Chicken Sternum Type II Collagen

Type II Collagen Peptides for Joint-Health Formulations

Chicken sternum-derived Type II collagen ingredient with a standardized collagen, chondroitin sulfate and hyaluronic acid matrix for B2B nutraceutical sourcing. Review the COA specifications, technical documentation and commercial supply options below.

Type II Collagen Peptides powder from chicken sternum
Source Chicken Sternum
Protein / Collagen ≥60% · Batch 68.0%
Chondroitin Sulfate ≥25% · Batch 26.2%
Hyaluronic Acid ≥5% · Batch 5.1%
II

Hydrolyzed vs. Undenatured Type II Collagen

This page is intended for ATNUTRA's Type II collagen peptide / hydrolyzed product line, not a native low-dose undenatured Type II collagen ingredient. The supplied COA itself identifies the product as “Collagen Type II” from chicken sternum and reports its composition; request the current TDS or process documentation when the hydrolysis designation is required for formulation, regulatory review or finished-product labeling.

Product Overview

Chicken Sternum Type II Collagen Matrix

The supplied COA identifies this ingredient as Collagen Type II originating from chicken sternum. Its composition is standardized around protein/collagen, chondroitin sulfate and hyaluronic acid, with additional controls for pH, ash, loss on drying, fat, bulk density, heavy metals, particle size and microbiology.

For procurement and R&D teams, this makes the product suitable for technical comparison based on measurable composition rather than unsupported absorption or disease claims.

COA Product Name Collagen Type II
Origin Chicken Sternum
Reference Batch 20260102
Mfg Date 2026/01/02
Expiry Date 2029/01/01
Net Packaging 20 kg / Carton
Reference Batch COA

Composition Snapshot

Reference-batch results are shown separately from specification limits. Request the current batch COA before final supplier qualification.

Protein / Collagen 68.0%
Chondroitin Sulfate 26.2%
Hyaluronic Acid 5.1%
pH 5.7
Bulk Density 0.44 g/ml
Total Bacteria 200 CFU/g
Technical Specifications

Type II Collagen COA Specifications

The table below reproduces specification limits and reference-batch results from the supplied COA. “Pass” indicates conformity where no numeric result is reported.

Test ItemSpecificationReference Batch Result
AppearanceWhite to Off-white PowderPass
OdorCharacteristicPass
Protein (Collagen)≥60.0%68.0%
pH4.0–7.55.7
Chondroitin Sulfate≥25.0%26.2%
Hyaluronic Acid≥5.0%5.1%
Ash≤8.0%6.3%
Loss on Drying≤10.0%6.48%
Fat≤2.0%Pass
Bulk Density0.4–0.5 g/ml0.44 g/ml
Heavy Metal≤10 ppmPass
Lead≤1.0 ppmPass
Arsenic≤2.0 ppmPass
Mercury≤0.5 ppmPass
Cadmium≤0.5 ppmPass
Particle Size100% Through 80 MeshPass
Total Bacteria Count≤1,000 CFU/g200 CFU/g
Yeast & Mold≤100 CFU/g20 CFU/g
SalmonellaNegativePass
Staphylococcus aureusNegativePass
Standardized Composition

A Three-Component Type II Collagen Matrix

The COA supports a formulation-oriented description of the ingredient through three measurable composition parameters rather than broad physiological claims.

01

Protein / Collagen ≥60%

The reference batch reports 68.0% protein/collagen against a minimum specification of 60.0%.

02

Chondroitin Sulfate ≥25%

The reference batch reports 26.2% chondroitin sulfate against a minimum specification of 25.0%.

03

Hyaluronic Acid ≥5%

The reference batch reports 5.1% hyaluronic acid against a minimum specification of 5.0%.

Formulation Pathways

Type II Collagen Peptides for Product Development

Evaluate dosage form, serving size, sensory performance and regulatory positioning in your finished formula before commercial scale-up.

01 / Joint Nutrition

Joint-Health Supplements

Use the standardized collagen, chondroitin sulfate and HA composition when developing joint-focused supplement concepts.

02 / Powder

Drink Powders & Sachets

Evaluate particle size, dispersibility, flavor system and finished-powder stability in the target serving format.

03 / Solid Dose

Capsules & Tablets

Review bulk density, excipient compatibility and target serving size for capsule or tablet development.

04 / Functional Food

Specialty Nutrition

Assess sensory, processing and market-specific regulatory suitability in the intended finished product.

B2B Qualification

What to Request from a Type II Collagen Supplier

Current SERP results for bulk Type II collagen emphasize source identity, COA/specification review, samples, packaging and technical documentation. Use these criteria during supplier qualification.

Current Batch COA

Confirm collagen, chondroitin sulfate, hyaluronic acid, heavy metals and microbiology on the commercial lot.

TDS / Processing Declaration

Confirm whether the commercial grade is hydrolyzed and document the processing designation used for your market.

Chicken Sternum Source Statement

The reference COA identifies chicken sternum as the origin; request current source and traceability documentation.

Sample for R&D Testing

Evaluate flow, sensory, dispersibility and compatibility in your actual dosage form.

Packaging & Commercial Terms

The reference COA records 20 kg net per carton and 23 kg gross per carton. Confirm current MOQ, availability and lead time separately.

Buyer FAQ

Type II Collagen Peptide Sourcing Questions

What is the source of this Type II collagen ingredient?

The supplied COA identifies the origin as chicken sternum.

What is the protein or collagen specification?

The COA specification is ≥60.0% protein/collagen. The reference batch reports 68.0%.

How much chondroitin sulfate and hyaluronic acid does it contain?

The specification requires ≥25.0% chondroitin sulfate and ≥5.0% hyaluronic acid. The reference batch reports 26.2% and 5.1%, respectively.

Is this the same as undenatured Type II collagen?

No. This page is intended for ATNUTRA's Type II collagen peptide / hydrolyzed product line, not a native low-dose undenatured Type II ingredient. Request the current TDS or processing declaration to document the exact commercial-grade designation.

Does the COA specify molecular weight?

No. The supplied Type II Collagen COA does not list a molecular-weight specification, so this page does not publish one. Request additional technical data if molecular-weight information is required.

What particle size and bulk density are specified?

The COA specifies 100% through 80 mesh and a bulk density range of 0.4–0.5 g/ml. The reference batch reports 0.44 g/ml.

What packaging is documented?

The updated reference batch uses 20 kg net per carton, with 23 kg gross weight per carton. Confirm current commercial packaging when requesting a quote.

Can I request a current COA and sample?

Yes. Contact ATNUTRA with the target application, destination market and expected volume to request current technical documentation and sample availability.

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