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4-(Methylamino)Benzoic Acid

    • Product Name 4-(Methylamino)Benzoic Acid
    • Alias p-Toluamide
    • Einecs 226-409-8
    • 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

    852697

    Chemical Name 4-(Methylamino)benzoic acid
    Molecular Formula C8H9NO2
    Molecular Weight 151.17 g/mol
    Cas Number 56-91-7
    Appearance White to off-white crystalline powder
    Melting Point 178-182°C
    Solubility In Water Slightly soluble
    Pka 4.2 (carboxylic acid group)
    Smiles CC1=CC=C(C=C1)N(C)C(=O)O
    Iupac Name 4-(methylamino)benzoic acid
    Storage Conditions Store at 2-8°C, keep container tightly closed

    As an accredited 4-(Methylamino)Benzoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The packaging for 4-(Methylamino)benzoic acid, 25g, is a sealed amber glass bottle with a tamper-evident cap and clear labeling.
    Shipping 4-(Methylamino)benzoic acid is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. Packaging complies with regulations for transport of chemicals. Proper labeling, documentation, and hazard information are included. During transit, temperature and handling precautions are maintained to ensure safety and prevent degradation or accidental release.
    Storage 4-(Methylamino)benzoic acid should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizing agents. Protect it from moisture, heat, and direct sunlight. Ensure proper labeling and restrict access to trained personnel. Store in accordance with local, regional, and national regulations to maintain safety and chemical stability.
    Application of 4-(Methylamino)Benzoic Acid

    Applications of 4-(Methylamino)Benzoic Acid in Industrial Manufacturing

    As a direct manufacturer, we supply 4-(Methylamino)Benzoic Acid to a select range of industrial sectors where the unique substitution pattern and functional properties of this compound match precise technical requirements. Below, we detail verified downstream application scenarios, each aligned with industry-specific protocols, manufacturing process stages, and defined product endpoints.

    1. Synthesis of Local Anesthetic Active Pharmaceutical Ingredients (APIs)

    Pharmaceutical firms utilize 4-(Methylamino)Benzoic Acid as an intermediate in the synthesis pathway for esters and amides relevant to local anesthetic drug production. Its methylamino group serves as a key precursor in the formation of the aromatic base, which is subsequently coupled or esterified depending on the target API structure. This segment demands a high compliance threshold and consistent lot-to-lot specification to ensure pharmacopoeial conformity—every batch integrates at defined stages in GMP-validated manufacturing, primarily in intermediate synthesis and final API assembly.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP/NF (United States Pharmacopeia/National Formulary) monograph alignment for intermediates
    • European Pharmacopoeia (Ph. Eur.) raw material standards
    • FDA 21 CFR Part 211 (Current Good Manufacturing Practice for Finished Pharmaceuticals, as relating to intermediates)

    Typical usage ratio

    • 0.7–1.2 molar equivalents per batch of target anesthetic, tuned based on yield studies and downstream stoichiometry

    Downstream process integration

    • Stepwise coupling in aromatic amide or ester formation reactors following nitration/reduction, generally after purification post-condensation

    Final product types

    • Pharmaceutical-grade anesthetic APIs such as Mepivacaine, Ropivacaine, or custom N-methylated derivatives

    2. UV-Absorber Additive in Specialty Polymer Compounding

    Polymer converters incorporate this compound as a building block in synthesizing custom ultraviolet-light absorbers for plastics exposed to outdoor or high-light conditions. The methylamino functionality supports downstream reactions to produce functionalized benzophenone or benzotriazole derivatives, which are compounded directly into engineering polymers through melt or solution blending to deliver stable light protection in finished thermoplastics.

    Industry compliance standards

    • REACH Regulation (EC 1907/2006) Substance Registration for chemical handling in Europe
    • ISO 9001 Quality Management System for plastics additive manufacturing
    • RoHS Directive 2011/65/EU (Restricted Substances: Electrical/Electronic Equipment)
    • ASTM D5208-01 Accelerated Weathering Test standards (applicability for evaluation, not registration)

    Typical usage ratio

    • 0.05–0.3% by resin weight, fine-tuned in masterbatch preformulation stages depending on UV durability targets and final application

    Downstream process integration

    • Entrance during polymer melt compounding (twin-screw extrusion) or solvent blending, immediately prior to pelletizing and downstream extrusion/injection

    Final product types

    • UV-resistant polycarbonate panels, automotive dashboard interiors, outdoor electrical housings, greenhouse rigid films

    3. Photoactive Agent Precursor for Specialty Dye Synthesis

    Dye manufacturers employ this raw material for developing functionalized azo or condensation dyes. Its methylamino substitution allows precise color modulation in diazotization-coupling operations. This scenario is highly formulary-specific, with batch design reflecting sought after spectral properties and process reproducibility in textile, photographic, or analytical colorant production. Each integration run synchronizes with precise reaction controls, yielding high-purity dye lots destined for controlled industrial uses.

    Industry compliance standards

    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals - Manufacturing Restricted Substances List) for textile and leather dyeing
    • EN 71-3:2019 (Safety of Toys – Migration of Certain Elements, for pigments in children’s articles)
    • OEKO-TEX® Standard 100 (Chemical Safety in Consumer Textiles)
    • ISO 14001:2015 (Environmental Management Systems in chemical manufacturing)

    Typical usage ratio

    • 0.6–1.0 molar equivalents relative to coupling substrate, adjustable by desired chromophore intensity and dye purity in pilot trials

    Downstream process integration

    • Utilization in diazotization and azo-coupling reactors, directly after pre-purification and pH adjustment, enabling controlled chromophore synthesis

    Final product types

    • Photoactive textile dyes, colorimetric analytical reagents, photographic filter dyes, specialty inkjet colorants

    4. Intermediate for Synthesis of Agrochemical Active Ingredients

    Agrochemical formulators require structurally differentiated benzoic acids for custom pesticide and herbicide synthesis. This compound provides a tailored aromatic scaffold for constructing amide, ester, or heterocyclic functional groups integral to newer actives. It integrates as a key intermediate in closed-system batch or continuous-flow synthesis, where traceability and contaminant control measure up to agrochemical regulatory protocols. The adoption basis centers on reactivity control, traceable quality, and compatibility with further chlorination, nitration, or amide coupling.

    Industry compliance standards

    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS) guidelines
    • EU Regulation (EC) No 1107/2009 for Plant Protection Products
    • ISO 9001:2015 Certified Agrochemical Manufacturing
    • CROP LIFE International Stewardship Guidelines

    Typical usage ratio

    • 0.8–1.5 molar equivalents per target molecule, selected per downstream coupling demands validated in laboratory scale-up

    Downstream process integration

    • Feeding into initial heterocycle formation or terminal amidation/esterification units, typically post-purification and pH neutralization, before formulation into technical grade actives

    Final product types

    • Herbicide parent compounds, pesticide active matter for emulsion concentrates, selective plant growth regulator intermediates
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    Certification & Compliance
    More Introduction

    Introducing 4-(Methylamino)Benzoic Acid: Experience Shaped by Chemical Manufacturing

    Understanding 4-(Methylamino)Benzoic Acid from the Manufacturer’s Floor

    Every batch of 4-(Methylamino)Benzoic Acid reflects years of process refinement and hands-on problem solving. This compound, sometimes recognized in research and synthesis circles as p-methylaminobenzoic acid, has earned attention both as an intermediate and end-use compound across a range of fine chemical, pharmaceutical, and specialty application areas. As the manufacturer, our perspective stems directly from the reactors and purification equipment, not from product brochures or after-the-fact marketing material.

    Formulation, Handling, and Consistent Output

    Producing 4-(Methylamino)Benzoic Acid at scale means balancing reaction efficiency and product purity. In our facility, this molecule comes to life by coupling precision temperature control and stringent filtration during amination and subsequent crystallization stages. Solid-state product emerges as a fine crystalline powder, white to off-white, carrying a characteristic, faint amine odor. Rigorous drying and sieving eliminate irregular particles, minimizing agglomeration for those working downstream.

    Our production lines rely on in-process analytics—think HPLC, melting point determination, and loss on drying tests. Results matter. Typical purity exceeds 99% by HPLC, keeping residual solvents and impurities well below recognized thresholds. Such practices, especially avoiding metallic contaminants or unwanted aromatic impurities, ensure repeatable assay and spectral data, which research chemists and production formulators both appreciate.

    The Working Role of 4-(Methylamino)Benzoic Acid

    Clear, proven pathways connect this acid to several real-world uses. As a manufacturer, we have seen it most frequently in custom syntheses and in the building of specialized pharmaceutical compounds, dyes, and imaging agents. Its para-methylamino functional group enables straightforward coupling for those who seek to further diversify the aromatic ring, introducing extended chains or activating groups through acylation, sulfonation, or cross-coupling methodologies.

    Beyond laboratory scale experiments, companies engaged in the hunt for next-generation active ingredients rely on this benzoic acid as a starting nucleus. Substantial activity comes from its ability to act as a stable intermediate—making it easy to protect, functionalize, or bridge to new structures. Demand isn't abstract; it comes from scientists who have encountered bottlenecks with less versatile substrates or who have found other aminobenzoic acids less easy to derivatize under mild conditions.

    Specification and Quality Emphasis: A Chemist’s Perspective

    Nothing slows a research campaign or production run like variable input quality. Our teams work closely with downstream users to ensure clear, detailed specifications, from particle size profile to trace metal analysis and solvent residue certifications. This outreach emerged from direct feedback. For instance, a scale-up gone wrong due to batch-to-batch inconsistency wastes both time and money. Real-world consequences drive us to update documentation, traceability, and lot records promptly.

    Our QC environment draws from pharmacopeial principles but recognizes the demands of those behind the bench. Testing covers melting point accuracy, water content (Karl Fischer titration), ultraviolet and IR signatures, and freedom from residual starting materials or side-products. This approach does not come from checklist thinking but grows out of listening to partner labs, catching issues before shipment, and troubleshooting via feedback loops with end users.

    Comparing 4-(Methylamino)Benzoic Acid to Other Benzoic Acid Derivatives

    Chemists face critical choices when selecting functional intermediates. The difference between 4-(Methylamino)Benzoic Acid and other benzoic acid analogues, such as para-aminobenzoic acid or meta-substituted acids, rests in the reactivity, steric profile, and compatibility with coupling reagents. We see direct substitution effects: the methylamino group at the para position helps moderate both electronic and steric hindrance, partially shielding the amine while maintaining carboxyl group accessibility.

    By experience, we see this compound outperform simple aminobenzoic acids in several synthetic schemes. The methyl group attached to the nitrogen offers greater hydrophobicity and increased stability in both acidic and basic media, translating to better shelf life and less risk of unpredictable side reactions. More than once, clients achieved higher yields or milder reaction conditions using our product, compared to unsubstituted or ortho/meta isomers.

    While the more common para-aminobenzoic acid (PABA) holds substantial historical value in dye and pharmaceutical chemistry, its basic nitrogen may lead to over-reactivity or competing amide formation under acidic coupling regimes. The methyl group on our product tempers that, making selective transformations more controllable. Comparing to unsubstituted benzoic acid, reactivity differences show up especially in N-acylation, reductive amination, and Suzuki-type cross-coupling chemistry, often reducing the likelihood of unwanted oligomerization or cross-linking.

    Unique Insights from Manufacturing Challenges

    Insights learned in an actual chemical plant rarely align with textbook recipes. Scale changes everything. Any process that works for a few grams in a glass flask might fail when ramped to several metric tons in stainless steel reactors. We encountered solvent management issues, inconsistent crystallization, and filter clogging over the years. None of these got solved overnight. Operators on night shift and R&D colleagues exchanged countless notes before optimizing reflux conditions, solvent swap procedures, and particle recovery.

    Iron contamination once presented a persistent headache, visible as faint pinkish tints in the finished product, sometimes only detectable by advanced spectroscopy. Stepping into the plant, we traced it back to impeller abrasion in high-shear zones. A full retrofit to lined equipment eliminated the risk, but the learning curve came the hard way. Such issues highlight the genuine value of in-house manufacturing knowledge versus theory-based advice from catalogues or traders.

    Robust waste management and solvent recovery make both financial and environmental sense. We operate distillation and solvent scrubbers, integrate feedback from local regulators, and track emissions data and effluent profiles. Operators engage in regular training to minimize exposure risks, and live data monitoring alerts us to untoward process deviations, maintaining product quality and workplace safety alike.

    Supporting Modern Industry Demands

    Trends in pharmaceutical R&D and specialty materials point to ever tighter specifications and more robust analytical reporting. Regulatory agencies look beyond nominal purity, eyeing potential genotoxic impurities and residual solvent risks right down to parts-per-million levels. Our in-house laboratory runs full spectra—HPLC, GC-MS, NMR, and ICP-OES—for every lot. We bank on real traceability, matching COA data with electronic batch records, not because a third party asks, but because this approach catches and corrects issues before they hit the customer’s receiving dock.

    Several downstream partners, drawing from life sciences, dyes, and emerging battery material sectors, now request bespoke grades or adjusted specifications for their advanced syntheses. We collaborate directly, sharing real insights from our scale-up trials—pointing out, for instance, which solvents best dissolve 4-(Methylamino)Benzoic Acid for high solids loading, or how to adjust pH buffering when using it as a coupling partner. The work extends past simple compliance, venturing into genuine process partnership.

    Addressing Supply Chain and Price Fluctuations

    Global raw material markets do not run on autopilot. Prices fluctuate, and occasional shortages of key precursor chemicals—like nitrobenzoic acid or methylamine—create both logistical and cost headaches. Rather than wait for aftershocks, we maintain multiple sourcing options for critical reagents and oversee robust inventory management on both raw materials and finished stock. This cushions our clients from sudden availability swings.

    Experience tells us that orders spike ahead of key industry conferences, patent filings, or government tenders. Predicting such cycles comes from years of tracking industry habits and open discussion with purchasing managers and formulation chemists. Customer requests for just-in-time shipments keep us nimble: regular audits streamline our response, keeping fulfillment reliable without bloated excess stock.

    Pushing Beyond the Basics: Collaboration and Customization

    Some applications require more than default chemistry. Whether it’s novel labeling studies in medicinal chemistry, development of new fluorescent tags, or constructing intricate heterocyclic scaffolds, our teams prioritize direct communication with R&D partners. We tweak particle size, moisture content, and purity levels according to use case, drawing on direct experience with scale-up batch processing and analytical troubleshooting.

    We take pride in sharing real data. Several biotech groups, facing process bottlenecks due to unpredictable melting behavior or persistent off-notes in their synthesized compounds, turned to us for solution development. Our willingness to provide early-batch samples, host site audits, and walk through our production records give peace of mind, not because a template says so, but because our reputation rises or falls with the integrity of what ships out our doors.

    Requests for documentation—ranging from detailed batch records to logistics traceability and confidential purity data—get handled hands-on. We keep customer feedback loops open, refining both our documentation and our actual processes based on robust dialogues, not canned responses.

    Stewardship: Environmental and Worker Safety

    Producing aromatic acids at industrial scale generates both effluent and vapor streams. Responsibility does not end with a neat COA. We designed our process to achieve minimal waste load, moving to more selective catalysts and improved solvent recycling. Employees participate in regular safety briefings, with clear protocols for handling, spill management, and respiratory protection. We monitor worker health and respond to potential irritant exposure situations with immediate countermeasures and medical support.

    Community relationships matter too. Regulators and neighbors visit, inspect, and ask questions. We support transparency, local hiring, and ongoing communication around emission controls. Genuine, open tracking of safety metrics, near-miss reporting, and compliance with regional environmental standards underpin both our license to operate and our long-term trust with customers.

    Navigating Change: Adapting to Regulation and Technology

    New regulations never emerge in a vacuum. Over the years, both chemical and pharmaceutical agencies ratcheted up expectations for reporting, impurity controls, and supply chain verification. Rather than simple compliance, we integrated digital batch records, improved change control, and layered digital signatures onto our documentation process. Practical experience adapting to these shifts allowed us to avoid shipment delays and costly recalls; our customers count on uninterrupted supply that also meets new benchmarks.

    Process technology advances also shape day-to-day reality. We retrofit automation where possible, not to do less, but to catch outliers quickly—unexpected color shifts, pressure deviations, or erratic solvent return. Real-time data displays empower shift supervisors to intervene early. Rather than cutting out the human link, our approach combines automated display with seasoned operator judgement, delivering precise, dependable output every cycle.

    Summary of Experience: Why Work Direct with the Manufacturer?

    A direct relationship with the manufacturer means more than a spot price or a product label. It is built on transparency and mutual reliability, especially during scale-up trials, regulatory inspections, or sudden technical hurdles. Knowing how every batch is made—and being able to trace product history or process tweaks—keeps both us and our long-term clients nimble and informed.

    Our methods start with raw material selection and continue through process monitoring, extensive analytics, and open dialog with our partners. Every lesson learned—be it from scaling up a novel synthesis route or troubleshooting a minor impurity—directly shapes the daily procedures and technical support we offer. Working directly allows for faster answers, real-time troubleshooting, and a level of product consistency that is difficult to match through distributors or speculative stockists.

    Over the decades, our manufacturing of 4-(Methylamino)Benzoic Acid developed by staying closely engaged both with scientific advances and the practical working concerns of research teams and industrial users. Continual investment in equipment, people, and analytical tools keeps us in line with evolving industry standards and customer aspirations. This approach offers more than just a product; it offers the assurance, technical backing, and flexibility required for both present and future needs.