granulation processes . Conforms to USP-NF, EP, JP, and ChP pharmacopoeias with CDE registration F20230000328. Typical use level: 0.5-15% w/w.

    Pharmaceutical Grade Carboxymethylcellulose Calcium (Carmellose Calcium, CMC-Ca)

    Product Overview

    Carboxymethylcellulose Calcium is the calcium salt of a polycarboxymethyl ether of cellulose . It is a multifunctional pharmaceutical excipient widely used as a disintegrant, binder, and diluent in oral solid dosage forms including tablets and capsules . Unlike its sodium counterpart, the calcium salt offers the advantage of sodium-free formulation, making it particularly suitable for cardiovascular and sodium-restricted patient populations .

    Product Identity:

    • Chemical Name: Carboxymethylcellulose Calcium / Carmellose Calcium

    • CAS Number: 9050-04-8 

    • CDE Registration No.: F20230000328

    • Pharmacopoeia Compliance: ChP, USP-NF, EP, JP 

    • Synonyms: Calcium carboxymethylcellulose, Calcium CMC, CMC-Ca, Carmellose Calcium 

    • UNII: UTY7PDF93L 

    • Appearance: White to yellowish-white or off-white powder, hygroscopic after drying 

    • Solubility: Practically insoluble in water, acetone, alcohol, and toluene; swells in water to form a suspension 

    Key Features & Benefits

    1. Superior Disintegration Mechanism

    • Water-insoluble but rapidly swells to several times its original volume upon contact with aqueous media 

    • Creates mechanical pressure that rapidly breaks apart tablets

    • Ensures fast and complete disintegration for enhanced drug dissolution

    • Performs well even in hard tablets where other disintegrants may not perform adequately 

    2. Multifunctional Excipient

    • Disintegrant: Primary function as tablet disintegrant at 0.5-15% concentrations 

    • Binder: Effective binder in wet granulation processes

    • Diluent/Filler: Can serve as tablet diluent

    • Suspension Aid: Used as suspension stabilizer in oral and topical preparations 

    3. Sodium-Free Advantage

    • Contains no sodium – ideal for cardiovascular drugs and sodium-restricted patients 

    • Addresses growing regulatory and patient demands for low-sodium formulations

    • Meets clean-label and health-conscious formulation trends

    4. Excellent API Compatibility

    • Particularly effective for cephalosporin drugs, with demonstrated dissolution improvement properties 

    • Good chelating structure benefits certain API classes

    • Compatible with a wide range of active ingredients including: Pioglitazone HCl, Aminophylline, Berberine HCl, Milnacipran HCl, Cefixime, Nicorandil, and many others 

    5. Superior Physical Properties

    • Excellent compressibility and tablet hardness

    • Maintains tablet integrity while ensuring rapid disintegration

    • Good flow properties for direct compression

    • Stable despite hygroscopicity – store in well-sealed containers 

    6. Regulatory & Quality Profile

    • Meets USP-NF, EP, JP, and ChP pharmacopoeia standards 

    • CDE registered (F20230000328) for Chinese market

    • GMP manufactured with rigorous quality control

    • Available with regulatory support for global filings

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