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Cyclobutanemethanol

    • Product Name Cyclobutanemethanol
    • Alias CBM
    • Einecs 207-360-0
    • 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

    203134

    Cas Number 3391-83-1
    Molecular Formula C5H10O
    Molecular Weight 86.13 g/mol
    Iupac Name Cyclobutanemethanol
    Appearance Colorless liquid
    Boiling Point 166-168 °C
    Melting Point −30 °C
    Density 0.947 g/cm3 at 25 °C
    Solubility In Water Moderately soluble
    Flash Point 73 °C (closed cup)

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

    Packing & Storage
    Packing Cyclobutanemethanol is packaged in a 100 mL amber glass bottle with a secure screw cap and appropriate hazard labeling.
    Shipping Cyclobutanemethanol should be shipped in tightly sealed containers, kept in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances. The package must comply with applicable chemical transportation regulations, including labeling as a flammable liquid if necessary, and handled by trained personnel using appropriate protective equipment.
    Storage Cyclobutanemethanol should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizers. Keep it away from direct sunlight and moisture. Store at room temperature and ensure containers are clearly labeled to prevent accidental misuse or exposure. Use proper chemical storage protocols at all times.
    Application of Cyclobutanemethanol

    Applications of Cyclobutanemethanol in Industrial Manufacturing

    Cyclobutanemethanol serves as a specialty intermediate in several advanced chemical manufacturing sectors owing to its unique cyclobutane structure and primary alcohol function. As the original manufacturer, we support formulators and plant managers with proven technical directions for incorporating cyclobutanemethanol into demanding industrial environments. Below, we present detailed application scenarios based on validated commercial practices and regulatory requirements across specialty chemicals, pharmaceuticals, agrochemicals, and advanced coatings fields.

    1. Pharmaceutical Intermediate Synthesis for CNS Drug Development

    Cyclobutanemethanol finds targeted use as a building block in the multi-step synthesis of central nervous system (CNS) active pharmaceutical ingredients, where the cyclobutyl motif confers unique pharmacological profiles. Medicinal chemistry groups employ its primary alcohol group for selective functionalization during lead optimization and scale-up. Its integration often occurs in protected intermediates for subsequent ring-opening, halogenation, or etherification to furnish final drug precursors.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP) General Chapters
    • EudraLex Volume 4 GMP Guidelines
    • REACH Regulation (EC) No 1907/2006 (substance registration)

    Typical usage ratio

    • Batch usage from 0.5 mol% to 1.8 molar equivalents, adjusting for reaction stoichiometry and step yield optimization in heterocyclic synthesis

    Downstream process integration

    • Charged at the key intermediate synthesis stage via Grignard reaction, or as a protected alcohol in multistep route assembly prior to final deprotection

    Final product types

    • Central nervous system drug candidates and intermediates
    • Small-molecule modulators containing cyclobutyl moieties
    • Active pharmaceutical ingredient (API) key starting materials
    • Chiral drug intermediates for lead compound libraries

    2. Agrochemical Intermediate in Selective Herbicide Manufacturing

    Crop protection formulators rely on cyclobutanemethanol for the synthesis of cyclobutyl-based heterocyclic building blocks integral to new herbicide actives. Its application as a functionalized ring allows high selectivity in C-C and C-O bond constructs during active molecule creation, addressing concerns of crop tolerance and target weed resistance by structural innovation.

    Industry compliance standards

    • FAO/WHO Specifications and Evaluations for Agricultural Pesticides
    • EPA 40 CFR Part 174 – Pesticide Act of 1996
    • ISO 9001:2015 certification for raw material traceability
    • Globally Harmonized System (GHS) labeling

    Typical usage ratio

    • Input at 0.8–3.5% w/w of initial batch mass, modulated for pathway efficiency and target product purity in multistep active ingredient synthesis

    Downstream process integration

    • Introduced during cyclobutyl ether or ester formation step in the synthesis sequence of new-generation pre-emergent herbicides

    Final product types

    • Herbicide technical concentrates featuring cyclobutyl substituents
    • Pre-emergence weed control products
    • Active ingredient intermediates for selective agrochemical agents
    • Cyclobutyl-fused heterocyclic herbicides commercialized for resistant weed management

    3. Specialty Monomer in High-Performance Polymeric Coatings

    Manufacturers of advanced coating systems employ cyclobutanemethanol as a reactive monomer to introduce controlled rigidity and molecular branching in specialty copolymer architectures. Its cyclic structure delivers tuneable hardness and scratch resistance, particularly relevant for automotive and electronics protective coatings with extended service lifespans under physical and chemical stress.

    Industry compliance standards

    • ISO 9001:2015 certified quality management systems in coatings production
    • DIN EN 13300 for paint and coating performance
    • European Chemicals Agency (ECHA) monomer restrictions under REACH
    • RoHS Directive 2011/65/EU (lead, chrome, mercury content)

    Typical usage ratio

    • Formulated as 1-5% by weight in resin pre-polymer blends, determined by desired crosslinking density and target film properties

    Downstream process integration

    • Copolymerized during backbone construction as a co-monomer with acrylates, maleates, or epoxies in prepolymer synthesis

    Final product types

    • Automotive OEM and refinish coatings with scratch/impact resistance
    • Electronics encapsulation polymer coatings
    • Protective anti-corrosive industrial paints
    • UV-curable high-solids lacquer formulations

    4. Fine Chemical Intermediate for Fragrance Ingredient Manufacture

    Producers of high-performance aroma molecules select cyclobutanemethanol as a precursor for synthesizing cyclobutyl ketones and alcohol derivatives used in specialty perfumery accords. The raw material’s compact ring system enables tailor-made, high-impact olfactory notes through oxidation and esterification transformations that are controlled under fine chemical production flows.

    Industry compliance standards

    • IFRA (International Fragrance Association) Standards and Guidelines
    • EU Cosmetics Regulation (EC) No 1223/2009
    • ISO 9001-certified aroma chemical manufacture
    • Hazard Communication Standard OSHA 29 CFR 1910.1200

    Typical usage ratio

    • Charged at 2–10% of batch volume for targeted transformations depending on conversion step type and expected aroma intensity in the final ingredient

    Downstream process integration

    • Brought in at the key alcohol oxidation or ketone functionalization stage to generate high-purity synthetic musks and woody base notes

    Final product types

    • Cyclobutyl-based aroma chemicals
    • Custom fragrance intermediates for perfumery accords
    • Synthetic musk and woody odorants
    • Fine fragrance and personal care blends with unique ring-structured notes

    5. Precursor in Advanced Polymer Crosslinker Production

    Cyclobutanemethanol is functionalized in the synthesis of specialty aliphatic crosslinking agents for high-durability polymers. Its ring system imparts spatial rigidity and enhances chemical resistance in downstream polyurethane, epoxy, or acrylic network-forming chemistry. Chemical engineers add it as a modular element to control crosslink density and, thus, the targeted performance profile of final thermoset materials.

    Industry compliance standards

    • ASTM D6358 – Standard Specification for Crosslinking Agents
    • ISO 14001 – Environmental Management in chemical plants
    • REACH downstream user conditions (Art. 37)
    • ECHA Classification, Labelling, and Packaging (CLP) Regulation

    Typical usage ratio

    • Used at 0.5-4 mol% relative to main chain agents, balanced to achieve designed network properties and chemical compatibility

    Downstream process integration

    • Fed into reactor during initial polyol or resin blend-up stage, prior to curing; participates in polyaddition or polycondensation reactions

    Final product types

    • Aliphatic polyurethane crosslinkers
    • High-solids two-component epoxy systems
    • Durable acrylic thermoset binders
    • Adhesive resins for specialty high-end applications
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    Certification & Compliance
    More Introduction

    Cyclobutanemethanol: Insight from the Manufacturer’s Floor

    Making Cyclobutanemethanol: Our Perspective

    Cyclobutanemethanol isn’t a common name outside certain corners of the lab, but anyone who’s spent time around practical organic synthesis knows what a useful building block it can be. We’ve spent years getting to know its quirks—from the challenges in scaling up its ring strain-driven production, to the daily diligence required during purification. Producing this compound calls for strict control over both temperature and pressure. If the chemistry veers even a little off track, unwanted side products creep in. This has taught our teams to favor batch consistency and robust monitoring.

    We run our main production using a high-purity model, usually with a minimum assay of 98%. For customers working in flavor intermediates, pharmaceuticals, or specialty polymer development, this degree of purity prevents unwanted reactivity in subsequent steps. Our reactors, fitted out for smaller volumes than commodity lines, handle about 500 kg per month. This pace prioritizes quality over scale, which fits most customers’ research and synthesis runs rather than bulk commodity blending.

    Handling and Physical Appearance

    Cyclobutanemethanol, C5H10O, appears as a colorless to faintly yellowish liquid at room temperature. Internally, our technical staff watches for any haze or color drift, as these can indicate trace impurities or oxidation from poor storage. The boiling point hovers in the 144–146 °C range. This helps in easy distillation for those needing to adapt our standard material further in-house. The faint, somewhat sweet odor isn’t a concern in well-ventilated process areas, but we still minimize open handling.

    Where Cyclobutanemethanol Finds Its Value

    This compound’s real value comes from its strained cyclobutane ring combined with a primary alcohol—making it more than just a curiosity on the shelf. Chemists favor this molecule as a starting point for creating a wealth of cyclobutylacetic acids, aldehydes, esters, and even certain carbocyclic drug scaffolds. In our experience, it gets used in the synthesis of antiviral and cardiovascular intermediates, but the bulk demand often comes from fragrance intermediates. The ability to introduce the cyclobutyl group onto more complex structures—without having to build a four-ring from scratch each time—saves months in upstream research.

    How We Ensure Reliable Quality—Based on Experience

    Years on the manufacturing floor have shown that off-the-shelf purity claims don’t always tell the full story. During repeated crystallizations and distillation cycles, even small handling mistakes—such as insufficiently dried glassware—can lead to water contamination. This affects both yields and downstream performance. We insist on water content below 0.1%, measured by regular Karl Fischer analysis. Routine checks flag both high and low pH excursions, as trace acids or bases will not only age the product prematurely but also interfere with customers’ sensitive reactions.

    Last year, a regular client flagged low conversion rates in a Grignard addition to Cyclobutanemethanol. After cross-checking, a subtle peroxide impurity cropped up. We traced it to steel joints that had recently been steam cleaned but not dried thoroughly. Making that link reinforced our strict drying and oxygen exclusion steps at every stage—lessons learned on the job, not just from textbook procedures.

    How Cyclobutanemethanol Stands Out from Other Alcohols

    In industrial circles, comparisons often arise between Cyclobutanemethanol and more common alcohols like benzyl alcohol or cyclopentanol. The key difference boils down to reactivity and the structure of the four-membered ring, which brings significant ring strain and distinctive physical properties. This ring strain can make it more reactive in certain chemical transformations—such as ring-opening reactions or cyclization steps—than similar five- or six-membered analogs.

    For colleagues working in pharmaceutical fine chemicals, adding a cyclobutyl scaffold at the right point in a synthetic route can sometimes unlock biological activity that eludes larger ring structures. For example, we’ve supported projects where this compound made possible selective derivatization in steroid frameworks without requiring high temperatures or super-stoichiometric forcing conditions. No one ever asks for Cyclobutanemethanol by accident—it’s brought in when standard alkyl groups aren’t enough for a synthetic challenge.

    Testing and Documentation—An Open Book

    Many years ago, we fielded lots of questions on batch traceability. In response, we began attaching full chromatographic profiles and water content reports to every shipment. Each drum and flask ships with a certificate of analysis (COA) that we actually sign by hand, not just print from ERP software. Analytical methods follow both in-house procedures and international standards, with gas chromatography (GC) and infrared (IR) spectra available upon request. Sometimes, an order needs extra trace-metal screening if a pharmaceutical company asks for it. This flexibility is built from real customer feedback, not just regulatory box-ticking.

    We’ve kept to a single standard model—minimum 98% purity—because running multiple specification lines didn’t make practical sense. This focus ensures every operator on our team handles each batch the same way, and that we spend our troubleshooting time learning from our own runs rather than patching together custom processes for each shipment.

    Storage, Transport, and Long-Term Stability

    Experience has taught us that storing Cyclobutanemethanol in tightly sealed glass containers under a nitrogen blanket slows degradation. Polyethylene or polycarbonate won’t survive repeated fills or rough transport, as the compound’s affinity for organic materials leads to slow migration and eventual contamination. We use amber glassware for light protection, especially for clients with long supply chains or extended field storage.

    Bulk drums ship on pallets lined with absorbent pads. This simple step came after a minor spill during a summer heat wave—a mistake not repeated. Cyclobutanemethanol holds up well at ambient temperatures, though we recommend cool, dry areas with regular venting for container rooms. Those doing repackaging or small-lot resales should carefully avoid high heat or direct light, as degradation speeds up in open or translucent containers.

    Comparison to Other Synthetic Starting Materials

    Some in R&D may wonder why choose Cyclobutanemethanol over less expensive or more plentiful starting points. Our experience shows that for certain intermediates, there is no ready substitute. Cyclopentanol or phenylmethanol can’t supply the molecular tension—the unique way the ring’s angle strain channels reactivity into new bonds—that makes Cyclobutanemethanol special. Simply put, if your synthetic plan depends on the four-membered ring, substituting would either require multi-step detours or higher temperatures that hurt overall selectivity and yield.

    Feedback from our clients in agrochemical development suggests that attempts to swap out Cyclobutanemethanol usually drop yields by over 20%. That margin can decide whether a project reaches pilot scale. Further, we’ve worked with academic partners who struggled with commercial alcohols clogging up their NMR analysis with impurities—something that tighter specs on Cyclobutanemethanol help prevent. These direct stories mean more than rehashed literature summaries.

    Safety, Hazards, and Responsible Practice

    Having this material on site doesn’t bring the same fire risks as larger alcohols, but general precautions still deserve attention. Our floor staff wears gloves and safety glasses, as even brief skin exposure can cause dryness or mild irritation. Inhalation risk stays low thanks to low volatility at standard process temperatures. Small leaks, if left unattended, might give off a faint odor but rarely trigger alarms. Still, our staff treats every handling station as a possible spill site, especially near filling tanks and open process lines.

    We publish full hazard data on SDS sheets, and any reactivity tests with strong oxidizers or acids follow published industrial hygiene guidelines. We have seen no serious incidents over a decade, but frequent training refreshers and strict container labeling prevent avoidable mix-ups. Safety at scale grows out of routine, and our teams bring real working experience—learned by repetition, not memo.

    Environmental Responsibility in Manufacturing

    We take waste minimization seriously. By cracking down on excess solvent use and improving capture after distillation, we’ve halved liquid effluent since 2018. The spent catalyst, once binned as general waste, now routes through a metals reclamation program. Less hazardous byproducts result directly from improvements our operators suggested after hands-on troubleshooting. These aren’t glamorous changes but they matter for long-term sustainability. For smaller quantity shipments, we use recyclable materials wherever possible. As a rule, our containers avoid halogenated plastics or single-use synthetics.

    Down the line, we encourage our customers to treat any Cyclobutanemethanol waste as they would other primary alcohols—through established incineration or waste-to-energy channels, never down municipal drains. Each order includes updated handling tips, based not just on regulatory requirements but on our own lessons from years spent managing production and spill response plans. No shortcuts, no half-truths.

    Feedstock Sourcing and Upstream Validation

    Nearly every production hiccup we’ve faced came from inconsistent feedstock—usually the cyclobutanone key intermediate. Our supply chain team now qualifies upstream sources through periodic audits. Suppliers must send samples from each batch before we issue new POs. Some came up short, and over time, we narrowed down our partners. In practice, this vigilance prevents last-minute scrambling and off-spec material. Reliable supply beats low cost at this level.

    Working with Clients—Real Cases, No Hype

    One of our more demanding customers, a university lab synthesizing non-standard nucleosides, ran into trouble with an overseas source. They switched to our grade, and the difference in baseline purity unblocked a stalled research milestone. Rather than vague promises, we provide chromatograms and batch narratives—our own chemists on the phone, not call center reps. This transparency builds more enduring relationships than price wars or quick turnaround pitches. Many returning clients have stayed with us for a decade or longer, training each new graduate student or technician with our process notes and application examples.

    Ongoing Improvements and Future Directions

    Our team constantly experiments with process tweaks, from glassware upgrades to automated solvent recovery. We cut production time by 30% over the past three years, not by cutting corners, but by understanding every step’s limits—air exclusion, solvent ratios, transfer lines, batch-by-batch verification of catalyst quality. These gritty, incremental improvements don’t often grab headlines. Still, the cumulative effect shows up in fewer out-of-spec warnings, steadier delivery times, and stronger lab-to-plant consistency for all users.

    Sometimes, we’re asked about custom derivatives: acetates, halides, or even isotopically labeled analogs. While not the bread and butter of our business, we take these as opportunities to deepen our own know-how. It’s common for a PhD student to call directly to talk through a difficult transformation or modification strategy. There’s no replacement for real conversation with someone who's mixed more than a few batches and dealt with every surprise a strained cycloalkyl alcohol can deliver.

    Informed by Decades of Hands-On Production

    At heart, our approach to Cyclobutanemethanol flows from real production experience. Every decision—spec selection, container choice, handling protocol—reflects lessons learned mixing, storing, and shipping thousands of liters over decades. The compound provides a precise tool for organic synthesis, and our job is to keep supply smooth, honest, and reliable. Those with synthetic ambitions trust us with their most demanding work not only because of what’s in the bottle but because of the know-how wrapped around it.

    For those who see value in a four-membered ring where reactivity and selectivity matter, Cyclobutanemethanol sits in its own league. We stand by the compound and the way we handle it, drawing on years of operations, troubleshooting, customer feedback, and plain hard work. Focusing on real outcomes beats chasing artificial scale, and keeping every part of the process transparent puts every user—chemist, engineer, or researcher—on steady ground.