Sodium Hyaluronate Ingredient
Sodium Hyaluronate Supplier | Ingredient for Supplement Formulation
Sodium Hyaluronate is the sodium salt of hyaluronic acid. For supplement formulations, the choice of grade is closely tied to molecular weight, dosage form and the way the ingredient behaves during processing.
Product Information
Sodium Hyaluronate at a Glance
The core identity and supplied product form.
Considérations relatives à la formulation
Molecular Weight Is a Key Sodium Hyaluronate Specification
Molecular weight is one of the main parameters used to distinguish Sodium Hyaluronate grades. It can influence viscosity and solution behavior, so the selected grade should fit the finished product and its processing conditions.
In Powder Formulas
For capsules, tablets and dry blends, the specification needs to work with the powder-handling requirements of the formula, including moisture and bulk-density considerations.
In Reconstituted or Liquid Systems
For products that are dissolved or reconstituted, viscosity, pH and solution appearance become more relevant during formulation trials.
Applications
Sodium Hyaluronate for Supplement Formulation
Sodium Hyaluronate is used in supplement concepts across solid and liquid formats, with the product format shaping how the ingredient is incorporated into the finished formula.
Santé des articulations
Used in joint-support supplement concepts and combination formulas designed around ingredients such as collagen, glucosamine or chondroitin.
La beauté de l'intérieur
Used in oral beauty formulas where Sodium Hyaluronate is selected as part of a skin-focused ingredient system.
Capsules et comprimés
Used in capsule and tablet formulas where Sodium Hyaluronate is incorporated with the other selected actives and excipients.
Powders & Drinks
Used in powder and beverage concepts where the ingredient is incorporated directly or dissolved during formulation.
Certificate of Analysis
Sodium Hyaluronate Specification
The table below records the specification and test results for the supplied batch.
| Test Item | Standard | Spécifications | Result |
|---|---|---|---|
| Apparence | QB/T 4576-2023 | White or almost white powder or granular | Qualifié |
| Hyaluronate de sodium | QB/T 4576-2023 | ≥92.0% | 93.08% |
| Glucuronic Acid | QB/T 4416-2012 | ≥43.5% | 45.02% |
| Poids moléculaire | QB/T 4416-2012 | Measured Value | 1.048 × 106 Da |
| pH (0.1%) | QB/T 4576-2023 | 6.0–8.0 | 7.10 |
| Perte au séchage | QB/T 4576-2023 | ≤10,01 TP3T | 8.0% |
| Résidus à l'allumage | QB/T 4576-2023 | ≤13.0% | 9.25% |
| Protéines | EP10.0 | ≤0.30% | 0.168% |
| Transmittance (0.1%) | QBT 4416-2012 | ≥99.0% | 99.9% |
| Densité en vrac | CP 2020 | Measured Value | 0.30 g/ml |
| Sulphate | WS1-(X072) 2011Z | ≤0.02 | <0.02 |
| Total Arsenic (as As) | QB/T 4576-2023 | ≤0.3 mg/kg | <0.3 mg/kg |
| Heavy Metal (as Pb) | QB/T 4576-2023 | ≤0.5 mg/kg | <0.5 mg/kg |
| Hg | T-SNHFA011-2021 | ≤ 0,1 mg/kg | <0.1 mg/kg |
| Cd | T-SNHFA011-2021 | ≤0.5 mg/kg | <0.5 mg/kg |
| Total Plate Counts | QB/T 4576-2023 | ≤ 100 UFC/g | < 100 UFC/g |
| Molds & Yeasts | QB/T 4576-2023 | ≤ 50 UFC/g | <50 CFU/g |
| Staphylococcus Aureus | T-SNHFA011-2021 | Négatif | Négatif |
| Pseudomonas Aeruginosa | QB/T 4416-2012 | Négatif | Négatif |
| Coli Group | QB/T 4576-2023 | Négatif | Négatif |
The certificate concludes that the batch complies with the stated internal control standard.
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