Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

3-Methyl-1-Phenyl-2-Butanone

    • Product Name 3-Methyl-1-Phenyl-2-Butanone
    • Einecs 244-975-7
    • 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

    955706

    Chemical Name 3-Methyl-1-Phenyl-2-Butanone
    Molecular Formula C11H14O
    Molecular Weight 162.23 g/mol
    Cas Number 16642-98-5
    Appearance Colorless to pale yellow liquid
    Boiling Point 262-263 °C
    Density Approximately 1.01 g/cm³
    Refractive Index n20/D 1.521
    Flash Point 110 °C
    Smiles CC(C(=O)CC1=CC=CC=C1)C
    Solubility Insoluble in water; soluble in organic solvents
    Synonyms 1-Phenyl-3-methyl-2-butanone

    As an accredited 3-Methyl-1-Phenyl-2-Butanone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 500g amber glass bottle is securely sealed, labeled "3-Methyl-1-Phenyl-2-Butanone," featuring hazard warnings and handling instructions.
    Shipping 3-Methyl-1-Phenyl-2-Butanone is shipped in tightly sealed containers to prevent leakage and contamination. It should be stored in a cool, dry, and well-ventilated area, away from incompatible substances. During transit, it must be protected from physical damage and comply with relevant chemical transportation regulations to ensure safety.
    Storage Store **3-Methyl-1-Phenyl-2-Butanone** in a tightly sealed container, placed in a cool, dry, and well-ventilated area away from direct sunlight and incompatible substances such as strong oxidizers. Keep the storage area free from ignition sources. Ensure containers are clearly labeled, prevent moisture contact, and handle only with appropriate protective equipment to avoid inhalation, skin, and eye contact.
    Application of 3-Methyl-1-Phenyl-2-Butanone

    Applications of 3-Methyl-1-Phenyl-2-Butanone in Industrial Manufacturing

    3-Methyl-1-Phenyl-2-Butanone serves as a specialty chemical intermediate adopted by multiple complex downstream sectors, where its defined structural and organoleptic properties contribute directly to target product identity and performance. The following sections provide detailed application areas based on real industry practices and process integration, summarized by our technical support and collaboration with downstream manufacturing partners.

    1. Fine Fragrance Compounding

    Perfumery manufacturers utilize this ketone as a character impact agent, particularly valued for its diffusive aroma profile and high stability in top-note formulations. It reliably provides lift and complexity in designer fragrance development, and survives both compounding and quality control cycles without oxidation or discoloration, a vital trait in luxury perfumery.

    Industry compliance standards

    • IFRA (International Fragrance Association) Standards and Amendments
    • REACH Regulation (EC) No 1907/2006 for ingredient registration and safety data
    • COSMOS Standard for Natural and Organic Cosmetics (where relevant for natural-inspired lines)
    • RIFM (Research Institute for Fragrance Materials) Safety Assessment Protocols

    Typical usage ratio

    • 0.02–0.25% by weight in finished fragrance oil; adjustment based on desired impact and regulatory threshold for final application

    Downstream process integration

    • Direct addition during mixing and blending at the fragrance compounding stage, before dilution in ethanol or fixative base

    Final product types

    • Luxury perfumes
    • Eau de toilette and cologne
    • Home fragrance concentrates
    • Personal care scented formulations

    2. Aroma Chemicals Synthesis

    Aroma chemical manufacturers employ this compound as a specific building block for the synthesis of complex flavor and fragrance intermediates, in both batch and continuous processes. Its keto group promotes selective condensation and ring-closure reactions essential in the creation of keynotes and synthetic aroma analogues targeting natural descriptors.

    Industry compliance standards

    • FEMA (Flavor and Extract Manufacturers Association) GRAS Listings (where relevant)
    • US FDA 21 CFR Part 172 (Food Additives Permitted for Direct Addition to Food for Human Consumption, limited to intermediates)
    • ISO 9001:2015 (Quality management systems in aroma chemical manufacturing)
    • EU FCM (Food Contact Materials) Regulations (for applicable process byproducts)

    Typical usage ratio

    • 5–15% as starting material in multi-step organic synthesis; precise ratios depend on target molecule and process yield optimization

    Downstream process integration

    • Charged as a key substrate in reactors during stage-specific condensation, acylation, or cyclization steps, with real-time process monitoring for conversion efficiency

    Final product types

    • High-purity synthetic musk derivatives
    • Cyclic aroma intermediates
    • Masking agents for flavor and fragrance bases
    • Key notes for specialty aroma accords

    3. Pharmaceutical Intermediate Synthesis

    Active pharmaceutical ingredient (API) manufacturers incorporate this substance as a critical intermediate, where its reactivity supports selective carbon–carbon bond formation leading to advanced pharmaceutical building blocks. Established use cases include small molecule drugs where stereochemistry and purity critically affect biological activity, with the process tightly controlled under GMP guidelines.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US Pharmacopeia (USP) and European Pharmacopoeia (Ph. Eur.) for intermediate handling and purity specifications
    • FDA cGMP (21 CFR Parts 210 & 211) for API production
    • EudraLex Volume 4 (EU GMP Guidelines)

    Typical usage ratio

    • 0.5–10 mol% relative to primary substrate, with scaling parameters defined by route of synthesis and target API requirements

    Downstream process integration

    • Introduced during core intermediate formation phase, prior to final purification and crystallization of pharmaceutical precursors; monitored for residual levels in compliance with reporting thresholds

    Final product types

    • Active pharmaceutical intermediates for neuroactive compounds
    • Chiral synthons for specialty drug classes
    • Custom pharmaceutical building blocks for CDMO workflows
    • API precursor batches for clinical and commercial supply

    4. Specialty Polymer Modifier

    Functional polymer producers integrate this ketone as an end-group modifier or chain transfer agent in specialty polymerizations, where its aromatic and aliphatic structure fine-tunes physical characteristics such as flexibility, melt flow index, and dielectric behavior. It enables precise molecular design for demanding electronics and coatings sectors.

    Industry compliance standards

    • ISO 9001:2015 for specialty polymer manufacturing
    • RoHS Directive 2011/65/EU for electronics polymers
    • ASTM D256 and D638 for evaluating polymer mechanical properties
    • UL 94 (Standard for Safety of Flammability of Plastic Materials)

    Typical usage ratio

    • 0.1–2% by mass as a co-monomer or chain transfer compound; dosage depends on targeted polymer attributes and application method

    Downstream process integration

    • Fed during batch or continuous polymerization reactions, with stepwise monitoring to maintain molecular weight distribution and compositional uniformity

    Final product types

    • Engineering thermoplastics for electronics
    • Flexible coatings for optical films
    • High-performance adhesives
    • Precision molded plastic components

    5. Flavour Ingredient for Non-Food Applications

    Manufacturers of non-food grade flavors in oral care deploy this substance as a characterizing agent in sophisticated aroma delivery systems such as toothpastes and mouthwashes. Its perceptible taste/aroma threshold and low volatility profile grant durability in branded consumer products, with stability verified in long-term accelerated shelf-life studies.

    Industry compliance standards

    • FD&C Act (US) regulations for indirect additives
    • ISO 16128 (Guidelines on technical definitions for natural and organic cosmetic ingredients)
    • Cosmetic Ingredient Review (CIR) Safety Assessments
    • EU Cosmetics Regulation (EC) No 1223/2009

    Typical usage ratio

    • 0.01–0.10% in finished oral care flavor base; the actual level selected after sensory panel evaluation and regulatory exposure calculations

    Downstream process integration

    • Mixed into flavor concentration premixes prior to blending with active oral care agents and humectants during toothpaste or mouthwash manufacturing

    Final product types

    • Flavored toothpaste
    • Mouthwash aroma bases
    • Chewing gum flavor concentrates (non-food, functional)
    • Cosmetic-grade breath fresheners
    Free Quote

    Competitive 3-Methyl-1-Phenyl-2-Butanone 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

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    3-Methyl-1-Phenyl-2-Butanone: A Closer Look From the Laboratory Bench

    Real-World Manufacturing Brings Reliability to Every Batch

    Over years of producing specialty ketones, 3-Methyl-1-Phenyl-2-Butanone stood out in our catalog for its purity, consistent yield, and reproducibility on scale. Our team moves the entire process under one roof—sourcing, synthesis, and quality checking. This single chain of control gives our chemists a clear view of raw material origin, batch conditions, and finished product attributes.

    We run this ketone through several distillation rounds and tight controls on moisture content because customers in fragrance formulation, pharmaceutical intermediates, and fine chemical synthesis want clean, reliable product with no unknowns drifting in from careless process shortcuts. Over time, building up our in-house protocols stopped headaches for formulators who once saw batches fail due to off-spec byproducts from poorly tuned columns.

    Understanding 3-Methyl-1-Phenyl-2-Butanone: Structure Shapes Function

    This molecule, sometimes called beta-methyl-beta-phenylbutanone, features a compact backbone with distinctive branching at the third carbon. That structure changes how it behaves compared to more common linear ketones like methyl ethyl ketone or acetophenone. The combination of the phenyl ring with a methyl group at the three-carbon position pushes electron density and gives its carbonyl group distinct reactivity for further modification.

    We learned early that this particular branching improves its odor profile—a bit brighter and more persistent than plain alkyl phenyl ketones. In the lab, that also means selective functionalizations become easier to control without unwanted side reactions, especially those leading toward chiral intermediates required for higher-value pharmaceutical targets.

    Precise Purity for Targeted Applications

    Our batches typically reach a minimum purity of 99%, measured by both GC and NMR, not simply by a single QC check. Moisture is kept below 500 ppm, a level we check at multiple points across the process. We’ve found that higher water content cuts performance in some catalytic reactions and causes problems in certain fragrance matrices. Our operations never rely on a one-size-fits-all drying step; instead, drying and final purification match the kind of downstream use intended by each client. This matters for people crafting complex blends, especially when minor impurities can change how a product behaves in solution or on the skin.

    We committed to using glass-lined and stainless steel reactors for every stage: this eliminates trace corrosion products, which once plagued early syntheses run in traditional vessels. Our technical staff runs spot tests weekly—and when needed, we break down reaction vessels for visual and analytical checks. This direct experience led us to scrap an entire reactor line in year three and start over with modern, more robust materials. The result: greater batch integrity, easier cleaning, fewer product recalls, and sharper analytical signals on every certificate we issue.

    Comparison: Where This Ketone Excels Over Its Siblings

    We often hear from development chemists who want to know what sets 3-Methyl-1-Phenyl-2-Butanone apart from standard chain ketones or even benzyl acetone. Side-by-side in the production environment, our experience shows a few notable differences.

    First, volatility is dialed back compared to simple straight-chain variants. This provides greater control for colleagues building fragrance bases where slow release or long-lasting notes are prized. In reaction development, its steric configuration better shields the carbonyl from nucleophilic attack, reducing formation of certain byproducts that demand costly downstream separation.

    Compared with acetophenone, adding the methyl group breaks symmetry in the molecule, which comes into play both in physical properties and in asymmetric synthesis. We noticed that enantioselective transformations targeting this ketone often give greater yields and cleaner products than routes with less branched analogs. These attributes lower resource consumption and cut cycle times—a real benefit for both our processing teams and the chemists who rely on us.

    Meeting Industry Demands: Real Challenges, Practical Solutions

    Demand for 3-Methyl-1-Phenyl-2-Butanone keeps climbing, especially from creators of fine fragrances and pharma intermediates facing shortages of quality raw materials. As a company making this material from the ground up, we have seen the risks tied to outsourcing any part of the chain. Off-the-shelf material procured from fragmented supply lines may come with trace contaminants, erratic purity, or hidden compliance liabilities. Some players in the industry pass along these inconsistencies to customers or only catch problems when end products fail analytical checks months later.

    To address these challenges, we hold regular meetings between synthesis, purification, QC, and logistics teams—not as a formality, but because our history includes times when a missed handoff led to lost time or off-spec product. Direct lines of communication cut these problems short. Equipment specialists and chemists swap notes daily about pressure swings, solvent load profiles, and lab-scale trial outcomes. If we change suppliers for any starting material, we run verification on two pilot reactions before bringing anything online, documenting performance and purity every step of the way.

    How Stringent Controls Add Value Downstream

    Our technical staff routinely discusses with end users the headaches of running less consistent material. In one case, a client’s fragrance blend had unexpected odor drift after shipping—using their retained sample and ours, we traced the issue to a trace impurity in a lot we acquired from outside, which slipped through because of lax supplier controls. This failure cost us money and time—but drove us back to single-source production methods and tighter batch release checks. We put in a double-check system at the loading dock and instituted random checks on stored lots. Since then, product liabilities have dropped to near zero.

    QC staff run routine checks that mimic real-world formulation conditions, dissolving samples in typical solvent blends and monitoring stability over weeks—not just at release, but in the months following. This practice grew from actual customer issues: batch-release QC alone can’t guarantee stability once material runs through a blending line and hits complex matrices. We built up our storage and testing program after learning that even a trace peroxide in the product could cause a batch to fail under light stress, even after leaving our plant well within spec.

    Specific Uses Backed by Practical Experience

    3-Methyl-1-Phenyl-2-Butanone fills a specialized role across several fields. In the fine fragrance industry, it’s valued for its warm, persistent scent and its ability to anchor base notes without overpowering brighter elements. Some clients use it as a fixative, noting its effects on projection and wear time in high-end formulations. Larger fragrance houses send us specifications tied not just to GC purity but to odor consistency, forcing us to dial in batch-to-batch reproducibility. No batch leaves the plant without passing a sensory panel when destined for this sector.

    Synthetic chemists, especially those crafting chiral intermediates, prize the molecule’s distinct branching. It opens up reaction routes to enantiopure building blocks that feed next-generation pharmaceuticals, particularly ones aiming for selective GRAS status. A trusted academic partner flagged that one pathway delivered yields 15% higher with our product than with the market standard—direct feedback driving tighter control at our front end. We have rebuilt purification pipelines after seeing minor byproducts frustrate asymmetric hydrogenations, learning that fractional distillation at reduced pressure, layered with flash column cleanup, delivers the cleanest product.

    Customers using the ketone as a crossover intermediate for agricultural actives require detailed impurity profiling and documentation. Over time, we assembled a comprehensive in-house database of typical residuals, covering both organic and inorganic traces. This approach arms regulatory teams with paperwork and transparency at audit time, not just a stamped “Certificate of Analysis.” We field direct calls from customers’ own quality auditors, ensuring data flows openly and accurately.

    Continuous Improvement—Leaning on Experience, Not Just Data Sheets

    Even with efficient protocols, every production run reminds our staff that chemistry doesn’t happen in a vacuum. Traditionally, season-to-season variation in raw material quality sits at the root of process drift. We moved to supplier qualification programs that push for complete disclosure of both source and process. We don’t buy on price or catalogue alone. Chemistry remains as much about relationships as precision.

    Our batch journals track everything from color changes in precursor feeds to operator observations at every step. These notes don’t just fill compliance folders; they feed our morning roundtable sessions, shaping small tweaks in temperature ramp rates, agitation timing, and solvent selection. At one point, a minor change in solvent source produced a subtle haze in the final product, only evident on close storage trials. We retraced steps, pulled retained samples, and worked back to adjust filtration media. The result: a clear, stable product that matches client expectation throughout its shelf life.

    Technology updates play their part. We invested in upgraded analytical equipment only after trialing new detectors and confirming they could pick up trace artifacts missed by standard FID. Weekly cross-training sessions give every operator a working understanding of how synthesis, purification, and QC connect. This hands-on familiarity with both gear and raw material makes the difference between mechanistic production and genuine control over end product quality.

    Balancing Scale With Responsibility: Environmental and Safety Realities

    Producing batches large enough to support commercial demand for 3-Methyl-1-Phenyl-2-Butanone carries responsibilities that go beyond paperwork. No synthetic campaign, no matter how efficient, runs risk-free. Our crews train on prompt response to process upsets—solvent recovery systems keep emissions down, and byproduct streams get tested before any disposal. Over the last two years, we cut waste by developing reclaim protocols for spent solvents, recapturing usable material and sending less chemical out for incineration.

    One practical lesson: strict housekeeping saves both money and safety incidents. We’ve tracked near-misses involving minor leaks and traced them back to equipment fouling, which can be prevented by regular cleaning and staff vigilance. We use anti-corrosive coatings in all high-risk lines, and spend time on staff walkthroughs before every major run, ensuring the entire team has a say in safe production. Our safety officer and senior chemists review every logged incident, treating near-misses as training gold, not just bureaucracy.

    Process documentation and closed-system handling play central roles in both plant and product safety. We built an in-house digital record system that links data from operations, lab verification, and warehouse management, so any deviation pops up in real time, long before reaching the loadout terminal. Customers shared horror stories of receiving contaminated material in poorly labeled drums from other suppliers; our serial traceability means every container can be tracked from synthesis batch to end user, preventing mix-ups and allowing instant recall if needed.

    Why Direct-from-Manufacturer Makes All the Difference

    End users increasingly ask tough questions about origin, compliance, and traceability. Working as manufacturers, not middlemen, means we don’t rely on speculation—we know exactly how each batch is made, what went into it, and what left the reactor. Feedback comes direct from laboratory benches or plant floors, feeding improvement ideas directly into R&D, procurement, and process control.

    Too many intermediaries in the chain bring confusion, delay, and sometimes double handling of problems, driving up cost without adding value. Our staff answers for every spec, every certificate, and every delivery, insuring that accountability stays in-house. That level of direct stewardship builds the kind of trust that carries across years and changing regulatory landscapes.

    Innovation Comes From Experience—And Listening Closely

    Markets evolve, regulations change, and new applications for 3-Methyl-1-Phenyl-2-Butanone appear yearly. We draw our greatest insights from speaking to users at every point in their own value chains—research chemists, QA officers, regulatory staff, and formulation teams. Every challenge they share pushes us to revisit methods, ask new questions about trace chemistry, or tweak sampling protocols so that answers travel faster from our lab benches to their QA desks.

    As the global chemical landscape continues shifting, the need for transparency, control, and continuous learning only grows. Collaborative improvement, open communication, and hard-won experience form the backbone of how we make 3-Methyl-1-Phenyl-2-Butanone—not just for compliance, but for the kind of reliability that’s earned batch by batch, not assumed by certificate.