Joint Health Ingredient
Vegan Glucosamine Ingredient Supplier
A defined glucosamine hydrochloride ingredient supplied for product development and specification review. The page below presents the product identity, tested batch record and complete analytical results without mixing batch data into the application or purchasing sections.
Product Identity
Vegan Glucosamine HCl
The fixed product details below come from the supplied Certificate of Analysis or the product identity documented with it.
Batch Record
Certificate of Analysis Batch Record
This section identifies the tested lot. The detailed release results follow in the technical table.
Technical Specification
Vegan Glucosamine HCl Specification & COA Results
Release limits, recorded results and analytical methods listed on the supplied certificate.
| Test Item | Specification | Result | Analytical Method |
|---|---|---|---|
| Identity & Physical Properties | |||
| Appearance | Crystalline powder | Complied | Visual |
| Color | White | Characteristic | Visual |
| Assay | 98.0% – 102.0% | 99.5% | USP40-HPLC |
| Identification |
A: Infrared absorption B: Chloride test C: Retention time D: Vegan Source |
Complied |
USP40 <197K> USP40 <191> HPLC In House Standard |
| Specific Rotation | +70.0° – +73.0° | +71.5° | USP40 <781S> |
| Residue on Ignition | NMT 0.1% | 0.04% | USP40 <281> |
| Loss on Drying | NMT 1.0% | 0.05% | USP40 <731> |
| pH | 3.0 – 5.0 | 4.1 | USP40 <791> |
| Contaminants & Inorganic Components | |||
| Heavy Metals | NMT 10 ppm | Complied | USP40 <231> method II |
| Arsenic | NMT 3 ppm | Complied | USP40 |
| Content of Sulfate | NMT 0.24% | Complied | USP40 |
| Microbiology | |||
| Total Plate Count | NMT 1000 cfu/g | <10 cfu/g | USP40 |
| Yeast & Mold | NMT 100 cfu/g | <10 cfu/g | USP40 |
| Salmonella | Negative | Negative | USP40 |
| E. coli | Negative | Negative | USP40 |
| Conclusion | |||
| COA Conclusion | Conforms to USP40 | Conforms | Certificate of Analysis |
Application
Formulation Formats
The ingredient can be evaluated for joint-health supplement products where glucosamine HCl matches the finished product requirement.
Capsules
Used in capsule formulas where the selected glucosamine form and powder characteristics fit the target serving and manufacturing process.
Tablets
Used in tablet formulas subject to the compression, excipient and processing requirements of the finished product.
Powder Products
Considered for powder-based supplements and blends when the material's physical and analytical requirements match the process.
Qualification
What to Confirm for Your Formula
These checks help determine whether the documented material fits the finished product before a commercial order is placed.
Product Specification
Compare your required ingredient identity and release limits with the applicable product specification and current lot documentation.
Processing Requirements
Confirm that the selected material fits your dosage form, blending process, handling conditions and intended market requirements.
Request Pricing & Product Information
Send your required quantity, application, specification and destination so the product information can be matched to your project.