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Aerosil 200

To guarantee the highest purity and efficacy, we adhere to strict global standards

Pharmaceutical Excipients

Aerosil 200

Aerosil 200 is a high-purity, hydrophilic fumed silica produced by the hydrolysis of silicon halides in a hydrogen-oxygen flame. It is a light, amorphous, white powder with a massive surface area of approximately 200 m2g. In the pharmaceutical industry, it is primarily valued as the industry-standard Glidant. By coating the surfaces of active particles, it reduces inter-particle friction and prevents static charges, ensuring an optimized and uniform flow of powders during high-speed tablet compression and capsule filling.

The product conforms to the specified requirements of the United States Pharmacopeia (USP), European Pharmacopoeia (EP), and/or British Pharmacopoeia (BP).
A detailed CoA is issued with every batch, outlining potency, purity profile, and microbiological testing verification.
A comprehensive Drug Master File is available to support registration submissions to regulatory authorities worldwide.
Production takes place in certified facilities that strictly adhere to current Good Manufacturing Practices (cGMP).
Functional Category:
Glidant, Thickening Agent, Suspension Stabilizer, and Tablet Disintegrant.
Appearance:
Extremely light, fluffy white powder; bluish tint in dispersed light (Tyndall effect).
Physical State:
Amorphous (Non-crystalline) – non-abrasive to manufacturing machinery.
Solubility:
Practically insoluble in water and organic solvents; soluble in hydrofluoric acid.
Tablets & Capsules

Powder flow improvement (Glidant).

Prevents bridging and sticking in hoppers; ensures dose weight uniformity in every unit.

Liquid/Oily Systems

Carrier for viscous oils.

Its high adsorptive capacity allows for the conversion of oils or liquid APIs into free-flowing, compressible powders.

Creams & Gels

Viscosity adjustment (Thickening).

Provides structural viscosity and prevents phase separation in semi-solid preparations.

Suspensions

Anti-caking agent.

Creates a physical network that prevents solid particles from forming a hard "cake" at the bottom of the bottle.

Regulatory Compliance

The product fully complies with the requirements specified in the United States Pharmacopeia (USP), the European Pharmacopoeia (EP), and/or food standards (FCC).

Chemical Inertness

As an inert material, it does not react with most APIs, ensuring long-term drug stability.

High Purity

Rigorously tested for heavy metals, chlorides, and moisture content (Loss on Drying).

Controlled Efficiency

Effective at very low concentrations (typically 0.1% to 1.0%), minimizing the impact on the final tablet size.

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