methyl 1-methyl-1,2,5,6-tetrahydropyridine-3-carboxylate hydrobromide (1:1)

    • Product Name: methyl 1-methyl-1,2,5,6-tetrahydropyridine-3-carboxylate hydrobromide (1:1)
    • Chemical Name (IUPAC): methyl 1-methyl-3,6-dihydro-2H-pyridine-3-carboxylate hydrobromide
    • CAS No.: 127903-73-3
    • Chemical Formula: C8H13NO2.BrH
    • Form/Physical State: Solid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
    • Price Inquiry: sales7@bouling-chem.com
    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    634402

    Product Name methyl 1-methyl-1,2,5,6-tetrahydropyridine-3-carboxylate hydrobromide (1:1)
    Cas Number 88071-99-2
    Molecular Formula C8H14BrNO2
    Molecular Weight 236.11 g/mol
    Appearance White to off-white solid
    Purity Typically ≥98%
    Melting Point 116-120°C
    Solubility Soluble in water and methanol
    Storage Temperature 2-8°C
    Synonyms Methyl 1-methyl-1,2,5,6-tetrahydropyridine-3-carboxylate monohydrobromide
    Smiles COC(=O)C1=CCN(C)CC1.Br
    Inchi InChI=1S/C8H13NO2.BrH/c1-9-5-3-7(4-6-9)8(10)11;h3-4H,5-6H2,1-2H3;1H
    Hs Code 29333999

    As an accredited methyl 1-methyl-1,2,5,6-tetrahydropyridine-3-carboxylate hydrobromide (1:1) factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 5 grams of methyl 1-methyl-1,2,5,6-tetrahydropyridine-3-carboxylate hydrobromide (1:1), with tamper-evident seal.
    Container Loading (20′ FCL) Container Loading (20′ FCL) for methyl 1-methyl-1,2,5,6-tetrahydropyridine-3-carboxylate hydrobromide: securely packed, moisture-protected, 20-foot container, custom pallets, hazard labeling, optimized space, compliant with chemical transport regulations.
    Shipping Methyl 1-methyl-1,2,5,6-tetrahydropyridine-3-carboxylate hydrobromide (1:1) is shipped in tightly sealed containers, protected from moisture and light. It is transported under ambient temperature conditions, with appropriate labeling for hazardous materials and in compliance with chemical shipping regulations. Ensure secure handling to prevent leaks or accidental exposure during transit.
    Storage Store methyl 1-methyl-1,2,5,6-tetrahydropyridine-3-carboxylate hydrobromide (1:1) in a tightly sealed container in a cool, dry, well-ventilated area, away from light and incompatible substances such as strong oxidizers. Keep at 2–8°C (refrigerated), protected from moisture. Ensure containers are clearly labeled and handled according to standard laboratory safety protocols.
    Shelf Life Shelf life: Stable for at least 2 years when stored in a cool, dry place, protected from light and moisture.
    Application of methyl 1-methyl-1,2,5,6-tetrahydropyridine-3-carboxylate hydrobromide (1:1)

    Purity 98%: methyl 1-methyl-1,2,5,6-tetrahydropyridine-3-carboxylate hydrobromide (1:1) of 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high yield and minimized byproduct formation.

    Melting point 178–182°C: methyl 1-methyl-1,2,5,6-tetrahydropyridine-3-carboxylate hydrobromide (1:1) with a melting point of 178–182°C is used in solid-state compound formulation, where it provides thermal stability during processing.

    Molecular weight 252.13 g/mol: methyl 1-methyl-1,2,5,6-tetrahydropyridine-3-carboxylate hydrobromide (1:1) at 252.13 g/mol is used in precision dosage drug delivery, where accurate formulation is achieved for targeted therapeutic applications.

    Particle size ≤ 50 µm: methyl 1-methyl-1,2,5,6-tetrahydropyridine-3-carboxylate hydrobromide (1:1) with particle size ≤ 50 µm is used in fine chemical synthesis, where rapid dissolution and homogeneous mixing are improved.

    Stability temperature < 100°C: methyl 1-methyl-1,2,5,6-tetrahydropyridine-3-carboxylate hydrobromide (1:1) with stability up to 100°C is used in temperature-sensitive process engineering, where compound integrity is maintained under controlled thermal conditions.

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    Certification & Compliance
    More Introduction

    Methyl 1-methyl-1,2,5,6-tetrahydropyridine-3-carboxylate Hydrobromide (1:1): In-Depth Insights From the Manufacturing Floor

    Introducing a Specialized Pyridine Derivative—Our Perspective as the Producer

    Years of hands-on chemical manufacturing have shaped the way we approach the synthesis and supply of methyl 1-methyl-1,2,5,6-tetrahydropyridine-3-carboxylate hydrobromide. Every batch reflects decisions made for purity, reliability, and consistency, guided by our experience with its unique chemistry. Not all chemical manufacturers tackle this molecule, which often lands on the desks of researchers or process development teams looking for precise reactivity in heterocyclic chemistry.

    Understanding Its Structure and Why Chemists Seek It Out

    Studies on functionalized pyridine rings often draw a dividing line between standard building blocks and those designed for very specific substitutions or reactivity. In this molecule, the tetrahydropyridine ring carries both a methyl and a carboxylate group, a combination that addresses challenges in selectivity during subsequent transformations. Its hydrobromide salt form alters solubility and reaction profiles compared to the more common hydrochloride analogues or free bases. Chemists involved in pharmaceutical R&D, or complex organic synthesis, regularly request it to introduce this framework in APIs or advanced intermediates.

    Building Consistency From Raw Material to Final Salt

    In production, the biggest concern is impurity control. Several routes can deliver this carboxylate, but only a few yield consistently low levels of related byproducts. Using in-house developed crystallization steps, we bring the hydrobromide out as a solid with reproducible melting range and fine particle shape. Each process step, from quenching to filtration, receives close monitoring—not out of habit, but out of recognition that inconsistent formation of the hydrobromide leads to clumpy material and tricky downstream purification for our customers.

    Large-scale synthesis has uncovered subtleties invisible during gram-scale preparation. The methyl group at position one, far from benign, can rearrange under stronger acid conditions or extended heating. Avoiding overbromination or decarboxylation requires precise temperature and pH tracking. Batches are routinely sampled at key points, ensuring that the finished product, by the kilo or the ton, stays true to assigned structure every time.

    Physical Characteristics—and Why They Matter Beyond the Lab

    In our experience, the physical form is often neglected until after the chemists receive their material. We pay attention to flowability, dustiness, and moisture uptake during isolation, not just for ease in handling but to improve weighing accuracy at the customer’s bench. The hydrobromide salt is hygroscopic, which influences both storage advice and delivery format. We keep our batches in tightly sealed containers, using inert lining where possible, so the carboxylate methyl ester does not degrade before reaching the hands of users.

    Purity Standards—Not Just Numbers on a Certificate

    We have come across a range of approaches to purity—some suppliers quote generic “over 98%,” ignoring the potential impact of byproducts. For this compound, minor ester hydrolysis or the presence of isomeric tetrahydropyridines hinders downstream synthetic steps. Our team relies on HPLC, NMR, and Karl Fischer titration methods selected for this molecule, not simply adapted from other generic pyridines. This lets us provide a practical guarantee of structure and content. Several customers reported reduced troubleshooting and higher yields since switching to our batches; this feedback directly informs process tweaks and upgrades in production.

    Application Experience—Where It Fits in Real-World Chemistry

    The main value of this chemical comes out in N-alkylation, Michael additions, and as an advanced precursor for nitrogen heterocyclic compounds. In-house synthesis routes for alkaloid analogues or pharmaceuticals find this derivative effective in building specific ring systems. We routinely collaborate with medicinal chemists who use it for introducing methylated tetrahydropyridine substructures where regioselectivity and stereochemistry are critical. Some routes toward anti-parkinsonian agents, for example, depend on the reactivity of the nitrogen and the stability of the carboxylate ester under various conditions.

    Our product’s reproducibility has cut timelines for scale-up or optimization. Clients in contract research or specialty pharma may previously have spent weeks re-running reactions due to batch-to-batch impurity drift. Our manufacturing approach, always verified by experienced analytical chemists before shipment, practically removes this uncertainty from their workflow and allows faster progress from proof of concept to pilot scale.

    Why the Hydrobromide Form Stands Out—A Chemical Producer’s View

    For many pyridine derivatives, the hydrochloride salt is common. We observed that the hydrobromide variant brings significant differences in downstream chemistry. Some research teams found that substituting the hydrobromide for the HCl salt changes selectivity in reductive aminations or hydrogenations—sometimes offering cleaner conversion, other times giving milder reaction conditions. We studied these effects by working alongside process chemists and adapting our supply accordingly.

    Handling and shipping the hydrobromide salt raise logistical and regulatory issues not encountered with the free base. The solid hydrobromide packs more densely, and with the right packaging, survives longer shipping routes exposed to variable temperature and humidity. End users in humid environments have shown appreciation for our product’s stability and extended shelf life, provided storage is maintained between 2–8°C and away from direct sunlight.

    Comparing with Analogues—What Sets Our Batch Apart

    Other methyl-substituted tetrahydropyridines look similar on paper but react distinctly in synthetic steps. We learned this through side-by-side studies requested by customers aiming to replace more hazardous or inconsistent intermediates. The carboxylate ester at the three-position increases solubility in many organic solvents, making it more versatile for both batch reactors and flow chemistry setups. Unlike unprotected amine analogues, our compound integrates with established protecting group strategies and allows for selective deprotection after target transformations.

    We receive frequent questions about substituting this product for pyridine-3-carboxylate or for the corresponding hydrochloride salt. Our hands-on verification, not just analytical printouts, guides these decisions. Sometimes the solubility profile or thermal stability advantages of the hydrobromide are decisive. In one instance, a client’s catalyst residue problem cleared up once they shifted from their previous HCl salt supplier to our hydrobromide batches—a difference confirmed with our own internal reaction trials.

    Addressing Sourcing and Scalability—Direct from the Synthesis Line

    Many organizations come to us after experiencing delays from traders or third parties. Our vertically integrated setup supplies the hydrobromide salt uninterrupted from synthesis, workup, and final refinement, directly to shipping. This cuts out common bottlenecks—lost paperwork, inadequate tracking, or exposure to unsuitable storage during transit. Scientists and procurement teams often express relief that their feedback loops straight back to the team responsible for the batch, which means real-time adjustments instead of slow bureaucratic fixes.

    Up-scaling the synthesis from research scale to pilot or commercial amounts taught us to solve new challenges with phase separation and crystallization. We design our reactors and downstream equipment specifically for this salt and continue to refine every stage based on field reports, analytical findings, and our own batch histories. Variations in raw input quality—such as bromide content or water traces—cannot always be assumed from supplier certificates, so our internal QA methods catch and correct before any impact on yield or performance occurs.

    Storage, Shelf Life, and Practical Use—Real-World Considerations

    Storage guidance comes not only from theoretical studies but from hands-on experience with heat, moisture, and packaging issues. We moved away from certain plastics after seeing slight changes in appearance or trace-level impurities migrate over time. Our packaging now involves laminated foil and low-permeability liners, reducing water ingress and accidental contamination. Customers using our product months after receipt continue to document consistent melting range and assay values, even under challenging warehouse conditions.

    As a manufacturer, our responsibility extends past the shipping dock. We actively document ambient stability, reactivity under light, and optimal conditions for both short-term and long-term holding. This ensures the methyl ester group holds up under diverse lab climates, reducing the risk of delayed or unexpected hydrolysis. For labs running parallel syntheses, this reliability translates into smoother workflows, more accurate planning, and simpler quality tracking.

    Feedback-Driven Process Improvements—Listening to End Users

    We maintain open lines between our chemists and scientists at client companies. Feedback on lot-to-lot performance, reaction outcomes, and analytical deviations feeds directly into batch record adjustments and next-phase process controls. Laboratory reports on application-specific issues—such as solubility shifts or observed off-color formation—prompt investigation at the manufacturing level, not just at sales or distribution. Several process improvements, including selective crystallization and controlled drying procedures, stem from conversation with those actually performing the chemistry.

    Our goal is not only to address complaints but to anticipate needs based on recurring findings. In the past, a percentage increase in methyl ester hydrolysis products nudged us to reevaluate our quenching temperature profile. Fielding questions on flow chemistry integration highlighted the benefit of producing a finer powder grade, which reduces undissolved residues in automated systems. These direct feedback loops shape both the design of the synthetic route and the way we handle finishing and quality checkpoints.

    Beyond Supply: Supporting the Next Generation of Research

    Manufacturing this carboxylate hydrobromide goes hand-in-hand with staying current on the needs of the research and pharma sectors. We regularly monitor literature and patent activity involving related pyridine derivatives to identify trends that may affect demand, handling requirements, or application specificity. Partnerships with academic labs and biotech startups keep us tuned to emergent applications, such as non-traditional reaction media or new solvent systems, ensuring that our offering remains relevant and meets changing chemical demands.

    Pharmaceutical development timelines put a premium on supply stability and data transparency. Our process focuses not only on analytical batch release, but on offering supplementary real-world use data that chemists can call on when troubleshooting or comparing performance. We see this as essential to building trust and supporting meaningful research progress, not simply fulfilling an order.

    Challenges We’ve Overcome — Real-World Manufacturing Stories

    Not every batch runs perfectly, and we have a history of confronting unexpected hurdles. Once, an incoming bromide salt with higher than anticipated water content triggered incomplete precipitation. Realization of the problem at the granulation step led us to intensify our incoming QC and verify reagent lots before committing to large-scale synthesis. Changes in regulatory requirements on precursors forced us to secure alternative sources and qualify backup suppliers, guaranteeing uninterrupted shipment to our partners through changing market conditions.

    Real incidents—such as container breaks in transit or customs hold-ups due to poorly filled paperwork—led us to overhaul our logistics documentation and then collaborate with shipping specialists to reinforce packing standards. We understand first-hand how value in the chemical supply chain goes beyond purity and specification; it comes down to reliability under unpredictable circumstances and readiness to respond quickly if anything goes off-course.

    Commitment to Quality, Safety, and Long-Term Scientific Impact

    Our commitment is ongoing. Manufacturing methyl 1-methyl-1,2,5,6-tetrahydropyridine-3-carboxylate hydrobromide forms part of a larger pledge to responsible chemical production. Creating reliable raw materials for intricate syntheses impacts not only the operation of today’s laboratories but the success of tomorrow’s therapies and technologies. Our onsite teams continue to refine every stage, share findings, and work hand-in-hand with our partners to advance the best possible outcomes in laboratory, pilot, and industrial settings.

    These efforts reinforce the reputation of materials coming directly from certified manufacturers. Years of accumulated knowledge mean each order reflects not just compliance but know-how—from synthesis and isolation to storage and dispatch. Whether for pharmaceutical development, fine chemical exploration, or cutting-edge academic projects, we bring focus, humility, and hands-on experience as the driving force behind this chemical’s journey from reaction flask to research bench.