Sodium Hyaluronate Powder Bulk

Cross-linked Sodium Hyaluronate Powder | Cosmetic Grade

Product Name: Sodium Hyaluronate Crosspolymer 

Cross-linking Agent: 1,4-Butanediol Diglycidyl Ether (BDDE)

Residual BDDE: ≤ 2 ppm (Strictly Trace Controlled via GC-MS)

Physical Form: 100% Pure, Unswollen Dry Powder

Grade: Specialty Cosmetic Grade / Bioactive Topical Grade

Appearance: White or off-white, free-flowing powder

Certificates: BRCGS, IFS, COSMOS Approved, Halal, Kosher, ISO9001

Sample Support: 10g – 50g Free Sample Available for R&D

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  • Description Description
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  • What is Cross-linked Sodium Hyaluronate Powder?


    Cross-linked Sodium Hyaluronate Powder is a macromolecular polymer of sodium hyaluronate (CAS: 153831-98-2) modified via covalent chemical cross-linking of linear sodium hyaluronate chains....... This modification transforms the standard linear configuration into a three-dimensional reticular net matrix. Compared to linear hyaluronic acid, this cross-linked structure exhibits elevated enzymatic resistance against native hyaluronidase degradation, establishing a breathable, non-occlusive hydrophilic protective mesh over the stratum corneum to significantly reduce transepidermal water loss (TEWL).

    The active material is processed and supplied as a 100% pure, unswollen dry powder, minimizing formulation volume constraints, unexpected pH shifting, and preservative incompatibilities typically associated with pre-solubilized hydrogels. This stable solid matrix allows R&D formulators to achieve predictable viscosity and controlled rheological profiles in topical cosmetic delivery matrices.

    Manufactured and distributed globally under validated quality protocols by Technologie printemps vert, the bulk raw material is optimized for long-lasting daily hydrators, sun care formulations, and protective skin-barrier serums. The analytical profile ensures standard-compliant purity thresholds and compatibility with organic and vegan clean-beauty cosmetic matrices.


    spécification

    Nom du produit

    Sodium Hyaluronate Crosspolymer

    CAS non.153831-98-2

    Cross-linking Agent

    1,4-Butanediol Diglycidyl Ether (BDDE)

    Residual BDDE≤ 2 ppm (Validated via GC-MS / Headspace)
    Assay (on dry basis)≥ 95.0% (Glucuronic Acid Content ≥ 45.0%)
    Physical Form100% Pure, Unswollen Dry Powder
    apparenceWhite or off-white, free-flowing powder
    Swelling Degree≥ 50 g/g (Water absorption capacity)
    Transmittance≥ 99.0% (0.1% aqueous solution after full swelling)
    pH Value5.5 – 7.5 (0.1% aqueous solution after full swelling)
    Protein Residue≤ 0.1%
    Loss on Drying≤ 10.0%
    Heavy Metals≤ 10 ppm (Pb ≤ 2ppm, As ≤ 1ppm, Hg ≤ 0.1ppm, Cd ≤ 1ppm via ICP-MS)
    Pesticide ResiduesCompliant with Global Cosmetic Regulatory Standards (Not Detected)
    Microbiological ControlTotal Plate Count ≤ 100 cfu/g; Yeast & Mold ≤ 50 cfu/g; Salmonella/E.Coli: Negative


    Learn More About Our Comprehensive Solution for Compliant and Stable Hyaluronic Acid Ingredient.

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    Quality & Compliance


    Bio-Synthesized Safety Profiling: Manufactured utilizing pure, non-animal derived substrates, guaranteeing a 100% animal-free and Non-GMO functional polymer matrix with zero BSE/TSE risk.

    Validated Cross-Linking Controls: Processed under precisely monitored cross-linking thermal cycles to ensure the absolute structural stability of the 3D polymer mesh, preventing temperature-induced matrix degradation or early gel cleavage.

    Minimal Cytotoxicity Risk: Advanced industrial purification protocols limit residual cross-linking agents to BDDE ≤ 2 ppm via GC-MS, systematically mitigating skin irritation and topical sensitization across commercial compounding runs.

    Rigorous Endotoxin Limits: Engineered with a controlled, low bioburden and strict endotoxin threshold, satisfying the safety criteria required for premium post-procedure skin barrier topicals and medical-aesthetic matrices.

    Global Market Clearance: The manufacturing and quality management systems of Green Spring Technology are fully certified under BRCGS, IFS, Halal, Kosher, and ISO9001 protocols. This comprehensive compliance infrastructure guarantees full alignment with US MoCRA, EU Cosmetic Regulation (EC) No 1223/2009, and international COSMOS/Ecert clean beauty regulatory standards.


    Green Spring Technology Certificates


    Key Advantages


    • Reticular Polymerization Technology: Engineered via a precise chemical sequence that locks linear chains into a highly uniform three-dimensional (3D) net matrix, eliminating batch-to-batch structural variance and physical degradation.

    • Extended Enzymatic Breakdown Resistance: The dense cross-linked lattice provides documented resilience against native cutaneous hyaluronidase, establishing a long-lasting, continuous protective moisture barrier on the skin surface.

    • Additive-Free Formulation Freedom: Processed and delivered as a 100% pure, unswollen dry powder containing zero preservative interferences or carrier solvents, providing R&D formulators complete control over active loading and pH management.

    • Seamless Viscoelastic Customization: Rapidly expands into a smooth, non-gritty hydrogel polymer upon hydration, demonstrating stable compatibility across a specific pH range of 5.5 – 7.5 with standard cosmetic thickening matrices.

    • Optimized Supply Chain Economics: Supplying a pure dry powder variant significantly reduces overseas shipping weight and storage volume footprints compared to pre-solubilized hydrogels, lowering the total cost of ownership (TCO) for industrial procurement operations.


    Applications

    • Long-Lasting Barrier Repair Systems: Hydrates and incorporates into anti-aging night creams, protective salves, and dry skin balms, forming a continuous, stable moisture network that resists enzymatic wash-off and environmental stress factors.

    • Post-Procedure Skin Conditioning: Formulated for soothing post-treatment hydrogels, topical recovery serums, and sheet masks, providing validated high viscoelastic cushioning to protect vulnerable dermal surface barriers.

    • Rinse-Off Cleansing Matrices: Maintains stable skin retention and efficient matrix deposition within surfactant systems, including facial washes, body cleansers, and scalp care treatments, providing documented deep post-wash hydration.

    • High-Performance Sunscreen Frameworks: Enhances film uniformity and active ingredient suspension metrics in mineral sunscreens, daily UV defense lotions, and protective primers, preventing formula cracking and structural settling.

    • Hybrid Color Cosmetic Formulations: Suspends inorganic pigments uniformly in liquid foundations, tinting fluids, and long-wear lip glosses, significantly improving smooth bendability and preventing mid-day dry patch accentuation.



    Technical FAQ


    Q1: What is the optimal hydration protocol to prevent particle clumping and gritty micro-gel formation?

    A1: Disperse the unswollen dry powder in deionized water at 20°C to 30°C (68°F to 86°F) using a low-speed propeller agitator at 300 to 500 RPM for 30 minutes. Allow the matrix to static-hydrate for 2 to 4 hours to reach peak swelling degree (≥ 50 g/g). Slurrying the powder with a glycol wetting agent at a 1:3 ratio prior to water exposure eliminates texture grittiness and accelerates hydration kinetics.


    Q2: Will high-shear homogenization or vacuum emulsification equipment rupture the 3D reticular matrix?

    A2: Excessive mechanical shear permanently degrades viscoelastic properties. To maintain structural chain integrity, high-shear rotor-stator homogenization must be limited to ≤ 3,000 RPM for < 5 minutes at temperatures below 50°C (122°F). For commercial manufacturing, introduction of the pre-swollen hydrogel polymer during the post-emulsification cooling phase via low-shear anchor mixing (30 to 60 RPM) prevents physical degradation.


    Q3: How does the cross-linked three-dimensional lattice respond to high electrolyte concentrations?

    A3: This covalent lattice physically locks water molecules within its reticular cells, outperforming linear polymers under salt strain. In formulation matrices containing up to 1.5% electrolyte salts (e.g., Sodium PCA, Magnesium Sulfate), the cross-linked hydrogel retains over 85% of its initial storage modulus (G'), maintaining film uniformity and preventing phase separation or formula settling.


    Why Partner With Green Spring Technology?


    • Rheological Calibration Alignment: Technical support packages provide complete shear-thinning curves and storage modulus (G') data charts to ensure the polymer characteristics align precisely with commercial high-shear compounding tank parameters.

    • Batch-Fidelity Cross-linking Density: Advanced matrix purification protocols stabilize a highly uniform cross-linking degree across commercial scales, preventing unintended viscosity shifting during massive production line warm-ups.

    • Anti-Hydrolysis Ocean Transit Guard: Bulk shipments are managed under strict quality protocols utilizing a critically low water-activity index and vacuum-sealed desiccant layering, eliminating the risk of premature moisture swelling during trans-oceanic transit.

    • Industrial Foam-Free Dispersion Engineering: Optimized particle kinetics from Green Spring Technology allow the cross-linked powder to undergo rapid wetting without air entrainment, substantially cutting down vacuum-deaeration cycle times during commercial manufacturing.

    • Compounding Scale-Up Safety Support: Established in 2000, the 26-year advanced bio-synthesis experience of Green Spring Technology provides industrial manufacturing operations with direct technical consultation for large-scale hydration and viscosity stabilization troubleshooting.


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