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HS Code |
742374 |
| Cas Number | 335-89-7 |
| Molecular Formula | C7F15NH2 |
| Molecular Weight | 399.11 g/mol |
| Iupac Name | 2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-pentadecafluorooctan-1-amine |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 154-156°C at 760 mmHg |
| Density | 1.73 g/cm³ at 25°C |
| Solubility In Water | Insoluble |
| Flash Point | >110°C (closed cup) |
| Vapor Pressure | 0.2 mmHg at 25°C |
As an accredited 1H,1H-Perfluoroheptylamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 1H,1H-Perfluoroheptylamine is supplied in a 25g amber glass bottle, tightly sealed, with hazard labeling and product information displayed. |
| Shipping | 1H,1H-Perfluoroheptylamine must be shipped in accordance with local and international regulations for hazardous chemicals. It should be packed in tightly sealed, compatible containers, cushioned to prevent breakage, and transported as per relevant guidelines for perfluorinated compounds, typically under a UN number, with appropriate hazard labeling and documentation. |
| Storage | 1H,1H-Perfluoroheptylamine should be stored in a tightly closed container in a cool, dry, well-ventilated area, away from direct sunlight, heat sources, and incompatible materials such as strong oxidizers and acids. Store at room temperature, avoiding moisture and ignition sources. Appropriately label containers and ensure access is limited to authorized personnel trained in handling perfluorinated compounds. |
Applications of 1H,1H-Perfluoroheptylamine in Industrial ManufacturingAs a trusted chemical raw materials producer, we support multiple industries by supplying 1H,1H-Perfluoroheptylamine strictly for established downstream segments. Our technical experience ensures consistent performance across specialized manufacturing processes. Below, we outline the principal industrial application scenarios, addressing the specific regulatory, formulation, integration, and finished product contexts for each. 1. Fluorinated Surfactant Synthesis for Firefighting Foams1H,1H-Perfluoroheptylamine serves as a key intermediate in synthesizing advanced fluorinated surfactants used in aqueous film-forming foams (AFFF) for fire suppression. Manufacturers rely on its unique perfluoroalkyl structure to increase film stability and burnback resistance, supporting rapid flame knockdown on hydrocarbon fuel spills while achieving compliance with updated environmental mandates. The exact incorporation level must be balanced based on target fluorine content and required surfactant properties for Type B fuel fire performance. Industry compliance standards
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2. Oil-Repellent Textile FinishesTextile finishing specialists use 1H,1H-Perfluoroheptylamine in fluoroalkyl functionalization for durable oil- and water-repellent treatments on performance fabrics. The amine group enables grafting to reactive sites on synthetic or blended fibers, resulting in superior repellency properties as measured by industry-standard methods. Dosage rates are refined per fabric structure, treatment bath, and final repellent performance metrics, specifically to prevent fabric hand alteration while maintaining robust repellency cycle counts. Industry compliance standards
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3. Hydrophobic Coatings for Electronic ComponentsDevice manufacturers implement 1H,1H-Perfluoroheptylamine when formulating hydrophobic and anti-wetting coatings for printed circuit boards and sensitive microelectronic assemblies. Its perfluoroalkyl chains permit uniform monolayer formation that blocks moisture ingress, crucial for reliability under high-humidity storage or operational environments. Dosing in the precursor blend is tightly controlled to avoid dielectric impact while achieving targeted surface energy reduction. Industry compliance standards
Typical usage ratio
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4. Anti-Fouling Additives in Industrial LubricantsLubricant compounders incorporate 1H,1H-Perfluoroheptylamine into advanced lubricant formulations to impart anti-fouling and low surface tension characteristics. These properties inhibit the deposition of contaminants in critical mechanical systems exposed to aggressive environments, such as food processing chains and turbine components. The addition rate directly affects boundary film formation and must be adapted to viscometric base fluids and specific machinery duty cycles while complying with lubricant-specific quality benchmarks. Industry compliance standards
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5. Process Reagents in Fluoropolymer ManufactureFluoropolymer producers leverage the selective reactivity of 1H,1H-Perfluoroheptylamine to introduce functional end-groups during controlled polymerization of specialty copolymers. This integration supports the customization of surface properties such as oil repellency and chemical inertness in the final polymer matrix without compromising thermal or mechanical stability. Precise metering ensures uniform chain functionalization and minimizes process-side reactions, strictly monitored under polymer production regulatory controls. Industry compliance standards
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6. Chemical Surface Modifiers for Analytical InstrumentationProducers of precision glassware and chromatography components use 1H,1H-Perfluoroheptylamine for chemical vapor deposition (CVD) of anti-adhesive, low surface energy films. This modification critically reduces analyte carryover and fouling in gas and liquid chromatograph columns, capillaries, and sample vials. Treatment levels must align with analytical purity requirements and instrument-specific retention time tolerances, supporting repeatable, high-accuracy measurements. Industry compliance standards
Typical usage ratio
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Every day, chemists in our production halls work with a variety of compounds, but few capture the unique blend of stability and versatility like 1H,1H-Perfluoroheptylamine. Known by its CAS number 423-38-1, this fluoroalkylamine features a perfluorinated carbon backbone capped by a primary amine group. Its formula, C7F15NH2, may look intricate, but it’s the practical implications that matter most in a lab or industrial setting. Over years of development and countless production runs, direct experience has taught us the real-world impact of adding this specialty chemical to a formulation, whether for high-performance coatings, surfactants, or advanced materials research.
At its core, our 1H,1H-Perfluoroheptylamine offers a string of fully fluorinated carbons—seven in a row—ending with a primary amine. The result: an unusual mix of chemical inertness from the fluorinated chain and reactive capability at the amine group. Many fluorinated compounds exhibit high resistance to solvents, acids, bases, and oxidative conditions, but once you try to build something with them—linking them into larger molecules or adjusting their surface properties—the chemistry gets tricky. That’s where this compound fits seamlessly. The NH2 end opens up routes for derivatization, coupling, and further reactions, while the perfluorinated tail gives those end products the durability and unique characteristics associated with high-end fluoro-materials.
Years on the synthesis line have shaped our standards for 1H,1H-Perfluoroheptylamine. Purity remains a focus, since side products and traces of other fluorinated amines can dramatically shift application results. After optimizing distillation and purification steps, we've consistently delivered material with a purity level above 98%, as measured by gas chromatography. Technicians also keep an eye out for water content and residual acids, which can creep in during certain steps of manufacture. In-house Karl Fischer titration and acid-base titrations keep those minor impurities under tight control, because customers in electronics, medical, and specialty polymer fields cannot tolerate variability.
Physical form matters just as much. Many other amines, especially non-fluorinated analogs, tend to be liquids or low-melting solids, and can present handling or storage challenges. Our 1H,1H-Perfluoroheptylamine has a boiling point in the range of 90–110°C at reduced pressure, and at room temperature it appears as a clear to faintly yellow liquid. Storage in sealed fluoropolymer vessels or glass avoids interaction with container materials—lessons learned from early tests that showed how some elastomers and ordinary plastics allowed for slow leaching or evaporation. Each batch leaves our plant stabilized and quantified for moisture, so it's ready for precise dosing in downstream applications.
Our production team first began making this molecule for customers looking to prepare perfluorinated surfactants with custom properties. The amine group lends itself to quaternization, acylation, and other modifications that introduce hydrophobicity, oleophobicity, or tune surface energy. In electronics, formulators have designed anti-static additives using derivatives of our material, allowing them to combine the best of polyfluorinated performance with a customizable head group. Stories from the field keep coming back to a central point: substitution with classic alkylamines simply cannot achieve the same low surface energy or durability.
In paints and coatings, technical feedback from R&D partners has confirmed the edge provided by the perfluoroheptyl chain. Resistance to fouling, chemical staining, and water repellency stand out in QUV weathering and chemical immersion tests. Customers working on stain-resistant fabrics and anti-fingerprint glass coatings often specify our amine due to ease of functionalization without sacrificing the benefits of perfluorination. Incorporation of the amine has enabled developers to join the perfluorinated chain to polymers, silicones, or crosslinkers, expanding the field for durable, high-performance surfaces. These results didn’t come by guesswork: successive iterations and collaborative trials between plant chemists and field users honed the methods and dosages until target performance numbers finally matched real-world needs.
Making and handling perfluorinated amines have presented our team with their own set of demands. Unlike traditional amines, perfluorinated versions tend to display reduced volatility but can emit strong, occasionally irritating vapors if not handled in ventilated environments. Our operators wear full respiratory protection and chemical-resistant gloves during transfer and blending. Standard procedures call for low-temperature distillation and transfer using closed systems, both to control emissions and minimize operator exposure.
In the early days, the answer to minimizing high-boiling residue and byproducts was not obvious. Heat decomposition can create ultra-fine fluorinated particles or acids, which are not only difficult to remove but also can cause traces of contamination in customers’ finished goods. Improvements in reaction control, raw material selection, and multi-stage purification have reduced these issues close to background levels—important for semiconductor and advanced electronics use, where even minor contamination spells trouble. Every drum now comes with a detailed certificate of analysis, produced in-house by staff who have seen first-hand how deviations can impact high-value projects.
No one working with fluorinated materials these days can ignore the tightening regulatory spotlight. Several countries have restricted the use of long-chain perfluorinated compounds, particularly those with more than eight fluorinated carbons. Our 1H,1H-Perfluoroheptylamine sits just under these thresholds, with seven fluorinated carbons, a fact plain to any regulatory officer inspecting facility output. Still, we’re not complacent. Recent European news and environmental reports prompt us to double-check product life cycle assessments, waste management systems, and emissions controls. We routinely update documentation and participate in industry dialogues so customers know they’re sourcing a product from a manufacturer that understands global compliance, not just immediate supply needs.
Waste handling isn’t an afterthought. As the team responsible for both synthesis and environmental monitoring, we recover solvents and neutralize byproducts on-site whenever practical. Analytical chemists routinely monitor effluent for traces of persistent fluorinated material, and any detected levels above trace background are reported and managed as hazardous waste according to international guidelines. It’s a balancing act between maximizing yield and minimizing ecological impact, but ongoing investment in abatement technology—such as carbon filtration and thermal oxidation—keeps us ahead of most competitors in compliance and stewardship.
Plenty of customers who come through our doors arrive curious—often skeptical—about what really sets 1H,1H-Perfluoroheptylamine apart from other available amines. Our on-site technical teams often demonstrate the practical differences with direct comparisons. Typical alkyl amines, for instance, lack the robustness against acids, bases, or organic solvents and cannot deliver the ultra-low surface energy critical to applications in high-end fluoroplastics or repellency coatings. Even among other perfluorinated amines, structure matters: switching out a perfluorohexyl or perfluorooctyl chain tangibly changes thermal properties, viscosity, vapour pressure, and downstream compatibility.
Our experience suggests that the seven-carbon perfluorinated backbone hits a sweet spot for both solubility in solvents like perfluorohexane and dimethyl sulfoxide, and reactivity in acylation or quaternization reactions. It’s neither too volatile nor too waxy for typical processes. In contrast, longer chains may suffer from excessive viscosity or regulatory constraints, and shorter chains may not deliver the fluorine-content needed for demanding applications. Years of scale-up experimentation have shown that using the precise homolog with the right number of carbons can be the difference between steady production and a headache of fouling, gelling, or unpredictable end-use results.
Our early efforts with 1H,1H-Perfluoroheptylamine happened in glassware: stirring, stripping, analyzing, and scaling cautiously to identify sources of impurity or instability. Once small-scale tests produced repeatable, high-purity outcomes, we transitioned to industrial-scale reactors with finely-tuned agitation, temperature zones, and inert gas blanketing. These choices matter far beyond laboratory curiosity. Even small design tweaks such as baffle placement or condenser geometry have had unexpectedly large impacts on product purity and yields.
We learned quickly the difference between a sample produced for academic research and drums shipped for industrial use. Overhead blending, filtration through PTFE and glass fiber media, and vapor-phase transfer protect the material from degrading or contaminating. Batch after batch, we document not only chemical composition, but also color, odor, and consistency—practical markers our customers rely on for visual quality assurance. In production, every kilogram counts, so reducing loss to residue and evaporation remains a daily focus. Maintenance teams receive regular training specific to perfluorinated systems, as residues left in transfer lines or vessels can present stubborn cleaning problems if overlooked.
Open lines of communication with users have shaped both our product and process. A client in industrial coatings once flagged inconsistency in coating thickness when changing to a newer batch: joint investigation revealed a subtle interaction with their proprietary crosslinker, traceable to a minor but measurable difference in free base content of our product. Others have provided us with samples of finished materials for reverse analysis, allowing us to adjust purification protocols and deliver tighter control on composition and residue. This feedback loop, built over years, keeps our teams humble and responsive—always searching for details that make tangible differences.
Collaboration doesn’t only mean one-way feedback from customers. Internally, production chemists, maintenance technicians, and plant safety teams hold regular debriefs to share discoveries and lessons learned. Every step, from the receipt of precursor fluoroiodides or telomer intermediates, through hydrogenation, to final distillation, represents opportunities for improvement and knowledge sharing. The pride of the plant comes not just from hitting yield targets or cost goals, but also from customers coming back for repeat orders, citing the reliability and performance of the material in their own finished products.
Some of our most important learning moments have come from troubleshooting problems. Early in scaling up production, operators noticed discoloration and an off-odor in a few batches, tracked down to trace iron contamination from a reactor seal. Process engineers adjusted the cleaning regimen and switched to more inert gaskets, preventing recurrences. Another incident involved handling a spill, when technicians revised protocols and personal protective equipment requirements. Every incident record gets reviewed so procedures adjust in real time—closing the gap between front-line reality and written SOPs.
Maintaining process repeatability demands constant attention. Basic rules of thumb—such as slow addition of reactants, close monitoring of temperature ramps, and staged purifications—have been honed by hard-earned mistakes. Especially with a specialty chemical like 1H,1H-Perfluoroheptylamine, small slips in timing or reagent addition can introduce impurities difficult to remove from the perfluorinated backbone. This discipline, built over long hours in the plant, is why customers stake their reputations—and their manufacturing lines—on our material rather than a faceless commodity product.
We view our responsibility for 1H,1H-Perfluoroheptylamine as ongoing. Chemists continue to explore new derivatizations, especially those aimed at combining perfluorinated performance with lower toxicity or improved degradability. Product stewardship means anticipating questions that researchers, regulators, and end-users will raise—about persistence, migration, or breakdown products. Already the lab team is investigating methods for catalytic or biological degradation, seeking to lower long-term environmental impact while keeping those signature properties that industry demands.
Collaborations with universities and industrial consortia keep us tuned to broader questions, such as safe handling in manufacturing environments and pathways for reuse or recycling. Recent tests have examined the use of perfluoroheptylamine derivatives in cationic surfactants, surface modifiers for advanced textiles, and additives in microelectronics. In each case, we supply small lots for early-stage research and adjust our process based on feedback, gradually scaling up once projects move towards commercialization. Direct interaction steers our research agenda far more than market trends alone. Our commitment remains grounded in how real people—engineers, operators, scientists—experience and rely on the material, batch by batch and year by year.
Working directly with 1H,1H-Perfluoroheptylamine, from pilot runs to full-scale manufacture, uncovers both the chemistry and human factors that define a reliable specialty chemical. Performance depends not only on molecular structure but also on consistent, attentive production—each variable tracked and improved with every cycle. The edge that this particular perfluorinated amine brings—solubility, reactivity, ruggedness and tailored surface properties—translates into high-value applications and satisfied repeat customers. As the manufacturer, we commit to not only refining our process, but also meeting the challenge of responsibly producing a substance with such specialized utility, supporting its use from first synthesis through to global deployment and eventual end-of-life.