Magnesium Lactate

Magnesium Lactate

Magnesium Lactate (C₆H₁₀MgO₆ · 2H₂O) is an organic mineral salt produced via the controlled reaction and crystallization of high-purity food-grade lactic acid with magnesium sources.
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Product Introduction

Magnesium Lactate (C₆H₁₀MgO₆ · 2H₂O) is an organic mineral salt produced via the controlled reaction and crystallization of high-purity food-grade lactic acid with magnesium sources. It functions primarily as a highly bioavailable mineral supplement and pH-buffering agent in functional foods, dietary supplements, and pharmaceutical formulations.
Manufacturing operations are conducted in dedicated synthesis facilities using 316L stainless steel reaction systems under FSSC 22000 and cGMP frameworks. Each production lot is quantitatively analyzed via complexometric titration and ICP-MS elemental screening to verify compliance with USP, FCC, and EP monographs.

 

Key Specifications

 

Test Parameter

Specification (USP / FCC)

Typical Batch Value

Analytical Test Method

Assay (Dried Basis)

98.0% – 101.0%

99.3%

EDTA Titrimetry

Magnesium Content

10.0% – 12.0% (Dihydrate)

10.6%

ICP-OES

Loss on Drying

14.0% – 20.0% (Dihydrate)

18.2%

Gravimetric (105°C, 4h)

Heavy Metals (as Pb)

≤ 10 ppm

< 5 ppm

ICP-MS

Lead (Pb)

≤ 0.5 ppm

< 0.1 ppm

ICP-MS

Arsenic (As)

≤ 1.0 ppm

< 0.2 ppm

ICP-MS

Cadmium (Cd)

≤ 1.0 ppm

< 0.1 ppm

ICP-MS

Mercury (Hg)

≤ 0.1 ppm

< 0.05 ppm

ICP-MS

pH (5% Aqueous Solution)

6.0 – 8.0

6.7

Potentiometry

Particle Size Distribution

95% pass 80 mesh

98% pass 80 mesh

Mechanical Sifting

 

Applications

 

Dietary Supplements: Compounded into hard capsules, chewable tablets, and effervescent powder systems to deliver high gastrointestinal tolerance and systemic absorption.
Functional Foods & Beverages: Incorporated into sports drinks, electrolyte waters, and nutritional bars for mineral fortification without metallic flavor distortion.
Pharmaceutical Industry: Utilized as an active pharmaceutical ingredient (API) intermediate and direct-compression mineral matrix in oral solid dosage forms. 

 

Product Grades & Options

 

Magnesium Lactate Dihydrate (Fine Powder): Milled to ≤ 80 mesh specifications, optimized for homogeneous dry-powder mixing and capsule filling.
Magnesium Lactate Dihydrate (Granular): Processed via wet granulation to improve flowability, minimize fine dust generation, and support high-speed tableting operations.
Custom Grades: Tailored particle-size distributions and low-microbial profiles available upon technical application review. 

 

Quality Control & Documentation

 

Production runs are governed by automated raw material dosing, closed-loop crystallization temperature regulation, and automated centrifugation.

 

Laboratory Validation: Outgoing lots are verified in our ISO/IEC 17025 accredited laboratory using HPLC for chemical purity and ICP-MS for heavy metal quantification.

Lot Traceability: Complete backward and forward tracking from raw lactic acid feedstocks to final packaged fiber drums.

 

Regulatory Dossiers Supplied:

Certificate of Analysis (COA) per production lot

Safety Data Sheet (SDS)

Non-GMO, Allergen-Free, and BSE/TSE Statements

Kosher and Halal Certificates

 

Packaging & Storage

 

Standard Packaging: 25 kg fiber drums lined with dual food-grade low-density polyethylene (LDPE) bags, secured with tamper-evident pull-tight seals. Palletized and stretch-wrapped for maritime and air transport safety.
Storage Environment: Store in tightly sealed containers in a cool, dry, well-ventilated warehouse. Protect from direct humidity and extreme heat.
Shelf Life: 24 months from the manufacture date in unopened original packaging. 

 

FAQ

 

Q: What differentiates Magnesium Lactate from Magnesium Oxide or Citrate?

A: Magnesium lactate contains approximately 10% elemental magnesium by weight and provides significantly higher aqueous solubility and gastrointestinal tolerance than oxide or citrate alternatives, minimizing laxative side effects in sensitive formulations.

Q: Does this product comply with USP and FCC monographs?

A: Yes. Synthesis, analytical testing, and final product release comply fully with current United States Pharmacopeia (USP) and Food Chemicals Codex (FCC) standards.

Q: What is the minimum order quantity (MOQ) for bulk shipments?

A: The standard MOQ is 500 kg (20 x 25 kg drums) to fit standard ocean freight pallet configurations. 1 kg sample quantities are available for R&D laboratory evaluation.

Q: Can the particle size distribution be customized for specific tableting machines?

A: Yes. Air-classifier milling systems allow us to adjust mesh size distributions to meet specific bulk density and flowability requirements for high-speed direct compression.

Q: What analytical methods are used for heavy metal verification?

A: Every production lot is analyzed using Inductively Coupled Plasma Mass Spectrometry (ICP-MS) to measure trace levels of lead, arsenic, cadmium, and mercury against strict threshold limits.

Q: How is batch-to-batch consistency maintained during production?

A: Consistency is controlled through automated reactor feeding, calibrated online crystallization monitoring, and a mandatory 3-year retention sample archive for every manufactured lot.

 

Request a Quote & Technical Documentation

 

Submit your technical requirements and commercial projections below to receive a formal quotation, current batch COA, and working sample within 24 business hours.
Required Inquiry Details: Target Grade (Powder/Granular), Annual Volume Projection, Port of Destination, and Specific Documentation Requirements (USP/FCC). 

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