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Arundic Acid

    • Product Name Arundic Acid
    • Alias ONO-2506
    • Einecs 691-110-4
    • 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

    815535

    name Arundic Acid
    chemical_formula C17H15NO4S
    molecular_weight 329.37 g/mol
    CAS_number 19485-54-4
    appearance White to off-white powder
    solubility Slightly soluble in DMSO
    mechanism_of_action Inhibitor of S100B synthesis
    primary_use Neuroprotective agent
    IUPAC_name 3-Phenyl-5-[(phenylsulfonyl)methyl]-2,4-oxazolidinedione
    Melting_point 155-157°C

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

    Packing & Storage
    Packing Arundic Acid, 5 grams: Supplied in a sealed amber glass vial, labeled clearly with product name, quantity, and safety information.
    Shipping Arundic Acid is shipped in secure, airtight containers to protect it from moisture and contamination. Packaging complies with standard chemical transportation regulations. It is labeled with clear hazard information and safety instructions. Shipment is typically made via ground or air freight, depending on destination and quantity, ensuring safe and compliant delivery.
    Storage Arundic Acid should be stored in a tightly closed container, protected from light and moisture. Keep it at room temperature, ideally between 2–8°C (refrigerated), and in a well-ventilated, dry area. Ensure storage is away from incompatible substances, and clearly label the container. Follow all relevant safety and handling regulations for chemicals in your facility.
    Application of Arundic Acid

    Applications of Arundic Acid in Industrial Manufacturing

    Arundic Acid, manufactured at our facility under strict quality controls, supports advanced chemical processes across multiple industrial sectors. Through our technical expertise, we ensure that each application complies with prevailing market and regulatory demands, delivering consistent performance for downstream producers.

    1. Pharmaceutical API Synthesis for Neurological Agents

    In pharmaceutical manufacturing, Arundic Acid functions as a key intermediate for the synthesis of neuroprotective active pharmaceutical ingredients (APIs), specifically for treatments targeting neurodegenerative diseases such as Alzheimer’s and Amyotrophic Lateral Sclerosis (ALS). Its use centers around the controlled formation of CNS-active molecules during multi-step organic synthesis. Production lines demand analytical-grade purity, controlled crystallization, and traceability for each input batch to meet strict pharmacological requirements. Manufacturers control residual solvent profiles and impurity thresholds based on pharmacopeia standards. The finished APIs proceed directly to formulation and clinical supply chains for oral dosage forms and injectable therapeutics.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP) – 21 CFR Parts 210/211 (US FDA)
    • European Pharmacopoeia (Ph. Eur.) monographs for CNS APIs
    • USP–NF standards for related substances, purity, and validation
    • ICH Q3A/B guidelines for impurities and residual solvents

    Typical usage ratio

    • Employed as an API intermediate at 0.25–1.5 molar equivalents in multi-step batch synthesis, based on exact target molecule; process R&D optimizes equivalents based on yield and impurity minimization.

    Downstream process integration

    • Introduced after initial aromatic coupling, entering the CNS-active ring construction step; purification follows with preparative chromatography or crystallization depending on synthetic route.

    Final product types

    • Finished APIs for oral solid dose (tablet, capsule)
    • Liquid and lyophilized injectables for neurology therapy
    • Bulk pharmaceutical intermediates for CDMOs

    2. Research-Grade Biochemistry Reagents

    Academic and biotech research institutions utilize Arundic Acid as a neuroinflammation modulator in vitro and in vivo. Application protocols commonly require high-purity lots (≥98%) with validated analytical certificates for reproducibility in cellular assays, biochemical studies, or preclinical animal models. Researchers dissolve the material in specific buffers or organic solvents depending on assay design, evaluating neuroprotective properties or glial cell modulation. Documentation includes batch traceability, low endotoxin content, and product release via independent labs. The material reaches downstream customers through direct supply or contract research partners executing neuroscience projects.

    Industry compliance standards

    • ISO 9001:2015 (Quality Management Systems for analytical manufacturing)
    • GLP (Good Laboratory Practice) documentation for reagent traceability
    • Institutional Animal Care and Use Committee (IACUC) references for in vivo use
    • Declaration of Research Use Only—non-GMP, not for therapeutic application

    Typical usage ratio

    • Applied at 1–50 μM in cell cultures; 1–50 mg/kg in animal studies, determined by principal investigator protocols and peer-reviewed literature references.

    Downstream process integration

    • Weighted and diluted by researchers before application to neuron-glia co-cultures, or prepared as injectable solutions for animal models of neurological disorders.

    Final product types

    • Preclinical assay kits
    • Custom research reagents for neuroscience
    • Contract research services involving neurodegenerative disease models

    3. Precursor in Fine Chemical Synthesis of Specialty Compounds

    Chemical manufacturers employ Arundic Acid for its unique aromatic structure during the development of high-value specialty compounds, including CNS-targeted probe molecules and advanced pharmaceutical building blocks. Fine chemical facilities require tight control of reaction temperatures, solvent environments, and catalyst systems for efficient incorporation. Material performance depends on stability during nitration, halogenation, or esterification steps, with batches certified for minimum impurity and moisture content. Resulting specialty compounds proceed to formulation or further derivatization based on contract manufacturing partner requirements.

    Industry compliance standards

    • REACH (Registration, Evaluation, Authorisation, and Restriction of Chemicals – EU regulations)
    • ISO 14001 (Environmental Management for chemical synthesis)
    • Hazardous chemical control—local government permits for precursor use
    • Custom specifications from downstream partners (analytical validation, impurity profiling)

    Typical usage ratio

    • Ranged at 0.1–2.0 equivalents per batch scale, adjusted according to specific downstream synthetic requirements and process mass intensity (PMI) calculations.

    Downstream process integration

    • Charged into reactor vessels following preliminary catalyst or solvent addition; enters stepwise amidation, aromatic substitution, or selective reduction reactions within multi-step synthetic workflows.

    Final product types

    • Advanced pharmaceutical intermediates
    • Neurobiological chemical probes
    • Reference standards for analytical chemistry

    4. Preclinical Drug Development Screening

    Contract research organizations and pharmaceutical developers require Arundic Acid for early-stage compound screening, assessing neuroprotective effects and mechanistic pathways in electrophysiological and biochemical assays. The material’s reproducibility in assay formats, low batch-to-batch variability, and traceability facilitate validation of results across multiple sites. Preclinical testing platforms specify purity parameters and release analytics to fit protocol endpoints. Compounds screened undergo lead optimization prior to regulatory submission or further animal model validation. The supply chain prioritizes rapid turnaround, detailed documentation, and technical support for assay troubleshooting.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP)
    • 21 CFR Part 58 (US FDA GLP regulations)
    • ICH M3(R2) guidelines on nonclinical safety studies
    • Material Transfer Agreements (MTA) for controlled research access

    Typical usage ratio

    • Used at 10 nM–100 μM in high-throughput screening plates, with concentration determined by assay sensitivity and the developmental stage of the candidate molecule.

    Downstream process integration

    • Solutions prepared by lab automation systems or manual pipetting, introduced into cell-based or receptor-binding assays that inform candidate selection and pathway analysis.

    Final product types

    • Screening libraries of CNS-active compounds
    • Electrophysiological assay kits
    • Custom-developed lead candidates for further medicinal chemistry
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    Certification & Compliance
    More Introduction

    Arundic Acid: Experience from the Manufacturer’s View

    Working hands-on with chemicals for decades means learning what makes one molecule stand out from the crowd. These aren’t lessons from textbooks—they come from thousands of production batches, feedback cycles, and a relentless push to meet the changing demands in neuropharmacology and beyond. Among the compounds we've handled, Arundic Acid has steadily gained traction as a research cornerstone, both in academic investigations and in early-stage pharmaceutical projects focused on nervous system protection and repair.

    A Closer Look at Arundic Acid

    Arundic Acid (also known in academic circles as ONO-2506 or 3-methylbenzyl-2-acetylamino-3-(4-hydroxyphenyl)propionate) captured researchers’ attention over twenty-five years ago with its role in modulating glial cell activation and its described neuroprotective effects. From our standpoint as chemical manufacturers, what matters most—apart from its molecular promise—remains consistency in synthesis, reliability in purity, and clear utility for our clients’ applications.

    We’ve standardized our processes to produce Arundic Acid in batches ranging from kilogram- to multi-hundred-gram scales, targeting 98–99% purity as confirmed by HPLC and NMR (proton and carbon). This achieves reliable results whether a researcher is conducting in vitro bioassays or scaling up to small animal studies. Over time, incremental investments in reactor volumetrics and purification columns have yielded not just higher output, but a noticeable reduction in the byproduct spectrum and more manageable waste streams, translating to predictable composition every time.

    Model and Specifications: No Room for Guesswork

    From the ground up, manufacturing Arundic Acid means walking the fine line between reliable synthesis and sustainability. The essential starting point, in our operations, is the correct sourcing of aromatic precursors and phenolic esters—each batch we accept hits a benchmark for trace metals, moisture content, and residual solvents. After refining substrate and catalyst loads during hydrogenation and esterification, monitoring the reaction kinetics closely, we press on with crystallization protocols derived from actual pilot-scale results instead of textbook theory.

    Each time the output drifts even half a percent off-spec on melting point or spectral signature, we halt for analysis. These checks have saved more than a few lots from expensive post-processing or failed customer applications. It’s a lesson burned into our workflow: quality has to be built into each process step, not tried at the endpoint. Our final product, white to pale yellow crystalline solid, typically maintains melting points around 122–124°C, with loss-on-drying routinely below 0.5%. Ash tests confirm complete removal of inorganic residues, supporting high reproducibility in downstream experiments. We monitor stability under ambient and refrigerated conditions for six to twelve months, offering data to clients who need to plan out their research timelines or stock management.

    Usage: Why Institutions Rely on Arundic Acid

    The main audience for Arundic Acid outside our factory is the research community working on neurodegenerative models and studies on glial inflammation. Academics, biotech companies, and pharmaceutical R&D teams make up most of our client base. Researchers usually dissolve the product in DMSO, ethanol, or saline for in vitro assays, or formulate into suspensions for in vivo neurological studies. Each year, we see more protocols testing its potential role in treating brain ischemia, traumatic brain injury, amyloid pathology, and more. This growth reflects a global hunger for new neuroprotective strategies as populations age and chronic conditions increase in frequency.

    Feedback reaches us straight from the bench. A research team might report on the compound’s activity profile against S100β expression in astrocytes. Others might run comparative trials between Arundic Acid and established glial inhibitors, probing subtle differences in toxicity or experimental reproducibility. Over time, our own familiarity with the molecule’s behaviors—solubility quirks, storage needs, interactions with glassware—lets us coach clients past early sticking points before they disrupt months of data collection.

    We field questions from institutions considering bulk purchases as their in vivo trial designs expand. For larger lots, some clients request finer particle sizes or micronization to improve dissolution, and we can modify our final process—usually by employing additional milling steps or adjusting solvent ratios—to accommodate those requirements. Our regular production cycle allows us to fulfill both small research orders and industrial quantities under the same consistent process.

    How Arundic Acid Differs from Other Analytical Compounds

    Walking down the production floor, it’s easy to spot which products require the most involved quality checks. Arundic Acid routinely sits on the shelf next to other neuroactive agents—sometimes side by side with riluzole, clozapine, or memantine. Still, every molecule brings its own quirks. We have learned that Arundic Acid’s biggest distinction, compared to related glial modulators, comes down to purity threshold, shelf stability, and the flexibility of supply.

    Our product—the direct result of controlled esterification and amide formation—rarely shows the same tendency toward oxidative decomposition that plagues some other benzamide derivatives. This means storage requirements impose less hassle for academic labs with only basic refrigeration. The photostability and absence of offending side-isomer peaks in quality control spectra allow researchers to focus on their own variables instead of chemical anomalies.

    Compared with other neuropharmacological agents, Arundic Acid offers a profile that supports longer shelf life and easier formulation. Some commonly discussed alternatives demand special handling atmospheres to prevent degradation or formation of unwanted hydrolysis products. By contrast, Arundic Acid remains stable in dry air, resists color changes, and holds up after repeated opening—attributes lab managers appreciate when running expensive studies on a tight timeline.

    Lessons from Batch to Batch

    From the vantage point of the production team, smooth manufacturing is about anticipating what could go wrong and removing those possibilities up front. Each batch we prepare flows through a staged gate system, with temperature, pH, and reaction time checks verified by staff instead of relying on automation alone. Over the years, this habit has led to process updates: we now employ automated leak and pressure detectors during hydrogenations, and we maintain redundant chromatographic lines for both process checks and final-release analysis.

    Every process adjustment stems from a real-world challenge. For example, initial production runs years ago revealed sensitivity to small changes in batch temperature during amide coupling—leading to inconsistent yields and variable impurity profiles. Unwilling to accept “normal” batch-to-batch fluctuations, our crew experimented with jacketed reactors, more precise temperature controls, and real-time HPLC monitoring. Now, even when raw material quality varies slightly, we catch deviations before they compromise the whole batch.

    Lessons aren’t always confined to process mechanics. We have witnessed research clients run into setbacks because of unanticipated solubility limits or reactivity with test buffers. In response, we not only share product specifications but maintain ready dialogue with technical teams, offering practical tips—like the optimum solvent mix, pH range for dissolution, and handling techniques to avoid static aggregation in powder forms.

    Tracing the Impact: From Factory to Lab

    The most satisfying moments in this kind of work come when academic articles, conference posters, and new patent filings mention successful applications based on our Arundic Acid. Having shipped to universities, biotech startups, and contract research organizations across multiple continents, we keep tabs on published outcomes and report summaries provided back to us by longtime partners. These stories often describe Arundic Acid’s unique role in reducing neuroinflammation or supporting white matter integrity in rodent models. Over time, the accumulated evidence builds a practical sense of where and how Arundic Acid adds direct value to scientific progress.

    We avoid making broad claims or leaning on unproven marketing. Instead, we reference specific published findings—in which our material contributed to the inhibition of S100β, demonstrated modulation of astrogliosis, or extended survival in certain animal models—spoken from actual delivery records rather than speculation. The feedback has pushed us to improve not just the chemical itself, but shipping protocols, shelf-life analysis, and even packaging to minimize transit-time impact, especially for international clients facing longer customs windows.

    Sustainable Sourcing and Environmental Responsibility

    Years of manufacturing have taught us to respect both the resource inputs and the broader environmental impact of specialty chemicals. Our drive to achieve high purity in Arundic Acid doesn’t come at the expense of the environment. We choose starting materials verified for responsible sourcing, verify all supply chains for transparency, and handle waste streams with active recycling wherever practical. Production scale-up involves improving solvent recovery and switching to lower-impact catalysts while maintaining product consistency and yield. We worked with process safety experts to develop containment systems for both volatile and non-volatile process wastes, turning what once required costly off-site remediation into manageable in-house recycling or neutralization steps.

    Every few months, the team evaluates new options for greener solvents or streamlined reaction conditions. In several cases, these adjustments have led to measurable reductions in both hazardous waste generation and overall energy consumption per kilogram of product. We share these milestones openly with clients interested in life cycle analysis, knowing every entity in the chemical value chain is increasingly tasked with transparent reporting and responsible stewardship. Our commitment isn’t static; the drive for continual improvement ensures that tomorrow’s Arundic Acid remains every bit as reliable, if not more so, than today’s.

    Solving Real-World Issues: Feedback Loop with Researchers

    Trust builds slowly. By regularly inviting honest feedback from end-users, we’ve developed practical remedies for common lab issues. Take for instance the question of solubility—many researchers voiced concerns about dissolution times, which directly affect experiment setup and reproducibility. Listening to their hands-on problems, we now include an optimized solvent recommendation sheet with each shipment, summarizing concentration limits and agitation protocols based on observed lab results. For those facing supply chain bottlenecks, our supply planners forecast demand months in advance and keep buffered inventory, so institutions on tight grant deadlines don’t face material shortages midway through critical studies.

    We also stay on top of regulatory expectations. Our batches ship with complete documentation covering traceability, conformance certificates, batch analysis data, and SDS in standard formats. For export controls or new regulatory designations, dedicated compliance staff handle paperwork and stay engaged with emerging legal guidelines. This approach has kept international deliveries punctual and ensured our products enter research workflows without customs holdups or unforeseen interruptions.

    Focusing on What Matters

    From a manufacturer’s viewpoint, Arundic Acid is more than a tradename on a label. It’s a molecular tool developed through iterative learning, direct collaboration with scientists, and a drive for ongoing process refinement. The value stems from measurable outcomes: transparent quality assurance, clear feedback channels, and straightforward logistics, all grounded in practical know-how. With every order filled, our team applies years of hands-on experience to deliver reliable, high-quality material—ensuring that researchers relying on Arundic Acid can stake their ideas on a dependable foundation, batch after batch.

    Where many specialty compounds come with question marks about consistency and supply, we offer a record drawn from thousands of production hours, open dialogue with users, and practical engineering to balance performance and sustainability. That experience, more than anything, continues to shape how Arundic Acid contributes to the expanding field of neuropharmacology and beyond.