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(1S)-(+)-3-Carene

    • Product Name (1S)-(+)-3-Carene
    • Alias Delta-3-carene
    • Einecs 202-313-6
    • 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

    811862

    Iupac Name (1S)-3,7,7-Trimethylbicyclo[4.1.0]hept-3-ene
    Cas Number 498-15-7
    Molecular Formula C10H16
    Molar Mass 136.24 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 168–170 °C
    Density 0.864 g/cm³
    Optical Rotation [α]D20 +39° to +41° (neat)
    Refractive Index 1.476–1.478 (20 °C)
    Solubility In Water Insoluble
    Flash Point 42 °C (closed cup)
    Odor Sweet and pungent, similar to turpentine

    As an accredited (1S)-(+)-3-Carene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The (1S)-(+)-3-Carene is supplied in a 25 mL amber glass bottle with a secure screw cap, labeled for laboratory use.
    Shipping Shipping of (1S)-(+)-3-Carene should comply with regulations for flammable organic liquids. The chemical must be properly sealed in compatible containers, labeled with hazard information, and protected from heat and ignition sources. Transport must adhere to local and international regulations, such as DOT, IATA, or IMDG, ensuring safe and compliant delivery.
    Storage (1S)-(+)-3-Carene should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and direct sunlight. It should be kept away from oxidizing agents and acids. The storage area should be equipped for flammable liquids and comply with local fire and chemical safety regulations. Avoid inhalation and contact with skin or eyes.
    Application of (1S)-(+)-3-Carene

    Applications of (1S)-(+)-3-Carene in Industrial Manufacturing

    (1S)-(+)-3-Carene is a monoterpene hydrocarbon derived from turpentine oil, recognized for its unique chemical reactivity and olfactory properties. As a direct manufacturer, we supply this raw material to several advanced processing downstream sectors, supporting precise formulation needs, regulatory compliance, and integration into complex industrial workflows. Below are key application scenarios where our (1S)-(+)-3-Carene plays a critical role in end-user manufacturing.

    1. Fragrance Compounding for Fine Perfumery

    Perfumery formulators utilize (1S)-(+)-3-Carene as a building block to create complex natural accords, notably in pine, citrus, and floral scent compositions. Its distinctive fresh, woody aroma serves as both a top note ingredient and as a reactive substrate for synthesis of further aroma molecules. Master perfumers precisely dose this raw material to comply with global fragrance safety and allergen control regulations, while enabling the creation of stable and unique finished scents for high-value markets.

    Industry compliance standards

    • International Fragrance Association (IFRA) Standards
    • EU Regulation (EC) No 1223/2009 on Cosmetic Products
    • Cosmetic Ingredient Review (CIR) Safety Assessments
    • REACH Registration for Fragrance Ingredients

    Typical usage ratio

    • 0.05–1.5% of total fragrance concentrate, depending on target note profile and regional allergen restrictions.

    Downstream process integration

    • Added during the compounding stage, dissolved in a solvent such as ethanol or DPG; undergoes QC batch sampling for odor intensity and purity before being blended into bulk fragrance oil.

    Final product types

    • Fine perfumes, eau de toilette, personal care fragrances, home ambiance diffuser oils, and luxury scented candles.

    2. Synthesis of Pharmaceuticals and Terpenoid Derivatives

    Chemical and pharmaceutical manufacturers employ (1S)-(+)-3-Carene as a starting material for synthesis of active pharmaceutical ingredients, chiral synthons, and specific intermediates such as carvone and related oxygenated terpenoids. Its enantiomeric purity and reactivity underpin critical chemical conversions used in the production of anti-inflammatory agents, expectorants, and other specialty compounds under GMP-controlled environments.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP–NF Monographs for Terpene and Terpenoid Intermediates
    • European Pharmacopoeia Standards
    • 21 CFR Part 211 GMP for Finished Pharmaceuticals (where applicable)

    Typical usage ratio

    • Typically 1–5 molar equivalents as a reaction substrate in pharmaceutical synthesis, adjusted based on the desired yield and downstream conversion efficiency.

    Downstream process integration

    • Charged into reaction vessels as a purified feedstock following distillation; undergoes chemical transformation (e.g., oxidation, isomerization) monitored by HPLC/GC and enantiomeric excess analysis prior to isolation of pharmaceutical intermediates.

    Final product types

    • Terpenoid-based APIs, chiral building blocks, mucolytic drugs, and intermediates for further chemical synthesis in the pharma sector.

    3. Flavor Formulation for Confectionery and Beverages

    The food flavor industry applies (1S)-(+)-3-Carene as a volatile flavor component to impart piney, citrusy nuances in confectionery, gum, and selected beverage applications. It must meet rigorous food-grade standards, with careful attention given to its usage levels and trace analysis given potential allergenicity. Technologists select this raw material for tailored flavor profiles that require a subtle freshness and authentic natural notes, functioning both as a primary flavor agent and as a blending modifier.

    Industry compliance standards

    • Food Chemicals Codex (FCC)
    • 21 CFR §172.515 (Flavoring Substances and Adjuvants)
    • EU Regulation (EC) No 1334/2008 on Flavorings
    • ISO 22000 Food Safety Management

    Typical usage ratio

    • 0.0005–0.02% in finished food flavorings, with the precise threshold determined by regulatory limits and sensory panel result analysis.

    Downstream process integration

    • Introduced during liquid flavor compounding; homogenized under vacuum or low-shear mixing to achieve uniform distribution; subjected to GC-MS purity verification prior to downstream QA and bottling.

    Final product types

    • Chewing gum flavors, hard candy, citrus beverage bases, and aroma compounds for processed food.

    4. Manufacture of Synthetic Resin and Polymer Modifiers

    Producers of specialty resins use (1S)-(+)-3-Carene as a reactive monomer or diluent in synthesis of terpene phenolic resins, adhesive tackifiers, and high-performance coatings. Its defined boiling point and controlled polymerizability provide consistent batch-to-batch properties, while its integration enables fine tuning of resin solubility, glass transition temperature, and final adhesion characteristics as required by performance adhesive clients.

    Industry compliance standards

    • ISO 9001 Quality Management Systems for Polymer Manufacturing
    • REACH Registration for Monomer Supply Chain
    • ASTM D3317 (Adhesives: Tackifier Resins)
    • FDA 21 CFR §175.105 (Adhesives for Food Packaging, where intended for indirect food contact)

    Typical usage ratio

    • 10–30% by mass in terpene phenolic resin formulations, according to specific tack, softening point, and viscosity targets identified by lab testing and pilot runs.

    Downstream process integration

    • Metered into reactor during the initial resinification stage; mixed with phenol or alkylphenols and alkali catalysts; end-point characterized by melt viscosity and color before downstream strand-cutting or flake production.

    Final product types

    • Hot-melt adhesives, pressure-sensitive tapes, road marking paint binders, and specialty coating additives.

    5. Production of Natural Insect Repellents and Biopesticides

    Manufacturers of eco-friendly insect control agents select (1S)-(+)-3-Carene for its volatile scent characteristics and tested repellent effect. Its application as an active in biopesticide formulations ensures that finished products can claim natural origin and conform to organic agriculture input standards. Formulators optimize dosage to balance efficacy and regulatory residue limits, integrating this monoterpene into both liquid and solid repellent production streams.

    Industry compliance standards

    • US EPA FIFRA Biopesticide Registration
    • EU Regulation (EC) No 1107/2009 on Plant Protection Products
    • OECD Guidelines for Testing of Chemicals (Repellents and Attractants, No. 812)
    • NOP (National Organic Program) Input Standards for Organic Agriculture

    Typical usage ratio

    • 0.1–4% as active ingredient, fine-tuned based on target insect species, product format, and application guidelines.

    Downstream process integration

    • Added post-emulsification or during blending with other natural actives; subjected to GC purity verification and efficacy testing before packaging in consumer formats.

    Final product types

    • Natural insect sprays, mosquito coil actives, agricultural biopesticides, and organic farming pest management concentrates.
    Free Quote

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    Certification & Compliance
    More Introduction

    (1S)-(+)-3-Carene: A Closer Look at Our Terpene Production

    Producing (1S)-(+)-3-Carene brings its own set of challenges and surprises. As manufacturers who focus on turpentine derivatives, we understand that this bicyclic monoterpene sometimes hides in the background, overshadowed by pinene and limonene. We see this compound step up whenever our partners in flavors, fragrance, and chemistry want that clean, slightly woody note or seek a starting point for more complex synthesis work.

    Model and Key Specifications

    Our batches of (1S)-(+)-3-Carene consistently reach a purity above 98%. This kind of number never appears by chance. Distillation columns don’t forgive inattention, and raw gum turpentine varies with every harvest. Small shifts in feedstock composition or equipment parameters can nudge our content up or down, so we monitor each lot with GC. Specific gravity lands between 0.86 and 0.87 at 20°C, right where it ought to for real carene. Boiling point hovers from 168°C to 174°C, and that’s one value we watch because tighter fractions mean fewer side products. Our finished product remains a clear, colorless liquid, because any haze cuts into its use in downstream synthesis or perfumery.

    People often focus on those numbers, but the distinctive odor and chemical stability matter at least as much. The sharp, sweet-pine aroma comes through even in diluted samples. We test each drum since our customers will notice the faintest off-note once they start blending into aromas or flavors. Physical specification keeps us grounded, though handling and storing carene calls for a careful hand. Its low viscosity and volatility make it easy to transfer or evaporate, but spills often linger with a persistent odor. Regular checks prevent degradation from heat and light, which can turn a good batch into a write-off if ignored.

    Using (1S)-(+)-3-Carene: Insights from the Factory Floor

    Over the years, we’ve seen (1S)-(+)-3-Carene migrate through quite a few industries. Chemists in synthetic fragrance value its ability to serve as an intermediate for preparing more elaborate molecules. In this sector, our clients often call with urgent requests for batch consistency; if the chirality switches or impurity profile shifts, their syntheses miss the mark, and so do we. From our experience, carene accepts derivatization cleanly—epoxidation or hydration reactions reach high yields as long as the starting material stays within the required range.

    Flavor houses and perfumers come asking for a natural source, seeking the soft, resinous aroma carene imparts to essential oil blends. In those cases, origin stories matter. Citrus, pine, and turpentine feedstocks each throw subtle variations. We stick with gum turpentine so that our (1S)-(+)-3-Carene rides closest to the authentic forest fresh note. Downstream, this makes a difference for candle, soap, and detergent blends—small as the usage level may be. We’ve experimented in our own applications, and a touch of carene cuts through the “soapy” quality that synthetic mixtures sometimes bring. Unlike α-pinene or β-pinene, its aroma rounds out with a fruitier, almost candied edge.

    Despite these sensory perks, demand in the adhesives and resins market depends on chemical behavior more than fragrance. Here, (1S)-(+)-3-Carene acts as a monomer source or viscosity modifier. Sharp quality control and batch tracking become central, since side reactions in polymerization can lead to color or performance problems. Over several production seasons, our technical team has had to adjust reflux ratios and pressure settings to ensure we ship material that meets the narrow molecular weight distribution requirements our customers impose. One missed step and the whole shipment returns—no one wants a curdled resin or a sticky glue failing QC.

    What Sets (1S)-(+)-3-Carene Apart

    Our industry sometimes treats turpentine derivatives as interchangeable, but working in production shows the limits of this idea. (1S)-(+)-3-Carene doesn’t simply copy the effects of limonene, camphene, or pinene. Structurally, that extra five-membered ring drives its reactivity. Our chemists note that the hydration, halogenation, and rearrangement pathways diverge from the simpler monoterpenes, opening up unusual routes to novel molecules. Limonene oxidizes easily and offers a citrus note, but its oxidation products cause off-odors and shelf instability unless carefully managed. α-Pinene leans piney and turbid, but lacks the subtle sweet lift that (1S)-(+)-3-Carene introduces in fine fragrance or flavor settings.

    Synthetic routes involving (1S)-(+)-3-Carene give access to chiral intermediates unavailable from more abundant monoterpenes. This matters for specialty synthesis and fine chemicals, where enantiopurity affects both regulatory acceptance and end-use activity. More than a few clients have told us that only carene-derived derivatives match their performance, especially for chiral ligands or building blocks in pharmaceutical development. Our ongoing analytical support—chiral GC, NMR, and optical rotation checks—anchors our claims and helps answer the hard questions that researchers pose.

    From a performance angle, carene outpaces several competitors in stability. Its high boiling point keeps losses low, especially during high-temperature blending or compounding. Where limonene breaks down, carene keeps its profile intact. Raw batch testing supports what we’ve seen in finished goods—rancidity and oxidation rates remain negligible if storage follows best practices. Drums kept cool and sealed don’t show any major dimer formation or yellowing over months. That translates to fewer customer complaints and less waste overall.

    Challenges in Real-World Manufacturing and Distribution

    Refining (1S)-(+)-3-Carene at scale challenges our team in more ways than one. Turpentine, the primary raw material, shifts in composition all season long. Climate, pine species, and tapping practices contribute more complexity to the supply chain than many realize. Over the years, we’ve learned to hedge against these swings by collecting harvest data, logging yield shifts, and prequalifying each lot of gum. Sometimes a feedstock comes on the truck with lower than expected carene fraction. Other times, batch deviation arises from a tiny shift in distillation column temperature. Our operators walk the line between achieving top-purity carene and avoiding fraction co-distillation; the boiling points nestle so close together that losing the split by even a small margin can either waste raw material or cause purity to drop below acceptance standards.

    Once produced, storage and shipment form another bottleneck. Carene’s volatility and sensitivity to light require us to stick with stainless steel or coated drums, never clear plastics or unprotected containers. A queue of returned shipments early in our history taught the team hard lessons about logistics: don’t let product sit unsealed, keep out of direct sunlight, and push for climate-controlled transit, especially in hotter regions. Downstream, customers often call us to discuss drum handling or shelf life, since mishandling at their site can undo weeks of controlled production. Our technical service line logs these calls, seeking patterns to inform future production or packaging changes. We involve supply chain partners in the process, since everyone—from drum supplier to trucking fleet—plays a role in keeping carene batch integrity high.

    Policy and export regulations layer on more challenges. Monoterpenes cross legal thresholds for flammability and environmental hazard. Our compliance team prepares documentation at each stage, ensuring that shipments pass customs and satisfy environmental safety standards. Occasional site visits from regulatory agencies keep us sharp, checking that all storage tanks, labeling practices, and effluent streams meet strict standards. High batch traceability remains the best defense should questions arise—a lesson learned after one close call with an improperly labeled shipment. Customers in Europe and North America regularly request documentation on residual solvents, chiral purity certificates, and environmental footprint data. Auditors respond best to real records and clearly tracked workflows.

    Where We See (1S)-(+)-3-Carene Heading

    The industry signals new uses for (1S)-(+)-3-Carene. Aside from its established place in flavors, fragrances, and resins, researchers explore its role as a bio-sourced building block. Policies pushing for renewable chemical feedstocks benefit from carene’s renewable origin. In early pilots, green chemistry teams convert it into new polymers and specialty intermediates, aiming for biodegradable or low-toxicity applications. These are ambitious projects, with hurdles yet to be solved, but the interest highlights carene’s untapped value. We’ve hosted a few project teams in the plant; they bring their own analytics and help us see blind spots in our lab controls. Feedback cycles like this tighten our process and keep us on our toes.

    One reason (1S)-(+)-3-Carene stands out relates to its unique position between abundance and specialty. Pinewoods renewal places turpentine as a sustainable resource, and carene’s complexity offers more than just commodity value. As direct market feedback comes in, we focus on matching our batch documentation and production controls to the questions chemists pose. Every request for a new derivatization pathway or stability trial stretches our lab team and deepens our product understanding. Where new technical data emerges—from unexpected reaction byproducts to shelf life in exotic blends—we share findings within the team and integrate changes in the next production run. This back-and-forth with both research teams and regular buyers gives carene a collaborative edge that other monoterpene lines rarely achieve.

    Customers often compare our (1S)-(+)-3-Carene to products available from India, Brazil, or smaller regional distillers. Each supplier takes different approaches with fractionation and purification. Over more than a decade, we’ve dialed in our approach to meet both cost and technical demand. In several benchmark studies with large flavor and fragrance houses, our product repeatedly earns high marks for consistency and low off-note incidence. Key partners trust our documented chiral balance, knowing that the right optical rotation threads the needle for downstream syntheses. This doesn’t happen by accident—years of carefully recording outcomes and iteratively tightening process controls shape every drum we ship.

    Improvements and Future Solutions

    Scaling up carene operations means finding room for constant improvement. Our in-house R&D teams stay focused on optimizing cut points in our columns and improving activated carbon treatment protocols to further knock out trace contaminants. These process tweaks often start with a single troubleshooting call or rejected shipment. Data gathered in the field finds its way back to the lab, leading us to reevaluate baseline operating temperatures or update solvent rinse cycles. Over time, the little changes stack up—a subtle tweak to the vacuum system cuts impurity drag-through by half, or a new blending procedure gently boosts optical purity.

    Sustainability goals enter the conversation more frequently as well. Our procurement team partners with certified suppliers to secure renewable pine feedstock, prioritizing sources who follow strict conservation guidelines. In the last two years, we’ve launched projects to cut primary energy use during distillation and to improve solvent recycling onsite. Documentation of waste streams and emissions feeds directly into our environmental audits and helps us respond to customer requests for life-cycle data. These efforts not only make us a cleaner operation but also line up with the expectations of leading multinational buyers, who increasingly ask for proof of renewable sourcing and waste mitigation in the value chain.

    One future challenge centers on finding alternative uses for byproducts. Although (1S)-(+)-3-Carene makes up only a small fraction of turpentine, other components like limonene and camphene offer commercial value as well. Integrated extraction and purification can cut down waste, build new product lines, and help offset the costs of high-purity carene refinement. Our site teams work with revenue from byproduct streams—turpentine oil for disinfectants, residual pine oil as a solvent or cleaning agent—to keep the main operation cost-effective while reducing pressure on waste management. Tracking each side stream boosts both profitability and environmental stewardship, two goals that increasingly drive stakeholder decisions.

    Customers sometimes request custom blends or specific stereoisomers beyond (1S)-(+)-3-Carene itself. Meeting these calls forces us to rethink standard operating procedures and push for higher selectivity and better analytical screening. Dedicated process equipment and tighter control loops let us isolate fraction peaks more precisely, minimizing cross-contamination risk. Advanced chiral chromatography and multi-stage distillation—investments that seemed costly at first—now pay dividends in customer satisfaction and market reach. We’ve also rolled out real-time quality monitoring systems on the floor, so that errors surface and get addressed before a batch leaves the plant. This hands-on, data-driven approach keeps us nimble and trusted as demand patterns shift.

    Lessons from the Workshop and the Lab

    Our team has learned to trust both the lab notebook and the seasoned operator’s hunch. A well-maintained still matters as much as a calibrated GC. Oddly, some process changes first surface as anecdotes—one operator spots a shift in condensate odor, another tracks a small drop in distillation yield after a gasket swap. We encourage everyone who handles the product—from drum loaders to technicians—to record anomalies and speak up. Over time, these details feed back into small process improvements, reducing scrap and improving customer outcomes. Some of our best breakthroughs have come after following up on these small surprises.

    We also invest in regular training, both to keep up with new regulatory standards and to respond quickly to production shifts. That means revisiting safety protocols, updating job aids for remote diagnostics, and ensuring all staff—from lab analysts to maintenance—know where carene fits into the bigger picture. Education pays forward, not just in cleaner product but in stronger morale. Safety and traceability remain the cornerstones of our operations, values that we reinforce with every production meeting.

    Looking back, our journey with (1S)-(+)-3-Carene has proven surprisingly dynamic. Market forces, research needs, and regulatory scrutiny each push the bar a little higher. We embrace each change as another chance to refine our process, deliver cleaner product, and support customers tackling complex chemistry. Working hands-on means juggling raw material variability, technical troubleshooting, and new commercial demands—all while keeping the long game in mind. As science and industry crowd in on renewable chemistries, carene will keep making its mark as both a starting point and a fresh note in diverse formulas across the globe.