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Glycocholic Acid Sodium Salt

    • Product Name Glycocholic Acid Sodium Salt
    • Alias Glycocholate Sodium
    • Einecs 220-811-1
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    943453

    Chemical Name Glycocholic Acid Sodium Salt
    Cas Number 475-31-0
    Molecular Formula C26H42NNaO7
    Molecular Weight 505.60 g/mol
    Appearance White to off-white powder
    Solubility Soluble in water
    Melting Point 180-185°C (dec.)
    Storage Temperature 2-8°C
    Ph 1 Solution Approximately 7.5-9.0
    Purity ≥98%

    As an accredited Glycocholic Acid Sodium Salt factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Glycocholic Acid Sodium Salt, 10g, supplied in a sealed amber glass vial with a secure screw cap and appropriate safety labeling.
    Shipping Glycocholic Acid Sodium Salt is shipped in tightly sealed containers to protect it from moisture and contamination. It is typically packed in accordance with regulatory standards, ensuring safe handling during transit. The package is clearly labeled and may require temperature control or special handling as per safety guidelines.
    Storage Glycocholic Acid Sodium Salt should be stored in a tightly sealed container at 2–8°C (refrigerated), protected from light and moisture. Ensure the storage area is well-ventilated and free from incompatible materials. Prevent prolonged exposure to air. Proper handling and storage conditions help maintain the compound's stability and prevent degradation or contamination.
    Application of Glycocholic Acid Sodium Salt

    Applications of Glycocholic Acid Sodium Salt in Industrial Manufacturing

    As a direct manufacturer of Glycocholic Acid Sodium Salt, we focus exclusively on real, established downstream uses where this bile acid derivative provides functional value in demanding industrial production. Below, we detail its application in biopharmaceuticals, diagnostic reagent formulations, cell culture media, and high-precision bile salt chromatography standards, with a clear outline of sector-specific requirements, process integration, responsible dosage levels, and the types of finished goods produced by leading downstream users.

    1. Biopharmaceutical Active Pharmaceutical Ingredient (API) Synthesis

    Biopharmaceutical producers use Glycocholic Acid Sodium Salt in the enzymatic synthesis of semi-synthetic bile acid derivatives and as a solubilizing agent in the formulation of advanced oral drugs targeting liver and gallbladder conditions. The material’s high purity and consistent chemical profile support stringent batch-release criteria, and strict process validation protocols control its integration within the synthesis or blending steps, ensuring every lot supports regulatory drug registration. The usage ratio varies depending on the target API, balancing desired solubility, drug-release characteristics, and pharmacokinetic profiles.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP-US FDA 21 CFR Part 210/211)
    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.)/United States Pharmacopeia (USP) standards for bile acid derivatives
    • Chinese Pharmacopoeia (ChP) for APIs involving bile salts

    Typical usage ratio

    • 0.02%–1.5% w/w in oral formulation matrices, based on drug solubility requirements and target dosage form; precise ratio adjusted during pilot-formulation development

    Downstream process integration

    • Introduced post-synthesis for salt formation, or blended during granulation or solution preparation in the final drug formulation phase prior to tableting or encapsulation

    Final product types

    • Prescription pharmaceutical tablets/capsules for gallstone dissolution
    • Liver protective or regulator oral liquids and softgel products
    • Adjunct bile acid medications for specialized hepatic function therapy

    2. In Vitro Diagnostic (IVD) Reagent Formulation

    Major diagnostic reagent manufacturers utilize Glycocholic Acid Sodium Salt to formulate test solutions for biliary acid concentration assessment in clinical biosample analysis. Its controlled bile acid spectrum ensures consistent response curves in enzyme-linked or colorimetric assays. Downstream quality-controlled blending protocols emphasize batch uniformity, minimizing lot-to-lot variation in diagnostic kit performance. Reagent concentrations are determined according to the kit’s analytical sensitivity and targeted clinical use.

    Industry compliance standards

    • ISO 13485:2016 Medical Devices – Quality Management for IVD production
    • IVD Directive 98/79/EC (Europe) or IVDR (Regulation (EU) 2017/746)
    • FDA 21 CFR Part 820 (Quality System Regulation) for IVD manufacturers
    • Chinese YY/T 0316 for diagnostic kit process quality

    Typical usage ratio

    • 0.05–0.25 mmol/L in working diagnostic solutions; exact level determined by desired calibration curve and instrument-specific detection requirements

    Downstream process integration

    • Diluted and mixed with buffer solutions and enzyme systems in automated or semi-automated reagent blending systems during batch-assembly of liquid or lyophilized IVD kits

    Final product types

    • Clinical chemistry bile acid assay kits for serum and plasma analysis
    • Liver function screening panels for hospital laboratory use
    • Automated analyzer compatible diagnostic reagent packs

    3. Research-Grade Cell Culture Media Supplements

    Cell culture media producers serving biomedical research and industrial R&D add Glycocholic Acid Sodium Salt as a functional additive in specialized hepatocyte and biliary epithelial cell growth formulations. The compound supports in vitro studies on bile acid metabolism, toxicity screening, and gene expression in liver-pathology models. Reliable supplier-origin documentation and batch traceability safeguard the entire downstream workflow, from component weighing through final filtration and aseptic packaging. Media formulations balance effective cell growth with experimental reproducibility, often requiring custom supplementation concentration.

    Industry compliance standards

    • ISO 9001:2015 (Quality Management Systems for research reagents)
    • ATCC animal cell culture production guidelines
    • Good Laboratory Practice (GLP) for R&D reagent batches
    • USP General Chapter <1046> Cell and Tissue Culture Media

    Typical usage ratio

    • 0.01–0.05% w/v relative to total medium volume; adjusted according to cell type, project experimental design, and published reference protocols

    Downstream process integration

    • Pre-dissolved in basal medium during component addition, followed by sterile filtration and packaging into single-use or bulk bottles/tubes under aseptic conditions

    Final product types

    • Hepatocyte and bile duct cell culture media for academic and biotechnology R&D
    • Primary liver cell maintenance kits for toxicology testing
    • Custom media blends for pre-clinical pharmaceutical research

    4. Bile Acid Reference Standard for Chromatographic Analysis

    Producers of analytical standards and chromatography consumables employ Glycocholic Acid Sodium Salt as a high-purity reference substance for quantitative analysis of bile acids in pharmaceutical quality control, clinical research, and environmental monitoring. Every batch undergoes certified purity validation and detailed traceability, supporting downstream users in calibration of HPLC, LC-MS, or capillary electrophoresis platforms. Strict control of molecular structure purity minimizes analytical background interference, enabling reliable quantification even at trace-level detection.

    Industry compliance standards

    • ISO/IEC 17025:2017 (Testing and Calibration Laboratories Accreditation)
    • USP and Ph. Eur. guidelines for reference substance qualification
    • GLP for preparation and release of analytical reference standards
    • Internal SOPs for homogeneity and stability validation

    Typical usage ratio

    • Directly weighed as 10–50 μg/mL standard solutions for calibration curve preparation; concentration fine-tuned to instrument detection range and target matrix

    Downstream process integration

    • Dissolved in suitable analytical-grade solvents, then aliquoted into vials or ampoules for shipment under cold-chain or desiccated conditions to prevent degradation

    Final product types

    • Bile acid analytical reference standards for international laboratories
    • Multi-component bile salt calibration mixtures for pharmaceutical QC
    • Ready-to-use HPLC grade analytical kits
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    Certification & Compliance
    More Introduction

    Introducing Glycocholic Acid Sodium Salt: A Foundation for Precision in Biochemical Research

    Defining Glycocholic Acid Sodium Salt from a Manufacturer’s Perspective

    Working on the production floor and behind the lab doors, we’ve come to know Glycocholic Acid Sodium Salt for its directness and reliability. This bile acid derivative supports research applications that call for clear, predictable results. Our Glycocholic Acid Sodium Salt (Chemical formula: C26H42NO6Na) arrives as a fine, white to off-white powder, straightforward to handle and solubilize. Consistency in appearance and composition reflects years of batch optimization, quality tracking, and feedback from scientists who demand purity from each gram.

    We manufacture this salt using controlled enzymatic and chemical synthesis routes, prioritizing traceability of raw materials and eliminating impurities that can disrupt sensitive assays. Every container starts with a multi-step purification process, pushed to analytical standards by HPLC and mass spectrometry checks. If you work in the lab, that means less second-guessing and more trust in your calibration curves and reference materials. Specified water content, sodium counterion content, and glycocholic content always meet published benchmarks for research grade material, giving scientists confidence in repeat and multi-site studies.

    Functional Value in Biochemistry and Physiology Studies

    Over decades in chemical production, we’ve witnessed how a well-made glycocholate salt transforms experiment outcomes. Researchers in membrane transport and bile acid metabolism rely on exact sodium salt concentration to model biological processes faithfully. The glycine conjugation of glycocholic acid (versus taurine or unconjugated forms) supports work examining intestinal absorption, micelle formation, and the investigation of enterohepatic circulation. Our product dissolves swiftly in water or physiological buffers, which reduces prep time and avoids clumping or undissolved particulates that can affect downstream analytics.

    Researchers appreciate that our Glycocholic Acid Sodium Salt carries the authentic biochemistry found in mammalian systems. Used in cell culture, it influences gene regulation, aids solubilization of lipids, and serves as a nutritional element in organoid and hepatocyte models. In pharmacological work, analysts use it to test pharmaceutical absorption and interaction with bile salt transporters. Those manufacturing enzyme assays consider its purity critical for kinetic measurements. The stability of the sodium salt also prevents unexpected hydrolysis or pH shifts during long incubations, making it the reliable backbone for protocol standardization in published methods.

    Why Specifications Should Matter in a Research Product

    Long hours in manufacturing and the laboratory have taught us that not all glycocholate salts start equal. We focus on batch consistency, measured by assay (on dry basis), and elemental sodium content. Even modest discrepancies in sodium counterion or moisture can cause variances in buffer preparation or altered activity in sensitive transport assays. We keep our loss-on-drying values bounded to a strictly monitored margin, recognizing that some researchers map their buffer molarity to the fourth decimal place.

    Trace organic contaminants, such as related bile salts or unconjugated cholic acid, are segregated out during purification. This sharpens the contrast with off-the-shelf products from non-specialists, where co-eluting impurities can distort chromatographic peaks or generate noise in enzyme activity metrics. We build in batch-to-batch analytical comparisons, focusing on glycine-to-cholic acid linkage integrity, which impacts binding affinity and downstream biological relevance. Quality checkpoints do not end at synthesis— packaging in light-protective, airtight containers holds stability over the full shelf life promised.

    How This Product Differs from Other Bile Salts and Conjugated Acids

    Customers sometimes contrast glycocholic acid sodium salt with similar compounds: taurocholate, deoxycholate, or chenodeoxycholate. Our experience underscores the structural and behavioral distinctions. Glycocholic, with its glycine conjugation, carries a slightly more hydrophilic profile, forming micelles at different critical concentration points from its taurine analogs. Researchers looking for models of mammalian bile composition pick glycocholate salt because it mimics the metabolic routes and intestinal absorption seen in vivo. Deoxycholate, used as a potent detergent, disrupts cell membranes more harshly—unsuitable for work needing physiological integrity of membranes.

    Comparing glycocholic to its unconjugated parent molecule, glycocholate’s water solubility and buffering properties improve markedly. This reduces preparation time and avoids undissolved residue, important for microplate assays or automated liquid handlers. The sodium counterion itself offers advantages over potassium or calcium salts, dissolving in standard buffers without precipitation or side reactions. The stability profile adds robustness across varying temperatures, so both transport and storage maintain chemical identity and usability.

    Our Approach to Manufacturing: From Sourcing to Packaging

    Building Glycocholic Acid Sodium Salt as a manufacturer means mastering not only the chemistry but also the supply chain. We source raw bile acid from certified suppliers who document animal health and origin, meeting expectations for traceability. Glycine conjugation and sodium salification take place under controlled conditions, monitored by senior chemists with decades at the bench. Every batch faces a gauntlet of checks—NMR spectra, melting point, optical rotation, and solvent checks—guarding against surprises that can stall research timelines.

    We respond directly to feedback from long-term users who push the boundaries of cell culture, bioavailability, or metabolic flux analysis. Packaging has evolved with their demands, now relying on air-tight, opaque HDPE bottles with desiccants, sealed in tamper-resistant pouches. This approach prevents hydration drift and UV degradation during shipping and on the storage shelf. Careful labeling with exact batch data ensures that every researcher can replicate earlier protocols without confounding variation from the starting material.

    Supporting Trusted Outcomes in Academic and Industry Projects

    Our clients often share that mistakes in foundational reagents like bile salts ripple through months of work. By limiting lot-to-lot variation and controlling every specification, we remove a variable from complex pharmaceutical, food, or diagnostic projects. The cry for “batch stability” isn’t theoretical—it means reliable IC50 measurements, consistent results in growing 3D liver spheroids, or data reproducibility across teaching laboratories worldwide. We’ve adapted production runs to accommodate higher-output pharmaceutical research and provided high-purity analytical grades for long-form metabolomics or clinical biomarker validation.

    We don’t see our Glycocholic Acid Sodium Salt as a commodity. It’s a partner in the quietly demanding work of science—where one off-value, one distorted standard, can unravel a data set months in the making. Laboratory troubleshooting often circles back to the quality and source of simple reagents. By tightening control over every aspect—raw material integrity, chemical transformation, end-stage packaging—we build a track record of trust with university, hospital, and industrial teams alike.

    Points of Differentiation from Non-Manufacturer Sources

    Bile salts sourced from resellers or trading companies frequently present unknowns. We hear from researchers who encounter variable moisture content, off-odors, or ambiguous labeling on bottles marked generically. As a manufacturer, we deliver Glycocholic Acid Sodium Salt with a detailed Certificate of Analysis prepared for each lot, connecting every gram to a traceable record on our production line. Our technical team provides guidance on solubilization and storage, built on thousands of hours spent working with the product in a range of applications.

    We support queries from bench scientists and process engineers alike—grappling with dissolution protocols, buffer compatibility, or regulatory submissions. By producing at scale in-house, our operations shield researchers from global supply shocks or interruptions that often hit middleman distributors hardest. For clients running multi-year or regulatory-sensitive studies, that reliability means undisturbed timelines and data credibility. The feedback loop with users drives improvements back to our upstream processes—something traders or importers rarely offer.

    Understanding and Meeting Evolving Research Demands

    Change is constant in bioscience. Over the last decade, we’ve watched interest in bile acid transporters surge, driven by drug development for metabolic and digestive disease. Glycocholic Acid Sodium Salt, once quietly confined to basic physiology studies, now anchors cell-based reporter assays, NMR work, and pharmaceutical bioavailability testing. To keep pace, we’ve expanded production capacity and upgraded purification columns to minimize minor side-products—a move sparked directly from hearing about problematic background signals in mass spectrometry reports from client labs.

    At the same time, advances in organoid and tissue engineering place more demanding criteria on all media components. Bile acids aren’t just standard supplements; their batch quality influences everything from cell fate decisions to toxicity readouts. We’ve responded by providing additional, targeted analytical data in each lot certificate, accommodating requests for extra UV-Vis, elemental, or LC-MS scans. That willingness to push quality documentation deeper strengthens collaborative research and bolsters confidence for protocol publication or grant proposals.

    Addressing Frequent User Queries: Stability, Handling, and Storage

    Scientists using our Glycocholic Acid Sodium Salt ask about routine storage, handling, and compatibility with evolving protocols. From our hands-on perspective, we stress that storing the powder in a dry, cool environment—sealed tightly—prevents caking and maintains solubility for at least two years from packaging. Acid hydrolysis and photodegradation do not pose issues under normal laboratory conditions, thanks to our selection of both packaging materials and drying processes.

    Researchers often switch between concentrated stock solutions and single-use aliquots, depending on experiment scale. Our salt demonstrates predictable behavior in a wide variety of solvents, especially buffered saline and phosphate solutions commonly used in transport kinetics, enzyme work, or lipid micelle studies. If protocols require precise osmolarity or pH adjustments, we provide detailed elemental analyses to support accurate buffer construction. We recognize that clinical and translational workflows require not only chemical stability, but also reproducible dispersibility, minimizing batch-induced noise in longitudinal data sets.

    Enabling Better Outcomes: Supporting Regulatory and Industry Objectives

    Drug developers, food scientists, and clinical researchers count on authenticity and trace documentation. As bioequivalence and novel drug design focus increasingly on the subtle interactions of bile acids with transporters and nuclear receptors, regulators want assurance that all reagents trace back to controlled manufacturing environments. Our Glycocholic Acid Sodium Salt production lines meet strict internal, industry, and, where requested, GMP-aligned standards, supporting regulatory filings and published studies. Our supply chain transparency supports audits and repeat runs for regulated customers.

    We detect growing demand from industrial process engineers who look for predictable scale-up quality. Bulk batches for pharmaceutical or nutraceutical production must not introduce batch-to-batch drift or hidden process-altering byproducts. Thanks to our laboratory-to-plant feedback loops, we can expand production to meet ton-scale orders, while holding every lot’s purity and performance data to the same rigorous benchmarks as laboratory trial sizes. We avoid unexpected supply interruptions by safeguarding raw material routes and fostering long-term relationships upstream in the supply web.

    Future Directions and Continuous Improvement in Glycocholic Salt Manufacturing

    In-house R&D never stands still. Every month, scientists at collaborator labs update us with fresh demands—whether isoform-specific glycocholate analogs, customized salt formulations, or requests for microbially-sourced glycocholic acid to support non-animal workflows. We channel user feedback into process optimization, automation, and more extensive impurity profiling, aiming not only to keep up but to stay a step ahead of evolving research. Our internal target: remove every doubt about the consistency, performance, or biological fidelity of any batch delivered.

    We see ourselves not only as a supplier, but as long-term research partners. Trust emerges from continuous, open conversation about what works and what needs attention. This feedback shapes everything from reaction monitoring thresholds to stability and packaging upgrades. Each improvement in manufacturing processes reflects years of experimenting, troubleshooting, and listening to researchers. As methods and questions change, we adapt to the evolving research landscape, supporting more advanced applications.

    Direct Dialogue: The Value of Manufacturer Engagement

    Open lines of communication support ongoing improvement. Technical teams, from postdocs to production engineers, reach out with concerns—from solubility adjustment to batch certification questions. By handling technical support internally—citing firsthand experience with batches from start to finish—we close the guesswork that often accompanies products outside a manufacturer’s direct purview. We also track recurring queries or issues, using them as catalysts for batch refinement or additional documentation. Every direct conversation feeds back into better product, tighter tolerances, and greater transparency.

    We offer in-depth guidance for scaling from bench to pilot plant, recommend protocols for solution prep and storage, and troubleshoot compatibility with assay platforms. No generic helpdesk or delayed distributor response: just the perspective of scientists who’ve handled the salt throughout its lifecycle, from reaction vessel to finished product.

    Looking Ahead: Why Quality Matters More Than Ever

    With science moving toward more complex screening technologies, engineered tissues, and fine-grained metabolic analysis, the time spent on defining and controlling the quality of fundamental reagents like Glycocholic Acid Sodium Salt pays dividends in research certainty. Our manufacturing process—marrying analytical rigor, hands-on chemical production, and real-world feedback—supports not only robust experimentation today but also the scalable needs of tomorrow’s discoveries. We invite our clients to keep the dialogue going; every challenge faced in the lab sharpens our commitment to manufacturing excellence and to science done right, from the starting batch on up.