To catalogue

TYLOPUR® 90SH-15000SR

CAS Number
9004-65-3
EC Number
618-389-6
Chemical Name
Hydroxypropyl Methylcellulose

TYLOPUR® 90SH-15000SR hypromellose grades feature optimized viscosity, hydroxypropoxy content, and particle size to guarantee highly reproducible dissolution profiles in the production of extended release matrix tablets. It is fully compliant with USP, JP, EP and applicable in granulation or DC processes. Different viscosity grades are available according to your requirement.

Properties

Physical Form
  • Powder
  • Solid
Pharma and Nutraceuticals Functions
  • Binder
  • Controlled Release Agent
  • Extended Release Agent
  • Thickener
  • Viscosity Modifier

Product families

Applications

Healthcare & Pharma — Drug Delivery & Care Solutions
  • Transdermal
Healthcare & Pharma — Pharmaceutical Manufacturing
  • Excipients & Coatings

Product Families

Pharmaceuticals & Nutraceuticals — Excipients
  • Binders & Disintegrants
  • Formulation & Processing Aids
  • Modified & Controlled Release

Other characteristics

Brand
TYLOPUR
Functions

Binder, Controlled Release Agent, Extended Release Agent, Thickener, Viscosity Modifier

Dosage Form
Transdermal Patches
Certifications & Compliance

European Pharmacopeia (Ph. Eur.), GMP, Japan Pharmacopeia (JP), United States Pharmacopeia (USP)

Grade
Pharma Grade
Markets
Healthcare & Pharma
Appearance
Conforms
Technology
Pharmaceuticals & Nutraceuticals
Packaging Type
  • Boxes
  • Drums
Storage Information

Fiber drum (40-50 kg) with polyethylene single bag inside.; Big bag 1060 x w 710 x h 1250 mm (up to 1040 liters).; Keep dry. Store away from excess heat and sunlight.; Store preferentially in original packaging.

Chemical Inventories
  • AICS (Australia)
  • DSL (Canada)
  • EEC/EU
  • EINECS (EU)
  • ENCS (Japan)
  • IECSC (China)
  • KECI (Korea)
  • NZIoC (New Zealand)
Applications

Very sutaible for sustained Release (matrix Tablet).; Suitable for plaster/dermal patch

Regulatory Information
  • EU-Regulations
  • National regulations
Manufacturing Technology
  • Direct Compression
  • Dry Granulation
  • Wet Granulation
Certifications and Compliance
  • European Pharmacopeia (Ph. Eur.)
  • GMP
  • Japan Pharmacopeia (JP)
  • United States Pharmacopeia (USP)
Key Quality Attributes in Matrix Tablets
  • Decrease in initial erosion.
  • Slower drug release.
  • No effect on tablet hardness.

Technical data

Table 1 of 1

9 rows
CharacteristicValueUnitMethod
Viscosity1125 - 2100mPa.s—
Viscosity100 - 100000mPa.s—
Identification (A - E)Conforms—EP
pH5.0 - 8.0—EP
Loss on Dryingmax. 5.0%EP
Sulphated Ash/ Residue on Ignitionmax. 1—EP
Heavy Metalsmax. 20ppmEP
Methoxy Content27.0 - 30.0%—
Hydroxypropoxy Content4.0 - 7.5——

The Omnichem website uses cookies. By continuing to use the site, you consent to their use in accordance with our Privacy Policy and to the collection of analytics.