|
HS Code |
559332 |
| Chemical Name | 3'-Chloroacetophenone |
| Cas Number | 99-02-5 |
| Molecular Formula | C8H7ClO |
| Molecular Weight | 154.6 g/mol |
| Appearance | White to off-white crystalline powder |
| Melting Point | 53-56°C |
| Boiling Point | 263°C |
| Density | 1.22 g/cm³ |
| Solubility In Water | Slightly soluble |
| Flash Point | 128°C |
| Refractive Index | 1.564 |
| Smiles | CC(=O)C1=CC(=CC=C1)Cl |
As an accredited 3'-Chloroacetophenone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 100g amber glass bottle with a secure screw cap; labeled “3'-Chloroacetophenone,” hazard symbols, lot number, and supplier details. |
| Shipping | 3'-Chloroacetophenone is shipped in tightly sealed containers, complying with regulations for hazardous chemicals. It should be packaged to prevent leaks and labeled according to transport guidelines. During transit, use suitable secondary containment and ship via approved carriers. Store away from incompatible substances, heat, and moisture to ensure safety and maintain chemical integrity. |
| Storage | 3'-Chloroacetophenone should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from direct sunlight and sources of ignition. Keep the container away from incompatible substances such as strong oxidizing agents. Ensure it is labeled properly, and access is restricted to trained personnel. Follow all relevant local, state, and federal regulations for chemical storage. |
Applications of 3'-Chloroacetophenone in Industrial ManufacturingAs a direct manufacturer, we supply 3'-Chloroacetophenone for established industrial sectors where its unique molecular structure brings functional value through precise formulation, tight process control, and compliance-managed integration. Below, we describe primary downstream applications, covering standards requirements, technical usage insights, production role, and typical finished goods for each use case. 1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredient (API) SynthesisPharmaceutical manufacturers use 3'-Chloroacetophenone as a core building block for synthesizing key intermediates in numerous API production routes, especially those requiring substituted ketones for heterocyclic ring construction or as acylating agents. This material functions in early to mid-stage synthesis steps, acting as an acyl source or structural framework for active molecules. Its use must align with filing documentation and process validation protocols to ensure chemical traceability, impurity control, and compliance with regulated impurity thresholds in APIs. Industry compliance standards
Typical usage ratio
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2. Synthesis of Agrochemical IntermediatesAgrochemical formulation plants rely on 3'-Chloroacetophenone as a foundation in the batch synthesis of key herbicide, pesticide, and fungicide actives as well as intermediate molecules forming part of patent or off-patent product lines. Process engineers select this raw material when demanding controlled reactivity and precise steric effects, particularly for producing substituted benzene derivatives that expand the spectrum of agrochemical mode-of-action classes. Dosing and traceability remain tightly regulated based on residue studies, with QA sampling in each intermediate step. Industry compliance standards
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3. Precursor in Synthesis of Tear Gas FormulationsDefense and security sector chemical plants utilize 3'-Chloroacetophenone as a critical precursor for producing CS and CN-type non-lethal riot control agents. These applications require tightly controlled reaction conditions and absolute documentation for regulated handling. The compound undergoes condensation or halogenation, followed by blending with dispersant carriers and stabilization materials to ensure batch-to-batch reproducibility while observing controlled substance regulations and hazardous chemical protocols at every stage. Industry compliance standards
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4. Intermediate in Synthesis of Specialty Fragrance PrecursorsFine chemical producers employ 3'-Chloroacetophenone as an intermediate in the multi-step creation of aromatic compounds used in specialty perfumery and flavoring. Its chloro-substituted ring provides a scaffold for further alkylation or reduction, enabling the development of complex musky and green notes. This segment demands high purity, controlled impurity profiles, and color standards. QC units routinely screen for residual solvents and byproducts before downstream process units carry out final steps. Industry compliance standards
Typical usage ratio
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Producing chemicals on a large scale demands more than basic mixing or batch reactions. In our experience as a manufacturer, the backbone of any successful production run lies in the quality and consistency of each starting material. We find that 3'-Chloroacetophenone stands out among aromatic ketones for its reactivity and niche role across multiple sectors. Known by its IUPAC name, 1-(3-chlorophenyl)ethan-1-one, this compound delivers time and again for researchers and process chemists who require both selectivity and reliability in their syntheses.
Consistent batches require carefully managed synthesis routes. Our approach begins with secure sourcing for 1-(3-chlorophenyl)ethan-1-one, followed by purification steps designed to minimize byproducts. Trace impurities may not seem significant at first; after years of experience we have seen minor differences in starting material quality spiral into larger headaches for downstream reactions. Our analytical team monitors every lot with GC-MS verification and melting point confirmation so our partners avoid these costly disruptions.
The aromatic scaffold of 3'-Chloroacetophenone makes it an attractive starting point for both academic research and bulk synthesis in the pharmaceutical and agrochemical sectors. Its electrophilic carbonyl at the para-position from the halogen produces a subtle electronic effect chemists can rely on. Modifications at other positions on the phenyl ring often alter reactivity and selectivity, which is why we put special attention into source material traceability and analytical rigor.
The specifications stem from what our end-users have asked us to refine over years of continued supply. Each production lot offers a purity of at least 99 percent by area, as judged by GC. The substance appears as colorless to pale yellow crystals, with a distinct, crisp melting point around 53 to 55°C. Storage and handling feel straightforward, as stability under standard plant conditions rivals other halogenated acetophenones.
Fine-tuning the synthesis often requires a predictable nucleophilic profile. 3'-Chloroacetophenone carries its halogen on the meta-position, subtly influencing downstream chemistry—especially in Friedel-Crafts acylation or Suzuki-Miyaura coupling reactions. Judging by repeated customer feedback, competing products with ortho or para substitution tend to show either too much steric hindrance or unwelcome side reactions. The meta-chloro placement achieves a balance between accessibility for catalysis and sufficient ring activation, which increases overall process efficiency.
Smaller differences in melting range, crystal habit, or residual solvent content make a noticeable difference in large runs. We have optimized our final recrystallization and drying protocols to keep control samples representative of production-scale output. When production chemists contact us about reactivity or material performance, they are not looking for vague assurances; they come expecting a reproducible lot, with properties matching published standards.
The specific role of 3'-Chloroacetophenone in fine chemical synthesis makes it more than just a routine intermediate. We hear from our clients regularly about the benefits of using this compound as a precursor in heterocyclic chemistry, for example in synthesizing benzoxazoles, indoles, or related pharmacophores. Its defining blend of electronic effects allows for directional substitutions that other positional isomers do not replicate. This often leads to higher yields and fewer side products in multistep processes.
The pharmaceutical sector values compounds that simplify process steps. The carbonyl function on the ethanone moiety remains reactive while the meta-chlorine resists undesirable overacylation or rearrangement. This profile becomes indispensable during late-stage functionalizations, such as those in non-steroidal anti-inflammatory or central nervous system active drug candidates. Each kilogram supplied can represent weeks shaved off program timelines, provided that the compound stands up to scale.
Agrochemical developers look for intermediates like this when seeking selective synthons with the flexibility to accommodate additional heteroatom incorporation. The fine adjustment made possible by the meta-halogen motif opens the door for diversified library synthesis—a key part of finding new candidates for pest or weed control molecules. It’s a rare case where positional isomerism makes a dramatic difference in synthetic streamlining.
Polymers research and materials science teams have also shown interest in this compound, usually as a monomer precursor. The clean, predictable substitution pattern and moderate cost structure often tip the balance when evaluating new routes for specialty resins or performance additives.
Not every 3'-Chloroacetophenone shipment is created equal, and through repeat manufacture, we have learned which details tip the balance for commercial users. Some manufacturers chase down high batch volumes at the expense of careful purification; we balance both. By sticking to smaller, well-controlled batch reactors, we limit unpredictable byproduct formation and keep close tabs on each lot through in-process analytics.
Market trends show occasional surges in lower-grade imports. These often show lower purity levels and broader melting point ranges. Process chemists end up spending valuable time on downstream purification or troubleshooting. The feedback from our clients proves that investments in additional analytical steps pay back: batches that meet strict assay and impurity specs speed up both small and large scale synthesis, reducing costs from troubleshooting unexpected side pathways.
Direct production keeps us nimble. Trends in regulatory standards and safety documentation keep tightening, and since we control the synthesis all the way through to shipment, we update packaging and documentation rapidly to reflect evolving requirements. Maintained in-house expertise offers technical support based on hands-on laboratory experience, rather than relying on boilerplate answers from traders. For new applications, our development chemists review compatibility with related functional groups or recommend alternative halogenation positions that align with stability or downstream integration.
3'-Chloroacetophenone consistently turns up in projects where other acetophenone derivatives fall short. Subtle as the isomeric difference seems, a switch from meta- (3’) to para- or ortho- halogen placement causes significant changes in both chemical and biological results. In practice, para-chloroacetophenone (4’-isomer) often shows reduced reactivity under palladium-catalyzed coupling, while ortho-substitution introduces both steric hindrance and increased side product formation.
In analytical runs, even tiny differences in isomeric distribution may hamper the identification or purification of custom analogues. Our facilities achieve a consistently high selectivity during the electrophilic aromatic substitution step of chlorination, which points back to careful reactor design and monitoring protocols. Years of direct feedback have helped us tweak process parameters for maximal meta selectivity and minimal contamination from other position isomers.
We made the choice early on not to blend isomer streams, even during periods of elevated raw material cost. It seemed at the time like a challenge, but direct production control permits rigorous fractionation and targeted product isolation. The result for end-users comes in the form of predictable reactivity, so process R&D avoids late surprises from isomeric impurities. Pharmaceutical developers, in particular, have commented on smoother downstream steps because of higher feedstock selectivity.
Having handled thousands of kilograms across several facilities, practical concerns around storage and logistics matter just as much as laboratory specs. We stick to packaging formats that minimize contact with light and moisture, based on empirical stability data—not just standard practice. Low volatility and limited hygroscopicity mean this item remains workable in standard warehouse conditions, but customers moving to industrial scale should always consider a clean, dry space and secure secondary containment.
Documentation and labeling systems link every drum or bag with the specific lot analysis, so users can trace any anomalies rapidly. Our support teams field plenty of practical questions around shelf life and compatibility with downstream solvents, acid, or base. The answers always come from real-world storage and bulk transfer experience, not generic data sheet references. Regular field checks and mock recalls ensure that the material remains traceable from plant loading area to customer facility—not just on paper.
Supply chain upsets—from solvent procurement challenges to unplanned regulatory reviews—reveal why real manufacturing insight matters. Flexibility to scale up or slow down production, tweak delivery times, or accommodate shifting documentation norms only comes from hands-on familiarity with the material. Prompt, direct shipping, paired with reliable analytics, lets customers adapt their schedules without production loss.
Chemical handling responsibility goes beyond meeting batch purity cutoffs. Safety teams insist on up-to-date SDS and compliance paperwork before materials hit plant floors, so every batch ships with current documentation aligned with both local and international standards. Years of audit participation taught us to maintain transparent raw material traceability, which helps during internal reviews and regulatory updates.
3'-Chloroacetophenone does not fall into classifications for highly toxic or difficult-to-handle substances for most users, but we still encourage good practice. Direct handling with gloves and goggles forms standard plant procedure. Handling instructions specify well-ventilated areas, both for operator comfort and long-term systems integrity. For high-throughput systems, containment and air monitoring devices reduce risk further. Most of these practices reflect lessons gathered from the plant floor, rather than off-the-shelf recommendations.
Environmental responsibility means examining process steps for possible waste minimization or recycling opportunities. We feed back production-side solvent and reagent consumption patterns into ongoing reviews for greener process alternatives. This sometimes leads to tweaks in upstream synthesis to reduce chlorinated waste or solvent emissions. Our development team keeps track of emerging guidance around chemical discharge, keeping up with both regional and international frameworks. These incremental steps help support both long-term plant viability and better compliance confidence for our partners.
Supplying 3'-Chloroacetophenone over decades has revealed constant, often subtle pressure points—from raw material availability to unexpected downstream side reactions in customer processes. Customer feedback loops help us refine batch sizes, change reaction times, or adjust packaging formats. In more than one case, a customer’s process hiccup led us to revisit our purification train, discovering a tiny impurity that went under the radar with older test protocols.
A direct line to the manufacturing floor means batches can be made or held based on real usage forecasts rather than market guesswork. This minimizes both overproduction waste and under-supply risks. Technicians get involved early in understanding changes to reaction parameters or scale-up requirements, so the ship-to-plant connection remains practical, not theoretical.
Academic users have occasionally reached out about custom derivatives or unusual purity needs; our chemists work directly with them to clarify which grade or isomer they actually need. This back-and-forth saves resources on both sides, and through these collaborations, we have explored new applications, from catalyst testing to reference compound synthesis. The lessons we gather travel back to the main production line for future QC refinements.
Working with 3'-Chloroacetophenone highlights the tangible advantage of direct, on-site experience with every shipment. Maintaining deep control over analytical checks, synthesizing only high-selectivity batches, and keeping the supply chain transparent provide meaningful stability for partners navigating complex research or commercial landscapes.
End-users demand more than commodity-grade chemicals. They look for reliability, batch-to-batch reproducibility, and rapid support when variables change—whether driven by regulation, process scale, or new applications. Our history with this compound reflects practical lessons learned on the floor, and each improvement comes from active conversation with those who rely on it, not theoretical optimization.
Continued development will follow new directions in sustainable production, smarter waste management, and customized specifications. Our model prioritizes experience-driven solutions, because the stakes in chemical manufacturing always extend beyond the next delivery or production lot. Whether for senior scientists looking to scale campaigns, or process teams navigating supply chain bottlenecks, our commitment centers on sharing real insight, not just specifications. That approach lets our partners keep their projects moving—and keeps us learning.