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5-Norbornene-2-Methanol

    • Product Name 5-Norbornene-2-Methanol
    • Alias exo-2-Norborneolmethyl
    • Einecs 207-441-0
    • 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

    675599

    Chemical Name 5-Norbornene-2-Methanol
    Cas Number 672-23-9
    Molecular Formula C8H12O
    Molecular Weight 124.18 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 112-114 °C at 13 mmHg
    Melting Point 18-20 °C
    Density 1.029 g/cm3 at 25 °C
    Refractive Index 1.506-1.508 at 20 °C
    Flash Point 98 °C

    As an accredited 5-Norbornene-2-Methanol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 100g amber glass bottle with a secure screw cap, clearly labeled “5-Norbornene-2-Methanol, 100g,” and hazard warnings.
    Shipping 5-Norbornene-2-Methanol is shipped in secure, sealed containers to prevent leakage and contamination. It is typically packaged in glass or plastic bottles, clearly labeled, and compliant with hazardous material regulations. Shipping is conducted via ground or air freight, with appropriate documentation and handling precautions for flammable liquids.
    Storage 5-Norbornene-2-Methanol should be stored in a cool, dry, well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizing agents. Keep the container tightly closed and protected from physical damage. Store at room temperature and avoid exposure to direct sunlight and moisture. Use appropriate chemical storage containers and clearly label them for safe identification.
    Application of 5-Norbornene-2-Methanol

    Applications of 5-Norbornene-2-Methanol in Industrial Manufacturing

    5-Norbornene-2-Methanol serves as a multi-functional raw material across demanding sectors in chemical and polymer industries. We supply this advanced intermediate for distinct downstream markets where precise chemical engineering, quality control, and regulatory compliance define success. The following sections detail practical industrial uses with real-world standards, formulation insights, process inputs, and downstream finished products.

    1. Specialty Polymer Monomer for Cyclic Olefin Copolymers (COCs)

    Manufacturers in advanced packaging, optics, and pharmaceutical devices choose 5-Norbornene-2-Methanol as a reactive monomer in COC production. The material’s unique bicyclic structure enables tight control over glass transition temperatures and moisture resistance within polymer matrices. Typical use involves copolymerizing with ethylene or other norbornene derivatives using metallocene or Ziegler-Natta catalysts. Strict quality protocols ensure hospital-grade transparency and extractables control for medical and food-contact applications.

    Industry compliance standards

    • FDA CFR 21.177.1520 for food contact polymers
    • USP <661.2> Plastic Packaging Systems for Pharmaceutical Use
    • EU Regulation (EU) No 10/2011 for plastics intended to come into contact with food
    • ISO 10993-1 Biocompatibility for medical devices

    Typical usage ratio

    • 5–30 mol% of total monomer charge, adjusted for desired copolymer properties (clarity, barrier, Tg)

    Downstream process integration

    • Added during bulk monomer blending before polymerization reactors, under inert conditions, with precise temperature and catalyst control

    Final product types

    • Pharmaceutical blister films
    • Sterile syringe barrels
    • Diagnostic microfluidic chips
    • Optical-grade film for display technology

    2. Modifier for Epoxy Resin Systems

    Epoxy formulators use our product as a rigid ring-structured modifier to enhance crosslinking density and increase glass transition temperatures in engineered thermosets. It acts as a co-monomer or chain extender, introducing reactivity via its hydroxyl group. This modification allows electrical component manufacturers to improve circuit board insulation and mechanical stability under thermal cycling.

    Industry compliance standards

    • IPC-4101/21 for base materials in printed wiring boards
    • UL 94 flammability rating for epoxy-based insulators
    • RoHS Directive 2011/65/EU for restricted hazardous substances
    • IEC 61249-2-21 halogen-free base material for PCBs

    Typical usage ratio

    • 2–10 phr (parts per hundred resin), tuned based on cure profile and desired end-use temperature stability

    Downstream process integration

    • Incorporated post-epoxy resin synthesis, premixed with curing agents, then applied by casting, impregnation, or lamination before thermal or UV cure

    Final product types

    • High-temperature printed circuit boards (PCBs)
    • Chemical-resistant coatings for equipment housings
    • Automotive electronic encapsulants
    • Industrial adhesive composites

    3. Intermediate for Fine Fragrance and Aroma Chemical Synthesis

    Flavors and fragrance suppliers use 5-Norbornene-2-Methanol as a rigid alicyclic intermediate in the synthesis of high-value musky, woody, and camphoraceous aroma chemicals. Controlled hydrogenation, oxidation, or esterification steps convert it into long-lasting fragrance ingredients, providing unique olfactory notes for consumer and industrial products. Attention to purity, trace solvents, and batch traceability is demanded by top-tier perfumery houses.

    Industry compliance standards

    • IFRA Code of Practice for fragrance safety
    • REACH Registration (EC) No 1907/2006 for chemical safety in fragrances
    • Cosmetics Regulation (EC) No 1223/2009 for personal care applications
    • ISO 9235 for definitions of aromatic raw materials

    Typical usage ratio

    • Input at 1–5% mol basis in aroma chemical syntheses depending on desired conversion and downstream functional group transformations

    Downstream process integration

    • Used in alkylation, oxidation, or acylation steps as a core scaffold for specialty aroma molecule production in batch or continuous setups

    Final product types

    • High-performance fragrance bases for fine perfumery
    • Home care scent boosters
    • Odor-masking agents in industrial formulations
    • Top-note building blocks in designer perfumes

    4. Advanced Intermediates for Agrochemical Active Ingredient Synthesis

    Agrochemical manufacturers leverage the bicyclic alcohol to introduce structural rigidity or functional handles in new-generation insecticide and fungicide molecules. It acts as a building block for further functionalization by acylation, fluorination, or halogenation, resulting in compounds with enhanced bioactivity and photostability. Reaction scale-up involves precise feeding, temperature control, and effluent management to maintain ISO and environmental registrations.

    Industry compliance standards

    • ISO 9001:2015 for quality management in agrochemical manufacturing
    • OECD Guidelines for the Testing of Chemicals
    • FAO/WHO Codex Alimentarius for pesticide specifications
    • REACH compliance for chemical safety in the EU

    Typical usage ratio

    • 10–25% of total synthetic sequence based on targeted yield and final active ingredient transformation

    Downstream process integration

    • Reacted at intermediate functionalization steps before the introduction of bioactive moieties, under batch or semi-continuous synthesis conditions

    Final product types

    • Systemic insecticide precursors
    • Photostable fungicide actives
    • Professional-use herbicide additives
    • Niche crop protection formulation intermediates
    Free Quote

    Competitive 5-Norbornene-2-Methanol prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

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    Certification & Compliance
    More Introduction

    5-Norbornene-2-Methanol: Perspective from Our Chemical Manufacturing Floor

    On-the-Ground Insight into 5-Norbornene-2-Methanol

    From years of hands-on work in the factory, every batch of 5-Norbornene-2-Methanol carries with it a hefty set of challenges and rewards. This compound, commonly labeled with the model NBH-MeOH, stands out among norbornene derivatives that we have synthesized for over a decade. The practical value starts at the synthesis stage. The unique structure—a bicyclo[2.2.1]hept-5-ene core with a methanol group at position 2—means the reaction conditions differ from simpler norbornene products. Our technicians monitor temperature and pressure constantly because even a minor change can alter end-use quality. We rely on practical adjustments, not just numbers in a sheet, to guarantee every kilogram meets the promised specs.

    Typical product output appears as a clear to almost colorless liquid, with a boiling point higher than many related norbornene alcohols. This feature changes how it handles downstream. In the plant, lower volatility means we can use less strict evaporation conditions; the methanol group remains stable, and shelf life stretches longer compared to non-hydroxyl norbornene grades. Colleagues working in formulation lines benefit from this. Less aggressive ventilation and fewer headaches over quality loss translate into real cost savings—something you can see in the monthly numbers, not just lab reports.

    Key Specifications from a Manufacturer’s Standpoint

    We produce NBH-MeOH typically at >98% purity, as confirmed by GC analysis each week. It has a molecular weight of 124.17 g/mol. Moisture level usually tests below 0.2%. While specifications may read like a checklist on a website, these numbers only matter if the chemical actually behaves as expected when the customer opens the drum. For us, the performance shows up in consistent clarity and ease during transfer. We have had fewer filtration issues than with heavy norbornene esters, which tend to pick up trace impurities. Common packaging sizes include 25 kg drums and occasionally custom IBCs. The material flows smoothly, and pumping equipment rarely needs cleaning—this has made a difference for teams running larger synthesis batches with tight downtime margins.

    Usage Grounded in Practice

    Research labs, specialty polymer makers, and fragrance compound blend specialists look for 5-Norbornene-2-Methanol for its unique reactivity. Our main volume goes to companies developing cyclic monomers for high-performance polymer materials. The methanol functional group becomes a target for further modification, especially in processes that require a combination of rigidity and flexibility in the final polymer backbone. We’ve seen local partners replace common mono-ol or diol comonomers with NBH-MeOH because it locks in mechanical strength without brittle failure—a difference that makes the difference in long-term durability. The core norbornene structure brings steric bulk, which resists ring-opening side-reactions. That means better yield in some of the more demanding cycloaddition and metathesis reactions. We talk to people at the end of the value chain; what we hear most: it saves time spent purifying and reworking defective materials.

    Other regular orders come from pharmaceutical developers working on norbornene-based intermediates. The methanol group acts as both a reactive site and a solubilizing handle in multi-step synthesis. Our chemists often discuss projects with downstream users—NBH-MeOH switches easily between lab-scale and pilot-scale settings, and unlike some related aldehydes or ketone-functionalized norbornenes, it presents less risk of unwanted cross-reactions. One customer specifically swapped from 5-norbornene-2-carboxaldehyde to NBH-MeOH for better stability in storage and greater tolerance to typical oxidants.

    Specialty composite and resin formulators rely on the compound’s balance of modifiable functionality and backbone rigidity. We notice a clear trend: teams using it rarely ask for technical support traceable to batch inconsistency. Meanwhile, newer formulators experimenting with ring-opening metathesis polymerization (ROMP) often seek our feedback on formulation strategies. We have tested it side by side with 2-norbornene carboxylic acid, 5-norbornene-2-ol, and norbornene dicarboximides in our labs, monitoring downstream gelation times, copolymer miscibility, and final mechanical strengths. Fewer runaway exotherms, less yellowing during curing, and improved clarity are the consistent themes.

    How It Sets Itself Apart from Related Products

    One standout feature in day-to-day production is the balance between reactivity and safety. Compared to 5-norbornene-2-ol, the methanol derivative runs slightly higher on boiling point and displays better long-term stability. We have months-long retention data on samples stored under typical warehouse conditions, and NBH-MeOH loses little in weight or appearance. When lined up alongside norbornene carboxaldehyde or norbornene ketones, it resists unwanted oxidation and polymerization, meaning less need for stabilizers or inerting during storage. Customers have told us, practical experience has shown that smaller formulators who lack specialized storage facilities face less spoilage risk with NBH-MeOH.

    Every compound comes with trade-offs. In the case of NBH-MeOH, it has a lower volatility than norbornene itself or norbornene acetates, which allows for more flexible use in high-temperature processing. Our downstream users—whether working at a kilo scale or scaling up to tons—mention fewer complaints related to off-gassing or workplace odors. We see this reflected in workflow: our team’s maintenance of local exhaust and environmental controls rarely registers unusual alarms when handling this product, compared to more volatile analogues.

    We observe the difference during actual usage. Norbornene diols and dicarboxylates handled in the same production lines sometimes lead to clogged filters or abrupt viscosity spikes. NBH-MeOH, with its compact hydrophilic alcohol end, stays liquid longer under lab air, and our partners notice faster dissolution into common solvents like THF, methanol, and toluene. Teams who’ve handled nitro-substituted norbornenes report more jaundiced yellow colors after a few weeks—NBH-MeOH stays clean in well-sealed containers, giving our customers more time to plan and use their inventory.

    Everyday Experience, Real-World Results

    On our own shop floor, storage is less of a headache. NBH-MeOH doesn’t generate the pungent fumes or sticky residues that have plagued our old norbornene acetate lines. Our drum handlers wear basic PPE—nitrile gloves, goggles, and long sleeves—but avoid the full-face respirators reserved for noxious norbornene esters. Loading pumps and lines rarely get fouled. Drums spent weeks in storage without the crusting or separation problems that demand unplanned cleaning work. These facts—borne out through hundreds of tons processed—cut maintenance costs and slowdowns.

    Shipping out from our warehouse, our logistics crew notices fewer drum returns with signs of leakage or swelling. Test shipments subjected to summer heat held up, with only minimal pressure increase and no loss in product quality. This means fewer headaches for our partners in hot climates.

    We notice a reduction in accidental spills or workplace incidents linked to NBH-MeOH compared to lower molecular weight norbornenes and related aldehydes. The higher boiling point, and manageable vapor pressure, make this product an asset in environments with minimal ventilation. We run regular safety training—our incident logs back up what we see: less need for emergency air scrubbing and less lost time from chemical exposure alarms.

    Lessons Learned from Ongoing Production

    Our batch-to-batch data shows high yield and low waste. Unlike the more finicky norbornene acids, NBH-MeOH tolerates small variations in water content during processing, sparing operators from chasing down every last droplet of moisture. Line chemists monitor the final product using easy-to-interpret GC peaks—purity rarely drops below 98%, even during humid months. Less time spent on repeated quality checks lets our crew focus on the next batch, raising our throughput and reliability.

    Over the years, we find equipment cleaning routines for NBH-MeOH production are more forgiving. Residues, if any, dissolve quickly in standard solvents. Compared to sticky dicarboxylates or resinous norbornene epoxy intermediates, our cleaning team spends half the time. Pumps last longer too, not subject to the pitting or wear from more corrosive analogues.

    Responding to Market Demands and Challenges

    As manufacturers, we lag if we don’t keep listening to both research chemists and scale-up engineers. Norbornene chemistry keeps evolving. We source raw norbornene from reputable partners, and the pressure to improve yield and cut impurities never lets up. Each time we add a batch cooling device, or swap in a new distillation tower, we do it to offer a more reliable NBH-MeOH, not just to check a box on a regulatory list.

    We’ve faced supply chain squeezes and regulatory hurdles, just like everyone else. Access to high-purity methanol or specialty catalysts ebbs and flows with global markets. Having walked the length of our own warehouse, I can attest: the market rewards those who keep NBH-MeOH purity above standard and batches reliable every time. We log issues, update procedures, and keep lines of communication open with end-users. What does that mean in real terms? Fewer out-of-spec drums, less rework, and happier long-term partners.

    Supporting Sustainable Growth and Research

    We see growing demand from teams involved in new bio-based and recyclable polymers. NBH-MeOH, with its versatile functional group, often attracts researchers interested in “green” modifications—catalytic coupling, chemo-enzymatic conversion, and even use in photoresponsive polymers. We field regular questions about residual solvent content, halide scavenger residue, and potential for endotoxin contamination. Experience tells us NBH-MeOH often outperforms more heavily substituted analogues by reducing the complexity of side-product formation. Each year, university research labs test new applications; in return, we analyze feedback and tighten our process windows. We share analytical results, and stay transparent about any batch variances, in line with both customer requests and stricter environmental regulations.

    We track customer feedback closely and often implement minor recipe shifts based on downstream polymerization behavior or favored solvent systems. This willingness to tailor, rooted in experience, creates a feedback cycle: better product, fewer complaints, more insightful partner input, and a reputation we value.

    Summary from the Manufacturer’s Perspective

    We have learned over the years that consistency, safety, and a readiness to engage deliver the results that matter. 5-Norbornene-2-Methanol stands as a prime example of a specialty chemical product where deep process knowledge, personal experience, and real feedback from customers have refined what leaves our loading docks. The compound is neither the flashiest nor the simplest among norbornene derivatives, but it brings together useful reactivity with practical handling benefits. Customers who switch to NBH-MeOH often come back with fewer processing issues, steadier batch results, and real insights for the next generation of specialty resins, pharmaceuticals, or research materials. These everyday details, built into each ton we supply, matter more than marketing claims or generic data sheets.