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Methyl 2-Methylnicotinate

    • Product Name Methyl 2-Methylnicotinate
    • Alias methyl-2-methylnicotinate
    • Einecs 226-957-5
    • 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

    681955

    Chemical Name Methyl 2-Methylnicotinate
    Molecular Formula C8H9NO2
    Molar Mass 151.16 g/mol
    Cas Number 5470-70-2
    Appearance Colorless to pale yellow liquid
    Boiling Point 251-253°C
    Density 1.14 g/cm³
    Solubility Slightly soluble in water; soluble in organic solvents
    Smiles CC1=CC=CN=C1C(=O)OC
    Inchi InChI=1S/C8H9NO2/c1-6-4-3-5-9-7(6)8(10)11-2/h3-5H,1-2H3
    Flash Point 105°C
    Storage Conditions Store in a cool, dry, and well-ventilated place

    As an accredited Methyl 2-Methylnicotinate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 100 grams, tightly sealed with screw cap; chemical label displays "Methyl 2-Methylnicotinate," lot number, and hazard symbols.
    Shipping Methyl 2-Methylnicotinate is typically shipped in tightly sealed containers to prevent moisture or contamination. It should be transported in compliance with local and international chemical shipping regulations, often as a non-hazardous material. Store and ship in a cool, well-ventilated area, away from incompatible substances, and with appropriate labeling and documentation.
    Storage Methyl 2-Methylnicotinate should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as oxidizers. Keep it away from direct sunlight and moisture. Store at room temperature and ensure the storage area is equipped with appropriate spill containment and fire-fighting measures. Handle under a chemical fume hood if possible.
    Application of Methyl 2-Methylnicotinate

    Applications of Methyl 2-Methylnicotinate in Industrial Manufacturing

    Methyl 2-methylnicotinate supports several advanced industries as an essential intermediate, contributing well-defined performance characteristics to downstream synthesis and end-product quality. As the original manufacturer, we supply this material for specialized applications where defined technical standards, carefully controlled dosage, and reliable integration into proprietary process steps underpin safe and compliant manufacturing across high-value product lines. Below are key application segments with their technical requirements.

    1. Pharmaceutical Intermediate for Anti-Inflammatory Drug Synthesis

    Methyl 2-methylnicotinate functions as a building block for the synthesis of specific non-steroidal anti-inflammatory drug ingredients, serving regulated pharmaceutical supply chains operating under strict compliance oversight. Manufacturing sites require careful handling and process validation to maintain API purity and documentation for international market access. Dosage adjustments depend on batch target yield and impurity control, while process teams monitor reaction sequence optimization to meet in-process control (IPC) checkpoints.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) monographs for intermediates
    • US FDA 21 CFR Part 211 guidelines on finished pharmaceuticals
    • WHO GMP guidelines for pharmaceutical manufacturing

    Typical usage ratio

    • Batch input: 0.6–1.2 molar equivalents relative to starting amine or ketone precursor, depending on product target and impurity profile

    Downstream process integration

    • Added during the initial step of ester exchange or methylation, followed by purification before coupling or cyclization reactions
    • Monitored using HPLC for intermediate purity prior to final API formation

    Final product types

    • Pharmaceutical grade anti-inflammatory agents
    • Finished API intermediates for global generic drug manufacturing
    • Final solid-dosage forms (e.g., tablets, capsules, topical gels)

    2. Cosmetic Active Ingredient for Warming and Microcirculation Products

    Methyl 2-methylnicotinate is valued by personal care formulators for its controlled vasodilating effect, making it a preferred active ingredient in spa, massage, and skin-care lines focused on improved microcirculation and localized skin warming. Cosmetic companies require verifiable ingredient traceability for regulatory documentation and must optimize inclusion level for both efficacy and minimized irritation, requiring close collaboration with manufacturing QC.

    Industry compliance standards

    • EU Cosmetic Regulation (EC) No 1223/2009
    • US FDA Voluntary Cosmetic Registration Program (VCRP)
    • China NMPA Cosmetics Supervision and Administration Regulations
    • ISO 22716:2007 Cosmetics — Good Manufacturing Practices

    Typical usage ratio

    • Topical formulations: 0.1–1.0% by weight as an active, titrated based on product type and patch test results

    Downstream process integration

    • Incorporated during the final cooling phase of emulsion, ointment, or gel formulation, with rapid mixing under nitrogen to prevent degradation
    • Stability and efficacy verified by dermatological and in vitro vasodilation assessments

    Final product types

    • Professional massage creams and warming gels
    • Facial treatment masks and serums for microcirculation support
    • OTC cosmetic topical products

    3. Intermediate in Agrochemical Synthesis: Pyridine-Based Herbicides and Fungicides

    Agrochemical companies deploy this methylated nicotinate as a key intermediate for downstream synthesis of specific pyridine-derived active substances used in crop-protection products. The compound enables molecular modifications that optimize the performance and selectivity of formulated agrochemicals, and quality teams must document compliance with all relevant chemical safety and residue standards during scale-up.

    Industry compliance standards

    • FAO/WHO specifications for agricultural pesticides
    • REACH Registration (EC 1907/2006) requirements for chemical intermediates
    • ISO 9001:2015 (Quality Management, Agrochemical Manufacturing)
    • OECD Guidance Document on Residues in Crops and Foods

    Typical usage ratio

    • Input range: 0.8–1.0 mole per functionalized pyridine core, adjusted according to product structure and required biological activity

    Downstream process integration

    • Introduced in the pyridine ring derivatization step, followed by condensation or halogenation, and subsequently purified before formulation blending
    • Monitored for conversion rate and trace residual profiling at the intermediate stage

    Final product types

    • Pre- and post-emergent herbicide actives
    • Systemic fungicide intermediates
    • Finished agrochemical formulations for crop protection use

    4. Synthesis of Specialty Dyes for Industrial and Analytical Applications

    Colorant and analytical chemistry manufacturers select methyl 2-methylnicotinate as a precursor for unique substituted nicotinate-based dyes that provide performance properties such as UV-visibility, biological staining, or indicator function in laboratory settings. Downstream customers require reproducible hue and spectral data, necessitating precise control of input ratios and process purification for batch-to-batch consistency and regulatory colorant approval.

    Industry compliance standards

    • EU Regulation (EC) No 1907/2006 for chemical risk management (REACH)
    • US EPA guidelines for chemical manufacturing and dyes
    • Textile dye Oeko-Tex Standard 100 (where applicable)
    • ISO 9001:2015 for Quality Control in Chemical Synthesis

    Typical usage ratio

    • Input ratio: 1.0–1.5 equivalents to chromophore scaffold precursor, regulated by desired color shade and HPLC purity target

    Downstream process integration

    • Charged during the coupling or substitution phase in multi-step dye synthesis, then subjected to column chromatography and crystallization for final dye isolation
    • Each batch undergoes UV-Vis and IR analytical confirmation

    Final product types

    • Laboratory analytical stains
    • UV-indicator dyes for process QC
    • Industrial process-tracing colorants
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    Certification & Compliance
    More Introduction

    Methyl 2-Methylnicotinate: Insights from the Manufacturing Floor

    What Drives Our Focus on Methyl 2-Methylnicotinate

    Methyl 2-Methylnicotinate stands out as a fine, crystalline substance with a pale color, familiar to any technician or operator who has run syntheses for nicotinic acid derivatives. In our plant, this compound carries the model 98% min, reflecting not just the nominal purity on a label but the actual, routinely confirmed batch consistency we produce. Working with this material has taught us about the subtle differences between similar esters and how small process adjustments give a better yield and lower impurity profile.

    The synthesis routes we’ve calibrated draw on direct methylation to achieve selectivity at the desired position, which means fewer byproducts for downstream processing. Our technicians spend much of their time watching for temperature slopes and distillation rates, aware any deviation can bump up related substances that no analyst wants to see in a chromatogram. Handling raw feeds and solvents under proper reduction atmospheres prevents trace nitrosation, a detail overlooked by those not hands-on with reactors.

    Comparing to Related Compounds and the Question of Purity

    Discussion at the plant often involves comparisons between Methyl 2-Methylnicotinate and its more common cousins, like methyl nicotinate or ethyl 2-methylnicotinate. Each compound has different volatility, odor, and reactivity, and these play a big role in user choice. Methyl 2-Methylnicotinate brings a good balance between high reactivity for ester transformations and manageable odor, neither as sharp as methyl nicotinate nor as heavy as the butyl series. We see much cleaner conversion in coupling reactions, especially where active esters speed up pharmaceutical steps.

    Purity doesn’t just matter for numbers on a certificate; it dictates everything from color to storage stability. In-house, we filter out even minor colored impurities. Trace discoloration can point to oxidation or incomplete methylation, and our QC teams follow such hints back to their source in the batch logs. Differences in purity also show up during storage; higher residual starting material can mean slow hydrolysis, a problem for anyone packaging finished actives months later.

    Strengths Seen by Operators, Not Just Analysts

    The biggest feedback we hear from chemists is how this ester dissolves cleanly without the faintly sour residues of similar pyridine derivatives. We package the product tightly, working with lined drums or drums with inert liners as soon as cooling finishes — not out of habit, but learned from years of fighting trace moisture ingress and packing flaws. Handling crystalline materials daily has conditioned us to spot flow and caking issues, both of which can stem from how the product leaves the final drier. Operating centrifuges and vacuum driers, our team avoids excess particle shearing, which makes the final product less dusty and more free-flowing for mixing, minimizing inhalation and loss during handling.

    Industry users remark that this compound’s reliable melting range and low residual solvents reflect well on the yield and purity downstream. In our experience, a stringent distillation helps keep unwanted halides or residual acids out of the lot, both of which would give unpredictable results in pharmaceutical applications.

    Applications: As Seen on the Floor, Not Just in Literature

    Field reports from our customers run the gamut, but the core uses always reflect its role as an intermediate. Methyl 2-Methylnicotinate’s structure, which carries both a methyl ether and a substituted pyridine ring, gives it strong legs in the synthesis of skincare agents that benefit from nicotinic acid analogues. Chemists on the floor frequently see the product charged as a starting material for anti-inflammatory active ingredients, vasodilators, and nuclear receptor modulators, especially where achieving precise ester hydrolysis rates is crucial.

    On our shop floor, batches may head to another reactor for direct conversion into more complex esters or aromatic substitutions. Each shipment reflects decisions made by operators — controlling pH, dose rates for methylating agents, and dwell time in finishing vessels. Unlike standard methyl nicotinate, which tends to hydrolyze faster under mild conditions, Methyl 2-Methylnicotinate holds up longer in neutral media and only cleaves under more vigorous acid or base.

    Beyond pharmaceuticals, some partners report success using Methyl 2-Methylnicotinate in materials development, especially for films that require stability at high pH or for modified polyesters where substitution patterns affect cross-linking. Originally, some customers only knew of the compound for fragrance blends, but over the years, word has spread about its versatility in intermediates, and demand has shifted closer to regulated industries.

    Specifying What We Actually Make

    Every producer claims process know-how, but small differences show up on the floor: the anti-solvent precipitation we use leads to higher-density crystals than those made through direct evaporation. Tighter density means easier weighing and quicker charging to reactors — a difference that clear up after years of changing filtration speeds to control crystal habit.

    We keep water content as low as possible, below 0.3% by Karl Fischer titration on final lots. This small tweak, born from long hours during drying optimization, keeps peroxides and related side products low during storage, so the ester holds up. Routine checks with HPLC and NMR help us catch lots with small shifts in methyl positioning, a detail that can slip through less sensitive QC routines, leading to rework in more critical applications. From my perspective running batch records, errors that show up in pellet strength or reactivity often trace back to over-drying or improper loading, not always the faults listed on finished batch analysis sheets.

    Handling, Storage, and Production: Lessons Learned with Aging Infrastructure

    Older plants learn quickly how esters respond to air, light, and bad packing. Methyl 2-Methylnicotinate does not oxidize as rapidly as some unsaturated esters, but even so, we keep lots away from raw sunlight and high humidity. In one incident, a poorly sealed drum led to faint caramelization near the liner’s edge — a reminder to always work fast at the filling stage and use inert cover gas if weather turns sticky. Each batch is only as good as its path from the final dryer to the drum, a fact reinforced every quarter when we audit retained samples against the original batch.

    For shipment, we avoid bulk bags. Dense, smaller drums stack more safely, travel better, and give fewer caking complaints. Downstream, this translates into higher productivity. When partners report failure during formulation, the fix sometimes lies not in changing reactants but revisiting packing, storage, and transport. Long-term stability studies we run in-house support up to two years shelf-life under standard warehouse conditions — provided the original seal remains unbroken.

    Practical Differences: Methyl 2-Methylnicotinate vs. Methyl Nicotinate and Similar Esters

    People often overlook molecular detail, but anyone manufacturing on scale has to track how it plays out. Methyl 2-Methylnicotinate’s additional methyl group not only alters the physical characteristics — melting point, volatility, and reactivity — but it also affects both yield and downstream conversion efficiency. Standard methyl nicotinate brings higher volatility and more pungency, making closed vessel systems a requirement. Operators appreciate how our product lets them run with less odor and lower direct exposure risk.

    Some esters, like ethyl or butyl 2-methylnicotinates, don’t achieve the same sharp cut-off in chromatographic purity because their larger alkyl chains hold on to more by-product during synthesis. Through many pilot batches, we found that making the methyl ester lets us control reaction rate, cut time on the line, and push overall throughput. The final tetrahedral shape also means less residual solvent, reducing rinsing burdens.

    In direct blending, users find fewer odor complaints in confined environments and easier neutralization should waste handling be required. These practical differences drive customer loyalty as much as any COA guarantee, because the proof lies in day-to-day ease and clean batch histories.

    Manufacturing Practice: Leaning on What Works

    Our crews learned that simplicity brings success. Complicated setups cause maintenance headaches and batch variation. Consistent high-end purity — what we see with 98% min — only comes from keeping to a small set of validated, repeatable steps. Batch logs track not only temperatures and charges but operator interventions: slight variances in stirring speed or heat rate can decide final color, clarity, and yield. Building this knowledge takes years of seeing what works at every scale, from pilot drums to full tankers.

    Routine GC scans of headspace let us catch early hydrolysis or solvent residues before packing. Investing in in-line filters and dryers wasn’t an easy sell at first, but each upgrade means smoother operation and fewer customer complaints. The choice of reagents and careful elimination of inorganic by-products reduces both final waste and disposal costs. All these improvements build on experience, not theory, and we see real-world benefit in lower deviation rates and happier clients.

    Regulatory and Customer Requirements

    Increasing expectations from pharmaceutical and regulated industry buyers mean no shortcuts in documentation, traceability, or records. Each lot carries a full chain of custody, with digital and paper logs checked against operator sign-offs. Rather than relying solely on off-the-shelf methods, our in-house analytical team adapts protocols for key impurities, guided by what customers actually report as critical for their process.

    Throughout audits, regulators often zero in on solvent residues, trace metal content, and batch-to-batch uniformity. Maintaining this record, year in and year out, comes from close teamwork among production, QC, and maintenance staff. Years of plant feedback tells us nobody wants unexplained spikes of any non-listed element — so every container, valve, and pipe gets detailed tracking.

    From our side, handling all related documentation in-house adds to our workload but pays off as buyers’ trust climbs. Users in Japan or Western Europe often run more sensitive screens for low-level organics than others, and our internal standards follow these customers’ requirements. Sharing real batch records, not only summaries, keeps our credibility intact when issues crop up, and it makes future problem-solving far easier.

    Future-proofing our Supply and Manufacture

    Markets change, but the expectation for high-quality intermediates keeps rising. As larger buyers audit sustainability claims, our plant invests in waste reclamation for solvents and tight cycle control to limit energy consumption. Real energy savings came not from grand announcements but from small fixes: heat recovery from condensers, upgraded insulation, and predictive maintenance on driers. Each year, investment tightens up areas where batch deviation showed up. Keeping certifications current, especially those flagged by EU and US regulators, means constant process review and improvement, rooted in the daily work of operators and engineers.

    Plant managers reflect that the reputation we carry comes not from perfect marketing but from a steady record of reproducible, documented production. Every improvement runs through hands-on validation and in-situ testing, and only those showing benefit persist. Decisions on scaling, batch size, or new blends happen through direct experience with each generation of equipment. As demand moves from general industrial to higher-grade requirements, the skills built from decades on the floor help us stay prepared.

    What Using Methyl 2-Methylnicotinate Feels Like Downstream

    Customers tell us about fewer headaches in blending and less downtime. A consistent particle size flows smoothly in blenders, with minimal dust. Batches show low agglomeration, pointing to the tight controls in our drying and finishing processes. Downstream, this means higher first-pass rates, making production scheduling more predictable. Improvements didn’t come overnight; every reliable shipment reflects adjustments based on prior mistakes. Manual checks during packing, regular audits of returned drums, and detailed records of complaints and fixes build the knowledge base that leads to better products.

    In all steps, the aim is a product that starts out stable, behaves as expected, and helps customers innovate further without having to troubleshoot their raw material. Our technical service team, drawing on the same backgrounds as the batch operators, closes the loop between plant reality and lab innovation. Field visits and troubleshooting calls often draw on earlier incidents, talked out across production meetings and logged for future batches. This continual feedback loop keeps the focus on what truly matters: reliability, ease of use, and results you can see by eye and by instrument.

    Conclusion: Why Our Manufacturing Experience Makes a Difference

    Anyone can list product details or copy a certificate. Years spent on a production line, though, teach attention to detail that guides every day’s work. Our view on Methyl 2-Methylnicotinate draws on thousands of monitored batches and customer reports, tracked from raw material receipt to finished drum. The lessons learned — from dealing with failed batches, awkward packing, and evolving regulations — shape each improvement for the next. By keeping our manufacturing rooted in daily, documented practice, we serve customers who value straightforward quality and a partner who stands behind every drum.