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HS Code |
303195 |
| Cas Number | 35445-00-4 |
| Molecular Formula | C13H21NO |
| Molar Mass | 207.31 g/mol |
| Iupac Name | 4-(Heptyloxy)aniline |
| Appearance | Solid or crystalline |
| Melting Point | 39-41 °C |
| Boiling Point | 349.2 °C at 760 mmHg |
| Density | 1.0 g/cm³ (approximate) |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Smiles | CCCCCCCOC1=CC=C(C=C1)N |
As an accredited 4-Heptyloxyaniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, screw cap, hazard label, containing 25g of 4-Heptyloxyaniline; marked with product name, CAS, and supplier details. |
| Shipping | **Shipping Description for 4-Heptyloxyaniline:** This product is shipped in a tightly sealed container, protected from light and moisture. It should be handled as a laboratory chemical, compliant with all relevant transport regulations. Packaging ensures containment of any leaks and includes proper hazard labeling. Shipping is typically via ground or air courier under standard chemical transport conditions. |
| Storage | 4-Heptyloxyaniline should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizing agents. Keep the container tightly closed and properly labeled. Protect from direct sunlight and moisture. Use appropriate chemical storage cabinets, preferably those designed for organic chemicals or amines, to ensure safe handling and minimize risk. |
Applications of 4-Heptyloxyaniline in Industrial Manufacturing4-Heptyloxyaniline serves as a functional intermediate and coupling agent in multiple niche industrial sectors. As a direct manufacturer, we support leading downstream processing chains that prioritize high-purity inputs and highly controlled integration into formulation, synthesis, and conversion workflows. Each segment below outlines actual, compliant use cases where this specialty aniline derivative drives critical value in industrial production. 1. Liquid Crystal Intermediate for Advanced Display TechnologiesManufacturers of liquid crystal materials incorporate this compound as a key intermediate in the synthesis of ether-linked phenyl aniline structures for high-performance display panels. The alkoxy chain and amine functionality enable precise control of molecular orientation and dielectric anisotropy, crucial for thin film transistor-LCD and next-generation device architectures. Integration strictly adheres to high-purity (99.5%+) and low-metal specifications, with analytical verification required for each production batch. Industry compliance standards
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2. Synthesis of Polyimide Resins for Flexible ElectronicsChemical producers utilize this aniline as a monomer unit in polyimide resin synthesis via polycondensation with dianhydrides. The heptyl ether side chain introduces flexibility and enhances thermal and mechanical properties in resulting films. Strict polymer process control demands traceability from base material and thorough documentation of amine content and residual solvents to meet electronic substrate standards. Industry compliance standards
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3. Dye and Pigment Intermediate for Performance CoatingsProducers of specialty azo and anthraquinone dyes employ this chemical to introduce linear alkoxy substitution on aromatic ring systems, modifying color fastness and substrate affinity. Its controlled reactivity ensures batch-to-batch color consistency and end-user safety in high-value textile and plastic applications. Detailed handling and reporting are required to comply with global dye standards and customer audit trails. Industry compliance standards
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4. Intermediate for Liquid Crystal Polymer (LCP) CompoundsDownstream LCP compound manufacturers select this molecule for incorporation into high molecular weight poly(ester-imide)s. The tailored alkoxy group controls melt phase transitions and mechanical strength for demanding connector and micro-molding applications. Production closely monitors molecular weight distribution and color index, reporting trace impurity levels to maintain electrical performance in finished parts. Industry compliance standards
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5. Engineered Additives for High-Performance Epoxy FormulationsEpoxy system producers rely on this compound as a reactive diluent and property modifier in high-flex adhesives and encapsulants. The heptyl ether chain modifies cross-link density and imparts improved crack resistance without sacrificing dielectric strength. Adherence to electronic material QC protocols ensures the absence of ionic impurities and tight control of amine content in reactive blends. Industry compliance standards
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In our day-to-day operations as a chemical manufacturer, producing specialty anilines with consistent properties has remained a core focus. Among these, 4-Heptyloxyaniline stands out, not just for its chemical structure but for the kind of reliability it offers in diverse downstream processes. Chemists and formulation specialists regularly search for compounds that behave predictably under strict synthesis conditions. In our own work, the value in high-purity 4-Heptyloxyaniline translates directly to the success of advanced research and industrial production.
4-Heptyloxyaniline features a heptyloxy chain attached to the para position of the aniline ring. The added length of the alkoxy group changes both the solubility and the reactivity profile compared to lower alkoxy analogs. Over years of feedback from partner labs and direct use in our pilot projects, we have seen its value in areas where subtle adjustments to molecular flexibility and hydrophobicity dictate end-use performance.
Our 4-Heptyloxyaniline, offered under code HPA-7, emerges from a multi-step synthesis that leaves minimal trace impurities. Producing this compound at scale calls for careful fractionation and a clear understanding of how trace water or leftover reactants might impact both shelf life and functional use. Our analytical runs, using NMR and HPLC, show purity levels often exceeding 99%. From experience, allowing even minor oxidative degradation reduces usefulness in color-critical or electronic applications. For this reason, we pursue closed handling and quick isolation, supporting both purity and stability.
Batch-to-batch reproducibility matters. Some operations focus on throughput at the expense of final characteristics. Our teams have opted instead for controlled reaction times and the use of rigorously tested solvents. We have found that variations in heptyl group insertion can skew the melting point and shade reactivity, so we regularly analyze not just finished product, but also side fractions. Implementing this discipline, we have kept deviation in key tests well within industry norms.
In our own facility, 4-Heptyloxyaniline often serves as a key intermediate for azo dye manufacture. The long heptyl chain pushes dye molecules to display softer shades and greater plastic compatibility. Years of batch trialing taught us that shorter alkoxy anilines favor brighter, more blue-toned mixtures, but often fail to spread thoroughly in plastic hosts. 4-Heptyloxyaniline's chain length produces a noticeable upgrade in dispersion and processing temperature window. We have run those tests not only with conventional solvents, but with newer eco-friendly plasticizers that can throw lesser analogs out of solution.
Beyond colorants, the most interesting uses of 4-Heptyloxyaniline come through in liquid crystal research and as a specialized monomer component in advanced polymers. Our research and scale-up work sometimes revealed frustrations with inconsistent molecular orientation in final polymer films. Using our tightly controlled 4-Heptyloxyaniline, formulation scientists achieved more uniform alignment in experimental OLED backplanes and in trials for optical retardation films. The effect comes directly from the elongated alkoxy tail, which shapes both material flexibility and the ability to tune molecular order at specific orientations. In liquid crystal work, this feature is critical.
After years comparing batches of para-alkoxyanilines from butoxy through octyloxy length, we have documented distinctive trends. The jump from hexyl to heptyl substitution makes more difference than expected—especially for resistance to solvent evaporation and improved blending characteristics. With pentyl and hexyl versions, we noticed an increased tendency for phase separation in prepolymer mixes under stress. In our own accelerated aging tests, heptyloxy chains proved less prone to crystallization and produced more stable dispersions in high molecular weight matrices.
Customer labs have reported greater batch-to-batch yield certainty when using our HPA-7 in repeated organic syntheses. This comes down to consistent melting and boiling behavior, driven by the controlled length of the side chain. Reliable purification cuts down post-reaction cleanups on their end. In the hands of developers working on thermotropic polymers or responsive coatings, these subtleties reduce trial-and-error cycles. Our feedback loop with industrial partners revealed that cross-linked materials based on shorter alkoxy anilines sometimes crack or lose mechanical softness, confirming the importance of the heptyloxy group.
As for environmental or health concerns, we observed that the heptyloxy derivative volatilizes less readily than shorter chain analogs. This assists fume extraction and exposure management, particularly in confined or continuous-feed facilities. Despite this, we keep strict adherence to PPE protocols for our team. Our chemical hygiene measures extend through every stage—synthesis, filtration, and packaging.
Scaling up 4-Heptyloxyaniline production posed distinct challenges. Introducing a seven-carbon tail to aniline’s core structure lengthens every stage of the process. Solubility in reaction solvents shifts compared to shorter chain homologs, forcing us to adjust stirring speeds, cooling times, and extraction protocols. Early batches suffered from incomplete alkylation and trace polysubstitution, so our technical crew adapted workup procedures, sometimes switching solvent types mid-campaign. Each adjustment, even at the liter scale, affected not just output, but how reliable samples proved over six-month storage tests.
Through these efforts, we found the synthesis procedure favored by lab scale teams didn’t directly scale to our reactors without yield or quality setbacks. Rather than chasing textbook recipes, our team developed methods with staged additions and real-time monitoring, checking endpoint conversions regularly. This focus eliminated the headaches of rerunning incomplete batches and cut production losses. Several times, customer feedback from pilot orders led to changes in how we managed fractionation and drying, particularly for those using the compound in sensitive analytical or electronic devices.
Conversations with research-driven factories using our HPA-7 model often highlight how their older grades of para-alkoxyaniline left deposits on thermal nozzles or failed extraction standards. Integration of high-purity 4-Heptyloxyaniline marked a shift: more complete solvation, less frequent cleaning cycles, and less off-gassing at processing temperatures. This saves not only time, but also material in high-value coatings and electronic production.
Some customers trialed the compound as a hardener in custom epoxy blends. The heptyloxy side chain imparted increased compatibility with flexible polymers and reduced embrittlement at low temp cycling. In our own R&D group, material scientists picked up on these traits and created model high-resilience coatings able to withstand hard vacuum and temperature swings, which standard short chain analogs could not manage. Reliability in the final polymer matrix often comes down to the subtle interplay between molecular geometry and functional group distribution—points that only become clear after observation over hundreds of batches across several years.
Colorant designers in the textile sector using our 4-Heptyloxyaniline found improvements in wash resistance and color stability compared to standard butoxy or hexoxy grades. While direct evidence comes from side-by-side lab tests, the practical benefit comes alive in field reports, where treated textiles retained desired hues through repeated laundering and dye bath cycling. These kinds of results have reinforced our emphasis on detailed purity controls and storage conditions, since even minor contamination or degradation can show through under these real-world stressors.
Producing specialty aromatic amines like 4-Heptyloxyaniline takes patience and persistence. Over the past decade, our teams have found that meticulously managing every aspect from raw feedstock to the final shelf-stable form has built lasting relationships with industrial innovators. Whether for liquid crystals, engineering plastics, or next-generation dyes, reliability counts as much as initial inventive chemistry.
Chemists developing high-end coatings have reported fewer batch failures and increased throughput using our consistent-grade heptyloxyaniline. For example, in OLED research, variations in starting material structure can introduce artifacts during pixel deposition. Our focused oversight follows the compound’s journey right through to the packaging line, ensuring researchers and manufacturers face fewer unwanted surprises.
Our experience shows that even slight impurities or incorrect side chain lengths can undermine otherwise sound research. For this reason, every production campaign begins with updated specs, and our QC protocols adapt based on what we see at scale—whether that’s changing solvents or extending cooling times to whip out stray byproducts. In situations where formulation teams called out off-spec results, we responded with fresh samples, running full analytical workups side-by-side with customer teams to pin down the underlying issues.
Handling alkoxyanilines never ends at the reactor. From the time raw reactants enter our blending tanks, staff are trained to monitor fume characteristics and keep accurate logs at each checkpoint. Longer side chains like in 4-Heptyloxyaniline shift volatility downward, helping reduce emissions but prolonging solvent stripping steps. This adjustment pays off: lower emissions mean less environmental impact and improved safety conditions in the shop.
Disposal and waste handling remain critical. Residues of heptyloxyaniline can’t follow simple aqueous procedures. Our facility segregates organics for incineration and captures solvent residues for on-site distillation. Supporting the health of our team and the local environment, we have written procedures for both spill response and chronic exposure risk, developed from years of process safety experience. Local regulatory changes often prompt refinements to our handling steps, but practical know-how is what ensures consistency over time.
Often, new users overlook the extended shelf stability of our 4-Heptyloxyaniline. In practice, stored correctly, it resists oxidation longer than many shorter alkoxy relatives. Our packed drums, lined for moisture control, remain robust even in fluctuating warehouse conditions. In our own periodic QA spot tests, retained samples continue to meet spec months out from production, saving our customers from costly rework and unexpected failures.
Teams approaching us with novel applications—glass modifiers, surfactant builders, or unusual coupling agents—gain from our day-to-day operational perspective. Because our staff runs pilot lines side-by-side with production, we catch inconsistencies before they scale to problem batch sizes. For unique synthesis goals, we are able to suggest tweaks based on shared lessons from both troubleshooting and success stories. The dialogue with innovative partners ensures our workflow continually improves.
Sourcing raw materials from globally vetted suppliers and intensively tracking their lot histories, our staff minimize the risk of off-base material entering reaction streams. The experience built here enables quick course corrections: if a batch doesn't crystallize to the expected form, our QA team pounces on the root cause, adjusting temperatures or changing filtration media to keep the final product on spec. Long-term relationships with research organizations thrive on honesty about what works and what doesn’t.
Internal workshops and field visits to customer sites expand our perspective, building technical know-how that can transfer across many aromatic amine applications—not just those centered on 4-Heptyloxyaniline. Hearing from users contending with challenging melt flows, color shifts, or product losses under pressure cycles grounds our production strategy in practical results, not abstract theory. Bringing that feedback full circle, we pass both successes and mistakes into the next production planning round.
Professional manufacturing extends far beyond label claims or sales language. Supplying 4-Heptyloxyaniline for so many industry sectors leads us to maintain open records for every lot, from raw material certification through transport logistics. Our QA workflow doesn’t stop with one round of analytical checks—it lives in production logs, retained sample archives, and customer service reports. This discipline builds trust not just in product spec sheets, but in every use case that unfolds after delivery.
As regulations shift and customer requirements rise, our teams stay ahead with continuous training—hazard identification, spill control, and safe disposal are routine, not afterthoughts. The end use of 4-Heptyloxyaniline often lies in sectors subject to audit, so there's no shortcut in lot tracking or supply transparency. Whether supporting textile dye innovators or electronic display pioneers, our commitment remains: clarity, precision, and direct technical support.
Years of work developing 4-Heptyloxyaniline in-house taught us the necessity of tight process control, reciprocal partnership with users, and transparent trouble-shooting. Real chemical innovation doesn’t come from isolated lab experiments. It grows from honest feedback, resilience in face of production setbacks, and sustained attention to both chemistry and those relying on it. From piloting early reactions to full-scale logistical coordination, our staff backs each drum and lot with pride and responsibility. The distinctive properties of 4-Heptyloxyaniline arise not just from formula, but from the persistent commitment to meet real-world demands.