Magnesium Glycinate
Available documentation may include COA, TDS, MSDS, specification sheet, allergen statement, heavy metal and microbiology results, and Halal/Kosher statements where available. Additional Non-GMO, BSE/TSE, GMP, ISO or market-specific documents should be confirmed against the selected grade and supplier source before RFQ.
Product Overview
Magnesium Glycinate is a chelated mineral ingredient supplied in food supplement grade for capsule, tablet, powder blend, gummy and beverage-premix formulations. It is commonly positioned in calm, sleep and muscle-relaxation supplement concepts, and is selected by brands that want a well-tolerated magnesium form with clear mineral-content and contaminant control.
For B2B sourcing, the key purchasing and QC points are chelation form and ratio, elemental magnesium content, assay and identification, appearance, heavy metals, microbial limits, moisture, particle form, and batch-to-batch consistency. Buyers should confirm the target elemental-magnesium content and dosage-form fit before quotation, because capsule and tablet projects often specify a narrower particle-size or flow range than powder-blend projects.
Healtain supports purchasing, sourcing, QA and formulation teams by confirming the available grade, mineral content, sample availability, MOQ, lead time, packaging and documentation package before quotation. For quality and compliance context, buyers can review the Quality & Compliance page alongside this product page.
Applications
- Calm and sleep support capsules, tablets and powder blends
- Muscle relaxation and recovery formulas
- High-potency mineral blends requiring chelated magnesium
- Gummies and beverage premixes where taste and solubility are reviewed
- Private-label projects needing mineral-content and document confirmation
Recommended Dosage Forms
- Capsule
- Tablet
- Powder blend
- Gummy
- Beverage premix
FAQ
Q1: What specifications should be confirmed for Magnesium Glycinate?
Buyers should confirm the chelation form and ratio, elemental magnesium content, assay, appearance, moisture, heavy metals, microbial limits, particle form and the intended dosage form before quotation. Food supplement grade is the common starting point.
Q2: How is elemental magnesium content controlled?
Elemental magnesium content is a key QC item and should be reviewed against the selected grade and batch COA, because it determines how much finished-product magnesium can be delivered per serving.
Q3: Which dosage forms is it commonly used in?
Magnesium Glycinate is commonly evaluated for capsules, tablets, powder blends, gummies and beverage premixes. Capsule and tablet projects may need a specific particle-size or flow profile.
Q4: What documents can be requested?
COA, TDS, MSDS, allergen statement, heavy metal and microbiology results may be available, with Halal/Kosher and other market-specific documents confirmed against the selected grade and source.
Q5: How should MOQ, samples and lead time be confirmed?
MOQ, sample availability and lead time depend on the selected grade, stock and order quantity. Confirming these together with the specification and documentation package before ordering helps avoid delays.
Related Formulation Guide
For R&D and production planning, see How to Choose Particle Size and Flowability for Formulations.
Related Logistics Guide
For small order planning and freight cost control, see Why Small Bulk Ingredient Orders Have High Shipping Costs.
Related Products
RFQ Readiness
Assay, mesh, purity, source, carrier, dosage form and target application.
COA, TDS, MSDS, allergen, Non-GMO, Halal, Kosher or market files when available.
Evaluation sample, pilot order, bulk quantity, shelf life and packing preference.
Destination country, carton/drum/pallet details, lead time and shipment coordination.