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1-(2-Chlorophenyl)Acetone

    • Product Name 1-(2-Chlorophenyl)Acetone
    • Alias chloroephedrone
    • Einecs 205-685-2
    • 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

    764334

    Iupac Name 1-(2-chlorophenyl)propan-2-one
    Molecular Formula C9H9ClO
    Molar Mass 168.62 g/mol
    Cas Number 835-26-9
    Appearance Colorless to pale yellow liquid
    Boiling Point 120-122 °C at 15 mmHg
    Density 1.17 g/cm³ (approximate)
    Solubility In Water Low
    Synonyms 2-Chlorophenylacetone, 2-Chloro-1-phenyl-2-propanone
    Smiles CC(=O)CC1=CC=CC=C1Cl
    Inchi InChI=1S/C9H9ClO/c1-7(11)6-8-4-2-3-5-9(8)10/h2-5H,6H2,1H3
    Refractive Index 1.565 (approximate)
    Pubchem Cid 160812
    Flash Point 90 °C (approximate)

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

    Packing & Storage
    Packing 500 mL amber glass bottle with tamper-evident cap, labeled "1-(2-Chlorophenyl)Acetone," includes hazard warnings and batch number.
    Shipping 1-(2-Chlorophenyl)Acetone is shipped in compliance with hazardous materials regulations. It is securely packaged in sealed, chemical-resistant containers to prevent leaks and contamination. Proper labeling and documentation accompany the shipment, with handling instructions and relevant hazard warnings. Shipping may require ground or approved courier services, depending on local, state, and international laws.
    Storage 1-(2-Chlorophenyl)acetone should be stored in a tightly sealed container, away from heat, light, and sources of ignition. Keep it in a cool, dry, and well-ventilated area, segregated from incompatible materials such as oxidizing agents and strong acids. Ensure proper chemical labeling and store in accordance with local regulations and institutional safety protocols. Always use appropriate personal protective equipment when handling.
    Application of 1-(2-Chlorophenyl)Acetone

    Applications of 1-(2-Chlorophenyl)Acetone in Industrial Manufacturing

    1-(2-Chlorophenyl)Acetone serves as a significant intermediate across several industrial sectors, specifically where targeted chlorinated acetophenone derivatives are needed in controlled, high-purity processes. Our material meets rigorous consistency demands, bolstering the manufacturing reliability for specialty downstream products.

    1. Pharmaceutical Active Ingredient Synthesis

    In regulated pharmaceutical synthesis, 1-(2-Chlorophenyl)Acetone enters as a key intermediate for manufacturing select APIs and their precursors, including some restricted central nervous system actives. Operators integrate this raw material into multi-step reactions, requiring stringent process validation and multi-point in-process controls. Typical batch records specify dedicated containment protocols, with quality release only after thorough impurity profiling. Manufacturers leverage its chemical reactivity to achieve precise aryl-ketone incorporation, optimizing yield in complex coupling or reductive alkylation pathways relevant to the intended API. Formulation groups rigorously adjust for minimal residual solvent, ensuring compliance with global pharmacopoeia limits before proceeding to downstream isolation or tableting.

    Industry compliance standards

    • Good Manufacturing Practice (GMP) guidelines (ICH Q7)
    • USP-NF and Ph. Eur. monographs for finished APIs
    • ICH Q3A/B impurity requirements
    • FDA and EMA registration filings

    Typical usage ratio

    • Reaction mixture: 0.86 to 1.13 molar equivalents depending on target compound structure and yield optimization based on stoichiometry from development scale batches

    Downstream process integration

    • Charged early during ketone alkylation steps
    • Isolated post-reaction via solvent extraction or chromatographic purification
    • Quality checked by LC-MS/HPLC pre-release

    Final product types

    • Pharmaceutical active pharmaceutical ingredients (APIs) for clinical or commercial use
    • Small-molecule CNS intermediates

    2. Agrochemical Intermediate Production

    Major agrochemical manufacturers value 1-(2-Chlorophenyl)Acetone as a precursor for selective herbicide and fungicide molecules. Processing facilities frequently deploy this compound in Grignard, acylation, or halogen-exchange reactions to construct advanced heterocyclic systems. Operators measure input ratios precisely, aligning feedstock quantities with target pesticide batch size and regulatory method validation data packages. Post-synthesis, plants remove excess starting material and side products using multi-step solvent washes. Final product release always follows maximum residual level (MRL) compliance verification tied to global crop protection standards.

    Industry compliance standards

    • FAO/WHO maximum residue limits (MRL) and guidance specifications
    • ISO 9001:2015 for quality management
    • Country/regional PPP (plant protection product) registration dossiers (e.g., US EPA, EU REACH, China ICAMA)
    • OECD product characterization protocols

    Typical usage ratio

    • Batch synthesis: 0.90–1.05 molar equivalents relative to primary reactant; adjusted to maintain reaction completeness while limiting waste streams

    Downstream process integration

    • Introduced during the core condensation or substitution step in pesticide synthesis
    • Monitored for conversion rate by in-process GC-FID/HPLC
    • Subjected to multi-stage purification prior to formulation into technical-grade pesticide concentrates

    Final product types

    • Herbicide technical concentrates
    • Fungicide active ingredient intermediates

    3. Aroma and Fragrance Ingredient Manufacturing

    Flavors and fragrances companies exploit the unique chlorinated structure of this compound in the preparation of specialty aroma molecules, particularly for fine fragrance base notes and certain industrial deodorants. Formulation chemists map usage based on targeted scent profiles and IFRA (International Fragrance Association) safety guidelines. The material typically enters selective condensation, reduction, or Friedel-Crafts acylation routes, with QA/QC focusing extensively on organoleptic purity and allergenicity limits. Finished aroma blends must adhere to precise trace content levels, and manufacturers routinely monitor for compliance with international labeling and traceability requirements.

    Industry compliance standards

    • International Fragrance Association (IFRA) Standards
    • REACH/Toy Safety European Standard (EN 71-5) for toy perfumes
    • ISO 9235: Natural aromatics versus synthetics
    • Good Manufacturing Practice (IFRA/IOFI GMP)

    Typical usage ratio

    • Formulation: 0.1–2.5% by weight in aroma chemical syntheses; precise ratios depend on the desired fragrance intensity and regulatory thresholds

    Downstream process integration

    • Added as a core reactant during aroma intermediate creation
    • Purified by fractional distillation or preparative GC instrumentation
    • Quality confirmed by GC-olfactometry and allergen screening pre-blending

    Final product types

    • Fine fragrance intermediates
    • Industrial and homecare deodorant bases

    4. Specialty Dye and Pigment Intermediate Manufacturing

    Producers of high-performance dyes integrate this chemical into the synthesis of specialty aryl-ketone pigment intermediates, used in segments such as plastics coloration, fiber dyeing, and specialized printing inks. The reactivity profile supports tailored nucleophilic aromatic substitution and condensation chemistries under precisely controlled temperature profiles. Technicians record and verify weight-to-weight ratios, ensuring pigment precursors meet downstream chromaticity and lightfastness benchmarks. Quality teams analyze for chlorinated by-products, ensuring final outputs stay within regulatory impurity limits for polymers and textiles. Final pigment concentrates or masterbatches then supply customers in the plastics, fiber, and printing market.

    Industry compliance standards

    • ISO 9001:2015 for quality management
    • OEKO-TEX Standard 100 (class I–IV) for textile applications
    • EN 71-3 Safety of toys: Migration of certain elements
    • EU Ecolabel chemical requirements for dyes and inks

    Typical usage ratio

    • Dye intermediate batch: 1.00–1.35 molar ratios based on target pigment molecular design and reactivity

    Downstream process integration

    • Combined with nucleophile or dye precursor in batch reactors
    • Reaction endpoint controlled via UV-vis/LC spectrophotometry
    • Intermediates isolated and further condensed as required for final pigment type

    Final product types

    • Color pigment intermediates for plastics compounding
    • Synthetic dye precursors for textile fibers
    • High-purity ink colorants
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    Certification & Compliance
    More Introduction

    Understanding 1-(2-Chlorophenyl)Acetone: Beyond the Basics

    Long hours in the chemical plant have given us an appreciation for chemicals that never seem to complicate a process more than necessary. 1-(2-Chlorophenyl)Acetone isn’t the most glamorous name, but its value shows up every time our synthesis lines run without a hitch. When we fill drums with this crystalline intermediate, it demonstrates that practical molecular design can make direct contributions to the quality of downstream products. There’s always talk in the market about innovation, but this particular compound strikes a strong balance between reliability and reactivity. With plenty of years tweaking its production, our understanding comes from a hands-on perspective, not just product brochures.

    What Sets 1-(2-Chlorophenyl)Acetone Apart

    Chemists on our team keep 1-(2-Chlorophenyl)Acetone at the front of our inventory because it stands up to demanding reaction conditions without losing integrity. In daily operations, conversion rates matter more than theoretical yields on paper. We see few side reactions and fewer headaches in downstream separations, which means better results for end users. The presence of the ortho-chloro group gives selectivity during condensation reactions. Compared to unsubstituted phenylacetone, the chloro substituent influences both electron distribution and steric profile, giving rise to useful differences in product structure.

    We produce this acetone derivative with non-stop vigilance on process controls. There’s no shortcut around maintaining air-free conditions and tracking every exotherm in real time. Our batches get tested across multiple points by in-lab GC-MS and HPLC, not just a single pass at the end. Doing so avoids passing on contaminants further down the chain. Anyone who’s ever tried to clean up a batch with unknown byproducts understands why these choices matter. Consistency in purity isn’t a sales slogan; it decides if you spend the night at the plant fixing problems or if you get to go home on time.

    Molecular Details and Why They Matter

    1-(2-Chlorophenyl)Acetone’s CAS registry confirms its unique identity, but practical experience with this molecule tells more than numbers. Its molecular formula and weight differ slightly from standard analogues by only a single chlorine, but that presence changes the game in a big way for condensation and alkylation chemistries. Through sustained R&D, we’ve seen that these small differences in reactivity let customers adjust process temperatures and solvents, opening new windows for lab and plant operators looking for a competitive edge.

    Every lot we ship matches rigorous NMR and IR identity checks—experience in the lab teaches that you pick up on subtle shifts that mean a new impurity could be lurking. Keeping standard melting and boiling ranges consistent only comes from hands-on process tuning. With every completed batch, our staff learns more about how pressure, temperature, and solvent choice affect the isomer content or potential formation of byproduct chloroketones. That knowledge helps us refine not just our own synthesis, but our recommendations when asked for real-world feedback by end-users.

    Why Usage Context Dictates Success

    Customers ask if 1-(2-Chlorophenyl)Acetone can be swapped directly into places where plain phenylacetone once stood. Our answer comes from days spent running different trials, not from what the literature claims. That extra chlorine adds both bulk and new electronic effects, which most noticeably show up during subsequent coupling steps. In our own research and pilot runs, shifting over to this molecule makes a clear difference when looking for regioselectivity in ring closures or Friedel–Crafts-type alkylations.

    Pharmaceutical companies value this because it offers greater control over substitution patterns, especially in complex target molecules. Agrochemical users get a different benefit: increased robustness against unwanted side reactions, which results in fewer waste streams during scale-up. Fine chemical producers mention how the predictable fragmentation patterns during analytical testing make tracking impurities less complicated. Hearing about these downstream benefits reinforces why our focus on reproducibility at the manufacturing stage isn’t wasted effort.

    Comparing Against Structural Relatives

    It’s easy to presume that adding a single chlorine atom does little, yet direct process comparisons repeatedly illustrate the opposite. 1-(2-Chlorophenyl)Acetone outperforms unsubstituted phenylacetone when you demand selectivity in electrophilic aromatic substitution. We’ve learned which catalysts pair best through direct comparison—Lewis acid-catalyzed condensations using the chlorinated version often run at slightly lower temperatures, which directly cuts energy consumption in larger plants.

    Competing compounds like 1-(4-chlorophenyl)acetone land in a similar ballpark, but differences in reactivity and downstream suitability become obvious when developing scale-up protocols. Our customers highlight fewer complications in workup and purification steps, and bring up improved shelf life under suitable storage. These findings aren’t just statistics; they shape batch yields and waste disposal needs in real-world facilities. As a team rooted in chemical manufacturing, comparatives only matter if they mean fewer production stops and less waste troubleshooting.

    The Day-to-Day in Manufacturing: Challenges and Solutions

    Synthesizing 1-(2-Chlorophenyl)Acetone requires precise temperature profiles. Any deviation invites side products or batch loss. We rely on robust jacketed reactors, regular probe calibrations, and constant monitoring—not because we like gadgets, but because every missed detail tends to show up in yields and product color. Running through scale-ups, leftover chlorinated intermediates presented the toughest challenge. Rather than push them through the system, we invested in dedicated separation stages and solvent recovery, which let us isolate pure product without forcing downstream partners to deal with reprocessing issues.

    Handling raw materials stands near the top of the safety list—chlorinated benzenes and acetones exhibit volatility, and trace water kills selectivity during formation. We structure every batch to minimize downtime, practicing pre-dries with molecular sieves rather than assuming supplier solvents arrive at spec. For storage, glass-lined steel tanks have justified their cost. The risk of steel-catalyzed decomposition sits fresh in our minds after one batch in the early years developed off-odors by the end of the week. It’s these experiences that shape process discipline.

    The Role of Analytical Chemistry and Process Feedback

    Lab analytics anchor every decision in our plant workflows. Pre-shipment samples see more than just a single-technique check; our QC teams pull retention data, run stress tests, and confirm structural assignments using high-resolution spectra. Some partners only expect a basic purity readout, but our data set covers major and minor impurities, moisture by Karl Fischer, and traces of any unreacted starting materials. Applying these routines costs extra effort, but pays off when customer processes run without needing extra adaptation or error chasing.

    Tracking stability has kept our shelves in order during long-term stockholding. We found that 1-(2-Chlorophenyl)Acetone keeps best under dry nitrogen at moderate ambient temperatures, avoiding both sunlight and humid zones of the warehouse. We report impurity levels not only at shipping but again after set storage intervals, so end users plan their own storage and re-testing schedules. Every time a partner calls with a new requirement, feedback from our data logs reinforces or fine-tunes our internal controls.

    Regulatory and Environmental Considerations

    Responsible chemical production takes regulatory exposure seriously. Regulatory changes affect everything from permissible emission levels to tracking precursor shipments. Our facility aligns batch output with the current global and local statutes—compliance checks are more than paperwork since any deviation halts batch release. Our environmental controls focus on minimizing volatile organic compound emissions. Continuous scrubber monitoring tracks real-time outflow, since even trace releases of chlorinated solvents or ketones cause regulatory headaches and real health risks to local communities.

    Waste mitigation strategies extend from the shop floor to post-delivery. By-products from 1-(2-Chlorophenyl)Acetone synthesis get collected separately, and partnerships with chemical recyclers turn a portion of this material back into feedstock. Handling safety ties directly into our local permits; staff run through emergency containment and neutralization drills quarterly. Nobody in manufacturing underestimates the risk of chlorinated material in ground or water supplies, so mistakes inform stricter protocols and investments in better waste handling.

    Partnering with Customers: Experience from the Field

    Some of the most meaningful product improvements have come from honest exchanges with customers using 1-(2-Chlorophenyl)Acetone in new projects. Plant chemists, R&D scientists, or small-scale formulators call in with specific process challenges that textbooks don’t always cover. We respond with more than standard specs; our technical team relies on hands-on test runs, comparing process output under different catalyst or solvent schemes. That habit of feedback and improvement builds trust and leads to repeat partnerships.

    Adaptation stories surface every year—customers testing our material in heterocycle syntheses have reported new yield plateaus after switching from unchlorinated analogues. We’ve worked side by side through several scale-up days, troubleshooting live, adjusting feed rates, and reviewing NMR peaks together. These joint efforts erase the boundary between producer and user, focusing everyone on final product quality. Developing specifications that flex for slight process variation, rather than clinging strictly to theoretical ideals, lets more customers succeed without extra cost or rework.

    Ongoing R&D and Process Optimization

    Continuous process optimization remains one of our core strengths as a manufacturer, not just a supplier. We invest in every stage—from selection of chlorination agents and custom reactor design, through in-house process simulation tools that predict product distribution at scale. The lab group logs every experiment, cataloging catalyst performance and impurity profiles. Real-world runs always uncover new routes to improve product stability, manage energy costs, and sharpen the overall environmental footprint.

    Emerging green chemistry standards challenge us to question historic approaches. Experiments have focused on alternative chlorination strategies to reduce halogenated by-products. Adopting semi-batch operations and staged-reactor systems have slashed waste and tightened process controls. Reducing solvent load and maximizing recovery rates mean customers down the line handle less hazardous waste, and we run leaner with every finished lot. Every R&D effort ties directly to improvements customers recognize—either in more predictable running or easier workups at their own facilities.

    Looking Forward: Safe and Reliable Delivery

    Getting 1-(2-Chlorophenyl)Acetone to users safely closes the loop between manufacturing and real-world application. Pack-out teams emphasize sealed, contamination-proof drums, backed by full chain-of-custody documentation and hazard labeling that reflects experience, not just regulations. Our logistics partners understand the unique shipping risks accompanying chlorinated organics; training sessions keep everyone up to date. We inventory under tightly controlled conditions, giving customers confidence in shelf life for both immediate and long-term projects.

    Tracking and traceability have changed in recent years as regulatory agencies push for digital batch monitoring, and we’ve modernized accordingly. End-to-end batch records give full trace history, so any process anomaly gets traced within hours, not days. In the field, this means customers access technical support backed by real-time process insights instead of just a warranty clause. Our own staff treat shipment accuracy and technical transparency as non-negotiable.

    Practical Lessons from Decades on the Line

    Chemical manufacturing always carries surprises, and our time with 1-(2-Chlorophenyl)Acetone has taught us lessons that shape every new batch. Quality habits—double-checks, honest failure tracking, and routine process audits—define how consistently our product performs in partner labs. From fixing leaks on midnight shifts to debugging unexpected impurity peaks, we’ve seen improvements form in small, hard-won steps.

    We stay rooted in measurable outcomes. Customer feedback loops have inspired small tweaks that made significant differences. Managing raw materials, finessing reaction timers, and tripling effort in analytical verification all deepen reliability, not just for this acetone derivative, but for every future compound on the roster. Openness to new uses, new process adjustments, and honest reporting mean manufacturers and clients stand a better chance of building processes with fewer stoppages, safer workdays, and better long-term outcomes.

    Our relationship with 1-(2-Chlorophenyl)Acetone comes from the shop floor, not just catalogs. That’s what allows us to keep product quality high for every drum and every application, year in and year out.