|
HS Code |
771473 |
| Product Name | 4-(1H-Pyrrol-1-Yl)Benzoic Acid |
| Synonyms | 4-(Pyrrol-1-yl)benzoic acid; N-Phenylpyrrole-4-carboxylic acid |
| Molecular Formula | C11H9NO2 |
| Molecular Weight | 187.20 g/mol |
| Cas Number | 5575-16-8 |
| Appearance | Off-white to pale yellow solid |
| Melting Point | 221-225 °C |
| Solubility | Slightly soluble in water; soluble in organic solvents like DMSO and ethanol |
| Purity | Typically ≥ 98% |
| Storage Conditions | Store at room temperature, in a tightly closed container, protected from light and moisture |
As an accredited 4-(1H-Pyrrol-1-Yl)Benzoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The packaging contains 25 grams of 4-(1H-Pyrrol-1-yl)benzoic acid in a sealed amber glass bottle with a tamper-evident cap. |
| Shipping | The shipping of 4-(1H-Pyrrol-1-yl)benzoic acid is conducted in tightly sealed containers to prevent contamination and moisture exposure. The chemical is classified as non-hazardous but should be shipped following standard laboratory reagent handling procedures. Appropriate documentation accompanies the package, ensuring compliance with local and international regulatory requirements. |
| Storage | 4-(1H-Pyrrol-1-yl)benzoic acid should be stored in a tightly sealed container, protected from light and moisture, and kept in a cool, dry, and well-ventilated area. Avoid exposure to incompatible substances such as strong oxidizing agents. Properly label the container and store it away from direct heat sources to maintain the compound’s stability and prevent contamination. |
Applications of 4-(1H-Pyrrol-1-Yl)Benzoic Acid in Industrial ManufacturingOur production-grade 4-(1H-Pyrrol-1-Yl)Benzoic Acid is engineered for consistent performance across specialized chemical synthesis, advanced materials, and life sciences sectors. As a direct manufacturer, we enable downstream partners to optimize formulation precision and process reliability for next-stage industrial applications. 1. Pharmaceutical Intermediate SynthesisThis compound serves as a critical building block in the synthesis of heterocyclic pharmaceutical intermediates, especially for anti-inflammatory and central nervous system drug development. Its unique chemical profile ensures high selectivity in Suzuki coupling or Buchwald-Hartwig amination routes, supporting active pharmaceutical ingredient (API) production under current Good Manufacturing Practices. Our material undergoes rigorous QC testing to meet purity and trace impurity specifications required by licensed drug substance manufacturers. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. OLED Materials PrecursorThis aromatic pyrrole derivative is widely adopted in the manufacture of advanced organic electroluminescent materials, particularly for blue and green light emitting layers in organic light-emitting diode (OLED) displays. Its high oxidative stability and electronic conjugation allow fine-tuning of charge-transport and emission properties, supporting both research and industrial-scale OLED fabrication lines. Downstream producers select this material to achieve target thin-film uniformity, high quantum yield, and device longevity specifications. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Specialty Polymer Resin SynthesisIn the specialty polymer industry, this benzoic acid derivative enables production of high-performance conjugated polymers via step-growth or chain-growth routes, adding functional groups for improved mechanical strength and thermal stability. Our raw material enhances the molecular versatility of co-polyester and aromatic polyimide resins, which high-end producers use in electronics, aerospace composites, and filtration membranes. Manufacturers adjust monomer input to balance processability and end-use functionalization requirements. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Analytical Reagent ProductionThis compound is used as a fine chemical intermediate for the manufacture of analytical derivatization reagents and selective complexing agents in certified chemical analysis kits. Its molecular structure supports stable labeling, making it valuable in high-sensitivity qualitative and quantitative detection for academic research, clinical diagnostics, and environmental monitoring. Our plant follows full batch-to-batch identity confirmation and trace impurity controls for laboratory reagent grades. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
|
Competitive 4-(1H-Pyrrol-1-Yl)Benzoic Acid prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: admin@sinochem-nanjing.com
Flexible payment, competitive price, premium service - Inquire now!
4-(1H-Pyrrol-1-Yl)benzoic acid holds a straightforward story before it reaches the user. Throughout years in the chemical industry, turning raw aromatic compounds into high-purity, functional building blocks, I have seen demand for 4-(1H-Pyrrol-1-yl)benzoic acid grow in research labs and scaling pilot operations. We deliver this compound with a focus on what matters most to scientists: predictable behavior, consistent specs, and ease of integration into their workflow. In our work, the best chemistry is always the chemistry you can count on for yield and reproducibility rather than surprise. This attitude drives our day-to-day decisions on batch control, QC, and reliable shipping. Every time this benzoic acid derivative leaves our facility, it reflects our investment in good science as much as good manufacturing practice.
For this compound, the chemical designation leaves little room for confusion: 4-(1H-Pyrrol-1-Yl)benzoic acid describes a benzoic acid backbone with a pyrrole ring attached to the para position. Years back, developing the bench-scale protocol, we ironed out steps to favor high yield and purity. Final products meet high-performance liquid chromatography requirements, supporting consistent identification and functional application. Most users request this compound at a purity greater than 98% — a standard we maintain using silica gel chromatography and subsequent recrystallization.
Each batch is checked for melting point, appearance, and water content. The compound typically appears as a pale solid, avoiding clumping and offering an easy transfer to reaction vessels. We chose borosilicate packaging to maintain stability during storage and transit, based on direct feedback from partners handling sensitive syntheses. Our testing combines in-house infrared spectroscopy and NMR validation to support verification and trust in its performance.
This benzoic acid variant always shows up at key steps in medicinal chemistry and advanced material synthesis. Years ago, a major project required a functionalized aromatic platform less prone to side reactions than anilines or standard benzoic acids. Our 4-(1H-Pyrrol-1-Yl)benzoic acid brought a predictable mix of reactivity at the carboxylic acid and electronic modulation from the pyrrole ring. Researchers at a pharmaceutical scale-up project saw how easily it coupled for peptide conjugation and how well it resisted oxidative degradation. That immediate feedback encouraged us to keep refining our crystallization method, keeping impurities below the level that can trip up complex cascade reactions.
On the materials front, another story stands out. Catalysis researchers looking to anchor functional groups onto graphene or nanotubes sought out this benzoic acid. After integrating it into pilot runs, their feedback was unambiguous: the compound ensured tight, reproducible grafting and no cost in surface stability. The straightforward behavior during amide bond formation and reliable conversion to corresponding esters have kept it moving forward in academic and commercial electronics labs alike.
Standing back and comparing to other aromatic acids, several technical points arose where users hit trouble with supply from less focused sources. Some offer benzoic acid or pyrrole derivatives with mixed batches, broad melting points, or ambiguous color — all signs of competing by low price and compromising consistency. Our batches target the core need for single-lot homogeneity, eliminating the variability that creates headaches in long syntheses.
Our facility uses a fixed sequence in the synthesis — we rely on high-grade solvents and controlled temperature steps, and we keep strict oversight over catalyst loading. This blend of experience and straightforward, no-shortcut manufacturing keeps conversion rates close to theoretical. Whenever a batch falls short of our in-house cutoffs, it never sees final packaging. The difference over years of feedback is clear: fewer delays in process development, easier scale-up from milligram to kilogram scale.
Another key factor that sets 4-(1H-Pyrrol-1-Yl)benzoic acid apart from generic benzoic acids is the combination of electron-donating capacity of the pyrrole ring with the reactivity of the carboxylic group. Organic chemists looking to develop heterocycle-rich scaffolds for pharmaceuticals or custom catalysts take advantage of this dual behavior. Generic benzoic acids or simple pyrroles simply do not provide the same balance between solubility, reactivity, and resistance to over-oxidation. Synthetic challenges that often plague related acids, such as side-chain halogenation or unwanted ring-opening, occur less frequently in our product thanks to our selective purification stages and robust precursors, which we source directly.
Working on the manufacturing side, I regularly walk past reactors during quality checks, eyes and nose alert for batch differences. Time after time, researchers who come tour our facility mention the difference between what our 4-(1H-Pyrrol-1-Yl)benzoic acid brings and what they encountered elsewhere. These conversations stick with me. Sometimes they struggled with melting point drifts that translated into unpredictable yields. More than one lab sent us email updates once they switched — fewer byproducts, less cleanup, better downstream reproducibility.
For those using 4-(1H-Pyrrol-1-Yl)Benzoic acid in fragment-based drug design, the high purity supports crystallographic studies without background signals to confuse data sets. We learned this by supporting collaborations with structural biology core facilities: cleaner crystals, easier data interpretation. Analytical teams looking to trace subtle metabolites see fewer false positives from decomposition. Such direct benefits stem from sticking to a production model that favors small-batch precision when needed but still supports scalable, repeatable output.
Practical issues matter at scale. In one case, a customer struggled with atmospheric moisture uptake in benzoic acids from a previous supplier. They needed grams, not tons, but their research relied on consistent pKa and solubility. We adjusted drying conditions in the post-purification step and dropped surface moisture to levels well below 0.2%. Word soon reached us that their reactions stopped showing unexplained shifts. That’s how manufacturing decisions shape research outcomes.
Rigorous testing shapes much of our daily workflow, but we keep flexibility for those special cases that set custom requirements. Researchers sometimes request extra drying cycles, or alternate flask sizes, or even ask about compatibility with particular solvent systems. We take those queries seriously, drawing on direct experience and archived production data. Some users choose this benzoic acid for its tolerance of different coupling agents — dicyclohexylcarbodiimide, EDC, or even green chemistry alternatives. Every time a new process enters development, we compare the outcome against the in-house control sample, supporting customers at every stage from initial method development through pilot trials.
This adaptability often makes a tangible difference. A university group aiming to optimize esterification found that small tweaks in the post-reaction cleanup led to smoother final products. Working with them, we changed the solvent gradient during chromatography. Their comment after the run: less time spent correcting for baseline drift, and more time focused on innovation. Our support hinges on that cycle — feedback, adjustment, and shared success.
Storage and ease of handling often get little mention until trouble hits a workflow. Over the years, we fielded repeated questions about temperature control and light sensitivity. 4-(1H-Pyrrol-1-Yl)benzoic acid keeps well at room temperature, as long as containers remain sealed and protected from excessive humidity. Through targeted stability testing, we identified that freezing offers no major advantage unless solvents in use are unusually hygroscopic.
Users working on months-long projects want batches with reliable shelf life. We deliver with silica desiccants included, and we found that opening bottles only inside dry boxes keeps stock potent across multiple uses. Training new lab users in-house, we found that static buildup and cross-contamination sometimes halts pure syntheses. For that reason, we supply the product in anti-static vials for large orders, picking up on small but persistent challenges noticed after hundreds of scale-ups.
Our manufacturing philosophy leaves little space for compromise. Commitment to quality control begins with the lot record for each batch and reaches through to shipment. Choosing solvent grades, handling intermediates, and validating purification steps feels routine, but these steps make or break the compound’s reputation after delivery. We reject any containers that turn up off-color or fail dissolution tests in standard solvents.
Compliance with regulatory and safety frameworks guides our daily practices. No batch goes out without complete documentation of all reagents, trace impurity levels, and possible allergens. Risk mitigation does not serve as a buzzword here — it keeps projects, reputations, and research partners protected against unexpected delays. Our staff undergoes continuous training, using hazard analyses from prior incidents, building a learning environment that safeguards both producers and users.
We received a call last year from a long-standing customer: a regulatory agency needed rapid clarification of compound origin and synthetic steps. Since we keep all records digitized and accessible, delivering that confirmation took hours rather than days. This speed did not arrive overnight; it grew from constant review and a steady refusal to accept lowest-bid supplier attitudes in the specialty chemical sector.
In manufacturing specialty chemicals, communication with users and developers means staying responsive to changes in both practices and goals. Over countless projects, it became clear that every challenge pointed the way to better process design. Hearing from researchers who struggled to scale up “off-the-shelf” starting materials or who lost weeks tracking impurities in bought-in competitors gave real context to every tweak we made.
Continual engagement with research labs, pilot plants, and academic groups shows up in the product quality and the small features added to support everyday work. One research group used our benzoic acid in a combinatorial library build, cycling through multiple reaction platforms. They commented on the time they saved not needing to recheck by HPLC for each new batch — consistent product freed them to explore new space. Another team looking at metal-organic frameworks found side reactions dropped when switching to our lot, helping them report new results ahead of schedule.
Seeing the same names come up in our order system confirms the value of earning each return request. Researchers who move between companies or academic institutes write to ask for our benzoic acid by name, sometimes weeks after their old projects wrapped up. This continuity sends the strongest signal about the practical difference careful manufacturing imparts, and we take it as a responsibility.
We listen when feedback arrives, whether by technical report, email, or field visit. It shapes decisions we make in every quarter — adjusting drying when atmospheric moisture threatens, shifting suppliers if precursor quality tumbles, or revisiting all documentation if regulatory status shifts. Supporting real progress in research pulls us to keep finding benefits that extend past customer service platitudes.
Over a decade in the specialty chemicals sector, the definition of innovation shifted away from flashy marketing toward meaningful reliability. The real work focuses less on trying to outdo competitors on price or packaging and more on ensuring that the next gram of 4-(1H-Pyrrol-1-Yl)benzoic acid outperforms the last. Each time a user builds a new therapeutic scaffold or solves an electronic coupling problem with our product, we learn what matters. It comes down to trust earned by putting consistent, high-quality building blocks in their hands without excuses.
In a research climate chasing speed and impactful results, time matters. Our job is to remove the friction that comes from supply variation, shipping delays, or technical ambiguity. Getting the chemistry right from the start translates to saved runs, published papers, and successful patent filings downstream. Our commitment has been and remains to build in that reliability with each batch that leaves our facility.
Talk to any competitor and stories surface about the difficulties of delivering refined specialty products at scale. Raw material shortages, labor disruptions, or regulatory knots challenge anyone in the chemical space. What sets us apart boils down to a refusal to let those excuses filter into quality or user experience. Continuous improvement shapes our routine just as much as any periodic audit or annual target.
Our staff routinely steps outside standard procedures when unique problems demand a shift. If new analytical methods reveal subtle degradation not caught by baseline testing, we upgrade the detection suite. If a user proposes a green or alternative synthesis, our technical team runs the numbers, evaluates pilot runs, and returns a critical analysis grounded in our facility data. Change arises from trust in the experience behind each adjustment, not from checking boxes or meeting sales quotas.
Expertise, experience, authority, and trust form more than buzzwords for us — they ground daily work. From entering the plant to shipping out finished product, our employees embody years logged at the bench, troubleshooting routine syntheses, and engaging directly with client feedback. Authority comes from open documentation of each lot, cultivation of repeat partnerships with researchers, and response to regulatory requirements without shortcutting steps.
We treat trust as a living commodity. Every mishandled batch erodes confidence; every positive result deepens relationship. Consistent investments in staff, process upgrades, and transparent communications demonstrate our exercise of these commitments far beyond certifications or compliance paperwork. Experience shows us again and again — quality compounds start from quality control at every stage, and nothing replaces the satisfaction of helping push a research question forward via a sound, reliable chemical.
By learning from both successes and setbacks, refining production yet remaining flexible, and always driving at reproducibility and trust, we offer a foundation for innovation across chemistry disciplines. Each order of 4-(1H-Pyrrol-1-Yl)benzoic acid reflects a commitment shaped by hands-on work at every level of manufacturing. Direct application feedback shapes tweaks, keeping us accountable and moving quality upward. For research operations, pilot plants, or novel synthesis, this compound represents the intersection of process reliability, transparency, and shared scientific purpose.