Products

HyaSource® Care Sodium Hyaluronate Series

    • Product Name: HyaSource® Care Sodium Hyaluronate Series
    • Alias: hyasource-care-sodium-hyaluronate-series
    • Einecs: 231-791-2
    • Mininmum Order: 1 g
    • Factroy Site: Yudu County, Ganzhou, Jiangxi, China
    • Price Inquiry: admin@ascent-chem.com
    • Manufacturer: Ascent Petrochem Holdings Co., Limited
    • CONTACT NOW
    Specifications

    HS Code

    573180

    Product Name HyaSource® Care Sodium Hyaluronate Series
    Main Ingredient Sodium Hyaluronate
    Appearance White to off-white powder
    Molecular Weight Range Low, medium, and high molecular weights available
    Solubility Soluble in water
    Ph Value 5.0-8.0 (1% solution)
    Odor Odorless
    Application Area Cosmetics and personal care
    Functions Moisturizing, film-forming, skin conditioning
    Certifications ISO and GMP certified
    Storage Conditions Cool, dry place, protected from light
    Packaging Options Aluminum foil bags, fiber drums
    Shelf Life 24 months
    Origin China
    Brand FocusChem

    As an accredited HyaSource® Care Sodium Hyaluronate Series factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The **HyaSource® Care Sodium Hyaluronate Series** packaging features a white and blue box containing 100g sealed, moisture-proof foil pouches.
    Shipping Shipping for **HyaSource® Care Sodium Hyaluronate Series** is handled in compliance with industry safety standards. Products are securely packaged in sealed, airtight containers and shipped in temperature-controlled environments to maintain quality. Timely delivery and proper labeling ensure the chemical arrives safely and in optimal condition for pharmaceutical or cosmetic use.
    Storage HyaSource® Care Sodium Hyaluronate Series should be stored in a tightly sealed container, away from light, heat, and moisture. Store in a cool, dry place, ideally at 2–8°C. Avoid exposure to air and contaminants to preserve product stability and efficacy. Follow any additional manufacturer instructions for optimal storage and handling to maintain product integrity.
    Application of HyaSource® Care Sodium Hyaluronate Series

    Applications of HyaSource® Care Sodium Hyaluronate Series in Industrial Manufacturing

    As a direct manufacturer, we supply the HyaSource® Care Sodium Hyaluronate Series to major industrial sectors requiring precise moisture management and biocompatibility. Our material supports advanced formulation for global manufacturers in personal care, pharmaceuticals, medical devices, topical veterinary, wound management, and functional foods. The application details below reflect actual downstream usage in high-value markets, with attention to regulatory and process requirements.

    1. Skin Care and Personal Care Formulation

    Sodium hyaluronate is a staple for high-end moisturizers, serums, masks, and leave-on treatments. Our series offers molecular weights adapted for hydration modulation and sensory feel. Customers use our grade at critical points to establish film formation, water retention, and rapid absorption. This material supports stability in water-based emulsions and oil-in-water systems, integrating during the pre-cooling or final addition stage for batch uniformity verification. Typical products include intensive facial serums, premium lotions, and overnight creams targeting moisture retention and minimal irritation.

    Industry compliance standards

    • EU Cosmetics Regulation (EC) No 1223/2009
    • U.S. FDA OTC Monograph for Skin Protectants
    • ISO 22716 (Cosmetics GMP)
    • China National Standard GB/T 29665 (Cosmetics – Technical Specifications for Safety)

    Typical usage ratio

    • 0.05% – 1.0% by weight, depending on product viscosity, hydration level, and skin feel requirements. Higher molecular weight forms typically at 0.1%–0.3%; hydrolyzed/low-weight at up to 1% for daily dermal products.

    Downstream process integration

    • Dispersed in deionized water at 40–60°C under gentle agitation. Added during phase combination or as an end-phase cool-down component to prevent degradation. QC sampling aligns with viscosity and pH checks.

    Final product types

    • Moisturizing facial creams
    • Anti-aging serums
    • Sheet masks and hydrogel patches
    • Eye area treatments and lip balms

    2. Parenteral and Topical Pharmaceutical Dosage

    Pharmaceutical manufacturers deploy sodium hyaluronate for injectable viscosupplementation, ocular formulations, and topical pharmaceuticals. Our pharmaceutical grades support purity and endotoxin requirements necessary for integration in ophthalmic, intra-articular, and topical gel products. Material introduction typically occurs after sterile filtration or in closed-system aseptic blending to ensure integrity. The series provides support for sustained-release gels, artificial tears, and dermal wound gels.

    Industry compliance standards

    • USP-NF Monograph Sodium Hyaluronate
    • European Pharmacopoeia (Ph. Eur.) Monograph 1472
    • Japanese Pharmacopoeia (JP)
    • ICH Q7 GMP for Active Pharmaceutical Ingredients

    Typical usage ratio

    • 0.1% – 2.0% by weight; intra-articular injections up to 2.5% depending on molar mass and target rheology. Ocular drops typically at 0.1%–0.4%. Topical wound fillers at 0.2%–1%.

    Downstream process integration

    • Hydrated in WFI (Water for Injection) under aseptic conditions. Integrated post-sterilization filtration or in closed blending tanks. Final products packaged sterile. Endotoxin and bioburden control monitored throughout.

    Final product types

    • Pre-filled syringes for joint injection
    • Ophthalmic solutions and gels
    • Topical wound healing gels
    • Nasal irrigation solutions

    3. Wound Care and Advanced Dressing Materials

    Medical device companies employ sodium hyaluronate for hydrocolloid and hydrogel wound dressings, burn care sheets, and moist wound healing therapies. It acts as a non-cytotoxic moistening agent, delivering hydration at site-specific concentrations. Integration occurs via casting into cross-linked films, embedding in sponges, or pre-hydration into alginate sheets. The polymer’s biocompatibility assists in meeting clinical device criteria for non-irritancy and controlled exudate management.

    Industry compliance standards

    • ISO 10993-1 Biocompatibility Evaluation
    • FDA 21 CFR Part 820 (QSR for Medical Devices)
    • EU MDR 2017/745 Class IIb/III for Dressings
    • AAMI/ANSI/ISO 13485 Medical Devices QMS

    Typical usage ratio

    • 0.2% – 2% by weight within the formulated layer; ratio tailored to fluid absorption and substrate flexibility. Thicker dressings may use higher concentrations to enhance gelling and retention.

    Downstream process integration

    • Mixed with aqueous phase, optionally cross-linked with agents like calcium chloride. Applied prior to film casting, lyophilization, or freeze-drying. Final QC includes moisture content and sterile packaging.

    Final product types

    • Sterile hydrogel wound dressings
    • Hydrocolloid and foam dressings
    • Burn relief patches
    • Pressure ulcer treatment pads

    4. Veterinary Topicals and Injectable Solutions

    Veterinary pharmaceutical manufacturers rely on sodium hyaluronate for developing joint health injectables, dermatological gels, and eye care drops for companion animals. The raw material must comply with veterinary pharmacopeia standards and be suitable for animal biocompatibility. Material incorporation is batch-dependent and must maintain viscosity and clarity in the presence of other actives and preservatives. Processing includes sterile compounding and terminal filtration before filling.

    Industry compliance standards

    • Ph. Eur. and USP monographs
    • VICH GL9 (Good Manufacturing Practice for APIs in Veterinary Products)
    • FDA 21 CFR Part 514 (New Animal Drug Applications)
    • ISO 9001 for Veterinary Industry

    Typical usage ratio

    • 0.1% – 1.5%; intra-articular products often at 0.5%–1%. Ophthalmic animal drops typically at 0.1%–0.3%. Adjusted by species and anatomical site.

    Downstream process integration

    • Dispersed in sterile water, followed by pH adjustment and preservative addition if required. Added pre-filtration to ensure homogeneity. Filled under aseptic conditions into single- or multi-dose containers.

    Final product types

    • Equine joint injectables
    • Veterinary eye drops
    • Dermal gels for wound care in animals
    • Oral mucosa protectants for pets

    5. Oral Liquid and Solid Functional Food Supplements

    Health and nutrition brands utilize sodium hyaluronate in functional beverages, oral dispersible powders, and capsules targeting joint and skin health. Food-grade quality assures absence of contaminants and compliance with food additive regulations. Incorporation occurs in aqueous dissolutions for drinks or blending in powder premixes under low-moisture conditions. Usage varies according to labeling claims, serving sizes, and reduced calorie matrices, carefully avoiding residual taste or solubility issues in final formats.

    Industry compliance standards

    • GB 29924 (Chinese National Standard for Food Additives)
    • EU Regulation (EC) No 1333/2008 – Food additives
    • US FDA 21 CFR 184.1984 (Generally Recognized as Safe for direct food uses)
    • GFSI (Global Food Safety Initiative) benchmarked schemes

    Typical usage ratio

    • 10 mg – 200 mg per daily serving in solid dose; 0.01%–0.1% by weight in RTD beverages. Adjusted based on functional claim, solubility at ambient, and taste masking requirements.

    Downstream process integration

    • Dissolved in water for liquid fills prior to HTST/aseptic processing. Blended with maltodextrin or excipients for powder dosing. Segregated batching prevents humidity pickup. QC checks for purity and particle integrity.

    Final product types

    • Collagen booster drinks
    • Hyaluronic acid oral tablets
    • Granule sachets for direct consumption
    • Functional confectionery for skin hydration

    6. Contact Lens and Ocular Biopolymer Solutions

    Sodium hyaluronate is broadly implemented in the manufacture and packaging of contact lens storage, rinsing, and wetting solutions. Its viscoelasticity and film-generating properties assist in extending contact lens comfort and minimizing dryness on the ocular surface. Raw material integrates into isotonic buffered systems post-filtration. Pharma-grade QC ensures clarity, sterility, and ionic balance. Dosage and batch testing follow regional pharmacopoeia and medical device pre-market notification standards.

    Industry compliance standards

    • ISO 18369 (Contact lenses – Standard for solutions)
    • USP, Ph. Eur., and JP monographs relating to ophthalmic-grade excipients
    • 21 CFR 820 (Quality System Regulation for Medical Devices)
    • TGA (Australia) Conformity Assessment for Medical Devices

    Typical usage ratio

    • 0.05% – 0.3% in lens solutions; precise ratio determined by desired viscosity, lens material compatibility, and anti-adhesion requirements.

    Downstream process integration

    • Hydrated in sterile buffered saline under controlled agitation. Filtration through 0.2 μm prior to bottling. Final filling in aseptic lines with light-blocking packaging if required. Routine micro and physicochemical analysis for release.

    Final product types

    • Multipurpose contact lens solutions
    • Daily lens wetting drops
    • Lens cleaning and soaking fluids
    • Ophthalmic lubricating drops

    Free Quote

    Competitive HyaSource® Care Sodium Hyaluronate Series prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please contact us at +8615365186327 or mail to admin@ascent-chem.com.

    We will respond to you as soon as possible.

    Tel: +8615365186327

    Email: admin@ascent-chem.com

    Get Free Quote of Ascent Petrochem Holdings Co., Limited

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    Discovering the HyaSource® Care Sodium Hyaluronate Series: A Transparent Manufacturer’s Perspective

    Introduction: Genuine Manufacturing Insights

    Our work with sodium hyaluronate runs deep, going back decades in the chemical manufacturing space. We’ve seen customer needs shift and technology march forward, but one thing stays constant: end users rely on consistent, safe, and high-quality material. The HyaSource® Care Sodium Hyaluronate Series has grown directly from our daily manufacturing practices, ongoing R&D, and quality audits. As the actual maker—processing raw materials, running reactors, performing filtration and purification, and guiding every lot through its journey from wet synthesis to finished powder—our team sees every detail. Practical considerations at every treatment, filtration, and drying step shape the substance’s structure. We’ll share why this matters, how small differences shift application results, and why the HyaSource® Care series reflects our experience.

    HyaSource® Care’s Formula: What Consistency Really Means

    Sodium hyaluronate isn’t just an ingredient on a label. We choose fermentation strains, confirm water quality, and control temperature and pH every hour. Our base specification covers a range of molecular weights but each model in the HyaSource® Care line has a targeted window, driven by end use—cosmetic serums that aim for quick moisture without stickiness, viscoelastic components used in injectables, and long-lasting textures for leave-on treatments. Our process chemistry team tunes the fermentation and downstream purification to match each application’s requirements. Real experience tells us that environmental factors, batch sizes, and purification speed all influence results. The powder’s flow, solubility, visual clarity, and even how cleanly it rehydrates when mixed—these visible and tactile details trace back to our plant floor.

    Importance of Molecular Weight: Beyond Brochure Claims

    Discussing sodium hyaluronate means talking about molecular weight, since this property directly shapes each product’s feel, absorption, and final look, whether in a hydrogel mask, eye drop, or topical lotion. We make sure each HyaSource® Care grade lands comfortably within the promised range thanks to in-house GPC and viscosimetry. Higher molecular weights bring a more robust and slightly tacky touch—best for forming lasting films, moisture shields, or consistency boosters. Lower molecular weights spread rapidly and absorb better, suitable when thin, non-greasy formulations are prioritized. Some customers expect a powder that dissolves instantly; others focus on elastic texture after hydration. Our regular audits and field feedback point out that quick-dissolving, impurity-free hyaluronate, without dustiness or off-smells, comes directly from neat, well-controlled production equipment. Cosmetic developers and clinical trial partners have stressed, during visits and reviews, that predictable hydration, clarity, and viscosity mean fewer failed batches for them and more stable long-term results for their brands.

    Product Models: Practical Differences

    The HyaSource® Care Sodium Hyaluronate Series spans several defined models, with molecular weight as the primary distinction because it carries practical effects. Our High Molecular Weight (HMW, usually above 1,000 kDa) grades work well for forming an occlusive, flexible film on skin or mucosal surfaces. These batches demand longer fermentation and a careful balance of crosslink inhibitors during the process, and yield powders that hydrate into elastic gels. Middle Molecular Weight (MMW, typically 500–1,000 kDa) suits leave-on lotions, facial creams, and medical lubricants, with enough viscosity to thicken but not enough to create a sticky residue. Low Molecular Weight (LMW, commonly ranging from 10–300 kDa) dissolves much faster in cold water and blends into aqueous serums or topical injectables where enhanced skin penetration matters.

    Many formulators ask whether the series covers both cosmetic and medical grades. Our stack of batch records and end use feedback has shown that medical device partners need certified purity: low bacterial endotoxin, clear transmission, zero excipients. Cosmetic manufacturers might focus more on immediate texture or sensory testing, and pricing often shifts based on purity. HyaSource® Care's production line operates under ISO certifications, and each lot passes a battery of trace comingled tests, not only for molecular weight but for protein and nucleic acid contaminants. We frequently verify each spec—microbial purity, threshold for heavy metals, and visual clarity—since regulators, customers, and our own team walk the same shop floor.

    Specifications and Batch Results: The Line Between Routine and Excellence

    Numbers on paper tell only part of the story. A sodium hyaluronate batch should never carry odors, sticky clumps, or over-dried flakes. We evaluate each HyaSource® Care lot for bulk powder color, particle size distribution, density, and speed of hydration in controlled lab and bench trials. Particle size, ranged from ultra-fine for serums to macro-format granules for sheet masks, makes a difference in production speeds and finished product look. Occasionally, technical partners request tighter variance around moisture content or want the powder to behave a certain way in automated dispensing. We adjust our dryers, change sieve mesh, or slow down the blending cycle, because real machines and operator hands, not just test tubes, set our internal standards. This type of physical check—hand-mixing, filming, and rehydration testing—reflects habits built through years of chemical manufacturing.

    Each model in HyaSource® Care carries COA-backed results. Purity checks go beyond national standards, catching issues like pyrogen, protein, or multimer contaminants before the powder ever leaves the warehouse. Surface chemistry and trace residuals, critical in medical and injectable uses, depend not just on raw material choice but on line maintenance, cleaning protocols, and filter integrity. End-users who experience issues—unexpected color, dust, or slow hydration—rely on our willingness to review the full production batch, not just a supply invoice.

    End Use and Application: Customer Results Matter

    The true test for any batch is in use. R&D teams, cosmetic manufacturers, and device companies report their results after launching with HyaSource® Care. For hydrating sheet masks and serums, low- to middle-range MW grades give a light, refreshing texture, while HMW versions help create creamier, richer treatments. Hyaluronate’s rehydrated texture can show beads, lumps, or full transparency, depending on the lot and mixing process. Our shop floor team often hears when a batch “just works”—dissolving without residue, holding water in a finished product, performing well under consumer trials. These details land directly as feedback. Cosmetic chemists share concerns about sensitivity, skin feel, and stability. Medical device partners focus instead on absence of irritants, regulatory compliance, and sterilizability. These differences don’t come from a catalog; they come from directly listening to people who use each product and from our own in-house product trials.

    Some partners have developed their own use-cases distinct from industry norms. For example, a specialty wound care manufacturer needed a powder that could hydrate extremely rapidly in sterile conditions, without introducing foaming or off-tastes when mixed into a carrier gel. We modified dehydration stages, double-filtered the solution, and validated dust content batch by batch. In another case, a mask manufacturer required granular material that poured consistently on automated lines, while still hitting cost and purity needs. Each adjustment involved direct involvement on the shop floor, not abstract R&D proposals or templated protocols.

    Transparency in Sourcing and Traceability

    Customers in both medical and cosmetic fields expect raw material integrity. We open our factory to audits and maintain digital records, including all fermentation, purification, and drying steps. We regularly walk clients through traceability chains, showing how each raw input, fermentation culture, purification resin, and storage container is logged and reconciled. Some market shifts—such as customer concerns about regional origin or biofermentation versus animal-based sources—led us to tighten controls further. Our procurement and quality control teams check each input for consistent microbial profile, solvent residue levels, and batch-specific risk. In-house technicians connect COA and batch numbers to every lot. Every HyaSource® Care grade is made, stored, and tracked in a controlled-access area, and the team ensures the supply remains consistent through direct oversight rather than distant broker chains. Years of manufacturing sodium hyaluronate mean we stay a step ahead on transparency and traceability.

    Sustainability, Process Controls, and Operational Efficiency

    Environmental and sustainability concerns are growing across industries. Our team approaches waste reduction and green chemistry not as slogans but as plant-floor challenges: minimizing solvent use, reducing wastewater load, and recycling fermentation media where feasible. Drying and filtration steps use heat recovery and, when process permits, closed-loop air systems. By focusing on consistent fermentation yields for sodium hyaluronate, we keep raw waste low and spend more energy on purifying each lot instead of fixing defects after the fact. Powder packaging options, requested by customers for single-use or bulk transfer, continue to evolve based on recyclability. Next-generation projects target biodegradable packaging and reduced process carbon footprint. Each improvement follows direct feedback from our operators and technical team, not just a published goal; we believe sustainability must make our plant safer and more efficient before it makes its way into marketing or compliance reporting.

    Meeting Regulatory and Market Demands: Compliance Driven by Experience

    As regulators tighten controls, particularly for pharmaceutical and medical-use hyaluronate, our quality and documentation standards have evolved. Our QMS has faced dozens of site inspections, each bringing new learning and tighter recordkeeping habits. Cosmetic end users pay close attention to allergen, fragrance, and preservative residue risks, so every HyaSource® Care batch undergoes final rinse water monitoring and allergen risk assessment. New regulation in some regions now requires lot-level reporting on origin of raw material, full production timelines, and shipping records. Auditors often ask about training, routine maintenance logs, and incident reports—issues only manufacturers can answer confidently. We welcome these checks, since real batch-level history helps prevent even minor inconsistencies from reaching the customer. Where we see problems—occasional appearance issues, variable pour rate, or even rare foreign matter findings—we trace the issue back to the shift, machine, or filter that caused it, and adjust procedures at the root. This depth of compliance comes from long-time plant operators who understand both the science and the value of discipline.

    How HyaSource® Care Compares to Other Hyaluronate Grades

    Market comparisons often reduce sodium hyaluronate to cost per kilogram or published specification sheets. Our experience shows that the less visible details—flowability, absence of odor, particle size uniformity, predictable hydration—make the difference once the powder is in use. We see generic or broker-handled material fall short, drying into lumpy or discolored powder, or suffering during shipping because insufficient care went into final finish or packing. These details matter more than the published molecular weight average. HyaSource® Care maintains its clarity, structure, and shelf stability throughout logistics challenges; small but frequent differences in manufacturing input translate into a noticeable gain in product appeal and trust from customers. We know some supply chains obscure origin or blend multiple lots; our families and staff have stood behind every finished kilo, and that accountability flows directly to our customers.

    HyaSource® Care doesn’t rely on broker-accessible pools or re-labeled product. Each model sits in clean-room managed zones with batch numbers, logged operator inputs, and site-level controls, so every single drum or pack retains that original identity. Many downstream users come back not just for a molecular weight number but for the security of knowing what went into the raw material—because failed batches or recalls cost far more than slight savings. No one on our shop floor wants to send a batch out without knowing it will help improve finished goods, not cause another round of troubleshooting.

    Solving Problems: Real-World Scenarios

    Developers in personal care, medical devices, and specialty foods often face the hard reality that sodium hyaluronate is not a generic commodity. A Japanese dermal filler brand experienced repeated gel consistency failure with untraceable sources. After switching to HyaSource® Care, and multiple plant visits later, their process stabilized with clearer gel, predictable batch-to-batch flow, and fewer viscosity complaints—or, put more simply, less downtime and recall risk. A European allergy skin care brand needed assurance of no animal origin and zero environmental cross-contaminants. They audited our fermentation tanks, checked strain records, and ran their own random COA checks, which convinced their QA that trust comes from clear process transparency. In every case, we found that solving problems requires more than a spec sheet; it involves plant-level dialogue, hands-on trials, and true willingness to trace anything back to source.

    Food technologists, especially in functional beverages or oral supplements, bring a special set of concerns—taste masking, dispersibility, lack of off-flavores, and food safety require manufacturers to understand how sodium hyaluronate interacts with heat, acid, and storage conditions. Some test batches failed on taste, with “plastic” notes or cloudiness when using lower grade supply. HyaSource® Care’s food grade goes through additional polishing and enzymatic treatment to keep neutral flavor and optically clear solutions, as proven in multiple RTM (ready-to-mix) beverage launches. We welcome food partners to bring their toughest challenges to the plant so we can adapt steps or blend configurations directly on the shop floor. This flexibility arises from manufacturer-level control; no remote party can replicate the level of process adjustment that insider experience delivers.

    Continuous Improvement and Customer Partnership

    Long-term relationships build not from contracts but from working through problems together. Our own staff have accompanied customers through high-speed mask production runs, pilot plant scale-ups, and clinical trial batches. Every comment, complaint, or test result lands on the desk of our plant and quality teams. Sometimes improvements mean as little as changing sieve mesh, altering batch cooling rates, or modifying packaging film permeability to retain shelf moisture content. At other times, it calls for more investment—automation, robotics-assisted filling, electronic batch tracking.

    We keep internal records of every success and every failure, and our goal is to always convert critical feedback into changes at the plant. As one of our veteran operators says, “hyaluronate is simple on paper but shows its true quality only in use.” That’s why we keep listening, keep testing, and keep evolving. Customers build trust not just in a name, but in the lived reliability that comes from repeated batches delivering what’s promised with no excuses.

    Conclusion: Manufacturing with Integrity, Not Just Production

    Producing sodium hyaluronate for today’s advanced personal care and medical-focused industries means living up to high expectations every day. The HyaSource® Care Series is more than a label; it reflects the care, oversight, and pride our entire team puts into every lot. Experience shows that no amount of paperwork or marketing can substitute for production integrity—the discipline in clean work areas, meticulous record-keeping, and shared pride among plant staff and management. Customers who have visited our facility see a team invested in delivering real value, not chasing short-term volume.

    By staying close to our process and keeping open lines with partners in every industry we serve, we continue driving quality and reliability for the HyaSource® Care Sodium Hyaluronate Series. We welcome those seeking more than commodity supply—those who want a genuine partner on the manufacturing side, with the experience and transparency to back every gram—because our success lasts only as long as our customers’ products shine.

    Top