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HS Code |
596197 |
| Productname | 7-Bromoheptanenitrile |
| Casnumber | 4391-00-4 |
| Molecularformula | C7H12BrN |
| Molecularweight | 190.09 |
| Appearance | Colorless to pale yellow liquid |
| Boilingpoint | 112-114°C at 12 mmHg |
| Density | 1.27 g/cm3 |
| Refractiveindex | 1.475-1.480 |
| Flashpoint | 101°C |
| Smiles | N#CCCCCCCBr |
| Meltingpoint | - |
| Solubility | Insoluble in water; soluble in organic solvents |
As an accredited 7-Bromoheptanenitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 25g bottle of 7-Bromoheptanenitrile arrives in an amber glass container with a secure screw cap and hazard labeling. |
| Shipping | 7-Bromoheptanenitrile is shipped in sealed, chemical-resistant containers to prevent leaks or contamination. The package is clearly labeled with hazard warnings and handled according to regulations for toxic and irritant chemicals. It is transported under ambient conditions unless otherwise specified, ensuring compliance with all safety and regulatory guidelines for hazardous materials. |
| Storage | 7-Bromoheptanenitrile should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizers. Protect from moisture, direct sunlight, and heat. Store in a designated chemical storage cabinet, preferably for halogenated compounds. Ensure containers are properly labeled and handle with appropriate personal protective equipment. |
Applications of 7-Bromoheptanenitrile in Industrial ManufacturingAs the direct manufacturer of 7-Bromoheptanenitrile, we supply this raw material primarily to specialized chemical sectors where its distinct molecular structure supports complex synthesis routes. Below, we detail principal downstream applications based on practical industry requirements, regulatory frameworks, commercial processing, and finished goods manufacturing. 1. Pharmaceutical Intermediate SynthesisPharmaceutical companies employ 7-Bromoheptanenitrile as an intermediate in producing targeted active pharmaceutical ingredients, especially for APIs involving heptane carbon chains with functional nitrile groups. The compound provides a reliable building block for the stepwise assembly of heterocyclic structures and alkyl nitriles, contributing to the diversification of drug substance portfolios. Manufacturers actively select it for its stable reactivity in nucleophilic substitutions crucial to preclinical and clinical molecule synthesis, with ongoing quality and batch consistency meeting audit traceability for regulated market supply. Industry compliance standards
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2. Agrochemical Ingredient ManufacturingProducers of crop protection compounds incorporate this material to introduce functionalized carbon chains in the synthesis of select herbicides and insecticide intermediates. The nitrile moiety serves as a key anchor for ring closure or further halogenation steps, supporting development of agrochemical agents with defined selectivity and environmental profile. Strict adherence to traceability and impurity limits aligns with end-user safety and export market requirements. Industry compliance standards
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3. Specialty Polymer and Material ModificationIndustrial polymer synthesis operations utilize 7-Bromoheptanenitrile to introduce reactive nitrile side chains or halide groups in the formation of performance polymers designed for coatings, adhesives, or membrane applications. Its linear seven-carbon structure permits engineered flexibility and chemical resistance, and modification steps using this raw material often optimize the physical and thermal properties of engineered macromolecules used in demanding environments such as filtration or aerospace composites. Rigorous material documentation accompanies each batch for traceability. Industry compliance standards
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4. Organic Synthesis for Fine ChemicalsChemical manufacturers engaged in fine chemical production utilize 7-Bromoheptanenitrile for carbon chain elongation and controlled functional group transformations. Its reactivity enables production of specialty aldehydes, amines, and carboxylic acids with high positional specificity. These intermediate compounds serve analytical, diagnostic, and material science sectors, where batch-to-batch consistency and purity demand comprehensive process records and trace impurity management. Industry compliance standards
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Building molecules is our trade, and few building blocks show the steady reliability of 7-Bromoheptanenitrile, also known by its systematic name, 7-bromoheptanenitrile or 1-bromo-6-cyanohexane. Over years of refining our process, we’ve watched this specialty nitrile become an essential repeat-choice for fine chemical synthesis. It belongs to a small family of bromo-substituted aliphatic nitriles. Unlike versions with shorter or longer chains, or those with alternative halides, it opens certain doors with its carefully placed cyano and bromo groups. Simply put, it offers direct value as a key intermediate where the right balance between reactivity and chain length must be struck.
We synthesize 7-Bromoheptanenitrile using controlled halogenation of heptanenitrile, keeping moisture and oxygen in tight check to prevent side-chain oxidation or polymerization. Years spent tinkering have taught us the practical value of such process controls: by eliminating trace aldehydes and minimizing over-bromination, we increase both yield and purity. Finished product routinely comes off the line at 98% minimum purity by GC, with most shipments exceeding this target. Remaining organics fall within our set limits, including residual starting material and dibromo-heptanes—impurities that often disrupt downstream reactions if left unchecked.
Physical goods matter to a chemist even more than spectroscopic data. Our product presents as a clear, slightly yellow liquid, free-flowing down the reactor sleeve. Its boiling point sits solidly above 220°C under reduced pressure, letting it slot into heated reaction systems without unwelcome volatility or losses to the atmosphere. We avoid deep coloration and keep water content under 0.15%, knowing full well what even trace moisture can do to a Grignard or nucleophilic substitution downstream.
People working in the lab—not just behind a desk—reach for 7-Bromoheptanenitrile for several proven reasons. The molecule bridges two versatile worlds by marrying a reactive bromide with a terminal nitrile. It slides seamlessly into nucleophilic substitution chemistry, forming heptanenitrile derivatives through gentle alkylation or amination routes. Medicinal and agrochemical developers take advantage of the robust carbon-nitrogen triple bond, allowing the incorporation of the seven-carbon skeleton into more complex targets. In specialty polymer R&D, the compound acts as a functional modifier, introducing polar end-groups onto otherwise inert chains.
What makes this compound stand out in real-world syntheses, from custom research labs to scaled-up facilities, is the strategic separation between its two functionalities. The bromo end reacts smoothly in SN2 and SN1 chemistry, while the nitrile resists reduction or hydrolysis under neutral or slightly basic conditions. This allows two-stage reactions with excellent control, building up molecular complexity stepwise—something simply not possible with shorter homologues or with bromoalkanes lacking polar handles.
Manufacturing experience brings home an appreciation for subtle chemical differences. For instance, 6-bromohexanenitrile and 8-bromooctanenitrile both share the same functional motif as 7-Bromoheptanenitrile, but their chain length nudges physical and chemical properties in important ways. The six-carbon version produces compounds with tighter molecular packing, slightly higher volatility, and different solubility in nonpolar and polar media. Step up to eight carbons, and the end product feels waxier and resists incorporation into more polar end uses—less efficient coupling, more stubborn emulsions.
The seven-carbon middle ground avoids both extremes: its moderate chain offers better solubility in aprotic solvents, permitting extended reaction times and higher yields, while providing enough chain length for many pharmaceutical intermediates and surfactant backbones. Real users notice the difference in how these analogues behave, even if the data sheets look almost interchangeable. Experience tells us that transformations using 7-Bromoheptanenitrile frequently result in cleaner end products and more manageable workups, especially during column chromatography—a simple benefit, but one that matters in day-to-day lab operations.
Handling 7-Bromoheptanenitrile in our facility brings a set of best practices. Brominated nitriles need separation from alkali and strong oxidizers, as they otherwise take on a brown tint or emit faint almond-like odors from hydrolysis products. We fill drums and carboys using inert gas barriers, avoid ordinary steel containers, and insist on HDPE or glass lining for bulk storage tanks. Shelf studies indicate that, when kept below 25°C and dry, the compound keeps its color and purity for at least eighteen months. Operators in the plant got in the habit of cycling lot numbers and running small QA checks, catching any off-odors early before they migrate into customer supply chains.
End users tell us that these precautions pay off. Left uncapped or exposed to sunlight, the product attracts humidity and develops problematic amine or acid by-products. Small leaks in valve seals can go unnoticed if operators lack training, so we regularly run basic safety drills. We’ve learned, by fixing a handful of minor incidents quickly, that attentive storage and handling halves rejects and extends the working life of shipped material.
Over the last decade, regulatory agencies have taken a closer look at specialty nitriles in the context of chemical use reporting and safe handling. The production of bromoalkyl nitriles falls under several national and international oversight regimes, not least because some precursors also serve in the synthesis of regulated pharmaceutical compounds or specialty materials. We took steps early on to document each step of traceability and keep transparent batch records. Local regulators require regular reporting of emissions and effluent integrity, so we run environmental monitoring alongside product quality checks.
Internally, training sessions ensure employees and local emergency teams know how to spot and neutralize accidental releases. While the vapors at room temperature remain minimal, we insist on adequate exhaust scrubbing, using activated carbon beds and wet traps for any vented lines. We do this not because rules tell us to, but because mid-scale leaks in confined workspaces can cause headaches, sore throats, or, with larger spills, health symptoms for sensitive operators.
For our downstream customers, we advocate working in ventilated rooms, avoiding skin contact, and treating the compound as a flammable, irritant organic. Our data show that, though 7-Bromoheptanenitrile is not especially hazardous compared to related bromoalkanes, it demands respect in handling—accidents stem more from careless transfers or improper containment than from inherent chemical risks.
From a manufacturing stance, the most challenging demand is consistent supply. Feedstock volatility in butyronitrile and bromine markets sometimes rattles the forecast, making accurate lead times a daily struggle in tight markets. Early on, we set up dual sourcing on key intermediates and invested in storage tanks to buffer month-to-month swings. Our plant engineers spent long evenings forecasting, managing risks posed by shipping, seasonal storms, or export controls.
As manufacturers, we field the calls at midnight when a customer’s bench chemistry stops cold because a drum ran out or a shipment sat too long in a customs depot. In our experience, reliability means much more than ticking off a logistics box. We track every lot with unique batch IDs, maintain repeatable synthesis conditions, and keep lab notebooks open for customer queries—sometimes reviewing GC traces with counterpart scientists late at night to resolve questions over trace byproducts.
Customers often ask why this compound, rather than a simple alkyl bromide or another chain-length, deserves their investment. Experience tells us it’s not about molecular weight alone, but about tuning reactivity and compatibility to fit their own complex reactions. The presence of both a terminal nitrile and a bromine atom, separated by a six-carbon spacer, lets synthetic chemists introduce the right amount of lipophilicity while maintaining polar functionality. Scenarios in R&D that need robust coupling to nitrogen, oxime, or amine substrates benefit from precisely this sort of bifunctional intermediate.
We’ve seen customers in pharmaceutical synthesis migrate from five- and six-carbon analogues to seven, achieving more selective N-alkylation on sensitive APIs, reducing byproduct formation and improving yields. Polymeric material scientists value the consistent melting and compatibility of the seven-carbon derivative in block copolymer syntheses. The subtle difference in fatty chain length sometimes spells the difference between neat emulsification and gelling—something that lab theory seldom predicts, but bench results underline repeatedly.
Another subtle, but important difference involves odor and volatility. Customers working in fragrance intermediates or in open-system pilot plants notice fewer odor issues with the seven-carbon version, which, in practical use, reduces operator fatigue and complaints. In hot, humid environments, the seven-carbon derivative resists aerial loss and hydrolysis noticeably better, translating into tighter mass balances and less waste to remediate.
No product ever rolls off a chemical line in perfect form on the first try. We spent long periods battling byproduct formation—overbromination, unwanted cyclization, and formaldehyde contamination snuck into early lots and forced retooling of purification sequences. Sometimes, seemingly minor adjustments in temperature ramp or mixing order produced batches with bright yellow hues instead of the desired near-colorless finish.
Tackling these problems took more than adopting textbook purification. Our operators rotated shifts during critical runs; analytical chemists sampled at each stage, catching fluctuations before they cascaded into full-scale defects. If a drum failed color inspection, we learned to trace root causes back to tiny oxygen leaks or marginally degraded feedstock, rather than blaming operator error or over-relying on post hoc chemical correction.
On the commercial end, stories surface of delayed delivery due to customs issues, temperature excursions during transport, or end users unwittingly storing an open drum in a warm storeroom. We invested in product education, direct technical troubleshooting, and developed more rugged packaging for shipments crossing climate zones. Keeping stability bulletins current and sharing use-cases with partners trimmed unnecessary handling risks and fostered a more collaborative supplier-client relationship.
We manufacture molecules people put to use in real-world conditions, not textbook laboratories. The long hours in synthesis development, fine-tuning purification, and relentless focus on safety bring us closer to products that support innovation in pharmaceuticals, specialty chemicals, and advanced materials. The features that set 7-Bromoheptanenitrile apart—its measured polarity, reactivity, and solid chemical stability—have become clearer with every batch we make and every customer question we solve.
Ongoing feedback loops, open exchange with bench chemists and chemical engineers, and on-the-floor vigilance keep the product relevant even as synthetic methodologies shift and downstream requirements evolve. Quality didn’t come from theory, but from putting hands in gloves, feet on factory floors, and testing until the results met the real needs of industrial chemists.
As production chemistry evolves, so do expectations for purity, process transparency, and supplier accountability. We continue investing in process safeguards and new analytical techniques, unafraid to learn from the inevitable errors and near-misses that come with chemical manufacturing. Decades in the industry tell us each improvement in 7-Bromoheptanenitrile isn’t just a technical step, but part of a larger trust we build with the chemists and industrial users who rely on responsible sourcing and predictable quality.
Looking forward, we listen closely when end users ask about new synthetic targets, greener production methods, or alternative solvents. Working with partners developing biodegradable surfactants or complex pharmaceutical intermediates, we routinely modify reaction protocols, minimize waste, and adapt purification methods to suit emerging demands for cleaner profiles. Product evolution doesn’t happen in isolation; we treat every collaboration as a chance to refine what we supply and how we support clients from the bench to the warehouse.
Core to our approach is a straightforward belief: no two production lots look identical at the microscopic level, but repeatable quality comes from relentless attention to detail. Frequent feedback, benchmarking performance in actual use, and transparent reporting have helped us help customers mitigate risks, streamline processes, and innovate at pace with changing markets.
For us, 7-Bromoheptanenitrile represents more than a chemical SKU—it reflects learned experience, built trust, and a daily commitment to helping the next stage of chemical innovation move forward. Through many seasons and shifting industry demands, the product continues to earn its place on reaction benches and pilot plants worldwide. By committing to openness, continual process refinement, and an unvarnished sharing of successes and setbacks, we support the people who turn base molecules into tomorrow’s breakthroughs.