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Chondroitin sulfate

Chondroitin sulfate for food supplements: source species, grade choice, EU regulatory status and formulation notes for capsules, tablets and powders.

CAS 9007-28-7EC 232-696-9Joint & Connective Tissue

Technical data

CAS number9007-28-7
EC number232-696-9
Molecular formulaH2O4S.xUnspecified
Molar mass463.37 g/mol
HS code3913 90 00

Grades and forms of chondroitin sulfate powder

Chondroitin sulfate is a sulfated glycosaminoglycan, a polysaccharide extracted mainly from animal cartilage. Supplement manufacturers buy it as a powder, usually as the sodium salt. Three choices define the material: source species, the assay method behind the stated purity, and the physical form your format needs.

Source species is the first decision. Bovine, porcine, chicken and marine cartilage (shark and other fish) are the usual raw materials. Source affects the sulfation pattern, the molecular weight distribution, allergen labelling and how the finished product can be positioned. Material produced by microbial fermentation also exists, but its regulatory status must be checked before use.

Purity figures depend on the analytical method. Titration-based and chromatographic methods can give different results for the same lot. Compare offers only when the certificates of analysis state the same method and the same basis, as-is or dried.

Physical form follows the format. Fine powder suits capsules and drink powders. Granulated grades flow and compress better in tablets. State the source, assay method and form you need in the quote form; SoleChem sends the specification sheet and certificate of analysis with its quote.

EU regulatory status

Chondroitin sulfate is neither a vitamin nor a mineral. Directive 2002/46/EC harmonises only vitamins and minerals in Annexes I and II. Chondroitin sulfate counts as an “other substance”, and its use in food supplements is governed by national rules. Notification requirements and any maximum amounts differ by member state, so check each target market with its competent authority.

Regulation (EC) No 1925/2006 provides an EU procedure to prohibit or restrict other substances in Annex III. Confirm that no entry for chondroitin sulfate applies before launch.

Novel-food status depends on source and process. Fermentation-derived chondroitin sulfate must be checked against the Union list in Implementing Regulation (EU) 2017/2470, including its specifications and conditions of use. Cartilage-derived material should also be checked under Regulation (EU) 2015/2283. The novel food guide explains how to do this.

Animal-derived chondroitin sulfate may also fall under EU hygiene rules for food of animal origin; check the requirements that apply to your source. Marine material from fish may trigger an allergen declaration under Regulation (EU) No 1169/2011; see labelling a food supplement. Any claim on the label must follow Regulation (EC) No 1924/2006 and the EU Register of nutrition and health claims. The health claims guide covers the rules.

Formulation notes

Chondroitin sulfate is hygroscopic. Keep containers closed between uses and handle it in low-humidity rooms. In tablets, moisture uptake can soften cores during storage, so a moisture-barrier coating is common.

Servings declared on joint products are usually several hundred milligrams. In capsules, fill volume then sets the capsule count per serving, so check bulk density on the specification sheet early. Shell choice matters for positioning: gelatin shells add a second animal source, while HPMC shells do not.

In tablets, chondroitin sulfate is often combined with MSM, hydrolyzed collagen or hyaluronic acid. High active loads leave little room for excipients, so granulated grades help. Test hardness and disintegration on the full blend.

The material dissolves in water, which suits sachets and drink powders. Assess taste and colour in the finished matrix, as both vary with source and lot.

Label-claim arithmetic uses the assay on the certificate of analysis:

  • Powder per serving = declared chondroitin sulfate ÷ assay (as a fraction).
  • If the assay is on a dried basis, correct for the loss on drying stated on the certificate.
  • Add any overage after this step; the overage calculator handles it.

The formula and molar mass in the identity table describe the substance generically. Chain length and sulfation vary by source, so the specification sheet, not the registry entry, defines the material you buy. More ingredients of this type are listed under Joint & Connective Tissue.

Questions from buyers

Is the molar mass in the data table the molecular weight of chondroitin sulfate?

No. Chondroitin sulfate is a polymer of variable chain length, so the registry formula and molar mass describe the substance generically. If an average molecular weight is specified for a grade, it appears on the specification sheet.

Can marine chondroitin sulfate replace bovine material in an existing formula?

Not without review. Sulfation pattern, molecular weight distribution, allergen labelling and source declarations can all change. Requalify the new material against its specification sheet and certificate of analysis and update the label before switching.

Reviewed by Atakan Cilingir, Technical Sales Manager, SoleChem Kimya A.Ş. · Updated October 2026