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N-(5-Bromopentyl)Phthalimide

    • Product Name N-(5-Bromopentyl)Phthalimide
    • Alias 5-Bromopentylphthalimide
    • Einecs 612-131-7
    • 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
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    Specifications

    HS Code

    815964

    Product Name N-(5-Bromopentyl)Phthalimide
    Cas Number 52443-22-8
    Molecular Formula C13H14BrNO2
    Molecular Weight 296.16 g/mol
    Appearance White to off-white solid
    Melting Point 53-56°C
    Purity Typically ≥98%
    Solubility Slightly soluble in common organic solvents
    Density 1.43 g/cm³ (estimated)
    Smiles C1=CC=C2C(=C1)C(=O)N(C2=O)CCCCCBR
    Inchi InChI=1S/C13H14BrNO2/c14-8-3-1-2-7-15-12-9-5-4-6-10(9)13(16)17-11(12)15/h4-6H,1-3,7-8H2
    Storage Conditions Store at room temperature, in a dry and well-ventilated place
    Hazard Statements May cause irritation to skin, eyes, and respiratory system

    As an accredited N-(5-Bromopentyl)Phthalimide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing N-(5-Bromopentyl)Phthalimide, 25g, securely sealed in an amber glass bottle with tamper-evident cap and clear hazard labeling.
    Shipping N-(5-Bromopentyl)Phthalimide should be shipped in well-sealed, chemically-resistant containers, protected from moisture and direct sunlight. It should be clearly labeled and transported according to regulations for organic compounds. Ensure shipment complies with local and international hazardous material guidelines, employing appropriate cushioning and secondary containment to prevent leaks or contamination during transit.
    Storage Store **N-(5-Bromopentyl)phthalimide** in a tightly sealed container, away from moisture, heat, and direct sunlight. Keep it in a cool, dry, and well-ventilated chemical storage area, preferably in a designated cabinet for organic reagents. Avoid storing near strong oxidizers, acids, or bases. Ensure appropriate chemical labeling and restrict access to authorized personnel only.
    Application of N-(5-Bromopentyl)Phthalimide

    Applications of N-(5-Bromopentyl)Phthalimide in Industrial Manufacturing

    N-(5-Bromopentyl)phthalimide plays a key role in several advanced industrial sectors as a high-purity intermediate for specialized chemical synthesis. Below are major industry-specific applications carefully selected according to verified downstream use, describing each complete scenario from compliance standards through to the finished products manufactured in those sectors.

    1. Pharmaceutical Intermediate Synthesis

    Pharmaceutical companies use N-(5-bromopentyl)phthalimide in multi-step active ingredient production, particularly during the preparation of certain alkylated amines or heterocyclic building blocks. The material’s controlled reactivity supports nucleophilic substitution steps critical for synthesizing compounds such as antihistamines, anticonvulsants, or antidepressants. Integration requires strict traceability from batch to batch and an established impurity profile to satisfy regulatory submissions.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211 (cGMP for Finished Pharmaceuticals)
    • European Pharmacopoeia (Ph. Eur.) Monographs on intermediates
    • USP General Chapters <823> and <1079> for handling and quality assessment

    Typical usage ratio

    • 0.2–1.0 molar equivalents relative to primary amine or nucleophile, adjusted based on impurity control or alkylation efficiency requirements for each target API synthesis

    Downstream process integration

    • Charged during the alkylation step following initial condensation or cyclization, preceding purification or conversion to an amine or advanced intermediate

    Final product types

    • Pharmacologically active compounds, specifically intermediate skeletons for CNS drugs, analgesics, and custom pharmaceutical research chemicals

    2. Agrochemical Building Block Manufacturing

    Producers of specialty crop protection actives employ N-(5-bromopentyl)phthalimide in their flow chemistry lines, where it’s converted into complex side-chain extended amines and heterocycles. This intermediate enables refined control during the alkylation of selective agents, yielding finished actives with improved environmental breakdown or target specificity. All feedstock must comply with regional agrochemical safety and traceability requirements.

    Industry compliance standards

    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS) Specifications and Data Sheets
    • REACH (EC No 1907/2006) registration and supply chain traceability
    • ISO 9001:2015 Quality Management System in production plants
    • OECD Principles of Good Laboratory Practice (GLP)

    Typical usage ratio

    • 0.15–0.6 molar equivalents, depending on stoichiometry of targeted crop protection molecule and impurity control requirements across the reaction pathway

    Downstream process integration

    • Introduced at the alkylation or N-substitution stage in multi-step synthesis of amide, urea, or carbamate herbicides, followed by continuous purification and stabilization

    Final product types

    • Herbicide and pesticide active ingredients featuring branched or functionalized alkyl side chains
    • Precursor molecules for insect repellent formulations

    3. Advanced Organic Synthesis for Dye and Pigment Intermediates

    Colorant and pigment manufacturers source N-(5-bromopentyl)phthalimide as an alkylating agent in the synthesis of specialty dye intermediates, notably for producing functionalized aromatic amines that impart enhanced colorfastness or solubility. Processing requires rigorous adherence to hazardous substances guidelines due to the production of aromatic derivatives used in regulated markets such as textiles and inks.

    Industry compliance standards

    • OEKO-TEX Standard 100 for restricted substances in textile colorants
    • EU REACH Annex XVII (restrictions on certain aromatic amines/dyes)
    • ISO 14001:2015 environmental management in pigment plants
    • ZDHC (Zero Discharge of Hazardous Chemicals) guidelines for dye manufacturing

    Typical usage ratio

    • 0.1–0.5 molar equivalents relative to the aromatic amine core, with optimization according to desired color properties and residual bromine limits

    Downstream process integration

    • Added in the phase where side-chain functionalization of chromophoric cores occurs, typically before final purification and formulation of the dye or pigment intermediate

    Final product types

    • Disperse and reactive dye intermediates for textiles
    • Specialty pigments for digital and industrial printing

    4. Specialty Polymer Functionalization

    Chemical producers utilize N-(5-bromopentyl)phthalimide as a functional group donor in the synthesis of monomers and in chain-extension reactions, allowing the production of specialty polymers with pendant functional groups for use in high-value coatings, membranes, or adhesives. End-to-end material control ensures elimination of unreacted intermediates in compliance with application-critical regulations.

    Industry compliance standards

    • ISO 9001:2015 for quality system management in polymer plants
    • Regulation (EU) No 10/2011 on plastic materials and articles intended for food contact (where relevant)
    • ASTM D2569/D2569M for chemical resistance testing
    • UL 94 for flammability requirements in finished products

    Typical usage ratio

    • 1–5 wt% in monomer or pre-polymer feed, subject to chain-length and functional group density targets for the polymer being synthesized

    Downstream process integration

    • Introduced during solution or bulk polymerization to impart alkyl or functionalized side chains, followed by extrusion or casting for downstream shaping and curing

    Final product types

    • Functionalized polymers for specialty adhesives
    • Coating resins with enhanced surface reactivity
    • Membrane materials for industrial filtration

    5. Synthesis of Custom Research Reagents

    Research reagent suppliers and custom synthesis labs integrate N-(5-bromopentyl)phthalimide in the scalable laboratory routes for high-purity reference materials and analytical standards. Its predictable reactivity and compatibility with various protection-deprotection strategies makes it a standard intermediate for generating structurally diverse libraries of organyl compounds. All handling follows established laboratory safety and documentation protocols.

    Industry compliance standards

    • ISO/IEC 17025 for competence in testing and calibration laboratories
    • GHS classification and labeling requirements for research chemicals
    • Safe handling and transport per the UN Recommendations on the Transport of Dangerous Goods (UN TDG)
    • OECD GLP for traceable compound characterization

    Typical usage ratio

    • Usually 0.05–0.25 mmol scale per reaction for library synthesis; can increase to gram-scale for preparative research, with ratio based on designed yield per target analog

    Downstream process integration

    • Used in the early to mid-stages of multistep synthesis of target compounds, including during intermediate transformation for structural diversification

    Final product types

    • Reference standards for analytical method validation
    • Custom synthesis products for biological testing or screening campaigns
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    Certification & Compliance
    More Introduction

    N-(5-Bromopentyl)Phthalimide: Building Versatility Into Chemical Synthesis

    Introduction to Our Approach and Product

    For over ten years, our team at the manufacturing facility has worked closely with industries that rely on agile, practical solutions for specialty chemical synthesis. When we set out to refine the process for N-(5-Bromopentyl)Phthalimide production, we focused on reliability, purity, and ease of use for downstream chemistry. In practical terms, these goals translate to smoother workflows for our partners in pharmaceuticals, agrochemical intermediates, and material sciences.

    N-(5-Bromopentyl)Phthalimide has earned a permanent place on our product line because its brominated, phthalimide-protected backbone meets a real need in multi-step organic synthesis, especially in N-alkylation and nucleophilic substitution strategies. In the lab and at scale, chemists value a reagent that delivers predictable, controlled results. Mistakes in protecting group chemistry or halogen incorporation slow everything down. We designed this compound to minimize that kind of trial-and-error.

    Product Model and Core Specifications

    Our current model, processed under designation NPBI-5B, follows quality control standards that stem from firsthand feedback by medicinal chemists and process engineers. Each batch reaches a typical purity of 98% or above by GC, with a water content held below 0.2%. Particle size distribution, color, and handling characteristics stay consistent across lots, not because of marketing claims, but because we run these reactions daily and adjust parameters based on lab-scale observations. By holding to these benchmarks, we cut variability in downstream couplings, substitutions, and deprotections, which ultimately helps users meet their own project milestones.

    Our process team gets asked about byproducts and trace contaminants, as regulatory and GMP programs depend on tight analytical data. To address this, we use validated methods for bromide and phthalic acid residue detection and publish COAs with each shipment. We don’t rely on stock protocols. Instead, we tweak chromatography and crystallization steps between projects, learning from observed shifts in impurity profiles. This hands-on monitoring cuts requalification headaches later, so compound libraries or pilot batches keep flowing without interruption.

    Usage in Synthesis and Process Design

    In real-world settings, N-(5-Bromopentyl)Phthalimide steps in as a bridge between two often-contradictory objectives: introducing functional alkyl halides, and protecting nitrogen atoms during long synthetic sequences. Chemists trust this molecule to carry a heavy load because its phthalimide group defends against stray nucleophilic attack, and the terminal bromide stays reactive for substitution. Experience tells us that when using raw alkyl bromides direct from the shelf, mixtures and side products creep up. By locking the amine as a phthalimide, stray reactions drop, cleanup improves, and the final amine can be unmasked with hydrazinolysis or reduction.

    We’ve supplied NPBI-5B for key steps in routes making amine-linked small molecules, and for attaching tailored sidechains onto complex heterocycles. In medicinal chemistry, groups often use this compound to extend carbon chains or build linkers between functional motifs. In agricultural research and performance materials, the bromide handles substitution onto aromatics, or introduces tags for cross-linking experiments. End users choose it because they see less rearrangement, easier purification, and better yields versus processing free alkyl bromides.

    Several partners use this reagent for time-sensitive library synthesis—faced with an urgent SAR campaign, teams favor intermediates that react quickly and predictably under standard conditions. NPBI-5B proves flexible; it dissolves well in common solvents such as DMF, DMSO, and THF, while holding up under basic and mildly acidic environments. This versatility means fewer delays reworking protocols to adapt for solubility or decomposition. The process improvement may not always look dramatic from a management perspective, but at the bench, a consistently reactive halide protected by a sturdy imide speeds up discovery cycles.

    What Sets N-(5-Bromopentyl)Phthalimide Apart from Other Products

    As the manufacturer, we’ve compared this compound head-to-head with structurally similar alternatives: unprotected 5-bromopentylamine, shorter chain analogs, and other imide-protected halides. Feedback centers on two points—process reliability and downstream flexibility. Seasoned chemists spot the value in a five-carbon spacer: it bridges enough distance for bioconjugation or cross-linking, yet stays manageable in scale-up or downstream purification. Alternatives with fewer carbons tend to restrict conformational freedom or introduce solubility complications.

    Free 5-bromopentylamine, in our direct tests and partners’ bench work, wreaks havoc if not immediately consumed. It’s hygroscopic, often sticky, and prone to unwanted side reactions, especially with air, moisture, and microbial contaminants found in standard R&D environments. Our product side-steps those headaches. The phthalimide group protects the amine, meaning storage losses drop, weighing accuracy improves, and measured dosing into reactors works out in reality, not just on paper.

    Alternatives with different leaving groups—such as chloropentyl or iodopentyl phthalimide—have their place, but show tradeoffs between reactivity and cost. Bromide hits a sweet spot: it leaves cleanly under nucleophilic substitution without the volatility and toxicity issues attached to iodide, and avoids the sluggish reactivity sometimes recorded when using chlorides. Industry partners tell us their reaction times drop, and impurity levels stay lower in final products.

    Manufacturing: Reliability Built on Shop Floor Experience

    Every NPBI-5B batch originates from experience gained over thousands of liters or, in some cases, gram-to-kilo process development runs. In scale-up, we faced reality: solvents, temperature ramps, and crystallization conditions rarely operate as text-book-ideal. We learned to regulate exotherms before they happen, and listened closely when pilot plant operators reported color drift, clumping, or yield drop-off. Those moments drove incremental process tweaks that never show up on generic product datasheets, but they matter if customers count on timely, reproducible supply.

    Our operations do not outsource critical control steps, especially impurity purging and bromide quality checks. This direct oversight not only lets us catch out-of-spec material before it leaves the plant, but builds trust with scientists who remember which supplier batches made their process run smoother—and which caused delays. We established a feedback loop, sometimes inviting longtime partners to observe our plant runs or send their own chemists to audit our procedures directly. Ideas from those visits changed our solvent dry-down methods and adjusted quenching protocols, both steps that cut batch-to-batch differences in bromide content and hydrolysis risk.

    During the last three years, regulatory expectations for trace contaminants tightened across both European and Asian markets. Instead of scrambling to catch up and risking shipment delays, we integrated broader analytics: HRMS, trace bromination products via HPLC, and volatile residue scans that spot tank contamination long before it threads into finished batches. Over time, these measures pay off—but only if plant workers see direct results on their line. So we offer ongoing skills training, peer review of lot records, and direct incentive for reporting process drift. The expertise on our workflow grows with every new project, not because of outside mandates, but because we know mistakes grow more expensive the further they go down the line.

    Insight Into Supply Chain Resilience

    Several chemical suppliers missed deliveries in the past five years—often due to disruptions in bromine feedstock, or fluctuations in demand for side-products found in other commodity chemical streams. By managing in-house sourcing for key reactants, we avoid the worst effects of these swings. Our production schedules for NPBI-5B balance predictable monthly volume with enough capacity fluctuation to accommodate emergencies, including those triggered by new regulatory controls or transport bottlenecks.

    A recent story: in 2022, global shipping saw a spike in container hold-ups at key Asian ports. One major customer needed 300kg with a lead time of two weeks. Because our process does not depend on just-in-time bromine procurement or external contract drying, we re-allocated reactors and delivered in time, avoiding shipment delays that could have cascaded throughout the partner's clinical trial supply. This is the kind of reliability that the trading market seldom offers, but which practical chemistry demands.

    We’ve formalized these practices, keeping extra inventory of NPBI-5B and its intermediates, with documented emergency procedures for rapid re-qualification if an input supplier changes. Incoming raw materials get lot-tracked, and every process change stays recorded for both batch consistency and troubleshooting. These steps may sound simple, but after seeing what happens when a critical ingredient runs out industry-wide, we’ve learned to value patience and redundancy over maximum theoretical efficiency.

    Supporting Scale-Up: Lab, Pilot, and Full Commercial Production

    Many clients begin with small custom batches, then scale up as clinical programs or new materials gain traction. The feedback loop from their scale-up teams—troubleshooting agglomerate formation, off-odor development, or filtration speed—is central in refining our own protocols. In early-stage projects, flexibility to modify solvent systems, drying parameters, or packaging makes the compound easier for technicians to deploy outside the core research group.

    We don’t deliver surprise formulation changes mid-campaign. Users control sample volumes, packaging configuration, and delivery schedule. Packaging options for NPBI-5B range from gram units for analytical work to commercial drum shipments, all with interior liners to prevent oxidation or contamination. For global shipments, we employ double-verification on labeling and documentation, since documentation errors create regulatory headaches that bag down release and, in some cases, force expensive relabeling—and nobody wants that lost time.

    Scaling NPBI-5B beyond the lab bench introduces practical questions—especially for those worried about exothermic hazard, semi-volatiles, and workplace safety. We supply technical data from our own plant runs and provide hands-on troubleshooting if unexpected events crop up. On several occasions, our technical support staff traveled to pilot plants for on-site adjustment of process conditions. It makes a difference for chemists to see manufacturing staff who genuinely understand their workflows, instead of reading scripts prepared by outside marketers.

    Environmental and Regulatory Considerations

    As brominated intermediates receive increased environmental scrutiny, the pressure grows to minimize emissions, track waste streams, and document compliance. Our facility integrates closed-loop solvent recovery, bromide scrubbing during reaction and work-up, and targeted process water treatment that passes not only local limits but the more demanding thresholds set by multinational partners. We track and document every discharge, enabling safe adoption by customers who must report chain-of-custody and residual contaminant levels under global chemical regulations.

    Several larger buyers recently asked us to support ESG reporting on NPBI-5B: traceability, energy footprint, and lifecycle impact. Our plant audits each campaign’s actual energy, water, and solvent consumption, so we supply certificate and analytical documentation on request. These reporting measures arise not as a compliance burden, but because we've seen specialty chemical projects paused or blocked outright when paperwork fails to satisfy regulators. Reliable supply now means evidence-based transparency across the chemical’s entire lifecycle.

    To support users with different jurisdictional reporting needs, our documentation tracks starting material sources, trace impurity analysis, hazard handling procedures, and batch lot histories. Our team regularly updates SDS documentation to match the latest regulatory changes, communicating upticks in any listed restrictions or hazard statements. Where clients seek REACH, TSCA, or other region-specific compliance, we guide their teams through proper notification and certification steps, based on our experience managing these programs for similar compounds.

    Technical Support and Collaboration: Beyond the COA

    In practice, many challenges with N-(5-Bromopentyl)Phthalimide stem not from the core chemistry, but from context—solubility shifts, compatibility in emerging solvent-free systems, scale-up foaming, or sudden regulatory queries for manufacturing documentation. Our support team connects directly with process chemists, not through ticketing portals or generic responses, but through focused discussion of their actual processes. Multiple customers maintain annual partnerships, sending their own in-house samples for impurity benchmarking against our approach, or co-developing impurity studies to support their own application needs.

    Across projects ranging from drug discovery to next-generation functional materials, we hear recurring requests for documentation to back risk assessments, process development, or technology transfer. We maintain these resources in-house, revising based on new feedback, and make senior synthetic chemists—those who ran the development themselves—available for consults. Reliable chemical supply depends on more than just shipping grams or kilos; if a process team runs into trouble mid-route, or faces surprises in downstream purification, they know they can reach out for direct, informed support drawn from genuine shop floor and pilot plant experience.

    Our culture values direct language and practical answers over template responses, in part because we learned hard lessons trying to fix earlier problems with abstract assurances. If an issue crops up that our team hasn't seen, we look into the details—even inviting process partners to run side-by-side experiments or co-write process notes surrounding new controls or alternative raw materials. Through these exchanges, we capture experience-driven tweaks—new quenching order, additive selection, or slow dosing protocols—making synthesis more robust for everyone who relies on N-(5-Bromopentyl)Phthalimide as their platform.

    Looking to the Future: Demand, Development, and Sustainability

    Demand for NPBI-5B continues to shift along with innovation in pharmaceuticals, specialty polymers, and bioconjugation. As technology advances, the need rises for modular, reliable intermediates that can be modified quickly, adapted for new coupling partners, and incorporated safely into scale-up. Design teams want freedom to build new linkers, spacers, or N-functionalized scaffolds without the risk or mess of working with free alkyl bromides. Experience tells us that the combination of a phthalimide-protected amine with a five-carbon, brominated tail covers more territory than elemental building blocks alone. That’s why development teams looking to streamline their workflows and stay ahead of regulatory shifts seek out compounds with proven track records.

    We continue investing in technology upgrades, process analytics, and operator training to ensure each batch delivers performance and consistency. Rather than chasing commodity pricing or outsourcing critical steps, we aim to lead in transparency and reliability. As chemical markets grow more volatile and regulatory requirements grow steeper, the work done by manufacturing chemists—on the floor, not just in the boardroom—grows more important to science and industry alike.

    In every kilo of N-(5-Bromopentyl)Phthalimide shipped from our plant, there’s a story of hands-on experimentation, collaboration, and process evolution. We stand ready to work with those driving the next generation of chemical innovation, supporting their goals with steady supply, clear answers, and a commitment to practicality and quality in specialty chemical manufacturing.