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Porcine Deoxycholic Acid

    • Product Name Porcine Deoxycholic Acid
    • Alias Kybella
    • Einecs 206-132-7
    • 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

    726054

    Product Name Porcine Deoxycholic Acid
    Chemical Formula C24H40O4
    Molecular Weight 392.57 g/mol
    Appearance White crystalline powder
    Source Porcine (pig) bile
    Solubility Slightly soluble in water, soluble in ethanol
    Melting Point 178-185°C
    Cas Number 83-44-3
    Storage Temperature 2-8°C
    Purity ≥98%
    Odor Odorless
    Ph Value 6.5-8.0 (1% solution in water)
    Synonyms 3α,12α-Dihydroxy-5β-cholan-24-oic acid
    Application Biochemical research, surfactant, bile acid studies

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

    Packing & Storage
    Packing Porcine Deoxycholic Acid is packaged in a 25g amber glass bottle, sealed, labeled with product details, safety warnings, and batch information.
    Shipping Porcine Deoxycholic Acid ships in secure, airtight containers to prevent moisture absorption and contamination. It is classified as a non-hazardous chemical but should be handled with appropriate PPE. Packages are labeled per regulatory guidelines and shipped at ambient temperature unless otherwise specified, ensuring product integrity throughout transit.
    Storage Porcine Deoxycholic Acid should be stored in a tightly sealed container at 2-8°C (refrigerated) and protected from light and moisture. Store in a cool, dry, and well-ventilated area, away from incompatible substances. Ensure proper labeling and secure storage to prevent accidental usage or contamination. Avoid exposure to excessive heat and handle following standard chemical safety guidelines.
    Application of Porcine Deoxycholic Acid
    Purity 98%: Porcine Deoxycholic Acid with 98% purity is used in pharmaceutical synthesis, where it ensures high yield and reproducibility of active compounds. Molecular Weight 392.57 g/mol: Porcine Deoxycholic Acid with a molecular weight of 392.57 g/mol is used in bile acid research, where precise molecular mass supports accurate analytical quantification. Melting Point 178-181°C: Porcine Deoxycholic Acid with a melting point of 178-181°C is used in formulation development, where thermal stability maintains product consistency during processing. Solubility 50 mg/mL in DMSO: Porcine Deoxycholic Acid with solubility of 50 mg/mL in DMSO is used in in vitro cell studies, where high solubility enhances assay performance. Particle Size <100 μm: Porcine Deoxycholic Acid with particle size below 100 μm is used in topical delivery systems, where fine dispersion improves absorption rates. Stability Temperature 25°C: Porcine Deoxycholic Acid with stability at 25°C is used in controlled storage environments, where it prevents degradation during long-term storage. Endotoxin Level ≤0.1 EU/mg: Porcine Deoxycholic Acid with an endotoxin level of ≤0.1 EU/mg is used in injectable formulations, where minimized endotoxins ensure biocompatibility for parenteral applications. Ash Content ≤0.5%: Porcine Deoxycholic Acid with ash content ≤0.5% is used in laboratory reagent production, where low inorganic residue reduces contamination risk in sensitive experiments.
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    Certification & Compliance
    More Introduction

    Porcine Deoxycholic Acid: Experience from the Manufacturer’s Floor

    Real-World Insights on a Core Bile Acid Ingredient

    Porcine Deoxycholic Acid has stood out in our line-up for many years because it bridges biology and industrial application in a way few raw materials do. This isn’t just another white powder sitting on a shelf; it carries with it careful processing and a legacy of adaptation. On our production floor, we see every day how this secondary bile acid interacts with other substances and why customers, especially those in pharmaceuticals and specialized research, come back asking for it—and ask precise questions about purity, consistency, and sourcing.

    Manufacturing Roots and Batch Consistency

    A lot of deoxycholic acid on the market comes from a mix of sources—some bovine, some synthetic—so the question around why we focus on porcine often comes up. Over time, we’ve narrowed our process to collect and extract from high-quality porcine bile. The model 95% grade crystal, for instance, grows out of a multi-step filtration and crystallization protocol. We don’t just focus on a high HPLC purity figure; experts from QA pull random samples from each batch, sometimes drilling even into trace contaminants that don’t show up on most standard COAs.

    There is a noticeable difference at the end of each lot. Hands-on operators calibrate equipment ranges based on the feedback from these in-plant checks. The result: a material with a defined melting range, a reliable solubility profile, and no surprises downstream for formulators. Some clients have shared stories of lots from other sources causing instability in their finished product. Our internal chemists double down on consistency by tracing back minor variances and tightening process parameters. In a world where repetition counts, we have found that tiny shifts during the deconjugation or purification make a mark, so we invest real labor there.

    What Sets Porcine Apart—The Details That Matter

    The question we hear most from experienced formulators is: “What’s the difference between porcine and other sources?” While the base molecule, C24H40O4, remains the same, the trace lipid contaminants and even elemental residue from the animal’s diet can influence the profile of final lots. Porcine-sourced material tends to offer a slightly different trace fatty acid spectrum versus bovine, something we’ve seen corroborated by independent researchers and of course our own in-house mass spectrometry runs.

    Batches from pig sources generally produce a lighter, cleaner crystal. Users who need high-purity esters or salts for injection or lipolytic agents often spot minute differences—not just in impurity load-outs, but in the ease with which the finished API can be compounded. Some animal product purists ask about infectious risks. Our manufacturing protocol circumvents those concerns with multiple pathogen clearances, and routine PCR screens on each lot. We do not accept or process raw material without full traceability from the abattoir, with supporting documentation on diet and health management.

    Specifications and User Care on Factory Floor

    Our porcine deoxycholic acid most often comes in crystalline form at not less than 95% HPLC purity. Over the years, we’ve taken specifications further: each kilogram is double-vacuum packed on site, then scanned with FTIR to confirm molecular identity—these are steps that many traders skip, but we find avoid headaches on the receiving end. End-users usually dissolve it in organic solvents for formulation or use as a reference standard; our technical support hears plenty of reports about rapid, clean solubilization due to our focus on fine crystalline structure.

    We have never needed to add anti-caking agents or other extenders. Many synthetic alternatives lack the lipid “background” which gives our product a close match to natural bile environments—especially relevant in pharmaceutical and clinical settings. For those working in cosmeceuticals, the day-to-day differences are real: a certain creaminess and flow during emulsification stands out when using high-grade porcine-sourced acid versus generic grades.

    Experience from Botanicals to Biologics

    Standing inside our facility, it's clear that incoming questions are growing more sophisticated. Researchers have started asking our team to help differentiate between porcine and bovine origins with respect to bioassays. Some overseas partners cite regulatory preferences for porcine versus bovine origin due to BSE controls, especially in East Asia and some European markets. Because our team runs both public and proprietary screening assays, we can answer with full batch documentation, not just verbal assurances.

    Porcine bile acids also see demand from biologists tracing gut flora-bile interactions, who increasingly want batch-to-batch consistency on a molecular level. We have responded by introducing full batch certificates showing not only standard purity but also detailed spectroscopic overlays, microbial limits, and even heavy metal breakdowns. Some teams have asked for full quantified datasets, and we provide those on request for R&D programs.

    Supporting Clinical and Cosmetic Manufacturing

    In clinical research, the source and specification of deoxycholic acid make a difference. Injectable lipolysis products, for example, require precise knowledge of the acid origin and processing steps. We have participated in collaborative projects where even minute variance in the acid’s physical properties can alter the needle response or skin tissue reaction. In those cases, we supply not only the material but also product history, spectroscopic confirmation, and our in-house analytics. Researchers developing new APIs for metabolic or hepatological investigation depend on this kind of transparency.

    The cosmetic field has its own challenges. Cream developers and solution formulators frequently share concerns about shelf-life, phase separation, and color retention. Through our steady QA programs, we have seen our product consistently outpace generic alternatives in creams and serums. There’s a larger discussion around integrating our deoxycholic acid in advanced skin therapy protocols, and we are continuously expanding pilot-scale offerings to support these innovators.

    What Goes Into Quality: From Raw Material to Final Product

    We work with large, traceable porcine suppliers, many of whom we have visited personally. It’s not just about extracting the raw bile—it’s also about how the pigs are raised, their feed composition, and even small details like antibiotic treatment cycles. Every input makes its way into the analytical fingerprint of our finished batches, so we keep communication lines open, accepting only partner farms with rigorous documentation.

    After arrival, raw materials undergo rapid cold-chain transfer and immediate processing. Extraction starts within hours—anything longer and risk of degradation grows. Our process involves several stages of filtration, precipitation, and refinement, followed by slow crystallization. Each batch goes through full chromatography and spectroscopic reads to confirm structure and watch for contamination.

    The people on our floor bring decades of hands-on knowledge. Some have worked up from basic extraction lines to lead entire QA teams; they’re the first to spot process shifts or unexpected test values. Their experience feeds directly into every decision we make, from minor equipment calibrations to broader process redesign.

    Meeting Regulatory Demands and Documentation Expectations

    Regulations have become tighter, and different markets expect extensive transparency on animal sourcing. We have responded with voluntary batch certifications, offering trace documentation on animal origin, feed sources, and production timelines. Many partners request both animal health and anti-microbial records; our support team prepares those with every order for research or clinical supply.

    Standard setting bodies such as the USP or EP outline purity and contaminant limits, but we have found several customers—those working in advanced biologics, for example—require full impurity profiling beyond basic standards. For these, we offer full-run HPLC chromatograms, NMR proof, heavy metal checks, and spectrometric overlays. Where some suppliers rely on generic third-party documentation, our certifications reflect daily, in-house monitoring.

    A Legacy of Demand and Performance Feedback

    Feedback from downstream users shapes how we refine our offering. Several years ago, clinical users raised recurring issues with solubility and small particulate formation. Our technical team spent months retooling the filtration step, working late into the night, discarding several runs that didn’t meet standards. The current product has resulted from these iterative improvements, not theoretical optimization. In the real world, this work cuts down reprocessing and product recall risk for our customers.

    Cosmetic industry users have asked us to further hone color and clarity. One collaboration with a skin therapy company resulted in fine-tuning the moisture control steps, leading to better long-term stability in finished creams. Our engineers and QA testers prefer this partnership approach—something you only get with direct manufacturer-to-customer relationships. We know how the material behaves in actual product recipes because we listen to chemists and developers, and we invite feedback at every stage.

    Impacts of Source Material and Handling on Applications

    The value of deoxycholic acid depends on the actual bioactivity profile achieved in practice—not just a calculated assay value. As a raw material, porcine-sourced grades seem to deliver a closer fit to certain in vivo and in vitro systems where researchers and clinicians want to mirror natural bile acid composition. Batch-to-batch reproducibility has become even more important as global supply chains grow more complex. By handling all processing and QA ourselves, without relying on third parties, we can promise genuine continuity to demanding labs.

    The differences show up not only in technical data but also in day-to-day lab performance. For example, our staff often hears about product behavior in liposome encapsulations, topical agents, and oral delivery vehicles. We know, based on multiple case reports, that some grades sourced from mixed animals leave behind residues or undetectable contaminants that interact with lipids in unplanned ways. Our focus on porcine-only, with meticulous clean-up, reduces those unknowns for our partners.

    Forward-Looking: Addressing New Challenges in the Field

    Research teams working on metabolic syndromes or liver conditions are once again increasing their expectations of raw materials. As more biosafety and environmental guidelines come into force, we find the current standard of transparency isn’t enough. That’s driving us to deepen traceability, documenting everything from abattoir handling to final QA. Our perspective from daily manufacturing keeps us tuned into these changes and ahead of emergent requirements, before they become industry-wide mandates.

    We’re keeping an eye on movements towards more sustainable, humane practices in sourcing. Many partners ask us about animal welfare, antibiotic usage, or environmental impact linked to sourcing. We respond with open process audits. Our technical teams are right now evaluating options such as lower-impact extraction solvents, integrated waste water handling, and reduced transportation distances. This is real, difficult work, requiring investment and both technical and logistical experience—something we’ve built through producing these products in-house for decades.

    Conclusion: Value from Experience at Every Step

    The journey from raw porcine bile to a clean, high-spec deoxycholic acid crystal is no straight line. Every batch involves scientists, machine operators, QA leads, and frontline staff bringing practical know-how to bear at each stage. Over years, we’ve adapted not by following trends but by responding to direct user feedback, regulatory pressure, and our own observations from the floor. For those who care about reliability, performance, and true traceability, these lessons matter far more than any product sheet or marketing claim. As we move forward, the insights from daily manufacturing—real work, real process—will continue to shape what we offer to research and formulation teams worldwide.