MEDIOCON INC offers Quatrefolic® [(6S)-5-Methyltetrahydrofolic Acid, Glucosamine Salt], an advanced form of folate based on the glucosamine salt of the naturally occurring (6S)-5-methyltetrahydrofolate (5-MTHF).
Quatrefolic® represents a reduced and active form of folate and is designed as a source of folate for dietary supplements, nutraceutical formulations and suitable food applications. The official Quatrefolic® information identifies it as the glucosamine salt of (6S)-5-methyltetrahydrofolate.
Unlike folic acid, 5-MTHF is already in a reduced folate form. Quatrefolic® uses glucosamine as the salt-forming component and is described by its manufacturer as offering improved water solubility compared with the calcium salt of 5-MTHF.
The ingredient has received regulatory recognition in multiple markets. The Quatrefolic® manufacturer states that FSSAI approved (6S)-5-methyltetrahydrofolic acid glucosamine salt as a new food additive in February 2019.
EFSA identifies the compound as (6S)-L-5-methyltetrahydrofolic acid, glucosamine salt and reports a molecular formula of C20H25N7O6 · 2C6H13NO5, molecular weight 817.80 g/mol, and CAS Registry Number 1181972-37-1 for the glucosamine salt.
MEDIOCON INC supports sourcing and supply of Quatrefolic® / 5-MTHF glucosamine salt according to customer requirements, grade and applicable quality documentation.
| Parameter | Specification |
|---|---|
| Appearance | Typically yellow to orange/yellow powder |
Mediocon Inc is a GMP-certified API manufacturer and bulk pharmaceutical ingredient supplier based in Aurangabad, Maharashtra, India. We specialise in supplying Quatrefolic® 5-MTHF Glucosamine Salt Manufacturer & Supplier in India | MEDIOCON INC (CAS 1181972-37-1) and over 1,000 other Active Pharmaceutical Ingredients, excipients, herbal extracts, and nutraceutical ingredients to pharmaceutical manufacturers worldwide.
Our Quatrefolic® 5-MTHF Glucosamine Salt 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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