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Methyl 4-Chlorophenylacetate

    • Product Name Methyl 4-Chlorophenylacetate
    • Alias methyl_4_chlorophenylacetate
    • Einecs 219-009-9
    • 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

    768135

    Chemical Name Methyl 4-Chlorophenylacetate
    Molecular Formula C9H9ClO2
    Molecular Weight 184.62 g/mol
    Cas Number 2116-84-9
    Appearance Colorless to pale yellow liquid
    Boiling Point 257-259 °C
    Density 1.204 g/cm3
    Refractive Index 1.537
    Solubility In Water Insoluble
    Smiles COC(=O)CC1=CC=C(C=C1)Cl
    Purity Typically ≥98%
    Storage Conditions Store at room temperature, tightly closed
    Flash Point 112 °C
    Synonyms Methyl p-chlorophenylacetate

    As an accredited Methyl 4-Chlorophenylacetate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 250g of Methyl 4-Chlorophenylacetate is packaged in a sealed, amber glass bottle with a tamper-evident screw cap.
    Shipping Methyl 4-Chlorophenylacetate is shipped in tightly sealed containers to prevent leakage and contamination. Packaging complies with regulatory guidelines for chemical transport. The container should be clearly labeled, handled with care, and kept away from incompatible substances. During transit, it must be protected from extreme temperatures, physical damage, and moisture.
    Storage Methyl 4-Chlorophenylacetate should be stored in a cool, dry, and well-ventilated place, away from incompatible substances such as strong oxidizers. Keep the container tightly closed and protected from light. Store at room temperature, and avoid moisture exposure. Ensure the storage area is equipped with spill containment and clearly labeled. Follow all local, state, and federal regulations for chemical storage.
    Application of Methyl 4-Chlorophenylacetate

    Applications of Methyl 4-Chlorophenylacetate in Industrial Manufacturing

    Methyl 4-Chlorophenylacetate is an essential specialty intermediate used by manufacturers across several downstream chemical sectors. Its well-characterized reactivity and stability make it valuable for the production of advanced active ingredients, intermediates, and fine chemicals where controlled functional group transformation is critical. Below are key industrial application scenarios in which this raw material contributes to consistent process yields and end-product quality.

    1. Pharmaceutical Intermediate Synthesis for CNS Active Compounds

    Pharmaceutical manufacturers incorporate this aromatic ester as a building block in the synthesis of central nervous system (CNS) drug intermediates, particularly for selective CNS depressants and anticonvulsant active ingredients. By leveraging the compound’s chlorinated aromatic structure, process chemists achieve necessary functionalization steps during multi-stage synthesis, supporting stringent impurity profiles required for regulated markets.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211 (Current Good Manufacturing Practice for Finished Pharmaceuticals)
    • European Pharmacopoeia (Ph. Eur.) standards on API and intermediates
    • China GMP (2020 Edition)

    Typical usage ratio

    • Ranges from 0.5 molar equivalents to 2.2 molar equivalents, adjusted by stepwise transformation yield and target API complexity.

    Downstream process integration

    • Introduced at the intermediate coupling step for acylation and functionalization reactions, prior to cyclization or heterocycle construction during API ingredient assembly.

    Final product types

    • API intermediates for benzodiazepines and structurally related CNS actives
    • Purified CNS depressant precursors
    • Synthetic intermediates for new chemical entity (NCE) R&D pipelines

    2. Fine Chemical Synthesis of Fragrance Ingredients

    Manufacturers operating in the aroma chemical sector employ this methyl ester for synthesis of engineered aromatic fractions used in fragrance compounding. Its controlled release of 4-chlorophenyl moieties streamlines ester interchange, acylation, and etherification transformations, which must meet safety and olfactory purity benchmarks demanded by personal care and home care end users.

    Industry compliance standards

    • IFRA (International Fragrance Association) Standards and Guidelines
    • EU REACH Regulation (EC) No 1907/2006 for chemical safety
    • ISO 9235:2013 (Aromatic Natural Raw Materials Vocabulary)

    Typical usage ratio

    • 0.8% to 2.5% by weight of total synthetic precursor charge in fragrance base ingredient production, according to formulation volatility and desired olfactory threshold.

    Downstream process integration

    • Charged into batch reactors during ester exchange or as a limiting reactant during aromatic aldehyde synthesis stages within multi-step organic transformations.

    Final product types

    • Fine fragrance intermediates for perfumery bases
    • Aromatic aldehydes and acetals for flavor and fragrance compositions
    • Specialty odorants for detergent, fabric care, and personal hygiene markets

    3. Agrochemical Active Ingredient Manufacturing

    In crop protection chemical production, the compound serves as a crucial protected intermediate in synthetic routes toward herbicide active molecules. The para-chloro benzyl motif enables scalable functionalization—such as alkylation or hydrolysis—for actives where precise substitution patterns drive field performance and regulatory acceptance.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products (FAO/WHO Joint Meeting on Pesticide Specifications, JMPS)
    • US EPA FIFRA (Federal Insecticide, Fungicide, and Rodenticide Act) process requirements
    • ISO 9001:2015 Quality Management System for Agrochemical Manufacturing

    Typical usage ratio

    • Varying 1.0–1.7 mole equivalents, based on process pathway efficiency and conversion rates in target agrochemical syntheses.

    Downstream process integration

    • Fed as a blocking group reagent during the early functional group introduction phase or as a protected intermediate subject to subsequent de-esterification in the synthesis of target herbicides.

    Final product types

    • Herbicide actives with para-chlorobenzylamino or -phenoxy structures
    • Analytical standards for agrochemical residual analysis
    • Agrochemical intermediates for further derivatization

    4. Custom Synthesis for Photoinitiator and UV Absorber Precursors

    Specialty chemical producers integrate this methyl ester as a source of chlorinated aromatic carbon frameworks in the multi-step synthesis of photoinitiators and ultraviolet (UV) absorber intermediates. Its incorporation enables tailored substitution patterns essential for the development of advanced resins, coatings, and plastic additives meeting rigorous performance and regulatory requirements.

    Industry compliance standards

    • EU Regulation (EC) No 1272/2008 (CLP) on classification, labeling, and packaging of chemical substances
    • ISO 9001:2015 Quality Management Systems in specialty chemical production
    • RoHS Directive 2011/65/EU for restricted substances in electrical and electronic equipment

    Typical usage ratio

    • 1.2%–3.5% by total reactor charge mass for intermediate batch runs, depending on the quantum yield and targeted end-use application spectrum absorption.

    Downstream process integration

    • Incorporated at the aromatic precursor step of photoinitiator manufacture or as a chlorinated side-chain source prior to condensation/polymerization in UV absorber intermediate production.

    Final product types

    • Photoinitiator monomers for UV-curable coatings and inks
    • UV stabilizer intermediates for plastic masterbatches
    • Performance resins for automotive coatings and optical applications
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    More Introduction

    Methyl 4-Chlorophenylacetate: Direct Insights from the Production Floor

    Hands-On Introduction to Methyl 4-Chlorophenylacetate

    Crafting Methyl 4-Chlorophenylacetate has put us face-to-face with both the science and the day-to-day realities of the chemical world. As a team anchored in manufacturing, the tangible details matter to us—what goes into each batch, how precise our process can be, and what users actually experience down the line. This compound serves a specialized world. It’s not a household name, but those working in fragrance development, pharmaceuticals, and advanced materials recognize the significance of every molecule.

    Our production batch goes under the microscope each shift. There’s a rhythm to this: loading the methyl ester model—most buyers prefer the high-purity, white crystalline variation—keeping an eye on the melting point, handling the raw materials with respect for what they bring to the table. Lab work and machine checks produce the transparency that builds trust, whether providing raw compounds for synthetic routes or small-scale process chemicals for research teams.

    Why This Compound Carries Weight in the Lab and on the Line

    Not all phenylacetates are born equal. Through our production runs, the tweaks in methylation and the presence of a chlorine atom at the 4-position set this compound apart from others in the phenylacetate family. Subtle shifts in its structure don’t just show up in the numbers—they drive reactivity patterns, stability profiles, and downstream application results.

    Methyl 4-Chlorophenylacetate slots into synthesis pathways that other esters just can't handle as cleanly. In fine chemical development and pharmaceutical intermediates, the balance between reactivity and selectivity brings real benefits. Many colleagues in R&D pointed out how small changes in molecular design—such as introducing that single chloro substituent—create significant improvements in reaction sequences or product yields.

    Our Approach: Precision, Experience, and Consistency

    Off-the-shelf solutions rarely match the insights that come from operating reactors and troubleshooting the unexpected. Methyl 4-Chlorophenylacetate’s synthesis draws on over a decade of hands-on learning. Each purification cycle, every minor adjustment to solvent temperature, and every note carried forward from nightshift technicians shapes our current process. No shortcut replaces methodical, experience-based repetition.

    The finished batches undergo rigorous purity assessments using gas chromatography and HPLC. Technicians record yield and purity as a second nature. We have learned, sometimes the difficult way, that even a fractional shift in process controls—airflow over the condenser, washing timeframes—can impact crystalline formation and stability. Factoring in those operational details makes a difference that frequently goes unnoticed by distributors but matters to end-users who require chemical consistency.

    Differences that Define This Phenylacetate

    Our plant produces several methylated phenylacetates. Placing 4-chloro on the ring delivers two main differences. First, it changes the electronic distribution, making Methyl 4-Chlorophenylacetate behave differently under catalysis or in coupling reactions compared to compounds like methyl phenylacetate or methyl 2-chlorophenylacetate. Second, the chlorine’s position influences how well downstream reactions run, especially in the context of pharmaceutical or fine agroscience synthesis.

    I’ve watched research clients choose Methyl 4-Chlorophenylacetate for projects where slight increases in reactivity or predictable leaving group behavior are critical. This is not just a matter of numbers—it's about the confidence researchers gain over hundreds of syntheses when one substrate delivers reliable, phase-to-phase results. Colleagues in aroma chemical manufacturing also notice how it produces estery, subtly chlorinated notes, favoring it over similar compounds for certain fragrance constructions.

    Specifications and Handling, Drawn from Routine Practice

    Typically, our product exits the final filtration at over 98% purity. Standard deliveries arrive as fine, nearly white crystals or powder. Melting points land close to 65-69°C—a measure confirmed with every lot, since slight deviations may signal off-spec batches or the need for adjustment in the distillation step.

    We’ve found that customers working on pharmaceutical intermediates need this narrow melting range to confirm compound identity. Experienced chemists often check these simple specs before trusting the batch for synthesis.

    From a plant operator’s perspective, handling requires careful attention to temperature—avoid sustained exposure to high heat and segregate it from strong acids or bases. Storage in non-reactive, airtight containers away from direct sunlight not only preserves product clarity but also keeps its subtle aromatic profile intact. By monitoring humidity on the floor, we can prevent unwanted clumping and degradation—this reduces waste for both us and our downstream users.

    Applications: Where Utility Meets Reliability

    The reach of Methyl 4-Chlorophenylacetate goes well beyond the lab notebook. In synthesis, it steps up as a key building block for active pharmaceutical ingredients and pesticide analogues. This methyl ester finds its place in creating intermediates for drugs and research chemicals that demand high purity and predictable reactivity.

    Our partners in the fragrance sector use it to introduce understated depth—its aromatic signature is nuanced, just distinct enough to differentiate a formulation. Other analogues produce sharper, more volatile notes, but our product’s stability supports slow-release formulations and complex blends. There’s a quiet pride in hearing a fragrance chemist point out that the stability of a batch held up over months, even under challenging storage, thanks in part to the purity and handling knowledge applied on our production floor.

    Researchers value this compound for cyclization and alkylation studies. The 4-chloro group opens a different set of possibilities compared to its unsubstituted cousin, enabling routes that wouldn’t otherwise be feasible or economical. Tried-and-tested batch records have shown time and again that the right starting material means fewer failed experiments, improved yields, and tighter analytical profiles.

    How Methyl 4-Chlorophenylacetate Compares to Similar Compounds

    Direct production experience taught us the practical differences among phenylacetate derivatives. Methyl phenylacetate, for example, serves as a more basic starting point, less selective, and with a different reactivity window. Its lack of halogen often makes downstream bromination, chlorination, or further substitution necessary.

    Methyl 2-chlorophenylacetate has seen use in select syntheses, but the positional isomerism causes noticeable differences in physical properties—lower melting point, altered odor, and changes in reactivity for subsequent steps. The 4-position chlorination in our product maintains a stronger electronic withdrawal, leading to better yields in electrophilic aromatic substitution, a feature especially valuable in certain pharmaceutical intermediate production.

    In repeated head-to-head lab runs, switching out the methyl group for ethyl or using different aromatic substitutions can create higher volatility or less robust crystalline integrity. That constant scrutiny—testing batches with subtly different substitutions—lets us confirm why Methyl 4-Chlorophenylacetate earns repeat requests from critical users.

    Our Production: Challenges and Continuous Lessons

    Conversations about quality do not just happen in meeting rooms for us—they unfold on the plant floor, in the middle of early-morning shifts, between maintenance checks and final recertification steps. The main challenge remains ensuring that each lot matches not only the specification but carries the physical consistency and performance that experienced users expect.

    Scaling up from pilot to full-scale runs forced us to rework agitation systems and rethink how we approach solvent recovery. Lost yield at this stage costs not only raw material but credibility. That means monitoring temperature distribution, avoiding overconcentration, and constant team supervision rather than trusting every instrument’s output at face value. Only after many real-world cycles—maintenance hiccups, power fluctuations, seasonal humidity changes—did we refine our routines so extensively.

    Comparing each run’s HPLC outflows, noting subtleties in crystal habit, or even smelling a freshly opened drum became part of batch release. No third-party handler can understand those early warning signs as intimately as someone who's stood at the centrifuge, scraping out product or troubleshooting a jacketed vessel’s cooling phase.

    Supporting Claims: Real Results in End-Uses

    Pharmaceutical customers have reported stepwise gains in yield and purity after fine-tuning their reactions with our batches, backed up by blinded lab studies. One research team moved from 82% yield to over 90%, pinpointing the consistent melting point and low impurity signatures as instrumental in reducing their purification steps.

    Feedback loops run both ways—researchers working on novel active ingredients provide insights into batch-to-batch behavior, which then fuels internal process revisions. That collaborative approach isn’t always visible from an outside view, but the chain reaction—one good batch driving a successful project, which returns to improve our next run—has built a production culture that prioritizes shared results, not just dispatch numbers.

    In fragrance, specialists have commented on the codependence between chemical quality and the integrity of olfactory notes in complex blends. Variability in crystallinity, influenced by precise synthesis time and cooling rates, has, on occasion, led to differences in how a fragrance holds over time or under varying climate conditions. By tracking those microvariables, and feeding field feedback back into our plant procedures, we manage to keep outcomes consistent—from the first test vial to batches used in primary formulation.

    Solutions for the Problems We Face

    Every plant operation faces bottlenecks. For us, contamination turns out to be less of an issue than process drift due to aging equipment or seasonal variation. Subtleties like slightly altered solvent evaporation rates bring bigger surprises than any theoretical risk flagged by auditors. Constant training and clear documentation help address these, but practical skills—knowing how to spot the first sign of off-smell or discoloration—matters most.

    To avoid supply interruptions, we build redundancy into raw material sourcing and invest in preventive maintenance cycles. Attempts to automate everything reach a point of diminishing returns; hands-on review before final packing still catches discrepancies that analytics sometimes miss, whether that’s a slight tan cast in a batch or a microcrystalline shift.

    Our quality team has also established relationships with users’ downstream chemists, trading back every anomaly they spot in reaction, odor, or physical appearance. These conversations—sometimes informal, sometimes meticulously written—remain the backbone of truly reliable product output, especially for compounds like Methyl 4-Chlorophenylacetate, where minor variables translate to major impacts in end-use.

    What It Means to Be the Manufacturer: Accountability and Perspective

    Watching a product move from raw material to finished chemical, witnessing each part of the batch journey, ingrains a distinctive sense of accountability. The weight of each finished drum is not just a number in the ledger, but proof of all the moments work went right—or wrong. Methyl 4-Chlorophenylacetate is more than a line-item or a reagent ID. Users trust its performance through repeated campaigns, and the final outcome reflects every person who loaded, checked, tested, and packed along the way.

    From the production side, each feedback message—whether routine praise or a troubleshooting alert—rings with lessons close to home. Our collective experience with refining this compound has shaped not only product quality, but the evolution of in-plant systems, the robustness of our training, and the responsiveness of our support team. Manufacturing teaches the hard truth faster than any business review—a shortcut leads to headaches, a missed step leads to downtime, and attention to detail keeps production on track.

    Perspective for Current and Future Users

    For customers weighing the practical difference between our Methyl 4-Chlorophenylacetate and similar esters, experience from the reactor floor speaks louder than a technical data sheet. Reliable performance comes from hundreds of hours in process review, open exchange with real-world users, and working through each seasonal challenge that production throws our way.

    Our commitment unfolds in each lot—measured by purity, reactivity, and user satisfaction, not by abstract standards. End-users—the researchers crafting next-generation actives, the perfumers designing signature notes, the pharmaceutical teams demanding stepwise fidelity—push us to stay sharp and responsive. From a manufacturer’s view, delivering Methyl 4-Chlorophenylacetate isn’t just about meeting technical specifications. It’s about enabling successful outcomes, every time, through a chain of shared knowledge and concrete experience.

    Looking Forward: Responsible Practices and Continuous Advancement

    Over time, tighter regulatory oversight and increasing sophistication in both synthesis and analytics have raised the bar for chemical production. We’re not immune. Meeting compliance is part of the job, but true advancement means actively seeking improvement—testing greener alternatives for solvents, reevaluating waste management, auditing equipment, and implementing routine skills updates for the team. Cleaner product streams and safer work conditions naturally follow.

    Feedback from industry partners sensing subtle trends or shifts in their finished products prompts us to revisit even long-standing routines. This safeguards not just our reputation, but our partners’ R&D trajectories. Every improved separation technique, every better method for monitoring trace impurities, or safer workflow iteration brings incremental, practical value.

    That philosophy—a balance of hands-on know-how and willingness to learn—defines our ongoing relationship with Methyl 4-Chlorophenylacetate manufacture and supply. The result is not just a reliable product, but a foundation of trust and practical support built up, one batch at a time, where the stakes for failure or success are both real and immediate.