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HS Code |
135073 |
| Cas Number | 7785-26-4 |
| Molecular Formula | C10H16 |
| Molecular Weight | 136.24 g/mol |
| Iupac Name | (1S,5S)-2,6,6-trimethylbicyclo[3.1.1]hept-2-ene |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 155-156 °C |
| Density | 0.858 g/mL at 25 °C |
| Optical Rotation | [α]D20 = -45° to -51° (neat) |
| Flash Point | 33 °C (closed cup) |
| Solubility | Insoluble in water; soluble in organic solvents |
As an accredited (1S)-(-)-Alpha-Pinene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle labeled “(1S)-(-)-Alpha-Pinene, 98%, 100 mL.” Features hazard symbols, lot number, and safety instructions. |
| Shipping | (1S)-(-)-Alpha-Pinene is classified as a flammable liquid. It should be shipped in tightly sealed, approved containers. In transit, it must be clearly labeled, protected from heat, ignition sources, and sunlight, and comply with local and international shipping regulations (such as DOT, IATA, or IMDG guidelines for hazardous materials). |
| Storage | (1S)-(-)-Alpha-Pinene should be stored in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and direct sunlight. Keep the container tightly closed and protected from moisture. Store separately from strong oxidizing agents and acids. Ensure appropriate labeling and use explosion-proof electrical equipment as alpha-pinene is flammable and can form explosive mixtures with air. |
Applications of (1S)-(-)-Alpha-Pinene in Industrial Manufacturing(1S)-(-)-Alpha-Pinene is a key monoterpene raw material widely adopted by downstream chemical manufacturers in the synthesis of value-added products. As a direct producer with advanced distillation capability and traceable sourcing, we supply consistent (1S)-(-)-Alpha-Pinene to support high-precision applications across several specialized industrial segments. Below, we detail practical downstream cases in which our material is an essential feedstock, highlighting regulatory compliance, actual formulation roles, process junctions, and representative finished goods in each scenario. 1. Manufacture of Terpineol for Fragrance and FlavorsLeading fragrance formulators and flavor houses use (1S)-(-)-Alpha-Pinene as a primary starting material for the synthesis of alpha-terpineol. Through finely controlled catalytic hydration and subsequent isomerization processes, manufacturers achieve high-purity terpineol fractions that align with international organoleptic and purity benchmarks needed in luxury perfumes, detergents, and flavoring agents. Industry compliance standards
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2. Synthesis of Camphor for Pharmaceutical ApplicationsPharmaceutical processors utilize (1S)-(-)-Alpha-Pinene as the precursor in a multi-step oxidation and rearrangement sequence to manufacture synthetic camphor. This camphor later serves as an active or auxiliary ingredient in topical analgesics, vapor rubs, and medicinal ointments, meeting strict pharmacopoeia criteria for medicinal purity. Industry compliance standards
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3. Resin and Adhesive Production for Industrial CoatingsIndustrial resin formulators incorporate (1S)-(-)-Alpha-Pinene in the synthesis of polyterpene resins, which are further processed into tackifiers and adhesion promoters in the manufacture of high-performance adhesives and industrial wood coatings. Strict control over the polymerization parameters ensures compliance with segment-specific mechanical and migration standards. Industry compliance standards
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4. Production of Insect Repellent ActivesSpecialty chemical companies rely on (1S)-(-)-Alpha-Pinene as a synthetic intermediate for generating derivative compounds such as borneol and isobornyl esters, both of which function as active components in insect repellents and natural pesticide formulations. This integration demands careful material tracking and process validation to meet agrochemical and biocide safety laws. Industry compliance standards
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5. Synthesis of Chiral Building Blocks for Agrochemical IntermediatesMajor agrochemical manufacturers use (1S)-(-)-Alpha-Pinene as a source of chiral frameworks in multi-step synthesis routes for specialty intermediates, including enantiomerically pure synthons required in fungicides and insecticide active ingredient development. These routes call for advanced chiral synthesis control and documentation to conform to emerging global pesticide standards. Industry compliance standards
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As a chemical manufacturer with decades of experience in terpene isolation and purification, we’ve witnessed the growing appreciation for products like (1S)-(-)-Alpha-Pinene across multiple industries. This compound’s significance comes not from synthetic mimicry, but from meticulous extraction, separation, and quality management, processes we have refined year after year. The result stands far apart from low-grade alpha-pinene or racemic pinene blends. With the (1S) enantiomer, the chemical structure shapes not only the aroma but the way the ingredient interacts in each application, from fragrances and flavors to chemical synthesis.
Pinene exists in nature as two main isomers: (1S)-(-)-Alpha-Pinene and (1R)-(+)-Alpha-Pinene, each recognized by its distinct optical activity and slightly different olfactory profile. The (1S)-(-)-enantiomer dominates in certain botanical sources, particularly European pine trees. This chiral purity matters to downstream chemists and formulators. Many applications, especially in aroma chemistry and pharmaceutical synthesis, demand single-enantiomer materials to achieve desired physiochemical properties, reaction outcomes, and regulatory compliance.
Unlike many mixtures offered by traders or commodity suppliers, we use targeted fractionation methods that rely on expertise built from process control rather than simple steam distillation. Our field teams procure feedstock from long-term partners, selecting only those lots that yield the highest ratio of (1S)-(-)-Alpha-Pinene after processing. The raw sap undergoes precise fractionation, removing non-terpenic impurities, then further separation until laboratory results confirm a high-reliability, single-enantiomer product. We continually test for trace chiral impurities, sulfur compounds, and aldehydes—byproduct markers that affect odor, stability, and downstream reactivity.
Customers who formulate fine fragrances, flavors, and advanced chemical intermediates consistently look for purity above 96% for (1S)-(-)-Alpha-Pinene. In lower grades, even trace levels of the (1R) isomer or co-eluting terpenes introduce off-notes and reduce product performance. Our batches undergo both gas chromatography and specific rotation validation, anchoring each lot to its chiral fingerprint.
We guarantee clarity free from cloudiness and suspend particulate, because haze and micro-droplets complicate automated dosing equipment. Our analyzers measure specific gravity and refractive index at controlled temperatures, flagging any deviation that might impact large-scale blending pipelines or manual mixing in smaller laboratories. In all our years of handling pinenes, we’ve learned that even small inconsistencies can propagate into costly, unpredictable variables for industrial and artisanal customers alike.
With the increase in regulatory checks, such as those enforced by REACH, IFRA, and FDA counterparts around the globe, customers need trackable, reproducible lots. For this reason, each production run is fully documented, and we retain retained samples for every order.
The (1S)-(-)-Alpha-Pinene we produce finds its way into a spectrum of applications. In perfumery and flavorings, this enantiomer delivers a crisp, evergreen freshness that cannot be duplicated by using synthetic blends or racemic pinene. Expert noses in perfumery and flavor design can distinguish subtle nuances that arise from pure (1S)-(-)-Alpha-Pinene—nuances that manifest as nuances of forest, herbal, or terpene sharpness, forming the backbone of top notes in colognes, room sprays, or high-quality extracts for culinary use.
Chemical synthesis leverages (1S)-(-)-Alpha-Pinene as a critical carbon skeleton for producing complex intermediates, including bicyclic terpenoids, resins, and natural product derivatives. Enantioselectivity in starting materials accelerates complicated reduction reactions and chiral transformations, translating to higher efficiency and lower waste. Small inconsistencies in enantiomeric ratios at the source force downstream processes to contend with reaction byproducts and reduced yields.
Even outside of chemical and aromatic uses, this pinene isomer enters the market as a renewable feedstock for specialty adhesives, solvents, and even chiral auxiliaries for asymmetric synthesis. Our facilities, with equipment dedicated purely to pine terpenes, reduce risks of cross-contamination and batch memory—a lesson from years spent responding to sensitive customers in electronics and pharmaceutical pre-cursors.
Decades in the field have reinforced the reality that supply security means more than a filled order book. We maintain relationships with foresters to ensure sap harvesting follows robust environmental protocols. The collection and extraction process reflects the principles of circular chemistry—we recover process water and recycle solvents after each cycle, with active monitoring to avoid cross-variable contamination.
On the ground, temperature swings, transport issues, and even slight shifts in pH during initial extraction impact enantiomeric purity. Early mistakes, like allowing sap to rest too long before fractionation, cost us yield and market confidence. Over time, our teams developed time-tested routines—proximity to forest sources, staggered collection, and rapid transfer—minimizing degradation and conformational changes in alpha-pinene content.
Our reactors and distillation columns undergo regular passivation and recalibration to keep batch-to-batch performance consistent. Data from the past decade shows that many rejected batches across the industry come from inconsistent separation techniques, especially when feedstock quality varies. Investments in automation, in-line sensors, and human oversight have helped us consistently hit the chiral purity marks our customers expect.
We practice full vertical integration, from feedstock sourcing to final packaging. Internal tracking codes link every unit to its lot, raw batch, and even the forest stand where the pine originated. Long-standing clients appreciate the degree to which we can recall historical data—chemical fingerprint, temperature logs, maintenance records for the separation columns used, and final lab QA checks—especially as regulatory pressure grows.
Our team maintains forward-looking documentation suitable for demanding auditors. From our experience, transparency brings confidence in markets as varied as flavorings, environmental solvents, and advanced materials. End-user chemists in multinational labs, as well as boutique formulators, gain direct access to product development and quality assurance teams, not just to sales orders.
A common point of confusion arises for buyers seeking general “alpha-pinene”, “terpene concentrate”, or even pure limonene. True (1S)-(-)-Alpha-Pinene differs not just by molecular structure, but by supply chain, process, and suitability for demanding applications. Alpha-pinene from commodity sources often comprises mixtures, sometimes with more of the (1R) isomer or with co-extracted beta-pinene, limonene, and non-terpenic volatiles.
The chiral nature of (1S)-(-)-Alpha-Pinene offers distinct reactivity and olfactory notes—a factor crucial to high-impact value streams like flavor and pharmaceutical synthesis. Clients have learned, sometimes painfully, that low-cost, racemic pinene introduces unpredictable outcomes in multi-step reactions or high-sensitivity fragrance systems. For example, racemic pinene from global spot markets may arrive with up to 10% other terpenes, leading to off-odor, discoloration, or lower batch yields for fine chemicals.
Limonene, another major cyclic monoterpene, shares structural similarities but brings a citrus profile, unlike the green-pine freshness of (1S)-(-)-Alpha-Pinene. Limonene’s use in cleaning or food applications differs, and technical substitution for true alpha-pinene fails in both aromatics and synthesis where chiral specificity and reactivity dictate outcomes.
Beta-pinene, typically co-produced in pine resin streams, brings its own set of handling and application criteria. It lacks the sharp, herbal-fragrance note of alpha-pinene and reacts differently in organic synthesis. Many end users conflate these pinenes, only to discover downstream issues with color stability, solubility, and chemical consistency. Having navigated countless technical support requests over time, our technical team spends considerable resources helping customers identify the right isomer for their end use.
Our experience shows ecological stewardship stands at the core of long-term terpene production. Pine forest extraction must strike a balance between productivity and forest regeneration. We select forests managed under sustainable certification and maintain ongoing dialogue with local harvesters—sharing knowledge, supporting training, and directly monitoring sap yields. This approach emerged after observing erosion and habitat loss in overloaded pine stands managed by short-term resellers, which led to both lower long-term yields and regulatory concerns.
Resource efficiency continues through the plant. By investing in low-energy fractionation and solvent recovery, we reduce emissions and raw material waste. Our closed-loop extraction and purification lines not only meet regulations, but help us maintain purity standards. Employee input plays a key role—over the years, line workers have suggested process improvements that now set our operation apart. For instance, ongoing collaborative experiments with resin stripping temperatures have allowed us to further increase yields of the (1S) isomer, all while reducing unwanted byproducts.
Global demand for high-purity (1S)-(-)-Alpha-Pinene increases every year, driven by new applications in pharmaceuticals, cosmetics, and sustainable chemicals. Seasonal bottlenecks, climate impacts, and shifts in regulatory thresholds pressure producers to innovate. We’ve mitigated harvest volatility by using long-term forward contracts, diversified forest supply partners, and adaptive processing facilities that run year-round.
As new industries emerge, end users ask for more stringent impurity limits and supply transparency. We’ve responded with regular process audits, expanded laboratory capacity, and real-time data reporting accessible to customers. For example, certain aroma formulators require lower than 100 ppm trace oxygenates due to the risk of premature oxidative odor. Our continuous fractional distillation, paired with inert-gas blanketing during transfer, achieves these benchmarks.
We also confront price volatility due to supply imbalances or jumps in demand for downstream goods like pharmaceuticals. Rather than shift the costs onto the customer, we work collaboratively—sharing forecasts, scheduling capacity, and offering storage agreements on-site. Our experience in previous market disruptions underscores the importance of reliability and communication.
In flavor and fragrance labs, formulators leverage (1S)-(-)-Alpha-Pinene in high-impact green, pine, and forest notes. These are sometimes deployed at less than 0.5% in the finished product, yet the difference in bright, clean aroma is perceptible even at low concentrations. In one collaboration with a major beverage flavor lab, our selective extraction process allowed their product to clear repeated sensory evaluation rounds, whereas previous batches with mixed pinene failed due to secondary notes.
Pharmaceutical chemistry groups focus on chiral purity for precursor synthesis leading to compounds such as terpineol and camphor derivatives, where racemic pinene, even at 98% purity, proved unsuitable due to stability and yield issues in the final step. A process audit with this partner pinpointed the need for improved storage and transfer conditions, which our operations implemented. The result: reduced decomposition and more predictable conversion in scaled chemical transformations.
Similar narratives come from adhesive and specialty polymer producers. Their lines demand consistently low sulfur and no off-spec terpenes. Sudden changes in supplier purity or process stability previously caused production halts and waste. With our vertically integrated production and strict QA, they maintain smooth runs, predictable curing profiles, and end-use compliance.
True technical advancement emerges not from isolated academic work, but through years of batch processing, feedback from formulators, and inevitable troubleshooting. We invest directly in process improvements—such as more selective chromatography, low-pressure fractionation, and on-line purity monitoring—driven by real needs in the field, not just in-house innovation for its own sake.
Technical teams, many with over 20 years of laboratory and plant experience, bring insight about how minor plant operations, like cleaning protocols or timing distillation runs relative to harvest cycles, impact overall purity. Over time, we realized minimizing oxygen exposure, optimizing atmosphere controls, and integrating rapid cooling after distillation boosted enantiomeric retention and stability—a competitive edge our customers experience in practice.
We continue to share these developments with our customers, from process flow adjustments that enhance reproducibility, to chemical analysis improvements that inform better risk management downstream. Open channels of communication with field chemists ensure ongoing improvement.
Future trends in green chemistry, regulatory tightening, and sustainability will continue to shape the market for (1S)-(-)-Alpha-Pinene. Researchers press forward with chiral syntheses, looking for more selective, eco-friendly ways to use this building block. Our investments in both people and equipment reflect a company-wide commitment to anticipating needs, not just reacting to the shifting market.
Recent interest in renewable platform chemicals has spotlighted pinenes as both green solvents and enantiopure intermediate sources. We’ve seen early-adopter formulators in electronics and polymers push for even higher chiral stability. To meet these requests, we run parallel development lines, testing new fractionation and monitoring methods, while also training the next generation of plant operators and process chemists in advanced pinenes management.
From years of supplying to both high-volume and artisanal customers, we know consistency forms the backbone of trust in every chemical transaction. Our people build quality into each step, and our customers’ feedback translates into improved process performance and product characteristics.
(1S)-(-)-Alpha-Pinene serves demanding industries that cannot afford variable materials. By controlling the whole production stream—from sustainable pine collection to highly selective fractionation and relentless quality checks—we provide a chiral terpene with documented consistency. The added value is not only in purity percentages, but in the reliability, transparency, and ongoing technical improvements built from real-world experience across broad markets. Customers count on us for much more than a commodity; they trust our dedication to continuous improvement, stewardship, and hands-on support at every stage of production and application.