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Cyclopentylpropionyl Chloride

    • Product Name Cyclopentylpropionyl Chloride
    • Alias Cyclopentylpropionyl chloride
    • Einecs 'EINECS 211-742-6'
    • 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

    723278

    Productname Cyclopentylpropionyl Chloride
    Casnumber 6287-50-9
    Molecularformula C8H13ClO
    Molarmass 160.64 g/mol
    Appearance Colorless to pale yellow liquid
    Boilingpoint 120-122°C at 20 mmHg
    Density 1.03 g/cm³
    Refractiveindex 1.455-1.457
    Purity Typically >98%
    Solubility Reacts with water, soluble in organic solvents
    Storagetemperature Store at 2-8°C
    Flashpoint 99°C
    Chemicalclass Acyl chlorides

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

    Packing & Storage
    Packing Packaged in a 500 mL amber glass bottle with a secure screw cap, featuring a hazard label and tamper-evident seal.
    Shipping Cyclopentylpropionyl Chloride is shipped as a hazardous material, typically in sealed, corrosion-resistant containers to prevent moisture and air exposure. Containers are clearly labeled with appropriate hazard symbols and handled according to international transport regulations. Transport occurs under controlled temperature conditions, ensuring safety and chemical stability during transit.
    Storage Cyclopentylpropionyl chloride should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from moisture. Keep it away from heat, direct sunlight, incompatible substances such as strong bases, alcohols, and oxidizers. Store under inert atmosphere (e.g., nitrogen) if possible. Protect from physical damage and label containers clearly. Use secondary containment to prevent spills.
    Application of Cyclopentylpropionyl Chloride

    Applications of Cyclopentylpropionyl Chloride in Industrial Manufacturing

    Cyclopentylpropionyl Chloride supports a range of synthesis steps for pharmaceutical intermediates, specialty agrochemicals, and select fragrance ingredients. As a direct manufacturer, our focus stays on integration into advanced organic synthesis pipelines, strict batch traceability, and technical optimization for downstream processors. The following sections detail verified industry applications, highlighting unique requirements and practical information for each scenario.

    1. Synthesis of Active Pharmaceutical Ingredient (API) Intermediates

    This acyl chloride functions as a critical acylating agent during the assembly of designated nitrogen-heterocycle intermediates in controlled pharmaceutical manufacturing. Our product enters the targeted amidation and esterification stages, providing a reactive site for subsequent substitution and cyclization conducted under cGMP environments. Customers adopt this input for bridging steps in central nervous system and cardiovascular compound lines, integrating it with established reaction sequences for API intermediate construction. Chromatographic and impurity control aligns with strictly regulated pharmaceutical supply chains.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP) General Chapters for Chemical Intermediates
    • European Pharmacopoeia (Ph. Eur.) Requirements for Excipients and APIs
    • China GMP Certification for Pharmaceutical Raw Material Production

    Typical usage ratio

    • 0.8–1.2 molecular equivalents relative to amine or alcohol reactant, adjusted for exact intermediate reaction stoichiometry to avoid over-acylation.

    Downstream process integration

    • Introduced in a controlled acylation reactor at the intermediate stage, following nitrogen base addition and anhydrous conditions, monitored by in-process HPLC to determine end-point for subsequent reaction quenching.

    Final product types

    • Piperidine- or pyrrolidine-based pharmaceutical intermediates
    • Key building blocks for synthetic analgesics
    • Precursor molecules for antihypertensive agents

    2. Agrochemical Active Ester Synthesis

    Within agrochemical manufacturing, downstream processors incorporate this intermediate during the acyl chloride stage to introduce cyclopentylpropionyl groups to aromatic or heteroaromatic nucleophiles for advanced ester synthesis. QC focuses on minimizing residual chloride and optimizing conversion rates for herbicide and insecticide molecule frameworks subjected to field regulatory review. Our production ensures consistency for customers formulating high-purity pesticide esters targeted at resistant pest populations.

    Industry compliance standards

    • FAO/WHO Specification and Evaluations for Agrochemical Technical Materials
    • REACH Regulation (EC No 1907/2006) for Manufacturing and Import in the EU
    • ISO 9001 Certified Quality Management Systems for Agrotech Production
    • US EPA Registration Guidance on Pesticide Technical Grades

    Typical usage ratio

    • 1.0–1.3 mol equivalents relative to alcohol or phenol nucleophile, slightly excess to drive quantitative esterification without leaving excess starting acid chlorides, which require post-reaction scrubbing steps.

    Downstream process integration

    • Added after solvent selection and base addition in batch or continuous-flow reactors; undergoes immediate nucleophilic substitution followed by aqueous washing and neutralization before product isolation.

    Final product types

    • Specialty herbicide esters
    • Synergist intermediates for insecticidal formulations
    • Cyclopentyl-derivative active compounds for crop protection blends

    3. Advanced Fragrance Ingredient Synthesis

    Manufacturers of aroma chemicals employ this specialty acid chloride in the Friedel–Crafts acylation of aromatic substrates for the creation of novel musky and woody olfactory notes. It finds precise dosage when customers demand clean cyclopentyl moiety introduction free from unwanted byproduct notes in large-scale perfumery compound production. Formulators leverage tightly specified purity, ensuring compliance with global fragrance safety standards and IFRA-restricted substance validation throughout the entire production batch.

    Industry compliance standards

    • International Fragrance Association (IFRA) Guidelines on Restrictive Use
    • EU Regulation (EC) No 1223/2009 on Cosmetics
    • GHS/CLP Labeling and Handling Provisions
    • ISO 9235:2013 for Aromatic Raw Materials

    Typical usage ratio

    • 0.7–1.4 molar equivalents to the aromatic substrate; adjusted based on desired acylation mono- versus di-substitution and minimization of side reactions in olfactory note profiling.

    Downstream process integration

    • Introduced at the acylation step, after AlCl3 or related Lewis acid catalyst loading, followed by purification by distillation or fractional crystallization to provide odor-pure intermediates for subsequent blending.

    Final product types

    • Musky/woody aroma compounds
    • Fragrance intermediates for fine perfume bases
    • Specialty olfactory additives for personal care and home fragrance

    4. Custom Synthesis of Specialty Polymers

    Polymer industry customers integrate this acyl chloride as a chain-modifying reagent in the step-growth synthesis of cyclopentyl-functionalized polyesters and polyamides. Technical users require detailed batch COA documentation supporting integration into R&D and pilot-scale reactors. This intermediate ensures the controlled insertion of 3-cyclopentylpropionyl functionality, enabling end-use processors to tune thermal stability and mechanical profile of advanced specialty polymers. These polymers meet application-specific standards for non-food technical markets.

    Industry compliance standards

    • ISO 9001 for Quality Management in Polymer Synthesis Plants
    • ASTM D883 Standard Terminology for Plastics
    • EU Regulation (EC) No 1907/2006 (REACH) – Monomer Registration/Reporting
    • TSCA Inventory Compliance for US Polymer Commercialization

    Typical usage ratio

    • 0.5–1.0 molar ratio based on target polymer backbone sites for functionalization; customized to control distribution and maintain processable molecular weight range.

    Downstream process integration

    • Metered injection into closed reactor systems following diol or diamine substrate addition; chain propagation occurs under inert atmosphere until conversion monitoring (e.g., by FT-IR) prompts quenching and downstream extrusion or casting.

    Final product types

    • Cyclopentyl-modified engineering polyamides
    • Specialty polyesters for technical film applications
    • Cyclopentyl-functional oligomer building blocks
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    Certification & Compliance
    More Introduction

    Cyclopentylpropionyl Chloride: From Production Floor to Practical Chemistry

    Understanding What We Make: A Chemist’s Perspective

    Every batch of Cyclopentylpropionyl Chloride (CPPC) tells a story about technical meticulousness, real-world challenges, and a constant push for reliable quality. In our decade of manufacturing specialty acid chlorides, CPPC earns special attention on the production floor. With a molecular structure built around a cyclopentyl moiety joined to a propionyl chloride group, this compound catches the eye of those developing new pharmaceuticals and custom intermediates. Its molecular formula: C8H13ClO lets us trace purity and verify batch consistency through each production cycle. The CAS number 3328-12-9 is a reference point for those who already track this compound in their R&D pipelines.

    Industrial synthesis of CPPC requires careful orchestration. We start with high-purity cyclopentylcarboxylic derivatives and carry out chlorination reactions under anhydrous conditions. Corrosive byproducts must be contained, and the purity target usually sits above 98% by GC, with colorless to pale yellow liquid as the expected outcome. Batch after batch, our reactor setups have taught us to respect the small parameters that keep this molecule stable—air-tight systems, chilled condensation, and strict exclusion of water. Each operator understands how fuming acid chloride vapors behave and adjusts glassware and safety protocols accordingly.

    We log each step, not because paperwork makes things safer, but because in acid chloride chemistry, small mistakes don’t stay small for long. By investing in dedicated glass-lined reactors and rigorously training our team, we continue to maintain reaction selectivity and minimize exothermic runaway risks. Raw material chain-of-custody checks mean every drum of CPPC we ship shares a direct trace from initial reagents to sealed product container.

    How Cyclopentylpropionyl Chloride Gets Used in Our Customers' Hands

    In practical chemistry labs, CPPC acts as a building block for more than just academic curiosity. Ask anyone in custom organics production. This reagent sparks interest because it adds the cyclopentylpropionyl group efficiently to nitrogen and oxygen nucleophiles. Amides, esters, and substituted ketones all emerge from judicious use of CPPC as an acylation agent. When working through medicinal chemistry requests, we see growth in demand from companies screening novel cyclopentyl-substituted compounds for biological activity. Small molecule libraries, API precursor syntheses, and analog optimization—all depend on scalable, reliable access to rarer acid chlorides like CPPC.

    Pharmaceutical teams value CPPC’s unique reactivity profile. The cyclopentyl group introduces ring strain and spatial effects, giving downstream products characteristics unattainable using linear propionyl chloride or bulky aromatic variants. In the field, the physical properties matter. CPPC’s boiling range—typically between 110-115°C at reduced pressure—lets chemists manage distillations and avoid hydrolytic degradation common in more sensitive acid chlorides. For scale-up or process chemistry, these real-world handling advantages shave time off development timelines.

    On the pilot scale, solvent compatibility becomes a deciding factor. CPPC dissolves readily in halogenated hydrocarbons, ethers, and some aromatic solvents. Each route designer who’s tried to template a new functional group across a molecular scaffold knows that acyl chloride selection can define an entire project’s feasibility. Unlike more volatile or polymerization-prone analogues, properly stabilized CPPC resists premature hydrolysis even at several liters scale with overhead agitation.

    Agrochemical firms and fine chemical makers utilize CPPC to tailor molecular frameworks for actives and intermediates. The cyclopentyl moiety introduces distinct stereochemical bulk, which can create effective barriers to unwanted metabolic breakdown in both plant and veterinary applications. We’ve seen project teams consider CPPC to replace straight-chain variants when seeking improved environmental fate or pharmacokinetic profiles, particularly for molecules flagged as too flexible or too quickly metabolized in vivo.

    Differentiating Cyclopentylpropionyl Chloride from Other Acid Chlorides

    Comparing CPPC to other acid chlorides, the distinction runs deeper than just the atomic arrangement. Take propionyl chloride, benzoyl chloride, and pivaloyl chloride—each sees widespread use, but their reactivity, safety profile, and application space diverge sharply from CPPC. Linear acid chlorides like propionyl chloride introduce simple alkyl groups, resulting in less steric hindrance and faster nucleophilic addition rates. This can be a blessing during routine synthesis, but for projects requiring controlled selectivity, CPPC’s cyclopentyl group offers a moderating influence.

    Benzoyl chloride, with its aromatic core, brings both increased stability and unique reactivity to the table. Aromatic acid chlorides sometimes suffer from poor solubility or slower reaction kinetics, especially in hindered systems. CPPC splits the difference: it introduces a non-aromatic cyclic ring, balancing reactivity with physical ruggedness. Researchers interested in modifying enzyme substrates or tuning ligand frameworks find this feature compelling.

    Another practical difference emerges during product workup. Routine acid chlorides often undergo rapid hydrolysis, leading to pungent byproducts and yield losses. In hands-on experience, CPPC resists unintended reaction during short exposures to ambient humidity, granting lab staff extra flexibility as they set up columns or transfer liquids. This is no license to ignore safety or inert atmosphere standards, but years in manufacturing have shown that small increments in reagent robustness translate into cost savings and smoother pilot runs.

    Pivaloyl chloride carries impressive steric bulk, but often introduces handling hazards thanks to its volatility and the risk of rapid polymerization. CPPC, thanks to its cyclic structure, doesn’t suffer the same level of volatility risks or monomer instability. Stability improvements simplify container selection and storage conditions on both the manufacturer side and at customer warehouses.

    Sourcing Quality: Manufacturing Lessons Learned

    In manufacturing CPPC, supply consistency and purity drive repeat orders more than any marketing claim could. Technicians know that a batch containing low-level side products like cyclopentanecarboxylic acid or excess unreacted starting material will upend a process run down the supply chain. We couldn’t afford to ignore trace contaminants, so we developed closed-loop feedback between our QA lab and plant floor. Gas chromatography and NMR screening on every lot is not just a box to tick, but an ongoing risk mitigation effort. We keep our downstream partners informed with clear documents, typically providing GC trace data, water content analysis, and confirmation of physical properties before shipment.

    We don’t approach CPPC as a commodity. Each lot must achieve uniform reactivity, which is only possible by tuning chlorination ratios and maintaining absolute dryness from start to endpoint. On one occasion, a minor leak in our condenser introduced water vapor, resulting in a sub-standard batch. Immediate corrective action saved the lot, but the lesson endures: precise control over every system parameter makes the difference between a trusted supplier and unreliable stock.

    Long-term experience shapes the way we store and ship CPPC, too. Exposure to trace moisture or UV light alters the compound over days. Glass bottles with PTFE-lined caps, dry nitrogen blanketing, and rapid, tracked logistics allow us to reassure buyers that the contents arriving at their door remain unchanged from the moment they left our filling line.

    Practical Risk Management for Users and Makers

    No acid chloride deserves casual handling, and CPPC is no exception. Rigorous attention to PPE—gloves, goggles, full shielding—minimizes human exposure and keeps teams safe during sampling and transfer. The vapor irritates mucous membranes, and contact with skin leads to burns typical for acid chlorides. Our staff receives ongoing hazardous material training and works with acid scrubbers active throughout the extraction process.

    Each drum we fill carries signs of corrosive hazard. We stay up to date on regulatory requirements, share revised SDS sheets with every client, and encourage buyers to discuss new safety protocols or disposal questions. Our in-house engineering team invented a drum coupling system that allows customers to draw CPPC directly into closed reactors, minimizing atmospheric exposure. The quieter incident log is proof that small changes in transfer technology can make a noticeable difference in safety outcomes.

    Those less familiar with specialty acid chlorides may not grasp the value of production traceability or fail-safes in delivery. Our years of shipping to both domestic and export markets anchor our focus on compliance—clear labeling, lot tracking, and adjusted shipping routes during adverse weather keep our products in spec and on schedule. No shortcuts or improvisations exist when sending hazardous goods—a lesson reinforced by every shipment sent and every customer inquiry handled on a Friday afternoon.

    What Sets Cyclopentylpropionyl Chloride Apart in Custom Chemistry

    Out of hundreds of specialty acid chlorides running through our plant, CPPC stands out for the breadth of its synthetic utility. Its unique balance between steric protection and reactivity leads to downstream products unavailable through common alternatives. Medicinal chemists value how it inserts conformational rigidity, providing differentiated analogs during SAR (structure-activity relationship) studies. Agrochemical designers deploy it when patenting new pesticide scaffolds, often crediting the cyclopentyl unit with improvements in target selectivity or soil behavior.

    Our long-term partners have recounted production bottlenecks fixed by switching from linear acid chlorides to CPPC. Investigating a medicinal analog, one R&D group doubled their desired yield using CPPC to provide steric selectivity in an amidation step, avoiding side reactions that plagued their previous protocol. These successes, while confidential in detail, confirm the reputation CPPC holds in advanced synthesis applications.

    We advise anyone considering CPPC to approach it as a specialty tool. Properly understood, its quirks and advantages can make or break a project. Factory-trained support staff field technical questions about solubility issues, co-solvent selection, and scale-up compatibility on a weekly basis. Many first-time buyers, unsure about reaction exothermicity or required base quench conditions, call us for hands-on troubleshooting. Decades making and selling CPPC have taught us that expert technical assistance isn’t icing on the cake—it’s essential to project success.

    The Role of Cyclopentylpropionyl Chloride in Today’s Chemical Industry

    Regulatory agencies worldwide increase scrutiny on hazardous substances, tightening acceptable limits for acid chlorides in end products. As manufacturers, we continually adjust our quality systems and invest in better process controls to align with changing standards. CPPC doesn’t face some of the tougher volume restrictions imposed on chlorinated aromatics, but customers count on us to stay ahead of new monitoring rules. Our plant operators track every update from chemical control agencies and preemptively adjust batch management, anticipating emerging compliance needs—whether in documentation, contamination thresholds, or waste handling.

    Sustainability matters. For years, acid chloride producers carried a reputation for process waste and fume challenges. In our shop, emission treatments and closed-loop solvent management minimize off-site impact. Cyclopentylpropionyl chloride production generates hydrochloric acid vapors; our scrubbers capture them and feed the acid stream to neutralization tanks, supplying a chemical plant that runs with as little environmental legacy as possible. Routine audits by third parties reinforce our internal drive to leave no corner unattended. Customers and regulators alike welcome the attention to clean chemistry, and we see repeat business as organizations put greater scrutiny on upstream supplier practices.

    Waste minimization turns into tangible efficiencies. Our practices reduce raw material losses, lower utility consumption, and shave downtime. CPPC doesn’t get produced as a sideline while we focus on bigger volume commodities—it earns its place through quality, stable supply, and responsiveness to feedback from some of the world’s pickiest customers.

    Anticipating Challenges, Shaping Solutions

    Every year brings supply chain shifts. Raw materials tighten; shipping routes face new scrutiny. Making CPPC has meant keeping adaptable, whether it’s qualifying new sources of cyclopentyl starting materials or developing alternative synthetic routes when regulatory risk shifts. Our technical staff work closely with procurement, sourcing sustainable feedstocks whenever possible and conducting full analytical verification with every substitution.

    Transport and storage challenges never disappear in acid chloride manufacturing. Logistics partners trained in hazardous goods management understand the importance of unbroken temperature control and humidity exclusion. Missteps aren’t just costly—they become learning opportunities. Routine shipments cross climate zones, revealing weaknesses in thermal insulation or sealing. We focus on batch stability, monitoring every outbound drum for signs of contamination or pressure variation, and promptly recall or replace any lot falling below specification.

    Customer education continues as an essential part of our everyday. Sales staff share handling tips, describe correct dilution protocols, and document past troubleshooting steps to help new users avoid common mistakes. More direct experience with the chemistry and logistics of CPPC makes all parties better equipped, safer, and more efficient.

    Why Transparency and Support Matter

    Our plant’s approach to Cyclopentylpropionyl Chloride starts and ends with accountability. Customers don’t just buy a barrel; they expect certainty—about reactivity, supply timelines, and what’s not in the drum. Whenever a batch approaches our minimum purity threshold, managers sign off on reprocessing before it leaves the line. Customers see the results—clear, repeatable reaction profiles and minimal downtime over the years.

    We actively encourage partners to communicate concerns about storage, shipment, or application. Our technical team doesn’t hide behind formulas or jargon—they deliver plain answers backed by real evidence and years of hands-on problem-solving. Feedback flows both ways. Adjustments and clarifications inform our next round of process improvements.

    The chemical industry rewards reliability. By putting experience ahead of empty assurances, by measuring, testing, and listening, we’ve carved out a reputation as dependable producers of Cyclopentylpropionyl Chloride. Honest, science-driven answers continue to inform our every interaction. Through decades of combined chemical manufacturing, we’re reminded each day why the fine details of making and supporting specialty reagents matter.