Buy High Purity Injection Grade Sodium Hyaluronate Powder pH 6.0-7.5 Manufacturer, Suppliers

Injectable grade sodium hyaluronate is produced using advanced microbial fermentation technology and undergoes multiple purification processes, resulting in ultra-high purity, excellent biocompatibility, and strict control over endotoxin and impurity content. Its pH value remains stable within the physiological range of 6.0–7.5, which helps improve product stability and good compatibility with human tissues, thereby reducing irritation and ensuring safety for clinical use.

Product Description

Product Specification
Product Name Sodium Hyaluronate
Chemical Formula (C14H20NNaO11)n
Chemical Structure Sodium Hyaluronate Chemical Structure
CAS No. 9067-32-7
Appearance White, fine powder
Assay 95.0%~105.0%
Solubility Soluble in water
Heavy metals ≤10ppm
Protein ≤0.1%
Bacterial endotoxins ≤0.05IU/mg
Source Microbial fermentation
Our Advantages
Ten Years of Focus
We have focused on supplying injectable-grade sodium hyaluronate raw materials for many years, accumulating mature production experience and industry understanding, enabling us to better meet the needs of medical aesthetics, ophthalmology, and joint applications.
High Quality and Stability
We have established a strict quality control system. Each batch of products undergoes multiple tests to ensure high purity and strong stability, meeting injectable application standards.
Flexible Samples and Packaging
We support small-scale testing and multiple packaging specifications, and can provide customized solutions according to customer needs, facilitating R&D and practical application.
Certifications and Qualifications
We have passed international certifications such as ISO and GMP. Our production and management meet pharmaceutical-grade standards, with complete documentation and traceable quality.
Global Export Experience
We possess extensive experience in export and customs clearance, are familiar with the requirements of various countries, and have stable logistics channels to ensure efficient and safe delivery.
Client Case
Client Background & Challenges
Our client is a company specializing in the development of injectable cosmetic products, primarily including mesotherapy and dermal fillers. During product development and registration, the client had stringent requirements for sodium hyaluronate raw materials, particularly regarding safety and stability. However, in the initial supplier collaborations, the client encountered significant problems: high endotoxin levels in the raw materials, making it difficult to meet injectable-grade standards; significant quality fluctuations between different batches, affecting formulation stability; and the supplier's inability to provide complete and standardized quality documentation, hindering the registration process. These issues directly impacted product development progress and market launch plans.
Our Solution
To address the client's high standards for injectable applications, we provided high-purity injectable-grade sodium hyaluronate raw materials, focusing on controlling endotoxin levels and microbial indicators to ensure the product met stringent safety requirements. Simultaneously, by optimizing the fermentation and purification processes, we achieved stable control of molecular weight distribution, ensuring consistency between batches. Furthermore, based on the client's specific formulation needs, we provided customizable molecular weight ranges and related technical parameters, along with complete quality documentation, including Certificate of Analysis (COA), endotoxin test reports, and microbial limit data, thus comprehensively supporting the client's R&D and compliance application efforts.
Results & Client Feedback
After adopting our raw materials, the client successfully completed internal quality validation, significantly improved formulation stability, and effectively controlled batch-to-batch variations. Simultaneously, comprehensive technical documentation greatly enhanced the completeness of registration materials, accelerating the product filing and approval process. The client reported that their end products met expected standards in terms of safety and user experience, and highly praised the consistency and reliable supply of raw materials. This has led to the establishment of a long-term and stable cooperative relationship between the two parties.
Frequently Asked Questions
Q1: What is the source of your Sodium Hyaluronate raw material?
Our Sodium Hyaluronate is produced through microbial fermentation, ensuring high purity, consistent quality, and safety suitable for pharmaceutical and injectable-grade applications.
Q2: How do you ensure the product is safe for injectable applications?
We strictly control critical safety parameters, keeping bacterial endotoxins at ≤0.05IU/mg, heavy metals at ≤10ppm, and protein levels at ≤0.1% to fully comply with injectable-grade requirements.
Q3: Can you provide customized molecular weight ranges?
Yes, we can provide customizable molecular weight ranges and technical parameters tailored to your specific formulation and development needs.
Q4: What standard certifications do you hold?
Our production processes and management systems comply with pharmaceutical-grade standards and hold international certifications such as ISO and GMP, ensuring complete quality traceability.
Q5: What documentation is provided with the product?
We supply comprehensive documentation with our products, including Certificates of Analysis (COA), endotoxin test reports, and microbial limit data, to facilitate your R&D and registration processes.
Q6: Do you support testing samples and flexible packaging?
Yes, we support small-scale testing by providing samples and offer multiple packaging specifications to fit different stages of your formulation R&D and production.

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