Chicken Sternum-Derived Ingredient
Type II Collagen Powder Manufacturer & Supplier
Chicken sternum-derived Type II collagen powder for supplement manufacturers and ingredient buyers, supported by batch specifications, application information and commercial supply details.
Product Profile
Chicken Sternum-Derived Type II Collagen Powder
This dry powder is supplied as a B2B collagen ingredient for oral supplement formulation and commercial raw-material sourcing.
Ingredient Positioning
The product is positioned for supplement manufacturers evaluating a chicken-derived Type II collagen ingredient in dry-powder form. Technical qualification should be based on the current specification and lot documentation rather than on assumptions drawn from other Type II collagen grades.
Product Identity
The supplied documentation identifies the material as chicken sternum-derived Type II collagen powder. It does not define the grade as hydrolyzed, native or undenatured, so those processing forms should not be treated as interchangeable with this product.
Technical Specification
Type II Collagen Powder Specifications
Review the reference batch against the stated composition, physical, heavy-metal and microbiological requirements used for raw-material quality evaluation.
| Test Item | Test Method | Specification | Batch Result |
|---|---|---|---|
| Composition & Physical Properties | |||
| Collagen | Kjeldahl method | ≥60.0% | 68.4% |
| Mucopolysaccharides | CPC | ≥25.0% | 25.6% |
| Appearance | Visual Testing | Off-white to light yellow powder | Pass |
| Odor | Sensual Testing | Characteristic | Pass |
| Ash | GB5009.4-2016 | ≤8.0% | Pass |
| Loss on Drying | USP731 | ≤10.0% | 8.04% |
| Fat | CP Appendix VII H | ≤2.0% | Pass |
| Particle Size | Through Sieving | 100% through 100 mesh | Pass |
| Heavy Metals | |||
| Heavy Metal (AFS) | AFS | ≤10.0 ppm | ≤10.0 ppm |
| Mercury | AFS | ≤0.1 ppm | ≤0.1 ppm |
| Arsenic (As) | AFS | ≤1.0 ppm | ≤1.0 ppm |
| Cadmium | AFS | ≤0.2 ppm | ≤0.2 ppm |
| Lead | AFS | ≤0.1 ppm | ≤0.1 ppm |
| Heavy Metal (AOAC) | AOAC | ≤10 ppm | Pass |
| Microbiological Testing | |||
| Total Bacteria Count | USP2021 | ≤1,000 CFU/g | 300 CFU/g |
| Yeast & Mold | USP2021 | ≤100 CFU/g | 30 CFU/g |
| Salmonella | USP2022 | Negative | Pass |
| Staphylococcus aureus | USP2022 | Negative | Pass |
Batch results: Lot 20260309 · Report issued March 16, 2026. Results may vary by lot within the stated specifications.
Formulation Applications
Type II Collagen for Oral Supplement Development
The dry powder can be evaluated in common oral dosage forms. Final suitability depends on target serving size, excipient system, processing conditions and the performance requirements of the finished formulation.
Capsules
Evaluate powder flow, fill volume and compatibility with the complete excipient system when developing capsule products.
Tablets
Review blend uniformity, compression behavior and the contribution of other formulation components during tablet development.
Powder Blends
Assess mixing behavior, sensory characteristics and serving-format requirements when incorporating the ingredient into dry blends or sachets.
Sourcing Considerations
Qualifying the Correct Type II Collagen Grade
Type II collagen ingredients can be offered in different processing forms. For this product, sourcing decisions should follow the identity and specification documented for the supplied grade.
Confirm Product Identity
Use the supplied product specification to confirm source, physical form and composition. Do not substitute hydrolyzed, native or undenatured terminology unless the current product documentation explicitly supports it.
Match the Dosage Form
Evaluate the powder within the intended capsule, tablet or dry-blend system. Finished-formula requirements determine whether the ingredient is suitable for the planned manufacturing process.
Review the Current Lot
Use the current specification and lot-specific COA during purchasing review. Reference batch data on this page provides context, while commercial qualification should follow the documentation for the lot being offered.
Commercial Supply
Bulk Type II Collagen Supply for Supplement Manufacturers
Packaging, lot documentation and purchasing follow-up support B2B buyers moving from technical evaluation to commercial sourcing.
Packaging & Shelf Life
Net weight: 20 kg / drum
Gross weight: 23 kg / drum
Reference lot manufacture: March 9, 2026
Reference lot expiry: March 8, 2029
Purchasing Review
Share the required quantity and destination when requesting a quotation. Current availability, order terms and lot-specific documentation can then be reviewed for the material being offered.
B2B Ingredient Inquiry
Discuss Your Type II Collagen Requirements
Share your formulation context, required quantity and destination so the inquiry can be matched to the relevant technical and commercial information.
Project Context
Tell us the intended dosage form, destination market and stage of product development.
Technical Fit
Identify the product specification and batch documentation needed for your ingredient qualification process.
Commercial Follow-Up
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