Bulk Bone Broth Protein Ingredient

Beef Bone Broth Protein Powder for Nutraceutical Formulations

High-protein Beef Bone Broth ingredient for B2B sourcing, with a NLT 97% protein specification and 3,000–5,000 molecular-weight range. Review batch analytical data, technical qualification points and commercial sourcing requirements below.

Beef Bone Broth Protein powder for nutraceutical formulations
Protein Specification NLT 97%
Batch Protein Result 97.2% Dry Basis
Molecular Weight 3,000–5,000
Bulk Density 0.37 g/ml
Product Overview

High-Protein Beef Bone Broth Powder

The Certificate of Analysis identifies the material as Beef Bone Broth and controls protein, molecular weight, ash, loss on drying, pH, heavy metals, melamine metabolites, bulk density, sodium and microbiology.

For formulation and procurement teams, the key differentiator on this page is measurable batch composition. Claims about collagen type, amino acids, glucosamine, chondroitin, hyaluronic acid, grass-fed sourcing or extraction process should only be added when separate current technical documentation supports them.

COA Product Name Beef Bone Broth
Batch No. BB260403
Production Date Apr.02, 2026
Date of Analysis Apr.09, 2026
Date of Expiry Apr.01, 2029
Batch Quantity 2,000 kg
Batch Analytical Data

Batch BB260403 Snapshot

Batch values are displayed separately from specification limits so procurement and R&D teams can distinguish the product standard from the tested result.

Protein 97.2% Dry Basis
Molecular Weight 3,000–5,000
Ash 1.05%
Loss on Drying 5.98%
pH 5.3
Sodium 0.04%
Technical Specifications

Beef Bone Broth Protein Specifications

Specification limits and tested batch results are reproduced from the supplied analytical certificate. Values not shown on the certificate are not added to the table.

Test ItemSpecificationBatch ResultTest Method
CharacteristicLight yellow granule, 60 meshSensual Test
ProteinNLT 97%97.2% (Dry Basis)Kjeldahl Method
Molecular Weight3,000–5,0003,000–5,000Gel Chromatography Method
AshNMT 2.0%1.05%U.S.P. / N.F.
Loss on DryingNMT 8.0%5.98%U.S.P. / N.F.
pH5.0–6.55.3Japanese Pharmacopoeia
Heavy Metals (Pb)NMT 20.0 ppm<20 ppmNa2S Colorimetric
Arsenic (As2O3)NMT 1.0 ppm<1.0 ppmAtomic Absorption Spectrometer
Chromium<2.0 ppm<2.0 ppmAtomic Absorption Graphite Furnace
Melamine (Metabolites)NegativeNegativeHPLC
Bulk Density>0.35 g/ml0.37 g/mlU.S.P. / N.F.
Sodium<0.7%0.04%ICP-MS
Total Bacterial<1,000 CFU/g300 CFU/gUSP 2021
Yeast and Mold<100 CFU/g30 CFU/gUSP 2021
E. coliNegative / 10gNegativeUSP 2021
Coliform GroupNegative / 10gNegativeUSP 2021
LeadNMT 1.0 ppm<1.0 ppmICP-MS
Mercury (Hg)NMT 0.1 ppm<0.1 ppmICP-MS
CadmiumNMT 0.1 ppm<0.1 ppmICP-MS
Technical Qualification

What the Analytical Data Supports — and What to Request Separately

Current SERP competitors frequently add collagen, amino-acid, grass-fed and clean-label claims. For supplier qualification, keep those claims separate from what the batch analysis actually proves.

Supported by the Batch Analysis

These properties are explicitly reported in the supplied certificate.

ProteinNLT 97%; batch result 97.2% dry basis
Molecular Weight3,000–5,000 by gel chromatography
Physical PropertiesAsh, moisture, pH, bulk density and 60-mesh characteristic
Contaminant ControlsHeavy metals, arsenic, chromium, melamine, lead, mercury and cadmium
MicrobiologyTotal bacterial, yeast & mold, E. coli and coliform results

Request Before Making Additional Claims

These points are not established by the supplied analytical certificate.

Raw Material & Process DeclarationExact bovine material, manufacturing flow and extraction/hydrolysis description
Amino-Acid ProfileGlycine, proline, glutamine, EAA/BCAA and other individual amino acids
Collagen CompositionDo not state Type I/III or collagen percentage without supporting analysis
Natural ActivesHA, glucosamine, chondroitin and mineral claims require product-specific data
Label & Source ClaimsGrass-fed, dairy-free, hormone-free, BSE/TSE, allergen and country-of-origin documentation
Formulation Pathways

Beef Bone Broth Protein Powder for Product Development

These are formulation formats to evaluate during R&D. Finished-product claims, nutrition positioning and processing suitability should be confirmed independently.

01 / Powder

Protein Drink Powders

Evaluate dispersibility, flavor system, protein target and serving size in the finished powder blend.

02 / Savory

Instant Broth Concepts

Assess taste, salt system, seasonings, aroma and reconstitution performance for savory products.

03 / Nutrition

Functional Nutrition

Use the documented protein specification as one input when developing high-protein nutrition concepts.

04 / Blend

Protein Blend Systems

Evaluate sensory and functional compatibility when combining bone broth protein with other animal or plant proteins.

B2B Sourcing

What to Request from a Beef Bone Broth Protein Supplier

Current SERP results for commercial bone broth protein emphasize protein assay, source, samples, packaging and technical documents. Separate verified data from marketing language.

Current Batch COA

Confirm protein, molecular weight, physical parameters, contaminants and microbiology on the lot being qualified.

Raw Material & Process Documentation

Request the manufacturing flow and source declaration if your label depends on bone, broth or process-specific positioning.

Amino-Acid / Collagen Data

Request separate analysis before using collagen, glycine, proline or other amino-acid claims.

R&D Sample

Test taste, odor, color, dispersibility and compatibility in your actual finished-product system.

MOQ, Packaging & Lead Time

The certificate records a 2,000 kg batch quantity, not a commercial pack size or current inventory commitment.

Beef bone broth protein quality testing and technical qualification
Buyer FAQ

Beef Bone Broth Protein Sourcing Questions

What is the protein specification for this Beef Bone Broth Protein?

The product specification is NLT 97% protein. Batch BB260403 reports 97.2% protein on a dry basis.

What is the molecular weight range?

The specification and batch result both report a 3,000–5,000 molecular-weight range using gel chromatography.

Does the COA prove Type I and Type III collagen content?

No. The analytical certificate does not report collagen type or collagen percentage. Separate product-specific testing is required before publishing Type I/III claims.

Does it contain glucosamine, chondroitin or hyaluronic acid?

Those components are not quantified in the supplied analytical certificate. Do not present them as standardized product features without additional supporting data.

What is the bulk density and sodium level?

The bulk-density specification is >0.35 g/ml with a batch result of 0.37 g/ml. Sodium is specified at <0.7% and the batch result is 0.04%.

Is this product grass-fed or dairy-free?

The analytical certificate does not establish grass-fed, dairy-free, allergen, hormone-free or BSE/TSE status. Request the relevant current declarations before using those claims.

What is the commercial packaging and MOQ?

The certificate shows a 2,000 kg batch quantity but does not specify packaging or MOQ. Request current commercial terms for your destination and expected volume.

Can I request current technical documents and an R&D sample?

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

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