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HS Code |
935467 |
| Chemical Name | N-Methylanthranilic Acid |
| Cas Number | 119-30-2 |
| Molecular Formula | C8H9NO2 |
| Molecular Weight | 151.17 g/mol |
| Appearance | White to off-white crystalline powder |
| Melting Point | 85-89 °C |
| Boiling Point | 344.8 °C at 760 mmHg |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Density | 1.25 g/cm3 |
| Iupac Name | 2-(Methylamino)benzoic acid |
| Pubchem Cid | 8727 |
| Smiles | CNc1ccccc1C(=O)O |
As an accredited N-Methylanthranilic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250g of N-Methylanthranilic Acid, packaged in a sealed amber glass bottle with a tamper-evident cap and detailed labeling. |
| Shipping | N-Methylanthranilic Acid should be shipped in tightly sealed containers, protected from moisture and light. It must be clearly labeled, handled as a chemical reagent, and transported according to local, national, and international regulations. Avoid exposure to incompatible substances; ship with appropriate documentation, including Material Safety Data Sheet (MSDS) and hazard classification if applicable. |
| Storage | N-Methylanthranilic Acid 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 strong oxidizers. Protect from moisture and direct sunlight. Ensure appropriate labeling and store at room temperature. Follow standard laboratory safety procedures, including the use of secondary containment to prevent spills and exposure. |
Applications of N-Methylanthranilic Acid in Industrial ManufacturingAs an established producer of N-Methylanthranilic Acid, we supply this intermediate to specialized sectors that require stringent quality consistency and clear regulatory traceability. Below we outline the main industrial segments leveraging our material, each characterized by distinct formulation practices, sector-specific regulatory frameworks, and end-use product types. 1. Pharmaceutical Dye Intermediates for API SynthesisAPI manufacturers employ N-Methylanthranilic Acid in the controlled synthesis of specialized pharmaceutical dye intermediates, particularly those necessary for coloring and marking active ingredients and excipients. It plays a crucial role in the preparation of azo and related dyes, directly influencing bioavailability markers and quality control agents used in solid oral dosage forms. Due to the highly sensitive nature of its application, all handling and dosing procedures observe strict traceability throughout batch synthesis. Industry compliance standards
Typical usage ratio
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2. Agrochemical Intermediate Synthesis (Auxin Analog Derivatives)Manufacturers in the agrochemical sector use our N-Methylanthranilic Acid as a starter molecule for the synthesis of plant growth regulator (auxin) analogs. Chemical processing plants utilize its aminobenzoic backbone in multistep functionalization, ultimately delivering active compounds formulated into commercial plant protection or plant growth regulator products. Strict adherence to agricultural chemical legislation and traceability for environmental safety underpins all downstream usage. Industry compliance standards
Typical usage ratio
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3. Dye and Pigment Manufacturing for Industrial TextilesLeading producers of technical and industrial textiles use our material in the synthesis of high-fastness anthraquinone and azo dyes. It introduces methyl-substituted aminobenzoic moieties that confer specific shade, dispersibility, and migration resistance, benefiting processes where stringent color reproducibility is essential. Application occurs strictly in compliance with environmental and user safety regulations aimed at minimizing residuals and migration into natural matrices. Industry compliance standards
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4. Optical Brightener Enhancer for Paper and Pulp ChemicalsPaper and specialty board manufacturers rely on N-Methylanthranilic Acid in formulations that enhance the brightness performance of optical brighteners and fluorescent whitening agents. Its incorporation enables modification of styryl and benzoxazole derivatives, delivering improved blue-white shading and boosting the perceived whiteness of coated and uncoated papers. All use follows distributor-specific environmental compliance and consumer safety guidelines relevant to fiber-based substrates. Industry compliance standards
Typical usage ratio
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5. Synthesis of Aroma Chemicals for Perfume IngredientsThe fragrance industry synthesizes key aroma molecules using N-Methylanthranilic Acid as an intermediate for producing methylated or ester-functionalized derivatives, essential for floral, fruity, and musky base notes. These derivatives appear in high-purity aroma compositions where batch reproducibility and trace-level impurity control are mandatory for global fragrance compliance and toxicological certification. Industry compliance standards
Typical usage ratio
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Since our early days in organic synthesis, N-Methylanthranilic Acid (model code 119-30-2, or NMAA, as some labs call it) has proved indispensable in the portfolios of both traditional chemistries and modern material science. Many in the field have asked why this particular aromatic acid stands out, especially considering its close relatives on the anthranilic acid spectrum. Production requires a commitment to purity, steady hands during methylation, and attention to moisture and trace metal content—details only the manufacturer controls at scale.
Like other key intermediates, this compound appears as a white or nearly white crystalline powder under strict process management. Our reactors rely on well-maintained temperature ramps and monitored agitation to avoid overmethylation and color impurities. Purity levels hold steady above 99 percent HPLC (USP standard), which allows downstream chemists to avoid chromatographic headaches. We screen each lot for residual solvents and ensure minimal levels of heavy metals, as these jeopardize both compliance and reaction performance in later stages.
Labs won’t soon forget the difference between running a synthesis with our material compared to lower-grade, high-moisture lots. Moisture, when not kept below 0.5 percent (a figure we measure through Karl Fischer titration), introduces hydrolysis risks—not just theoretical, but costly in active ingredient losses for those producing dyes or pharmaceuticals.
As manufacturers, we understand what reliable supply means. Many alternatives and derivatives exist within the aromatic acid family: anthranilic acid itself, o-toluidine, methyl anthranilate. Each fills a niche, yet N-Methylanthranilic Acid’s particular methyl substitution changes not just its reactivity but where it fits into entire production processes.
N-Methylation of the amino group yields a compound best suited when chemists require selectivity in acylation and condensation reactions. This has shaped its use in both fine chemicals and specialized pharmaceuticals. Compared to anthranilic acid, for example, our product’s extra methyl group blocks unwanted ortho-substituent reactions, reducing byproduct formation for those in dye manufacture or drug discovery. It saves time, solvent, and the occasional headache—no small matter on repeated kilo scales.
Some downstream companies still attempt to synthesize NMAA in-house starting from raw anthranilic acid and formaldehyde. Experience shows the small savings vanish when yields slip below 80 percent or purification drags through extra washes. We built our process to eliminate these recurrent bottlenecks. Our reactors operate semi-continuously, giving consistent conversion. Less downtime, higher yields, more control—experience teaches there’s no substitute.
We know the demands for narrow melting point ranges and sub-percent purity variations aren’t just documentation exercises. Dye producers using N-Methylanthranilic Acid as a precursor for azo pigments find that deviations of even 0.2 percent in purity can shift shade formation. Chemists working on nonsteroidal anti-inflammatory drugs (NSAIDs) lean on our guaranteed low-ash lots to avoid unpredictable pharmacological impurities. Whether for analytical standards in GC-MS or preparative HPLC, our material maintains particle size consistency so that weighing errors and deliquescence don’t erode process reliability.
Some customers with older synthesis routes ask about direct substitutions for methyl anthranilate or o-anisidine. From process troubleshooting to scale-up, our manufacturing team has guided several clients through head-to-head tests. NMAA’s unique structure all but ends the risk of nitrosamine contamination during downstream amide formation. More than one client has remarked that using our product cut reprocessing cycles by six percent over a full production year.
N-Methylanthranilic Acid occupies a daily place in our drums and Super Sacks not because of hype, but because end-users trust its track record—from sunfast dyes to pharmaceutical intermediates to metal complexation agents. In dye synthesis, the amino methyl group influences the brightness and lightfastness of pigments. In synthetic routes for antispasmodic compounds, this compound’s a proven performer, delivering predictable yields and potency batch after batch.
Some opt for it in lubricant additive exploration, attracting metal ions in formulations designed for engine wear testing. Analytical labs order by the kilo to assess impurity profiles in dye and bulk drug production. Plant engineers tackling waste stream challenges have used the compound’s chelating properties to reduce heavy metal discharge in process effluent. The applications keep evolving—reflecting decades of cross-disciplinary research.
Working on the manufacturing end, we see the challenges small inconsistencies pose for end-users: caking powders, erratic melting points, invisible impurities surfacing during crystallization. Our multi-step purification, supported by real-time GC-MS and IR spectroscopy, allows for rapid lot release without sacrificing quality. Those differences don’t show up on a standard spec sheet—but they make all the difference in a production environment.
We invested in automated packing lines to reduce foreign particle risk and oxidation. Exposure to air is kept below three minutes per batch, and each drum arrives nitrogen-flushed. International partners appreciate that our documentation tracks back to raw material batch numbers; our record-keeping gives full lot traceability up to five years post-shipment.
Feedback from pharmaceutical pilot plants taught us that even trace phthalate or silica stabilization residues invalidate entire campaigns. Once, a dye works flagged off-quality runs due to legacy wooden pallets contaminating open bags. We redesigned packaging and switched to medical-grade liners—no more surprises.
Transparency matters. Some chemists express caution over aromatic amine intermediates, linking them to safety and environmental risks. Our plant uses closed-system methylation and exhaust scrubbing to reduce personnel exposure. Annual audits led us to invest in wastewater controls that bring chemical oxygen demand (COD) values far under statutory thresholds. Any nonconforming batch is never released to market—either recycled in-process or destroyed under supervision.
Many new customers check for sustainable practices and want clarity on our supply chain. We source raw materials from ISO-certified partners and maintain regular supplier audits. Our methylation agents no longer rely on formaldehyde, reducing both emissions and operator hazards. Several years ago, persistent smell issues in some competitors’ lots came from uncontrolled side reactions, something we addressed through catalyst and base screening; our product simply handles better.
In the real world, consistent regulatory compliance in the EU, US, and East Asia doesn’t happen by accident. Our in-house quality team handles registration paperwork, offers full MSDS access, and partners with customers facing regulatory audits. Addressing allergenic and toxicological concerns, we reformulated and tested according to updated REACH and TSCA guidance.
The field continues to shift. Clients in flavor and fragrance chemistry ask how N-Methylanthranilic Acid fares against methyl anthranilate. The answer depends on synthetic goals—our product’s N-methyl substitution blocks esterification, providing an advantage when direct acid functionality is sought. Meanwhile, process chemists in electronics use the acid moiety to bind metals during film deposition, benefiting from our batch-to-batch reproducibility.
We’ve seen pigment manufacturers trial both o-toluidine and N-Methylanthranilic Acid for copper phthalocyanine synthesis. The latter’s performance reduces bleed and increases solubility in water-based systems, critical in eco-labeled inks. Our sales engineers help labs forecast demand, reserve drum lots during raw material bottlenecks, and troubleshoot purification hiccups from lab to tonne scale.
As electric vehicle batteries and OLED applications expand, we collaborate with innovators to tweak particle size distribution and packing density for their specialty needs. Open feedback keeps us refining our process, often leading to better outcomes on the plant floor.
Direct comparison with anthranilic acid, o-toluidine, or methyl anthranilate makes clear that the right choice depends on reactivity, environmental constraints, and downstream process design. Our production team spent years optimizing for customer priorities—low water content, high purity, tight particle size. These choices pay off where process failures sting most: recurring filter clogging, color drift in pigments, or failed regulatory batches.
Our commitment to research doesn’t end at the gate. Product managers track customer complaints, sample returns, and off-spec feedback. These data points drove us to lower heavy metal specs and switch filtering systems, even when older standards seemed “good enough.” Experience inside the plant has shown that pushing for higher benchmarks, even if unnoticed by most, earns long-term partnerships based on trust and real-world performance.
Responsible chemical production today goes beyond making a “good product.” We lead by example—phasing out hazardous reagents, reducing water usage via closed-loop systems, and ensuring byproduct treatment matches both local law and the expectations of global customers. Our environmental team meets regularly with local agencies, sharing findings and benchmarking against industry averages. Improvements here aren’t marketing—each step forward improves life in and beyond the plant.
Many buyers appreciate our openness surrounding energy use and greenhouse gas reporting. We actively monitor and report Scope 1 and 2 emissions, using this data to optimize utility needs and invest in efficient heat recovery. By focusing on continuous improvement—whether in solvent recovery, staff safety, or emission trapping—we demonstrate that fine chemicals production doesn’t mean sacrificing stewardship.
Years of hands-on experience have taught us that value in a product like N-Methylanthranilic Acid comes not from technical jargon, but from trust, repeatable performance, and dedication to better practices. From raw material checks to finished drum inspection, our entire team stands behind every lot we deliver. For those building new synthetic pathways, chasing yield improvement, or meeting ever-tougher global standards, we bring both expertise and willingness to adapt. The journey from aromatic amine to finished specialty product runs through our reactors, labs, and shipping docks—consistency, care, and partnership at every stage.
In the end, our product’s role emerges within the larger world of chemical innovation, sustainability, and customer need. We continue listening, learning, and improving, confident that our direct experience as real manufacturers—managing the supply chain, tuning the process, and addressing customer challenges—makes all the difference where it counts.