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Eudragit Rl CAS NO 51822-44-7
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CAS No.:51822-44-7
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
Eudragit RL is a high-quality, cationic copolymer of ethyl acrylate, methyl methacrylate, and a low content of methacrylic acid ester with quaternary ammonium groups. This unique composition provides a pH-independent, sustained-release mechanism crucial for advanced pharmaceutical formulation. It is an essential excipient for manufacturers developing controlled-release solid oral dosage forms, such as tablets and pellets, where precise drug delivery is required.
Application
- Sustained-Release Tablet Coating: Primary application for creating water-insoluble, pH-independent, and permeable film coatings that control the diffusion of active pharmaceutical ingredients (APIs).
- Matrix Tablet Formulation: Used as a release-retarding agent in matrix systems for extended drug release profiles.
- Pellet and Granule Coating: Enables the functional coating of multi-particulate dosage forms for tailored release kinetics.
- Combination with Eudragit RS: Often blended with Eudragit RS to fine-tune the permeability and mechanical properties of the final film for specific release targets.
- Pharmaceutical Research & Development: A key polymer for pre-formulation studies and the development of novel controlled-release drug delivery systems.
Basic Information
| Product Name | Eudragit RL |
| CAS No. | 51822-44-7 |
| Molecular Formula | (C5H8O2)x·(C4H6O2)y·(C7H14NO2)z |
| Molecular Weight | ~150,000 g/mol (Typical average) |
| Synonyms | Eudragit RL 100; Eudragit RL PO; Poly(ethyl acrylate-co-methyl methacrylate-co-trimethylammonioethyl methacrylate chloride); Ammonio Methacrylate Copolymer, Type A (USP/NF); Cationic Methacrylic Acid Copolymer; Acryl-EZE; Kollicoat EMM 30 D; EUDRAGIT® RL |
| EINECS | 257-390-8 |
Quality Control
Our Eudragit RL is manufactured and tested to meet stringent pharmaceutical excipient standards. Quality is assured through a comprehensive battery of tests including identification, assay, and impurity profiling. Certificates of Analysis (COA) are provided with each batch, confirming compliance with relevant pharmacopoeial monographs such as USP/NF (Ammonio Methacrylate Copolymer, Type A) and Ph. Eur.
Storage
Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at a controlled room temperature (15-25°C). This product is hygroscopic (moisture-sensitive); the original container must be kept tightly sealed to prevent moisture uptake, which can affect its flow and processing properties.
Specification
| Item | Specification |
|---|---|
| Appearance | White or off-white free-flowing powder |
| Identification (IR) | Conforms |
| Assay (Dry basis) | ≥ 98.0 % |
| Viscosity (20% in acetone) | 10 - 25 mPa·s |
| Residue on Ignition | ≤ 0.3 % |
| Heavy Metals | ≤ 20 ppm |
| Loss on Drying | ≤ 5.0 % |
| Quaternary Ammonium Groups | 4.5 - 7.0 % |
| Residual Monomers (GC) | ≤ 0.3 % total |
Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.
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