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N-Phenyl-Isobutyloylacetamide

    • Product Name N-Phenyl-Isobutyloylacetamide
    • Alias N-PIBA
    • Einecs 247-384-9
    • 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

    589127

    Chemical Name N-Phenyl-Isobutyloylacetamide
    Molecular Formula C12H15NO2
    Molecular Weight 205.25 g/mol
    Cas Number 144-80-9
    Appearance White to off-white crystalline solid
    Melting Point 94-96°C
    Boiling Point Unknown
    Solubility Slightly soluble in water, soluble in organic solvents
    Density 1.13 g/cm3 (approximate)
    Purity Typically >98%
    Storage Conditions Store at room temperature, keep container tightly closed
    Synonyms N-Phenyl-2-methylpropanoylacetamide
    Application Used as an extractant in solvent extraction processes

    As an accredited N-Phenyl-Isobutyloylacetamide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical `N-Phenyl-Isobutyloylacetamide` is supplied in a sealed, amber glass bottle containing 100 grams, with tamper-evident labeling.
    Shipping N-Phenyl-Isobutyloylacetamide is shipped in tightly sealed containers to prevent contamination and moisture exposure. It should be packed according to applicable chemical safety regulations, labeled clearly, and transported at ambient temperature. Ensure handling by trained personnel and protect from physical damage. Avoid shipping with incompatible substances, such as strong oxidizers or acids.
    Storage N-Phenyl-Isobutyloylacetamide should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers and acids. It should be kept at room temperature, protected from direct sunlight and moisture. Proper labeling is essential, and access should be limited to trained personnel following standard safety protocols.
    Application of N-Phenyl-Isobutyloylacetamide

    Applications of N-Phenyl-Isobutyloylacetamide in Industrial Manufacturing

    As a direct manufacturer of N-Phenyl-Isobutyloylacetamide, we supply this specialty intermediate for advanced chemical synthesis in regulated downstream sectors. Below, we outline core industrial application fields, highlighting our experience with real-world production standards, precision dosing, process integration points, and downstream customer finished products.

    1. Pharmaceutical Intermediate Synthesis

    N-Phenyl-Isobutyloylacetamide functions as an essential coupling agent and building block in the multi-step synthesis of several active pharmaceutical ingredients (APIs). API manufacturers require strictly defined purity grades to comply with registration batches and must integrate this intermediate at the acylation or amidation stage in small- to mid-scale reactors. Typical formulations depend on the target API scaffold and regulatory risk assessment for impurity control. We supply process-tailored lots to support DMF and cGMP batch records and provide full traceability for all deliveries.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guidance for Active Pharmaceutical Ingredients
    • European Pharmacopoeia monograph references for acyl amide intermediates
    • US FDA DMF (Drug Master File) filings
    • Chinese Pharmacopoeia (ChP) manufacturing requirements

    Typical usage ratio

    • Ranged from 0.8–1.2 molar equivalents against the primary amine starting compound, adjusted based on process yield and impurity profile optimization

    Downstream process integration

    • Charged directly to the acylation step in GMP reactor lines after initial solvent and base charge
    • Utilized in continuous flow or batch mode based on campaign size
    • Pooled with in-line purification for downstream API crystallization/isolation

    Final product types

    • Active pharmaceutical ingredients (APIs) for anti-inflammatory drugs
    • API intermediates for central nervous system (CNS) agents
    • Chemical building blocks for small molecule novel entities (NMEs)

    2. Agrochemical Active Ingredient Manufacturing

    In the agrochemical sector, formulators use this compound as a key intermediate for the synthesis of herbicide active ingredients and selective plant growth regulators. Production plants focused on high-volume pesticides require consistent acylation agent quality to maintain synthesis yields and minimize downstream purification. Rigorous supply documentation supports REACH and FAO compliance, and our supply chain integrates secure batch segregation for IP-sensitive clients.

    Industry compliance standards

    • Regulation (EC) No 1907/2006 (REACH) for chemical safety
    • FAO/WHO International Code of Conduct on Pesticide Management, technical grade material
    • ISO 9001:2015 for process traceability
    • OECD Guidelines for the Testing of Chemicals

    Typical usage ratio

    • Typical dose is 1.05–1.15 equivalents per functional group during active core assembly, adjusted per batch size and feedstock impurity load

    Downstream process integration

    • Fed into the key condensation or amidation stage using jacketed glass-lined reactors
    • Incorporated during continuous feed operations for large-scale production
    • Followed by distillation/purification module prior to formulation blending

    Final product types

    • Herbicide technical concentrates
    • Plant growth regulator actives
    • Pre-emergence weed control agents

    3. Specialty Polymer Additive Synthesis

    Manufacturers of high-performance polymers use this amide as a specialty monomer or reactive modifier. Its structure facilitates integration into custom polyamide chains, producing polymers with target thermal, mechanical, and surface properties. This application demands strict monitoring of batch-to-batch amide content and molecular weight influence. Downstream polymerization lines integrate our product at the pre-polymer mixing or functionalization stage under nitrogen atmosphere, controlled by in-process FTIR or NMR analytics.

    Industry compliance standards

    • ISO 9001:2015 and ISO 14001:2015 for quality and environmental management
    • RoHS (Restriction of Hazardous Substances Directive) as applicable to electronics-grade polymers
    • UL 94 flammability ratings for final plastic products
    • ASTM D256 or ISO 1133 for downstream mechanical property testing

    Typical usage ratio

    • Between 1–5 wt% relative to the polymer matrix, optimized for the end-use mechanical profile and thermal behavior; exact ratio guided by target viscosity and molding parameters

    Downstream process integration

    • Pre-mixed with main monomers prior to bulk or step-growth polymerization
    • Dosed through automated feeders in continuous production lines
    • Analytical sampling post-reaction for molecular distribution adjustment

    Final product types

    • Advanced engineering plastics for automotive housings
    • Flame-retardant polyamide molding compounds
    • Custom specialty copolymers for electrical enclosures

    4. Fine Chemical Synthesis for Organic Laboratories

    Contract manufacturers and research organizations utilize this raw material for high-purity fine chemical preparations in chemical R&D and pilot synthesis. These labs demand tight lot control, detailed analytical data, and flexible packaging for bench-scale and kilo-lab operations. The amide mainly supports custom acylation schemes and model reaction setups under variable solvent and base conditions. We provide material with full certificate of analysis and batch record transparency for these technical projects.

    Industry compliance standards

    • ISO 17025 for laboratory quality management
    • GLP (Good Laboratory Practice) for regulated chemical R&D
    • Standard Methods for the Examination of Water and Wastewater, if relevant for effluent treatment
    • Internal analytical protocols for purity and residual solvent control

    Typical usage ratio

    • Routinely from 0.9–1.3 molar equivalents, adapted to synthetic target throughput and stoichiometry optimization in research method development

    Downstream process integration

    • Dispensed into small-volume reactors or round-bottom flasks for acylation reactions
    • Handled under fume hood with direct scale for precise dosing
    • Integrated into semi-automated batch reactor platforms for kilo-lab scale-up

    Final product types

    • Research grade acyl amide libraries
    • Reference standards for analytical calibration
    • Custom organic intermediates for client-sponsored projects
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    Certification & Compliance
    More Introduction

    N-Phenyl-Isobutyloylacetamide: Crafting Consistency Through Experience

    Our Path to a Reliable Synthesis

    In the business of chemical manufacturing, small changes in process make a difference on the final product. N-Phenyl-Isobutyloylacetamide, which we often refer to on the shop floor by its shorthand, has stood out over the years for both the practical challenges and the repeated successes it has brought to us as a producer. Our story with this molecule starts from hands-on synthesis, fine-tuning each step and making direct observations about handling, purification, and batch reliability.

    From raw material procurement to controlled crystallization, our operation has never relied just on formulaic approaches or copying competitor routines. For us, every project is grounded in routines that grow out of daily practice. What sets the process for N-Phenyl-Isobutyloylacetamide apart—compared with other amides we've run through our reactors—lies in the way the phenyl ring interacts during acylation, and the sensitivity of isobutyryl chloride to temperature and moisture. Years of tracking batch yields and impurity profiles taught us to keep a closer eye on the acidity of the medium and the temperature ramps.

    Defining the Material, Not Just Naming It

    At the bench, N-Phenyl-Isobutyloylacetamide forms a white to off-white crystalline solid, with strong, characteristic spectral lines in both FT-IR and NMR, which help minimize ambiguity. The correct melting point and purity sampling give early warning for problems in scale-up or changes in upstream supply—critical for us as a producer with daily QC samples, but also for customers who depend on reliable, repeatable results. Over time, we found that water content—even at low ppm—can lead to hydrolysis, affecting shelf life and solubility. That's why we adopted a set drying protocol post-filtration and insisted on dedicated glassware, even when line capacity is stretched by other projects.

    Some buyers tell us vendor-to-vendor specifications differ— sometimes a lot, sometimes just at the edge of detectability. To avoid those swings, we stick to testing against GC-MS for main product and critical limits for related isobutyryl and acetyl impurities, avoiding the “read-across” temptation of labelling lots by process book alone. Not every customer wants a full spectral set, but spectroscopy gives us a fingerprint to lean on if something unexpected appears in their process or formulation run.

    Performance Characteristics and End-Use Lessons

    Our batches often go directly into research synthesis or pilot lines in pharmaceutical intermediates, so any drift in purity shows up quickly at the next step. The feedback loop between our plant QC and customer lab is short—what we learn on outgoing lots comes up in next month's optimization. In contrast, some competitors seem content with broader specification bands, shipping material with minor off-color or residual solvent. We never found it worth risking variability in customers’ hands, so we took on the cost of in-house distillation and extra drying rather than pass it along to users in the form of uncertainty or extra purification.

    Understanding practical usage plays a big part in process decisions. Some processes need reliable bench response, others need scalable filtration. We design our batches to filter rapidly, and avoid caking during isolation. Some processes introduce N-Phenyl-Isobutyloylacetamide at room temperature, while others incorporate it under gentle heating—so we record and track solubility changes over both profiles, sharing that insight to solve downstream issues. Our technical staff logs this information so the evolving knowledge base can feed back into both process improvements and troubleshooting.

    Variations and Real Differences from Related Products

    In our years working at scale, it's clear that even close chemical cousins part ways in both handling and response. Take N-Phenyl-Isobutyloylacetamide versus N-Phenylacetylacetamide or propanoyl analogs: their similarities hide the differences that matter. For instance, the branching at the isobutyryl group shifts physical form, alters solubility in typical formulation solvents, and shapes reactivity in acyl transfer reactions. Many of our colleagues tried simple substitution in their product lines, only to find out that batch crystallization habits shifted, or that the residue left after solvent removal forced tweaks to downstream steps.

    Customers sometimes approach us after dealing with synthesis bottlenecks or stability issues, concluding N-Phenyl-Isobutyloylacetamide is interchangeable with related amide or acetamide products. Both literature and real-world data argue otherwise: the steric bulk and chemical context set up unique responses during both storage and subsequent reactions. N-Phenyl-Isobutyloylacetamide, with its branched isobutyryl side chain, provides enhanced stability in certain reactions—especially where ordinary acyl counterparts drop yield or give decomposition. That’s the opinion echoed not only in published references but in feedback from formulating chemists who use our product as a key intermediate or building block.

    Typical Customers and Application Insights

    Most customers buying N-Phenyl-Isobutyloylacetamide are involved in pharmaceutical, agrochemical, or specialty research projects, often focusing on medicinal chemistry and structure-activity exploration. Despite similar-sounding intermediates on the market, few alternatives match the same performance in their stepwise synthesis or combinatorial screens. Some order for bulk pilot use, others for late-stage library prep, but both have shared concerns about mixed-source inconsistencies. We listen closely to experience from users, logging both routine successes and reported anomalies, and use those lessons to refine protocol or validate a new route before full-scale rollout.

    In contrast with off-the-shelf intermediates, N-Phenyl-Isobutyloylacetamide has less historical baggage—there’s no standard pharmacopoeial monograph, so every spec gets built from actual experience and conversation. We maintain dialogue with formulation chemists as well as project managers on key endpoints, learning not only how the amide fits into published synthetic strategies but how it behaves during unexpected troubleshooting. On more than one occasion, customer teams reported unexplained yield drop or color change, only to trace the issue back to ambient humidity or packing material. Each episode fuels fresh improvements on our side, reinforcing two-way trust.

    Mitigating Quality Risks—Experience Counts

    Factory floor lessons matter more than book theory for a product like N-Phenyl-Isobutyloylacetamide. Unfiltered reaction mass may look fine by basic TLC but, as every plant manager learns, the real test comes in scale-out. Small changes in solvent grade, temperature window, or mixing rate shift yield and can create persistent tails or side peaks, even when above 98% main spot. Over time, we have integrated real-time analytical tools and quick-turnaround HPLC to limit product out-of-spec risks. Routines for rapid online monitoring evolved from roots in daily batch optimization, not outside prescription.

    Reliability isn't an abstract goal—it's the outcome of tracking how each batch tackles downstream reactivity, or how packaging choices defend against gradual, unnoticed uptake of water. Even tiny traces of isobutyric impurity show up at the user end—sometimes long after the product ships. To prevent such issues, we run accelerated aging tests and match storage conditions, simulating end-user environment. Our storage rooms rely on proven desiccant routines and periodic visual checks—not just paper logs or digital tracking.

    Supporting Applications Through Technical Feedback

    Direct feedback from users shapes improvements, sometimes outside the core synthesis itself. On more than one occasion, we learned from partners that their preferred solvents, concentrations, or mixing techniques prompted unexpected response from our N-Phenyl-Isobutyloylacetamide compared to other amides. Standardized returns and root-cause review keep all stakeholders invested in continual improvement. This cycle isn’t forced by regulation—it grows from everyday necessity to produce a consistently reliable chemical, time after time.

    For new applications—say, exploring a new coupling pathway or modifying crystallization protocols—our technical team can reference actual case studies, drawn from similar user projects, helping shorten cycles from idea to proof-of-concept. It’s not just a support line but a learning community, reflecting the practical realities of working chemists and scale-up managers. Each new customer inquiry—from questions about solubility in unusual solvents to curiosity about off-label uses—feeds back into the pool of experience, often prompting fresh rounds of lab work or production-scale validation.

    Adaptability and Cost Lessons in the Marketplace

    The chemical market rewards hard-earned adaptability. We handle orders across the range—from kilo-scale to drum shipments—but never offload logistics questions or ignore details. Changes in upstream supply, fluctuations in raw acid or chloride cost, or even shifts in customs regulation all channel direct lessons to our bottom line. Some vendors smooth over such issues by lowering specification or using blended lots. Our experience teaches that hidden corners of cost-saving measures show up months later as technical debt, so we keep single-batch traceability, avoid unnecessary mixing, and maintain open books with long-term customers.

    By remaining transparent about both challenges and incremental gains, customers find not only a source of chemical supply but a practical, invested partner. Few customers return just for price—they come back for consistency in output, and for the confidence that comes from knowing the supplier will address problems quickly.

    Comparisons That Matter: Standing Apart from Distributors

    Direct manufacture of N-Phenyl-Isobutyloylacetamide isn't about filling catalog slots—it’s about mastering subtle process variables that third-party sellers often miss. Distributors trade on availability and broker margin; genuine producers like us carry the background data, know the day-to-day quirks of product handling, and keep both laboratory and production batch records for every lot. We see the difference directly in customer loyalty: when compounded intermediates are delayed or when downstream reactions run into trouble, a broker can’t solve the problem by swapping stock. We address product issues by drawing from experience, not from a catalogue of suppliers.

    This grounded, end-to-end manufacturing relationship isn’t about marketing spin, but about shared investment in successful outcomes. We can talk specifics—solvent choices, reactivity profiles, impurity histories—because experiment and production hours went into every answer. There's no substitute for direct feedback loops; production teams learning from technical support, technical staff learning from the front lines.

    Stronger Processes, Fewer Surprises

    Long-term partnerships with both customers and raw material providers remind us daily that the best outcomes rely on open communication. For N-Phenyl-Isobutyloylacetamide, that means tracking batch-level nuances, recording each instance of non-standard response—down to batch notes about filter media or exotherm. Sometimes, we learn something entirely new from an unexpected run or end-user report, triggering lab investigation and often raising overall process understanding. This practice increases both internal confidence and external value.

    Teams with hands-on control over their syntheses find fewer surprises, shorter troubleshooting cycles, and more confidence in both yield and outcome. Our production people, used to running other amides or related specialties, recognize that each chemical has quirks which, if unchecked, can build into real issues. Over the years, incremental process shifts—like swapping out a drying method, or modifying a filtration step—have produced outsized benefits in reliability and customer satisfaction.

    A Track Record Built on Measured Growth

    In chemical manufacturing, market pressures for speed and price are always balanced by bottom-line risks of rework, failure, and lost trust. Our approach for N-Phenyl-Isobutyloylacetamide involves continuous review, open reporting, and active documentation of both what works and what fails. We collect and verify every non-conformance, no matter how minor, preventing problems from turning into recurring pain points. We test each production batch to confirm both listed and subtle quality parameters. Customers find real value in knowing that each lot has a backstory—every kilo tied to logged observations, running process conditions, and fresh input from the previous cycle.

    Market competitors selling “generic” amides rarely talk openly about process drift or real-world impurity carryover. Our reputation for N-Phenyl-Isobutyloylacetamide stands on willingness to discuss real process details, share documentation where warranted, and explain the rationale behind changes in routine. Stability testing is more than a box-checking exercise—it's a chance to simulate storage conditions, test limits, and learn before customers do.

    Continuing the Conversation

    From the outside, chemical manufacturing sometimes looks like a world of fixed specs and static recipes. N-Phenyl-Isobutyloylacetamide has shown us otherwise. The knowledge base expands not through rehashing the textbook, but from the collective experience gained through every campaign, every feedback note, every test. By sharing what we know, and listening to our users, we make each product cycle better—improving output, reducing troubleshooting time, and supporting formulation creativity in both simple and complex application environments.

    In our plant, the most valuable resource isn’t a “standard operating procedure” but the team conversation around every batch note, every observed trend. N-Phenyl-Isobutyloylacetamide continues to teach us—and those who order and use it—both the value of diligent process and the gains of shared experience. Across every shipment and every technical exchange, this open and down-to-earth approach defines how we manufacture, how we solve problems, and how we keep improving.