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HS Code |
508697 |
| Chemical Name | 1-Benzylpyrrole |
| Molecular Formula | C11H11N |
| Molar Mass | 157.21 g/mol |
| Cas Number | 2141-37-5 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 274-276 °C |
| Melting Point | -5 °C |
| Density | 1.045 g/cm³ |
| Solubility In Water | Insoluble |
| Refractive Index | 1.586 |
As an accredited 1-Benzylpyrrole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 100 mL, sealed with a screw cap, labeled “1-Benzylpyrrole” with hazard warnings and batch information. |
| Shipping | 1-Benzylpyrrole is shipped in tightly sealed containers, protected from light, heat, and moisture. It is classified for transport as a chemical substance and should be handled according to standard safety regulations, including appropriate labeling and documentation. Ensure the packaging prevents leakage and complies with local and international shipping standards for chemicals. |
| Storage | 1-Benzylpyrrole should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizers. Keep the container tightly closed and properly labeled. Protect from direct sunlight and moisture. Store at room temperature and ensure that storage conditions comply with all relevant safety and regulatory guidelines for handling organic chemicals. |
Applications of 1-Benzylpyrrole in Industrial Manufacturing1-Benzylpyrrole serves as a critical intermediate in specialized sectors across chemical manufacturing. As the original producer, we focus on real-world downstream industries where this material is integral to established processes and strictly regulated applications. The following application sectors highlight differentiated uses based on authentic industrial practice, regulatory adherence, and formulation needs. 1. Active Pharmaceutical Ingredient (API) Synthesis for CNS AgentsPharmaceutical manufacturers employ 1-Benzylpyrrole as a core intermediate in the multi-step synthetic routes for several central nervous system (CNS) drug candidates. Its unique structure enables the specific construction of substituted pyrroles crucial in advanced psychiatric and neurological disorder therapies. Our material enters initial coupling stages, impacting final API yield and purity. Every commercial API customer requires traceability and documentation fully aligned with regional and global standards, demanding strict batch control and advanced impurity profiling throughout the manufacturing chain. Industry compliance standards
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2. Specialty Dye and Pigment Synthesis (Indole and Pyrrole Derivatives)In the performance pigment and dye industry, downstream producers utilize 1-Benzylpyrrole to access custom indole-based chromophores and specialized pyrrolic pigments for printing inks and plastics coloration. Its usage directly influences hue, stability, and lightfastness in the final colorant. Specialty pigment manufacturers operate under stringent QC protocols to ensure color reproducibility and compliance with global chemical safety laws for both technical and consumer-facing markets. Industry compliance standards
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3. Agrochemical Intermediate (Heterocyclic Active Ingredient Synthesis)Producers of advanced agrochemical active ingredients use 1-Benzylpyrrole in constructing heterocyclic moieties of selective fungicides and insecticidal compounds. These applications require compliance with agroscience regulatory frameworks and deep process know-how to meet efficacy, safety, and environmental standards. Formulators regulate the presence and transformation of benzylpyrrole derivatives to safeguard both final activity and toxicological profile of the crop protection product. Industry compliance standards
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4. Functional Materials: Organic Electronics (OLED/Hole Transport Layer Synthesis)Manufacturers of organic electronic components, such as OLEDs and advanced hole transport layers, integrate 1-Benzylpyrrole derivatives into custom molecular scaffolds to modulate charge mobility and layer morphology. Material traceability and narrow impurity profiles are essential for downstream performance in high-value device fabrication, where end users demand batch-to-batch optical and electronic consistency. These industries require trace-level analysis to ensure compliance with both electronic gradeware standards and regional substance control regulations. Industry compliance standards
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Every year, we produce hundreds of metric tons of specialty heterocyclic compounds for advanced applications, and 1-Benzylpyrrole holds an essential spot on our roster. This molecule, with CAS number 3510-66-5, comes off our reactors in clear, consistent quality because we follow process controls we've honed over 15 years making pyrrole derivatives. Some chemicals come and go in demand; 1-Benzylpyrrole remains a staple because of its broad use in organic synthesis, pharmaceutical research, and even in new material development.
Users who work with pyrrole derivatives know the headaches surrounding unwanted byproducts and batch inconsistency. In the early days, we spent late nights tracing sources of discoloration and trace impurities. Over time, in-house analytics revealed that even a tiny impurity—like a methylated isomer at 0.2%—can ruin downstream reactions. We retooled our purification, switched to high-purity starting pyrrole, and built QA steps after every isolation and distillation. That's why our 1-Benzylpyrrole comes through GC-MS at >99.5% purity and consistently passes NMR for residual solvent and aromatic content.
This product stands out for its compatibility across several synthetic routes. In medicinal chemistry labs, it often serves as a building block for functionalized heterocycles or as an intermediate for alkaloid analogues. Sometimes new clients ask whether benzylpyrrole survives Grignard or Friedel–Crafts conditions. In-house data shows our product's stability through these reactions. Many chemists conducting library synthesis find the benzyl group resists oxidation and moderate base conditions, making it adaptable to multi-step synthesis.
We assign this product our internal model number—BZP-99-05—to designate its specification and production origin. Each manufacturing batch receives full traceability documentation. More than once we've had a pharma partner request detailed batch histories after scaling up pilot campaigns. Delivering on this need, our ERP system records vessel numbers, operator logs, and final analytical data, ensuring transparent batch validity. That way, R&D or scale-up doesn’t come with unwelcome surprises at kilo scale.
Our years of partnership with R&D labs taught us to keep specifications tight and real: GC purity above 99.5%, water content <0.1%, and a transparent yellow-to-colorless appearance. We ship by glass or fluorinated bottles to eliminate contamination—a practice we learned the hard way after a one-off shipment reacted with plastic in warm weather. There’s no secondary solvent residue, just trace t-butanol from the final recrystallization, never exceeding 0.03%.
Clients developing OLED materials sometimes need higher volumes or different solvent traces to match their process, but most customers find our default preps satisfy routes from Suzuki couplings to N-alkylation. Wherever possible, we've eliminated heavy metal catalysis from our process, further cleaning up analytical background for end-users.
Direct feedback from researchers revealed students and chemists alike choose 1-Benzylpyrrole when they must quickly install a protected nitrogen atom, then release it cleanly in final steps. In contrast to N-methyl or N-phenylpyrrole, the benzyl group brings reliable protection while being easy to remove under hydrogenolysis or TFA cleavage. Because pyrrole rings are sensitive to oxidation, we keep all steps under nitrogen and recommend clients open drums in gloveboxes or under argon for large-scale uses.
In our own test reactions, 1-Benzylpyrrole handles electrophilic substitutions or cross-couplings without decomposing. Comparatively, N-methyl analogs scramble in strong acid. New users are often surprised the benzyl group does not alter the electronic distribution in the pyrrole ring as drastically as phenyl or tosyl groups, so reactions proceed in higher yield. This trait makes it a favorite for those synthesizing fragments for drug discovery or materials science prototypes.
We produce 1-Benzylpyrrole in ISO-certified reactors. Raw materials start with commercially sourced pyrrole, then pass through our in-house benzylation route. Over the last decade, supply chain disruptions in benzyl chloride forced us to secure dual-sourced inventory and lock annual contracts to protect client timelines. Our team learned to work closely with freight carriers for quick customs turnaround; one stuck shipment of 5 kg delayed a cancer research project for weeks. Now, orders come with real-time tracking and direct logistics support.
Globally, demand for heterocycles like 1-Benzylpyrrole shows no signs of slowing—especially with an uptick in small-molecule immunology candidates and OLED blue-emission calibrants. Our analytics lab catches even sub-ppm benzylpyridinium impurities, making our material suitable for high-sensitivity applications. When working with customers in the electronics field, we document every trace contaminant and adapt packaging for moisture-sensitive material. This product’s clean, high-purity profile means chemists spend less time on pre-reaction clean-up and more on research.
People often ask us about storage. This compound's volatility and light sensitivity demand rust-free, airtight containers, stored cool and dark. Long ago, we learned sunlight turns open bottles yellow, generating benzyl radicals that can eventually lead to tar. For this reason, all warehouse staff get regular training, and expired bottles are quarantined and tested before rework or disposal.
Critical incidents teach hard lessons. Years ago, a shipping error sent product ground instead of air, and customs heat spoiled a batch. Now, thermal loggers sit inside every shipper. One time, a client in Sweden reported trace polymers—we traced those to excess moisture condensation in the warehouse. We installed new HVAC ducts and record RH% daily. Clients can always request COA data and our storage conditions by batch.
We also make N-Methylpyrrole and N-Phenylpyrrole. Unlike those, 1-Benzylpyrrole’s N-substitution allows more flexibility both in reaction scope and protection-deprotection strategies. N-Methyl analogs often deliver slightly better solubility in apolar solvents but trigger side reactions during oxidation. The bulkier N-Phenylpyrrole stands up under harsher conditions, but many cross-coupling partners prefer the benzyl derivative due to its clean removal and unperturbed aromatic pi-system. In our own scale-up work, we’ve found N-benzyl-protection much easier to cleave by catalytic hydrogenation, as opposed to N-phenyl which requires stronger chemical reduction.
Structural analogues sometimes include N-tosyl or N-carbamoyl protection. These block sites even better but complicate final molecule deprotection, and bring unwanted sulfur or urea residues into assays. 1-Benzylpyrrole stays cleaner—both in final product and in lab protocols—avoiding extra chromatography or sulfur removal. For researchers optimizing multi-step routes, fewer contamination headaches mean better turnaround and more reproducible screening.
Pharmaceutical discovery teams report using our material at scales from gram to multi-kilo for starting fragments, especially in structure-activity relationship studies. Some use it as a handle for N-functionalization, then cleave the benzyl group to reveal free pyrrole for cyclization reactions. Peptide and macrocycle chemists find benzyl groups easy to track and remove, catching minimal byproducts in LC fractions. We’ve worked with OLED material manufacturers scaling up from bench to pilot runs, where batch-to-batch consistency prevented scrap and enabled direct transfer to coating lines.
A few synthetic chemists came back after switching to suppliers offering only technical grade material, complaining about column fouling and yield drop. After troubleshooting, we offered tailored purification for them, and their work built our practice of running bespoke batches as collaborative projects when warranted. Our regular clients routinely request analytical data packs beyond the COA, including NMR, GC-MS, residual solvent, and heavy metals—underscoring the importance of transparency and adaptability in practice.
From the beginning, our approach has been to engage users with honest conversation about what lab-scale or commercial chemists actually encounter. We don’t hide the bumps along the supply chain, nor do we gloss over variations that can occur outside strict QA controls. Our team responds quickly when clients report issues—even arranging split-sample analyses from both ends to confirm purity or resolve disputes. This direct communication loop has improved our manufacturing, packaging, and customer service, and shaped the feedback-driven evolution of how we present and deliver our 1-Benzylpyrrole.
We maintain complete batch histories. So, if a research group later notices something unusual, we can trace every source lot, operator, and analytical run performed. Around 2018, two clients flagged outlying IR absorptions. We traced them to a single raw material batch, recalled all affected product, and adjusted supplier approvals to prevent recurrence. Lessons like these make us proudest—not in avoiding fault, but in fast, evidence-based correction and learning.
Concerns about chemical sustainability prompt us to take every reasonable step toward greener production. Our benzylation uses mild bases and recyclable solvents, minimizing excess hazardous waste. Waste pyrrole and solvent get processed in an on-site reclamation unit, and our plant staff are trained to recognize and mitigate environmental risks unique to this molecule—mainly vapor emissions and wastewater load. Routinely, waste streams undergo in-house GC trace analysis before discharge, ensuring we meet and exceed local and international guidelines.
Safety matters, at every step. 1-Benzylpyrrole vapors irritate, especially in summer. Our floor staff use fume extraction and wear full dermal protection, and all transfer steps happen in closed loops to minimize exposure. Information on handling goes beyond formal safety docs: we deliver real-world tips from the shop floor—like avoiding aluminum utensils that react under high humidity, and never pipetting by mouth, no matter how seasoned the chemist.
Many research projects increasingly demand scale, rapid shipment, and flexibility in product specs. Over time, we’ve responded by modularizing our reactors, running both research and commercial scale in parallel, and maintaining buffer inventory so bulk and small orders are both possible. Electronic order status, raw material trace, and full QA docs travel with each shipment, because rapid transparency at each point has proven the simplest path to trust.
Some users have requested greener, solvent-less synthesis or to limit halide contamination for use in sensitive pharmacology assays. We’ve got projects underway to realize these goals. Laboratory-scale pilots already show promise for catalytic benzylation and solvent minimization. Once proven robust, these methods will transfer to production scales, reducing both cost and waste.
New regulations and client standards mean ongoing adaptation—in packaging, documentation, and analytics. Our team keeps training in the latest ISO, cGMP, and environmental best practices, and we seek user feedback for continuous improvement. In this way, every kilogram of 1-Benzylpyrrole delivered draws on a live, ever-evolving practice, not just a static set of datasheets.
As direct manufacturers, our expertise with 1-Benzylpyrrole doesn’t come from reading brochures or relaying third-party claims. It’s built over thousands of batches, countless conversations with researchers, and decades learning what goes wrong between flask and reactor. Each cycle in the plant sharpens our understanding and quality, so that advanced chemistry, R&D, and new materials start with confidence—right from our line.
For those working on the next molecule that drives pharma, electronics, or next-gen materials, reliability in the starting block matters. Our open-door approach, real batch data, and readiness to solve problems as they arise turns 1-Benzylpyrrole from a commodity to a partner in innovation.