|
Parameter |
Details |
|
Chemical Name |
Microcrystalline Cellulose |
|
Molecular Formula |
(C₆H₁₀O₅)n |
|
CAS Number |
9004-34-6 |
|
Appearance |
White to off-white odourless powder |
|
Moisture Content |
NMT 5.0% |
|
pH |
5.0 – 7.5 |
|
Grade |
Pharmaceutical / Food / Nutraceutical |
|
Packaging |
25 kg polylined fibre drums |
Excipient variability is one of the less-discussed but genuinely disruptive problems in tablet manufacturing. When the MCC in your formulation behaves differently batch to batch in particle size distribution, moisture content, or compressibility index, it shows up in tablet hardness, disintegration time, and coating adhesion. The formulation did not change. The excipient did.
As reliable Microcrystalline Cellulose Manufacturers in India, every batch is tested for particle size, moisture content, bulk density, pH, and compressibility before release. CoA, MSDS, and grade compliance documentation are standard with every order.
It is one of those excipients that appears in more formulations than most people realise, and yet, the number of suppliers who can deliver it consistently across grades, particle sizes, and documentation requirements is smaller than the market size suggests.
As established Microcrystalline Cellulose Suppliers in India, we supply across pharmaceutical tablet manufacturing, nutraceutical capsule and supplement production, and food processing applications. Different buyers come with genuinely different needs. A formulation team developing a new direct compression tablet needs a specific particle size grade with reproducible compressibility data. A food manufacturer needs food-additive certified material with clean labelling compliance. A nutraceutical company scaling from development to commercial production needs a supplier whose batch consistency does not shift when the order volume increases.
We handle all of these without minimum order thresholds and without any reduction in documentation quality between a small development quantity and a full commercial consignment. The CoA, grade compliance papers, and MSDS that accompany a 5 kg development order are prepared to the same standard as those that ship with a bulk commercial delivery because your formulation validation depends on that consistency from the very first batch you work with.
Exceptional Binding Strength: acts as a dry binder in direct compression tabletting, reducing the need for wet granulation and simplifying the manufacturing process.
Superior Compressibility: produces tablets with consistent hardness and low friability, even at lower compression forces.
Natural Disintegrant: absorbs water rapidly and swells to promote fast tablet disintegration and reliable drug release
Improved Flowability: enhances powder blend flow in high-speed tablet presses, reducing capping and lamination issues
Chemically inert: compatible with a wide range of APIs without interaction, making it suitable across therapeutic categories
Low Moisture Sensitivity: maintains performance under varying humidity conditions when stored correctly
Clean Regulatory Status: approved under USP, BP, EP, and food additive regulations globally.
Direct compression and wet granulation tablet formulations across pharmaceutical and nutraceutical segments.
Capsule filling as a diluent and flow aid for low-dose active ingredients.
Food products as a texturiser, anti-caking agent, and fat replacer.
Dietary supplement tablets and chewable formulations require high compressibility.
Cosmetic and topical formulations require an inert, stable powder carrier.
As a certified Microcrystalline Cellulose Exporter in India, we at 3PPL always create all export documentation - full export documentation, CoA, MSDS, Commercial Invoice, Packing List and Mandatory Compliance Papers for each of our International Sales, before each sale leaves our manufacturing facility.
For further information about Microcrystalline Cellulose and its related grade specifications/particle size requirements, quantities and delivery lead times, please contact our 3PPL Team.