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4-Bromo-1-Butamine Hydrobromide

    • Product Name 4-Bromo-1-Butamine Hydrobromide
    • Alias 4-Bromobutylamine hydrobromide
    • Einecs 276-907-6
    • 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
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    Specifications

    HS Code

    824574

    Name 4-Bromo-1-Butamine Hydrobromide
    Cas Number 5118-13-8
    Molecular Formula C4H11Br2N
    Molecular Weight 245.95 g/mol
    Appearance White to off-white crystalline powder
    Melting Point 218-220 °C (dec.)
    Solubility Soluble in water
    Purity Typically ≥98%
    Storage Temperature 2-8°C
    Synonyms 4-Bromobutylamine hydrobromide
    Smiles BrCCCCN.Br
    Inchikey CDVAPKSUZQSBOK-UHFFFAOYSA-N

    As an accredited 4-Bromo-1-Butamine Hydrobromide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

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    Application of 4-Bromo-1-Butamine Hydrobromide

    Applications of 4-Bromo-1-Butamine Hydrobromide in Industrial Manufacturing

    Our facility produces 4-Bromo-1-Butamine Hydrobromide for specialized synthetic routes across advanced chemical industries. This section details verified downstream manufacturing scenarios where this intermediate is actively employed, outlining compliance frameworks, typical usage concentrations, downstream process roles, and the major finished goods manufactured by end users.

    1. Pharmaceutical Active Ingredient Synthesis

    Major pharmaceutical producers incorporate this material during the development of various API side chains, particularly in the custom synthesis of small-molecule drugs involving aminobutyl linkers. The compound often enters multi-step reactions for building nitrogen-containing scaffolds needed in targeted therapies and CNS drug analogues. Accurate management of purity and trace impurities is enforced at each synthesis stage.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP-NF monograph criteria for related intermediates (as applicable)
    • EU GMP Directive 2003/94/EC
    • Pharmacopoeial heavy metal and impurity limits

    Typical usage ratio

    • 0.5–1.2 molar equivalents relative to core substrate; chemists tailor the charge based on reaction selectivity, batch size, and byproduct minimization

    Downstream process integration

    • Charged into the reaction vessel during nucleophilic substitution or reductive amination stages after protective group installation; isolated intermediates undergo sequential coupling or cyclization according to target molecule design

    Final product types

    • Custom API precursors
    • Specialty CNS active compounds
    • Branched amine-containing oncology drug intermediates

    2. Agrochemical Intermediate Production

    The agrochemical industry applies this compound as a functionalized amine source in the assembly of advanced crop protection actives. Chemical process engineers use it during scalable routes for building blocks required in selective herbicides and insecticides, especially where enhanced water solubility or biological targeting is critical.

    Industry compliance standards

    • FAO/WHO Pesticide Specification and Evaluation
    • ISO 9001-certified agrochemical QC systems
    • Occupational exposure concentration as per EH40 HSE
    • REACH registered for manufacturing and supply in the EU

    Typical usage ratio

    • Standard addition at 1.0–1.6 equivalents, according to the acylation or coupling stage; engineers optimize to maximize reaction yield and minimize excess

    Downstream process integration

    • Added in semi-batch reactor setups upon completion of substrate activation; typically followed by phase extraction, purification, and drying prior to downstream derivatization or formulation into technical concentrate

    Final product types

    • N-alkylated herbicide core intermediates
    • Aminobutyl-functional insecticide synthons
    • Custom pesticide building blocks for contract development

    3. Biochemical Labeling Reagents Manufacturing

    Our chemical is a critical intermediate for companies manufacturing bifunctional reagents used in targeted protein labeling and bioconjugation kits. Fine chemical producers utilize the primary amine function for introducing reactive handles, facilitating covalent attachment to biological macromolecules in research-grade diagnostics and proteomics.

    Industry compliance standards

    • ISO 13485:2016 for medical device reagents
    • OECD Guidelines for Testing of Chemicals
    • Good Laboratory Practice (GLP) for raw materials
    • Certification of Analysis (CoA) per shipment for trace contaminants

    Typical usage ratio

    • Low loading: 5–15% w/w in typical labeling reagent synthesis, adjusted depending on linker length and conjugation chemistry

    Downstream process integration

    • Incorporated during intermediate formation step for bifunctional linker synthesis, preceding downstream activation with NHS esters or maleimides for further conjugation

    Final product types

    • Protein/antibody labeling reagents
    • Crosslinker derivatives for cell imaging
    • Bifunctional linkers supplied to diagnostics kit assemblers

    4. Functional Polymer Modifier Synthesis

    Specialty polymer manufacturers use this raw material as a functional monomer or chain extender in the production of modified polyamides and block copolymers. The aminobutyl group introduces tailored reactivity and controlled chain flexibility, which are required in engineering high-performance, chemically resistant resins applied in electronics and automotive coatings.

    Industry compliance standards

    • ISO 9001:2015 for polymer manufacturing
    • ASTM D256 for impact resistance in finished plastics
    • RoHS Directive 2011/65/EU for hazardous substances in electronics polymers
    • EN ISO 1043-1 polymer classification

    Typical usage ratio

    • 2–8% w/w of total monomer charge, revised per desired mechanical and physical property endpoints in the final polymer matrix

    Downstream process integration

    • Metered into prepolymer reactors during chain extension or end-group modification phase, post-initial polymerization; undergoes controlled extrusion and pelletizing before downstream compounding

    Final product types

    • High-strength modified polyamide resins
    • Multifunctional block copolymers for E&E encapsulation
    • Adhesion-promoter masterbatches for specialized coatings

    5. API Linker Manufacture for Antibody-Drug Conjugates

    Specialized biopharma supply chain manufacturers use this compound for the synthesis of aminobutyl linkers tailored for antibody-drug conjugate (ADC) payload attachment. In these processes, the compound's structure enables selective conjugation chemistry, supporting the development of bioactive linker-payload formats meeting modern precision oncology delivery requirements.

    Industry compliance standards

    • ICH Q11 for development and manufacture of drug substances
    • EMA/CHMP guideline on antibody-drug conjugate development
    • ISO 14644 for cleanroom processing
    • USP <1043> Ancillary Materials for Cell, Gene, and Tissue-Engineered Products

    Typical usage ratio

    • 0.8–1.5 molar equivalents, selected based on targeted linker density on antibody scaffold and controlled by in-process analytical monitoring

    Downstream process integration

    • Activated with appropriate crosslinkers during linker-payload synthesis, then purified and formulated for downstream bioconjugation to monoclonal antibody backbones

    Final product types

    • Cleavable ADC linker intermediates
    • Stabilized bioconjugation reagents
    • Payload attachment modules for contract ADC developers
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    More Introduction

    Introducing 4-Bromo-1-Butamine Hydrobromide: A Strong Foundation for Chemical Synthesis

    Molecular Model and Specifications

    Those who spend any time in a laboratory will eventually run into compounds that quietly carry entire projects forward. 4-Bromo-1-Butamine Hydrobromide belongs to that category: a building block in organic synthesis with a reputation for reliability. Carrying the molecular formula C4H11Br2N, it introduces both flexibility and function to research and industrial applications. Chemists value this compound for its high purity, typically offered at greater than 98%. It stands as a white, solid salt, distinct from the base form of 4-bromo-1-butamine thanks to the stabilization provided by the hydrobromide addition. This hygroscopic characteristic means it absorbs water readily, so tight storage is a wise practice.

    Versatility and Use in Chemistry

    If you’ve ever tried piecework in peptide synthesis or linked molecules to surfaces in medicinal chemistry, you already know why amines like this matter. The butyl chain fitted with a bromo handle holds up well to diverse reaction conditions. It reacts smoothly with nucleophiles, making it a functional partner in alkylation and amination steps. Medicinal chemists seeking to create novel amine-linked scaffolds often turn to this compound. It lends itself to preparing biologically active molecules, and the bromine opens up further modifications by providing a reactive point for substitution. This isn’t abstract lab talk—it’s the type of compound that lets a researcher take a concept on paper and put flesh to it in glassware.

    Chemical suppliers distinguish this Hydrobromide from its free base sibling for good reason. Free base 4-bromo-1-butamine brings challenges with odor, volatility, and stability. Turning it into the hydrobromide salt renders it less volatile and more manageable. Safe handling always matters, and anyone in the lab knows the difference between a stable salt and a reactive oil. It's no accident that many protocols reference the hydrobromide as a starting material, particularly when consistency and repeatability are non-negotiable requirements.

    Real-World Impact and Differences from Related Chemicals

    Start comparing this compound to other short-chain alkyl bromides and you’ll realize not all amines behave alike. Some, like 1-bromobutane, don’t even bring an amino group to the table, so the range of applications narrows quickly. 4-Bromo-1-butamine hydrobromide not only acts as an alkylating agent but also contributes as a nucleophile when that amine is what you need for selective synthesis. Its position—the bromine at the terminal carbon and the amine at the opposite end—dictates which reactions succeed or stall. Try running some comparable syntheses with 3-bromo-1-propylamine hydrobromide and you'll end up with different yields, reactivity profiles, and likely a changed approach.

    In pharmaceutical research, the utility stretches well beyond lab curiosity. This compound forms a backbone for selective ligands used in target binding studies. Technicians count on its purity and physical stability to avoid spending hours troubleshooting unreliable reagents. During my own time in process development, switching from the free base to this salt version cut down waste and sticky cleanups. From undergraduate teaching labs up to GMP manufacturing suites, the call for reliable amines keeps growing.

    Safety, Storage, and Practical Considerations

    Handling this salt avoids the strong, unpleasant odors of the base, but it still pays to respect its toxicity and reactivity. Wearing gloves and goggles shouldn’t be up for debate—and in my experience, keeping silica gel handy extends its shelf life. It's tempting to view reagents as just interchangeable lines on a spreadsheet, yet anyone who’s confronted a clumpy, degraded bottle knows the frustration of lost time and blown budgets. Labs running on thin margins can’t afford to skimp on quality control, so product form and packaging play into daily operations.

    The stability of the hydrobromide salt simplifies shipping and storage. Unlike many liquid amines, you won’t face leaks or rapid degradation under reasonable conditions. Over the years supporting different pipelines, our teams found that using the right salt improved inventory longevity. This matters when projects span months or years, where replacing key reagents mid-stream can derail productivity and add approval headaches.

    Synthetic Pathways and Benefits in Research

    In advanced synthetic projects, versatility often wins out over novelty. 4-Bromo-1-butamine hydrobromide proves its worth by serving as a key intermediate. Whether reacting with strong nucleophiles or forming heterocycles by intramolecular cyclization, the compound doesn't box you into a corner. That’s a comfort when project timelines slip and researchers scramble for controllable variables.

    Take for instance the synthesis of substituted pyrrolidines—a motif central to many drug candidates and natural products. Using this hydrobromide salt, chemists introduce the butylamine chain in a single, tidy step and avoid messy phase separations. A similar analog lacking the hydrobromide would quickly form byproducts or evaporate in open reaction setups. Trust grows over time, so when a compound demonstrates reliable performance across hundreds of runs, it earns respect from both junior bench workers and principal investigators.

    Modern Challenges and Solutions in Chemical Supply

    In the crowded chemical supply market, labs have learned the hard way not to cut corners. Product consistency varies wildly by supplier and by batch. Counterfeit chemicals represent a growing threat as demand for amines spikes worldwide. Even experienced researchers have run into mislabeling and subpar materials. Years ago, a project I joined lost weeks to an impure batch sourced through a discount distributor. Once our procurement pivoted to hydrobromide forms with independent lot analysis, irregular results faded away.

    Some might see product authentication and supplier vetting as a bureaucratic drag, but steady supply chains form the backbone of real progress. Ecological impacts, waste reduction, and cost management hinge on choices like salt form, packaging, and storage practices. In fact, advanced characterization—like NMR or mass spec checks for each lot—doesn’t just boost confidence; it stops avoidable hazards before they spread. Trusting supply partners with GMP documentation, full disclosure, and batch testing isn’t a luxury in today’s landscape.

    Innovation and Future Applications

    Innovation in chemical synthesis keeps ratcheting up demand for smart, predictable reagents. 4-Bromo-1-butamine hydrobromide slots into green chemistry frameworks with less waste generated due to easy handling and high conversions. Researchers focused on developing sustainable chemistry appreciate reagents that don’t clog filters or require intensive remediation steps. Swapping from the free base to hydrobromide almost always means less solvent use during workups, a welcome change in labs chasing lower environmental footprints.

    With the growth of complex small molecule therapeutics, this compound’s dual nucleophilic and electrophilic properties come into sharper focus. Biotechnology researchers exploring conjugation chemistry rely on the clean amine group to tether linkers, dyes, and even antibody fragments. Peptide chemists, joining the hunt for next-generation antibiotics and probes, slot it into synthesis routes where classical bromides fall short. Over the past decade, more synthetic protocols cite this hydrobromide salt than older analogs, a practical sign that industry recognizes its edge.

    Looking at chemical innovation through the lens of accessibility, production of 4-Bromo-1-butamine hydrobromide faces fewer regulatory bottlenecks than controlled substances and highly toxic alkylators. Lower hazard ratings enable broader use in teaching and training programs, where the aim should be skill development and reproducible science. Increased transparency on purity, impurity profiles, and procurement traceability empowers those teaching chemistry to focus on core skills instead of wrestling with unreliable reagents.

    Regulatory and Environmental Responsibility

    Environmental stewardship has crept from the periphery to the center of chemical manufacture and distribution. Supply chains today face public and regulatory scrutiny on everything from packaging to disposal methods. As a non-volatile salt with manageable toxicity, 4-Bromo-1-butamine hydrobromide stands out compared to more hazardous amines. Facilities can streamline waste handling, cutting costs while reducing risk.

    Regulators keep a close eye on solvent emissions and halogenated waste. In this sphere, the hydrobromide salt meets compliance needs more easily than some predecessors or close relatives. My own experience handling waste management showed a marked difference in regulatory paperwork and cost when packaging and disposal switched from free base forms to stable salts. Small reductions in volatility and solubility add up, especially over a year’s worth of production runs.

    Lessons from the Lab: Why Details Matter

    Lab veterans pass on lessons the hard way: don’t underestimate how a single reagent can shape a project’s trajectory. I recall supervising a summer internship program where students repeatedly contaminated glassware with volatile alkyl amines. Adopting this hydrobromide version cut headaches overnight. Labs saw lower contamination levels, fewer abandoned experiments, and shorter clean-up times. While textbooks may gloss over such day-to-day realities, the choice of starting material ripples through even the most routine work.

    Precautions still matter, of course. Hydrobromide salts must be kept dry to prevent caking or hydrolysis, but in practice, these conditions are easier to maintain than with odorous, oily free bases. Research teams report more reproducible results simply by swapping their standard amine for this salt form. That predictability saves time and money, not to mention credibility when sharing data for peer review.

    It’s easy to underestimate compound selection until unforeseen problems crop up halfway through a synthetic series. Even with the best intentions, mistakes multiply when controls lack reliability. Choosing robust, stable salt forms like this hydrobromide upholds the culture of careful science that experienced chemists insist on. Facility managers and bench chemists alike gain an extra buffer against day-to-day variability, which is no small accomplishment.

    Supply Chain Resilience and Quality Assurance

    Recent disruptions in global supply chains have shown just how important quality is—not only of the product but of the documentation and sourcing behind it. Labs forced to swap suppliers with little notice now know that having a trusted, well-characterized reagent on the shelf can keep timelines on track. Price often dominates procurement decisions, and some stakeholders question the premium for high-quality salts. Yet the fallout from a poor batch—ranging from failed syntheses to lost grant funding—underscores why details matter.

    As organizations ask more of their chemistry labs, from rapid scale-up to parallel synthesis, the margin for error narrows. That's where the reliability of hydrobromide salts proves its worth. Lower volatility means less loss during weighing and transfer, a mundane yet critical advantage in both milligram and kilogram scale chemistry. Over my years working on both exploratory projects and scale-up, robust material handling reduced waste and minimized downtime across stages—a critical component of modern efficiency.

    Community, Collaboration, and Shared Knowledge

    No laboratory stands alone anymore. Collaboration has become the engine for most scientific breakthroughs, and the need for standardized materials only grows. 4-Bromo-1-butamine hydrobromide performs as a dependable contributor in shared research environments. Networks of researchers spanning institutions take for granted that a common starting point translates into comparable outcomes. Without stable and reproducible core reagents, benchmarks and replicability go out the window.

    More journals and funding agencies insist on specifics: purity certification, documented origins, and analytical verification for every core reagent. This hydrobromide salt simplifies those approvals, with suppliers typically providing thorough certificates of analysis, impurity data, and full traceability. In my own group, we shifted protocols toward standardized salts a few years back after a spate of irreproducible results. The change cut down follow-up experiments required to confirm preliminary findings, letting postdocs focus on innovation rather than troubleshooting.

    Conclusion: Building Trust Through Quality Reagents

    Every innovation in science rests on a foundation of reliable basics. 4-Bromo-1-butamine hydrobromide embodies that principle: a substance that, while unglamorous, helps unlock new discoveries every day. From improving safety in undergraduate teaching labs to supporting sophisticated drug discovery, its profile as a stable, pure, and well-understood reagent cements its place in modern chemical practice. Choosing robust materials benefits everybody—researchers, institutions, and society—by driving efficiency, promoting consistent results, and supporting the kind of shared progress that uplifts the entire field.