NewHa+® crosslinked HA is available in a cosmetic-grade powder and an injection-grade gel. Each form has its own specification, quality profile and intended development route.
NewHa+® Crosslinked Sodium Hyaluronate is a crosslinked HA product family. Buyers may also encounter the names Crosslinked Hyaluronic Acid, Crosslinked HA and Sodium Hyaluronate Crosspolymer. The gel form may be described as a crosslinked hyaluronic acid hydrogel.
The powder is a dry raw material for topical cosmetic formulation work. The gel is a prepared viscous system for evaluation by qualified organizations developing regulated injectable products. They are not same: each form has its own specification, COA and technical approval route.
| 项目 | 详情 |
| Product family | NewHa+® Crosslinked Sodium Hyaluronate |
| Page reference | CAS 105524-32-1 |
| Available forms | Cosmetic-grade powder; injection-grade gel |
| Powder appearance | White or off-white powder or fibrous particles |
| Gel appearance | Transparent or semi-transparent viscous colloid without visible foreign matter |
| Powder content | 95.0%–105.0% on the dried substance |
| Powder molecular weight | Reported result: >3.0 × 10⁶ Da |
| Gel pH | 6.5–7.5 |
| Gel dynamic viscosity | 45,000–120,000 mPa·s |
| Documents | Separate reference COAs for powder and gel; request current documents for the selected grade |
| MOQ and lead time | 已根据当前报价确认 |
| Grade and form | Key characteristics | Typical selection context | Main technical focus |
| Cosmetic-grade powder | White or off-white powder or fibrous particles; content and molecular-weight reporting on the powder specification | Topical cosmetic formulation development, including water-rich and emulsion systems | Dispersion, hydration, clarity, pH, viscosity, preservative compatibility and finished-formula stability |
| Injection-grade gel | Transparent or semi-transparent viscous colloid; defined particle-size, rheology, extrusion, sterility and endotoxin criteria | Regulated injectable-gel research, product development and quality evaluation by qualified organizations | Rheology, particle-size distribution, extrusion behavior, degradation, sterility, endotoxin and packaging compatibility |
The powder and gel are not alternative packaging formats for the same grade. Choose by application and form first, then compare the relevant content, molecular-weight, rheology, particle-size and microbiological criteria.
The powder grade is a dry Crosslinked Sodium Hyaluronate raw material for cosmetic formulation work. Its reference COA covers identity, solution appearance, pH, content, molecular-weight reporting and microbiological quality.
The table separates the acceptance criteria shown on the reference COA from its reported batch result.
| Test item | Reference acceptance criterion | Reference batch result |
|---|---|---|
| 外观 | White or off-white powder or fibrous particles | 符合 |
| Glucuronic acid reaction | Purple-red reaction under the stated identification procedure | 符合 |
| 溶液外观 | 透明；A600 nm ≤0.01 | Clear; A600 nm = 0.001 |
| pH | 5.5–8.0 in a 0.5% solution | 7.6 |
| Light transmittance | Clear; T550 nm ≥99.0% | 99.6% |
| Burning residue | ≤18.0% | 17.1% |
| 干燥损失 | ≤15.0% | 11.7% |
| 蛋白质含量 | ≤0.1% | <0.05% |
| Bacterial endotoxins | <0.5 IU/mg | <0.5 IU/mg |
精华液和精华
The powder grade can be assessed in water-rich serums and essences that use Sodium Hyaluronate Crosspolymer as a humectant and skin-conditioning ingredient. Establish a suitable dispersion process, then assess clarity, pH, viscosity and preservative compatibility before scale-up.
Gels and Mask Essences
Crosslinked HA powder can be considered for gels and mask essences where formula texture is part of the development target. Assess uniform dispersion, final viscosity, microbial control and package stability.
面霜和乳液
In emulsions, the powder grade may be introduced through an aqueous-phase process established for the finished formula. Assess compatibility with emulsifiers, electrolytes, preservatives and other polymers, then verify viscosity and stability before scale-up.
The gel grade is a transparent or semi-transparent viscous colloid with defined osmotic pressure, particle-size, rheology, extrusion, residue, sterility and endotoxin criteria.
It is intended for evaluation by qualified organizations developing regulated injectable products. The grade and its COA do not by themselves establish finished-device approval or market authorization.
| Test item | Reference acceptance criterion | Reference batch result |
| 外观 | Transparent or semi-transparent viscous colloid without visible foreign matter | 符合 |
| Effective usage amount | 90%–120% of the labeled amount | 111% |
| 鉴别 | Meets the stated requirements | 符合 |
| UV absorption at 260 nm | ≤1.0 | 0.24 |
| UV absorption at 280 nm | ≤1.0 | 0.19 |
| pH | 6.5–7.5 | 7.2 |
| Osmotic pressure | 270–350 mOsmol/kg | 334 mOsmol/kg |
| Heavy metal content | ≤5 μg/g | 符合 |
A reference COA shows the available test profile and one batch result. Commercial qualification should use the current specification and the lot-specific COA for the applicable powder or gel batch.
| 文档 | 可用性 |
|---|---|
| Powder reference COA | Available for the cosmetic-grade powder |
| Gel reference COA | Available for the injection-grade gel |
| Current product specification or TDS | Request for the selected form and grade |
| 每批次专属的合格证书 | Request for the applicable commercial batch |
| Additional quality or destination-market documents | Include the country and required document scope in the enquiry |
1.改善皮肤屏障
2.减少角质层的水分流失
3.抗紫外线侵入
4.保持数倍的水分
5.形成牢固的表面保护膜
6.透明质酸是人体内天然存在的物质，因此非常安全。它可以被人体完全吸收和代谢。交联透明质酸钠凝胶具有良好的生物相容性，具有抗透明质酸酶降解的能力，从而使透明质酸能够在体内长期存在，稳定地发挥其独特的物理和化学特性。.
7.交联透明质酸钠凝胶具有良好的支撑力、粘度和弹性，不易扩散和移位。因此，它具有良好的填充和塑形效果，而且塑形持续时间长。.
8.新陈代谢的速度是均匀的。吸收速度与每个人皮肤的饱满度和紧致度有关。.
100克/瓶、500克/瓶、1公斤/瓶。
Standard pack size, alternative packaging, sample quantity, MOQ and lead time are confirmed with the current quotation.
These terms may differ between the powder and gel because the two forms have different handling, packaging and project requirements.
No. The cosmetic-grade powder is intended for topical formulation work, while the injection-grade gel follows a separate specification and development route. Each form has its own COA.
No. It is a raw-material gel for regulated product development.
Yes. Renew can compare the requested limit and test method with the available powder or gel specification. Include the intended application in your enquiry.
Yes. Request the cosmetic-grade powder, injection-grade gel or both. Sample quantity and availability are confirmed by grade; include the intended application and destination country.
MOQ, sample quantity and lead time are confirmed with the current quotation.
Provide the required form, target specification, estimated quantity, application, destination country, packaging request and document list. Renew will confirm the applicable grade, sample status and commercial terms.
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