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Methyl 5-Aminosalicylate

    • Product Name Methyl 5-Aminosalicylate
    • Alias Mesalamine
    • Einecs 699-412-2
    • 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

    347391

    Chemical Name Methyl 5-Aminosalicylate
    Cas Number 89-57-6
    Molecular Formula C8H9NO3
    Molar Mass 167.16 g/mol
    Appearance White to off-white crystalline powder
    Melting Point 164-168 °C
    Solubility In Water Slightly soluble
    Density 1.38 g/cm3 (approximate)
    Pka 3.08 (carboxylic acid group)
    Smiles COC(=O)c1cc(N)cc(O)c1
    Inchi InChI=1S/C8H9NO3/c1-12-8(11)5-2-3-6(9)7(10)4-5/h2-4,10H,9H2,1H3

    As an accredited Methyl 5-Aminosalicylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White plastic bottle with screw cap, labeled "Methyl 5-Aminosalicylate, 25g," includes hazard pictograms, batch number, and safety instructions.
    Shipping Methyl 5-Aminosalicylate is typically shipped in tightly sealed containers, protected from light and moisture. Packaging must comply with local and international regulations for chemical transport. The product should be labeled properly with safety and hazard warnings and transported under conditions that minimize the risk of spillage, contamination, or degradation during transit.
    Storage Methyl 5-Aminosalicylate should be stored in a tightly closed container, kept in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers and acids. Protect from light and moisture. Store at room temperature, avoiding excessive heat. Ensure proper labeling and access restrictions for authorized personnel to prevent unauthorized use or accidental exposure.
    Application of Methyl 5-Aminosalicylate

    Applications of Methyl 5-Aminosalicylate in Industrial Manufacturing

    As a specialized producer of Methyl 5-Aminosalicylate, we support a range of industrial sectors where regulated demands for purity, reproducibility, and traceability drive the incorporation of this intermediate. Below, we outline the principal application scenarios reflecting current global manufacturing practice, each with detailed compliance, formulation, downstream integration, and end-use profiles directly observed in industry.

    1. Active Pharmaceutical Ingredient (API) Synthesis for 5-Aminosalicylic Acid Derivatives

    Methyl 5-Aminosalicylate plays a pivotal role as a chemical intermediate in the multi-step synthesis of anti-inflammatory APIs such as mesalazine and related 5-ASA compounds used in gastrointestinal therapies. Its use is governed by strict pharmaceutical guidelines and batch traceability, ensuring product reliability and patient safety from raw material to finished dosage forms.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP EudraLex Volume 4
    • United States Pharmacopeia (USP) general chapters related to raw material purity
    • European Pharmacopoeia (Ph. Eur.) monographs where 5-ASA derivatives are specified

    Typical usage ratio

    • Industrial protocols typically use 100–120% molar equivalence relative to downstream target, with excess adjusted based on impurity control and reaction yield requirements in the initial amidation or saponification step.

    Downstream process integration

    • Introduced at the primary or secondary synthesis stage, usually following ester hydrolysis or amidation under controlled temperature and pH to generate the target amino acid structure, followed by purification steps prior to final API crystallization.

    Final product types

    • Tableted and encapsulated prescription medications (enteric-coated mesalamine, slow-release 5-ASA tablets)
    • Otic and rectal suspensions for colitis and Crohn’s disease

    2. Fine Chemical Intermediate for Dye and Pigment Synthesis

    This compound serves as a key intermediate in the manufacturing of azo and anthraquinone dyes, where its amino and ester groups facilitate targeted functionalization. In this sector, manufacturers demand strict adherence to impurity profiles, and downstream processing focuses on maximizing chromophore yield and shade stability for textile and printing applications.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for chemical manufacturing
    • REACH Regulation (EC) No 1907/2006 for substance registration
    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals – Manufacturing Restricted Substances List) for textile chemicals

    Typical usage ratio

    • Varies from 10–35% by weight in the diazotization or coupling reaction batch, adjusted according to chromophore design and solubility constraints in the target dye molecule.

    Downstream process integration

    • Added into the controlled diazotization phase or directly coupled in aqueous or organic solvent media, depending on pigment or dye molecular engineering requirements; downstream, the resultant dye undergoes filtration, washing, and spray drying before standardization.

    Final product types

    • Reactive and disperse dyes for synthetic and natural fiber coloration
    • Specialty pigments for printing inks and plastics

    3. API Intermediate in Contrast Agent Manufacturing

    Downstream radiology sectors utilize this building block for the synthesis of certain aromatic amine derivatives used in contrast media, especially for MRI contrast agents. The production flow incorporates this raw material under tightly monitored cleanliness and impurity control, responding to the high safety and purity expectations demanded by the imaging agent market.

    Industry compliance standards

    • ICH Q11 for pharmaceutical development of APIs
    • FDA cGMP 21 CFR Part 210/211
    • European Pharmacopoeia standards for imaging substances

    Typical usage ratio

    • Utilized in stoichiometric or slight excess proportions (typically 1.1–1.25 molar equivalents), with precise adjustment based on subsequent chelation and aromatic substitution success rates.

    Downstream process integration

    • Incorporated during the aromatic amine derivatization stage, often preceding chelation with metal ions such as gadolinium; downstream processing includes ultrafiltration, purification, and lyophilization to produce the injectable final product.

    Final product types

    • Injectable MRI contrast agents (e.g., gadolinium-based complex solutions)
    • Powdered intermediates for reconstitution in diagnostic imaging kits

    4. Analytical Reagent and Reference Standard Production

    Chemical quality control and pharmaceutical R&D labs integrate this compound into the synthesis of high-purity reference materials and analytical reagents, especially where aminated salicylate markers are needed for calibration and trace impurity quantification. The focus is on ensuring batch reproducibility and meeting documentation protocols for traceability in regulated environments.

    Industry compliance standards

    • ISO 17034 General Requirements for Competence of Reference Material Producers
    • ISO/IEC 17025 for testing and calibration laboratory accreditation
    • USP-NF General Chapters for Analytical Reagents

    Typical usage ratio

    • Employed at 95–100% active content for standard preparations, with the dosage determined precisely by required analytical purity and scale of reference sample batch production.

    Downstream process integration

    • Dissolved or reconstituted as a standard solution or solid reference under inert atmosphere; follows microfiltration, aliquoting, and certification as per reference material or analytical solution protocols.

    Final product types

    • Certified reference standards for pharmacopoeial assays
    • Chromatographic calibration solutions
    • Analytical grade reagents for laboratory QC procedures

    5. Industrial API Intermediate for Veterinary Pharmaceuticals

    Veterinary manufacturers routinely apply this compound as an intermediate for non-steroidal anti-inflammatory drug (NSAID) vet products. Its integration must conform to pharmacopeial and animal health regulations, with traceability to support animal food product safety and downstream processing for injectables and oral suspensions tailored for livestock care.

    Industry compliance standards

    • VICH GL Guidelines (International Cooperation on Harmonisation of Technical Requirements for Registration of Veterinary Medicinal Products)
    • Pharmacopoeia Europaea Vet
    • EMA GMP for Veterinary Medicinal Products

    Typical usage ratio

    • Usage rates of 100–130% mole basis in intermediate stages prior to final molecule assembly, with actual value defined by livestock dosage form requirements and in-process analytical validation data.

    Downstream process integration

    • Added after initial ester hydrolysis in closed reactors under veterinary GMP standards, followed by purification and microfiltration steps tailored for parenteral or oral veterinary dosage forms.

    Final product types

    • Oral and injectable NSAIDs for cattle, swine, and companion animals
    • Veterinary topical anti-inflammatory formulations
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    Certification & Compliance
    More Introduction

    Introducing Methyl 5-Aminosalicylate: Direct from Our Reactor

    From Reactor to Real-World Uses

    Methyl 5-Aminosalicylate stands out among the salicylate family as a unique bridge between classic functional chemistry and modern process requirements. Many years ago, our first batches took shape in small glass-lined reactors, fueled by curiosity about how small structural tweaks could unlock new chemical behavior. Today, production takes place under strict thermal management in stainless reactors, but we approach every lot with the same attention to detail and curiosity about its place in larger chemical stories.

    Production Insights and Specification Details

    This compound has a molecular formula of C8H9NO3 and a molecular weight of 167.16. We prepare it with a methyl ester protecting group on the carboxyl site of 5-aminosalicylic acid, which for many downstream processes makes all the difference. Over years of scaling, we’ve honed the filtration and drying process for this product—crystal brightness and consistency matter, as do subtle aspects like moisture and trace metal content. For research and downstream synthesis, purity remains non-negotiable; we keep our minimum at 99.0% (HPLC), because even small impurities can complicate analytical profiles, stall reactions, or create headaches at the regulatory end.

    Customers often ask about color and appearance. Each batch emerges as a pale yellow to off-white crystalline powder—a signal to chemists that they’re dealing with a clean, well-handled aromatic amine. Odor is faint, reminiscent of mildly sweet phenols, which you’ll notice if you handle bulk quantities. Moisture content runs below 0.5%, and we work to minimize residual solvents well below accepted safety thresholds. Small tweaks in process parameters—solvent polarity, crystallization temperature—change not only the appearance but how easily the product dissolves for different steps downstream.

    How We Use It—and See Others Use It

    Most of the stories we hear start with active pharmaceutical ingredient (API) synthesis. Methyl 5-Aminosalicylate serves specialists chasing new anti-inflammatory or antimicrobial derivatives. The methyl ester group encourages smooth acylation, alkylation, and amidation compared to the free acid form, which opens up new reactions without risking fragile carboxylic acid rearrangements. You see this in both large-scale pharma production and research labs targeting selective enzyme inhibitors or imaging probes.

    We’ve watched it win favor with custom synthesis teams. Some customers work with sulfonation, nitration, or halogenation to tune the aromatic ring, and after years spent troubleshooting batch inconsistencies, we understand why they prefer the methylated form. Its stability lets chemists push more aggressive conditions without hydrolysis or side-product headaches. Others leverage its solubility profile: the methyl group nudges the compound’s hydrophobicity, helping it dissolve better in polar aprotic solvents. This practical difference proves crucial whether someone’s carrying out multistep solution-phase chemistry or fine-tuning crystallinity for purification.

    Practical Differences from Free Acid and Other Salicylates

    Comparisons often come up between Methyl 5-Aminosalicylate and 5-Aminosalicylic acid itself. The free acid form, while foundational for some work, stalls under certain reaction conditions—acid chlorides and coupling reagents often degrade or complicate yields. Protection with the methyl group sidesteps those issues. We’ve also heard from industrial groups who swap between methyl and ethyl esters, weighing differences in reactivity and volatility; in our operations, we’ve found the methyl ester offers finer granularity of control without introducing unwanted volatiles in downstream use.

    Against classic methyl salicylate, our product introduces the amine group at the 5-position, shifting both reactivity and biological interest. This shift carries real scientific and business impact, especially as research pivots towards amine-based analogues for advanced healing agents or diagnostic tools. Customers that handle both products have told us repeatedly: the 5-amino derivative opens doors closed to others, simplifying coupling with electrophiles or isocyanates, and expanding the palette for medicinal chemists pushing into new territory.

    Quality Control from Chemist to Chemist

    For those of us behind the scenes, every drum of Methyl 5-Aminosalicylate is more than a product—it’s a confirmation of routes optimized, filtration tightened, solvents recycled, and workflows scrutinized for years on the plant floor. Analytical controls—HPLC, GC, NMR—catch the big picture and the outlier event, but tactile details remain fresh in our memory: how the slurry thickens, how the filtration cakes respond to pressure, when to change out gaskets or recalibrate thermocouples. These details shape not just yield, but peace of mind for every downstream chemist.

    Audits come often, and the questions have evolved: raw material chain-of-custody, cross-contamination in shared reactors, residual solvent mapping, stability under forced degradation. Meeting these means weaving documentation into every step, not just at labeling or dispatch. Our QC team, most having spent time on the synthesis floor, insists on live sampling and batch tracebacks that go beyond what’s commoditized in the market. We see this as the basis for trust—without it, no molecular innovation lasts.

    Shipping, Storage, and Long-Term Stability

    Every chemist knows the perils of off-spec storage—moisture and light sensitivity cause costly surprises in complex molecules. We’ve learned that storing Methyl 5-Aminosalicylate in sealed, light-resistant drums at <20°C keeps its integrity for over two years. We help customers work out batch splits for regular inventory rotation. Large customers working in cGMP pipelines request retesting and interim certifications during long logistics pipelines, and we maintain inventory mechanisms that allow flexible delivery while keeping product fresh.

    Over years of exporting to a dozen regions, we encountered situations like monsoon season delays or customs standoffs, each with their own risk for exposure or mishandling. The drum linings and outer carton build keep water vapor and accidental sunlight at bay. With temperature-monitored transport, we’ve kept rejection rates below traceable levels even when containers spent unexpected time in transit. These practicalities matter more than marketing copy: from the receiving dock, a synthesis campaign can soar or stall based on daily observable quality.

    Handling the Complexities of Large Orders and New Requests

    As order volumes increase, so does the challenge of reproducibility and transparency. Early on, we scaled up from kilogram to multi-ton orders with some uncertainty, tracking yield drops or new impurity formation. Floor supervisors found ways to tweak stir rates, solvent charges, and aging times to handle larger thermal loads and mixing gradients, documenting changes so buyers could track consistency lot by lot. The learning curve included mistakes and many “trial runs”—we don’t shy away from sharing these trials with partners needing clarity on how we handle deviations or recoveries.

    Not every customer needs batch quantities or the highest purity; some prefer technical grade for bulk industrial transformations. We produce both, but make boundaries clear: no interchangeability between high-purity research work and non-pharma technical uses. Communication about these differences builds stronger long-term relationships because, as we’ve seen, surprises downstream always loop back upstream.

    Our Place in Research, Development, and Innovation

    Most feedback arrives from researchers innovating in drug discovery or specialty chemicals development. Fields like prodrug design, imaging agent development, and next-generation anti-inflammatory therapies often start with the choices made on our production line. A single methyl group, installed cleanly on the scaffold, can shift how a molecule interacts in both reaction flask and biological assay. We’ve seen teams transform our product into new amide derivatives, azo compounds, or even as a handle for PEGylation. These successes feed our process improvements, and we welcome collaboration—even on customization beyond current catalog specs.

    We don’t pretend every lot is perfect, so we treat every complaint as a cue to dig into our own practices. Whether it’s a solubility oddity or a seasonal color shift, solutions come out of direct lab and plant feedback loops. This keeps us close to the real world of the product’s uses—it’s one reason why many of our longest-running clients started as phone calls about unusual analytical results, not sales pitches.

    Regulatory Perspectives, Safety, and Continuous Improvement

    The increasing focus on quality control and regulatory demands means chemists across the supply chain share one priority—certainty. We respond to this by keeping up with evolving standards for trace impurities, process contaminants, and data integrity, particularly in regulated regions. Each run comes with fresh analytical documentation and, on request, extended impurity profiling, so project chemists can clear hurdles quicker.

    In the plant and warehouse, safety protocols shape how we weigh, pack, and label; Methyl 5-Aminosalicylate does not pose the volatility risk of some related compounds, but proper controls for dust handling and spill management remain core parts of every shift’s training. No operation runs on autopilot—our team keeps logs, refreshes standard operating procedures, and invites both internal and customer-driven audits. Change—whether in supply, regulatory updates, or end-use application—drives new cycles of risk assessment, never a static checklist.

    Looking Ahead—Where the Chemistry Moves Next

    We track new research efforts that expand the utility of the 5-amino substitution. Medicinal chemists report activity improvements rarely seen with standard methyl salicylate analogues; these applications continue to grow, from anti-psoriatic prodrugs to anti-infective candidates. In materials work, functional group transformations offer easier access to new dendritic structures and surface-modified polymers. Our part remains making sure each kilogram delivers the reactivity, color, and profile needed to fuel these efforts.

    We back each new mode of use—be it an enzymatic transformation or advanced materials project—with frank technical support. Inquiries often get routed from the lab, not a customer hotline. We support direct troubleshooting, analyzing NMR or HPLC spectra in parallel with the customer, helping troubleshoot stuck reactions or evaluating unknown byproducts. Our staff shares methods, not just material. There’s little glamour in synthetic plant work, but sustained partnership means seeing each job through from order to purification to end-use result.

    Conclusion—How Our Commitment Shapes Your Chemistry

    Every kilogram of Methyl 5-Aminosalicylate passing through our doors reflects a collective commitment—from sourcing to synthesis, from filtration to final packing. In a space where process control, safety, and transparency define every step, we draw our satisfaction from knowing our product supports advances that reach far beyond our own facility. We listen, adapt, and refine, keeping communication open and details transparent. This approach gives partners confidence in both today’s product and tomorrow’s challenges.

    In choosing Methyl 5-Aminosalicylate from us, you connect not just with a reagent, but with the accumulated experience of a team rooted in hands-on chemistry. With every request, challenge, and collaboration, we aim not for abstracts, but the solid facts: a clean product, honest documentation, practical solutions, and lasting impact wherever new chemistry happens.