MEDIOCON INC supplies BioSil® / Choline-Stabilized Orthosilicic Acid (ch-OSA®) as a specialty nutritional ingredient for nutraceutical and dietary supplement applications.
ch-OSA® is a complex consisting of orthosilicic acid (OSA) stabilized with choline. The manufacturer describes ch-OSA® as its patented choline-stabilized orthosilicic acid complex.
Because ch-OSA® is a complex rather than a single conventional chemical substance, a single molecular formula, molecular weight or CAS number should not be assigned to the complete ingredient without reference to the specific technical specification.
For commercial use, the exact silicon content, choline content, concentration, physical form, purity and other analytical parameters should be confirmed from the applicable product specification and batch COA.
ch-OSA® combines orthosilicic acid, described by the manufacturer as the biologically active form of silicon, with choline, which stabilizes the orthosilicic acid.
The manufacturer's current information identifies silicon and choline as the key nutritional components of ch-OSA®. Its labeling describes silicon in the form of choline-stabilized orthosilicic acid.
BioSil/ch-OSA® is positioned as a specialty ingredient for dietary supplement formulations rather than as a pharmaceutical API.
The ch-OSA® complex is naturally formulated as a liquid, although finished BioSil products may use different dosage forms.
BioSil / Choline-Stabilized Orthosilicic Acid may be used in:
Mediocon Inc is a GMP-certified API manufacturer and bulk pharmaceutical ingredient supplier based in Aurangabad, Maharashtra, India. We specialise in supplying BioSil (Choline-Stabilized Orthosilicic Acid) Manufacturer & Supplier in India | MEDIOCON INC and over 1,000 other Active Pharmaceutical Ingredients, excipients, herbal extracts, and nutraceutical ingredients to pharmaceutical manufacturers worldwide.
Our BioSil (Choline-Stabilized Orthosilicic Acid) Manufacturer & Supplier in India | MEDIOCON INC is manufactured under strict quality management protocols compliant with WHO-GMP, ISO 9001:2015, and major pharmacopoeial standards (IP, BP, USP, EP). Every batch undergoes full analytical testing before release with a Certificate of Analysis.
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