METHOCEL™ K15M S HPMC - Specialty

1 of 40 products in this brand
METHOCEL™ K15M S HPMC - Specialty, identified as cellulose ethers and hypromellose, functions as a rheology modifier, ensuring consistency in formulations. Notably, it possesses the property of being water-soluble, making it suitable for various applications.

Functions: Controlled Release Agent, Rheology Modifier

Chemical Name: Hydroxypropyl Methylcellulose

Chemical Family: Cellulose & Cellulosics, Cellulose Ethers

Labeling Claims: APE-free, Aflatoxin-free, Allergen-free, Aluminum-free, Antibiotics-free, BSE-free, Bisphenol Derivatives-free, CMR Substances-free, Caffeine Free, Dairy-free, Diethylene Glycol-free, Dioxane-free, Dye Free, Endocrine Disruptor-free, Ethylene Glycol-free, Fungicide-free, Gluten-free, Glycerin-free, Halal, Herbicide-free, Hormones-free, Iodide-free, Irradiation-free, Kosher, Latex-free, Monosodium Glutamate (MSG)-free, Mycotoxins-free, Natural Latex Rubber-Free, Nitrosamines-free, Non-GMO, Organic, PAH-free, PFAS-Free, PFOA-free, PFOS-free, PHO (Partially Hydrogenated Oil)-Free, PVC-free, Palm Oil-free, Paraben-free, Persistent Organic Pollutants (POP)-free, Pesticide-free, Phthalates-free, Plasticizer-free, Potassium-free, Preservative-free, Quaternary Ammonium Salt-Free, Sewage Sludge Free, Sugar-free, TSE-free, Tributyltin (TBT) - Free, VOC-free, Vegan, Vegetarian

Certifications & Compliance: Chinese Pharmacopeia (ChP), Directive 1333/2008/EC, Directive 2009/48/EC, Doping-Free, EU Cosmetic Regulation 1223/2009 Compliant, European Pharmacopeia (Ph. Eur.), FDA 21 CFR 101.9, FDA 21 CFR 172.874, FDA 21 CFR 174.5, FDA 21 CFR 175.105, FDA 21 CFR 175.300, FDA 21 CFR 176.170, FDA 21 CFR 176.180, FDA Compliant, FDA Food Safety Modernization Act (FSMA), FSC Certified, FSSC 22000, GMP, Generally Recognized As Safe (GRAS), Halal, ICH Q3C, ISO 14001, ISO 50001, ISO 9001, Indian Pharmacopeia, Kosher, Nagoya Compliant, National Formulary (NF), OEKO-TEX Compliant, Organic Certified, Orthodox Union Kosher, Regulation (EC) No. 1333/2008, Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1169/2011, Regulation (EU) No. 1272/2008, Regulation (EU) No. 1829/2003, Regulation (EU) No. 1830/2003, Regulation (EU) No. 2022/1396, Regulation (EU) No. 231/2012, Swiss Ordinance (SR 817.023.21), Turkish RoHS Regulation, USDA Organic, United States Pharmacopeia (USP), Waste Electrical & Electronic Equipment Directive (WEEE), cGMP

Dosage Form: Tablets

Synonyms: 2-Hydroxypropyl methyl cellulose ether, Cellulose hydroxypropyl methyl ether, Hydroxypropyl methyl cellulose ether, 2-Hydroxypropyl methyl cellulose, Hydroxypropyl methyl cellulose, Methyl hydroxypropyl cellulose, Hypromellose, HPMC, Hypermellose

  • TypeDocument Name
  • Brochure

    IFF Pharma Solutions Portfolio Brochure

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  • Brochure

    METHOCEL™ Cellulose Ethers Brochure

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Enhanced TDS

Identification & Functionality

Features & Benefits

Applications & Uses

Properties

Physical Form
Soluble In
Typical Properties
ValueUnitsTest Method / Conditions
Moisture Content (as Packaged)max. 7.0%PSM 100667
Viscosity (at 20°C, 2%)10,000 - 18,000mPa.sUbbelohde, PSM 101662
Composition
ValueUnitsTest Method / Conditions
Hydroxypropoxyl Content7.0 - 12.0%PSM 100755
Methoxyl Content19.0 - 24.0%PSM 100755
Sodium Chloride Contentmax. 2.0%PSM 100755
Screen Test
ValueUnitsTest Method / Conditions
Screen (< 420 micron through 40 U. S. STD. Sieve)min. 99%-
Note
  • All section names come under PHS.
  • The following specifications apply to sealed, unopened containers stored under the recommended conditions for the duration of the shelf life.
  • This product is not intended for use as a direct food additive or in pharmaceutical applications.

Regulatory & Compliance