Hyaluronate sodium - ≥95%, wt30,000-50,000 , CAS No.9067-32-7

CAS: 9067-32-7 Cat. No.: H758875 Formula: (C14H21NaNO11)n   Numero EC: 618-620-0
Disponibile su ordine
GRADE & PURITY ≥95% wt30,000-50,000
Synonyms
Sodium hyaluronate
Storage
Store at -20°C,Argon charged
Shipped In
Ice chest + Ice pads
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Size
Germania (EU)
USA*
Price
Qty
5mg
H758875-5mg
Su ordinazione · 8–12 settimane
121,40€
25mg
H758875-25mg
Su ordinazione · 8–12 settimane
468,49€
Enter a quantity for the sizes you want to add.
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Why this grade

≥95%, wt30,000-50,000 for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at -20°C,Argon charged Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 174 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Panoramica

Hyaluronic acid was partially degraded by hyaluronidase and separated by gel filtration HPLC. Hyaluronic acid oligosaccharides with different degrees of polymerization (DP4-20) and low molecular components with DP>20 were prepared.

Specifications

Sinonimi
Sodium hyaluronate
Specifiche e purezza
≥95%, wt30,000-50,000
Condizioni di conservazione di stoccaggio
Store at -20°C,Argon charged
Spedito in
Ice chest + Ice pads
Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.
Purezza
≥95%
Nomi e identificatori
Sorrisi canoniciCC(=O)NC1CC(C(OC1OC2C(C(C(OC2C(=O)[O-])O)O)O)CO)O.[Na+]
InChIKeyMAKUBRYLFHZREJ-JWBQXVCJSA-M
INCHI1S/C14H23NO11.Na/c1-4(17)15-5-2-6(18)7(3-16)24-14(5)26-10-8(19)9(20)13(23)25-11(10)12(21)22;/h5-11,13-14,16,18-20,23H,2-3H2,1H3,(H,15,17)(H,21,22);/q;+1/p-1/t5-,6+,7-,8-,9-,10+,11+,13-,14+;/m1./s1
Isomeri SMILES CC(=O)N[C@@H]1C[C@@H]([C@H](O[C@H]1O[C@H]2[C@@H]([C@H]([C@@H](O[C@@H]2C(=O)[O-])O)O)O)CO)O.[Na+]
WGK Germania 3
RTECS MT7250000

Documentazione

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic oxygen compounds
ClasseOrganooxygen compounds
SubclassCarbohydrates and carbohydrate conjugates
Intermediate Tree Nodes Sugar acids and derivatives
Direct ParentGlucuronic acid derivatives
Alternative Parents Disaccharides  Oxanes  Pyrans  Acetamides  Secondary alcohols  Carboxylic acid salts  Secondary carboxylic acid amides  Hemiacetals  Polyols  Acetals  Oxacyclic compounds  Carboxylic acids  Monocarboxylic acids and derivatives  Hydrocarbon derivatives  Organic oxides  Organic sodium salts  Organic zwitterions  Organonitrogen compounds  Carbonyl compounds  Organopnictogen compounds  Primary alcohols  
Molecular FrameworkAliphatic heteromonocyclic compounds
Substituents Glucuronic acid or derivatives - Disaccharide - Oxane - Pyran - Acetamide - Carboxamide group - Carboxylic acid salt - Hemiacetal - Secondary alcohol - Secondary carboxylic acid amide - Acetal - Carboxylic acid derivative - Carboxylic acid - Oxacycle - Monocarboxylic acid or derivatives - Organic alkali metal salt - Polyol - Organoheterocyclic compound - Organic nitrogen compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organonitrogen compound - Alcohol - Organopnictogen compound - Primary alcohol - Organic sodium salt - Organic salt - Organic zwitterion - Aliphatic heteromonocyclic compound
DescrizioneThis compound belongs to the class of organic compounds known as glucuronic acid derivatives. These are compounds containing a glucuronic acid moiety (or a derivative), which consists of a glucose moiety with the C6 carbon oxidized to a carboxylic acid.
External Descriptors Not available
Struttura 3D
Modello di struttura chimica interattiva





Certificati (CoA, COO, BSE/TSE e tabella di analisi)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

4 results found

Lot NumberCertificate TypeDataOggetto
E2609444Certificate of AnalysisApr 28, 2026 H758875
E2609458Certificate of AnalysisApr 28, 2026 H758875
J2514800Certificate of AnalysisAug 05, 2025 H758875
J2514801Certificate of AnalysisAug 05, 2025 H758875
Proprietà chimiche e fisiche
SensibilitàMoisture sensitive;heat sensitive
Domande frequenti e articoli
An Introduction to Research-Grade Carbohydrates: Decoding the “Glycan Language” and a Product-Selection Guide (with Tables 1–3)
Understanding Hydrophilic Polymers in Aqueous Systems: Hydration Mechanisms, Structural Knobs, and Task-Oriented Selection Guide (Including Tables 1–3)
Biomedical Polymer Insights: Role-Based Task Map, Six Key Material Levers, and a Risk-Driven Evidence Chain (including the Product Navigation Guide and Product Tables 1–3)
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Research Value of Polyelectrolyte Multilayers: Layer-by-Layer Design of Interfacial Composition, Mass Transport, and Function
Key Judgments in Medical Hydrogel R&D: From Polymer Source and Crosslinking Strategy to Sterilization Planning, Scale-Up Feasibility, and Quality Control
Injectable Thermosensitive Gels: Gelation Behavior, Rheological Properties, and Drug Release Characteristics
Applications of Enzymatic Protein Crosslinking Systems in Gel Construction and Functional Evaluation
Designing Hydrogel Scaffolds as Programmable Cell Microenvironments: From Click-Chemistry Functionalization to 3D Cell Culture Experimental Design
Thickening, Suspension, Auxiliary Stabilization, and Agglomeration Mechanisms of Xanthan Gum in Personal Care Formulations: From Molecular Structure to Processing Applications
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What Is Synthetic Biology? The Industrialization Pathway from Upstream Reagent Toolchains to Biomanufacturing Applications
Performance Sources and Formulation Applications of Enzyme-Based Ingredients in Daily Chemical Products: Fermentation Transformation, Enzymatic Reactions, and Application Principles
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Probiotics, Prebiotics, and Postbiotics in Skin Care: Conceptual Distinctions, Mechanisms of Action, and Their Applications in the Care of Dry, Itchy, and Rough Skin
How Do Collagen Peptides Act on the Skin? From Surface Hydration and Percutaneous Delivery to Fibroblasts and Collagen Homeostasis
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Structure and Functions of Fibronectin: Cell Adhesion, Cutaneous Wound Repair, and Topical Applications
Mechanism of Action of Tranexamic Acid in Pigmentation Care: From the Plasmin System to Regulation of Inflammation-Driven Pro-Melanogenic Signaling
Moisturizing Mechanisms of Tremella fuciformis Polysaccharides: From Polysaccharide Structure and Hydration Rheology to Dynamic Film Formation on the Skin Surface
Multilevel Moisturizing Mechanisms of Sodium Hyaluronate and Its Derivatives: Molecular Weight Modulation, Crosslinking, Acetylation, and Major Sites of Action
Skin Mechanism of Action of Pro-Xylane: From C-Xyloside Priming and CS/DS Chain Remodeling to the Dermal–Epidermal Junction
How Does Collagen Tripeptide Act on the Skin: Stratum Corneum Delivery, Matrix Protection, and Regulation of Collagen Homeostasis
What Is “Plant Collagen”? Distinguishing Ingredient Types, Structural Differences, Production Methods, and Skincare Effects
The Combination Logic of Palmitoyl Tripeptide-1 and Palmitoyl Pentapeptide-4: Skin Delivery, Matrix Signaling, and Regulation of Collagen Homeostasis
Mechanistic Basis of Acetyl Hexapeptide-8 in the Management of Expression Lines: SNARE Complex Interference, Constraints on Percutaneous Delivery, and Combination Strategies
How Ectoine Regulates Skin Hydration: Zwitterionic Structure, Preferential Hydration, and Barrier-Support Mechanisms
Structure, Emollient and Moisturizing Effects, and Source Identification of Squalane: From Complete Hydrogenation of Squalene to Stable Isotope Analysis
Citations of This Product
Calcolatori di soluzioni
Recensioni

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