Pharmaceutical-grade purity compliant with USP/NF, EP, and JP monographs.
Highly water-soluble with rapid hydration and low solution viscosity at typical formulation concentrations.
Excellent film-forming capability for controlled-release and immediate-release oral solid dosage forms.
Non-ionic, pH-independent solubility ensures consistent performance across gastrointestinal pH ranges.
Low endotoxin and microbial burden, validated for use in sterile and non-sterile parenteral and oral applications.
Binders and matrix formers in direct compression and wet granulation tablets.
Controlled-release polymer in hydrophilic matrix tablets for sustained drug delivery.
Film-coating agent for taste masking, moisture protection, and modified release profiles.
Viscosity modifier and stabilizer in liquid and semi-solid pharmaceutical formulations.
Excipient in ophthalmic solutions and injectables requiring low-viscosity, non-irritating cellulose derivatives.
| Chemical Type | Non-ionic cellulose ether derivative (hydroxypropyl substitution) |
| Product Form | White to off-white free-flowing powder |
| Appearance | Odorless, tasteless, fine particulate powder |
| Primary Applications | Oral solid dosage forms, film coatings, ophthalmic solutions, injectables |
| Key Features | USP/NF/EP/JP compliant, low viscosity grade, rapid hydration |
| Benefits | Enhanced tablet disintegration, robust film integrity, compatibility with wide API range |
| Storage Conditions | Store in original container at 15–30 °C, protect from moisture |
| Regulatory Status | DMF on file with FDA; listed in FDA Inactive Ingredients Database (oral, ophthalmic, injectable routes) |
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E-mail: wangxingqiang@ericwchem.com
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