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HS Code |
433881 |
| Name | 4-Iodopentylbenzene |
| Cas Number | 134647-13-7 |
| Molecular Formula | C11H15I |
| Molecular Weight | 274.14 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 312°C |
| Density | 1.425 g/cm³ |
| Refractive Index | 1.570 |
| Purity | Typically ≥97% |
| Solubility | Insoluble in water; soluble in organic solvents |
| Flash Point | 139°C |
As an accredited 4-Iodopentylbenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of 4-Iodopentylbenzene, sealed with a screw cap, labeled with chemical information and hazard warnings. |
| Shipping | 4-Iodopentylbenzene is shipped in sealed, chemical-resistant containers to prevent leakage and contamination. It should be transported according to local and international hazardous material regulations, kept away from heat, flame, and incompatible substances. Proper labeling and documentation are required, ensuring safe handling during storage and transit to the destination. |
| Storage | 4-Iodopentylbenzene should be stored in a tightly sealed container, protected from light, moisture, and incompatible substances such as strong oxidizers. Keep it in a cool, dry, and well-ventilated area, ideally within a chemical storage cabinet designed for hazardous organic compounds. Ensure labeling is clear and comply with all relevant chemical safety regulations for safe handling and storage. |
Applications of 4-Iodopentylbenzene in Industrial ManufacturingAs a direct manufacturer of 4-Iodopentylbenzene, we supply this specialty intermediate across distinct industrial sectors where aryl iodides play a specific functional role. Our technical expertise ensures customers achieve precise integration of this material in demanding downstream syntheses. Below we outline verified application scenarios, compliance frameworks, recommended usage levels, process integration points, and representative end products, supporting our partners’ consistent quality and regulatory conformity. 1. Pharmaceutical Intermediate Synthesis for Active Pharmaceutical Ingredients (APIs)Originating at the intermediate stage of API production, 4-iodopentylbenzene participates as a key arylating agent in palladium-catalyzed cross-couplings. This stage allows for selective introduction of iodinated aromatic side chains essential to targeted APIs, especially in oncology and CNS drug candidates. Our product directly integrates into medicinal chemistry campaigns and pilot-scale process routes validated under international GMP environments, where reagent traceability and impurity control determine project viability. Industry compliance standards
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2. Agrochemical Intermediate for Selective Herbicide SynthesisLeading agrochemical manufacturers use 4-iodopentylbenzene as a core intermediate in constructing alkylated aromatic rings crucial for next-generation selective herbicides. Iodinated intermediates allow precise substitution patterns during synthesis, affecting bioactivity and field stability. We supply to downstream processors who must balance process yield, batch consistency, and regulatory supply chain audits for active ingredients sold in regulated agricultural markets. Industry compliance standards
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3. Advanced Material Monomer for Liquid Crystal Display (LCD) Precursors4-Iodopentylbenzene serves as a specialty monomeric precursor in synthesizing highly ordered aromatic materials used directly in LCD alignment layers and anisotropic conductive films. Its tailored alkyl-aryl structure is critical for tuning the thermal and optical properties of downstream functional layers. Producers in the electronics chemicals sector integrate our product to maintain strict control over molecular orientation and purity required in flat panel display manufacturing. Industry compliance standards
Typical usage ratio
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4. Specialty Intermediate for Aromatic Dye Synthesis in Laboratory ReagentsLaboratory and diagnostic reagent manufacturers employ 4-iodopentylbenzene as a specialty aryl-alkylating agent in synthesizing novel aromatic dyes. The controlled introduction of the iodopentyl side chain imparts unique spectral properties critical to sensitive analytical and staining reagents. Our supply supports end-users requiring trace-level impurity profiles and certified analytical documentation for research and clinical settings. Industry compliance standards
Typical usage ratio
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5. Intermediate in Fine Chemical Synthesis of Flavors and FragrancesProducers of fine flavor and fragrance chemicals utilize 4-iodopentylbenzene as a building block to introduce controlled aromatic and alkyl motifs. The material enters critical stages where subsequent functionalization (e.g., oxidative cleavage or substitution) generates value-added aroma compounds designed to meet market profiles for food and cosmetic ingredients. Only facilities with full analytical and traceability infrastructure handle such synthetic intermediates, ensuring conformance with market-specific purity and allergen statements. Industry compliance standards
Typical usage ratio
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Competitive 4-Iodopentylbenzene prices that fit your budget—flexible terms and customized quotes for every order.
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In our work as a direct manufacturer, every compound has a story behind it—rooted in the hustle of the workshop, the diligence of our chemists, and the pressures and opportunities revealed by our clients. 4-Iodopentylbenzene stands out in our product portfolio, not just for what it is, but for what it unlocks. This specialty aromatic, mapped as 1-iodo-4-pentylbenzene and listed under CAS number 72456-12-1, has been occupying a particular niche in applied research and fine chemical synthesis. Its chemical simplicity hides its value: a single iodo atom perched at the para position of the pentyl-substituted benzene ring, a structure deliberately assembled to deliver reactivity when most other alkylbenzenes stall.
From our experience, the raw appeal of 4-iodopentylbenzene does not just come from theoretical reactivity. Feedback from our partners in the pharmaceutical and agrochemical industries keeps reinforcing its practical benefits. This compound enables Suzuki and Heck couplings that other pentylbenzenes fail to deliver. The iodine group, adjacent to a flexible five-carbon tail, acts as a reliable exit point for a broad set of cross-coupling reactions, allowing chemists to build complexity onto aromatic frameworks with straightforward procedures. Quality starts at the molecular level—impurities or isomeric noise chip away at downstream efficiency. That’s why our synthesis routes center on single-step iodination with high regioselectivity, driven by controlled temperature reaction, stoichiometric precision, and precise catalysis.
Years of manufacturing experience have taught us that process impurities create hidden costs. We address these at each batch stage, blending hands-on analytical chemistry with controlled crystallization to turn out a clear, off-white crystalline product. Typical purities run above 98%, verified by HPLC and NMR, because even minor byproducts can poison catalysis stages when clients scale things up. During recrystallization we’ve optimized conditions for both recovery and cleanliness. The product’s melting point generally falls within a tight range, and we regularly run custom NMR scans as requested for customers working on regulatory filings. Such care matters most for R&D teams under pressure to demonstrate purity and batch-to-batch reproducibility to their decision-makers.
Our standard 4-iodopentylbenzene comes as a crystalline powder, packed in moisture-resistant containers to hold stability through transit and storage. Packing options range from 100 gram bottles up to multi-kilogram bucket units, all filled from one lot to ensure consistency. What differentiates our offering comes from direct synthesis and batch scaling—not pieced together by traders, but managed by the same technical supervisors we trust with our other halogenated benzenes.
We maintain assay specs of 98% minimum by HPLC for routine orders, sometimes higher for custom syntheses aimed at med-chem programs. Color metrics keep yellowness index low, because even a tinge can indicate residual iodine or over-oxidized products creeping through a run. Moisture levels seldom rise above 0.1% by Karl Fischer, a useful check since excess water can trigger decomposition or side reactions when clients use the product as a reactant.
Our documentation responds to regulatory and analytical queries: Certificate of Analysis traces each batch; NMR, GC-MS, and IR spectra available for deeper dives. What we don't do—unlike third-party suppliers—is stretch the truth about handling or purity. Every spec listed is built from tests conducted in-house, on our own equipment, overseen by our team from raw materials through to finished product.
Customers often ask what lifts 4-iodopentylbenzene above alkylbenzenes with lighter halogens or different alkyl chains. In many lab settings, bromo or chloro-alkylbenzenes seem cheaper, but we’ve seen how iodinated versions like this one routinely outperform their rivals in catalytic coupling. The larger radial size and higher electron-donating profile of iodine enable palladium and nickel catalysts to latch on, cleave, and swap the iodo group with new partners more efficiently.
The five-carbon n-pentyl chain attached at the para position creates a unique blend of hydrophobicity and functional reach. Unlike shorter alkyl substituents, such as methyl or ethyl, this extended side-chain presents two key benefits. One: it improves solubility for non-polar solvents and matrix resistance in polymer or material science applications. Two: it brings a consistent scaffold for constructing target molecules, such as specialty intermediates and advanced building blocks for materials with specific surface properties. We’ve worked directly with innovators chasing new polymers, who report that such side chains anchor additional substituents without excessive steric barrier.
Pharmaceutical teams value this compound for small-molecule programs, especially where heteroaromatic coupling or late-stage arylation is needed. Some traditional alkylbenzenes introduce unwanted branching or side products, while our 4-iodopentylbenzene—thanks to the straight alkyl chain and para substitution—avoids much of the regioisomeric confusion that plagues similar phenyl iodides. Our factory’s ability to supply uniform isomeric distribution means fewer headaches during impurity analysis or process validation.
Agrochemical researchers have told us this molecule has a sweet spot: enough hydrophobicity to anchor active ingredients in field formulations, while the iodo group signals a path to further functionalization or “late-stage diversification.” The architecture we offer keeps the product flexible for multiple design routes, not locking chemists into one downstream chemistry.
Some of our earliest runs met with unexpected challenges. Heat management became a big deal: pentyl chains handle elevated temperatures differently than shorter alkylbenzenes, and iodine’s reactivity doesn’t forgive off-key pyrosynthesis steps. We adapted by switching to lower thermal loads and tweaking our batch cooling cycles. This side benefit actually nudged up the batch purity, as less side-chain decomposition occurred. Lab feedback triggered tweaks in our silica-gel column runs, giving rise to consistently tighter spectral peaks.
Clients’ requests for packing in non-reactive liners shaped the way we handle shipments. Iodinated aromatics, with their reactivity, can sometimes “sweat” inside standard HDPE. So, we invested in lined steel drums for larger quantities, which also keep the product odor-free through long hauls. Every time a batch travels, it leaves with a QR code for direct batch tracing—our answer to the rising bar for supply-chain integrity.
Many buyers have shared that big distributors struggle to match specific batch requests with technical questions. We’ve tried to bridge this by direct dialogue: chemists on our side handle pathway clarifications, custom purity requests, and advise on storage against temperature or UV exposure. Our production teams track typical annual demand changes, so we always keep contingency batches for researchers needing an extra 100 grams overnight for an urgent run.
In the specialty aromatic market, many products tout “high purity” but fall short in measurable batch-to-batch consistency. Several competitors, mostly traders or repackers, will pool lots from various sources and pass them through rudimentary filtration and repacking. Our focus stays on single-run chemistry—meaning every kilogram comes from one controlled route. This guarantees not only match-up on melting point and color but also minimizes contamination with other alkyl halide isomers.
Traditional pentylbenzenes with chloro or bromo function sometimes get flagged as “manageable substitutes,” but anyone running cross-coupling or direct arylation knows they introduce unwanted byproducts. Iodine substitution at the para position speeds up oxidative addition, widens coupling conditions, and drops the requirement for activating additives or harsh bases in the reaction mixture. The upshot? Fewer surprises, higher yields, and easier purification—value every lab can count in savings at the scale-up stage.
Some manufacturers offer iodo-substituted phenylenes with branched alkyl tails, like isopentyl or tert-pentylbenzenes, in search of solubility boosts or selectivity. We’ve produced and tested these internally, and results suggest diminishing returns: more branching means more steric drag during coupling and a harder time achieving full conversion in common catalysts. Straight-chain pentyl keeps things predictable—an edge consistently confirmed in our pilot studies and clients’ feedback loops.
By managing all synthesis, purification, and QA steps ourselves, our team addresses off-normal requests, such as deuterated standards or higher-purity sub-batches for reference work. These often require in-process adjustments on the fly, another reason being a manufacturing-first supplier allows for quick turnarounds and tailored batch tracking—out of reach for third-party brokers.
We’ve watched our 4-iodopentylbenzene move through the hands of polymer scientists, pharma innovators, agrochemical researchers, and custom synthesis groups. In polymer science, formulators reach for it because the pentyl side chain offers flexibility within polymers, improving plasticizers and surface effects—especially in block copolymer settings where aromatic reagents need predictable reactivity and bulk compatibility. Teams pushing boundaries in OLED and photonics research request this molecule for fine-tuning optical properties or introducing anchor points for heavy metal ligands.
Drug discovery groups have shared their experience swapping our product for less reactive halogenated benzenes. Benchtop reaction yields improved, and the product’s lack of isomeric drift kept cleaning steps short. Medicinal chemists typically need minor modifications of the core aromatic ring—our product’s iodo group serves as a versatile leaving group, surviving pre-functionalization without activating the pentyl tail or causing off-target reactions.
In the agro sector, we’ve supplied teams who modify the compound to make advanced pest management agents. The balance of nonpolarity and reactivity means they stay stable in oily matrices but offer anchor points for building new active molecules. Smaller groups working on niche applications have explored it as a chemical handle for attaching dyes, or for synthesizing radio-labeled reference materials for environmental studies.
Every user group has one concern in common: reliability of supply and consistency. A single “soft” batch costs time and credibility in regulated settings. We run our QA on every lot, not just the first, and maintain archival records for customers facing regulatory audits down the line. Our technical support pivots to keep pace with new literature and regulatory changes, keeping the feedback pipeline open between chemists, operations, and users.
Iodinated aromatics, by nature, force scrutiny for environmental handling, waste disposal, and long-term storage. Early on, we received reports of slow decomposition if exposed to sunlight or trace metal catalysts left in old flasks. Our response: light-resistant packaging, stability studies tuned to both tropical and temperate climates, and recommendations for handling in everyday lab settings. Routine packaging has gotten stronger and our support materials now include practical storage guides—orthodox to seasoned chemists, but practical for new R&D hires facing complex safety regulations.
The other challenge—purity drift over time—called for changes in our warehouse management. We now keep a rotating stock to keep age to a minimum, ship only from verified runs, and implement batch tracking by handheld scan at every transfer point. We maintain a feedback line for customers facing custom purity hurdles in highly regulated product lines. If a customer needs further purification—removal of potential heavy metals or sub-ppm water content—we batch and ship extra-analysed lots typically within one week, as everything stays under our direct control.
Scalability often surfaces as a sticking point. Small-batch suppliers may provide a high-purity sample but drop the ball at kilo-scale needs for process optimization. Our shop floor was built for kilogram to multi-ten-kilo orders. The experience taught us several scaling tips. Careful cooling, continuous agitation, steady feed—not shortcuts that would sacrifice quality for metric tons versus grams. These steps, adjusted over years of trial and process control investment, guide successful large-batch client projects and reinforce trust as research teams move from milligram samples to full scale-outs.
We do not stand still on our synthetic methods for 4-iodopentylbenzene. New catalysis reports, regulatory shifts, and green chemistry demands keep us watching the literature and consulting specialists. We use new reaction media as they prove reliable. If a more sustainable iodo-source or greener solvent cuts waste, we bring it to management for review and validation. The pull from users in demanding industries pushes our team to avoid complacency—if a cleaner run is available, or a custom spec needed, we make that change. That’s one edge that can’t be manufactured by copy-paste trading operations.
Direct lines to our technical and quality teams keep user questions central to our reminders for improvement. Whether the request comes from a pharma line chemist or an agrochemical application lead, we prefer to hear about problems directly and act, rather than let issues percolate through layers of distribution. Our standing approach is: prompt transparency, willingness to adjust, full batch traceability, and a human voice from our company chemists and production staff. That culture, shaped over years on the factory floor, will always guide how we treat every new batch of 4-iodopentylbenzene leaving our loading dock.
Manufacturing 4-iodopentylbenzene takes equal parts craft and care—fine-tuning conditions batch by batch, listening to customer demands, and building real substance into the supply chain. The combination of direct manufacturing oversight, practical hands-on chemistry, and open feedback loops helps us avoid the pitfalls of generic commodity trading. In keeping with the best practices in chemical manufacturing and ethical supply, we document every lot, respond to client needs, and keep product evolution continuous.
What distinguishes our 4-iodopentylbenzene is not only the batch purity or clever packing. It’s the reliability our teams stake their name on, and the knowledge clients share back to make every new production run smoother and stronger. With every request, every order, and every challenge solved together, the cycle builds lasting trust—and another set of advances in research, from the most basic bench chemistry to the most ambitious applied syntheses.