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1-Bromobutane

    • Product Name 1-Bromobutane
    • Alias n-Butyl bromide
    • Einecs 203-695-5
    • 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

    962301

    Cas Number 109-65-9
    Molecular Formula C4H9Br
    Molar Mass 137.02 g/mol
    Appearance Colorless liquid
    Odor Sweet, chloroform-like
    Boiling Point 101.7 °C
    Melting Point -112.5 °C
    Density 1.276 g/cm³
    Refractive Index 1.4390
    Solubility In Water 0.61 g/L (at 20 °C)
    Flash Point 32 °C (closed cup)
    Vapor Pressure 24 mmHg (at 25 °C)
    Logp 2.9

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

    Packing & Storage
    Packing 1-Bromobutane is packaged in a 500 mL amber glass bottle with a secure screw cap and detailed hazard labeling.
    Shipping 1-Bromobutane is classified as a hazardous material for shipping. It should be transported in tightly sealed, chemically resistant containers, clearly labeled, and handled according to international regulations. Shipping must comply with DOT, IATA, and IMDG rules, and packaging should prevent leaks and breakage. Avoid exposure to heat, ignition sources, and incompatible substances.
    Storage 1-Bromobutane should be stored in a cool, dry, well-ventilated area away from sources of ignition and incompatible materials such as strong oxidizers. Keep the container tightly closed and protected from direct sunlight. Store in a labeled, corrosion-resistant container. Protect from moisture and keep away from heat and flame. Use secondary containment to prevent leaks or spills.
    Application of 1-Bromobutane

    Applications of 1-Bromobutane in Industrial Manufacturing

    As a specialized manufacturer committed to stringent quality controls, we supply 1-Bromobutane as an essential intermediate across multiple chemical processing sectors. Our production supports the demanding process requirements and compliance standards of industrial clients who rely on consistent performance in downstream transformation and advanced formulation development.

    1. Synthesis of Pharmaceuticals: Active Pharmaceutical Ingredients (APIs)

    Pharmaceutical manufacturers utilize 1-Bromobutane for introducing butyl groups during the alkylation of core structures in active pharmaceutical ingredient synthesis. This intermediate plays a critical role in the preparation of various APIs through nucleophilic substitution reactions, especially where butylation provides pharmacologically active attributes or improves molecule stability. Precise control over reactant ratios and reaction conditions is required, as regulatory authorities mandate complete traceability and impurity control from raw material through the finished drug substance.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) and United States Pharmacopeia (USP) monographs for relevant APIs
    • 21 CFR Part 210/211 (FDA cGMP for pharmaceuticals)
    • Directive 2011/62/EU (Falsified Medicines Directive)

    Typical usage ratio

    • 0.5–1.2 equivalents relative to the core substrate, adjusted according to targeted yield and minimization of by-products in each batch synthesis step

    Downstream process integration

    • Integrated as the alkylating agent during the main nucleophilic substitution reaction step of the chemical synthesis route; followed by work-up, purification, and crystallization prior to API isolation

    Final product types

    • Butylated sulfonamides
    • Alkylated pyrimidines
    • Quaternary ammonium-containing pharmaceuticals
    • Intermediates for local anesthetics

    2. Manufacture of Quaternary Ammonium Salts for Surfactants

    Producers of cationic surfactants apply 1-Bromobutane for butyl group introduction into tertiary amines during alkylation, forming quaternary ammonium salts. Strict batch-to-batch reproducibility is critical for these processes, as the end-use application performance depends on the precise hydrophilic-lipophilic balance attributable to the butyl substituent. Chemical engineers govern stoichiometry tightly to maximize formation of targeted quaternary compounds and reduce unreacted amines and secondary alkylation side products.

    Industry compliance standards

    • ISO 9001:2015 (Quality Management System for chemical manufacturing)
    • REACH Regulation (EC) No. 1907/2006
    • OECD Guidelines for Testing of Chemicals
    • Specific customer acceptance standards for purity and color by downstream detergent manufacturers

    Typical usage ratio

    • 1.0–1.1 molar equivalents to tertiary amine base, modified depending on desired chain length and conversion efficiency

    Downstream process integration

    • Charged directly to reaction vessels as alkylating agent, followed by controlled heating and phase separation; the resulting quaternary ammonium salts are then neutralized and purified for use

    Final product types

    • Fabric softener concentrates
    • Antistatic textile additives
    • Phase transfer catalysts
    • Cosmetic conditioning agents

    3. Agrochemical Active Ingredient Synthesis

    Leading agrochemical companies deploy this chemical for the N-alkylation of heterocyclic cores in systemic and contact pesticide synthesis. By employing it as a butylating agent, formulators can tune solubility and bioactivity attributes in herbicide and fungicide molecules. Safe incorporation into batch and continuous-flow synthesis units is managed with strict environmental monitoring and compliance to regulations on chemical agent handling during downstream transformation and product finishing.

    Industry compliance standards

    • FAO/WHO Good Manufacturing Practices for Pesticide Production
    • Regulation (EC) No 1107/2009 (EU Plant Protection Products Regulation)
    • ISO 14001 Environmental Management
    • Globally Harmonized System of Classification and Labelling of Chemicals (GHS)

    Typical usage ratio

    • 0.8–1.3 equivalents relative to the parent heterocycle or amine, varied depending on target yield and minimization of residual starting material in crude mixture

    Downstream process integration

    • Fed into butylation step reactors after initial core synthesis; product is purified using solvent extraction and distillation before formulation into granules, liquids, or concentrates

    Final product types

    • Butylated pyridine and triazole herbicides
    • Fungicidal active compounds
    • Pesticide intermediates destined for further functionalization

    4. Fragrance and Flavor Ingredient Manufacturing

    Within the fragrance and food additive industries, technical teams exploit this molecule as a controlled alkylating agent, especially for forming butyl-substituted aromatic esters and ethers with improved volatility and olfactory properties. Due to its reactivity profile, thorough removal of impurities and residual bromide is required before incorporation into compositions intended for direct food or cosmetic contact, demanding high-precision formulation and advanced analytical verification at every stage.

    Industry compliance standards

    • IFRA (International Fragrance Association) Standards
    • FCC (Food Chemicals Codex)
    • 21 CFR Part 172 (FDA – Food Additives Permitted for Direct Addition to Food)
    • ISO 22716 (Cosmetics Good Manufacturing Practices)

    Typical usage ratio

    • Typically 0.9–1.0 equivalent per aromatic substrate; exact dosage adjusted according to desired ester/ether yield, with minimized bromide ion residues

    Downstream process integration

    • Introduced in batch synthesis post-aromatic substrate dissolution, undergoing controlled alkylation followed by multi-stage distillation and final purification for safe use in fragrances and flavors

    Final product types

    • Butylbenzoate and butylphenol esters (fragrance base notes)
    • Butylated vanillin derivatives
    • Food-grade flavoring components for beverages and confectionery

    5. Specialty Solvents and Extraction Media

    Chemical processing plants engaged in specialty solvent production leverage this raw material as a building block for synthesizing butylated ethers and advanced solvent blends, particularly where selective solvency and favorable volatility are needed. Plant operators carefully control the alkylation and purification sequences to meet application-specific purity, color, and odor specifications, while complying with solvent use legislation and minimizing hazardous by-product generation.

    Industry compliance standards

    • EPA 40 CFR Part 63 (Hazardous Organic NESHAP requirements)
    • EN 16766 (European standards for solvent purification)
    • ISO 9001 for solvent manufacturing operations
    • REACH registration for downstream solvent applications

    Typical usage ratio

    • 1.0 equivalent to substrate for etherification; ratio may increase up to 1.3 equivalents dependent on required product purity and process yields

    Downstream process integration

    • Charged during initial alkylation/etherification steps within solvent blend synthesis reactors, then processed via vacuum distillation and stringent dryness controls before blending

    Final product types

    • Butyl ether solvents for paints and coatings
    • Special-purpose cleaning agents
    • Hydrocarbon extraction media
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    Competitive 1-Bromobutane prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    1-Bromobutane: A Versatile Alkylating Agent Straight from Our Reactors

    Real-World Manufacturing—Why Purity and Consistency Matter

    In our daily work at the plant, 1-bromobutane stands out as a practical, clear liquid that brings real value to industrial chemistry. This simple alkyl halide, with the chemical formula C4H9Br, has become a staple for anyone who demands straightforward performance in organic synthesis. In our manufacturing lines, we emphasize full control over every batch, aiming for high assay levels, low moisture content, and the clean profile that downstream chemists depend on.

    The making of 1-bromobutane calls for a direct approach. We use n-butanol as the starting point, running it through a controlled halogenation process to attach the bromine atom to the straight-chain butane backbone. This gives a linear, primary alkyl halide—meaning the bromine sits at the end of the chain, not tucked onto a branch. That spatial arrangement influences both reactivity and the way the molecule behaves during further transformations.

    Customers ask about differences from related compounds. Compare it to 2-bromobutane, a secondary bromide. In 1-bromobutane, the bromine is always at the terminal carbon. This difference matters for lab and plant chemists wanting precise predictability in substitution or elimination reactions. With our tight grip on process conditions, you get a product that reacts cleanly, favoring one type of outcome. The secondary bromides tend to yield more complex mixtures, especially under competing SN1/SN2 or E1/E2 conditions. If you value clean conversions with minimal side products, 1-bromobutane easily stands apart.

    Our reactors frequently produce both technical and premium grades. Technical grade covers most routine organic syntheses. When the application calls for fine details—like transparent pharmaceuticals, electronic intermediates, or demanding catalysts—we push moisture and halide byproducts down to trace levels, keeping the purity above 99 percent. We draw on years of process control to ensure that every bottle and drum meets the level of cleanliness that labs and industrial plants insist on. After years in this business, we know an overlooked impurity or an out-of-specification moisture content can derail an entire process campaign. To avoid surprises, we’ve tightened our distillation, nitrogen blanketing, and batch analysis steps to minimize those risks.

    Supporting Innovation in Synthesis

    Chemists working in pharmaceuticals, agrochemicals, flavors, and specialty chemicals count on 1-bromobutane for its ability to introduce a four-carbon chain with a reliable leaving group. It’s a workhorse for Williamson ether synthesis, forming butyl ethers that show up in everything from active pharmaceutical ingredients to automotive fluids. Because of its primary position, 1-bromobutane also makes nucleophilic substitutions straightforward. You can attach butyl groups to alcohols, phenols, or amines with consistent yields—no messy byproducts, no mystery side reactions, no scrambling at the carbon center.

    We field many requests for bulk orders from manufacturers preparing intermediates like butylated pharmaceuticals. Time after time, process chemists confirm that our product maintains tight quality and reliability during scale-up. In our experience, even simple reactions reveal their true colors on a manufacturing scale. Subtle impurities, a slight excess of water, or a batch-to-batch shift in bromine content can foul up a whole production train, leaving sticky residues or off-color distillates. That’s why we stay committed to detailed analysis after distillation and before packing. The lessons we’ve learned from past campaign troubles now inform every new lot’s release profile.

    For research environments, 1-bromobutane brings something more—predictability and adaptability. Students and researchers can count on a familiar, well-mapped reaction partner, making it easy to test new synthetic schemes or optimize older routes. Labs often choose our chromatography-grade 1-bromobutane, especially where trace metals or halide ions might disrupt catalysis or NMR studies. Our team is always looking to boost these qualities, understanding how a clean baseline lets discoveries happen faster.

    Model, Packaging, and On-Site Handling

    Across our production lines, we’ve standardized several models aimed at different industry needs. Bulk runs for large-scale intermediates favor 200-liter drums, with vented closures and specialized linings to prevent product loss during temperature swings. Smaller lots—5 or 20 liters—meet the expectations of research teams or smaller specialty chemical producers.

    Handling 1-bromobutane calls for routine care but no extraordinary demands. The liquid boils around 101°C; it shows a dense, sweet odor like other simple alkyl bromides. Its volatility means we focus on drum sealing, vapor recovery lines, and regular headspace checks. No packed drum leaves our warehouse without leak testing and compatibility review on all closures. Over years of shipping at varying climates, we’ve tuned our procedures to minimize venting and keep the chemical as fresh on arrival as when it leaves the stills.

    On the user side, we regularly share our own in-plant handling protocols. Our operators use gloves, goggles, and local air extraction as a matter of daily practice. These protections balance the product’s reactivity and its moderate toxicity. From loading tanks to sampling intermediate streams, we reinforce this guidance with real-world case studies—no one benefits from process interruptions or unplanned exposures.

    The Real Differences: 1-Bromobutane Compared to Other Alkyl Halides

    Manufacturers and formulators often ask why 1-bromobutane should be selected over alternatives. For most substitution reactions, the primary carbon center at the end of the chain offers the cleanest and most controlled pathway for introducing butyl groups in both nucleophilic and some elimination reactions. This keeps byproduct formation low, which is especially important in multi-step pharmaceutical synthesis or high-value specialty chemical production.

    Going up the chain to 1-bromohexane or 1-bromooctane, you find similar profiles in terms of reactivity, but the physical properties—boiling points, viscosities, and solubility—shift in ways that complicate downstream processing or blending. 1-bromobutane does not suffer from the waxy, sluggish behavior of higher homologs, and keeps distillation practical at laboratory and pilot scale.

    Comparing the bromobutanes to the chlorinated or iodinated butyls, bromine hits a Goldilocks zone. The bromo group leaves more readily than chlorine in nucleophilic substitutions, giving higher yields in many cases. Iodides react even faster, but are less robust during handling and much pricier per kilogram—the bromines strike an effective middle ground for value and reactivity. Drawing from experience, most of our longtime customers find 1-bromobutane outperforms 1-chlorobutane when the need is for efficient alkylation under reasonable lab or plant conditions.

    The story changes slightly when working with shorter-chain bromides, like bromoethane or bromopropane. Those have higher volatility, more challenging flammability, and weaker partitioning into organic layers. 1-bromobutane, by contrast, can be transferred, stored, and disposed of with fewer flash point or evaporation concerns—at least at lab and pilot levels.

    Sustainability and Continuous Improvement

    Running a chemical manufacturing site means thinking beyond price or reactivity. We pay close attention to environmental and safety profiles, both inside the plant and downstream. Brominated compounds have a reputation for persistence and toxicity—historical accidents have taught the industry to keep a close eye on air emissions, waste water, and potential residues.

    To that end, we have shifted much of our waste capture to closed-loop scrubbing. Each bromination run runs through secondary absorbers to pull down trace HBr and organic residues before any vent gas hits our flares or external atmosphere. What started as a regulatory necessity became a source of process savings, since we rework recovered bromine into new batches. Plant teams update protocols every quarter to keep ahead of reporting and minimize carrying costs from hazardous waste handling.

    On customer request, we offer full traceability of raw materials, including details on bromine and butanol sources. Many buyers once demanded only paperwork; now, due to increased end-market scrutiny in pharma, electronics, or European manufacturing, both chain-of-custody and sustainability credentials move to the fore. Our staff invests the time to comply with REACH documentation, transportation regulations, and emerging Chinese and US rules targeting halogenated chemical production. Those hurdles take both steady paperwork and shop-floor discipline—one missed parameter or poorly-documented shipment can mean lost market access for us and our partners.

    Long term, our R&D team works to shrink the environmental impact. Enzyme-catalyzed halogenations and continuous-flow microreactor approaches look promising for bromobutane, potentially reducing waste and off-gassing. We’ve piloted a few runs: lab feasibility looks strong, process yield approaches parity with traditional batch chemistry, and no single-use solvents are needed. These projects grow out of the day-to-day realities of chemical operations, not venture capital pitches. If a process saves time, reduces utility bills, or wins regulatory clearance with fewer headaches, you can bet our team evaluates it for plant-scale rollout.

    Applications That Drive Demand

    If you walk the racks in our warehouse, you’ll find 1-bromobutane heading out in dozens of directions. Large-scale pharmaceutical houses use it as a building block for beta-blockers, angiotensin inhibitors, and non-steroidal anti-inflammatories. Agrochemical firms rely on it to build up four-carbon side chains in selective herbicides or insecticide precursors. The flavors and fragrance world takes advantage of butyl ethers or butyl-substituted benzenes, carrying a subtle, flexible sweetness across a range of profiles. Lubricant formulators build advanced esters and sulfonates where the even chain-length of n-butyl proves essential for predictable viscosity and performance.

    Electronics and specialty material makers see value as well. As printed circuit board resins grow more complex, a well-defined, pure alkyl halide can make all the difference in trace impurity profiles or performance under heating. Our experience shows that process engineers trust that each charge of bromobutane will meet not just purity, but the low water and halide side content required to prevent failure in sensitive downstream polymerizations.

    Solvent use plays a smaller role, but still crops up in custom synthesis. Our plant keeps 1-bromobutane volumes flexible enough to serve both large, routine chemical campaigns and the occasional, short-run specialty order. Decades on, we’ve learned not to treat any customer as “typical”—each run gets its own logging, sampling, and double-checking. Human error creeps in whenever complacency replaces follow-through, so we stick to hands-on, practical checks by operators who know what baseline looks and smells like.

    Future Challenges and the Need for Teamwork

    Each year brings shifts in regulation, market demand, and customer expectations. Increased focus on “greener” substitutes sparks research into ways to make each run of 1-bromobutane safer, cleaner, and more energy efficient. Customers ask for halogen recovery, closed drums, and chain-of-custody documentation in more detail. We embrace those changes—each process improvement or documentation update adds both to customer confidence and our own operational security.

    Global shipping and logistics headaches remain a constant headache for all chemical producers. Temperature swings or rough transit can stress closures, change headspace, or, in worst cases, contribute to leaks or cross-contamination. Our logistics team reviews each batch, collaborates with trusted forwarders, and regularly updates packaging specs when performance data suggests improved closures or liner systems. Over time, these small tweaks reduce both cost and risk.

    Feedback loops between plant staff, technical customers, and operations drive most product improvements. We never push through a change—be it in process, packaging, or QC method—without a real-world benefit. Only lessons learned from tough campaign failures or quality incidents spur meaningful changes, and our ongoing investment in operator training and customer communication keeps the product line strong.

    Why 1-Bromobutane Endures in Industrial Chemistry

    Decades into production, 1-bromobutane still finds its place at the center of efficient alkyl group installation and reliable, scalable synthesis. Chemists who value clarity—both in chemical structure and finished outcome—keep coming back to the straight, four-carbon chain with its terminal bromine. The feel of the product, familiarity of the handling, and the directness of the reaction pathways all combine to keep it relevant in modern chemistry.

    Manufacturing 1-bromobutane remains a practical science. It combines thoughtful process control, real-world logistics, regulatory attention, and a steady focus on customer feedback. We constantly upgrade specifications, invest in greener processes, and train plant crews to stay ahead of new challenges. Every batch benefits from the practical lessons etched by years in chemical production. From everyday alkylation to breakthrough research, each drum and bottle shipped from our site reflects the history and care that sets direct manufacturing apart.