Pharmaceutical-grade purity compliant with USP/NF, EP, and JP monographs for excipients.
Controlled viscosity profile optimized for aqueous immediate-release and sustained-release oral dosage forms.
Excellent cold-water dispersibility with rapid hydration and minimal gel lump formation.
Highly consistent batch-to-batch performance due to stringent GMP manufacturing controls.
Non-ionic, non-toxic, and non-allergenic—suitable for sensitive patient populations including pediatric and geriatric formulations.
Viscosity modifier and binder in direct compression and wet granulation tablets.
Matrix-forming polymer in controlled-release oral tablets and capsules.
Stabilizer and suspending agent in oral liquid suspensions and syrups.
Rheology modifier in topical gels and ophthalmic solutions.
Film-forming agent in pharmaceutical coating systems and buccal films.
| Chemical Type | Methyl hydroxyethyl cellulose (MHEC) — non-ionic cellulose ether |
| Product Form | White to off-white free-flowing powder |
| Appearance | Free-flowing, odorless, fine particulate powder |
| Primary Applications | Oral solid dosage forms, liquid suspensions, topical gels, ophthalmic preparations |
| Key Features | USP/NF, EP, and JP compliant; GMP-manufactured; low microbial burden |
| Benefits | Enhanced dissolution control, improved tablet mechanical strength, robust suspension stability |
| pH Range (1% aqueous solution) | 5.0–8.0 |
| Loss on Drying (LOD) | ≤ 7.0% w/w |
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E-mail: wangxingqiang@ericwchem.com
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