Kollicoat® IR

1 of 8 products in this brand

Kollicoat® IR is a white to faintly yellow free-flowing powder. The polymer consists of 75% polyvinyl alcohol units and 25% polyethylene glycol units. The product also contains approx. 0.3% colloidal anhydrous silica to improve its flow properties. As a result of its structure, the polymer dissolves very readily in acidic, neutral and alkaline aqueous media.

Chemical Name: Polyvinyl Alcohol-Polyethylene Glycol Copolymer

CAS Number: 96734-39-3

Functions: Binder, Film Former, Matrix Forming Agent

Dosage Form: Spray

Labeling Claims: Halal, Non-GMO, Not Engineered With Nanomaterials, Peroxide-free, Sustainable

Certifications & Compliance: European Pharmacopeia (Ph. Eur.), FDA Compliant, FSSC 22000, Hazard Analysis Critical Control Point (HACCP), ISO 14001, ISO 9001, International Standards For Phytosanitary Measures No. 15 (ISPM 15) Compliant, Japanese Pharmaceutical Excipients (JPE), OHSAS, REACH Exempt (Europe), United States Pharmacopeia (USP), cGMP

Technical Data Sheet

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Identification & Functionality

Chemical Name: Polyvinyl Alcohol-Polyethylene Glycol Copolymer
Country of Origin: Germany
Ingredient Origin: Non-Animal Origin,
Synthetic
Pharma & Nutraceuticals Functions: Binder,
Film Former,
Matrix Forming Agent
Technologies: Pharmaceuticals & Nutraceuticals
Product Families: Pharmaceuticals & Nutraceuticals — Excipients
Binders & Disintegrants,
Other Excipients,
Pharmaceutical Coatings

Features & Benefits

Labeling Claims: Halal,
Non-GMO,
Not Engineered With Nanomaterials,
Peroxide-free,
Sustainable
Key Benefits: Water-soluble film former for instant release coatings

High pigment-loading capacity

Excellent wet binder

Easy processing due to low solution viscosity and very fast dissolution

No peroxide formation

Applications & Uses

Markets: Healthcare & Pharma
Applications: Healthcare & Pharma — Drug Delivery & Care Solutions
Oral,
Topical,
Transdermal
Dosage Form: Spray
Manufacturing Technology: Wet Granulation

Properties

Physical Form: Powder,
Solid,
Suspension,
Tablets
Appearance: White to faintly yellow free-flowing powder
Soluble in: Water
Composition

Regulatory & Compliance

Certifications & Compliance: European Pharmacopeia (Ph. Eur.),
FDA Compliant,
FSSC 22000,
Hazard Analysis Critical Control Point (HACCP),
ISO 14001,
ISO 9001,
International Standards For Phytosanitary Measures No. 15 (ISPM 15) Compliant,
Japanese Pharmaceutical Excipients (JPE),
OHSAS,
REACH Exempt (Europe),
United States Pharmacopeia (USP),
cGMP
Chemical Inventories: TSCA Exempt (USA)
Grade: Pharma Grade

Packaging & Availability

Packaging Type: Drums
Packaging Information: 0.5KG Plastic bottle (Sample)

20KG Plastic drums

Storage & Handling

Storage Information & Retest Period: Store in tight containers and protect from light.

Retest Period : 36 months