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Cis-2-Hydroxy-3,4,5-Trimethyl-2-Cyclopenten-1-One

    • Product Name Cis-2-Hydroxy-3,4,5-Trimethyl-2-Cyclopenten-1-One
    • Alias Methylcyclopentenolone
    • Einecs 629-497-2
    • 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
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    Specifications

    HS Code

    309582

    chemical_name Cis-2-Hydroxy-3,4,5-Trimethyl-2-Cyclopenten-1-One
    molecular_formula C8H12O2
    molecular_weight 140.18 g/mol
    CAS_number 4753-74-6
    appearance Colorless to pale yellow liquid
    boiling_point 110-112°C at 10 mmHg
    density 1.04 g/cm³
    flash_point 105°C
    solubility Soluble in organic solvents such as ethanol and ether
    refractive_index 1.488–1.493
    odor Sweet, caramel-like
    storage_conditions Keep container tightly closed in a cool, well-ventilated area
    synonyms Cis-homofuraneol, 3,4,5-Trimethyl-2-cyclopenten-1-one, 2-Hydroxy

    As an accredited Cis-2-Hydroxy-3,4,5-Trimethyl-2-Cyclopenten-1-One factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The packaging is a 25-gram amber glass bottle with a tightly sealed cap, clearly labeled with the chemical name and safety information.
    Shipping Cis-2-Hydroxy-3,4,5-Trimethyl-2-Cyclopenten-1-One is shipped in tightly sealed containers, protected from moisture, heat, and direct sunlight. It must be handled as a chemical substance, complying with relevant transport regulations and labeling requirements. Appropriate documentation accompanies the shipment to ensure safety and regulatory compliance during transit.
    Storage Store **Cis-2-Hydroxy-3,4,5-Trimethyl-2-Cyclopenten-1-One** in a tightly sealed container, away from direct sunlight and sources of heat or ignition. Keep in a cool, dry, and well-ventilated area, separate from oxidizing agents and acids. Ensure the storage space is clearly labeled and restrict access to trained personnel to prevent accidental exposure or contamination.
    Application of Cis-2-Hydroxy-3,4,5-Trimethyl-2-Cyclopenten-1-One

    Applications of Cis-2-Hydroxy-3,4,5-Trimethyl-2-Cyclopenten-1-One in Industrial Manufacturing

    Cis-2-Hydroxy-3,4,5-Trimethyl-2-Cyclopenten-1-One is utilized as an advanced chemical intermediate across several high-value production sectors. We supply this raw material directly from our own facilities to ensure strict batch quality, process consistency, and repeatable integration into downstream manufacturing. Below, we detail key industrial applications and compliance guidelines for this specialty compound.

    1. Fine Fragrance Compound Synthesis

    Perfumery houses and aroma chemical manufacturers leverage this ingredient in the formulation of specialty aldehydic fragrance bases. Its cyclopentenone core introduces musk and floral notes with thermal and oxidative stability during high-shear mixing or vacuum distillation. Manufacturers control addition during the heart note blending stage, enabling nuanced odor profiles in premium perfumery concentrates and specialty aromas for toiletries.

    Industry compliance standards

    • IFRA Code of Practice (applicable limits per finished fragrance category)
    • EU Regulation (EC) No 1223/2009 (Cosmetics)
    • ISO 9235:2021 (Aromatic raw materials)
    • REACH Regulation (EC) 1907/2006 for registered substances

    Typical usage ratio

    • 0.05% to 0.8% of total fragrance concentrate; adjusted based on desired musk intensity and regulatory threshold for end-use type (e.g., fine perfume vs. deodorant)

    Downstream process integration

    • Introduced during the controlled blending of aroma raw materials under nitrogen atmosphere to avoid oxidation, before compounding into alcohol or oil carriers and filtering prior to packaging

    Final product types

    • Eaux de parfum
    • Luxury body sprays
    • Cream-based perfumed lotions
    • Personal wash fragrance concentrates

    2. Flavor Additive Intermediate for Food Ingredients

    Food ingredient manufacturers apply this compound to synthesize distinct, thermally stable flavor notes, especially in designer meat or savory analogs. Its molecular structure supports Maillard-type flavor systems while maintaining clarity and shelf life during high-temperature cooking or spray-drying. Addition is regulated and monitored for dosage, ensuring compliance and sensory reproducibility.

    Industry compliance standards

    • FCC (Food Chemicals Codex) Monograph references
    • EU Flavouring Regulation (EC) No 1334/2008
    • JECFA food additive safety assessments (where applicable)
    • US FDA 21 CFR Part 172 (Food Additives Permitted for Direct Addition to Food for Human Consumption)

    Typical usage ratio

    • 3 ppm to 60 ppm in finished food flavorings; optimal range determined via GC-MS batch analysis and flavor panel evaluation per formula

    Downstream process integration

    • Added post-reactive flavor precursor blending and before top note adjustment during vacuum evaporation or microencapsulation for powdered food flavorings

    Final product types

    • Processed meat flavor enhancers
    • Soy-based burger flavors
    • Snack seasoning blends
    • Instant soup flavor bases

    3. Pharmaceutical Synthesis Intermediate

    Pharmaceutical manufacturers utilize this compound as a key building block in the development of selective active pharmaceutical ingredients (APIs). Its functional groups enable site-selective derivatization for targeted molecular scaffolds, especially in anti-inflammatory and central nervous system drug research. Controlled addition during synthesis requires strict process validation and documentation to comply with pharmaceutical regulations.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP/NF General Chapters (United States Pharmacopeia)
    • European Pharmacopoeia Monographs (where applicable for process intermediates)
    • 21 CFR Part 210/211 (US cGMP for finished pharmaceuticals)

    Typical usage ratio

    • Variable, typically 0.5 to 1.2 molar equivalents relative to coupling reactant; determined by desired scaffold yield and downstream purification requirements

    Downstream process integration

    • Incorporated via stepwise addition in multi-stage synthesis, often in presence of protecting groups or organometallic reagents, followed by high-vacuum distillation and intermediate crystallization

    Final product types

    • API intermediates for non-steroidal anti-inflammatory drugs (NSAIDs)
    • Small molecule CNS agents (in research and development pipelines)
    • Selective ligand precursor compounds
    • Chiral catalyst scaffolds

    4. Specialty Resin and Polymeric Modifier Production

    Leading manufacturers of performance polymers and specialty resins incorporate this cyclopentenone-based molecule as a structural modifier to improve resin flexibility, impact resistance, and thermal color stability. Its keto-hydroxy functionalities promote co-polymerization or chain termination benefits, especially in prepolymer synthesis for high-gloss, high-solid coatings and adhesives. The input level is tightly specified and monitored to control finished material properties.

    Industry compliance standards

    • ISO 9001:2015 Certified Quality Management for production lots
    • ASTM D256 (Standard Test Methods for Impact Resistance of Plastics)
    • RoHS Directive 2011/65/EU for restricted substances in end-use polymer systems
    • REACH Annex XVII (Polymer ingredient restrictions for EU applications)

    Typical usage ratio

    • 0.3% to 2.5% by weight relative to prepolymer resin formulation; input rate adjusted based on target viscosity, cure profile, and downstream mechanical testing feedback

    Downstream process integration

    • Dosed during resin prepolymerization, under controlled temperature and pH, prior to chain extension or cross-linking; subsequent sampling for QC/gel permeation chromatography

    Final product types

    • Automotive clear coat binders
    • Impact-modified epoxy adhesives
    • Specialty UV-curable print coatings
    • Flexible synthetic varnish bases

    5. Fine Chemical Intermediate for Agrochemical Synthesis

    Agrochemical producers employ this substrate for constructing advanced crop protection agents. Its substituted cyclopentenone ring supports synthesis of herbicide and fungicide intermediates with engineered stability and specific bioactivity profiles. It is applied during key-stage condensation reactions under inert atmosphere, supporting both pilot-scale and commercial production under sector-specific controls.

    Industry compliance standards

    • FAO/WHO technical guidelines for pesticide active ingredients
    • OECD Principles of Good Laboratory Practice
    • ISO 17025 (Testing and calibration laboratories for agrochemical QC)
    • REACH Regulation (EC) 1907/2006 substance registration

    Typical usage ratio

    • Usually 0.65 to 1.3 molar equivalents per synthetic step, subject to process development scaling and target yield in the development of actives or adjuvants

    Downstream process integration

    • Added in early-stage synthetic pathway, typically via Grignard or Michael addition, with temperature and pH control to optimize conversion and minimize byproduct formation

    Final product types

    • Selective herbicide intermediates
    • Fungicidal active ingredient precursors
    • Insecticide scaffold chemicals
    • Specialty agrochemical additive hosts
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    Certification & Compliance
    More Introduction

    Cis-2-Hydroxy-3,4,5-Trimethyl-2-Cyclopenten-1-One: Manufacturer’s Perspective

    Real Challenges and Achievements in Fine Chemical Production

    As a team that’s worked in chemical manufacturing for over two decades, we know the hurdles and rewards in bringing advanced molecules from the bench to industry scale. Cis-2-Hydroxy-3,4,5-Trimethyl-2-Cyclopenten-1-One is one such specialty compound that stands out not just for its unique structure but for the opportunities and challenges it presents across fine chemical, fragrance, and pharmaceutical sectors. Let’s break down what this molecule offers, why its production isn’t straightforward, and what sets it apart from other cyclopentenones or related intermediates.

    Understanding the Molecule: Structure and Real-World Relevance

    This compound features a cyclopentenone core with three methyl groups clustered around the 3, 4, and 5 positions and a hydroxyl group hanging off the 2-position, locked into a cis configuration. Such functionalized cyclic ketones attract attention for their reactivity, flavor nuances, and as chemical building blocks. The methyl arrangement creates steric effects, making substitution reactions specific and limiting side-product formation—a clear benefit when refining downstream applications.

    What matters in an industry setting is the predictability and purity such a profile brings. Unsubstituted cyclopentenones and their trans-isomers have broader reactivity and lower selectivity in fragrance compositions or pharma intermediates. Our variant narrows down byproducts and batch variability due to locked cis-stereochemistry. Synthesis routes for this molecule require careful temperature and catalyst control, and the choice of solvent can mean the difference between consistent yields and costly rework.

    From Synthesis Floor to Finished Barrel: The Value of Direct Production

    As manufacturers, we appreciate firsthand that a clean supply chain starts at the reactor. There’s no middlemen padding cost or muddling lot histories. We keep a trained eye on every batch, running GC and NMR at multiple steps—not just to chase certificates but to keep each lot as close to 100% as possible. Here, we avoid residual solvents that muddy formulations in end-user processes. An off-the-shelf product from distributors may bear the same name, but without direct control, you never really know the contamination risk or consistency batch to batch. For users in fragrance creation or sensitive pharmaceutical synthesis, that difference is not academic—it’s risk or reward in each run.

    The Demands of High Specification: Why End-Use Dictates Process

    End users in research and industrial settings drive specification demands up. Low water content matters for those feeding cyclopentenones directly into further condensation or reduction steps; even trace moisture can throw a reaction or lead to hydrolysis issues. We routinely run Karl Fischer titrations and limit handling steps to reduce atmospheric contact. Fragrance formulating requires not only molecular purity but exclusion of trace organics that could taint aroma. Our customers bring these challenges to us, pushing us to use only the cleanest glassware and to monitor levels of minor isomers beyond basic HPLC standards.

    Our process incorporates fractional vacuum distillation as a final polish for every batch. The tight cut window ensures only the target cis isomer hits the drum while minimizing thermal decomposition. It’s labor-intensive, but it eliminates the tailing impurities we’ve seen in samples produced elsewhere. Industries moving from pilot to production demand evidence of this consistency. Past experience with other substituted cyclopentenones—where uncontrolled process leads to broad isomer mixes—taught us the value of strict distillation controls.

    Spotting the Differences: Not All Cyclopentenones Are Created Equal

    A side-by-side of our product with more common cyclopentenones, especially trans-isomers or those lacking methylation at key positions, shows striking differences. The cis-2-hydroxy arrangement alters reactivity in aldol and Michael reactions. The triple methyl groups block certain undesired reactive sites, granting more predictable outcomes in multi-step synthesis. In flavor and fragrance, this selectivity translates to brighter, more focused aromatic notes. Other cyclopentenones often include a harsher, less nuanced character, while the methylated cis version imparts deeper, rounder notes valued by skilled perfumers.

    From our own comparison trials, formulating with less-substituted or isomerically impure cyclopentenones leads to more batch variation, instability during long-term storage, and complications in downstream purification. Our approach, shaped by years of feedback from users, builds on this accumulated experience: push for the precise isomer, keep byproduct content below 0.2%, and never relax standards even under deadline.

    From R&D Requests to Commercial Scale: Adapting to Customer Needs

    The story of our involvement with cis-2-hydroxy-3,4,5-trimethyl-2-cyclopenten-1-one didn’t begin with bulk sales. Years ago, researchers in a leading fragrance lab approached us about achieving a specific isomer purity that wasn’t on the market. The challenge wasn’t limited to making a few grams under academic conditions, but realizing reproducible scale-up. Early batches looked clean at small scale, but as we reached 100-liter reactors, we found subtle side reactions emerging. This insight, the kind that only comes from direct production, reshaped our purification protocols and taught us that scale-up is rarely a linear path. Lasting partnerships grew from this transparency and iterative process.

    Unlike larger, commodity-focused players, we don’t see the benefit in mass-producing a catch-all profile that fits many uses only fitfully. Each client’s application—whether in chiral pharmaceutical synthesis or bespoke aroma formulation—calls for its own approach to trace impurity removal or stabilization. Our process recipes reflect these lessons, with feedback loops driving ongoing improvements. Over the years, we’ve learned adjustments at the solvent removal stage, changing column packing in fractional distillation, and tweaking catalyst amounts can change everything about the final product’s usability and shelf life.

    Regulatory Considerations: What Compliance Demands, Process Ensures

    As regulations around complex organics tighten, especially for applications in pharma or food-contact materials, trace contaminants become a hot-button concern. Third-party-sourced material leaves gray areas that compliance teams dread. Our hands-on management of every step—from raw chemical vetting to batch record retention—gives certainty. We’ve worked through regulatory audits where proving solvent recycling steps and purity documentation made the difference between approval and shipment delays. Each documentation step isn’t just paperwork for us—it’s insurance against lost trust and business.

    Our investment in analytical resources isn’t limited to passing certifications. Analytical repeats are run not only at batch release but at stability intervals, as some clients store this compound for months or years before use. If an impurity emerges late, we take that learning straight back to our process, tightening controls or swapping out any raw input that falls short. It’s the kind of closed-loop, practical quality assurance that only direct production can support.

    Technical Barriers and Practical Solutions: It’s More Than Just Mixing and Heating

    Cyclopentenones, especially those with multiple methyl groups and precise stereo requirements, challenge even experienced chemists. Methylation, for example, brings with it both steric and electronic complications. At the 3, 4, 5 positions, the methyl groups crowd the ring, and pressure or temperature changes can swing selectivity to unintended byproducts. During hydroxylation at the 2-position, reagent choice must avoid over-oxidation and preserve the ring integrity.

    We’ve found that conventional base- or acid-catalyzed methods won’t cut it for this molecule. Years of process trials led us to settle on a protected intermediate approach, using silyl or acetal groups at key steps, stripped off only after the main framework is intact. This limits migration or ring-opening side reactions. Some suppliers take shortcuts here and risk more isomeric contamination, particularly hard to spot if analysis stops at TLC or basic HPLC. Our labs go further, using 2D NMR to check for cryptic impurities that might elude simpler tests.

    Thermal control is non-negotiable. Even a two-degree swing at final distillation can change the impurity profile and knock long-term stability. We maintain strict batch logs, built over years of iteration, that record minute process shifts so we can trace root causes instantly. Other producers may not go to this granularity, but we find it critical for repeat orders and for troubleshooting customer feedback.

    Application Pathways: Listening to the Market

    We pay attention to where this molecule finds the most impact. In our own experience, advanced fragrance compounds benefit most from consistency and purity. The methyl-crowded, cis-hydroxyl profile boosts tenacity and fixes aroma notes effectively, avoiding the off-odors some other cyclopentenones introduce as they degrade. Perfumers searching for roundness and warmth, especially in sophisticated base notes, value this product as a key ingredient.

    In synthetic chemistry, this compound’s selective reactivity at open positions simplifies protection-deprotection strategies, making downstream modifications more efficient. Our process-origin material gives medicinal chemists a clean scaffold—proven by years of customer reactions—without fighting side products that muddy chiral separations or push yields down.

    We’ve supplied kilo lots for pharma intermediate research, where every stray isomer means another round of purification before pilot scale-up. Additional requests come from material science teams exploring new polymers and specialty resins, where the cyclopentenone core introduces ring strain and flexibility unattainable from other cyclic ketones. None of this is theoretical: project teams report higher consistency from our batches compared to generic sources, informing us (and our peers) of best practices based on practical experience.

    Breaking Down the Real-World Benefits

    Consistency is currency in manufacturing. Clients know that a verifiable, high-purity cis-2-hydroxy-3,4,5-trimethyl-2-cyclopenten-1-one lets them go further, faster. Their reactions work as intended, without stops for pre-cleaning or purification. We hear about off-market variants showing variabilities in both isomer content and trace residue levels, sometimes enough to tank a scale-up trial. Our batches, tracked back to the day, time, and operator, sidestep those headaches—and that edge, over time, saves real budgets and reputations.

    The choice of materials, glassware, and scale-up parameters roots itself in our experience. Over the years, we’ve upgraded from pilot glass stills to corrosive-resistant steel, ensured systems prevent cross-contamination, and run regular blank tests to benchmark against our own past lots. Some may see this as redundancy. We see it as delivering on each promise of batch-to-batch sameness, a trait that high-tech fragrance and pharma processes put to the test daily.

    Limitations and Risk Mitigation Approaches

    No manufacturing process is risk-free. Our own struggles with batch yield swings and impurity spikes taught us to build greater redundancies. Having parallel production trains has made a difference, reducing downtime and giving cushion against raw material hiccups. Close relationships with glassware and catalyst suppliers come from the costly lessons of unexpected delays or batch failures. Every process tweak is vetted through trial production before hitting commercial runs.

    Other producers sometimes shortcut risk mitigation, assuming process drift will average out. Our history tells us otherwise. Small anomalies snowball on large production runs. This is where direct manufacturer oversight becomes critical. By handling every step, from raw chemicals through shelf-stable drums, we spot issues early, catch outliers, and maintain a closed feedback loop with customers. The result? Fewer surprises, better returns, and real stability for project timelines and quality requirements.

    Feedback-Driven Improvements: Learning With Each Order

    Working as a manufacturer rather than a third party means hearing directly from those who use our products every day. Each complaint or suggestion becomes fuel for process improvement. Several years back, one customer noticed a slight, recurring off note in a fragrance base using our product. Far from dismissing this as formulation error, we went back to batch records, pulled retained samples, and found a trace impurity below standard detection levels. After refinement, follow-up feedback saw not just a return to normal quality but new business as the word spread.

    This kind of relationship, where information flows in both directions, isn’t possible for traders or resellers. Our technical staff routinely follows up after delivery, requesting updates on how the product performs in-process, and, when needed, sending technical reports to align on troubleshooting. It moves our production standards beyond checklists to real, tested solutions.

    Environmental Commitment: Responsible Manufacturing in Practice

    With rising demand comes responsibility. The process for cis-2-hydroxy-3,4,5-trimethyl-2-cyclopenten-1-one, rich in methylating agents and specialized solvents, creates both chemical and logistical waste challenges. Over the past decade, our facility invested in advanced solvent recycling and emission controls. By reclaiming and purifying used solvent on-site, we not only cut cost, but also significantly reduce environmental load. Wastewater from each run passes multiple recovery stages before discharge, and we regularly exceed local compliance benchmarks as part of our standing operations—not just a showcase event for auditors.

    We keep records of carbon impact per batch, using these data not only as a reporting metric but to drive ongoing reduction projects. Sustainable manufacturing isn’t a catchphrase; it’s a necessity if future supply is to remain secure and long-term partnerships flourish. These investments, borne of real practice, reinforce our stake in both industry success and environmental responsibility.

    Looking Forward: Innovation and Collaboration

    Markets change as fast as the projects on our production schedule. We have seen growing interest in new derivatives and higher-purity grades of cis-2-hydroxy-3,4,5-trimethyl-2-cyclopenten-1-one. Today’s synthesis routes may become tomorrow’s legacy if new applications demand even tighter impurity limits or tailor-made molecular profiles. Our R&D group works alongside customers exploring next-generation fragrance bases or innovative pharmaceutical scaffolds. Direct access to the manufacturing process means we can rapidly prototype updates, test substitutes for restricted substances, and validate scale-up strategies in real time.

    Open, ongoing dialogue with both long-term and first-time clients shapes our innovation agenda. Their challenges, deadlines, and feedback spiral directly into our batch sheets, leading to more robust, responsive industrial chemistry. We don’t lock into legacy methods when evidence points to better alternatives, often shifting raw material sources or process parameters as new data emerges. These choices benefit the whole marketplace—every order builds industry wisdom.

    Conclusion: Manufactured Value, Proven in Each Drum

    Ultimately, producing cis-2-hydroxy-3,4,5-trimethyl-2-cyclopenten-1-one isn’t about shipping boxes with a familiar label. It’s about making each shipment count for the teams who rely on chemical building blocks to propel discovery and make market-ready formulations. Manufactured with pride, care, and a steady hand, our product speaks through its performance in the lab and the plant.

    Direct manufacturer oversight—every step, every drum—translates into tangible benefits: proven purity, documentable consistency, and real-world fit for demanding applications. Our doors are always open to those who want to learn more, test a sample, or see first-hand how practical chemistry, attentive listening, and a relentless pursuit of better production results meet the ever-rising bar of today’s specialty chemical world.