|
HS Code |
954364 |
| Chemical Name | (+/-)1-(1-Naphthyl)Ethylamine |
| Cas Number | 3886-69-9 |
| Molecular Formula | C12H13N |
| Molecular Weight | 171.24 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 282-284°C |
| Melting Point | 2-5°C |
| Density | 1.08 g/cm³ |
| Refractive Index | 1.654 |
| Purity | Typically ≥98% |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Smiles | CC(N)C1=CC=CC2=CC=CC=C12 |
| Storage Conditions | Store at 2-8°C, tightly closed, protected from light |
| Synonyms | α-(1-Naphthyl)ethylamine; 1-Naphthyl-1-ethylamine |
As an accredited (+/-)1-(1-Naphthyl)Ethylamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | White, opaque screw-cap plastic bottle containing 25 grams of (+/-)1-(1-Naphthyl)Ethylamine, labeled with chemical name, CAS, and hazard warnings. |
| Shipping | (+/-)1-(1-Naphthyl)Ethylamine is shipped in tightly sealed containers under inert atmosphere to prevent oxidation and contamination. Packages are labeled according to chemical safety regulations, with protection from light, moisture, and extreme temperatures. Handling follows hazardous material guidelines, and shipping complies with all local and international chemical transport regulations. |
| Storage | (+/-)1-(1-Naphthyl)ethylamine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizing agents and acids. Store at room temperature (15–25°C). Keep away from sources of ignition, moisture, and excessive heat to maintain chemical stability and prevent hazardous reactions. |
Applications of (+/-)1-(1-Naphthyl)Ethylamine in Industrial ManufacturingOur factory-grade (+/-)1-(1-Naphthyl)Ethylamine supports advanced chemical synthesis across multiple downstream sectors. Below, we detail specific applications for this raw material along with sector-specific standards, formulation ratios, processing routes, and commercial end uses. 1. Chiral Intermediate for Pharmaceutical API SynthesisPharmaceutical manufacturers use (+/-)1-(1-Naphthyl)Ethylamine as a crucial chiral amine intermediate during the enantioselective synthesis of beta-blockers, antidepressants, and other active pharmaceutical ingredients (APIs). Its distinct configuration assists in constructing target molecules with precise stereochemistry required for pharmacological activity. Production facilities integrate this raw material within reductive amination and asymmetric synthesis steps, ensuring batch-to-batch consistency in the final API’s optical purity. Quality assurance includes regular analytical qualification per regulatory authority specifications, and processing equipment must meet stringent cross-contamination prevention measures. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Dye Intermediates in Organic Pigment ManufacturingPigment and dye manufacturers employ this amine for coupling with diazonium salts in the synthesis of high-performance azo and anthraquinone dyes. Its structure imparts specific chromatic and fastness characteristics demanded in automotive, plastics, and textile applications. Downstream producers optimize batch recipes using precise stoichiometry to balance potency, brightness, and end-use stability. Compliance includes adherence to environmental regulations regarding aromatic amine content and effluent discharge, with full traceability and analysis of illicit amine byproducts. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Ligand for Asymmetric Catalysis in Fine ChemicalsChemical processors integrate this amine as a base structure for producing chiral ligands, which are essential in catalytic systems for enantioselective hydrogenation, hydroformylation, and addition reactions. The resolved enantiomers or derived phosphines optimize conversion rates, selectivity, and enantiomeric ratios in value-added fine chemical manufacture, especially for agrochemical intermediates and high-performance materials. All catalyst production and usage conform with operational safety and batch consistency protocols, involving real-time reaction monitoring and stringent moisture and air exclusion. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Analytical Derivatization Agent in Chromatographic AnalysisSpecialty laboratories and analytical standards manufacturers use (+/-)1-(1-Naphthyl)Ethylamine for derivatization of carboxylic acids, carbonyls, or other chiral analytes prior to quantification or enantiomeric purity analysis by HPLC or GC. Its use produces UV-active or fluorescence-tagged analytes, improving detection limits and facilitating precise chiral separations. Procedures require careful control of stoichiometry, with excess amine removed by preparative separation. Reagent quality and batch documentation must conform with analytical reference material requirements and avoid contamination by byproducts or isomers. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
5. Additive in Advanced Polyimide Resin SynthesisHigh-performance polymer manufacturers utilize this amine for chain extension or end-group modification in polyimide resin production. Its inclusion helps manage molecular weight distribution, improves thermal stability, and modulates optical properties critical for electronic substrates and display films. Processing requires exact dosing and slow addition at controlled thermal profiles to prevent premature side reactions. Manufacturers conduct end-group analysis and perform all synthesis steps under anhydrous and cleanroom-grade conditions to meet stringent electronic grade quality. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
|
Competitive (+/-)1-(1-Naphthyl)Ethylamine prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: admin@sinochem-nanjing.com
Flexible payment, competitive price, premium service - Inquire now!
Working daily in our production facility, one gets to see firsthand how the demand for precision-crafted chiral amines has expanded across fine chemicals and pharmaceuticals. Among them, (+/-)1-(1-Naphthyl)Ethylamine has become essential on account of its role in chiral resolution and catalyst development. Its structure, characterized by the 1-naphthyl group attached to an ethylamine backbone, gives it a solid foundation for stereochemical transformations and asymmetric synthesis. Our team, through years spent refining batch parameters and scaling up technology, consistently delivers this product in a racemic mixture—meaning both R- and S-enantiomers present—which many researchers value for flexibility at the initial stages of compound development or resolution studies.
There is a difference between manufacturing for the open market and producing for specific, outcome-driven customers who rely on batch-after-batch reproducibility. Customers in pharma R&D, academic settings, and custom synthesis rely on subtle controls during amine condensation, solvent purity, and purification—details which are critical, because inconsistent impurities or even slight deviations in isomer ratios can disrupt downstream application. By staying in close conversation with colleagues in the laboratory and on the application side, we continue to focus manufacturing runs on actual end-use requirements, not just on paperwork targets.
Chemically, (+/-)1-(1-Naphthyl)Ethylamine holds its own as a strong intermediate for asymmetric catalysts, chiral auxiliaries, and ligand synthesis—delivering its value both as a resolution agent and as a moiety for further functionalization. Our experience highlights that its naphthalene component offers desired pi-stacking interactions in asymmetric environments, and the ethylamine group allows for direct derivatization. These chemical features are why process chemists and academic researchers look for purity levels above 98 percent, NMR traceability, and low water content, especially when used for the hand-off between discovery chemistry and early pilot scale.
Many newcomers to the market treat production numbers as the main selling point—purity over 98%, low residual solvents, and tight controls on optical activity. What ongoing conversations with downstream users reveal, though, is that repeated real-world performance distinguishes one manufacturer from another. We spend just as much energy on maintaining consistent melting point ranges, tight batch-to-batch color, and minimizing trace contaminants that can cause trouble in follow-up coupling or reductive amination steps.
Our standard specification for (+/-)1-(1-Naphthyl)Ethylamine includes a distinct melting point range, which is checked visually by our QC staff using established capillary tube methods. Batch homogeneity checks with thin-layer chromatography provide a rapid screen for possible aromatic impurities, and extensive attention goes to moisture content—important especially for those using it as a building block in water-sensitive routes. We run each finished lot against reference standards that have been stringently checked in-house, and third-party confirmation is available for projects that require rigorous documentation validation, such as new drug application filings or new methodology publications.
Lots are tested by proton and carbon NMR, ensuring spectroscopic fingerprinting aligns with known reference patterns. This process helps catch any batch-specific by-products or aromatic over-hydrogenation residues, which if present at higher levels, can undermine complex transformations in a customer's workflow. High-performance liquid chromatography further verifies purity and detects trace side-products common to the synthesis route. As a manufacturer, we know that this hands-on approach and the willingness to cross-examine every batch against previous lots makes a decisive impact down the line. End-users rely on the certainty that they’re working with the same product each time—not variants drifted off-spec through supply chain shortcuts.
From daily production meetings to night shifts running kilo-scale reactions, the value of experience cuts through theory. Having operated multiple synthetic routes for (+/-)1-(1-Naphthyl)Ethylamine—Grignard reactions, reductive amination, direct alkylation—we compare the tradeoffs in yield, aromatic substituent control, and cost. By refining routes through iterative testing and pulling in feedback from pilot projects, we’ve learned that robust output does not only rely on textbook chemistry; it requires persistent attention to input raw materials, reagent quality, and equipment cleaning protocols.
For instance, starting with freshly distilled 1-naphthaldehyde and high-purity alkylamines, we control humidity and temperature to avoid formation of unwanted secondary amines. Any aromatic over-substitution or amine oxidation must be purged through repeated distillations, which can appear minor but have lasting effects on trace impurity profiles. Experienced chemists track batch production logs for subtle indicators like color changes during distillation or slight gas evolution, knowing these can correlate with higher downstream defects or changes in melting point behavior. These habits, learned through years of hands-on work, mean that product reaching customers matches intended specifications in more than just outward appearance.
Supplying research- or GMP-grade materials introduces elevated requirements. We equip our facilities with controlled environments, regular equipment maintenance, and documented staff training, all aimed at preventing cross-contamination between aromatic amines and other classes. Our in-house guidelines, rigorously enforced, help keep amine oxidation at bay and deliver batch purities that genuinely support demanding research. The end result is a product that remains in the correct isomeric and chemical state from our reactor through to the customer’s bench.
Having dealt with the ups and downs in both generic and custom manufacturing, we see clear distinctions between standard bulk-grade (+/-)1-(1-Naphthyl)Ethylamine and our specialized product. Market-grade material, especially that sourced through indirect supply chains, often shows wider batch variation, higher color and odor levels, and more pronounced trace contamination. We’ve received feedback from research groups and pilot plants about issues with unknown peaks in chromatograms or persistent residues in reaction work-ups. Tackling these complaints shaped our investment in additional purification steps—fractional distillation or selective recrystallization—based on what the application truly demands.
Through dialogue on multiple project collaborations, it became clear that some customers request enantiomerically enriched material or require cyclization impurities to be diligently removed. For these demands, we build custom process routes: chiral resolution using tartaric acid derivatives, or switch to chromatographic separation on chiral silica if higher optical purity is necessary. Our facility's flexibility accounts for these application-driven differences, offering not just bulk racemic material, but scalable solutions for both R&D and pilot-plant quantities of enantiomer-specific amines. This means less troubleshooting and wasted time for customers who operate at the boundary between discovery and robust commercial production.
Comparing (+/-)1-(1-Naphthyl)Ethylamine to similar amines—such as isopropyl-phenylamines or other alkyl-naphthylamines—reveals its unique naphthalene aromaticity and hydrophobic profile, which support selectivity in chiral ligand frameworks and as resolving agents. Many customers try to substitute with structurally analogous amines, but their work quickly shows that aromatic stacking or solubility profiles shift, undermining intended outcomes in asymmetric catalysis or crystallization trials. By maintaining access to high-purity naphthyl-ethylamine, research and process teams avoid difficulties tied to less selective analogs and inconsistent end-product behaviors.
Used in asymmetric synthesis, (+/-)1-(1-Naphthyl)Ethylamine plays a central part as a chiral resolution agent and as a core fragment in constructing complex organic molecules. It stands apart when building transition metal catalysts, especially in enantiopure ligand construction for fine-tuned hydrogenations and cross-coupling. It also supports diastereomeric salt formation, a classic route for separating racemates in pharmaceutical pipelines—giving chemists an edge when resolving tricky intermediates or preparing pure drug candidates.
Customers engaged in discovery chemistry often rely on its compatibility with orthogonal protecting groups, while scale-up teams use our consistently pure product to minimize batch-to-batch recalibration in pilot plant optimization. Research teams use (+/-)1-(1-Naphthyl)Ethylamine when evaluating new stereoselective methodologies because its aromatic bulk offers more pronounced selectivity compared to simpler alkyl amines. Having a trusted source for this intermediate means less concern about oxidation, trace aldehydes, or inconsistent color in coupling and downstream reactions.
Lab experience shows that solvent choice, temperature management, and even addition rates of the amine influence final outcomes in multi-step routes—especially those involving chiral separations or ligand-metal assembly. We know that a well-matched batch of amine, free from problematic by-products or air-sensitive residues, makes the difference between success and the necessity to rework an entire project. Considerable time spent talking to chemists using NMR and mass spec day in, day out has taught us the importance of keeping main and side products to an absolute minimum, refining process stability, and supporting published literature with genuine reproducibility.
Many research teams share stories about purchasing lower-cost amines, only to face unpredictable results or the need for extensive pre-cleanup. What saves the day is working directly with a manufacturer capable of tuning the process to remove glycol and aromatic aldehyde residues, manage water content, and support custom documentation for regulatory or publication needs. The direct feedback loop between our manufacturing team and product users ensures that we’re not simply meeting the minimum standard, but anticipating shifts in use cases and planning for tighter impurity tolerances.
Difficulties arise when secondary suppliers or traders intervene in the chain. Product sitting too long in inappropriate storage or shipped improperly accumulates problematic coloration or forms by-products, which then materialize as extra peaks in downstream reactions. Our own logistics team coordinates rapid shipment, temperature control where needed, and clear shelf-life labeling—a level of visibility not often possible when purchasing from resellers or bulk traders. To ensure further reliability, our production team batches (+/-)1-(1-Naphthyl)Ethylamine only to order for larger volumes, tracking raw material lot numbers, and documenting all cleaning and process conditions.
With new advances in asymmetric catalysis and medicinal chemistry, research partners increasingly provide specific requests: optically enriched material, formulation in specific solvent systems, or delivery in moisture-protected packaging. Our QC analysts collaborate with users to align documentation—COAs, spectra, impurity profiles—as a standard practice not as an exception. This builds trust in complex projects, where moving from milligram research scale to pilot-kilo demands not just paperwork but direct, transparent partnership.
The field of fine chemical production never stays still. Each year our team sees shifts in demand toward higher selectivity, reduced environmental impact, and closer compliance with international standards. Increasing attention to green chemistry requires not only minimum waste generation, but also careful control of auxiliary reagents, waste solvent handling, and batch yield optimization. Working with (+/-)1-(1-Naphthyl)Ethylamine, the goal is to maintain purity, cost-effectiveness, and continuity while also reducing the production footprint. Recent investments in closed-loop solvent systems, vacuum distillation, and automated monitoring help us meet these challenges without sacrificing product quality.
From our perspective, robust product and reliable supply are not points of pride—they’re a daily responsibility. Whether chemistry teams use this amine as a tool for enantioselective synthesis or as a stepping-stone for more complex transformations, they need to know batches remain consistent, documentation stays thorough, and technical questions receive real answers. Our entire operation, down to sample dispatch and customer feedback, turns on relationships built through support, transparency, and a focus on what actually makes the difference at the bench and in the plant.
As new methodologies and reaction paradigms emerge worldwide, our product development and quality control teams stay attuned to published research and internal feedback. The lessons gleaned from both small lab-scale preparations and industrial production cycles feed back into tightened process parameters, raw material vetting, and collaborative method validation. The journey to ever-higher standards is shaped directly by those using (+/-)1-(1-Naphthyl)Ethylamine in leading research, and as manufacturers, we commit to meeting those standards each day we come to the plant.
Every batch of (+/-)1-(1-Naphthyl)Ethylamine represents a link in a much larger chain—from raw material selection to researcher application. Our deep focus on process rigor, real-world documentation, and ongoing customer support enables chemists to hit their marks in asymmetric synthesis, chiral separations, and complex molecule construction. Open lines of communication, continual process refinement, and an uncompromising approach to quality shape a product that delivers—not just in theory, but in the realities of daily work at the laboratory and pilot plant scale.
As new fields of discovery open and demands intensify, our continued investment in people, process, and technology defines the difference between ordinary and trusted supply. We respect the material, the craft, and the partnerships built around this essential intermediate, and we look forward to supporting new discoveries with the same standards of excellence we have built over decades of manufacturing experience.