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1-(4-Fluorophenyl)-2-Methyl-2-Propylamine

    • Product Name 1-(4-Fluorophenyl)-2-Methyl-2-Propylamine
    • Alias 4-FLUOROISOPROPYLAMPHETAMINE
    • Einecs 'EINECS 628-416-2'
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    775592

    Iupac Name 1-(4-Fluorophenyl)-2-methyl-2-propylamine
    Molecular Formula C10H14FN
    Molecular Weight 167.23 g/mol
    Appearance Colorless to pale yellow liquid or solid
    Boiling Point Estimated ~230-250°C
    Density Approx. 1.0 g/cm³ (estimated)
    Solubility In Water Moderate to low
    Flash Point Estimated ~100°C
    Structure Smiles CCC(C)(N)C1=CC=C(C=C1)F
    Pka Estimated ~9-10 (amino group)
    Odor Amine-like

    As an accredited 1-(4-Fluorophenyl)-2-Methyl-2-Propylamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White HDPE bottle with tamper-evident seal, labeled “1-(4-Fluorophenyl)-2-Methyl-2-Propylamine, 100 g,” with hazard and handling information.
    Shipping **Shipping Description:** 1-(4-Fluorophenyl)-2-methyl-2-propylamine should be shipped in a sealed, labeled container, protected from moisture and extreme temperatures. Transport must comply with local and international regulations for hazardous chemicals. Ensure secondary containment and include the appropriate safety data sheet (SDS). Handle only by trained personnel with chemical handling certification.
    Storage Store **1-(4-Fluorophenyl)-2-methyl-2-propylamine** in a tightly sealed container, in a cool, dry, well-ventilated area, away from sources of ignition, excessive heat, and direct sunlight. Keep away from strong oxidizing agents, acids, and bases. Refrigerate if specified by the manufacturer. Always wear appropriate personal protective equipment (PPE) when handling and follow all relevant chemical safety protocols.
    Application of 1-(4-Fluorophenyl)-2-Methyl-2-Propylamine

    Applications of 1-(4-Fluorophenyl)-2-Methyl-2-Propylamine in Industrial Manufacturing

    1-(4-Fluorophenyl)-2-Methyl-2-Propylamine serves as a critical intermediate in specialized sectors of the pharmaceutical and fine chemicals industries. Consistent quality and adherence to industry-specific regulations remain central throughout its integration into diverse downstream manufacturing processes. Below we outline several established real-world application scenarios, each shaped by sector-specific technical, compliance, and processing practices.

    1. Pharmaceutical Synthesis: Selective Serotonin Receptor Modulator API Intermediate

    This amine functions as a building block for the manufacture of select serotonin receptor modulator active pharmaceutical ingredients (APIs), particularly in the mental health medication sector. Producers rely on its fluoroaromatic profile to construct drug molecules targeting major depressive disorder treatments through precise, multi-step organic synthesis.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP, US FDA 21 CFR Part 210/211)
    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) and United States Pharmacopeia (USP) monograph requirements for pharmaceutical intermediates
    • DMF or CEP registration for regulated market supply

    Typical usage ratio

    • Integrated at 1.1–1.5 molar equivalents relative to the substrate in stepwise synthesis; exact ratios depend on route optimization and scale-up kinetics

    Downstream process integration

    • Introduced during the reductive amination sequence after initial aromatic halogenation, followed by catalytic hydrogenation and purification

    Final product types

    • Pharmaceutical-grade APIs for antidepressants, serotonin modulators, and related CNS drug classes

    2. Agrochemical Synthesis: Precursor for Arylamine Herbicide Development

    Within the global crop-protection industry, manufacturers use this compound as a precursor in multi-step synthesis for selective arylamine-based herbicides. Its substituted fluoroarene ring aids in the development of bioactive molecules targeting broadleaf weeds while providing environmental metabolite control in compliance-heavy jurisdictions.

    Industry compliance standards

    • REACH (EC 1907/2006) registration for chemical intermediates
    • OECD Guidelines for the Testing of Chemicals
    • ISO 9001:2015 for process consistency and quality control
    • Global GAP Hazard Analysis & Risk-Based Preventive Control (HARPC), where applicable

    Typical usage ratio

    • 0.7–1.3 equivalents in key condensation or amination reactions, with adjustments based on desired selectivity and impurity threshold management

    Downstream process integration

    • Reacted post-fluorination with isocyanates or carboxylic acids to generate active herbicide intermediates; handled in closed batch systems due to toxicity profile

    Final product types

    • Technical-grade and formulated herbicides for pre- and post-emergent agricultural use

    3. Fine Chemical Manufacture: Intermediate in Fluorinated Fragrance Ingredient Synthesis

    The fine chemicals sector leverages the compound’s aromatic fluoro functionality for constructing specialty fragrance molecules. These fluorinated amines contribute volatility and persistence to industrial-scale fragrance bases for the personal care and home care markets, adhering to stringent raw material traceability and toxicological safety reviews.

    Industry compliance standards

    • IFRA Code of Practice for fragrance ingredient management
    • EU Regulation (EC) No 1223/2009 on Cosmetic Products, specifically Annex II (prohibited substances list)
    • ISO 22716: Good Manufacturing Practices for Cosmetics
    • RIFM (Research Institute for Fragrance Materials) toxicological evaluation requirements

    Typical usage ratio

    • Between 0.2–0.6 equivalents depending on end-use olfactory performance requirements and blending tolerances in downstream synthesis

    Downstream process integration

    • Fed as a nucleophile in alkylation and acylation steps to generate tailored fluorinated aromatic ketones or amides, followed by distillation and analytic profiling

    Final product types

    • Intermediate fragrance compounds used in perfumes, detergents, and personal care formulations

    4. Advanced Material Synthesis: Monomer for Specialty Polymeric Materials

    Polymer chemists utilize the amine’s controlled reactivity for the creation of non-conventional monomers used in advanced performance resins targeted at electronics encapsulants, adhesives, and specialty coatings. The fluorine atom provides improved chemical resistance and glass transition temperature enhancements while satisfying progressive material certification reviews.

    Industry compliance standards

    • ISO 10993 for polymeric materials intended for limited medical device encapsulation (where relevant)
    • UL 94 flammability testing for electronic housing polymers
    • RoHS Directive 2011/65/EU on hazardous substances in electrical and electronic equipment
    • ASTM D638: Standard Test Method for Tensile Properties of Plastics

    Typical usage ratio

    • Utilized at 0.5–1.2 equivalents relative to comonomers in step-growth polymerizations, adjustable for target molecular weight and crosslinking degree demands

    Downstream process integration

    • Charged during controlled polycondensation with acid chlorides or isocyanates under inert conditions; process closely monitored for monomer conversion and fluorine retention

    Final product types

    • High-performance fluorinated resins for conformal coatings, specialty adhesives, and microelectronic encapsulation materials
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    Certification & Compliance
    More Introduction

    Introducing 1-(4-Fluorophenyl)-2-Methyl-2-Propylamine: A Manufacturer’s Perspective

    The Heart of Fine Chemical Innovation

    Producing 1-(4-Fluorophenyl)-2-methyl-2-propylamine has given us a unique vantage point on what precision and reliability mean in specialty chemical manufacturing. On the shop floor, the difference between a mediocre product and a dependable one starts in the planning and doesn’t end until the last drum leaves our warehouse. There is no shortcut in maintaining product purity and primary amine retention when working with substituted phenylamines, especially with the tricky 4-fluorophenyl ring in play.

    This compound, recognized for its position as a synthetic building block in both pharmaceutical innovation and advanced material research, has carved out a niche that continues to grow. The 4-fluorophenyl group brings extra reactivity to the table, while the methyl and propyl substitutions encourage careful balance—without these, the molecule loses the characteristics industry chemists rely on.

    Commitment to Specification: What Makes This Product Different

    We have spent years refining methods to maintain batch consistency. Tight control over the temperature and reagent ratios during amination ensures high selectivity toward the desired structural isomer. Each batch undergoes analysis through high-performance liquid chromatography and gas chromatography. This routine guards against common issues, like byproduct formation or leftover starting material, which often slip past less rigorous inspection.

    In our facility, we recognize that users of 1-(4-fluorophenyl)-2-methyl-2-propylamine require narrow impurity profiles. Minor changes in impurity content, especially halogenated trace contaminants, end up amplified further down the synthesis chain and could sabotage entire processes. This adds complexity but delivers what matters: confidence in each supply lot.

    Working with a Tricky Compound: Daily Realities in Manufacturing

    Handling aromatic amines with fluorinated substituents is not routine business. Both in synthesis and purification, our teams pay special attention to waste handling, as fluoride-containing byproducts can cause equipment corrosion and demand compliant disposal contacts. During purification, standard distillation doesn’t suffice. Careful vacuum distillation and, where needed, recrystallization from optimized solvent systems help isolate the product as free-flowing crystals or a steadily dosed oil. This is where experience counts.

    If the process slips, contamination with unreacted precursor or side-chain isomers undermines application value and builds headaches for clients downstream. Once, early in scale-up, a subtle variation in solvent polarity during washout produced unexpected retention of a propylated impurity. Since tightening solvent specs, our repeatability has improved, bringing QA inspection pass rates up and overall customer satisfaction along with it.

    Meeting Pharmaceutical and Advanced Materials Demands

    In pharmaceutical R&D, this amine often acts as a key intermediate for crafting active compounds set to enter clinical trials. Regulatory expectations are inflexible regarding known and unknown impurities. Our process documentation accompanies each lot, containing not only the typical purity figures but a complete impurity breakdown. We noticed a rise in audits seeking proof of robust traceability, so we strengthened our in-house tracking from raw material sourcing through each synthetic stage.

    For researchers working on advanced polymers or surface coatings, reactivity and shelf life take center stage. The presence of the 4-fluorophenyl substituent gives the molecule tuned electron density, leading to faster coupling or crosslinking reactions in certain applications. Rather than rely on generic amine intermediates, customers turn to our offering to achieve property profiles that basic benzylic amines can't match.

    Why Purity and Handling Matter: Hard Lessons on the Production Line

    Purity, in our experience, does not exist as a checkbox. It is the difference between smooth downstream conversion and columns clogged with tarry, useless material. In one instance, a change in a supplier’s aniline brought an unexpected impurity into our input stream, requiring discontinuation of our trusted jobber until we sourced raw material meeting our stricter in-house spec. Ever since, we established incoming material screening—not only for assay, but for IR-identifiable structural variances.

    Most users underestimate the trouble low-level halogenated impurities wreak on later steps, especially in palladium-catalyzed couplings. Having spent long evenings cleaning fouled reactors ourselves, we now deliver full impurity spectra per batch. This transparency lets our customers plan ahead, schedule less unproductive downtime, and avoid last-minute troubleshooting when a reaction misbehaves.

    Shelf Life, Storage, and Stability: Beyond the Basics

    Few intermediate producers will stress long-term product stability, but based on years witnessing spontaneous discoloration or slow degradation in improperly sealed containers, we put special effort into packaging. The free amine can absorb atmospheric carbon dioxide, souring the product if left unsealed too long. We ship each lot under carefully controlled conditions, with tamper-evident seals and desiccant packs if shipped over long distances. End-users who appreciate this added care report fewer issues with unexpected reactivity losses.

    We maintain regular re-testing for stored inventory batches and recall products well before measurable degradation can occur. This policy ensures our outgoing shipments perform as expected, even after months in transit or storage. Learning from a notorious shipment lost to months in a customs warehouse, we improved both our shipping containers and batch documentation, reducing risk for everyone in the supply chain.

    Application Area Insights: Learning from Customer Experience

    Customers and partners regularly share feedback about their success or struggles with this compound. We’ve learned that not everyone prioritizes the same parameters. Drug discovery teams highlight the importance of batch-to-batch consistency, especially for scale-ups from milligram runs to multi-kilo campaigns. Minor inconsistencies can translate to wasted days or costly retesting, especially if a timeline depends on an aggressive clinical pipeline.

    In advanced coatings or functional polymer labs, even subtle differences in product appearance—such as a faint tint, which can signal trace oxidation—matter. Over time, adjustments to our in-process sampling and improved inert handling have resulted directly from these discussions. We actively collect and apply insights from each delivered batch to tighten our operation, which helps not only us but the R&D teams counting on our supply stability.

    Comparing 1-(4-Fluorophenyl)-2-Methyl-2-Propylamine With Similar Materials

    Our clients sometimes ask if using a 4-chlorophenyl or an unsubstituted phenyl analog will offer similar reactivity or reliability. Experience proves that the fluorinated variant runs faster in nucleophilic aromatic substitution contexts, often providing cleaner conversions and yields in coupling chemistry. The relatively low toxicity and volatility, compared to their chloro- or bromo-phenyl cousins, provides a noticeably safer handling profile in practice.

    With the methyl and propyl substitutions in the side chain, 1-(4-fluorophenyl)-2-methyl-2-propylamine often finds favor where branched alkyl amines improve solubility, boost molecular interaction, or shape pharmacokinetic properties in lead molecules. This is not a niche effect; many of our customers discovered significant performance increases by moving from more linear or less substituted analogs. The specificity of this combination—fluorine para to a methyl/propylated amine—has unlocked new pathways for them as well as for our in-house research teams.

    Innovation in Warranty and Support: Standing by Our Work

    Manufacturing a specialty compound like this never ends at a purchase order. Each batch ships with a support offering based on decades of cumulative expertise in both bench chemistry and industrial scale-up. If a client runs into an unexpected issue—such as solubility mismatches, application-specific contamination concerns, or unforeseen stability problems—we provide direct, informed support.

    We have walked the same terrain: Have you ever performed a process validation run only to see byproducts where you expected none? Our team will dive into the roots of a problem, from batch records to analytical re-tests. Occasionally a customer has alerted us to a unique artifact in an unfamiliar application; we treat these as learning experiences. Each report closes a feedback loop, and we log every resolution for both internal training and procedural upgrades.

    Supply Chain and Reliable Delivery: Behind the Scenes

    Manufacturing capacity and reliable turnaround on specialty chemicals depend on a steady, resilient supply chain. Investing in multiple sources for fluorinated building blocks proved wise during supply shocks. By maintaining deep partnerships with trusted vendors and reinforcing local logistics, we keep lead times short even as demand swings.

    The realities of shipping hazardous chemicals mean delays can and do occur, yet we build safety stock both on-site and at local distribution points closest to major research hubs. This buffer has proven essential during unforeseen events—regulatory holdups, weather disruptions, or sudden surges in customer demand. Thanks to preventative planning, our fill rates stay high, and we rarely force users to substitute inferior analogs due to stockouts.

    The Bigger Picture: Compliance and Long-Term Security

    As regulations for amines tighten worldwide, our compliance protocols keep us ahead of shifts in reporting and documentation. We maintain third-party certified quality management protocols, file safety evaluation data, and track all exports in compliance with destination country requirements. Our legal and EH&S teams keep us continuously briefed on regulatory updates—every compliance certificate and test result is stored digitally and physically for full traceability.

    From the initial feasibility runs to multi-ton commercial shipments, our process engineers track and minimize waste generation and emissions. We manage spent solvents through approved waste vendors and minimize energy consumption by targeting more selective, lower-temperature syntheses wherever feasible. These choices come from both operational necessity and a commitment to social responsibility. No corner goes unexamined in our process audits, which, in our experience, deliver consistently better results for both our partners and the communities near our facilities.

    Continuous Improvement: Lessons Earned, Not Bought

    Real insight comes from facing bottlenecks, breakdowns, and technical surprises head-on. Five years ago, we overhauled our reactor design after discovering that trace side-chain rearrangement could occur at scale, a problem invisible during gram-scale trials. Since transitioning to upgraded agitation and heat transfer equipment, lot-to-lot reanalysis proved the fix paid off: Product quality stabilized above industry benchmarks, and customer complaints fell off.

    We continue to prioritize open communication with users. Their feedback often points out subtle shifts in performance—differences that only reveal themselves during application, not in routine QC. Each season brings new process tweaks, new analytical capabilities, and better packaging designed to withstand global logistics. Our trajectory as a manufacturer rests not only on initial product merit but on what we learn from every application, every return, every unexpected anomaly.

    Why Established Manufacturing Matters in the Age of Specialty Chemicals

    As novel drugs, advanced polymers, and performance chemicals capture more of the market, supply chain risk rises for all players. The days of relying on generic bulk commodity chemicals belong in another era—today’s researchers and developers count on source transparency, reproducibility, and ironclad documentation.

    Direct-from-manufacturer experience in making and supporting 1-(4-fluorophenyl)-2-methyl-2-propylamine means more than simply hitting a spec sheet. We’ve seen what fails without vigilant process control and what succeeds when issues are addressed proactively. That long view, in our estimation, serves not just our bottom line, but every scientist, engineer, and product developer who stakes their project’s promise on high-quality inputs.

    Looking Forward: Manufacturing for Tomorrow’s Demands

    Certain trends have made themselves clear. Demand for specialized amine building blocks grows each year, informed by more ambitious pharmaceutical and materials science programs. Customers expect not just raw material but robust assurance, rapid troubleshooting, and flexibility to match changes in research direction.

    Our approach places these values at the core of production and customer service. Every improvement, from extra in-process controls to live technical support, comes from the lessons learned adapting to evolving needs. We stake our reputation on not just delivering a product, but delivering on partnership—with accountability at every step, and a focus that reaches beyond the immediate sale toward a sustained role in your project’s success.