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HS Code |
786248 |
| Product Name | 2-(4-Nitrophenyl)Propionic Acid |
| Cas Number | 5741-04-8 |
| Molecular Formula | C9H9NO4 |
| Molecular Weight | 195.17 |
| Appearance | Yellow crystalline powder |
| Melting Point | 144-146 °C |
| Purity | Typically ≥98% |
| Solubility | Slightly soluble in water, soluble in ethanol and DMSO |
| Storage Temperature | Store at 2-8°C |
| Iupac Name | 2-(4-nitrophenyl)propanoic acid |
| Smiles | CC(C1=CC=C(C=C1)[N+](=O)[O-])C(=O)O |
As an accredited 2-(4-Nitrophenyl)Propionic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle labeled "2-(4-Nitrophenyl)Propionic Acid, 25g," with hazard symbols and batch information, securely sealed for transport. |
| Shipping | 2-(4-Nitrophenyl)Propionic Acid is shipped in tightly sealed, chemical-resistant containers to prevent contamination and leakage. It is handled as a hazardous material, requiring appropriate labeling and documentation. Shipments comply with international regulations for transport of chemicals, ensuring temperature control and safety measures during transit to protect both handlers and the environment. |
| Storage | 2-(4-Nitrophenyl)propionic acid should be stored in a tightly sealed container within a cool, dry, and well-ventilated area. It must be kept away from sources of ignition, incompatible substances such as strong oxidizing agents and bases, and direct sunlight. Handling should occur in areas with suitable exhaust ventilation, and containers must be clearly labeled to prevent accidental misuse or contamination. |
Applications of 2-(4-Nitrophenyl)Propionic Acid in Industrial Manufacturing2-(4-Nitrophenyl)Propionic acid serves as a critical intermediate for multiple fine chemical processes, supporting manufacturers across specialty chemical, pharmaceutical, and advanced materials sectors. We supply industrial-grade material tailored for direct use in actual production environments. Below, we outline its most relevant applications based on real downstream requirements and regulatory demands. 1. Non-Steroidal Anti-Inflammatory Drug (NSAID) Intermediates ManufacturingMany pharmaceutical companies utilize this acid as a precursor to synthesize selective COX-2 inhibitor NSAIDs. The process requires precise nitration and reductive steps to obtain specific pharmacophores. In dedicated GMP manufacturing suites, technicians incorporate this intermediate after core condensation reactions, which directly determines synthetic yield and impurity profiles. End-use pharmaceuticals undergo validation according to global submission dossiers. Industry compliance standards
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2. Liquid Crystal Intermediate for Advanced Display MaterialsThe electronics chemical sector uses 2-(4-nitrophenyl)propionic acid as an intermediate when synthesizing specific liquid crystal monomers required for TN and IPS display production. Strict control of isomeric purity and trace metal content supports stable molecular alignment and reduces optical failure rates. The compound enters the workflow post-alkylation, allowing for precise functionalization steps used by Japanese and Korean panel manufacturers. Industry compliance standards
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3. Specialty Dye Intermediate for Azo Pigment SynthesisPigment and dye manufacturers select this material for its ideal electron-donating and withdrawing group functionality, which improves molecular definition in azo and disperse dye production. During coupling stages, precise stoichiometry yields pigments with enhanced lightfastness and dispersion. The acid’s nitro configuration facilitates robust chromophore anchoring, critical for automotive and plastics-colorant applications. Industry compliance standards
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4. Chiral Building Block in Fine Chemical SynthesisProducers of advanced fine chemicals use this compound as a key chiral handle in the enantioselective synthesis of specialty organics. Laboratories and industrial facilities value the carboxyl and nitro functional groups, enabling diastereoselective transformations essential for agrochemicals and flavors manufacturing. The compound typically enters chiral resolution steps, allowing downstream target molecules to meet strict enantiomeric excess thresholds. Industry compliance standards
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Working in chemical manufacturing gives a person a view from the floor—well beyond dusty datasheets. Over the years, I’ve watched 2-(4-Nitrophenyl)propionic acid leave our kettles in ton-lots and drum shipments. This compound stands out not because of any universal magic, but because the industry keeps coming back for it, cycle after cycle. Its yellow hue and distinct crystalline form mark it out from more common benzoic or cinnamic analogs. In this commentary, I want to cut through the search engine jargon and reach the heart of what really matters about this product, and why it earns a permanent slot on our reaction schedules.
Walking into our reactor hall five years ago, an R&D chemist and I watched the pilot batch solidify under vacuum. The goal: a solid intermediate for niche pharmaceuticals. Traditional propionic acids lacked the aromatic nitro function, limiting subsequent coupling and reduction steps. Shortly after successful pilot runs, demand from small-molecule research labs started trickling in. This wasn’t an accident. Customers had spoken: alternative aryl compounds brought too many side products from over-nitration, or gave unreliable yields in Friedel-Crafts conditions.
2-(4-Nitrophenyl)Propionic acid caught the perfect intersection between chemical robustness and downstream flexibility. The propionic side chain proved stable under mild base, unlike the more sensitive ethylenic bridges seen in similar analogs. This foundation stabilized production schedules, supported scale-up, and kept our repeat customers happy. What started as a single-use pilot soon became a mainstay, with tweaks to crystallization protocols earning a few in-house nicknames for especially clean batches.
Mixing the ingredients is just step one. Our technical staff watch the compound’s warm yellow tint develop, checking for the signature luster under warehouse lights. Why does this matter? Visual checkpoints keep tabs on purity before instruments confirm analytical results. With some compounds, color means nothing. Here, a faded or muddy appearance tells production to re-check the batch. We learned, year after year, which indicators signal off-target ortho substitution, or leftover base contaminants.
2-(4-Nitrophenyl)propionic acid, in its pure state, brings advantages during further synthesis. The para-nitro group resists unwanted side-reactions under several reducing and coupling conditions. We see this play out when customers report fewer chromatographic separations, especially in gram or kilogram lab runs. Our chromatography team sometimes handles comparable materials. The extra cleanup required for isomeric impurities can slow an entire facility, so consistency in this product lifts operational bottlenecks for our clients.
Handling practicalities aren’t just whiteboard talk—they translate to lower losses and cleaner glassware every time the drums get hauled out of storage. Our containers see less caking, less static adherence, and a sharper edge to the melting end-point. This is not true of every substituted propionic acid that moves through our plant; those with only methyl or unsubstituted aryl groups tend to track more dust and moisture issues, particularly during our region’s humid months.
People new to 2-(4-nitrophenyl)propionic acid manufacturing ask, “Why this backbone? Why carry a nitro group?” Much of the answer comes down to downstream applications and easy transformations. Medicinal chemists tell us the para-nitro moiety offers a separate window for reduction. It converts smoothly to the amine, sidestepping more complicated protection steps required by meta or ortho-nitro analogs. That gives scientific buyers a cleaner path to building specific pharmaceuticals or imaging agents.
Years on the production line taught us which reaction conditions deliver the cleanest profile. Sulfonic acid catalysis, followed by temperature ramping, and close monitoring at a handful of critical endpoints—this isn’t just for regulatory paperwork. As process manufacturers, every lost percent on purification eats into efficiency and sustainability. Waste disposal for side-products builds up on the nerve-ends of operators and finance managers alike.
Feedback loops start on the shipping dock and go backward to synthetic design. Some earlier models of this compound suffered in high heat. We re-engineered isolation equipment to cut down on premature decomposition. The R&D team switched from batch to semi-continuous crystallization, nudging the particle size distribution tighter. These in-house improvements sounded minor, but led to better flow in customers’ powder feed hoppers. Sometimes the best evidence comes when complaints stop—not when a flashy data point rolls in.
The chemical catalogs overflow with substituted propionic acids. Some are cheap and plain—think phenylpropionic acid without electron-withdrawing blocks. Others add functional groups to every position on the benzene ring, pursuing new selectivities or regulatory clearances. What sets 2-(4-nitrophenyl)propionic acid apart has never been about volume production. Instead, it balances reactivity, safety, and historical trust in performance.
Compared to simple phenylpropionic analogs, the nitro substitution sticks out. Classic propionic acids run into side-interactions when researchers expose them to strong oxidants, or need electron-deficient arenes. The nitro group, in this context, brings a unique polarity to the table—tuning not just reactivity, but solubility in a way the unsubstituted backbone cannot. From a manufacturing stance, attempting to graft alternative functional groups after-the-fact brings more steps, each with their own yield penalty and regulatory review.
Meticulous tracking of batch analytics shows another edge: isomer content. Our protocols nearly eliminate ortho- and meta- substituted contaminants, which matters a great deal in medicinal chemistry. Some other producers accept higher impurity percentages, betting their end-users will clean them up downstream. We never took that risk, after damaging a client’s column years ago with a poor shipment. Over-purification costs time and money, and facing the honest mistakes of an earlier supplier has shaped our stubborn focus on batch purity.
Next, compare technical handling. 2-(4-Nitrophenyl)propionic acid shows more shelf stability and less tendency to absorb atmospheric moisture than many of its cousins. That means easier warehouse management and longer shelf life. These aren’t marketing slogans—they drive real procurement choices in small-molecule synth labs. Scientific buyers don’t want to redry powders if they can avoid it, and our records of batch returns underline that point every fiscal quarter.
Our clients’ chemists concern themselves less with the bulk product, more with fresh reactions. Over time, we hear about three main uses on the receiving end of our barrels: active pharmaceutical ingredient synthesis, fine chemical intermediates, and reference material standards.
Pharmaceutical groups often use the acid as a scaffold to synthesize anti-inflammatory candidates, or to build molecular fragments for CNS drugs. The compatibility of the para nitro group in their reduction and amination sequences keeps appearing in R&D feedback. By offering a clean-cut starting point, the acid streamlines column purification, often allowing researchers to skip steps that competing acids force them to include.
In fine chemicals, the compound’s unique electronic profile draws attention for more than just pharmaceutical work. Dye and pigment researchers experimenting with azo-coupling gravitate toward this particular structure. Its controlled electron density supports vibrant colors and consistent uptake in polymer host matrices. 2-(4-Nitrophenyl)propionic acid resists the oxidative degradation that limits the shelf life of other intermediates, making it a workhorse for innovative new dye blends.
Universities and analytical laboratories add another layer—here, the product acts as a calibration standard. Consistent melting point, batch-to-batch identity, and minimal isomer drift keep the acid reliable during regular control work. In these contexts, the story isn’t about creative reactivity—it’s about certainty for downstream analysis, and our batch records reflect several years of stable results under controlled storage. This is less dramatic than preparing new molecules, but crucial for labs running tight quality control.
Seasoned buyers don’t just glance at price sheets. They circle back for materials delivering tangible efficiency in their pipelines—fewer vacuum failures, less need for extra purification steps, more predictability with sensitive reduction chemistry. The outer world fixates on data points; inside manufacturing, it’s about which product gives a batch operator a calm day instead of a troubleshooting marathon.
Customer calls over the years log a few themes. Purity, always. But after that comes consistency. No two recrystallizations run on exactly the same clock. Only a tightly controlled process, carefully scaled and attentively run, produces the harmony that downstream users crave. One call from a frustrated lab head made our technical staff revisit filtration speeds and solvent washes. These changes translated into shorter drying times and less risk of contamination, paying off in repeat orders from some of the hardest-to-please research departments.
In every cycle, the feedback loop matters. Packaging preferences—whether high-density PE drums, or soft sachets for just-in-time use—get logged and reviewed by plant managers. Real-world packaging choices come out of years of client collaboration, not from a generic industry playbook. Each tweak, each failed run, each successful quarter brings new lessons, and our view stays grounded in what gets research done, not what reads well on a website.
Scaling up 2-(4-Nitrophenyl)propionic acid never looked tidy in textbooks. At two tons per batch, small impurities hide out and multiply unless every step gets fine-tuned. Local solvent availability and environmental handling requirements forced early changes to our processes—less reliance on aggressive chlorinated solvents, a tighter solvent recovery loop, modest tweaks in cooling rates to keep exotherms managed. The initial yield sacrifices made us nervous, yet, with each iteration, the waste streams dropped and batch success ticked up.
The team’s collective experience stuck with them in those moments. A sudden hotspot in the reactor? Temperature probe recalibrations. Unsettling trace of meta-isomer? Revisit raw material lots, review every cleaning step. Many facilities can pump out reaction products on paper, but only sustained attention to the ugly details delivers reliable commercial shipments per customer deadlines. We discovered that no single analytics run beats years of hands-on daily logs, visual checks, and persistence. There are no shortcuts in chemical manufacturing.
Every so often, new environmental standards bring a scramble. The industry drift toward green chemistry asks for gentler oxidants and cleaner energy integration. We paired up with suppliers offering robust, low-impact acids. Upgraded our fume handling after one too many alarms. The results: cleaner exhaust, leaner energy bills, and fewer agency inspections. Our staff adapted, adjusting schedules and training documentation. Sustainability on the shop floor doesn’t work as a half-measure; every marginal fix factors into the ledger over time.
No product comes to life without reliable upstream suppliers. The sourcing of critical building blocks for 2-(4-Nitrophenyl)propionic acid depends on decades-old partnerships. Price wars occasionally drive competitors toward riskier vendors—often at purity’s expense. We learned to invest in long-term relationships with trusted suppliers, visiting facilities and tracking certifications firsthand.
Trace contaminants, often overlooked by casual buyers, consistently cripple batch runs at the kilogram scale. Even robust reaction profiles fall apart facing nitrite or heavy metal impurities. We took hard-won lumps in the early days—imperfect audit trails, a delivery gone sour, a week lost to rework. Today, pre-shipment screening and in-house NMR quality checks flag trouble before full batch-release. New staff learn this lesson quickly, realizing that upstream diligence drives productivity in every shift.
Chasing high-purity 2-(4-Nitrophenyl)propionic acid, we come back again and again to the fundamentals—solid phase control, optimal solvent ratios, proper washing sequences. Our team tracks melting point, color, and FT-IR patterns before signing off a truckload shipment. Not every batch lives up to the highest standard; tight in-process control and early catch of off-spec material keep customer complaints to a minimum.
Laboratory and production staff don’t rely on hope—they log, track, adjust, and learn. No sleight-of-hand will ever replace accumulated experience for getting reproducible product on schedule. Failures, tough as they are, shape the confidence in current equipment and procedures. The margin in well-run plant operations is not found in technical jargon, but rather in fewer reworks, safer personnel, and satisfied customers who stick around year after year.
Over the past five years, patterns in end-user requests told their own story. Analytical labs, in particular, started demanding lower limits on both inorganic and organic side-products. Research teams in Europe pushed for smaller lots, better shelf life, and lower environmental impact. Those shifts sent our facility management back to raw material sourcing, utility upgrades, and batch scheduling.
Placing customer feedback at the front of every improvement cycle, we adjusted production for more flexible batch sizes. Added new analytical checkpoints, not just at the finish line but throughout the process. Experienced technicians consult directly with R&D buyers; any claim of boundary-pushing innovation gets grounded in what the lab can actually deliver. Inhouse discussions became more open about near-misses, improved process visibility, and the logic of every decision.
Firms clinging to “good enough” lose ground over time. By treating each request as the first proof-of-concept, our site has shifted a ragged trial batch into a reliable product year after year. End users point out strengths as well as limitations honestly, and their experience informs not just next month’s blend, but the next generation of process improvements. There is no shortcut in manufacturing chemistry—the fastest learn quickly to adapt and iterate based on user data, not dogma.
Creating batches of 2-(4-Nitrophenyl)propionic acid stands as more than a technical exercise. From selecting clean reagents to loading the final container, every process step builds confidence not just for us, but for the wide spectrum of applications downstream. Our experience teaches that transparency and open response to feedback matter just as much as instrumental analysis.
Many chemical plants run production lines efficiently, but building long-term relationships with specialty compound buyers relies on proven, repeatable product. Research teams run time-sensitive projects that tolerate little downtime. Knowing their supplier listens, documents, adjusts, and delivers consistent material has real value—especially in a sector where every process is one faulty lot away from a month-long delay.
With every order and every challenge, our understanding of this compound deepens. We track changing regulatory and market demands, maintain detailed logs, and invest in better environmental systems. Our longest-standing customers have stuck with us through the usual industry shakeups, and each new project reaffirms why close manufacturer–client collaboration yields results. The story of 2-(4-Nitrophenyl)propionic acid can’t be written in generic prose—it is told in clean glassware, high yields, steady reactions, and lasting partnerships.