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Cholic Acid Methyl Ester

    • Product Name Cholic Acid Methyl Ester
    • Alias Methyl cholate
    • Einecs 221-143-6
    • 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
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    Specifications

    HS Code

    462145

    Productname Cholic Acid Methyl Ester
    Casnumber 3779-95-1
    Molecularformula C25H42O5
    Molecularweight 422.60
    Appearance White to off-white solid
    Meltingpoint 122-125°C
    Solubility Soluble in chloroform, methanol; slightly soluble in water
    Purity Typically >98%
    Storagecondition Store at 2-8°C
    Synonyms Methyl cholate

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

    Packing & Storage
    Packing Cholic Acid Methyl Ester is packaged in a 1-gram amber glass vial, tightly sealed, labeled with product details and safety information.
    Shipping Cholic Acid Methyl Ester is typically shipped in tightly sealed containers to prevent exposure to moisture and air. It should be packed in accordance with chemical handling regulations, using protective materials to avoid breakage. During shipping, the package must be labeled appropriately and kept away from incompatible substances, heat, and direct sunlight.
    Storage Cholic Acid Methyl Ester should be stored in a tightly closed container, protected from moisture and direct sunlight. Keep it in a cool, dry, and well-ventilated area, preferably at room temperature (15–25°C). Avoid exposure to strong oxidizing agents. Ensure proper labeling and restrict access to trained personnel. Always follow local regulations and safety protocols for chemical storage.
    Application of Cholic Acid Methyl Ester

    Applications of Cholic Acid Methyl Ester in Industrial Manufacturing

    Cholic Acid Methyl Ester serves as a critical intermediate and functional additive in several advanced industrial sectors. As a direct manufacturer, we supply this compound for specialized uses where control of purity, process integration, and compliance with regulatory standards are essential for downstream production success.

    1. Pharmaceutical Steroid Synthesis

    Pharmaceutical manufacturers use Cholic Acid Methyl Ester as a building block in semi-synthetic steroid APIs. The compound enables selective modification of the bile acid backbone, which is essential in the production of hydrophilic bile acids and corticoid precursors. Process engineers introduce the methyl ester at specific steps during molecular derivatization, benefiting from precise control over functional group transformations and improved product yields while conforming to stringent QC protocols.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia Monograph 04/2014: 1331
    • United States Pharmacopeia (USP) standards for bile acid intermediates
    • FDA 21 CFR Part 210/211 for finished drug manufacturing

    Typical usage ratio

    • 0.8–1.2 molar equivalents per API intermediate batch; actual ratio optimized according to desired downstream conversions and target impurity profile

    Downstream process integration

    • Raw material charging into esterification or reduction vessels during the early phase of steroid skeleton modification
    • Supplies the methyl group for subsequent hydrolysis, hydroxylation, or oxidation pathways
    • Allows integration into multi-step batch or flow processes with in-process analytical control

    Final product types

    • Semi-synthetic bile acid drugs (e.g., ursodeoxycholic acid derivatives)
    • Corticoid intermediates
    • Bile acid-based novel therapeutic candidates
    • GMP-grade pharmaceutical actives

    2. Bioconversion Feedstock for Cholane Derivatives

    Industrial biotechnology producers employ Cholic Acid Methyl Ester as a specific substrate in microbial biotransformation processes. The methyl ester enhances solubility and membrane transport properties, permitting more efficient enzymatic conversions to secondary bile salts or rare cholane derivatives. This raw material supports process intensification by controlling substrate inhibition and improving the selectivity of hydroxylation and oxidation reactions performed by engineered strains or immobilized biocatalysts.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for Biotech Process Manufacturing
    • REACH registration for safe chemical use
    • EU Regulation (EC) No 1907/2006 for chemical substances in industrial applications
    • Guidelines for Novel Microbial Fermentation Processes

    Typical usage ratio

    • 5–50 g/L substrate loading in fermentation or bioreactor systems, tuned for cell type, catalyst specificity, and conversion yield

    Downstream process integration

    • Feeding to bioreactors prior to start-up or as a continuous substrate dosing during the bioprocess cycle
    • Direct addition into enzymatic transformation steps for conversion to target cholane molecules
    • Integration with in-line substrate feeding and automated QC monitoring for residual raw material

    Final product types

    • Rare secondary bile acids
    • Hydroxylated cholane derivatives
    • Precursor materials for API synthesis
    • Industrial-grade biotransformation intermediates

    3. Reference Standard Manufacturing for Analytical Laboratories

    Laboratory reagent producers and certified reference material suppliers value Cholic Acid Methyl Ester for primary standard calibration solution preparation. Its defined purity and stable methyl ester group make it a practical control for quantitative assay method validation, including LC-MS and NMR characterization of bile acids, enabling analytical laboratories to execute traceable and reproducible test results during both research and regulatory lot release testing.

    Industry compliance standards

    • ISO/IEC 17025 for competence in testing and calibration laboratories
    • ISO Guide 34 for reference material production
    • Ph. Eur. standards for chemical reference substances
    • USP Reference Standard requirements

    Typical usage ratio

    • 100 μg/mL–1 mg/mL in calibration solution, accurately weighed and diluted as per method SOP; mass adjusted for purity by certificate

    Downstream process integration

    • Weighing, dissolution, and dilution into solvent as initial calibration stock
    • Use in preparation of multi-component bile acid reference sets
    • Quality assurance batch documentation linking lot traceability to COA records

    Final product types

    • Certified reference materials (CRMs)
    • Analytical standards for FDA and EMA submission analyses
    • Calibration solutions for LC, HPLC, GC, and mass spectrometry
    • Research grade primary standards

    4. Chemical Reagent Feedstock for Organic Synthesis

    Specialty chemical manufacturers utilize Cholic Acid Methyl Ester as a precursor for custom organic synthesis. Controlled methylation enables selective protection of carboxyl groups, facilitating subsequent derivatization or ring-opening reactions. The ester provides improved handling characteristics and compatibility with various solvent systems, proving advantageous for scale-up operations requiring defined input purity and reproducible conversion rates in the creation of novel specialty organics.

    Industry compliance standards

    • ISO 9001:2015 for specialty chemical production
    • REACH compliance for manufacturing and import
    • Globally Harmonized System (GHS) for safe handling and labeling
    • Company-specific cGMP (for pharmaceutical-grade applications)

    Typical usage ratio

    • Varies between 1–2 molar equivalents depending on synthetic scheme; adjusted according to protection-demethylation kinetics and downstream reaction pathway

    Downstream process integration

    • Charging to synthesis reactors as a protected starting material
    • Sequential derivatization with custom functional groups under mild ester-protective conditions
    • Demethylation or hydrolysis to regenerate the carboxylic function as dictated by process needs

    Final product types

    • Novel cholic acid derivatives
    • Advanced intermediates for further fine chemical or pharmaceutical transformation
    • Organic synthesis probes for R&D
    • Customized cholic acid-based conjugates
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    Certification & Compliance
    More Introduction

    Cholic Acid Methyl Ester: Consistently High Purity Fuels Advanced Research

    As specialists in the synthesis and manufacture of bile acid derivatives, we've seen Cholic Acid Methyl Ester take a unique spot in many laboratories and industrial projects worldwide. Few substances offer the stability, consistent reactivity, and tractable properties that researchers expect when working on complex synthetic pathways. This compound, a methylated form of cholic acid, serves both as a key intermediate and as a building block for further chemical transformations. Processes requiring nuanced control over molecular architecture—such as drug discovery, metabolism studies, or pharmaceutical formulation—depend on reliable input materials. Having worked closely with many of the leading academic and industrial teams, we understand the importance of integrity in each batch delivered.

    Product Model and Purity Standards

    Each shipment of Cholic Acid Methyl Ester carries a model number that traces back to the synthesis batch, ensuring seamless recall and documentation for regulatory or R&D purposes. The product consistently falls within a purity range exceeding 98%, characterized by a nearly colorless to faintly yellow crystalline powder. High-Performance Liquid Chromatography (HPLC) and Nuclear Magnetic Resonance (NMR) support these claims, which we verify with each lot. With a molecular formula C25H40O5 and CAS number 3160-86-7, the integrity of the methyl ester is central to its behavior in downstream reactions. In daily practice, that purity translates to dependable reactivity, crucial when your experiments or productions hinge on the reliability of every milligram you introduce.

    During manufacturing, temperature, pH, and solvent systems directly influence the final ester profile. Multiple filtration steps and careful purification routines guard against cross-contamination from closely related bile acid analogues. We adapt and tune our process to meet not just the written specifications, but the practical requirements of modern organic synthesis. Over time, feedback from medicinal chemists and process engineers has shown us that small fluctuations in impurity profiles may introduce noise or misleading by-products into target reactions. By maintaining tight control over the methylation and subsequent crystallization phases, we consistently avoid the pitfalls of variable raw material performance.

    Versatile Usage Across Sectors

    Cholic Acid Methyl Ester serves roles in many fields. As an esterified derivative, it offers better organic solubility compared to its parent acid, which often leads to improved handling in non-aqueous reaction media. Many teams find its value in modification reactions, such as selective hydrolysis or ester exchange, supporting the design of custom bile acid derivatives for metabolic tracers or pro-drug design. Its role doesn’t end at synthetic chemistry. In life sciences, Cholic Acid Methyl Ester supports metabolic pathway mapping, often serving as a labeled substrate in enzymology or as a reference standard for analytical quantification.

    We've shipped this ester to researchers investigating gut-liver microbial interactions and others exploring cholesterol metabolism through isotopic labeling. Our contacts in custom API synthesis often request the compound as a precursor for more complex amphiphilic molecules. In practice, the methyl ester enjoys broader compatibility with organic solvents and reagents than the free acid, cutting down the time spent on pH adjustments or neutralization steps. Even seemingly minor properties—such as the melting range of 118–122°C—have implications for storage, transportation, and scale-up operations.

    Distinctive Features and Real-World Advantages

    Differences between Cholic Acid Methyl Ester and other cholic acid derivatives matter when process efficiency and data quality are on the line. Unlike the sodium or potassium salts of cholic acid, the methyl ester finds use in nonpolar and slightly polar solvents without introducing counter-ions or causing phase separation. Cholic acid itself often causes issues in organic synthesis routes due to its strong carboxylic acid function, prompting unwanted reactions unless handled with extreme care. The methyl ester, by masking that reactive carboxyl, allows for much cleaner transformations where selectivity or protection is needed.

    Compared to ethyl or benzyl esters, the methyl ester strikes a practical balance between reactivity and stability. The methyl group is easier to remove under mild conditions than bulkier alkyl groups, avoiding harsh saponification or hydrogenolysis steps that might damage sensitive structural motifs. Higher esters may linger in reaction mixtures and complicate product isolation, while methyl esters can be smoothly converted or cleaved once their protective function is complete. In peptide conjugation, the choice of the ester group directly affects yield and purity, making methyl the preferred option in many bio-conjugation strategies.

    Quality Control and Transparency

    Consistent results start with rigorous controls. Every batch undergoes a series of chromatography, spectroscopy, and melting point analysis to affirm that the product aligns with stringent pharmaceutical and research standards. Over years in operation, we've maintained complete traceability from raw starting materials to the packaged product, eliminating guesswork and providing reassurance to clients who demand unwavering quality. Controlling for trace metal content, residual solvents, and polymorphic variability forms the backbone of our daily operations. Samples showing even slight deviation from target parameters are rejected and never leave the facility.

    Feedback loops between our QC laboratory and production team drive ongoing improvements. Subtle process tweaks, such as adjusting recrystallization solvent ratios or refining temperature gradients, directly boost final purity and stability. We also maintain open channels with customers for technical support, troubleshooting unexpected analytical results, or advising on best uses for the compound based on accumulated internal and field data. This two-way exchange of knowledge means our Cholic Acid Methyl Ester evolves in step with industry needs, rather than lagging behind.

    Scale-Up Experience and Reliable Supply

    Scaling from gram-level laboratory syntheses to multi-kilogram industrial runs poses many practical challenges. Over the years, our production team has optimized each step, from the initial cholic acid isolation—sourced from highly controlled biological streams—to final esterification and drying. At scale, solvent recycling and waste handling affect both cost and environmental footprint. We recover and recondition solvents wherever possible, while ensuring their quality supports the exacting requirements of API or research material synthesis.

    Many laboratories tell us stories of interrupted projects due to unreliable or inconsistent raw materials. Our scale-up protocols, refined through experience and aligned with global best practices, support uninterrupted supply. Each lot matches defined chemical and physical characteristics, greatly reducing project downtime stemming from unexpected impurity or physical variation. Handling large-scale requests sometimes presents logistical hurdles, especially under fluctuating global demand, but our established infrastructure allows for flexibility without sacrificing quality. Overruns and contract manufacturing experience have enabled a system ready for sudden spikes in demand.

    Regulatory Recognition and Application Insight

    Many institutions examining bile acids and their derivatives for pharmaceuticals or food additives must answer to strict regulatory scrutiny. Our manufacturing operations make room for full documentation at every synthesis and handling step. Third-party audits, including cGMP certification for select product lines, require a commitment that extends far beyond routine paperwork. We keep comprehensive batch histories and analytical records, making document submission efficient for customers navigating regulatory checkpoints worldwide.

    Such transparency serves both seasoned practitioners and newer entrants in the bile acid space. For those exploring biosynthetic pathways of hepatic metabolism or creating cholic acid-derived product screens, knowing the chemical origin and purity profile matters as much as understanding the underlying biochemical rationale. Advanced analytical support often clarifies questions surrounding identification, quantitation, or secondary impurity presence—issues that can derail lengthy research timelines if not addressed upfront. Extensive experience with legal, regulatory, and import requirements has positioned us as a partner ready to help researchers and developers clear both scientific and administrative hurdles.

    Supporting Sustainable Development

    Responsible handling of raw materials and processing reagents sits at the core of our operations. Cholic Acid Methyl Ester production begins with biological inputs, making traceability and sustainability central to our planning. Working closely with upstream suppliers, we've helped put in place systems that minimize environmental disruption and maximize resource recovery, ensuring both consistent feedstock and reduced ecological impact. Modern purification methods—including chromatography recycling and precision solvent removal—contribute to a smaller waste profile. It’s not only about meeting compliance or certification targets but finding efficient ways to reuse and reduce at each step.

    Within our own facility, closed-loop water systems, energy-efficient distillation, and targeted solvent filtration further support these sustainability goals. Customer collaborations often prompt us to adapt or refine our processes for improved green chemistry performance, translating to tangible reductions in chemical usage and greenhouse gas participation. By staying engaged in emerging discussions about sustainable pharmaceuticals, we continue finding ways to lower our resource use while maintaining the purity and reliability users demand.

    Direct Feedback Shapes Product Evolution

    We see innovation arise organically through close collaboration with downstream users. Clients working in analytical chemistry often provide challenging feedback about detection limits, matrix effects, or secondary reactivity in complex sample backgrounds. At the bench and during pilot runs, these comments have prompted us to shift small but significant aspects of our manufacturing sequence: for example, improving the drying protocol to minimize trace moisture, or refining filtration steps to better capture micro-impurities before final packing.

    Clients in custom alkaloid synthesis and metabolic research invite us to joint troubleshooting sessions. Through shared analytical data and real-world application stories, we adapt our process to fine-tune performance for emerging challenges. For example, one major research group alerted us to intermittent color variation in a multi-step workflow; our investigation traced the issue to a previously unrecognized interaction with a by-product from an upstream esterification step. By addressing this at the source, we eliminated a mystery that had troubled several teams.

    Transport, Storage, and Practical Handling Benefits

    Laboratories working in both academic and industrial spaces depend on materials that hold up under regular shipping and storage conditions. Cholic Acid Methyl Ester offers favorable shelf stability, with resistance to hydrolysis in ambient air much greater than the parent acid. Hazmat handling requirements remain minimal due to the compound’s low volatility and benign hazard profile, so most teams can move, store, and weigh the material with standard laboratory precautions. No need for specialized equipment, which can hold up projects or drive up operational overhead.

    Storage in a sealed, non-reactive container at room temperature maintains the compound’s integrity for months, reducing risk for loss through decomposition or unwanted side reactions. The powder’s low hygroscopicity helps avoid clumping or handling loss, especially valued during weighing and dissolution. Shipping partners have consistently met our requirements, avoiding temperature excursions or excessive handling, so clients open their shipments to find intact product, not inconsistent aggregates or decomposed residues.

    Working With Researchers: Solutions and Support

    Having walked through the fine details of application-specific requirements with our partners, we’re equipped to offer more than an off-the-shelf product. Through hundreds of interactions—sometimes as simple as packing advice, at other times running parallel purity checks with a customer's analytical group—we help resolve bottlenecks before they threaten workflow. Many users return, not just for another bottle, but for the assistance they receive in understanding how this particular methyl ester fits into newer synthetic or analytical strategies. In cancer biology and microbiome research, for example, our support has helped teams fast-track their method validation procedures using product with documented lot-to-lot consistency.

    For those expanding into bile acid analog development, matching the chemical and physical properties of the methyl ester can determine whether a project advances. Detailed application notes, shared insights on analytical method optimization, and quick turnaround on technical queries ensure clients are always ready for the next step. Some teams push the boundaries of detection and sensitivity; others need the compound to initialize or serve as an internal standard in larger automated screens. We stay involved through the lifecycle of product use, updating datasets and supporting modifications to address new problem sets as science progresses.

    Challenges and Ongoing Improvements

    Markets for advanced chemical products rarely stay static. Demand shifts, regulatory insights, and discoveries in biochemistry or drug development prompt us to adjust. Maintaining scalable and reliable production requires foresight and willingness to innovate. From procurement of base cholic acid with greater traceability, to improving downstream esterification efficiency, we treat each new inquiry as an opportunity to refine our methods.

    At times, raw material shortages or sudden surges in custom orders stretch our systems. Our built-in redundancies, regular supplier audits, and continuous staff training have allowed us to weather unexpected shifts. In parallel, our network of distribution partners extends our reach while letting us maintain the close, technically oriented relationships that define our business model. As feedback from new markets accumulates, whether about solvent compatibility, analytical method trends, or upcoming regulatory changes, we integrate this knowledge to fuel both incremental and stepwise improvements.

    A Commitment to Integrity and Collaboration

    Reliability, transparency, and technical competence define our approach to Cholic Acid Methyl Ester manufacturing. Every kilogram that leaves our facility reflects the lessons learned through decades of chemical synthesis, customer interaction, and evolving application requirements. For organizations unraveling metabolic pathways or scaling up new pharmaceuticals, this compound provides a well-characterized, adaptable foundation. We rely on direct, ongoing dialogue with users to ensure our product remains relevant, responsive, and ready to support scientific and industrial progress.