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N-(Hydroxymethyl)Benzamide

    • Product Name N-(Hydroxymethyl)Benzamide
    • Alias Benzamide, N-(hydroxymethyl)-
    • Einecs 429-290-1
    • 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

    127898

    Chemical Name N-(Hydroxymethyl)benzamide
    Cas Number 7473-21-8
    Molecular Formula C8H9NO2
    Molecular Weight 151.17 g/mol
    Appearance White to off-white solid
    Melting Point 104-107°C
    Boiling Point No data available
    Solubility Soluble in water and most organic solvents
    Density No data available
    Inchi Key GDCUZRITQZSYNN-UHFFFAOYSA-N
    Smiles C1=CC=C(C=C1)C(=O)NCO
    Storage Conditions Store at 2-8°C, in a cool, dry place
    Purity Typically ≥98%

    As an accredited N-(Hydroxymethyl)Benzamide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing N-(Hydroxymethyl)Benzamide, 25g, is supplied in an amber glass bottle with a secure screw cap and detailed labeling.
    Shipping N-(Hydroxymethyl)Benzamide is shipped in tightly sealed, chemical-resistant containers to prevent moisture and contamination. Transport complies with regulatory guidelines for laboratory chemicals, ensuring proper labeling and documentation. The package is handled with care to avoid damage, and temperature control is maintained if specified by manufacturer recommendations or material safety data.
    Storage N-(Hydroxymethyl)benzamide should be stored in a tightly sealed container, protected from light and moisture, at 2-8°C (refrigerator conditions). Keep it in a well-ventilated, cool, dry area away from incompatible substances such as strong oxidizing agents. Handle under an inert atmosphere if possible, and follow all relevant safety regulations and guidelines to prevent degradation or hazardous reactions.
    Application of N-(Hydroxymethyl)Benzamide

    Applications of N-(Hydroxymethyl)Benzamide in Industrial Manufacturing

    As a direct manufacturer of N-(Hydroxymethyl)Benzamide, we focus on industrial-grade applications that directly integrate this intermediate into high-value synthesis and downstream processing. The segments detailed below reflect genuine global practices and regulatory requirements relevant to real production environments.

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

    This intermediate plays a critical role in the stepwise synthesis of certain benzamide-structured active pharmaceutical ingredients, including anticonvulsants and anti-inflammatory agents. Custom synthesis routes use precise raw material grades to satisfy stringent purity and traceability demands. Our material supports the manufacture of cGMP-compliant APIs by maintaining batch traceability and impurity thresholds suitable for DMF and ANDA submission. During process optimization, this intermediate integrates in the penultimate condensation step, where functional group protection and deprotection dictate downstream yield. Continuous monitoring during the reaction and purification steps supports high-purity end products and efficient regulatory clearance for further formulation.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 210/211 (FDA cGMP Regulations)
    • EP, USP, and JP monographs for final APIs
    • Controlled batch traceability for DMF filing

    Typical usage ratio

    • Typically ranges from 1.05 to 1.25 molar equivalents, adjusted based on final API structure and impurity carryover restrictions.

    Downstream process integration

    • Acts as a core building block during condensation or amidation steps
    • Introduced post-initial ring closure or side-chain protection phases
    • Subject to purification (recrystallization or chromatography) before final API crystallization
    • Integration prior to regulatory sampling and stability testing

    Final product types

    • Finished pharmaceutical APIs (tablets, injectables, controlled-release formulations)
    • Specialty benzamide-based drugs
    • Intermediates for central nervous system (CNS) therapeutic agents
    • API samples for clinical trial supply

    2. Intermediate in Agrochemical Synthesis

    Manufacturers in crop protection use this intermediate for the preparation of specific herbicide and fungicide actives. The raw material enters during the amidation or acylation steps, where precise molecular substitutions determine biological activity and selectivity. During process scale-up, attention to trace contaminant profiles aligns with regulatory pesticide residue tolerances. Solutions for this segment require robust process documentation and real-time impurity control, which support global product registrations and compliance with major regulatory bodies. Process engineers select reaction temperatures and solvents according to target activity, often requiring adaptation for different active ingredient families.

    Industry compliance standards

    • FAO/WHO Specifications for Pesticide Products and Formulations
    • ISO 9001:2015 Quality Management in agrochemical production
    • EU REACH registration compliance
    • Integrated pest management (IPM) residue requirements

    Typical usage ratio

    • Between 5% and 12% by mass in intermediate reaction mixtures; actual ratio depends on target molecule backbone and downstream methylation requirements.

    Downstream process integration

    • Added after initial aromatic ring substitutions
    • Incorporated into liquid-phase batch reactors for amidation
    • Followed by hydrolysis, neutralization, and filtration onsite
    • Direct feed to crystallization for downstream technical concentrate formulation

    Final product types

    • Active herbicidal technical concentrates (TC)
    • Systemic fungicidal technical-grade products
    • Microencapsulated crop protection actives
    • Precursor solutions for formulation-grade pesticide products

    3. Monomer Modifier in High-Performance Polymer Synthesis

    Producers of specialty polymers, such as polyamides and functionalized polyesters, use this raw material to introduce hydroxymethyl and amide groups for enhanced thermal and chemical stability. The additive acts as a chain stopper or functional group modifier, which permits control over degree of polymerization and tailored glass transition temperatures. Our product supports scalable melt or solution polymerization processes, ensuring minimal side reactions and maintaining consistent molecular weight distributions. Downstream users control the ratio precisely to manage flow properties critical for specialty film, automotive, and fiber applications.

    Industry compliance standards

    • ISO 9001:2015 for polymer manufacturing
    • EN 71-3 (Safety of Toys - migration of certain elements) for specific end-uses
    • EU REGULATION (EC) No 1907/2006 (REACH) - Polymer registration, monomer tallying
    • RoHS restriction compliance for polymer electronics parts

    Typical usage ratio

    • Typically 0.5–3% by weight as a chain modifier; adjusted based on target molecular weight and film flexibility requirements.

    Downstream process integration

    • Introduced before final polycondensation stage
    • Fed directly into polymerization reactor with other monomeric precursors
    • Monitored for in-process viscosity and chain extension parameters
    • Removal via vacuum stripping if excess unreacted intermediate detected

    Final product types

    • High-performance films and copolymer membranes
    • Specialty nylon fibers for automotive interiors and industrial filters
    • Modified polyesters for heat-resistant coatings
    • Technical resins for electronics housings

    4. Specialty Reagent in Laboratory Fine Chemical Production

    Custom synthesis labs and fine chemical producers select this compound as a controlled reagent for the functionalization of aromatic amides and for the preparation of analytical standards. It acts as a mild hydroxymethylating agent to derivatize sensitive functional groups in complex molecules, useful in both routine R&D and analytical reference synthesis. Purity and analytical traceability are mandatory at this level, with batch-specific certification provided for trace components. The ability to adjust reagent amounts enables precision in preparative organic syntheses, particularly where high selectivity or low byproduct rates are critical.

    Industry compliance standards

    • GLP (Good Laboratory Practice) for client analytical projects
    • ISO 17025 accreditation (testing/calibration laboratories)
    • Internal quality specifications for custom synthesis (purity, trace metals, residual solvents)
    • Material safety data alignment to OSHA 29 CFR 1910.1200

    Typical usage ratio

    • Commonly 1.0–1.2 equivalents per target molecule; modifiable for excess-driven reactions or trace-labeling preparation.

    Downstream process integration

    • Added post-initial substrate preparation in controlled lab synthesis
    • Metered into glass reactors or automated micro-scale synthesis modules
    • Monitoring by HPLC or TLC during reaction to ensure completeness
    • Removed via rotary evaporation or column chromatographic techniques before final product isolation

    Final product types

    • Analytical reference standards
    • Pharmacological research intermediates
    • Custom agrochemical intermediates for structure-activity studies
    • Fine chemical derivatives for catalog supply
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    Certification & Compliance
    More Introduction

    N-(Hydroxymethyl)Benzamide: From Chemical Factory to Your Workflow

    Direct Insights from the Manufacturer’s Floor

    N-(Hydroxymethyl)benzamide stands out because it was designed for those who want reliability in the lab and at industrial scale. Our team at the plant works with this compound every day, transforming simple raw materials into a finished chemical that meets challenging technical needs. After years dealing with shifting purity standards and handling odd requests from synthetic chemists, we understand the little things that turn a batch from good to truly dependable.

    Drawing on decades of manufacturing know-how, we make N-(Hydroxymethyl)benzamide as pure, consistent, and clean as possible. Consistency means fewer surprises. Chemists want the same reaction today as they got last year, and production teams want powder that handles without odd lumps or moisture. When our batches roll off the line, lab technicians can count on steady quality. For us, that means monitoring every step: checking for unwanted byproducts, keeping water content below strict thresholds, and watching for contaminants that might slow a reaction or alter results.

    What N-(Hydroxymethyl)Benzamide Does in Real Lab Work

    The reach of N-(Hydroxymethyl)benzamide covers a few distinct areas. It’s most valued as an intermediate in organic synthesis—especially where selectivity and clean reaction profiles matter. Most researchers use this molecule when constructing complex benzamide structures or exploring modifications on an aromatic backbone. In routine daily production, we see most orders from labs running pharmaceutical research, fine chemicals, or specialty polymers. They want reproducible reactions where the starting material performs the same way every time.

    Behind every order there’s often a specific request for certain particle sizes or moisture content. Some customers need tight handling on residual solvents. We use detection methods like HPLC and NMR to guarantee these properties. For any technical expert, knowing impurities sit well under 0.5% means less risk for troublesome side reactions or failed runs later. No one likes to retest over a contaminated material, and we’ve lived through our share of challenging audits. Our quality team doesn’t clear a drum without that extra round of inspection, which has helped us pass some grueling customer assessments over the years.

    What Makes this Material Unique

    Over the years we have worked with a range of N-substituted benzamides, both as side-chain variants and as core reagents. N-(Hydroxymethyl)benzamide carves out its own niche because the presence of the hydroxymethyl group creates both a reactive handle and a capacity to influence solubility profiles. That single methylene and hydroxy functionality opens pathways for both direct acylation and further modification. We’ve seen it serve as a scaffold for advanced intermediates in custom syntheses, where controlling reactivity matters.

    Compared to the simple parent benzamides, this product introduces both polar and nonpolar characteristics. It balances more readily between organic and aqueous solvents, depending on the system. Chemists tasked with choosing a starting material look at more than just the structural change; the whole downstream set of workflows varies based on this property. In-house, we often carry out pilot-scale drying and crystallization runs to dial in the best process for both free-flowing powder and minimum solvent waste. Supply teams don’t appreciate waste, and neither do we, so we keep the physical characteristics tight to the published range.

    Specifications: Beyond the Numbers

    Every batch we ship comes with a full supporting analytical profile: melting point, purity by HPLC, residual solvents levels, and moisture by Karl Fischer titration. Years back, we realized that customers don’t just read a report—they run their own cross-checks. One time, a customer flagged a faint impurity at 0.3% which could have risked their patented synthesis. Our team traced it back to a minor drying step equipment issue. Since then, every maintenance cycle comes with both mechanical review and a trial run before we ever switch back to production mode. These practices show up in the consistent specs:

    Physical handling properties such as flow and compressibility matter for those automating their dispensing or dosing lines. Several larger clients run this product through feeders and expect it to behave predictably—no bridging, clumping, or flow hesitations. We learned through unhappy customer returns that not every batch is perfect, so now we spend a chunk of time on physical checks in addition to standard analytics.

    Why Usage Matters in a Crowded Chemical World

    While formulas may look similar on paper, N-(Hydroxymethyl)benzamide offers a reliable solution for synthetic routes needing both stability and fine-tuned reactivity. Many classic benzamides serve as stable scaffolds, but the hydroxymethyl derivative does more—it enables the introduction of further modifications without excessive effort. Our clients tell us they pick this one for points in a pathway where a side reaction could ruin yields, or when cleaner work-up processes make life easier. Beyond research and scale-up, some pilot-scale pharma groups switched from older benzamide variants because of tighter analytical profiles and easier downstream purification.

    The world isn’t short on amides. There are plenty of acetyl, propionyl, or methyl derivatives. What draws difference is that single hydroxymethyl group. Not only is it a ready site for alkylation, but it also forms hydrogen bonds that can influence reaction medium choice and crystallization. In our scale-up facility, the tweak in physical properties meant revamping an entire drying process. A lot of pain went into learning the quirks, but now our teams run the material through closed transfer system lines and shorter hold times. These changes improved batch uniformity and cut the risk of contamination.

    Facing Challenges in Production and Handling

    In any factory setting, seemingly small faults can ripple through and cause bigger issues. Moisture control rises to the top in our work. Beyond packaging improvements, we started pulling more frequent statistical checks of humidity in storage. Sometimes, lot variation crept in when an operator switched from silica-dried bins to batch totes. The consequences showed up three months later as sticky material or inconsistent dissolution in customer labs.

    Another ongoing challenge comes from waste minimization in solvent selection. Five years ago, most batches used a single classic solvent, but as regulations changed, demand grew for less hazardous alternatives. We faced real trouble getting early test lots to match the specs of traditional material; product solubility or color sometimes shifted. Not every substitution succeeded. Today, we draw on a wide array of process routes, pulling from proven flow chemistry steps where possible. Maintaining performance standards with new inputs takes more lab and pilot time, but we see that investment paying off with better downstream feedback and lower regulatory hurdles.

    What Differentiates it from Other Products in Our Portfolio

    Having produced both standard benzamide and N-substituted analogues for years, the practical differences between each class become clear as usage feedback rolls in. N-(Hydroxymethyl)benzamide’s value sits in both reactivity and the subtle physical differences that end up mattering on the shop floor or the research bench. We have seen our regular customers walk away from older methyl or ethyl benzamide variants as their specs grow tighter, especially in regulated or patent-heavy fields like pharma research.

    Handling presents another key point. Some amides clump or cake with modest changes in humidity, but this compound tends to resist those issues when carefully packed. Teams in the warehouse favor it for better shelf-life and less rework. The apparent simplicity of just swapping a side group can mask a world of difference in application—chemically, physically, and operationally. Our ongoing investment in high-sensitivity analytics and tighter controls show up as straightforward savings for our users: less downtime, less loss, and fewer headaches.

    Supporting Reliable Research and Manufacturing

    People rely on the materials they know will work year after year. Labs doing long-term method development have told us that supply chain uncertainty sits among their biggest pain points. With N-(Hydroxymethyl)benzamide, those clients report fewer interruptions, fewer worries about last-minute batch requalification, and smoother transitions from kilogram to multi-ton scale runs. We believe this comes down to the investment in consistent processing and real-world feedback from customers. Our process changes weren’t dreams schemed up in boardrooms; they were responses to failed intermediate reactions, downstream bottlenecks, or unhappy project managers over the years.

    The world of fine chemicals never sits still—standards climb, regulatory pressures shift, and end-users ask for lower impurities and smaller ecological footprints. Our product reflects this pressure. For those scaling new pharmaceutical entities, building dye intermediates, or driving research forward, this small molecule plays a key supporting role. As regulations evolve, our shift in solvents, reduction in hazardous waste, and tighter moisture controls have meant our clients spend less time auditing and more time working.

    Continuing to Improve and Solve Problems

    No process ever stays perfect. We keep adding new measurement steps and customer-driven pilot tests. Any time a batch comes back with problems, the whole production team reviews what went wrong—just as we did shifting away from problematic solvents or fixing a crystallization hang-up that led to unreliable powder density. Feedback loops between clients’ downstream processing and our own teams have cut batch variation. Customers focusing on high-throughput synthesis appreciate not just the purity but also steady handling and less remixing. Periodic internal reviews push our plant chemists to try out updated drying or milling equipment when new issues crop up.

    For those concerned with regulatory compliance, we work closely with quality system auditors. Requests for new analytical screens or process improvements from clients don’t go to a black hole. We’ve installed more in-line monitoring and rapid analytics, particularly as we see more clients running tighter in-process checks. These continuous improvements benefit everyone—better traceability, fewer delays, and clearer audit trails.

    Closing Thoughts on N-(Hydroxymethyl)Benzamide’s Real-World Benefits

    Among all the options on the market, N-(Hydroxymethyl)benzamide holds its place for those who need reliability and strong technical performance every time. Our years of manufacturing experience have ingrained a focus on the details—purity, moisture, handling, and prompt adaptation to new challenges. By working hand in hand with researchers, production managers, and quality teams, we have shaped a process that delivers what modern labs and factories demand. For those who value steady results and direct support, this product fits naturally into demanding synthetic workflows.

    Making chemicals is not just about formulae or machines; it’s about listening to the people at the bench, on the packaging line, and in the customer’s plant. Choosing N-(Hydroxymethyl)benzamide from us connects you directly with a manufacturing team invested in both technical precision and practical support. That combination keeps research moving forward and keeps established production lines on track year after year.