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N-(4-Bromobutyl)Phthalimide

    • Product Name N-(4-Bromobutyl)Phthalimide
    • Alias 4-Bromobutylphthalimide
    • Einecs 629-005-6
    • 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

    427721

    Chemical Name N-(4-Bromobutyl)phthalimide
    Molecular Formula C12H12BrNO2
    Molecular Weight 282.14 g/mol
    Cas Number 3981-14-2
    Appearance White to off-white solid
    Melting Point 65-68°C
    Boiling Point No data available
    Density No data available
    Solubility Slightly soluble in water; soluble in organic solvents
    Purity Typically ≥98%
    Storage Conditions Store at room temperature, keep dry and airtight
    Smiles BrCCCCN1C(=O)c2ccccc2C1=O
    Inchi InChI=1S/C12H12BrNO2/c13-7-3-4-8-14-11(15)9-5-1-2-6-10(9)12(14)16/h1-2,5-6H,3-4,7-8H2

    As an accredited N-(4-Bromobutyl)Phthalimide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Sealed amber glass bottle containing 25 grams of N-(4-Bromobutyl)Phthalimide, labeled with safety data, lot number, and hazard symbols.
    Shipping N-(4-Bromobutyl)phthalimide should be shipped in tightly sealed containers, protected from moisture and light. It must comply with local and international regulations for hazardous materials. Suitable packaging includes chemical-resistant bottles with cushioning, clearly labeled with hazard information, and accompanied by a safety data sheet (SDS). Typically shipped via ground or air freight services.
    Storage Store N-(4-Bromobutyl)phthalimide in a cool, dry, and well-ventilated area, away from direct sunlight, moisture, and sources of ignition. Keep the container tightly sealed and away from incompatible materials such as strong oxidizing agents. Use appropriate, labeled containers to prevent contamination and accidental release. Follow all relevant safety and handling guidelines for organic chemical storage.
    Application of N-(4-Bromobutyl)Phthalimide

    Applications of N-(4-Bromobutyl)Phthalimide in Industrial Manufacturing

    As an original chemical producer, we supply N-(4-Bromobutyl)Phthalimide to OEM manufacturers, process integrators, and R&D labs across key fine chemical and pharmaceutical sectors. This intermediate enables precise transformations needed in advanced organic synthesis, specialty polymer modification, and active pharmaceutical ingredient (API) building blocks. Below, we detail representative industrial application scenarios with practical technical specifications.

    1. Active Pharmaceutical Ingredient (API) Intermediate Synthesis

    Pharma manufacturers utilize this compound during multistep API synthesis, frequently as an alkylating agent for controlled introduction of protected amino groups. Typical processes include N-alkylation reactions in the manufacture of antipsychotics and antiepileptics, where strict impurity control and batch reproducibility are mandatory. Downstream, it enables selective deprotection in later stages for API finalization.

    Industry compliance standards

    • ICH Q7A: Good Manufacturing Practice Guidance for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Parts 210/211
    • European Pharmacopoeia (Ph. Eur.) monographs
    • Chinese Pharmacopoeia (ChP) for registered APIs

    Typical usage ratio

    • Applied in 1.05–1.15 equivalents vs. the nucleophile; slight excess ensures full conversion.
    • Exact molar ratio adjusted based on reactant reactivity and lab validation runs.

    Downstream process integration

    • Charged post-initial protection in multi-step syntheses.
    • Employed during high-purity staged batch processing with solvent controls.
    • Removed or transformed by standard deprotection or reduction in subsequent operations.

    Final product types

    • API key intermediates for CNS medications (e.g., antipsychotic agents)
    • Intermediate blocks for antiviral and hormone drugs
    • Custom pharma project intermediates (contract or proprietary)

    2. Specialty Agrochemical Active Intermediate Manufacture

    Producers of selective herbicides and insecticides employ N-(4-Bromobutyl)Phthalimide as a chemical handle for alkylation steps in constructing bioactive molecules. The compound’s leaving group efficiency and stability under typical agrochemical conditions facilitate reliable industrial conversion for scalable pilot and commercial manufacturing.

    Industry compliance standards

    • FAO/WHO Specification and Evaluation for Plant Protection Products (FAO/WHO SEPPP)
    • US EPA 40 CFR Part 158: Data Requirements for Pesticides
    • REACH Regulation (EC) No 1907/2006 for raw material registration
    • ISO 9001:2015 for process and QC documentation

    Typical usage ratio

    • Generally used at 1.10–1.25 molar equivalents per active intermediate substrate.
    • Optimized according to desired conversion rate in batch or semi-continuous flow setups.

    Downstream process integration

    • Fed into closed reactor systems post-activation step.
    • Participates in substitution or condensation reactions before further derivatization.
    • Phthalimide group remains as intermediate protection until terminal processing.

    Final product types

    • Pyridine herbicide intermediates
    • Phenoxy acid herbicide building blocks
    • Custom pesticide and plant growth regulator synthons

    3. Functional Polymer Modification

    In engineered plastics and specialty resin production, our compound serves as a monomer modifier, introducing functional amine groups for compatibility or crosslinking. R&D and commercial scale users implement this step to create custom-imparted adhesive polymers, high-performance elastomers, or biocompatible coatings. It reacts under catalytic or photo-initiated conditions, accommodating a range of backbone systems.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems
    • ASTM D256 for impact resistance (for final plastics)
    • REACH Polymer Registration and EU RoHS compliance for formulated materials
    • GMP principles for medical-grade intermediate polymers (ISO 13485 where relevant)

    Typical usage ratio

    • Modifying agent content typically 0.5–2.5% by weight depending on target polymer functionality.
    • Ratio optimized experimentally based on backbone reactivity and product requirements.

    Downstream process integration

    • Introduced during pre-polymer mixing or chain-extension stages.
    • May participate in in-situ functionalization or post-reactor batch blending.
    • Residuals fully removed or neutralized by downstream purification and curing.

    Final product types

    • Custom polyamides and polyimides for electrical insulation
    • Adhesive resins used in automotive assembly
    • Functionalized polymer beads for chromatography supports

    4. Synthesis of Molecular Probes and Linker Chemistry in Research

    Biotech and diagnostics developers employ N-(4-Bromobutyl)Phthalimide in linker chemistry for the attachment of dyes, affinity tags, or bioactive ligands. The molecule's defined alkyl chain and phthalimide-protected amine allow orthogonal post-synthetic modifications suitable for small molecule probes, labeled peptides, and oligonucleotide conjugates.

    Industry compliance standards

    • ISO 9001:2015 for R&D material traceability
    • GLP (Good Laboratory Practice) for preclinical tools
    • USP <1058> for analytical quality control
    • No direct FDA pathway for research-use-only (RUO) chemicals, but documentation follows ISO/GLP standards

    Typical usage ratio

    • Amount varies with conjugation protocol, commonly 0.8–1.2 equivalents with respect to target sites on macro/micromolecules.
    • Ratios set based on maximizing yield and minimizing unreacted linker.

    Downstream process integration

    • Applied to pre-functionalize solid supports for peptide synthesis.
    • Used in solution-phase coupling with probe compounds, activated resins, or modified oligos.
    • Processed alongside analytical monitoring steps to assure purity.

    Final product types

    • Fluorescent peptide probes for cell imaging
    • Affinity resins for protein purification
    • Bio-conjugates for R&D diagnostics
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    Certification & Compliance
    More Introduction

    N-(4-Bromobutyl)Phthalimide: Reliable Building Block for Synthesis

    An Inside Perspective From Our Lab to Yours

    Every batch of N-(4-Bromobutyl)phthalimide that leaves our plant tells a part of a larger story. Years of synthesis experience have taught us which details truly matter in specialty intermediates like this one. We know our customers weigh quality, constancy, and process performance before anything else. Based on steady research in our facility, we continue to optimize routes and choose raw materials that provide reliable yields and subtle benefits in isolation and purification.

    Understanding The Product: Chemical Profile, Appearance, and Use Cases

    N-(4-Bromobutyl)phthalimide—C12H12BrNO2—stands out as a vital alkylating agent in the field of organic synthesis. We deliver it as a white to off-white crystalline powder, manufactured in lots ranging from gram to multi-kilogram scale. Experienced researchers often seek out this compound for its reactivity at the terminal bromide and the robust stability lent by the phthalimide moiety during multi-step syntheses.

    In practical terms, our own chemists have leveraged this intermediate most often for the Gabriel synthesis route when introducing protected amine groups. This protection not only avoids side reactions but also simplifies purification at later steps. The product holds up well during storage, a feature many chemists find useful when timelines stretch or scale-ups demand a reliable stock. Solubility favors common polar solvents—especially DMF and DMSO—which streamlines reaction planning in medicinal chemistry settings and with polymer precursors.

    Why The Manufacturing Approach Matters

    Margins for error in specialty chemistry remain narrow. Unlike catalog houses that source from brokers or traders, we oversee each step, from phthalic anhydride derivatization through to the careful halogenation that introduces the butyl bromide. This grants us the flexibility to monitor impurity profiles and optimize crystallization for every order. We have learned from experience that small differences in the control of bromobutyl introduction can lead to variable levels of side-products, which, in the worst cases, can stall an entire synthesis campaign downstream.

    Our control over the full process has allowed us to push reproducibility further. Rejection of out-of-spec material—rather than creative blending or dilution—has kept our lot-to-lot consistency in line with the expectations of process chemists. Downstream, this translates into predictable reaction kinetics and minimized troubleshooting for those using the product in their routes. We hear often from long-term industrial partners who rely on our batches to behave the same every time, especially in pilot and scale-up settings.

    Comparisons to Related Intermediates

    We produce a handful of related N-alkylphthalimides in parallel with the 4-bromobutyl version. The chain length or halogen identity offers chemists a menu of selectivity options, but each comes with quirks. For example, the chloro analog might cost a fraction less, but the lower leaving-group ability requires harsher conditions, which can induce overalkylation or by-product formation in certain reactions. The iodide tends to jump the reactivity level, proving useful in some nucleophilic substitution schemes, but shelf stability takes a hit, and cost per kilo sees a sharp rise due to raw iodine pricing.

    Looking at shorter alkyl chains, the N-(3-bromopropyl)phthalimide sacrifices some flexibility in downstream functionalization. Longer analogs, such as the N-(6-bromohexyl)phthalimide, can introduce steric issues or lessen solubility, making isolation more cumbersome. Field chemists have shared this feedback in one process optimization meeting after another. The four-carbon backbone in the N-(4-bromobutyl) option continues to show the sweet spot between reactivity, stability, and accessibility.

    Practical Challenges and Solutions in Handling and Sourcing

    Chemists dealing with our product rarely complain about ease of use, though we still recall years back when a batch was held up during recrystallization because the operator underestimated the role of water content in the final product. Advancements in drying technology and more deliberate control of atmospheric exposure have since alleviated many headaches, reinforcing how even minor hands-on production changes translate to real increases in yield and downstream reliability.

    Several teams working on scale-up have noted the importance of container compatibility and minimizing exposure to light and oxygen during storage. Overpacking and vacuum-sealing each batch has become our routine. It was tempting in earlier days to cut corners on these steps to move material out quicker, but past customer feedback and our own process lessons showed that surface oxidation quickly erodes not just purity, but confidence in the material overall.

    How Applications Drive Manufacturing Choices

    Many customers—academic, pharmaceutical, and specialty chemical—tell us they value the mild phthalimide protection for its selectivity in alkylation reactions. In drug discovery, this is often the difference between a route that scales cleanly and one that stalls under harsher conditions. A significant portion of our production supports those making protected amines and intermediates for further N-deprotection transformations. Reliability through each scale has given several contract research organizations comfort in running month-long campaigns without fear of batch-to-batch surprises or sourcing delays.

    Several specialty polymer firms use this material to anchor side-chains during copolymerizations, leveraging the controlled reactivity of the N-(4-bromobutyl)phthalimide under conditions that would otherwise degrade more labile intermediates. The manufacturing process we use avoids residual acid or base, as we have calibrated post-synthesis washing based on direct end-user input about downstream catalyst compatibility. Each season brings a new request for optimized parameters or expanded lot size, and we remain dedicated to meeting these evolving needs with production runs that we personally oversee.

    Quality Control—Lessons From the Shop Floor

    Quality for us is more than a checkmark on a certificate; it’s the product of hands-on detail. Batch testing with up-to-date analytical tools—NMR, GC-MS, and HPLC—plays a daily role in identifying outliers early. We’ve found that running chromatographic comparisons between process samples and reference spectra from established databases has helped pinpoint marginal impurities that, left unchecked, could compromise end-product functionality.

    We don’t just trust certificates on paper. Our in-process testing sheds light on measurable attributes such as color, melting range, and moisture content. In one instance, a seasonal shift in humidity altered crystal habit, affecting drying time, and thus final purity. By rotating to a controlled reactor environment and installing dedicated air dryers, we stabilized output and avoided further recurrence of the issue. Word spread within the chemist community, and new customers cited these first-hand stories as reasons for switching their supply.

    Feedback Loop: Customers Inform the Next Batch

    The field experience of our users continually shapes the product. Researchers who run high-throughput alkylation assays often share detailed yield and side-product data. More than once, this has prompted us to review purification steps or even pursue a new solvent crystallization recipe to boost final assay results. Pharmaceutical clients have asked for tighter particle size requirements, stating it impacts their mixing efficiency and scale-up yields. We’ve met these requests by tweaking mill settings and adding inline sifting to our final handling.

    Direct communication with scientists using our N-(4-bromobutyl)phthalimide lets us see beyond the drum or bag and learn how each lot performs in actual conditions. Surveillance doesn’t stop at the warehouse door. Our team regularly follows up on post-delivery performance, and we log user suggestions, issues, or even praises as feedback that flows straight into our continuous improvement meetings.

    Pitfalls of Non-Integrated Sourcing

    Companies that acquire intermediates through brokers or resellers often report challenges when tracing product origin. We see frequent cases where untracked handling or absence of documentation results in small but significant quality lapses. From our angle, control over every manufacturing step lets us backtrack any anomalous result, dig into the cause, and deliver solutions—be it a simple adjustment in raw material sourcing or a tweak to post-synthesis purification.

    We’ve noticed that switching sources, even for minor inputs such as phthalic anhydride, can subtly influence end-quality due to impurity carryover. Our own records track each lot’s journey from raw material to shipment, and we include supplementary spectral data with every dispatch to satisfy internal and customer audits. This thorough recordkeeping builds lasting trust, especially with partners in regulated industries.

    Working With Environmental and Regulatory Concerns

    In our region, compliance with environmental norms remains a moving target. Brominated intermediates generate regulatory attention owing to disposal and emissions issues. We approach solvent recovery and halide waste with closed-system capture and recycling. By investing in local treatment partnerships, we contribute to safer handling not just for our site, but for the broader community. Practical stewardship comes from combining on-the-ground operator vigilance with management investment in updated waste-processing units.

    Documentation for our material covers hazard labeling, transport, and disposal as required under international shipment conventions. Chemists in regulated settings can access full disclosure on processing aids, residual solvents, and storage stability, further reducing barriers to approval for new process trials. Years of supplying contract manufacturing organizations have given us a keen sense of where documentation gaps commonly arise or slow down onboarding, so we prepare each order to match these industry expectations.

    Supporting Innovation: Customization and New Derivatives

    Beyond the core compound, feedback from research partners occasionally leads to new derivatives or batch modifications. Teams working on next-generation surfactants have requested chain modifications, and we have responded by adapting our N-alkylation conditions and testing methods. Flexibility on our synthesis line lets us divert part of a batch for custom runs without disrupting regular deliveries, allowing collaborators to explore structure-activity relationships without long delays or material shortages.

    Though our foundation lies in N-(4-bromobutyl)phthalimide, we regularly invest in small run explorations for emerging N-alkylphthalimide variants, especially where there’s strong application feedback from the field. Requests like this often push us to upgrade reactor automation or trial greener halogenation procedures, since internalizing these requests preps us for the next wave of chemical demand.

    Price, Supply, and What Drives Trust

    No resource in our field stays untouched by global raw material cost shifts or changes in logistic infrastructure. Periodic spikes in bromine pricing ripple through to the final product, but our buyers have come to expect consistent, transparent communication about expected timelines and cost projections. Shortages in key feedstocks spur us to maintain redundant supplier networks, but we prioritize material traceability ahead of short-term price gains.

    Seasoned buyers know the pitfalls of cost-cutting on fine intermediates. The “best deal” rarely holds up under scrutiny if it demands process adjustments or brings an extra round of troubleshooting in the lab. A growing segment of our partners has moved away from spot buying and toward long-term arrangements not out of habit, but because experience has shown the hidden value in consistency. This confidence, built on open channels and direct lab-to-client relationships, keeps process innovation moving and manufacturers focused on core targets without constant disruption.

    Looking Ahead With N-(4-Bromobutyl)phthalimide

    From our earliest syntheses to the advanced routes shaping today’s pharmaceutical and specialty chemical innovations, direct experience has underlined the value of in-house synthesis, hands-on quality assurance, and a permanent dialogue with practitioners. N-(4-Bromobutyl)phthalimide stands as a case study in how manufacturing discipline, practical chemistry, and customer feedback come together to deliver a building block that supports invention, not just routine repetition.

    Every package reflects the lessons learned handling kilo-scale reactions and collaborating with scientists who demand reliability and openness. For those developing new products, optimizing existing routes, or seeking material for established programs, we see our relationship as more than supply and purchase. Instead, each shipment is another step in a network of technical partnerships, where expertise moves both ways and every lot delivered is another chance to prove the value of manufacturing know-how in fine chemicals.