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HS Code |
405216 |
| Chemical Name | 4,4'-Stilbenedicarboxylic Acid |
| Cas Number | 1761-61-1 |
| Molecular Formula | C16H12O4 |
| Molecular Weight | 268.27 |
| Appearance | White to off-white powder |
| Melting Point | 295-298°C |
| Solubility In Water | Slightly soluble |
| Density | 1.43 g/cm³ |
| Pubchem Cid | 23005 |
| Smiles | C1=CC(=CC=C1C=CC2=CC=C(C=C2)C(=O)O)C(=O)O |
| Inchi | InChI=1S/C16H12O4/c17-15(18)11-1-5-13(6-2-11)7-9-14-3-8-12(10-4-14)16(19)20/h1-10H,(H,17,18)(H,19,20) |
| Storage Conditions | Store in a cool, dry place; keep container tightly closed |
As an accredited 4,4'-Stilbenedicarboxylic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 100g quantity of 4,4'-Stilbenedicarboxylic Acid is packaged in a sealed, amber glass bottle with a secure screw cap. |
| Shipping | 4,4'-Stilbenedicarboxylic Acid is shipped in tightly sealed containers to protect it from moisture and contamination. Store and transport at room temperature, avoiding extreme heat and direct sunlight. Label per relevant chemical regulations, ensuring appropriate documentation for safe handling, transit, and delivery. Handle with standard laboratory protective measures during receiving and unpacking. |
| Storage | 4,4'-Stilbenedicarboxylic Acid should be stored in a tightly closed container in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizing agents. Protect from moisture and direct sunlight. Recommended storage temperature is ambient (room temperature) unless otherwise specified by the manufacturer. Handle under proper laboratory conditions using appropriate personal protective equipment. |
Applications of 4,4'-Stilbenedicarboxylic Acid in Industrial ManufacturingAs a direct producer of 4,4'-Stilbenedicarboxylic Acid, we support downstream businesses in multiple value-driven sectors where the material's chemical characteristics are critical to formulation performance, regulatory compliance, and process reliability. Below you will find key application scenarios where clients integrate this raw material into specialized workflows, with details on compliance, formulation guidance, production stages, and resultant finished goods. 1. High-Performance Polyester Resin for Engineering PlasticsLeading engineering plastics manufacturers incorporate 4,4'-Stilbenedicarboxylic Acid as a co-monomer during the synthesis of polyesters to enhance thermal stability, rigidity, and UV-resistance. Unlike standard aromatic acids, its linearity and extended conjugation facilitate polymer chains with superior mechanical strength, enabling downstream fabricators to meet strict regulatory demands, especially in automotive and electronic connector components. Industry compliance standards
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2. Fluorescent Whitening Agents for Textiles and PaperProducers of optical brighteners select 4,4'-Stilbenedicarboxylic Acid as a principal intermediate when manufacturing stilbene-based optical brighteners, thanks to its conjugated double bonds which deliver high absorption in the UV region. This raw material enables brightener resins that impart vivid brightness and desirable white tones to both cellulosic textile and paper surfaces, even at low dosages. Process controls ensure the material meets purity levels vital under regional consumer safety standards for products in direct skin or food contact. Industry compliance standards
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3. Monomer for Polyimides in Display and Electronics FilmsPolyimide manufacturers rely on the rigidity and planarity of stilbenedicarboxylic moieties to construct high-performance film monomers. These films serve as dielectric layers, flexible circuitry bases, or alignment layers in advanced display production. The distinctive aromatic linker allows for a balance of flexibility and dimensional stability, meeting both the physicochemical and dielectric property thresholds required by high-frequency electronic manufacturers. Industry compliance standards
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4. Cross-Linking Agent in UV-Curable CoatingsManufacturers developing advanced UV-cured coatings for plastic and composite substrates employ this acid as a multifunctional cross-linker, benefitting from its conjugated double bonds to facilitate rapid photoinitiated curing. The molecular configuration helps increase cross-link density and surface hardness, particularly in clear coats for automotive lamp housings and precision optical elements. Tight control of purity and particle size distribution supports applications requiring defect-free surfaces. Industry compliance standards
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5. Building Block for Advanced Polyesters in Membrane TechnologyMembrane manufacturers in gas separation and liquid filtration sectors apply this diacid as a monomer to tune polymer microstructure, increasing selectivity and chemical stability of polyester-based membranes. Its integration delivers improved resistance to fouling and solvent damage, extending functional lifetime—qualities demanded in industrial and environmental filtration modules. Consistent molecular purity ensures compliance during scale-up and regulatory audits. Industry compliance standards
Typical usage ratio
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4,4'-Stilbenedicarboxylic acid stands out as a key intermediate in advanced chemical synthesis. As a manufacturer, we have been working with this material for years, watching its role in research and industry develop faster each season. The backbone of this compound features two benzoic acid moieties connected by a trans-ethylene bridge, which gives it both rigidity and symmetry. Chemists value this molecular structure for good reason—these characteristics directly affect downstream reactions, especially in applications like coordination chemistry, polymer science, and specialty materials.
We ship large lots of this compound in powder form, tightly sealed to protect its integrity from atmospheric moisture and possible contamination. The product flows freely and appears white to off-white, reflecting high purity. Our in-house team maintains a minimum purity specification above 99% by HPLC, and batches consistently hit this mark thanks to controlled reaction and purification processes developed over a decade of continuous improvement. Melting point range sits around 314–316°C based on direct thermal analysis, making it well-suited for robust processing environments.
Polymer manufacturers value this molecule for one key reason: it brings a unique combination of rigidity and conjugation into copolymer chains. Polyesters built using 4,4'-stilbenedicarboxylic acid gain mechanical strength and elevated thermal resistance. We have supported several clients pursuing next-generation engineering plastics and high-performance fibers where brittleness or deformation at high temperature threaten the end use. The structured, stiff backbone provided by this acid goes further than standard terephthalic or isophthalic acids, especially in demanding scenarios. Without the ethylene bridge, many aromatic acids can’t deliver this combination of planarity and rigidity.
In pigment and dye manufacturing, the conjugated system becomes even more relevant. The extended π-system interacts with light efficiently, which has prompted ongoing research on new classes of optical brighteners and organic semiconductors. From our perspective, stability remains one of the main attractions. Formulators see little color drift and good performance in ultraviolet-stressed environments. Our QC data from five-year-old retained samples show negligible decomposition—a sign of real chemical resilience in storage and application.
Coordination chemistry represents another growth sector. Metal-organic frameworks often require linkers with two or more reactive sites and precise geometry. 4,4'-stilbenedicarboxylic acid serves as a top candidate, enabling researchers to build MOFs with tailored pore structure and gas-uptake properties. Our feedback from university and private R&D customers highlights reproducible results and easy purification of product trace metals, reducing downstream work.
From the standpoint of practical manufacturing, we’ve trialed and supplied a full range of aromatic dicarboxylic acids. Several differences separate 4,4'-stilbenedicarboxylic acid from its peers. Phthalic acid and terephthalic acid dominate mass-market industrial production, largely because of feedstock availability and historical process investment. These molecules perform well in established plastics such as PET, but their chemical backbones lack the extended conjugation made possible by 4,4'-stilbenedicarboxylic acid. We see this difference most clearly in electronic materials and specialty coatings where optical and thermal requirements push beyond what saturated aromatics can handle.
Isophthalic acid sits closer in use to terephthalic but still lacks the planarity and either trans- or cis- bridge awarded by stilbene. Comparing mechanical properties of final copolymers, we observe increases in modulus and glass transition temperature using the stilbene version. Downstream, customers report improved dimensional stability and less creep over long thermal cycles.
If other unsaturated aromatic acids are considered, such as biphenyl derivatives, they often elevate hydrophobicity or rigidity but introduce processing complications with solubility or reactivity. Our process for stilbenedicarboxylic acid creates a balance between workable solubility, a non-hygroscopic powder, and ease of handling in ordinary lab or plant settings. End users work with the product under fume hoods, using standard acidic or basic dissolution protocols, without clogging or precipitation problems reported in extended storage.
Any manufacturer working at scale knows production doesn’t forgive lapses in consistency. During the purification phase, we prioritize crystal habit and particle size distribution. A batch with unequal particle size complicates metering, transfer, and reaction kinetics. We learned early that slow crystallization and repeat washing during the final stages create a product that feeds smoothly whether you’re building a pilot reactor run or charging a full-scale extruder for thermoplastic synthesis. Customers often return for multiple lots through the year—requesting repeatable quality so process parameters don’t change unexpectedly.
Our purity cutoff came after evaluating polymer performance and asking for feedback from the molding operations we supply. Contaminants, even at 0.5 percent, introduce off-odors, reduce tensile strength, and discolor transparent applications. Chromatography traces, oxide content, and water titration data backed up the purchasing managers when they explained failures in field trials. Today, we run five separate quality checkpoints from the crude reaction stage to the bagged final lot. Every batch includes an HPLC trace and a COA run by independent in-house staff—not just relying on automated instruments.
We’ve also invested in packaging. Customers often lose value due to caking or atmospheric contamination. Our packaging uses five-layer foil barriers and inert gas purges, not simple polyethylene liners. Storage trials in tropical and arid climates have shown near-zero increase in water content after one year sealed—well below the detection limit of most Karl Fischer titration setups. No buyer likes surprises hidden in their drum or intermediate bulk, so we inspect every lot for pinholes and run vacuum decay testing on random bags from every order.
Changing regulations have prompted many chemical manufacturers to assess the impact of their intermediates—especially in export-heavy sectors. Stilbenedicarboxylic acid currently avoids the risk flags imposed by more reactive or toxic aromatics, such as anhydrides or heavily substituted benzenes. Its modest hazard profile and easy cleanup make it preferable on the plant floor and at end-of-life. We follow GHS labeling, including dust hazard statements, but users rarely report skin irritation or respiratory issues when working with standard PPE.
We’ve pursued greener synthesis methods based on continuous-flow oxidation, reducing both waste output and raw material losses compared to traditional batch setups. Downstream, customers in Europe and Japan asked about trace solvent residues, prompting us to upgrade purification cycles and document solvent recovery rates for our foreign shipments. Our annual audits certify that residuals stay far below national import thresholds.
Many buyers now need full traceability. We document each batch with timestamped records of raw source, operator, and process deviations. This level of transparency adds cost but gives peace of mind. For customers developing drugs or food-contact materials, having access to our process logs and validation records shortens their own market approval timelines. Even with regulatory schemes shifting frequently, especially regarding SVHCs and recycling obligations, we keep pace through constant process reviews and annual third-party audits.
The biggest issues raised by our customers relate to dissolving efficiency and end-use stability—particularly when scaling up R&D results to production volumes. In larger blends, solubility in custom solvents can slow down tank cleaning or clog filters. We keep records of solution handling from multiple customer lines and share these findings proactively; pre-warming solvents and staged charge rates typically reduce these common bottlenecks. We supply a technical summary note with each shipment based on these learnings, not just a loose MSDS.
Some polymerizers have tested custom particle milled lots, hoping for faster solubility. We ran these as special orders, but the overall balance between dusting and dissolution speed brings diminishing returns. Particle size consistency outperforms extreme fineness by a wide margin—an insight shared by several coating formulators running semi-continuous lines.
In end-use cases like advanced coatings, customers have raised questions about yellowing or optical clarity after UV exposure. Stilbene-based materials resist this shift far better than biphenyl and most naphthalene derivatives. We perform accelerated aging and reference sample retention in our own technical center, running side-by-side sample arrays exposed to real sunlight and artificial lamps. Color retention ranks in the top third of all aromatic dicarboxylic acids we work with, explained by the stability of the trans-stilbene core. This same property deters oxidative decomposition during long-term storage—an important detail for buyers committing to multi-ton lots.
Researchers keep finding new uses for this compound. Recent literature and patent filings suggest growing interest in electronic materials, such as OLEDs and organic field-effect transistors. We track these developments closely, working with R&D scale partners to tweak our purification parameters and reduce the trace metal footprint. Where traditional uses demand minimal solubility and high thermal resistance, electronics-grade material requires even higher purity and careful lot certification, with a focus on elements like iron, copper, and other transition metals. Each time a new use case emerges, we evaluate the process and update our documentation accordingly.
We’ve launched a dedicated feedback portal for customers to report process integration issues and improvement ideas. Many incremental changes originated from practical shop floor experiences rather than academic research. One flexible bag design came directly from a customer’s report of handling inefficiencies during overnight reactor startups. The QA team reviews every suggestion and feeds actionable items back into our plant upgrade roadmap. This direct manufacturer-to-user exchange, without reseller barriers, sharpens both our processes and our understanding of real-world application demands.
We see continued demand from the MOF and specialty resin sectors. Modifications to the base acid—such as controlled partial hydrogenation or tailored salt formation—open up further application territory. We regularly test alternative synthesis and purification runs, capturing new market opportunities or regulatory shifts as soon as they appear.
As bulk suppliers and hands-on process engineers, we know the nuance comes from daily experience. 4,4'-Stilbenedicarboxylic acid has moved from an academic curiosity into a practical tool across industries. Its technical profile—combining rigidity, conjugation, and symmetrical functionality—delivers a toolkit unavailable with mass-market dicarboxylic acids. The feedback from real processors, working long shifts in unpredictable environments, has taught us that purity, consistency, and responsiveness matter more than any brochure or product code.
Challenges remain, especially in pushing scale and certification further for tomorrow’s advanced materials. We approach this by continuous process evaluation, maintaining close communication with producers, and staying ahead of evolving standards. The story of this molecule is still being written by those who handle it every day, building something new with every batch.