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1-Chlorocarbonyl-1-Methylethyl Acetate

    • Product Name 1-Chlorocarbonyl-1-Methylethyl Acetate
    • Alias Acetic acid, 1-chlorocarbonyl-1-methylethyl ester
    • Einecs 'EINECS 249-317-9'
    • 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

    602979

    Chemical Name 1-Chlorocarbonyl-1-Methylethyl Acetate
    Molecular Formula C5H7ClO3
    Molecular Weight 150.56 g/mol
    Cas Number 35180-01-9
    Appearance Colorless to pale yellow liquid
    Boiling Point 162-164°C
    Density 1.19 g/cm3
    Solubility In Water Reacts with water
    Purity Typically >97%
    Refractive Index n20/D 1.425-1.429
    Flash Point 55°C
    Storage Conditions Store in cool, dry place under inert atmosphere

    As an accredited 1-Chlorocarbonyl-1-Methylethyl Acetate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Brown glass bottle, 500 mL, tightly sealed with a PTFE-lined cap, labeled with hazardous material symbols and clear chemical identification.
    Shipping Shipping for **1-Chlorocarbonyl-1-Methylethyl Acetate** requires secure, leak-proof containers, clearly labeled according to hazardous material regulations. It should be transported under controlled temperature conditions, avoiding heat and moisture. Proper documentation, including safety data sheets, must accompany all shipments. Comply with all relevant local, national, and international chemical transport regulations.
    Storage Store 1-Chlorocarbonyl-1-methylethyl acetate in a cool, dry, well-ventilated area away from sources of ignition and moisture. Keep container tightly closed and protected from direct sunlight. Segregate from acids, bases, and oxidizing agents. Use appropriate chemical-resistant containers and secondary containment to prevent leaks. Handle under a fume hood with proper personal protective equipment to minimize exposure.
    Application of 1-Chlorocarbonyl-1-Methylethyl Acetate

    Applications of 1-Chlorocarbonyl-1-Methylethyl Acetate in Industrial Manufacturing

    As the original manufacturer of 1-Chlorocarbonyl-1-Methylethyl Acetate, we provide this specialty intermediate to select downstream sectors requiring high-purity reagents for targeted synthesis purposes. The following sections highlight key application scenarios where current industry adoption, compliance, dosage, integration, and end use are clearly established through long-term manufacturing partnerships.

    1. Active Pharmaceutical Ingredient (API) Intermediate Synthesis

    API production facilities use this intermediate primarily in acylation and esterification steps during the synthesis of specific small molecule drug candidates and licensed generic actives. Its high reactivity and targeted acyl transfer capability allow for efficient synthesis of molecular structures that require acyloxy side-chain introduction. The integration must maintain strict process containment and batch reproducibility regulations set by global agencies.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • USP, Ph. Eur., JP (as applicable for API destination markets)
    • FDA 21 CFR Parts 210/211 (if exported to US market)
    • EU EudraLex Volume 4 (for Europe)

    Typical usage ratio

    • 0.3%–1.2% (w/w relative to the core API synthesis batch; adjusted based on desired ester chain and side-group modification requirements during step-wise synthesis)

    Downstream process integration

    • Introduced in closed reactor vessels after primary amination or amidation reaction; utilized under low-moisture and controlled temperature conditions to ensure controlled acylation and minimize byproducts

    Final product types

    • Pharmaceutical actives and intermediates for anti-infectives, cardiovascular treatments, and CNS agents

    2. Agrochemical Technical Intermediates Manufacturing

    Within the agrochemical sector, technical-grade use focuses on the synthesis of certain herbicide and insecticide intermediates where controlled acyl group transfer is a key step in obtaining structure-specific activity. Plants manage hazardous nature and controlled dosing within strict limits to avoid formation of unwanted chlorinated byproducts. Long-standing environmental and residue compliance systems apply to this segment.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products (FAO/WHO/UNEP)
    • REACH registration (Europe)
    • China Pesticide Registration Requirements (Ministry of Agriculture and Rural Affairs)
    • ISO 9001 Quality Management Systems

    Typical usage ratio

    • 0.8%–2.5% (as weight percent of total batch in multi-step synthesis of technical intermediates for final agrochemical formulation; adjusted to match active ingredient yield targets and downstream purification requirements)

    Downstream process integration

    • Charged to jacketed, stirred reactors after halogen exchange reactions; utilized during acylation step before neutralization and crystallization of technical-grade pesticides or intermediates

    Final product types

    • Key intermediates for pyrethroid insecticides and select selective herbicide actives

    3. Fine Chemical Synthesis for Photographic Chemicals

    Producers of high-purity esters and organic halides for specialty photographic and imaging chemicals incorporate this molecule into targeted synthesis of acyl-based developers and coupling agents. Strict feedstock traceability and contaminant specifications govern input quality, as even minor impurities impact downstream light sensitivity and color fastness of end-use emulsions and developer solutions.

    Industry compliance standards

    • ISO 18911:2010 Image stability of photographic images
    • RoHS Restriction of Hazardous Substances (for certain EU-destined optical products)
    • ISO 9001 (Quality Management for fine chemical synthesis)

    Typical usage ratio

    • 0.5%–1.7% by weight per formulation batch, optimization based on required reactivity and purity thresholds for light-sensitive intermediate production

    Downstream process integration

    • Fed to intermediary synthesis stage following base hydrolysis or amidation, often under inert atmosphere to suppress unwanted side reactions

    Final product types

    • Photographic developer esters, film coupling agents, specialty color-forming agents

    4. Polymerization Agent in High-Performance Polymer Manufacturing

    Manufacturers of engineered thermoplastics and copolymers use this raw material as a reactive chain-capping and functional group-introducing agent, particularly during step-growth polymerization of specialty polycarbonates and polyesters. Precise control of its addition at the oligomerization phase determines final polymer molecular weight and acidity profile, impacting performance consistency in industrial, automotive, and electronics grade materials.

    Industry compliance standards

    • ISO 9001 and ISO 14001 (Quality and Environmental Management Systems)
    • UL 94 (for flame retardancy assessment of final polymer components)
    • RoHS and REACH (for polymers supplied into electronics and EU export market)

    Typical usage ratio

    • 0.2%–0.6% (weight percent relative to total monomer input, finely adjusted by inline NMR or GPC monitoring of molecular weight growth)

    Downstream process integration

    • Metered addition post-initiation and during second half of step-growth polymerization, frequently integrated via precision dosing pumps to maintain reaction homogeneity

    Final product types

    • High-performance polycarbonate resins, specialty copolyester pellets, electronics-grade molding compounds

    5. Flavor and Fragrance Ester Intermediate

    Certain flavor and fragrance houses employ this intermediate for synthesis of custom-designed esters where precise control over acyl group attachment is needed to meet international organoleptic standards and ensure batch-to-batch consistency. Downstream blending requires official food-grade compliance documentation and trace solvent residue analysis in line with international ingredient norms.

    Industry compliance standards

    • FEMA (Flavor and Extract Manufacturers Association) GRAS status
    • IFRA (International Fragrance Association) Code of Practice
    • US FDA 21 CFR 172 (for approved flavoring substances)

    Typical usage ratio

    • 0.1%–0.4% (w/w in the context of targeted flavor/fragrance ester synthesis, varied to match final impact and solvent blend characteristics as determined through gas chromatography QC)

    Downstream process integration

    • Added after initial alcohol precursor distillation; utilized in small-scale reactor vessels for esterification reactions, followed by vacuum distillation and solvent stripping

    Final product types

    • Specialty fruit esters, aroma intermediates, stabilizers for fragrance compositions
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    Certification & Compliance
    More Introduction

    1-Chlorocarbonyl-1-Methylethyl Acetate: Practical Value Rooted in Manufacturing Experience

    Direct from Our Production Line: Crafting Consistency and Reliability

    For over two decades, our team has made 1-Chlorocarbonyl-1-Methylethyl Acetate on a commercial scale. Each batch passes through a meticulous process, honed by repetition and real-world trials rather than just textbook theory. Rather than treat this molecule as a checklist item, we view it as a tool that delivers measurable value to downstream manufacturing. Our process control keeps its purity consistently above 98%, supporting those looking for a high-quality intermediate in their chemical synthesis or pharmaceutical development programs. We run frequent checks, drawing on both chromatography and titration, to prevent surprises at the back end.

    Understanding Its Practical Role

    1-Chlorocarbonyl-1-Methylethyl Acetate offers a unique combination of a reactive acyl chloride with a protected ester group, making it widely useful as a key intermediate. Whether you work in fine chemicals, active pharmaceutical ingredient (API) synthesis, or specialty polymers, you likely value both the reactivity and the selective protection that this molecule provides. Its structure often lets chemists introduce functionality at the carbonyl site while controlling hydrolysis and transesterification risks. In our experience, most customers use it to build larger, more complex molecules, taking advantage of its clean leaving group and the stability of the acetate moiety during multi-step procedures.

    Our Approach to Specifications and Quality Control

    Every specification that leaves our facility traces back to lessons learned on the production floor. Yield drift, color change, and trace impurity issues have all served as signals for us to improve. Our current specification for industrial-grade 1-Chlorocarbonyl-1-Methylethyl Acetate puts the minimum purity at 98% by GC, with water content always kept below 0.2%. Acidity and residual solvents get checked at multiple stages, not just the tail end, because a missed detail early on can cost an entire batch later. For customers with stricter needs, such as those manufacturing injectable-grade intermediates, we provide custom documentation and extended trace analysis on request. We hold samples from each lot for two years, giving partners peace of mind about reproducibility.

    Why the Model We Offer Matters

    Some chemical companies cut corners by blending lots or taking short runs from tollers, leading to inconsistencies and unexplained variances in the final product. We avoid these pitfalls by controlling each step from raw material sourcing to final filling. Our approach eliminates batch-to-batch guesswork and ensures a predictable outcome for your own synthesis, from gram-scale trial through to commercial volumes. Our facility’s reactor capacities let us meet demand spikes without rush-induced error, and our direct production translates into faster batch release and convenient supply chain planning.

    Reliable Handling and Transport

    From our own logistics lessons, we know bulk acyl chlorides present both reactivity and transport hurdles. When we pack 1-Chlorocarbonyl-1-Methylethyl Acetate, we use UN-rated containers lined with specially selected seals. This prevents leaks and minimizes moisture ingress, which can degrade the chloride function. Our shipment partners go through an onboarding process, so everyone along the chain is aware of the compound’s sensitivity. We prefer rapid, direct routes to avoid prolonged storage or handling mishaps, protecting customers’ confidence with every delivery.

    Key Differences from Closely Related Products

    Chemists often face choices between structurally similar acyl chlorides and acetates. Many ask what sets 1-Chlorocarbonyl-1-Methylethyl Acetate apart from simpler acetyl chlorides or more common pivaloyl chlorides. The answer lies in the dual functional groups present. The acyl chloride segment makes it a strong electrophile that moves reactions forward efficiently, whether forming amides, esters, or acid anhydrides. The acetate protects against unwanted cross-linking and side reactions—properties not often seen in plain acetyl chloride, which is more prone to hydrolysis and less selective in coupling reactions. Compared to t-butyl-based derivatives, 1-Chlorocarbonyl-1-Methylethyl Acetate balances both reactivity and moderate steric hindrance, reducing by-products and boosting overall yield.

    Firsthand Use Cases: Chemistry in Practice

    On the customer side, we see most demand from synthetic routes where selective carbonyl introduction is critical. Some pharmaceutical partners use 1-Chlorocarbonyl-1-Methylethyl Acetate in stepwise amide bond formation, appreciating the stability offered by its acetate group under mild conditions. In the polymer sector, formulation chemists choose it when they need a clean acyl source without the volatility and unpredictability of other low-boiling acyl chlorides. The ester moiety gives it a handle for later transformations, adding flexibility to synthetic planning. Our experience tells us that once a process engineer sees its impact on reducing rework and purifying product, they rarely return to single-function reagents.

    Troubleshooting Challenges and Shared Lessons

    While making or handling this compound, learning often comes from what doesn’t work. Acid chlorides have a notorious reputation for hydrolysis. Any trace of moisture leads to HCl gas formation, pressurizing containers and generating corrosive by-products. Early in our history, we dealt with a few such incidents before adjusting our drying protocols and container specs. Now we run full moisture scrubs across the filling line and limit stock aging, decreasing the risk to nearly zero. For partners who store this material, we recommend a dry nitrogen blanket and non-reactive stoppers; many have found this simple practice eliminates off-spec events.

    The Value of Direct Manufacturer-Partner Dialogue

    Discussions with R&D chemists, quality managers, and process development teams often reveal pain points before they become bigger problems. One generics company, struggling with drop-in product from two sources, traced their synthesis issues to variance in acid content, which only our in-house control caught during a routine audit. After a collaborative troubleshooting session, we supplied tailored lots with adjusted moisture and acid specs. Their yields improved by 7%, and they reduced downstream column filtration. These kinds of success stories build long-term confidence, far beyond the specifications you might find in a standard PDF sheet.

    Environmental and Safety Commitments on the Ground

    Making and handling acid chlorides means facing tough environmental and safety realities. Our site engineers oversee a closed-loop washing system, scrubbing off any off-gas before discharge. Water-reactive by-products don’t simply get diluted—they’re neutralized in a controlled reactor and checked for full deactivation. Our team holds quarterly drills for handling leaks or exposure events, and we have not had a reportable environmental spill in over a decade. These details matter both to end-users and to our own staff, grounding our safety culture in daily practice, not just policy or paperwork.

    Supporting Customization and Process Transfers

    Many manufacturers express concern about changing intermediates during a late process stage. We tackle this by supporting small-lot pilot programs, letting customers see fit-for-purpose results before a full switchover. With in-house analytical capability, we simulate storage or transit stress, then offer product stability reports on request. Our staff chemists help bridge technical gaps, reporting findings directly rather than filtering them through sales channels. We find this transparency builds mutual trust and avoids project delays.

    Never Underestimate the Value of Predictability

    The more complex your molecule, the more you need predictable ingredients. We base our processes around reduction of risk—from avoiding batch contamination to documenting every critical control point. A few years ago, an agrochemical company tried to switch mid-project from our product to a cheaper alternative, only to encounter a jump in side reactions during scale-up. Their troubleshooting uncovered trace impurities in the replacement batch—not detectable in quick-release tests but enough to cause trouble on a hundred-kilo scale. On returning to our material, they immediately regained batch quality. This kind of firsthand outcome reinforces why direct sourcing from vetted manufacturers matters for high-stakes synthesis.

    Traceability and Audit Support in Real-World Terms

    Customers with strict audit needs—whether for regulators or internal QA—find that direct manufacturer records streamline review and certification. We archive every batch’s analytical data, from raw sodium metal quality in the initial step to the final Karl Fischer titration for water content. When faced with tighter controls brought in by national authorities, our full documentation means paperwork aligns with what’s in the drum. This saves time during site audits and reassures both our end-users and their regulatory counterparts. We view traceability as a working habit, not a burden.

    Innovating Beyond Routine: R&D and Co-Development Stories

    Every few quarters, we collaborate on new derivatization projects. These efforts often reveal new facets of 1-Chlorocarbonyl-1-Methylethyl Acetate’s reactivity and help customers unlock efficiencies. On one recent project, a research group aimed to streamline carbamate intermediate synthesis for a novel API. Working closely, we modified our work-up to deliver an ultra-low moisture variant. This technical tweak eliminated extra drying steps at their site, saving energy and batch time. We see such co-development not as an extra service, but as part of our job. The chemical industry’s pace rewards producers who stay hands-on and continuously adapt, rather than standing still with fixed product definitions.

    Differences in Cost Structure and Availability

    As primary producers, we can offer stable, predictable supply that’s not subject to the swings seen in traded intermediates. Direct sourcing lets us absorb raw material price movement with minimal effect on delivered costs. We rarely face backorders, due to forward planning and the ability to produce just-in-time lots. This supports partners during unpredictable demand spikes. For those who have experienced bottlenecks from smaller traders or overseas resellers, our approach removes many of the headaches—especially in the current global logistics climate.

    Beyond Commodity Thinking: Trust Built by Direct Manufacturing

    Some might place 1-Chlorocarbonyl-1-Methylethyl Acetate in the “commodity” column, but our experience has shown just how much nuance matters. Two batches, matched by CAS number, can behave very differently during a scale-up or GMP qualification. Minor shifts in residual acid or acetate content affect performance. Our on-site control and end-to-end accountability mean we catch things fast, make process improvements quickly, and stand behind every delivery. For us, batch-to-batch reliability is not just a slogan—our customer feedback and consistent repeat orders prove its fundamental importance, especially in sectors where a small deviation results in major cost overruns.

    Perspective from a Manufacturer’s Floor: Continuous Learning and Real-World Feedback

    Our factory has seen its share of surprises—unexpected reactivity during hot months, shifting impurity profiles with new solvent lots, or sudden surge orders. Each episode taught us the real-world behavior of this compound, far more than lab-scale pilot work ever could. Instead of hiding challenges, we communicate them early. Years ago, we noticed a trace impurity forming during longer holding times near the filling line, which could only be resolved by shortening exposure and adjusting storage temperature. These hands-on adjustments set manufacturers apart from mere traders, keeping end-users fully informed and minimizing disruption.

    Supporting Research, Development, and Continuous Flow Applications

    Our relationship with research teams remains ongoing, as more pharmaceutical and materials science customers adopt continuous flow systems. Using 1-Chlorocarbonyl-1-Methylethyl Acetate in flow chemistry settings demands both clean product and rapid response to questions about reactivity or side products. We run micro-pilot reactors to replicate customer conditions and share notes where we see pressure, temperature, or mixing impacting yield. Our joint troubleshooting often leads to mutual improvements—either in feedstock purification or line-specific methodology. In these cases, flexibility and technical openness prove more valuable than published specs alone.

    Learning from User Feedback: Closing the Quality Loop

    Some of our best process improvements result from real user feedback. One specialty chemical firm alerted us to a faint haze forming during their late-stage work-up, which had not been flagged in our QC protocol. Co-investigation revealed a low-level interaction with a storage additive in their reactor. We responded by reviewing additive compatibility and updating our internal procedure. As a result, their next batches ran clean, and we updated our documentation to prevent similar issues for others. Direct dialogue and willingness to modify practice remain critical to both product improvement and customer confidence.

    Looking Forward: Responding to Industry Demands with Agility

    We track downstream trends and anticipate how demand for intermediates like 1-Chlorocarbonyl-1-Methylethyl Acetate will evolve. As the pharmaceutical sector shifts toward green chemistry and lower-waste workflows, we prepare to support customers with batches free of class one solvents or using updated purification. We invest in reactor upgrades and analytical tools not just for internal requirements, but to help our customers meet their own sustainability and compliance goals. Our open, experience-driven approach gives production managers, bench chemists, and executives the confidence that changing regulatory or industry standards won’t surprise them at a critical moment.

    Final Thoughts: Manufacturing Perspective in Every Drum

    Each delivery of 1-Chlorocarbonyl-1-Methylethyl Acetate contains both the molecule and the manufacturing expertise behind it. From process optimization to hands-on troubleshooting and adaptation, our team stands on experience gained daily. The end result is more than a chemical—it’s a practical tool, shaped by learning, partnership, and the practical realities of scale production. For anyone looking to strengthen their own synthesis or secure reliable process outcomes, working directly with experienced manufacturers transforms an ordinary intermediate into a strategic asset.