| Product Name | Sodium Hyaluronate |
| Chemical Formula | (C14H20NNaO11)n |
| Chemical Structure |
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| CAS No. | 9067-32-7 |
| Appearance | White, fine powder |
| Assay | ≥99.5% |
| Solubility | Soluble in water |
| Heavy metals | ≤10ppm |
| Protein | ≤0.1% |
| Bacterial endotoxins | ≤0.5IU/mg |
| Source | Microbial fermentation |
Produced using advanced microbial fermentation technology, resulting in high purity and low impurities, meeting the stringent standards for ophthalmic product raw materials.
Can absorb a large amount of water, forming a long-lasting moisturizing layer on the ocular surface and reducing tear evaporation.
The unique viscoelasticity of sodium hyaluronate improves ocular surface lubrication, relieving dryness, foreign body sensation, and fatigue.
As a naturally occurring polysaccharide in the human body, sodium hyaluronate exhibits good safety and tolerability.
Supports various small packaging sizes, suitable for laboratory research and development, formulation testing, and small-scale production.
Manufactured and quality-controlled according to pharmaceutical-grade standards. The production environment and testing processes are strictly regulated, meeting the high requirements for raw material quality and safety in pharmaceutical and ophthalmic products, providing a reliable guarantee for related formulation development.
Advanced purification processes effectively control impurity levels, resulting in a low endotoxin and protein residue content, further enhancing its safety and biocompatibility. Suitable for ophthalmic formulations with high purity requirements.
Precise molecular weight control during production ensures sodium hyaluronate maintains a stable molecular weight range and good viscosity, contributing to improved formulation stability and product performance.
Exhibits excellent water solubility, rapidly dissolving in aqueous systems to form a homogeneous solution. It also demonstrates good stability in formulation systems, facilitating its application in various ophthalmic formulations.
Different packaging specifications can be provided according to customer needs to meet various usage scenarios, including R&D, pilot-scale testing, and large-scale production, improving ease of use and transportation safety.
Our Sodium Hyaluronate is produced through advanced microbial fermentation technology, ensuring high purity, low impurities, and excellent safety.
Yes, the product is manufactured and quality-controlled in strict compliance with pharmaceutical-grade quality standards, making it highly reliable for pharmaceutical and ophthalmic formulation development.
Our purification process maintains extremely low impurity levels: bacterial endotoxins are controlled at ≤0.5IU/mg, and protein content is ≤0.1%.
It exhibits excellent water solubility, dissolving rapidly in aqueous systems to form a highly homogeneous and stable solution.
Yes, we support flexible packaging sizes tailored to various application needs, including laboratory research and development (R&D), pilot-scale testing, and large-scale manufacturing.