Glucosamine sulfate sodium chloride (2NaCl) is a stabilized sulfate form of glucosamine developed for industrial supplement production. The sodium chloride complex preserves structural integrity during handling, blending, and storage, supporting consistent potency across manufacturing processes. This USP-grade material serves as a joint health ingredient for manufacturers producing capsules, tablets, and combination formulas for cartilage support applications.
The sodium chloride complex structure maintains the integrity of glucosamine sulfate through common production steps, including material handling, ingredient blending, and warehouse storage. This formulation supports consistent potency retention throughout manufacturing workflows, making it suited for high-volume production environments. The material works as a base ingredient for both single-ingredient and multi-component joint health products, with performance that aligns with standard supplement production workflows.
Produced in alignment with USP standards, this glucosamine sulfate 2NaCl follows defined purity thresholds and impurity controls. Assay on dried basis falls within 98.0% to 102.0%, with controlled levels of organic impurities, elemental impurities, and residual ethanol. Physical properties such as mesh size and bulk density are standardized to support routine processing in capsule filling, tableting, and powder blending lines. These controlled specifications support formulation reproducibility for commercial production lines.
Below is the complete specification sheet for this USP-grade glucosamine sulfate sodium chloride:
Test Item | Specification |
|---|---|
Appearance | White to off-white crystalline powder |
Identification | A. Infrared Absorption B. Identification Tests – General, Chloride and Sodium: Meets the requirements C. The retention time of the glucosamine peak of the sample solution corresponds to that of the standard solution, as obtained in the Assay D. Sulfate: In the test for Content of Sulfate, after the addition of barium chloride TS, a white precipitate is formed |
Assay (on dried basis) | 98.0% – 102.0% |
Specific Rotation | 50° – 55° |
pH (1% solution) | 3.0 – 5.0 |
Loss on Drying | ≤ 1.0% |
Sulfate Content | 16.3% – 17.3% |
Chloride Content | 11.7% – 13.0% |
Inorganic Residue (as salts) | 23.5% – 25.0% |
Sodium | Meet requirement |
Organic Impurities | Conforms to USP-NF |
Elemental Impurities | Complies with USP <232>/<233> |
Ethanol | ≤ 5000 ppm |
Physical Properties | |
Mesh Size | 100% through 30 mesh (As per customer requirements) |
Bulk Density | ≥ 0.6 g/ml |
Heavy Metals | |
Heavy Metals | ≤ 10 ppm |
Lead (Pb) | ≤ 3 ppm |
Arsenic (As) | ≤ 3 ppm |
Cadmium (Cd) | ≤ 1 ppm |
Mercury (Hg) | ≤ 0.1 ppm |
Microbiological Limits | |
Total Aerobic Count | ≤ 1000 CFU/g |
Yeast & Mold | ≤ 100 CFU/g |
Escherichia coli | Negative |
Salmonella | Negative |
Staphylococcus aureus | Negative |
Coliforms | Negative |
This glucosamine sulfate sodium chloride ingredient is formulated for use in joint health supplement production, with adaptability across multiple industrial applications. It fits into various product formats and formulation designs for commercial production. Common uses include joint health capsules and tablets, where standardized particle size and bulk density support consistent filling and compression performance. It also works in powder nutritional blends, where uniform mixing behavior supports even distribution of active ingredients across batch runs.
The material shows compatibility with other joint support ingredients, including chondroitin sulfate, MSM, and collagen. This compatibility allows formulators to develop multi-component joint health products using a single glucosamine source. It is suited for both single-ingredient SKUs and complex combination formulas in commercial production, supporting flexible product line development for enterprise customers.
Production takes place under ISO, HACCP, and GMP-aligned conditions. Halal and Kosher certification options are available for markets that require these credentials. All production and testing processes follow USP requirements to support regulatory compliance for finished products sold in global markets. These systems support traceability and process control throughout the production cycle.
Each production batch comes with a corresponding Certificate of Analysis (COA). Additional technical documentation including Technical Data Sheets (TDS) and Material Safety Data Sheets (MSDS) are available upon request. Standardized production workflows support reproducible quality across batches, supporting long-term formulation consistency for enterprise customers. Controlled processing parameters reduce variation between production runs.
Bulk order volumes are supported to match high-volume manufacturing demand. Export-oriented service structures support cross-border commercial procurement, with flexible quotation options for different order sizes. Technical inquiries receive structured response to support formulation evaluation and production planning for business buyers. Long-term supply cooperation arrangements are available for ongoing production needs.
The sodium chloride complex stabilizes the glucosamine sulfate structure, helping preserve active ingredient integrity during handling, blending, and storage. This structure supports consistent potency through standard manufacturing and storage workflows.
Each batch includes a dedicated COA. TDS, MSDS, and quality system documentation are available to support customer audits and technical evaluation processes for industrial clients.
Yes, this glucosamine sulfate 2NaCl is compatible with chondroitin sulfate, MSM, collagen, and other common joint health ingredients. It is suited for use in multi-component supplement formulations for commercial production.
For pricing details, sample requests, or technical support related to USP grade glucosamine sulfate 2NaCl, contact our team to receive targeted support for your production and procurement needs.
