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HS Code |
874898 |
| Chemical Name | (1R,2R,5R)-(+)-2-Hydroxy-3-pinanone |
| Cas Number | 77832-71-0 |
| Molecular Formula | C10H16O2 |
| Molecular Weight | 168.23 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 263-265 °C |
| Density | 0.991 g/cm³ |
| Optical Rotation | [α]D20 +47° (c=1, CHCl3) |
| Purity | Typically ≥98% |
| Smiles | CC1(C)CCC2(C1C(=O)C(O)C2)C |
| Inchi | InChI=1S/C10H16O2/c1-7-3-4-8(2)10(7,5-6-7)9(12)11/h8,11-12H,3-6H2,1-2H3/t8-,10-/m1/s1 |
As an accredited (1R,2R,5R)-(+)-2-Hydroxy-3-Pinanone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 25 grams, tightly sealed with a screw cap, labeled with product name, CAS number, hazard warnings, and supplier details. |
| Shipping | (1R,2R,5R)-(+)-2-Hydroxy-3-Pinanone is shipped in secure, tightly sealed containers to prevent leaks or contamination. The package is clearly labeled according to regulatory standards, and shipped at ambient temperature unless stated otherwise. Handling and transport comply with chemical safety regulations to ensure safe delivery. |
| Storage | (1R,2R,5R)-(+)-2-Hydroxy-3-Pinanone should be stored in a cool, dry, and well-ventilated area, tightly sealed in its original container. Protect from light, moisture, and incompatible substances such as strong oxidizers. Store away from sources of ignition and direct sunlight. Ensure proper labeling and keep out of reach of unauthorized personnel. Use secondary containment to prevent accidental spills or leaks. |
Applications of (1R,2R,5R)-(+)-2-Hydroxy-3-Pinanone in Industrial ManufacturingAs an established upstream producer, we supply (1R,2R,5R)-(+)-2-Hydroxy-3-Pinanone to key downstream manufacturers who require high-purity chiral building blocks. Our material is consistently chosen for specialty applications in advanced synthesis, fragrance ingredient compounding, and pharmaceutical intermediate processes. The following sections illustrate its targeted industrial integration. 1. Synthesis of Chiral Pharmaceutical IntermediatesOriginating from our production lines with high optical purity, this compound serves in the manufacture of chiral intermediates for targeted active pharmaceutical ingredient (API) synthesis. Downstream processors value its unique bicyclic skeleton and well-defined configuration, which facilitate stereo-controlled transformations in complex drug molecule construction. Industry compliance standards
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2. Fine Fragrance and Aroma Ingredient FormulationSpecialty aroma compound manufacturers consistently select this hydroxy-pinane compound for its distinct woody-camphoraceous profile and chiral character, enabling differentiating notes in fine fragrance and high-end flavor applications. Its stability in formulation prevents off-note generation during blending and compounding. Industry compliance standards
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3. Agrochemical Active Ingredient DesignLeading agrochemical synthesis operations use (1R,2R,5R)-(+)-2-Hydroxy-3-Pinanone as a molecular precursor for enantioselective crop protection agents. Its well-defined structure supports the creation of actives with improved selectivity and environmental decomposition profiles. Industry compliance standards
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4. Synthesis of Terpene-Based Specialty ChemicalsOur customers in the specialty chemical sector require (1R,2R,5R)-(+)-2-Hydroxy-3-Pinanone to enable the manufacture of terpene-derivative compounds featuring precise stereochemistry for use in resins, adhesives, and advanced polymer additives. Its defined chiral center is crucial for subsequent modification reactions. Industry compliance standards
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Every chemist in the factory knows the moment: the sweet, woody scent drifting from the distillation column that tells us (1R,2R,5R)-(+)-2-Hydroxy-3-Pinanone has emerged from raw pinene. This molecule stands out for its purity and high optical activity. Through hands-on process refinement, controlling temperature shifts and reaction times to fractions of a minute, we keep each batch consistent and highly refined. Each operator tracks the process in real time, adjusting every parameter for the tightest stereochemical selectivity.
Ours is not a “close enough for handwaving” operation. Maintaining 98% or better enantiomeric excess never happens by chance. A single pressure drop or unstable mixing and the yield drops, wastes spike, and the purity plummets. We catch it in the moment, not in postmortem. That’s a lesson learned from many pilot runs, a fair share of ruined reactants, and constant communication amongst the synthesis, purification, and analysis teams.
In our plant, we identify this batch as Model R-2H3P, distinguished by its absolute configuration and consistent analytical readout. Our sticks and liquid samples show a dense, colorless material with a faint, earthy-green aroma. Color, optical rotation, and refractive index remain dependable—HPLC reports bear numbers, but our scientists have an eye for crystalline structure and the smell that signals a clean run.
Our staff learned years ago to measure trace metal content, moisture, and volatile impurities using direct techniques. These tests shape the batch just as much as the temperature dials. GC-MS, NMR, and Karl Fischer titration work back-to-back on every run and are cross-checked obsessively. Raw numbers drive confidence, but repeat experience cements trust.
There’s another dimension often overlooked: sustainability and safety in manufacturing. Starting from pine-based natural precursors allows us to avoid over-reliance on fossil-based feedstocks. Closed loop operations and solvent reclamation reduce hazards and meet environmental targets. We keep direct oversight on each step—no middlemen, no outsourced shortcuts, only our team and our equipment between raw material and product.
The market holds a few analogues: 2-hydroxy-3-pinone isomers, racemic forms, and the more generic monoterpenoids from bulk suppliers. The difference appears immediately for anyone who’s worked with stereochemistry. Our (1R,2R,5R)-(+)-2-hydroxy-3-pinanone shines for its enantiomeric purity, physical stability, and batch-to-batch consistency. Racemic or poorly resolved mixtures never match its aroma or its selectivity in further syntheses.
Synthetic chemists and perfumers reach for this material because the rotational configuration delivers unique reaction control. For chiral building blocks, a single stereoisomer creates predictability in asymmetric catalysis. Our team has learned that contaminants, no matter how slight, can cloud a complex natural flavor or disturb a reaction outcome, introducing noise in NMR spectra or altering conversion rates. Purity isn’t marketing; purity translates to reliable outcomes, less troubleshooting, and more confidence at scale.
Compared to aldehydic or ketonic analogues, this hydroxy-ketone gives creative flexibility in fragrance design and organic synthesis. Its secondary alcohol group resists quick oxidation, yet undergoes tailored reduction or acylation. That means more selective transformations and less byproduct management on the back end for both pharmaceutical intermediates and specialty perfume materials. We see this play out in factory process logs every month—less downtime, smoother purification, and less solvent use.
Industrial customers come with specifications honed over years of practical work. A gentle shift in optical activity or a drop in purity triggers entire plant-wide quality reviews. Product developers credit (1R,2R,5R)-(+)-2-hydroxy-3-pinanone with stability in formulations. Whether designing novel aroma compounds or advanced monoterpene derivatives, our chemists understand firsthand how compromised source material adds days of extra troubleshooting. Consistent output, guided by real, working chemists, keeps us ahead of these headaches.
Most people see a product label or a flask; our team sees the path from pine trees to clean, bottled hydroxy-pinanone. We know which pinenes yield the best precursor, recognize smells, and pay attention to fraction cuts during distillation. Only solid, hands-on manufacturing delivers a hydroxy-pinanone suited for modern needs.
In fragrances and flavors, this compound adds depth, resilience, and a green-woody undertone sought by experts in fine fragrance and household blending. Adding just a fraction can brighten citrus notes or lend natural authenticity to pine, mint, and woody scents. Product developers have reported success with this ingredient, citing not only the olfactory strength but the ability to persist in formulations without rapid breakdown.
Organic synthesis labs use (1R,2R,5R)-(+)-2-hydroxy-3-pinanone as a chiral building block, particularly where selective catalytic reactions need a stable, optically active substrate. Industry feedback tells us it works as an intermediate in antiviral, anti-inflammatory, and other advanced fine chemical preparations. Process engineers count on its stability in multi-step reactions, seeing first-hand that minor isomeric impurities—so easy to miss in less controlled plants—may derail yield or require costly reprocessing unless tightly controlled.
Industrial cleaners and household product makers have included test batches of hydroxy-pinanone for its scent and low toxicity. Chemists on our floor track VOC evaporation rates and residue formation, learning through test batches how this molecule integrates with surfactants and other modern cleaning actives. It holds up under storage without yellowing or off-notes.
Research customers value this molecule for work in asymmetric synthesis and structure–activity studies. With every shipment, we field feedback from research users about clarity in NMR spectra, error-free chromatography runs, and high reproducibility. Seasoned scientists recognize the spectrum of minor impurities from common resold or repurified product. Batch-by-batch, our manufacturing team has responded to even tiny divergences, using cross-departmental feedback to push down unwanted variance.
Process optimization isn’t theory—it happens through tracked improvement, real-world troubleshooting, and commitment from the people who run the reactors, not just the quality assurance office. Our staff tracks every step: from feedstock selection and catalytic conversion through to in-line purification and small-scale blending. From experience, we know the pitfalls—unexpected shifts through plant steam failures, or the gradual creep of off-odors if a column’s packing wears out.
In every run, chemists in production and QC sign off on real checks. Each employee knows their work affects not just finished tests, but how our customers experience the product in the lab or in market. By owning each batch from source to bottle, we catch drift before it hits the loading dock.
Compared to broad-spectrum plant extract derivatives, or resold bulk hydroxy-pinanones, our internal controls back tight, repeatable stereochemistry. Batch histories, empirical trend charts, and real-time feedback make this possible. The emphasis has always been on eliminating sources of error before the raw material moves past the line.
Expertise in purification, built through repetition on the plant floor, sets our process apart. Each controlled fractionation step, every staged solvent removal, follows protocols developed by chemists whose careers depend on measurable output. This commitment to hands-on, on-the-ground control means our output matches published standards for purity and optical activity every time.
New opportunities emerge as research stretches the boundaries of monoterpene chemistry. Teams seek this type of hydroxy-pinanone to push new boundaries in selective synthesis. We’ve worked directly with academic and industrial partners, sharing batch data, running collaborative tests, and learning together from synthetic bottlenecks. A high-quality, consistent molecule allows researchers to jump directly into hypothesis testing, not waste cycles on avoidable purification.
Cosmetic chemists come back for this material because they know what happens in a poorly controlled batch: colors darken over time, unwanted side reactions occur, and final product scent shifts from green freshness to muddy sweetness. Stable odor and unchanging physical profile signal clean material, rooted in controlled, in-house manufacturing.
More manufacturers have realized the value of a direct supply. Without third-party repackaging, the material moves from our factory lab to customer bench with no shared intermediates. Tracking, tracing, and continuous improvement show up back in the lab as solvable, understandable outcomes, not nagging, mysterious inconsistencies.
The future of fine chemical production will always depend on skilled teams who spot unexpected shifts and act the same day. Overreliance on bulk intermediaries or generic commodity outputs inevitably introduces unwanted noise and traceable errors. Our own process history shows that the direct manufacturer’s viewpoint—caring about both the final product and every step upstream—minimizes blame games, shortens troubleshooting, and empowers fast solutions.
Customers have told us, again and again, that switching from repacked material to direct manufacturer batches halved their labwork headaches. The consistency pays off not just in paperwork but in measurable process efficiencies: lower waste, higher production yields, and better reproducibility. It’s not a sales pitch—factory chemists live with every batch, course-correct in real time, and are accountable for any out-of-spec product. This culture breeds trust, and it shows up in cleaner, stronger, more reliable (1R,2R,5R)-(+)-2-hydroxy-3-pinanone.
By keeping staff turnover low, fostering training across roles, and emphasizing in-person communication between synthesis, quality, and logistics teams, mistakes get noticed before they grow. We’ve found that empowering every operator not just to fix, but to question and improve, creates a lineage of knowledge that outlasts even the most advanced automation. No algorithm replaces a nose honed for odors signaling peroxide, or an eye for a shifting Kerr rotation.
Direct oversight of environmental responsibility also matters. By owning our solvent recovery, waste neutralization, and energy inputs, we cut down risk at the source. Our records draw a straight line from forest to finished hydroxy-pinanone, not just for compliance but for ongoing improvement. Customers running sustainable brands trust our attention to cradle-to-factory choices: renewable pine feedstock, reduced emissions, and honest process data.
Hydroxy-pinanone chemistry has moved fast over recent decades. We’ve seen demands for higher purity, lower residual solvents, and greater batch predictability take center stage as applications in research and industry mature. In our own experience, responding to these earned requirements has meant upgrading equipment, learning new purification methods, and collaborating openly with the most demanding clients. Each innovation shows up in the operating logs and, ultimately, in the reliability of the molecule delivered.
Factory chemists remain the first line of feedback: noticing shifting demand for new derivatives, fixing emerging process glitches, and working with customers in real time to troubleshoot any rare out-of-spec batch. From small-bottle research lots to ton-scale runs, the principles that set us apart—direct control, staff accountability, process transparency—make a tangible difference in the hands of end-users.
In the real world, shortcuts never pay. Those with deep practical experience spot the difference between a “good enough” batch and a world-class one before analysis even begins. Manufacturing (1R,2R,5R)-(+)-2-hydroxy-3-pinanone is less about talking up features and more about knowing the chemical inside and out: the way it smells, the way it forms crystals, the way it reacts under pressure or prolonged storage. By keeping every step close to home, we deliver something not just by the numbers, but by expertise built over years and measured in every delivery.