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HS Code |
406693 |
| Cas Number | 4549-31-1 |
| Molecular Formula | C7H14Br2 |
| Molecular Weight | 259.99 |
| Iupac Name | 1,7-Dibromoheptane |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 263-265 °C |
| Melting Point | -12 °C |
| Density | 1.529 g/cm3 |
| Refractive Index | 1.501 |
| Flash Point | 120 °C |
| Solubility In Water | Insoluble |
| Smiles | BrCCCCCCCBr |
| Pubchem Id | 12097 |
| Synonyms | Heptamethylene dibromide |
| Odor | Characteristic |
As an accredited 1,7-Dibromoheptane factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250 mL amber glass bottle with a secure white cap and safety seal, labeled "1,7-Dibromoheptane, 98%". Hazard symbols included. |
| Shipping | 1,7-Dibromoheptane is shipped in tightly sealed containers, typically made of amber glass or compatible plastic, to prevent leaks and degradation. Packages are clearly labeled with hazard warnings and handled as a corrosive, environmentally hazardous substance. Transport complies with relevant regulations like DOT, IATA, and IMDG for flammable and toxic chemicals. |
| Storage | 1,7-Dibromoheptane 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 moisture and direct sunlight. Use proper chemical storage containers, clearly labeled, and ensure secondary containment to prevent leaks or spills. Handle with appropriate personal protective equipment. |
Applications of 1,7-Dibromoheptane in Industrial Manufacturing1,7-Dibromoheptane is a specialized difunctional alkyl bromide employed as a building block in several high-value synthetic processes. Our facility supplies this chemical for use in core segments of chemical, pharmaceutical, and polymer manufacturing, serving clients globally with continuous quality control and full regulatory traceability. 1. Active Pharmaceutical Ingredient (API) Intermediate SynthesisIn pharmaceutical manufacturing, 1,7-Dibromoheptane acts as a bridging reagent for synthesizing key intermediates in the production of certain anti-viral and anti-hypertensive APIs. This compound provides an essential seven-carbon linker during the construction of complex heterocyclic structures via nucleophilic substitution, especially within custom and contract manufacturing projects. Downstream processors select it to meet both efficiency and regulatory demands in route scouting and API development, often optimizing batch and continuous process conditions for pharmaceutical yield and purity. Industry compliance standards
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2. Macrocyclic Polyether (Crown Ether) SynthesisSpecialty chemical manufacturers use 1,7-Dibromoheptane in oligomerization and macrocyclization reactions, most notably for producing crown ethers with seven-carbon bridges. The material acts as a critical dihalide in phase-transfer catalysis, enabling controlled ring closure with glycols or polyamines. Accurate stoichiometry and reaction control support consistent batch-to-batch outcomes, facilitating reliable operations for downstream formulators of select phase-transfer and extraction agents. Industry compliance standards
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3. Engineering Polymer Monomer PrecursorProducers of specialty engineering polymers utilize 1,7-Dibromoheptane as a bifunctional alkylating agent to generate linear or branched polymer backbones. The reagent's well-defined reactivity profile supports the synthesis of polyamides, polyimides, and block copolymers through nucleophilic substitution with diamines or diols. Careful dosage and rigorous impurity monitoring are necessary to prevent chain termination events, and downstream polymerization occurs under precisely controlled conditions to meet technical plastics specifications. Industry compliance standards
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4. Quaternary Ammonium Compound ManufacturingProducers of industrial biocides and functional surfactants use 1,7-Dibromoheptane as an alkylating reagent in the synthesis of quaternary ammonium compounds with controlled hydrophobic-lipophilic balance. The compound enables the introduction of straight-chain heptyl groups at each end of a nitrogen center to produce specialty cationic surfactants. Production facilities must optimize for yield and manage halide byproducts, particularly in continuous and semi-batch settings. Industry compliance standards
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5. Functionalized Organic Synthesis Intermediate (Specialty & Agrochemicals)Manufacturers of specialty fine chemicals and select agrochemical intermediates leverage 1,7-Dibromoheptane for introducing a controlled seven-carbon spacer via alkylation in multi-step syntheses. Its utility lies in supporting the spatial configuration of bioactive molecules where precise functional group placement is essential. Downstream operations incorporate it at defined coupling steps, often under anhydrous conditions, with strict adherence to purity and traceability criteria mandated by clients and regulators. Industry compliance standards
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Organic synthesis keeps evolving, but some materials stand out for the crucial role they play in connecting steps or opening new synthetic routes. 1,7-Dibromoheptane stands among these reliable components. As a manufacturer who has spent years refining both small and ton-scale batches of bromoalkanes, I have learned how much rests on the consistency and quality of this material. This compound, with the molecular formula C7H14Br2, brings two bromine atoms attached at each end of a seven-carbon straight-chain backbone. This structural feature opens a range of possibilities for building into larger, more complex molecules.
Purity defines the reliability of downstream results, especially in pharmaceutical intermediates or specialty polymers. Our experience pushes us to maintain 1,7-Dibromoheptane at a minimum purity of 98%, with moisture content kept far below detectable thresholds. Trace contaminants or extraneous halogenated byproducts always affect yields or catalyst lifespan during coupling reactions. For this reason, rigorous fractional distillation and multi-stage vacuum drying steps precede every lot leaving our plant. Over the years, we have seen how a few tenths of a percent in impurity can set back research or cause downstream quality failures. By continually fine-tuning distillation columns and performing regular GC-MS monitoring, we ensure consistent product and total bromine integration, so that our customers do not experience surprises during scale-up.
Although 1,7-Dibromoheptane sounds like a simple, straightforward dihalide, the characteristics can shift depending on how impurities are controlled and what source bromination method is employed. We prefer working with high-purity starting alcohols, since side-chain or ring-halogenated byproducts complicate separation and can poison sensitive catalysts. Careful attention to chlorinated byproducts results in a clear, water-white liquid, free from yellow or brown undertones that often point to iron or heavy metal contamination from equipment. The final product consistently measures a boiling range between 98 - 100 °C at 5 mmHg, which allows for reproducible handling even when customers transfer or store the chemical under inert gas systems.
Over the past decade, 1,7-Dibromoheptane has proved itself indispensable in developing C7 linkers and spacers for custom polymers and specialized active ingredients. Its appeal comes from the even placement of reactive bromine atoms on both chain ends, lending itself to symmetrical or “end-to-end” syntheses. Epoxy, polyamide, and polyether chain extensions often rely on these well-defined alkyl dihalides for efficient backbone elongation. In contrast to shorter bromoalkanes like 1,3- or 1,4-dibromopropane—butane derivatives, 1,7-Dibromoheptane delivers a much broader range between reactive points, enabling formation of flexible, less crowded molecular architectures. This helps maintain polymer solubility and processability—a feedback we hear regularly from specialty elastomer and membrane clients.
In pharmaceutical intermediate synthesis, it’s not rare for project chemists to come to us looking for clean, single-functionality chain-extensions without branching or unexpected isomerism. 1,7-Dibromoheptane gives the synthetic reliability needed for N-alkylation of diamines, stepwise etherification, and as a precursor in macrocycle closures. The seven-carbon span avoids the strain and torsion issues that arise in cyclization reactions when shorter chains force the molecular “ring” into unnatural spatial arrangements. We regularly supply gram to multi-kilo quantities to pilot plants looking to explore new cyclic compounds for antiviral and anti-inflammatory candidates.
Manufacturers constantly weigh chain length, reactivity, and processing safety. Shorter homologues such as 1,3- or 1,4-dibromoalkanes see use in cross-linking resins where compact spacers are needed. These, though, can trigger phase separation or stiffness issues in certain polymeric constructions. With 1,7-Dibromoheptane, it’s possible to walk a line between mechanical flexibility and chemical reactivity. Our polymer partners often point out that going longer (such as 1,10-dibromodecane) tips the balance toward excess plasticity or even crystalline domain formation, which undermines final application performance.
Shelf life and ease of handling also set this compound apart. Longer-chain dihalides tend to solidify at room temperature or develop waxy residues during storage. Our finished 1,7-Dibromoheptane remains fluid even in cooler storerooms, making it safer to measure and dispense without preheating. Fewer handling steps reduce risk, especially when operators work in large-volume environments or under manufacturer’s time pressure. Not all dibromoalkanes offer that kind of day-to-day practicality, especially in seasonal climates.
So often in chemical manufacturing, transitioning from bench to bulk throws up bottlenecks. We have worked with academic and industrial partners scaling from grams to hundreds of kilograms, and stepwise control of the 1,7-Dibromoheptane reaction always proves critical. Brominating heptan-1-ol through PBr3 or HBr ensures predictable chain integrity and minimal formation of internal alkenes or olefinic side products. Competing side-reactions can introduce unwanted “off-spec” molecules that compromise final performance. As manufacturers, we dedicate significant process development time to monitoring bromination parameters such as temperature, pH, and agitation setup. We have found that minor variations in input quality or reaction environment can shift impurity profiles significantly—a detail that often goes unappreciated until end-users encounter off-odors, unexpected color, or poor yields.
Bulk buyers come to rely on this product not just for purity but also for real-world logistical convenience. We pack our 1,7-Dibromoheptane only in high-integrity steel drums or coated HDPE containers with full inert atmosphere sealing. Over the years, we’ve handled requests to custom-fill smaller flask sets for rapid prototyping or provide multi-ton blends for continuous processing customers. Being a direct producer, everything is under our roof—no guessing on origin, storage conditions, or integrity of seals. Reliability in this way has become a major concern as international logistics and regulatory requirements tighten.
With the growth of custom-engineered materials, demand for selectively functionalized alkyl chains keeps rising. Epoxy resin producers depend on 1,7-Dibromoheptane to introduce flexible domains within rigid cross-linked matrices. Our product gives them greater leeway when fine-tuning glass transition temperatures or modifying impact resistance. Polyethylene glycol and polyamide process engineers favor the extra chain length for linking two different polymer blocks—creating products that stand up both chemically and physically to ever more demanding environments.
In surfactant synthesis, controlled chain length limits product foaming and optimizes wetting profiles. We have supplied this compound for nonionic surfactant programs intended to address textiles, water treatment, and advanced oil recovery systems. Organic intermediates built off 1,7-Dibromoheptane often serve as foundational reactants for custom cationic surfactant lines, especially where longer chain analogs become too hydrophobic or difficult to emulsify.
Safe handling and compliance have become more challenging each year. Since 1,7-Dibromoheptane finds itself regulated under several environmental and occupational exposure frameworks, having full vertical control is essential. We pre-screen every batch for residual free bromine and monitor air quality in the production hall, so operators do not face hidden respiratory hazards. Regular investment in abatement and containment means emissions stay well below published limits, and we share our long-term monitoring data openly with both customers and local agencies.
Traceability also matters. Our production records detail every batch’s journey from initial heptanol to final sealed drum. Repeat customers value quick access to full lot information, since a single outlier can undermine confidence and even recall finished consumer goods. Our internal analytics team checks each shipment with up-to-date analytic methods. In more than a decade, this open approach has helped us work through customs clearances and cross-border regulatory changes without shipment delays or customer headaches.
Procurement teams often ask why buying directly from a manufacturer—rather than through a trading house—matters. In bromoalkane chemistry, even a small slip in process consistency can multiply downstream costs. As process engineers, we see this all the time: an unexpected surge in color, a sharp off-odor, or new peaks in GC analysis change profile reliability during R&D and pushback downstream rework or troubleshooting. By producing 1,7-Dibromoheptane ourselves, every raw material, vessel, and packing material meets our own internal standards, not just those of third-party brokers. We train our staff to spot minute differences and follow up any deviation—something that only comes through years of hands-on production experience.
Beyond purity, direct production allows us to remain flexible as technology or end-user preferences shift. We receive requests for custom stabilizers or for modification to viscosity profiles—needs that cannot be filled by a static datasheet product. Working directly with formulation chemists, we can pilot lot-size adjustments or introduce in-process controls to meet new synthesis methods. This ongoing dialogue translates into faster optimization cycles and fewer project delays, since feedback moves both ways between shop floor and user lab.
Shipping and storage reshape chemical performance as much as initial purity. We handle drum and bulk container shipments worldwide. To protect against hydrolysis and accidental release of hydrogen bromide, containers never travel or sit exposed. Every step from filling to loading follows strict inerting and pressure-testing protocols. Our own field staff audit supply routes to confirm that transporters avoid prolonged exposure to temperature swings or light.
Long-term storage means thinking beyond standard practices. We often advise partners to store in tightly closed original drums, shielded from light and outside heat sources; this preserves the product’s low-moisture guarantee. Even a small introduction of atmospheric water can set off hydrolytic changes that pose risks down the line. We outfit each shipment with sealed sample vials that customers can test for any sign of mishandling without compromising container integrity. Though these details add upfront effort, we have found they practically eliminate lost inventory or disruption from batch variability.
Our improvement process draws directly on ongoing plant observations and end-user interaction. Customer complaints almost always point to root causes far earlier in the manufacturing chain. Addressing the issue of trace iron content in the early 2010s led us to upgrade all product-contact piping to inert, corrosion-resistant alloys. Outgassing or unexpected moisture led to facility-wide upgrades in vacuum and venting lines, reducing contamination risk for every subsequent batch. The improvements stick because they reflect both floor-level realities and technical wish lists from R&D partners.
Close work with regular clients feeds our drive for process excellence. By sharing sourcing constraints or sudden changes in demand, customers help us set up surge capacity ahead of spikes in global raw material flows or regulatory changes. More than once, we have flown out teams to troubleshoot not only our own materials but also site-specific use, helping chemists get back on schedule. These relationships, built on shared problem-solving and technical openness, anchor our ongoing commitment to reliability and product evolution.
Trends in specialty materials point continuously toward more challenging targets and greater regulatory oversight. 1,7-Dibromoheptane remains uniquely valuable in providing consistent, scalable C7 bridge formation with predictable end-group reactivity. Our history bears this out in both routine and breakthrough applications, from polymer additives to exploratory pharmaceutical intermediates. By focusing on incremental process improvements, safety, and direct customer communication, we aim to keep this product at the heart of innovation—reliable, accessible, and ready to meet the next generation of chemical challenges.
From the first kilo run to high-volume annual supply contracts, 1,7-Dibromoheptane has always rewarded care in sourcing and production. Maintaining stable quality and chemical integrity comes from hands-on plant management, direct experience with diverse end uses, and a steady commitment to open dialogue. The future of this product will keep drawing strength from enduring partnerships with R&D labs and technical teams, finding new ways to solve familiar and emerging challenges across the global chemical industry.