Pharmaceutical-grade hydroxyethyl cellulose (HEC) compliant with USP/NF, EP, and JP monographs.
Highly consistent rheology and viscosity performance across batches, ensuring robust process control in manufacturing.
Excellent water solubility and rapid hydration without clumping or gel lumps, even under high-shear mixing conditions.
Non-ionic, low ionic sensitivity, and compatible with a broad range of active pharmaceutical ingredients (APIs) and excipients.
Stable across pH 3–11 and tolerant to moderate heat, supporting sterilization and long-term formulation stability.
Ophthalmic solutions — as a viscosity-enhancing and mucoadhesive agent for sustained residence time on the ocular surface.
Topical gels and creams — providing structure, suspension stability, and non-tacky sensory profile.
Oral liquid suspensions — enabling uniform API dispersion and preventing sedimentation during shelf life.
Controlled-release tablet coatings — offering film-forming integrity and controlled erosion kinetics.
Injectable suspensions and depot formulations — acting as a biocompatible suspending and stabilizing polymer.
| Chemical Type | Hydroxyethyl cellulose (HEC), non-ionic cellulose ether |
| Product Form | White to off-white free-flowing powder |
| Appearance | Odorless, fine granular powder |
| Primary Applications | Pharmaceutical formulations: ophthalmic, topical, oral, injectable, and coating systems |
| Key Features | USP/NF, EP, and JP compliant; low heavy metals; low microbial limits |
| Viscosity (4% aqueous solution, 25°C) | 30–50 mPa·s (as specified per batch certificate) |
| Substitution (DS/MS) | DS ~2.3–2.6; MS ~2.8–3.2 |
| Residue on Ignition | ≤1.0% |
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E-mail: wangxingqiang@ericwchem.com
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