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4-Amino-3-Methoxybenzoic Acid

    • Product Name 4-Amino-3-Methoxybenzoic Acid
    • Alias 4-Amino-m-Anisic acid
    • Einecs 220-724-8
    • 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

    983982

    Cas Number 610-95-7
    Molecular Formula C8H9NO3
    Molecular Weight 167.16
    Iupac Name 4-amino-3-methoxybenzoic acid
    Appearance Off-white to beige solid
    Melting Point 196-198 °C
    Solubility In Water Soluble
    Density 1.336 g/cm³ (calculated)
    Smiles COC1=CC(=C(C=C1N)C(=O)O)
    Purity Typically ≥98%
    Storage Temperature Store at room temperature
    Synonyms p-Amino-m-anisic acid

    As an accredited 4-Amino-3-Methoxybenzoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 25g package of 4-Amino-3-Methoxybenzoic Acid comes in a sealed amber glass bottle with a printed hazard label.
    Shipping 4-Amino-3-Methoxybenzoic Acid is shipped in tightly sealed containers to prevent contamination and moisture absorption. The package is labeled appropriately according to chemical safety standards and handled with care. During transit, it is protected from extreme temperatures and direct sunlight. All shipments comply with relevant local and international transport regulations.
    Storage 4-Amino-3-Methoxybenzoic Acid should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from direct sunlight and sources of ignition. Keep it away from incompatible materials such as strong oxidizing agents. Store at room temperature and protect from moisture. Ensure proper labeling and follow all laboratory safety guidelines during storage and handling.
    Application of 4-Amino-3-Methoxybenzoic Acid

    Applications of 4-Amino-3-Methoxybenzoic Acid in Industrial Manufacturing

    4-Amino-3-Methoxybenzoic Acid serves as a critical intermediate in multiple industrial sectors. Our material supports diversified manufacturing pipelines, meeting strict downstream specifications for pharmaceuticals, dyes, and specialty chemicals. Below are detailed, sector-specific application scenarios based on our manufacturing expertise.

    1. Pharmaceutical Intermediate for Antihypertensive APIs

    Pharmaceutical producers use 4-Amino-3-Methoxybenzoic Acid to synthesize benzoic acid derivatives incorporated in antihypertensive active pharmaceutical ingredients (APIs), such as those in the angiotensin II receptor antagonist class. The raw material enters amidation, esterification, and acylation steps to introduce functional groups needed for biological activity. Quality control involves HPLC purity checks and in-process residue monitoring to comply with drug standards at every batch. Manufacturers adhere to validated synthesis protocols for batch-to-batch consistency and define the stepwise integration with other advanced intermediates. Our technical support includes custom particle size distribution upon request to match reaction kinetics in proprietary drug pathways.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • EU Pharmacopoeia monograph 01/2008:0201 for related substances
    • USP <795> for pharmaceutical compounding
    • 21 CFR Part 211 (US FDA cGMP for finished pharmaceuticals)

    Typical usage ratio

    • Component represents 10–35% by weight of total intermediate blend; final molar ratio tailored to target API structure, reaction yield, and residual impurity control

    Downstream process integration

    • Introduced at step 3 or 4 of multi-stage synthesis after halogenation/aromatic substitution
    • Reacted in pressure reactors for amidation with precise temperature control
    • Immediately filtered and washed to remove process salts before further condensation

    Final product types

    • Losartan potassium API
    • Candesartan cilexetil intermediates
    • Other angiotensin receptor antagonist APIs
    • Custom benzoic acid-based drug compounds

    2. Dye and Pigment Synthesis

    The compound functions as a functionalized aromatic amine building block in high-performance azo and anthraquinone dyes. Dye manufacturers employ our material in the diazotization step, where the amino group enables coupling with electron-acceptor moieties, yielding intense pigments. The process demands strict pH and temperature regulation to prevent side reactions and maximize color yield. Final pigments originate from carefully formulated blends responsive to textile and plastic end-use conditions. Regular QC sampling during synthesis and blending ensures uniformity in chromatic output and avoids unwanted byproducts.

    Industry compliance standards

    • OEKO-TEX Standard 100 for regulated amine content in dyes
    • REACH Annex XVII (EU) for aromatic amine restrictions
    • ISO 105-X12 for color fastness to rubbing
    • ISO 9001 process quality framework for dye batching

    Typical usage ratio

    • Pigment formulation typically includes 4–12% by weight of this intermediate, depending on specific tone and coverage strength; precise percentage set through pilot batch trials

    Downstream process integration

    • Loaded at the primary diazotization stage in aqueous or solvent phase
    • Coupled to chromogenic compounds using continuous-feed reactors
    • Isolated by filtration, then purified by repeated crystallization and washing

    Final product types

    • Reactive azo textile dyes
    • Disperse dyes for synthetic fibers
    • Anthraquinone pigment preparations
    • Composite color masterbatches for plastics

    3. Specialty Chemical Synthesis: Photoinitiator Manufacture

    Electronics chemical producers integrate this raw material in the creation of photoinitiator molecules, especially monomers utilized in UV-curable coatings, inks, and adhesives. The product’s methoxy and amino functionality yields selective reactivity in condensation and cyclization reactions critical for photoinitiator properties, such as absorption wavelength tuning. Each production run receives analytical verification of amine purity to avoid downstream polymerization inhibition. The photoinitiator synthesis workflow involves closed-system handling with solvent recovery and in-line process analytics. Trace-level detection of potential contaminants assures consumer electronics and packaging compliance.

    Industry compliance standards

    • ISO 14001 for chemical production environmental management
    • RoHS Directive 2011/65/EU for electronics chemicals
    • REACH Article 33 substance communication obligations
    • Chemical Safety Assessment (CSA) per ECHA guidelines

    Typical usage ratio

    • Incorporated as 5–20% weight fraction in precursor blend; adjusted according to target photoinitiator quantum efficiency and photo-absorption profile

    Downstream process integration

    • Charged at first condensation stage using automated dosing
    • Undergoes cyclization with acid catalysts in continuous reactors
    • Final photoinitiator isolated by vacuum distillation and flash chromatography

    Final product types

    • UV-curable ink photoinitiators
    • Coating and adhesive initiator agents
    • Specialty polymers for electronic displays
    • Photoresist chemicals for microfabrication

    4. Flavors and Fragrances Intermediates

    Aromatics producers in the flavors and fragrances sector employ this compound to supply key intermediates required for generating synthetic musks and complex aromatic aldehydes. The methoxybenzoic structure lends itself to methylation, oxidation, and nitration chemistry implemented under strictly inert conditions. We control metal catalyst residue below regulatory thresholds and manage dehydration stages with precision. Each batch adheres to material traceability from raw material to finished aroma compound, suitable for food and cosmetic regulatory review. Application-specific particle size customizations are available on request.

    Industry compliance standards

    • IFRA Standards for fragrance substance purity and traceability
    • 21 CFR 172.515 (US FDA) for synthetic flavoring substances
    • EU Regulation (EC) No 1334/2008 for flavoring substances
    • GMP for Cosmetics ISO 22716 in aroma manufacturing

    Typical usage ratio

    • Blend rate from 2–8% by weight in fragrance intermediate synthesis; optimized by targeted molecular transformation and downstream yield in aroma complexity

    Downstream process integration

    • Dosed at initial aromatic methylation or amine protection stage
    • Further reacted via nitration, oxidation, or etherification under batch or semi-batch conditions
    • Final intermediates isolated by column purification and subjected to GC quality release

    Final product types

    • Synthetic musk intermediates
    • Aromatic aldehyde bases for fine fragrances
    • Flavoring compounds for food applications
    • Cosmetic aroma chemicals
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    Certification & Compliance
    More Introduction

    4-Amino-3-Methoxybenzoic Acid: A Closer Look from the Factory Floor

    Stepping onto a chemical plant floor, you pick up patterns in the way raw materials arrive, products depart, and supervisors jog careful notes on every docket. Among the range of aromatic compounds, few names pop up as regularly in production meetings as 4-Amino-3-Methoxybenzoic Acid. Working here, you learn its role extends further than a simple catalogue entry. Every batch that comes off our reactors has a purpose designed by real-world demand, not just trade scripts or datasheets. Years in the business shape a different perspective about why such a compound matters and where its differences stack up against similar products.

    Better Chemistry Starts with the Molecular Backbone

    The structure of 4-Amino-3-Methoxybenzoic Acid, known by its CAS number 604-30-0, stands out in our product line because of its substitution on the benzoic acid ring. Those familiar with the synthesis process spot how the para amino group and meta methoxy group set this compound apart. The factory’s process technicians work with these features daily: precision in temperature control, pH, and reaction time, all to ensure clean substitution and robust yields.

    Our main output is a pale, off-white crystalline solid with a melting point in the range you’d expect from a well-bonded aromatic with limited steric strain. Regular HPLC analysis confirms an assay above 99%, keeping customer labs from frying columns or chasing tricky contaminants. The crude product after work-up is filtered to remove trace byproducts and dried carefully—moisture content remains low, so downstream process lines stay unclogged and stainless steel doesn’t develop surface corrosion.

    Where 4-Amino-3-Methoxybenzoic Acid Goes to Work

    A customer rings up the tech team with a request for a dye intermediate. Almost always, they’re asking for a compound that handles nucleophilic substitution with a handle to direct further functionalization. Our acid group presents just that: sharp carboxylic reactivity for salt formation or peptide linkage, while the para-amino and meta-methoxy allow controlled, predictable behavior in substitution. We send out tech sheets, but our sales managers find that many clients already did their homework—they know the value of this compound in specialty dyes and advanced pharmaceuticals.

    In pharmaceutical synthesis, 4-Amino-3-Methoxybenzoic Acid earns attention as a starting block for certain active drug compounds, benefitting from the way the substituents direct addition in subsequent reactions. Research chemists leverage these features for selective derivatization, a step that can save precious time and solvents in scale-up. In dyes and pigments, the stability of the aromatic ring—and the fine-tuned solubility from the methoxy—translates directly into batch-to-batch reliability and even color distribution.

    Choosing Our Process: Quality Differences That Show in the End Product

    Many manufacturers prepare substituted benzoic acids using multi-step syntheses that chase conversion at the expense of yield or purity. We’ve found that careful attention at the nitration and methylation steps reduces the burden on the final purification stage. In practice, this means fewer batch losses, manageable solvent usage, and tighter quality windows. Inspectors from large buyer facilities remark on the low residual solvents in our product—just a reflection of our investment in solvent recovery and dedicated distillation lines.

    Some competitors try to push turnovers by cutting purification time or running reactors hotter. We’ve run those experiments in our pilot bays. The finished material may show higher color or a sharp off-odor, sometimes not caught until a customer’s application fails QA. Over the years, engineers insisted on slow, controlled heating and staged crystallization, which gives us a sharp melting point and no unpleasant side reactions.

    Risk, Reliability, and Process Adaptation

    Down in the plant, every batch tells a story about risk. Lower-quality intermediates infect the value chain, leading to failures under scale. Once, a solvent delivery showed residual water in one tank. We traced a drop in crystallinity in the affected run and had to reprocess the entire batch. Since then, stricter water control and inline monitoring keep the process on track. These changes don’t just protect the factory’s bottom line—they prevent headaches for R&D chemists in labs miles away.

    Over the years, some pharmaceutical projects come in with tighter specs for trace amines. Frequent cleaning and dedicated vessels help us avoid cross-contamination with other para-substituted benzoic acid derivatives. We chart batch histories and notify clients if a run comes within any flagged margin. An open-door policy with auditors, combined with detailed process records, builds trust with each shipment.

    Environmental Practices Rooted on the Production Floor

    Working with aromatic compounds means handling acids, bases, and organics carefully. Older colleagues carried plenty of scars from under-protected work in the 1980s and 1990s. As regulation tightened, many producers groaned. We saw it as a way to strengthen both product quality and worker safety. Our process waters feed into a treatment plant; acid byproducts either get neutralized or recovered. Solvent recycling isn’t just a buzzword tossed in ESG reports; the savings show up in monthly chemical purchase logs.

    Compared to other benzoic acid derivatives, the process for 4-Amino-3-Methoxybenzoic Acid produces lower aromatic emissions with the right controls. Regular scrubber maintenance and leak checks are just routine. Batch sheets capture every input and output, a story of resource efficiency that many customers now ask about before asking price.

    The Market View from the Shop Floor

    Most customers come to us expecting a certain level of quality, but they come back because the product performs the same every time. Whether it lands in a pharma project or pigment manufacture, many report no sticky residues in lines or shipment delays due to failed tests. We ship in well-sealed drums or bags, moisture locked out. For those scaling up, we support with documentation to show batch variability, not just standard CoA printouts.

    Our API-destined batches stand out because of our investment in cleaning validation and allergen control—steps sometimes skipped by general-purpose plants. The story behind every kilogram remains clear in our records: who made it, on which line, with what trace impurity profile. And should a customer ever question a spot result, we answer with real records and on-the-ground photos.

    Comparisons with Other Benzoic Acid Derivatives – What Actually Changes

    4-Amino-3-Methoxybenzoic Acid differs from unsubstituted benzoic acid in more than just name. In the facility, the synthetic route changes the entire material flow. Introduction of the methoxy group changes reagent compatibility, shifting away from more aggressive conditions used with, say, 4-nitrobenzoic acid synthesis. Methoxy substitution also alters solubility in organic and aqueous phases; technicians prepping for crystallization recognize how subtle tweaks in pH guide product precipitation.

    The amino group on the para position opens the door for controlled diazotization and coupling reactions—making the compound essential for more than half of our dye intermediate business. We’ve noticed our long-standing relationships with dye manufacturers focus on those substitution patterns, particularly when purity and placement dictate downstream color performance.

    Why Customers Insist on Real Manufacturing Roots

    We sometimes receive requests from traders or brokers seeking custom packing or documentation. Often, they haven’t set foot in a plant or faced the constraints of real production assets. Our R&D engineers spend weeks building out pilot runs just to shave redundancies or solvent waste, not because the specification says so, but because handling waste on a real shop floor costs money, labor, and risk. The value in this compound—and all our output—is in predictable, honest quality, the sort that keeps respirator filters clean, tank bladders free from unexpected swelling, and site supervisors focused on process control rather than reactivity hazards.

    Direct production connects us with challenges unique to difficult intermediates. Early in our process line development for 4-Amino-3-Methoxybenzoic Acid, strange color fractions and inconsistent reactivity signalled issues with reagent supply—methylating agents online contained trace sulfur that found its way into product streams. Only by working daily on-site could our techs double-check supply spec sheets and trace the root cause. That level of attention defines manufacturing-led supply chains.

    Lessons From Continuous Operation

    Running the same plant day after day, lessons pile up. On 12-hour night shifts, production leaders adapt as equipment ages and reagent markets swing. Ensuring the 4-Amino-3-Methoxybenzoic Acid line stays competitive means continuous reinvestment and troubleshooting. Crystal sizing, for instance, determines how batches flow, pack, and blend—experience taught us which filters plug quickest and which dryers best handle the end material.

    Small changes ripple downstream. A tweak to dryer temperature, tested by our operators over several shifts, cut energy use and improved powder flow. The results saved labor on manual re-breaking. Over several fiscal years, continuous small improvements stack up to bottom-line gains that benefit everyone from shift workers to engineers.

    Looking Forward: Meeting Evolving Demands

    Researchers in drug development approach us with tighter impurity specs as global standards rise. Rather than shift blame or source rougher intermediates, our solution comes in investment—in-line monitoring, batch archiving, better raw input tracing, and frequent retraining of operators. Real improvements require time and money, but skipping these steps never pays off in the long run. It isn’t enough to meet minimums; client feedback and post-market reports always push us to strive higher.

    For new industrial dye formulations, changes in environmental regulation mean lower allowable amines and fewer halogenated impurities. Anticipating those rules lets us modify processes in advance, giving our partners in textile and coatings peace of mind that today’s material won’t fall out of spec after regulatory change.

    Our Take on Sustainable Value and Factory Pride

    Conversations with long-term employees reveal the pride in crafting batches that get high marks, not just from in-house QA but also from customer labs around the world. Veteran operators know which critical points catch errant acidity, drag in moisture, or result in slightly off-shade product. Their stories shape the protocols and batch records used by new hires.

    As sustainability pushes forward in specialty chemicals, real attention from the factory floor—recycling tanks, cleaning up spills fast, recovering waste heat—keeps our reputation strong. 4-Amino-3-Methoxybenzoic Acid serves as a measure of these values: a compound that reflects not just organic chemistry on paper but the practical wisdom gathered from hands-on manufacturing work.

    Bringing It All Together: A Manufacturer’s Perspective

    Through more than a decade of operation, we’ve learned substance matters. Customers want more than passable specs—they rely on us for usability, traceability, and consistency batch after batch. Meaningful partnerships start with experience rooted directly in chemical production: sharing real production parameters, opening up our process for inspection, and standing behind reliable shipping standards.

    Every kilogram of 4-Amino-3-Methoxybenzoic Acid carries stories from the plant floor—adjustments made, obstacles overcome, standards maintained, and continuous improvement. That depth doesn’t appear in a brochure but defines real specialty chemical manufacturing. By starting from actual production experience, we assure customers and partners that today’s product remains just as reliable and trustworthy as the first batch ever processed here.