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HS Code |
651725 |
| Chemical Name | 1,3-Phenylenediacetic Acid |
| Cas Number | 613-06-3 |
| Molecular Formula | C10H10O4 |
| Molecular Weight | 194.18 g/mol |
| Appearance | White to off-white crystalline powder |
| Melting Point | 205-209°C |
| Solubility In Water | Slightly soluble |
| Boiling Point | Decomposes before boiling |
| Density | 1.38 g/cm³ |
| Smiles | OC(=O)CC1=CC(=CC=C1)CC(=O)O |
| Inchi | InChI=1S/C10H10O4/c11-9(12)5-7-1-3-8(4-2-7)6-10(13)14/h1-4H,5-6H2,(H,11,12)(H,13,14) |
| Pubchem Cid | 13002 |
As an accredited 1,3-Phenylenediacetic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | White plastic bottle containing 100 grams of 1,3-Phenylenediacetic Acid, labeled with product name, chemical formula, and handling precautions. |
| Shipping | **Shipping Description for 1,3-Phenylenediacetic Acid:** 1,3-Phenylenediacetic Acid is shipped in tightly sealed containers, protected from moisture and light. It should be transported at ambient temperature with proper labeling, and handled in accordance with local, state, and international regulations. Ensure packaging prevents leaks or contamination, and include safety documentation per chemical handling standards. |
| Storage | 1,3-Phenylenediacetic acid should be stored in a tightly closed container, in a cool, dry, and well-ventilated place. Keep away from sources of ignition, moisture, and incompatible substances such as strong oxidizing agents. Store at room temperature and protect from light. Ensure that proper labeling is in place, and use appropriate safety practices to avoid inhalation or direct contact. |
Applications of 1,3-Phenylenediacetic Acid in Industrial ManufacturingAs the direct manufacturer of 1,3-Phenylenediacetic Acid, we supply this specialty intermediate to various downstream sectors where its unique bifunctional structure supports complex molecular construction and targeted property modification. Below we present real-world industrial applications, each with detailed compliance, formulation, and technical integration data strictly based on established manufacturing practice. 1. Specialty Polyesters for High-Performance Coatings1,3-Phenylenediacetic Acid serves as a key comonomer in high-performance polyester resin synthesis, particularly for coil, can, and industrial maintenance coatings demanding precise glass transition and flexibility profiles. Producers incorporate it to tailor branching and enhance chemical resistance, using melt polycondensation or solution polycondensation under controlled pressure and temperature profiles. Its difunctional aromatic backbone differentiates polymer matrices, impacting final film performance in industrial curing and end-use exposure. Downstream QC teams carefully analyze molecular weight distribution and residual monomer levels to comply with performance and safety requirements. Industry compliance standards
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2. Advanced Polyamide Engineering PlasticsIndustrial processors use 1,3-Phenylenediacetic Acid as an aromatic dicarboxylic acid in solution polycondensation to produce specialty polyamides. Its unique meta-phenylene diacid structure affords precise control over crystallinity, melting temperature, and chemical resistance in engineering plastics required for electrical, automotive, and specialty mechanical applications. Direct dosing at the monomer charging stage ensures homogeneous distribution, while melt processing must account for moisture and stoichiometry to meet downstream compounding and molding criteria. Industry compliance standards
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3. Functional Monomer for Epoxy Resin ModifiersFormulators in epoxy resin industries integrate 1,3-Phenylenediacetic Acid to manufacture difunctional epoxy modifiers and specialty curing agents, especially for coatings, adhesives, and electronics encapsulation. By forming diacid-terminated or acid-anhydride-modified hardeners, users customize crosslink density and flexibility, adapting cure curves for both ambient and thermal post-cure conditions. The acid is typically reacted through esterification or directly with epoxy prepolymers under batch-controlled conditions to achieve consistent reactivity profiles in downstream QC. Industry compliance standards
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4. Precision Chain Extender for Polyurethane ElastomersIn specialty polyurethane elastomer manufacturing, 1,3-Phenylenediacetic Acid acts as an aromatic chain extender in isocyanate-polyol urethane synthesis. It enables control of mechanical properties—such as hardness, resilience, and thermal resistance—matching application targets in rollers, sheets, and seals. The acid is typically neutralized and converted to diol analogs or directly polymerized with excess isocyanate in prepolymer or one-shot processes. Quality control checks focus on NCO content, free acid levels, and finished elastomer uniformity to ensure application-specific standards. Industry compliance standards
Typical usage ratio
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Producing 1,3-Phenylenediacetic Acid comes with its own rhythm and set of considerations. Over the years, we have refined our process to ensure consistency, reliability, and supply. This compound, recognized by its systematic structure—two acetic acid groups attached to the meta positions of a benzene ring—has become a mainstay in some demanding applications. As a manufacturer, getting the details right makes all the difference.
Our typical product model focuses on high purity monohydrate and anhydrous forms, offering more than 99% assay by HPLC. Managing water content stays at the front of our minds, as moisture can compromise downstream reactions or product handling. Typical presentations include free-flowing white crystalline powders, without caking or discoloration—both are telltale signs of mediocre processing. Every batch faces rigorous checks for heavy metals, single impurity levels, and particle size distribution. We constantly monitor melting points and residual solvents, mostly by GC and classical chemistry.
Storing this compound requires thinking about temperature, humidity, and the potential for contamination. We package in lined drums or double PE/polymer bags, depending on the lot size and transport requirements. Each batch ships with a CoA, but we know paper doesn't compare to batch-level confidence built on years of repeatable output.
In specialty polymerization, 1,3-Phenylenediacetic Acid has gained value for its ability to provide a rigid backbone with decent flexibility—striking that balance isn't easy with many other aromatic diacids. The placement of the acetic acid arms on either side of the benzene ring enables distinct crosslinking, especially in advanced polyesters and polyamides. Epoxy formulations also benefit from this molecular geometry; certain resins end up less brittle and more resistant to heat cycle fatigue.
Another striking use is in pharmaceuticals. Medicinal chemistry teams use it as a synthon during multi-step synthesis, with its spatially defined carboxyl groups simplifying route planning to target molecules. Our direct conversations with research clients have made it clear: avoiding unwanted by-products in these reactions comes down to the quality of the diacid itself, especially with respect to metal trace content and dark spots in the powder after storage.
Photographic chemicals, niche electronic materials, and custom coatings find value in this specific spacing of the acetic groups. In our own troubleshooting, we found that 1,3-Phenylenediacetic Acid's distinctive ring substitution reduces unwanted polymer branching, a problem that crops up with 1,2- or 1,4-linked isomers.
Compared to phthalic acid (1,2-benzenedicarboxylic acid) or terephthalic acid (1,4-benzenedicarboxylic acid), 1,3-Phenylenediacetic Acid brings a unique meta-structure to the table. Those other acids, widely traded, show up everywhere, but their properties limit their role in tuned specialty polymers. The longer methylene spacers in our product allow designers to introduce just enough flexibility between the rigid ring centers, resulting in materials that stand up to repeated mechanical and thermal stresses.
Our production teams have learned firsthand that making this difference obvious isn't only about specifications. We see how formulations based on isophthalic acid (1,3-benzenedicarboxylic acid) often struggle with hydrolysis stability and stickiness under high humidity. By contrast, 1,3-Phenylenediacetic Acid’s slightly longer linking groups deliver improvements in processability and finished part longevity, especially in molded and extruded products used in demanding environments.
Even in pharmaceutical synthesis, the subtleties add up. Process chemists in our client teams report fewer side reactions with 1,3-Phenylenediacetic Acid compared to phthalic-based reagents. That cleaner reaction profile does not only ease downstream purification but also lowers raw material consumption and solvent use—two pain points in kilo-lab and pilot plant scales.
Crafting this compound above 99% purity keeps our technical team sharp. Early on, we encountered significant variability in oxidative coupling steps. Through relentless adjustment of temperature profiles, solvent ratios, and purification media, we dialed in a process that minimizes batch-to-batch drift. Whenever an impurity trend emerges in QC, we gather the chemists, retrace our changes, and scrutinize upstream suppliers for raw benzenes and reagents. Cutting corners in any of these areas will show up later in dissatisfied polymer or specialty chemical customers—and those relationships mean more to us than any certificate.
Maintaining consistent physical properties also takes commitment. Over time, we noticed subtle shifts in particle habit (needle vs. tabular crystals) when scaling up reactor sizes. This ended up influencing not only dissolution rates in customer processes but also the ease of final product handling in automated lines. We adjusted cooling rates, modified recrystallization solvents, and added secondary screening steps. Our warehousing team raised concerns about solidified lumps during the rainy season, so we replaced standard drums with vapor-barrier-lined containers. Solving these issues required more than theoretical optimization—real people, hands-on fixes, and feedback from users ultimately drove process improvements.
Every manufacturing run generates questions about reducing waste and ensuring safe handling. In the case of 1,3-Phenylenediacetic Acid, we focused on solvent recycling, minimizing acid/base effluent, and recovering mother liquor during recrystallization. The challenge: balancing the rigor of purification with the practical cost of operation. After multiple pilot trials, we implemented distillation systems to bring solvent recycle rates above 90%. This not only improves environmental impact—it makes us less vulnerable to sudden spikes in raw material prices.
Heavy metal traces can ruin whole batches for drug or electronic-grade applications, so we scrutinize all incoming catalyst lots and run regular spectrographic analysis down to the ppm level. Every production line team member commits to regular training in spill response, as even small amounts outside the correct containment add unnecessary risk. The most effective safety upgrades haven’t come from outside audits—they come from feedback loops with our operators who know the quirks of every vessel and valve.
We're also watching energy use. Heating and cooling cycles dominate the cost of goods for high-purity small molecules like this. By digitizing our control systems and adding feedback sensors, we shave hours off reaction times. This means less energy, less chance of off-spec byproducts, and more predictable batch cycles. We keep a running log of process improvements—not just for internal reviews, but because our end users have come to expect complete transparency about environmental and safety performance.
Many customers approach us with process frustrations: plugging in their reactors, handling dust, or coping with variable flow properties. Responding to that, we have adjusted drying parameters, packaging formats, and even post-processing (milling or agglomeration) to address these pain points. Learning how our material behaves in real-world scenarios has changed the way we think about surface area, static charge control, and storage conditions.
A polymer manufacturer once flagged delayed dissolution in hot melt blends. We narrowed the root cause down to a minor change in crystal morphology tied to a slightly lower cooling ramp. We reworked our stepwise cooling sequence and saw their blending time improve—not a fix you can guess from a spec sheet. In another example, a pharma chemist noticed residual color in solution, which we tracked to trace iron from a weld seam on an older tank. Swapping equipment cleared up the issue—once again highlighting the need for root-level investigation instead of bandaid solutions.
Some of our longest-standing relationships started with requests outside the standard offering: a different mesh range, custom moisture spec, or altered batch sizes. These conversations often reveal process mismatches that would otherwise go unnoticed until scale up. By sharing our technical data and listening to user stories, we have avoided costly missteps that can set back projects by weeks or months.
In the specialty chemical and life science sectors, supply interruptions create more trouble than fluctuations in price. Our investment in buffer stocks, dedicated production slots, and offline QC has proven essential. Disruptions can occur from upstream raw material shortages, logistics delays, or even sudden regulatory scrutiny. We keep a steady communication channel open with our supply partners, always double-sourcing the key raw materials the market tends to overlook (e.g., specialty benzenes and nitriles).
Traceability features in every shipment. We batch track all product not just for compliance, but for learnings across product generations. If a downstream problem appears, our records can pinpoint the exact timeline, feedstocks, and process tweaks that contributed. Sometimes, the fix has more to do with how a customer is handling a particular drum or integrating into their workflow—other times, it points directly back to a processing step. NYS, REACH, and cGMP audits happen without drama because everything sits at our fingertips, open for inspection or improvement.
As anyone in the field knows, quality does not just come down to meeting a spec. Consistency, transparency, and follow-through move the needle in real-world projects. We don't pretend 1,3-Phenylenediacetic Acid is a fit for every application—it's a specialized building block with valuable properties where it's needed. Yet, because of its structure, only careful handling keeps its advantages clear in downstream manufacturing. Variation in crystal size, surface quality, and even the faintest discoloration can signal deeper production issues. This is why our QC goes well beyond regulatory minimums: monitoring photometric properties, checking for micro-contamination, and always comparing against retained reference samples.
We see growing demand from advanced material developers, particularly those pushing for new blends in composites and flexible electronics. In conversations with these users, a common theme emerges: product performance is inseparable from supply chain trust and process feedback. Early access to pilot-scale lots lets them avoid scale-up surprises. That only works if the manufacturer stays committed to sharing information and continually improving core processes along with the customer.
As new fields—advanced coatings, energy storage materials, engineered pharmaceuticals—look to differentiate, the specifics offered by 1,3-Phenylenediacetic Acid become more valuable. Both the rigidity and controlled flexibility of its structure open up options that are hard to reach with shorter diacids. A few years back, a client worked on high refractive index films for display technology, seeking a smoother ration between flexibility and clarity. Standard phthalic or terephthalic acids failed performance tests, but 1,3-Phenylenediacetic Acid offered an edge in processability and end-use clarity.
From the pharmaceutical side, novel linker strategies for peptide and oligonucleotide therapeutics increasingly use meta-oriented diacetic acids. Our engagement with those teams has us exploring finer cuts of purity, narrowing allowable side impurity levels even further, and investigating trace contaminant removal using multi-stage column purification. For custom work, precision matters at every stage—batch-to-batch integrity saves decision time for researchers.
We believe that real value creation in specialty manufacturing begins with an equipped team, investment in core process controls, and a willingness to review both successes and setbacks. Over time, the lessons learned become encoded into every batch, quietly enabling the next generation of materials science and drug discovery.
Making and supplying 1,3-Phenylenediacetic Acid is a continuous process of learning, attention to detail, partnership, and technical honesty. It's a journey shaped by the realities of plant floors, shipping docks, and the lab bench, not just drawings or data sheets. By focusing on the critical needs of our partners and applying hard-won experience, we keep raising the bar on what this molecule can deliver—performance, reliability, and trust built on daily decisions in our factories and labs.