|
Parameter |
Details |
|
Chemical Name |
Dextrose Anhydrous |
|
Molecular Formula |
C₆H₁₂O₆ |
|
Molecular Weight |
180.16 g/mol |
|
CAS Number |
50-99-7 |
|
Appearance |
White crystalline powder |
|
Purity |
99% minimum |
|
Moisture Content |
NMT 0.5% |
|
Grade |
Pharmaceutical / Food |
|
Packaging |
25 kg polylined paper bags |
The distinction between Dextrose Anhydrous and Dextrose Monohydrate is easy to overlook at the procurement stage, as they are both glucose, and the price difference is rarely significant enough to flag. But inside a moisture-sensitive formulation or a direct compression blend where water activity has been carefully balanced, that difference in water content is not trivial. Formulators who have experienced the consequences of a supplier substituting one for the other without flagging the change tend to remember the lesson.
As reliable Dextrose Anhydrous Manufacturers in India, every batch is tested for purity, moisture content, specific optical rotation, heavy metals, sulphated ash, and microbial limits before dispatch. CoA, MSDS, and applicable pharmacopoeial compliance documentation travel with every order without needing to be requested separately.
As reliable Dextrose Anhydrous Suppliers in India, we supply this compound in pharmaceutical and food grades, tested, documented, and compliant with pharmacopoeial standards across every batch. Here is what it consistently delivers inside your formulation:
Water-free composition makes it the preferred glucose source in moisture-sensitive formulations, where even small amounts of bound water create stability or compatibility concerns.
Excellent compressibility supports direct compression tabletting without wet granulation, saving process steps and reducing manufacturing complexity.
Mild, pleasant sweetness makes it suitable for chewable tablets, oral powders, and paediatric formulations where taste directly affects patient compliance.
Rapidly absorbed energy source in intravenous and oral rehydration formulations across clinical and therapeutic settings.
Chemically compatible with a broad range of APIs and excipients under standard manufacturing and storage conditions.
Recognised under USP, BP, IP, and food additive frameworks, globally accepted across regulated markets without additional justification.
Direct compression tablet manufacturing diluent and filler in moisture-sensitive formulations where starch-based alternatives are unsuitable.
Chewable and orally dispersible tablets where natural sweetness improves palatability and reduces the need for added sweeteners.
Oral rehydration salts and electrolyte powders are the primary energy and osmolality contributors.
Parenteral nutrition and intravenous solution manufacturing, where anhydrous purity and low endotoxin levels are non-negotiable.
Food and beverage production as a fermentation substrate, sweetener, and energy source.
Nutraceutical and sports nutrition powders require a clean-label, rapidly available carbohydrate.
Microbiological culture media in laboratory and industrial fermentation environments.
International procurement of a pharmaceutical-grade compound like this is rarely one-size-fits-all. The documentation a clinical nutrition manufacturer needs for import clearance looks nothing like what a tablet formulator requires, and a food-grade buyer importing it for fermentation has different compliance expectations altogether. Getting that wrong at the export stage costs everyone time they did not budget for.
As experienced Dextrose Anhydrous Exporters in India, every consignment leaves with a fully prepared CoA, MSDS, pharmacopoeial compliance confirmation, moisture certification, commercial invoice, packing list, and destination-specific regulatory papers verified well before the shipment moves. Reach out directly to discuss grade specifications, quantities, and lead times.