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3,5-Dimethylpyrrole-2-Carboxylic Acid

    • Product Name 3,5-Dimethylpyrrole-2-Carboxylic Acid
    • Alias 3,5-Dimethyl-2-pyrrolecarboxylic acid
    • Einecs 606-162-6
    • 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

    155778

    Productname 3,5-Dimethylpyrrole-2-Carboxylic Acid
    Casnumber 55151-69-0
    Molecularformula C7H9NO2
    Molecularweight 139.15
    Appearance White to off-white solid
    Meltingpoint 140-144°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Storageconditions Store at 2-8°C, protected from light
    Purity Typically ≥ 98%
    Smiles CC1=CC(=C(N1)C(=O)O)C
    Inchi InChI=1S/C7H9NO2/c1-5-3-6(2)8-4-7(5)9/h3-4,8H,1-2H3,(H,9,10)
    Synonyms 3,5-Dimethyl-1H-pyrrole-2-carboxylic acid

    As an accredited 3,5-Dimethylpyrrole-2-Carboxylic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 5g amber glass bottle, sealed with a screw cap, labeled "3,5-Dimethylpyrrole-2-Carboxylic Acid," with safety and handling information.
    Shipping **Shipping Description:** 3,5-Dimethylpyrrole-2-carboxylic acid is shipped in tightly sealed, chemical-resistant containers to prevent moisture or contamination. It should be packed securely according to hazardous material guidelines, accompanied by proper labeling and documentation. During transport, it is kept away from incompatible substances and maintained at recommended temperature and handling conditions.
    Storage 3,5-Dimethylpyrrole-2-carboxylic acid should be stored in a tightly sealed container, protected from light and moisture, in a cool, dry, well-ventilated area. Keep away from incompatible substances such as strong oxidizers. Label the container clearly, and avoid excessive heat. Store in accordance with relevant safety and chemical storage guidelines. Handle with appropriate personal protective equipment.
    Application of 3,5-Dimethylpyrrole-2-Carboxylic Acid

    Applications of 3,5-Dimethylpyrrole-2-Carboxylic Acid in Industrial Manufacturing

    As a direct manufacturer of 3,5-Dimethylpyrrole-2-Carboxylic Acid, we supply this intermediate to a range of specialized sectors. Each industrial application involves unique compliance guidelines, formulation approaches, and processing steps, resulting in distinct final products across life science, chemical, and material industries.

    1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredient (API) Synthesis

    API producers incorporate 3,5-Dimethylpyrrole-2-Carboxylic Acid into targeted heterocyclic synthesis, especially for manufacturing anti-infective and anti-cancer compounds. Our material enters multi-step organic processes such as Suzuki coupling or ring formation, where it serves as a strictly defined starting material. Manufacturers perform continuous GMP audits, monitor impurities at every batch, and optimize ratios for step-yield and cost. The resulting APIs require full traceability, and we provide batch-level documentation supporting submission to health authorities in regulated markets.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • U.S. Pharmacopeia (USP) and European Pharmacopeia (Ph. Eur.) monographs for process intermediates
    • FDA 21 CFR Part 211 (for related impurities and process controls)
    • REACH Registration (if imported into the EU)

    Typical usage ratio

    • 0.07 to 0.18 molar equivalents relative to core scaffold; adjustments based on target compound or patent constraints

    Downstream process integration

    • Direct addition to heterocyclic assembly step (e.g., via condensation or coupling reaction)
    • Strict input control into reactor under nitrogen or argon atmosphere
    • Real-time monitoring of reaction progress and residual starting material
    • Purification of intermediates by column chromatography or crystallization

    Final product types

    • Antimicrobial drug substances
    • Oncology API intermediates
    • Heterocyclic core fragments
    • Synthetic drug building blocks

    2. Agrochemical Synthesis Precursor

    Leading pesticide and plant growth regulator manufacturers use 3,5-Dimethylpyrrole-2-Carboxylic Acid to introduce substituted pyrrole motifs into new-generation actives. The raw material is charged into chlorination or acylation stages under closed-system handling. Quality teams scrutinize input purity due to strict downstream residue limits. Batch records document ratios and traceability for field trial registration dossiers per country-specific regulations.

    Industry compliance standards

    • FAO/WHO Specifications for Technical Grade Active Ingredients
    • OECD Guidelines for the Testing of Chemicals
    • ISO 9001:2015 Quality Management System
    • Globally Harmonized System (GHS) for hazard communication

    Typical usage ratio

    • 0.10 to 0.25 molar equivalents per synthetic sequence, adjusted based on target molecule and desired biological activity

    Downstream process integration

    • Charged in the heteroaromatic ring-forming stage
    • Kept under reduced pressure to minimize volatilization loss
    • Subsequent attachment of functional groups (e.g., halogenation, sulfonation)
    • Crystallization and water washing for impurity removal

    Final product types

    • Active ingredients for herbicides
    • Fungicide precursors
    • Insecticide intermediates
    • Growth regulator actives

    3. Dye and Pigment Intermediate for Specialty Colorants

    Specialty dye producers select our 3,5-Dimethylpyrrole-2-Carboxylic Acid for synthesizing advanced pyrrolic chromophores and metal-complex dyes. The intermediate enables precise electronic modification for improved colorfastness or spectral properties. High batch-to-batch consistency is required to meet textile or ink sector batch release criteria. Feed ratios are determined by the color index standard and targeted absorption band. Trace non-detectable impurity levels are critical for regulatory filings and end-user certification.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (textile applications)
    • DIN EN ISO 105 (color fastness testing)
    • ETAD (Ecological and Toxicological Association of Dyes and Organic Pigments Manufacturers) code of practice
    • Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH) for pigment intermediates

    Typical usage ratio

    • 3% to 9% w/w of total dye batch; variation according to pigment chroma or shade depth requirements

    Downstream process integration

    • Incorporation during core chromophore construction or metal-complex formation
    • Pre-formulation blending with rare earth metal salts or azo linkers
    • Stepwise purification by solvent extraction and pH shift
    • Final particle sizing or dispersion for textile and ink compatibility

    Final product types

    • Reactive textile dyes
    • High-stability printing pigments
    • Fluorescent security inks
    • Laser printer toners

    4. Functional Polymer Modification for Electronic Materials

    Advanced materials manufacturers deploy 3,5-Dimethylpyrrole-2-Carboxylic Acid to introduce conjugated nitrogen heterocycles into specialty polymers. This functionality achieves tailored conductivity, charge mobility, or solubility improvements in electronics. Stringent in-house QC checks control oligomer distribution and ensure feedstock purity before polymerization. The integration ratio depends on application-specific property targets such as dielectric loss or glass transition temperature (Tg).

    Industry compliance standards

    • IEC 60695-2-10 (electronic material flammability testing)
    • RoHS Directive (2011/65/EU) compliance
    • ISO 9001 for production traceability and QA documentation
    • UL 94 plastics flammability rating (finished goods)

    Typical usage ratio

    • 0.2% to 3.5% by mass of total monomer feed, varied based on molecular weight and specific device requirements

    Downstream process integration

    • Premix in polymerization reactor feed
    • Copolymerization or side-chain grafting under controlled temperature and solvent system
    • Post-polymerization blending for composite material creation
    • Vacuum drying and compounding into film or pellet

    Final product types

    • Conductive polymer films for flexible electronics
    • Dielectric layers in printed circuit substrates
    • Encapsulation materials for semiconductor packaging
    • Anti-static coatings
    Free Quote

    Competitive 3,5-Dimethylpyrrole-2-Carboxylic Acid prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    Introducing 3,5-Dimethylpyrrole-2-Carboxylic Acid: Building Blocks Born from Experience

    In the world of pharmaceutical and specialty chemical synthesis, 3,5-Dimethylpyrrole-2-Carboxylic Acid turns up as a quietly essential intermediate. We’ve spent years perfecting its production so research teams can trust each batch, whether advancing a new active pharmaceutical ingredient or stepping through a cosmeceutical pipeline. Consistent quality isn’t just a bullet point on a spec sheet; it’s the quiet guarantee built into every flask we ship.

    The Model We Manufacture: Molecular Simplicity, Chemical Potential

    3,5-Dimethylpyrrole-2-Carboxylic Acid, with our internal product reference DMPC-02, features the core structure: a pyrrole ring carrying methyl groups on the third and fifth carbon atoms, alongside a carboxylic acid at the second position. The CAS number many chemists recognize is 269-36-9, grounding our batches in established literature. Over time, we’ve observed that this specific substitution pattern is more than chemical trivia; it shapes reactivity and controls downstream chemistry.

    Our batches typically run with purity above 98%, measured by HPLC and substantiated by in-house NMR analysis. Color remains pale and consistent because variable hues point to stray tars and unwanted polymers — a sign quality slipped. We keep a tight grip on moisture and residual solvents, since trace contaminants can destabilize sensitive syntheses downstream. These may look like small details, but after decades spent talking with formulation chemists and pilot plant supervisors, they’re often what separates a workable batch from a bottleneck.

    Why This Small Molecule Earns Its Place in Synthesis Labs

    Why do chemists choose this particular acid over similar pyrrole derivatives? From our experience supporting customers ranging from academic PIs to process development groups at multinational companies, three reasons come up repeatedly.

    First, the methyl groups at 3 and 5 block unwanted side reactions. Pyrrole rings run reactive, but those two methyls stop over-bromination and keep the ring from getting torn apart under mild oxidative conditions. This isn’t theoretical — on the plant floor, cleaner conversions lead to higher yields, less column time, and a much easier time scaling. Carboxylic acids on non-methylated rings often drift off course, producing hard-to-remove purple tars and resinous byproducts.

    Second, 3,5-Dimethylpyrrole-2-Carboxylic Acid behaves predictably under most peptide coupling conditions, protecting chemists from unwanted rearrangements. Nobody wants to walk into work on Monday to find last week’s coupling reaction mucked up by spontaneous decarboxylation or ring-opening. Those features matter less to a catalog chemist than to process chemists under time pressure, but they save real headache during weeks when a bench project pivots into pilot-plant demands.

    Third, the methylation pattern changes solubility and crystal habit. Long ago, before switching to our present crystallization regime, we saw some batches of unprotected pyrrole carboxylic acids cake up in storage — clumping so tightly they needed to be hammered loose from barrels. Methylated versions flow better and resist cakes, which translates to easier weighing, dissolution, and blending in real-world manufacturing environments.

    Direct Applications: More Than a Reagent

    Pharmaceutical teams often use DMPC-02 early in API synthesis. Its carboxylic acid can transform into amides, esters, and other aryl derivatives without excessive purification hassle. Teams pursuing macrocycles count on this intermediate because it consistently slides into coupling reactions, helping splice together hard-to-form rings. After supporting hundreds of these syntheses, we find that our low-impurity profile saves much downstream pain: less need for chromatography and fewer stubborn, polar byproducts sticking to glassware for hours.

    In pigment, dye, and specialty coatings laboratories, this acid ends up as a precursor in heterocyclic pigment development. Some teams have told us that the methylated ring delivers superior color-fastness after coupling, compared to un-methylated analogues that drift or bleach under UV. This property isn’t universal, but the difference crops up often enough for seasoned formulators to keep our product close at hand.

    Cosmetic ingredient developers rely on the compound for its well-characterized, clean reactivity. Their focus lies in safety, so every batch must meet low heavy metal and residual organics standards. Our purification processes target these specifically, using protocols we developed together with regulatory and toxicology consultants. Beyond meeting regulations, that attention reassures procurement officers who field regulatory audits and customer inquiries.

    Comparison: How It Stands Apart from Other Pyrrole Carboxylic Acids

    We make several pyrrole carboxylic acids, each finding its place where chemistry or process requirements dictate. DMPC-02 is not the cheapest to produce. Still, its methylation at 3 and 5 blocks oxidative hot spots, delivering robust shelf stability. By contrast, the parent pyrrole-2-carboxylic acid spoils quickly, browns rapidly upon air exposure, and fouls glassware unless stored cold and dry. Even in strictly controlled environments, we hear chemists struggle with early decomposition.

    Another frequent point is route flexibility. Customers who use 3-methyl or 4-methyl substituted acids face more isomeric impurities after scaling up. Their crude products may carry a smattering of polymethylated rings, leading to batch-to-batch variability. The 3,5-dimethyl arrangement, on the other hand, locks down the ring so it yields just what teams expect.

    Those working on scale-up processes think about filtration and crystallization. Early on, we tried to support a customer’s transition from flask to pilot reactor for an unmethylated pyrrole acid. Solubility swings and variable filterability held things up for weeks. After switching to the dimethyl version, filtration became as predictable as clockwork, and yield-standard deviation dropped from 7% to 2%. Though a small molecule, these process improvements ripple all the way up to project managers and QA reviewers.

    Production Experience: Meeting Modern Process Demands

    Our manufacturing team spends as much time troubleshooting glassware performance as we do tuning chemistry. In producing 3,5-dimethylpyrrole-2-carboxylic acid, we’ve learned packaging matters as much as synthetic know-how. Early adopters pointed out that improper packaging can cause slight degradation, turning a white to beige powder into a sticky, tan mess. We’ve shifted to anti-static, low-moisture liners and airtight drums for all shipments, following up after every warm-weather transit season to make sure material arrives unchanged.

    Temperature matters, both during synthesis and storage. Uncontrolled crystallization rates, or even short exposure to ambient humidity, can send batch quality spinning sideways. That first-hand experience led us to automate drying and package under low humidity with rapid, closed transfer. Years ago, we relied on simple bulk-scale tray drying — it cost us several thousand euros in rejected batches one summer, a lesson we felt in real time.

    Lab and pilot teams need reproducible, traceable supply. Our analytical staff subjects every lot to in-house NMR, LC-MS, and wet assays — not because regulations say so, but because a missed contaminant at this stage can snowball into days of wasted effort downstream. We keep back samples from every lot and track every re-test result. That audit trail is a living document, shaped by years of customer input and evolving quality expectations in pharma and specialty chemicals.

    Supporting Process Safety and Downstream Audit Readiness

    Modern regulatory environments require not just a clean product, but complete visibility into how it was made. Our chemists collaborate directly with purchasers on impurity profiling. For customers advancing toward clinical or cosmetic registration, we routinely deliver batch-level statements on route-of-synthesis, extracted residual solvent data, and heavy metal screening. This isn’t just paperwork; in an age where quality audits can delay or derail supply chains, being able to back each statement with a library of archived data pays long-term dividends.

    On occasion, development teams request impurity isolation or spike-in studies. We’ve built flexibility into our process to deliver material for method validation, not just production. Supplying that extra 10 grams of “worst-case” impurity can bring a registration project through the last mile of regulatory filing. We don’t treat customer requests like tickets in a help desk queue — our staff picks up the phone and walks through the technical justification for each batch and its documentation.

    Addressing Sustainability and Waste

    As global attention pivots toward sustainable chemistry, developers of intermediates like this acid face scrutiny over solvents, waste, and energy intensity. Our journey hasn’t been one of overnight transformation. In the past, old-school methods relied on chlorinated solvents at high temperature. Regulatory and cost pressures forced us to look for alternative routes — switching to greener methods pushed us to experiment with new oxidants and work-up conditions.

    We retired legacy purification steps years ago, motivated by both regulatory compliance and the prospect of saving on VOC control costs. Every time we revisited the synthesis plan, we discovered new bottlenecks, but also found ways to cut hazardous waste in half. Any batch failing to meet our purity needs is now sent through a dedicated reprocessing loop rather than landfill disposal, echoing an industry-wide effort to close the loop on specialty intermediate production.

    Customers increasingly ask for documentation supporting our sustainability claims. We share our solvent recovery statistics and waste minimization reports without reservation. Trust in the chemical supply chain grows slowly — a lesson reinforced by every audit, discrepancy, and feedback meeting over the past decade. We realize that no process stays perfect forever; new environmental targets keep us pushing to update practices well ahead of regulation.

    Optimizing the User Experience — The Real Test of Quality

    The real test for any intermediate lies outside our facility walls. Stability, purity, granulation, and shipment timelines all converge in the customer’s hands. We’ve watched operators fight stubborn, electrostatic powders that refused to meter cleanly into kilo-pilot reactors, so we invested in both packaging improvements and anti-caking processing. One mistake on our part slows down lines, inflates cost per kilo, or derails a customer’s development plan — chemical quality is just one piece of the puzzle.

    Custom work also finds a place in our portfolio. Research teams sometimes need variant batches adjusted to a precise assay — whether for solubility studies, process screening, or impurity handling. Our team can produce off-spec or high-spec variants quickly, supported by method development tailored to the customer’s requirements. These projects provide crucial feedback for our continuous improvement cycles, since real-life process challenges rarely match up with textbook conditions.

    Wrapping Up: Why Experience with the Molecule Is Worth More

    We’ve produced and shipped DMPC-02 for years, supplying multinational corporations and academic groups alike. Each shipment carries our accumulated lessons: from fine-tuning purification to avoiding common contaminants, ensuring shipments arrive dry and free-flowing, and backing claims with data that stand up to the most rigorous third-party audit. This isn’t just about a chemical name or a catalog entry — it’s about delivering a product with reliability and process fit.

    Every order placed stands as a small vote of confidence in our people, methods, and ongoing improvements. We continue to draw direct feedback from formulation chemists, production engineers, and sourcing specialists experiencing first-hand the strengths — and occasional limitations — of 3,5-Dimethylpyrrole-2-Carboxylic Acid. That feedback loops straight into our process reviews and investment decisions, ensuring our customers receive material that performs where it matters most: in their hands, in their processes, and in their products.

    Supporting Continued Progress in Chemical Synthesis

    We see 3,5-Dimethylpyrrole-2-Carboxylic Acid as more than an intermediate. It embodies what can happen when a producer works in lockstep with chemists, process engineers, and regulatory teams, adapting not only to evolving technical needs but also to shifts in supply chain expectations, sustainability goals, and real-world process challenges.

    Every season brings new requirements, whether for advanced crystal forms, lower impurity profiles, or custom packaging for challenging climates. Our goal centers on building trust batch after batch, knowing the next challenge often lies just outside today’s order book. The accumulated experience found in every lot of DMPC-02 sets a foundation for customers building safer, more efficient, and more sustainable chemical processes.

    We look forward to supporting your synthesis, sharing our own lessons, and helping advance chemical manufacturing with the reliability only long-term experience can bring.