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4-Iodobenzyl Bromide

    • Product Name 4-Iodobenzyl Bromide
    • Alias 1-Bromo-4-iodomethylbenzene
    • Einecs 'EINECS 219-059-8'
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    234411

    Product Name 4-Iodobenzyl Bromide
    Cas Number 19816-43-0
    Molecular Formula C7H6BrI
    Molecular Weight 312.93 g/mol
    Appearance White to off-white solid
    Melting Point 48-50°C
    Density 2.02 g/cm³
    Purity Typically ≥98%
    Solubility Slightly soluble in water, soluble in organic solvents
    Storage Temperature Store at 2-8°C
    Smiles C1=CC(=CC=C1CI)Br

    As an accredited 4-Iodobenzyl Bromide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 5-gram amber glass bottle, tightly sealed, labeled "4-Iodobenzyl Bromide," with hazard symbols, supplier details, and batch number.
    Shipping 4-Iodobenzyl Bromide is shipped in tightly sealed, chemically resistant containers to prevent leakage and contamination. It is transported under ambient temperature, away from light, heat, and moisture. Proper labeling and documentation are provided, following hazardous material regulations to ensure safe handling and compliance during transit.
    Storage 4-Iodobenzyl bromide should be stored in a tightly sealed container under a dry, inert atmosphere, such as nitrogen or argon, to prevent degradation. It should be kept away from light, heat, moisture, and incompatible substances like strong bases or oxidizers. Store at a cool temperature, preferably in a refrigerator or designated flammable chemical cabinet. Handle with appropriate personal protective equipment.
    Application of 4-Iodobenzyl Bromide

    Applications of 4-Iodobenzyl Bromide in Industrial Manufacturing

    4-Iodobenzyl Bromide supports multiple critical syntheses in advanced manufacturing sectors. Its unique reactivity and substitution profile enable key transformations in pharmaceuticals, agrochemicals, and specialized material intermediates. Presented below are principal downstream industrial applications with process, compliance, and formulation details.

    1. Pharmaceutical Intermediate Synthesis

    Pharmaceutical manufacturers employ 4-iodobenzyl bromide as a halogenated alkylating agent in the synthesis of benzylated active pharmaceutical ingredient (API) intermediates. It serves as a pivotal building block to introduce iodobenzyl functionality into drug candidates and finished actives, particularly in the preparation of beta-blockers, anti-depressants, or CNS compounds. Operators must control reaction parameters and impurity profiles to meet stringent registration batch requirements.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP and Ph. Eur. monographs (as applicable for intermediates)
    • FDA 21 CFR Part 211 (for finished drug substance)
    • Chinese Pharmacopoeia for APIs

    Typical usage ratio

    • 0.85–1.15 molar equivalents relative to nucleophilic precursor; lab to plant scale ratio adjusted for reproducibility and yield optimization

    Downstream process integration

    • Charged into controlled batch or semi-batch reactors during electrophilic benzylation stages
    • Used alongside catalysts in the presence of protective agents to avoid bifunctional over-reaction
    • Purification follows by chromatographic or crystallization procedures

    Final product types

    • Benzylated API intermediates (e.g., beta-blocker precursors, anti-inflammatory skeletons)
    • Specialty CNS drug scaffolds
    • Reference standards for regulated pharmaceutical synthesis

    2. Agrochemical Active Ingredient Synthesis

    The agrochemical sector uses this compound for selective alkylation to synthesize high-value crop protection actives, particularly in fungicides and growth regulators featuring substituted benzyl moieties. Formulators require precise molar adjustments to control residue profiles and enforce compliance with selectivity specifications relevant to agricultural chemical registrations.

    Industry compliance standards

    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS)
    • ISO 9001 for production traceability and batch consistency
    • China National Standard GB/T 19108–2011 (for pesticide technical material)
    • EU Regulation (EC) No 1107/2009 on plant protection products

    Typical usage ratio

    • 1.0–1.2 molar equivalents for mono-benzylation reactions; adjusted downwards for multi-step coupling or in-situ functionalization

    Downstream process integration

    • Enters synthesis chain at the core benzylation or halogen substitution step
    • Application in pressure reactors or continuous flow systems for bulk synthesis
    • Integrated intermediate compound purified before onward transformation to target pesticide or biostimulant

    Final product types

    • Iodobenzyl-containing fungicide actives
    • Herbicide intermediate compounds
    • PGR (plant growth regulator) active ingredients

    3. Advanced Materials and Specialty Polymer Precursors

    Advanced material and polymer manufacturers utilize this compound for functional monomer synthesis. It enables direct incorporation of iodobenzyl units into pre-polymer chains, enhancing electronic and photophysical properties for specialty polymers used in OLED displays, sensors, and controlled-release materials. Batch documentation and characterization meet REACH and environmental standards for specialty chemicals.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006 for new chemical substances
    • ISO 14001 for environmental management in specialty polymer manufacturing
    • RoHS, where electronic applications are involved
    • Technical standards for polymer purity and end-use electrical performance

    Typical usage ratio

    • 5–25% by weight when blended as a monomeric intermediate, depending on desired polymer architecture and target functionalization

    Downstream process integration

    • Introduced at monomer synthesis or bulk polymer modification step under inert atmosphere
    • Integrated via phase-transfer catalysis to minimize side-reactions and ensure chain uniformity
    • Final polymerization proceeds following block or random copolymerization protocols

    Final product types

    • OLED display backplane polymers and emissive layer additives
    • SENS electronic sensor films
    • Controlled-release membrane and film materials

    4. Synthesis of Radiolabeled Compounds and Diagnostic Agents

    In the chemical synthesis of radiolabeled agents for diagnostic imaging and research tracer studies, 4-iodobenzyl bromide provides a critical entry point for selective radioisotope exchange, particularly in the preparation of iodine-125 or iodine-131 labeled benzyl derivatives. High purity and traceability are mandatory to minimize cross-contamination and to ensure safety in radiochemical applications.

    Industry compliance standards

    • USP General Chapter <823> Radiopharmaceuticals for compounding and PET drugs
    • cGMP guidelines for radiochemical manufacture
    • ISO 2919:2012 for sealed radioactive sources
    • Relevant local atomic energy regulatory approvals (e.g., U.S. NRC, European Atomic Energy Community)

    Typical usage ratio

    • 0.9–1.05 molar equivalents at tracer or microgram scale, adjusted based on radionuclide dilution and specific activity target

    Downstream process integration

    • Enters nucleophilic substitution or isotopic exchange with radioactive iodine in hot cell or glove box
    • Repurified by HPLC or preparative TLC to isolate high-specific activity tracer
    • Integrated directly into radiolabeled imaging agent formulations for QC and dosimetry

    Final product types

    • Radiolabeled diagnostic tracers (e.g., for PET, SPECT)
    • Laboratory reference isotopes
    • Research-use-only imaging agents

    5. Organic Synthesis Building Block for Fine Chemicals

    Producers of fine chemical intermediates utilize 4-iodobenzyl bromide as a halide source in Grignard, Suzuki, or Stille coupling pathways to generate elaborated aromatic scaffolds. The material's dual halogen functionality supports stepwise functionalization in high-value organic syntheses for fragrance, specialty dye, or electronic intermediate markets. Careful tracking of batch purity and reactivity profiles remains important for downstream reaction control.

    Industry compliance standards

    • ISO 9001:2015 for chemical production traceability
    • GMP-like systems (as required for food-contact or fragrance intermediates)
    • Purity and impurity profiling per customer specification
    • REACH registration for new chemistries in the EU

    Typical usage ratio

    • 1.0 molar equivalent in typical cross-coupling reactions
    • Adjusted stoichiometry may be applied for side-chain modification or multi-step syntheses based on yield requirements

    Downstream process integration

    • Applied at core halide coupling, functionalization, or ring closure stage
    • Introduced alongside appropriate palladium, nickel, or tin catalysts for C–C bond formation
    • Product passed through extraction and crystallization to purify target intermediate

    Final product types

    • Elaborated aromatic building blocks for dye chemistry
    • Electronic material precursors
    • Specialty fragrance intermediates
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    Certification & Compliance
    More Introduction

    4-Iodobenzyl Bromide: Reliable Quality from the Source

    Direct Insights from the Manufacturer: Practical Experience with 4-Iodobenzyl Bromide

    Making 4-Iodobenzyl Bromide isn’t about copying a procedure in a lab book; there are dozens of small process tweaks that make or break a batch. Our plant has worked with halogenated benzyl intermediates for decades. Over these years, we’ve learned the quirks of every step, from carefully dried glassware to the temperature range where impurities threaten turnover. Nobody wants a process halted by a stubborn impurity or variability that throws downstream work out of calibration. Sterling consistency and high purity stem from attention at each stage, not just checking a box at QC.

    One thing we’ve seen time and again: users stress over trace byproducts or accidental cross-contamination both in research and commercial runs. Reagents like 4-Iodobenzyl Bromide go into reactions where a competing halogen, or even the ghost of hydrolysis, can cause headaches. You don’t want to check your NMR only to trace the culprit to a distant batch run under subpar conditions. Our customers aren’t buying a commodity—they’re partnering with makers who track every gram from starting material to packaged product. This is why chemists reach out directly to the source, asking detailed questions, requesting documentation, and seeking out sample lots to align their methods before scaling up.

    Deep-Dive into 4-Iodobenzyl Bromide Models & Specifications

    Talking about “models” for a specialty fine chemical involves granular specs: purity, water content, melting points, permissible limits for related species. In practice, requests focus on specific purity grades. For 4-Iodobenzyl Bromide, we customarily provide 98% and 99%+ GC and HPLC grades, both tailored for synthesis in active pharmaceutical ingredients, advanced monomers, or specialty ligands. The balance between purity and price makes a real impact depending on downstream needs. Why overspend for a grade targeted for drug substance if you’re making a straightforward intermediate? On the other hand, no one wants to hash out issues during a complex cross-coupling or SN2 reaction because of a hidden trace contaminant.

    Moisture is another sticking point where the raw metric alone doesn’t tell the whole story. Every batch is packaged under inert conditions to keep the bromide and iodide stable, since both react with traces of water and reduce the shelf life. Dip into a bottle stored with a broken seal and you’ll quickly discover degradation products—resulting in either junk for the next synthesis or, at best, unpredictable yield. If you’ve ever tried to decompose the origin of a reaction failure, you know just how much a few ppm of water or leftover oxidant can throw things off. We’re vigilant about it because customers bring those problems to us, science in hand, looking for answers.

    Current packaging options reflect these priorities. Amber glass vials with precisely tested PTFE liners beat commodity packaging every time for shelf life and functional storage. Amber stops UV-induced decomposition. The PTFE liners allow chemical stability over months. Bulk customers—scale up projects at larger kilo or drum loads—ask for inert blanks and special requests like vacuum-sealed pouches or custom bottlehead threading for glovebox handling. We believe every container affects product quality as much as batch synthesis itself.

    A Look at Real-World Usage: The Front Lines of 4-Iodobenzyl Bromide Applications

    The main demand for 4-Iodobenzyl Bromide today comes from medicinal chemistry and advanced material synthesis. On the pharma side, many teams use it as a building block for biologically active compounds. Its bulky iodo and bromo groups make it a powerful tool for cross-couplings, especially for those running Buchwald–Hartwig aminations, Suzuki-Miyaura couplings, or preparing custom-functionalized heterocycles. You find the best results using this compound where selectivity and signal purity matter—for instance, in radiolabeling studies, or for synthesizing complex APIs where direct introduction of high-purity benzyl groups enables downstream modification. The bromo group offers versatility as a leaving group; the iodo ring enhances further substitution by activating the aromatic core for later-stage functionalization.

    Polymer and material scientists utilize this molecule for introducing functional handles. Whether making custom block copolymers, attaching spacers in supramolecular assemblies, or adding anchor points for bioconjugation, reliability at the fine chemical scale is a sine qua non. Over the past decade, several academic reports rely on 4-Iodobenzyl Bromide for post-polymerization modifications and as a linker in advanced electronic materials. We have worked hands-on with research groups to provide lots that fit rigorous structure confirmation routines, both for one-off experimental projects and for scalable tech transfer to pilot plant scale-up.

    In practice, an end user often approaches us after a negative experience with low-grade intermediates. Problems come up fast: inconsistent NMR spectra, off odors (hinting at trace toluenes or benzaldehyde impurities), color shifts, and poor conversion yields. We’ve seen it all. Maybe a researcher sources a bottle from a distributor selling unlabeled or poorly stored stocks. The result? Lost weeks or even months of effort. As a producer, our whole operation is built to erase those headaches: dedicated clean rooms, regular audits of analytical methods, and long-term archiving of batch sample data. These steps aren’t marketing slogans—they keep intricate syntheses running and ensure valid, reproducible science.

    Comparison to Related Halobenzyl Compounds: What Sets 4-Iodobenzyl Bromide Apart?

    At a glance, chemists might see many halobenzyl bromide derivatives on paper and assume they behave the same. Anyone who’s run reactions long enough knows that’s not the case. The iodine atom in the para position completely changes the compound’s properties—the electron-rich ring reacts differently compared to chlorinated or fluorinated analogs. The steric and electronic influences at the 4-position mean reactivity towards nucleophiles, metal catalysts, and oxidants shifts, often dramatically. The unique dual halide setup sets up further transformation options that simply don’t exist for single-halide or ortho/meta-substituted variants.

    We’ve noticed, over the years, that customers who have tried to substitute 4-Iodobenzyl Bromide with related products—like 4-Chlorobenzyl Bromide or 3-Iodobenzyl Bromide—end up reporting surprises. Small tweaks in ring electronics pile up in unexpected results: sluggish reactions, poor selectivity, or generation of side products nobody anticipated. For example, the 4-iodo substituent can serve as a valuable synthon in sequential functionalization or metal-catalyzed cross-couplings where palladium or copper catalysis thrives. Remove or swap that iodine and whole routes shut down or switch selectivity. The bromomethyl group’s lability compared to chloride means easier alkylation under milder conditions, reducing byproduct formation and safeguarding sensitive intermediates—crucial for advanced or late-stage synthesis.

    Shelf life and stability, often overlooked, matter as well. Certain positional isomers or mixed halides degrade faster or are more susceptible to environmental factors, especially when using a distributor’s poorly tracked stock. By producing 4-Iodobenzyl Bromide fresh, on a regular campaign, and keeping tight control of purification, we provide assurance batch to batch—a guarantee we’ve maintained for years. Regular customers who monitor their own inventories notice the difference versus generic commercial stocks that sometimes sit for months on the shelf before shipping out without temperature logs or up-to-date analytics.

    Manufacturing Realities: Handling, Hazards, and Solutions

    Anyone manufacturing benzyl halides knows you’ve got to respect the chemistry. 4-Iodobenzyl Bromide isn’t inherently more hazardous than related halides, but it demands the right protocols: moisture control, absence of oxygen, the avoidance of open air at every stage. Benzyl bromides hydrolyze, and the byproducts can be unpleasant or, for poorly ventilated labs, hazardous. We use closed loops, scrubbers, and regular atmospheric monitoring to shield both product and personnel. Operators undergo training that goes beyond SOPs and digs into the actual chemistry—why a bit of extra drying agent can matter, how one hot day changes the plant’s pressure profile, how to catch a microscopic leak before it impacts yield. We learned long ago that the best way to ensure purity is to treat every step, from raw material procurement to final packaging, as if we’re making our own research compounds.

    On a practical note, we’ve adapted the manufacturing line to minimize exposure at all points. Loading, reaction, and workup occur in a controlled atmosphere. We store outgassed solvents and run clean-in-place regimens, not just because it reads well on an audit, but because it lets us sleep at night. Technicians responsible for the halogen reactors know the ins and outs of keeping batch-to-batch variability down to a minimum. This attention to detail gets reflected in downstream analytical reports. Our in-house lab runs NMR, GC-MS, and HPLC on every lot and keeps both digital and physical records for traceability.

    If you’ve ever had to troubleshoot a multi-step synthesis gone sideways due to unreliable starting materials, you’ll appreciate working with a direct producer that will chase down the root cause of impurity spikes or color changes, not just read back a certificate of analysis. This is why we keep lines open for technical feedback—not just for complaints, but to hear how the compound actually performs under different substrates, catalysts, or in scale-up runs. We tweak purification methods based on this feedback: sometimes a seemingly minor change unlocks new performance for all users.

    Meeting the Challenges: Quality as an Ongoing Process, Not Just a Metric

    The demands for specialty chemicals shift, fast. A few years back, few cared about completely metal-free lots, and halogen content drifted below strict ICH Q3D limits. Now, with regulatory guidance on metal traces and new applications in sensitive API steps, attention sways to new priorities. We adapt; we validate. Our team revises washing protocols, upgrades detection limits, and makes sure every supplier of raw iodobenzene and hydrobromic acid meets the latest European, U.S., and Asian compendial regulations. This isn’t corporate mandate—it’s the day-in, day-out reality for a group that lives and breathes high-purity intermediate production.

    Implementing live inventory tracking and on-the-fly analytics may sound trivial, but it’s the backbone of reliability. Orders from pharma clients fluctuate based on phase changes and regulatory timelines. Material for an early-stage screen might only require a few grams, but a phase III supply can jump to drum loads in weeks. Our job is to anticipate: scale up batches, stagger campaigns to meet surge demand, and maintain enough safety stock so that nobody faces a last-minute shortage. This means dusting off the oddball batch record or making a fresh run on short notice to help a research team salvage a critical project. Every employee in the plant knows we’re not just running a factory; we’re backing up scientific progress for clients who have no patience for uncertainty.

    Quality is more than batch analytics. It involves open dialogue with customers. Process tweaks and method validation loops aren’t marketing. They’re the difference between a supplier who really understands your project and one who just ships product by the ton. One recent request: a university group needed 4-Iodobenzyl Bromide stable for a month-long, open-vial, air-free catalytic screening test. Standard packaging didn’t cut it. We engineered a glovebox-compatible vessel and ramped up inert-atmosphere filling. Small customizations like these make a world of difference, especially when every data point matters.

    Waste, Ecology, and Future Trends

    Fine chemical production faces environmental scrutiny. Benzyl halides require thoughtful waste handling—aqueous, organic, and trace halide byproducts can cause local issues if discharged improperly. Our experience has driven us to invest in closed-cycle waste neutralization and careful separation of iodinated from brominated streams. Waste isn’t a back-end concern; it’s coordinated from the process design forward. Regulatory bodies take these matters seriously. Non-compliance isn’t just a liability; it undermines trust, and the knock-on effect travels up the value chain. From responsible solvent recovery to partnerships with local waste handlers, we commit research and capital to meet standards.

    We see growing interest in green synthesis, solvent reduction, and energy minimization. Our plant has piloted microreactor-based production of 4-Iodobenzyl Bromide, which reduces hold-ups and limits side product generation. We coordinate regularly with academic and industrial partners to assess new catalytic routes; when a greener, safer path appears, we test and tweak. We also share findings on impurity profiles and mitigation strategies through technical forums, because the customer’s success depends on transparent, up-to-date knowledge about the chemicals we make.

    Looking forward, regulation will only tighten. End-users and buyers expect better traceability, analytic transparency, and genuine support. This suits us fine; we’ve built our plant with those demands in mind. Nothing beats hearing a customer finish a synthesis cleanly, with no mystery signals, confident in every number on the analytic report. We’re privileged and obligated to keep improving—and we see every batch as a step toward both better chemistry and truer collaboration.

    The Manufacturer’s Perspective: Why Direct Sourcing Matters

    Working face-to-face with scientists transforms how we run the plant floor and how we think about manufacturing. A bulk trader never hears about the reaction bottlenecks, the headaches of spotty supply, or the big sigh of relief when a project finally hits its mark. We do. Those details fuel our determination. We’ve shipped urgent lots to rescue end-of-year grant runs, expedited specialized purification for clinical trial-grade lots, and fielded late-night questions during early-morning time zones. Producers focus on real-world impacts, not sales cycles. If a client sees a deviation, we push our internal reviews—not to assign blame, but to fix the cause and prevent the next slip.

    The future of fine chemicals, especially tailored halide intermediates, belongs to direct partnerships built on honest feedback, deep process knowledge, and the recognition that every bottle links to big ideas in the lab. Every gram we make, we’ve sweated over for reliability—because that’s what you expect from a chemical manufacturer embedded on the front lines of synthesis. If your project depends on consistency, transparency, and expertise, you’re welcome to test our process. We welcome every challenge and every collaboration, knowing our strongest endorsement is your trusted, repeated use.