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D(+)-2-Octanol

    • Product Name D(+)-2-Octanol
    • Alias D-1-Octanol
    • Einecs 208-975-7
    • 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
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    Specifications

    HS Code

    462491

    Product Name D(+)-2-Octanol
    Cas Number 6168-72-5
    Molecular Formula C8H18O
    Molar Mass 130.23 g/mol
    Appearance Colorless liquid
    Boiling Point 179-181 °C
    Melting Point -17 °C
    Density 0.822 g/mL at 25°C
    Optical Rotation +8° to +9° (neat)
    Refractive Index 1.429-1.433 (20 °C)
    Flash Point 68 °C (closed cup)
    Solubility In Water Insoluble
    Synonyms D-2-Octanol, (+)-2-Octanol
    Purity Typically ≥98%
    Storage Temperature Store at room temperature

    As an accredited D(+)-2-Octanol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The packaging for D(+)-2-Octanol 100 mL comes in a sealed amber glass bottle with a secure screw cap and clear labeling.
    Shipping D(+)-2-Octanol is shipped in tightly sealed containers made of compatible materials, typically glass or HDPE, to prevent leakage and contamination. During transport, it is kept in a cool, well-ventilated area, away from heat and ignition sources. Proper labeling and documentation in accordance with regulatory guidelines are required.
    Storage D(+)-2-Octanol should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as oxidizing agents. Keep the container tightly closed when not in use to prevent moisture absorption and contamination. Store in a chemical-resistant container, clearly labeled, and protect from direct sunlight and heat to maintain chemical stability and safety.
    Application of D(+)-2-Octanol

    Applications of D(+)-2-Octanol in Industrial Manufacturing

    As a manufacturer specializing in D(+)-2-Octanol, we support downstream producers with consistent material quality, regulatory alignment, and application knowledge across critical sectors. Below, we detail the principal industrial domains harnessing this raw material, the associated compliance benchmarks, representative formulation ratios, integration stages, and the finished goods generated.

    1. Plasticizer Intermediate Synthesis

    Producers in the plasticizer industry leverage D(+)-2-Octanol primarily for synthesizing specialty esters such as dioctyl phthalate (DOP) and dioctyl adipate (DOA). The material enters as an alcohol reactant during esterification, ensuring precise molecular branching required for high-performance, flexible PVC plasticizers. Formulators carefully calibrate addition ratios, balancing reactant load with conversion efficiency while upholding regulatory thresholds for phthalate and non-phthalate compounds. Demand stems from cable insulation, automotive interiors, and packaging film manufacturers who require stable long-chain plasticizers with consistent migration control and low volatility.

    Industry compliance standards

    • REACH Regulation (EC) No. 1907/2006—substance registration and safety measures
    • RoHS Directive 2011/65/EU restriction on hazardous substances
    • EN 71-3:2019 Safety of Toys—Migration of certain elements (for soft PVC toys)
    • ASTM D3421 for plasticizer volatility testing

    Typical usage ratio

    • Alcohol-to-acid molar ratio: 1.05–1.20:1 in batch esterification
    • Adjustment based on desired ester yield and reactant purity

    Downstream process integration

    • Charge as a core alcohol during esterification with phthalic or adipic acid
    • Post-esterification purification, followed by blending into PVC compounds

    Final product types

    • Dioctyl phthalate (DOP), dioctyl adipate (DOA) plasticizers
    • Synthetic leather and vinyl flooring
    • Flexible PVC cable insulation
    • Plasticized polymer sheeting

    2. Fragrance Intermediate Manufacturing

    Major fragrance compound manufacturers utilize D(+)-2-Octanol as a critical intermediate for producing octyl-based ethers and acetates used in luxury perfumes and household air freshening formulations. The alcohol undergoes selective acetylation or etherification in controlled reaction conditions, followed by rigorous distillation to meet IFRA purity and allergen standards. Producers employ analytical methods for trace by-product control, accommodating batch-to-batch ingredient audits required by end customers in the personal care and home fragrance segments.

    Industry compliance standards

    • IFRA International Fragrance Association Standards
    • EU Cosmetics Regulation (EC) No. 1223/2009
    • IFRA Analytical Best Practices
    • ISO 9235:2013 (Aromatic natural raw materials—Vocabulary)

    Typical usage ratio

    • Acetylation reaction: 1.10–1.15 molar equivalents vs. acyl donor
    • Adjustment for residual odor profile and compositional purity

    Downstream process integration

    • Introduced as an alcohol substrate in fragrance intermediate synthesis
    • Cascading through distillation columns for high-grade separation

    Final product types

    • Octyl acetate and octyl ether fragrance bases
    • Fine perfumery additives
    • Household deodorizer and fabric softener scents
    • Detergent fragrances

    3. Pharmaceutical Intermediate Production

    In the pharmaceutical chemical sector, companies employ D(+)-2-Octanol for the stereoselective synthesis of chiral intermediates, including octanol derivatives essential for APIs and excipients with specific enantiomeric configurations. The raw material’s defined optical purity allows for controlled enantioselective reactions, aiding downstream synthesis of drugs targeting CNS or cardiovascular indications. Process engineers maintain GMP validation and impurity profiling throughout the preparative stages, supported by traceability documentation required for regulatory submission.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guidance for APIs
    • US Pharmacopeia (USP) and European Pharmacopoeia (EP) specifications
    • FDA 21 CFR Part 210/211
    • ISO 9001:2015 Quality Management Systems

    Typical usage ratio

    • Reaction stoichiometry: 1.00–1.05 molar equivalents in chiral synthesis
    • Adjusted to minimize by-product formation per active synth route

    Downstream process integration

    • Initial chiral reactant in the preparation of enantiopure pharmaceutical intermediates
    • Sequential steps including crystallization, solvent exchange, and final purification

    Final product types

    • Enantiomer-specific drug precursors
    • Stereospecific pharmaceutical building blocks
    • API (Active Pharmaceutical Ingredient) intermediates

    4. Lubricant Additive Component Manufacturing

    Manufacturers of synthetic lubricant additives incorporate D(+)-2-Octanol as an aliphatic backbone in the production of high-performance esters and specialty surfactant agents. The alcohol’s branched structure imparts tailored lubricity, pour point depression, and solvency in finished automotive and industrial lubricating formulations. Production lines feed the compound into esterification or alkoxylation reactors, with QC teams conducting batch certification against gear oil and hydraulic fluid standards for OEM suppliers and maintenance operations.

    Industry compliance standards

    • ASTM D445/D2270 for viscosity index
    • API Service Categories (SN, CF)
    • SAE J183 Engine Oil Chemicals Standards
    • OEM-specific lubricant approval protocols

    Typical usage ratio

    • Formulation input: 5–12% by weight in synthetic ester lubricant additives
    • Ratio optimized for finished product viscosity and thermal stability

    Downstream process integration

    • Reacted with dicarboxylic acids under controlled esterification to yield base fluids
    • Fed directly as co-solvent or wetting agent in additive blending tanks

    Final product types

    • Synthetic base oils for engine and transmission fluids
    • Hydraulic oils and gear lubricants
    • Metalworking fluid additives
    • Multipurpose greases

    5. Coating and Resin Modifier Processing

    Coatings producers utilize D(+)-2-Octanol in synthesizing octyl acrylates and methacrylates, key monomers and co-monomers for creating durable, flexible resins. The raw material enables the formation of polymers offering improved gloss, weather resistance, and chemical inertness in exterior paints and specialty industrial coatings. Integration occurs in the monomer pre-polymerization step, where continuous fed-batch reactors optimize conversion rates and minimize residual alcohol levels, which is critical for regulatory VOC compliance and product performance in the construction and OEM finishing sectors.

    Industry compliance standards

    • US EPA 40 CFR Part 59 (National VOC Emission Standards for Consumer and Commercial Products)
    • ISO 9001:2015 for production quality management
    • EN 13300: Paints and varnishes - Water-borne coatings
    • ASTM D7767 - Standard Practice for Determination of Volatile Organic Compound Content

    Typical usage ratio

    • Feedstock: 0.5–5% of total monomer mass in acrylic/methacrylic resin synthesis
    • Adjusted according to resin hardness and target film flexibility

    Downstream process integration

    • Alcohol charged to esterification reactors for acrylate monomer production
    • Initiates polymerization or copolymerization stages for high-solid or solvent-based resins

    Final product types

    • Exterior architectural paints
    • Automotive primers and topcoats
    • Protective marine and industrial coatings
    • Plastic and metal adhesion primers
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    Certification & Compliance
    More Introduction

    D(+)-2-Octanol: A Reliable Choice for Modern Synthesis

    Experience and Consistency in D(+)-2-Octanol Production

    In chemical manufacturing, few products challenge us quite like D(+)-2-Octanol. The process starts with careful raw material selection, and every batch demands attention. D(+)-2-Octanol stands out because each step – from oxidation to purification – calls for precise controls. Drawing on decades in the plant, we understand that customers rely on reliable optical purity, consistent stereochemistry, and reliable supply. Our team controls enantiomeric excess by tightly managing reaction temperatures and catalysts. Experience shows us that a small deviation in those parameters leads straight to racemization, which can waste entire production runs. Quality here comes from skill, not luck.

    D(+)-2-Octanol, also called R-2-octanol, brings value through its unusual chirality. Unlike generic 2-octanol, this substance offers a high [D] optical rotation, which makes it valuable to pharmaceutical and fine chemical industries. It’s not just a solvent or a base reagent. Our partners use D(+)-2-Octanol in the synthesis of chiral intermediates, which means that stereochemistry, impurities, and even minor batch-to-batch differences matter. A product like this does not find its way into large-scale processes by accident. Customers return because every shipment gives them matching GC retention times and high enantiomeric purity. From our lab data, typical purity for our product exceeds 99%, and enantiomeric excess stays above 98% in continuous runs.

    Specifications and What They Mean for End Use

    We focus on maintaining a well-defined product specification, not to meet bureaucracy, but to translate directly into easier project management for our customers. Most of our D(+)-2-Octanol goes out as a clear, colorless liquid, with a boiling point between 176 and 178 °C under atmospheric conditions. At 20°C, its specific gravity ranges from 0.820 to 0.830, and we regularly check optical rotation for compliance with customer needs. Water content, residual solvents, and trace byproducts cannot go unchecked: we use GC and Karl Fischer titration in every lot, which keeps water content below 0.1%, letting formulation chemists skip tedious drying steps.

    Stereoisomeric purity shapes reactivity. End users in pharmaceutical synthesis require the D(+) configuration for downstream reactions, particularly where enzymes or chiral catalysts are at play. In fragrance intermediates, the D(+) isomer influences scent profile and product compliance. Failing to secure high isomeric purity usually invites regulatory headaches and wasted resources.

    An Insider’s Take on Production Challenges

    A growing number of customers ask about our production practices. Synthetic processes for D(+)-2-Octanol often use either fermentation followed by resolution, or stereo-selective hydrogenation. Both routes bring risks. In fermentation, costs can spiral as yields drop, and the product may pick up microbial residues or acetic acid traces. When doing asymmetric hydrogenation, catalysts must remain tightly controlled, as even minute contamination from heavy metals or unreacted substrate blocks downstream use in pharma. Our shop-floor team stamps out errors by doubling cleaning cycles on reactors and testing for trace palladium or rhodium after each run. Senior technicians know that this avoidance of cross-contamination protects both plant safety and customer reputation.

    Logistics play their part. D(+)-2-Octanol oxidizes in the presence of air, especially under sunlight, forming odorous acids. Warehousing specialists at our facility transfer product quickly to storage under nitrogen, in high-density drums or ISO tanks lined with passivated stainless steel. A careless hour in the wrong tank can trigger flavor complaints and product returns. Such small factors build trust when users realize every shipment smells and flows like the last.

    Why D(+)-2-Octanol Has an Edge Over Similar Alcohols

    Not all secondary alcohols work under the same reaction conditions. Take racemic 2-octanol or typical S(-)-2-octanol. These lack the specific chiral orientation demanded by many drug or agro-intermediate makers. Simple racemic mixtures often complicate downstream separation and can double the cost at the API stage. In our experience, users integrating D(+)-2-Octanol achieve shorter synthesis cycles and less waste during chiral resolution. The added upfront investment pays off by streamlining development, clearing up regulatory submissions, and supporting patent positions.

    Another hidden value appears in analytical chemistry. D(+)-2-Octanol helps labs calibrate chiral columns or validate new enantioselective methods. Our technical support has seen projects grind to a halt due to unrecognized isomeric mismatches. D(+) provides a sharp, unambiguous peak, supporting rapid trouble-shooting and saving project hours.

    Features That Set D(+)-2-Octanol Apart

    Every bottle or drum contains our assurance of full REACH registration and compliance with Chinese, Japanese, and US inventory requirements. We go well beyond simply ticking regulatory boxes. By controlling trace impurities, we see fewer complaints around odor, color, or delayed reactivity. Stability after six months of warehouse storage proves itself in customer applications, especially in research-scale orders that might sit on the shelf before use. Flexibility also sits at the core of our approach; we listen when customers request packed-in nitrogen, high-purity filtration, or specific drum materials to protect their own processes.

    We regularly analyze returned feedback and batch histories. That process taught us early on that customers working in chiral catalysis rarely tolerate trace dodecanol or longer-chain byproducts. Our customized distillation steps suppress such contaminants. Analytical records are open for customer review, giving transparency into every production run. This open-book approach underpins relationships, as nobody likes surprises in an industry that abhors uncertainty.

    How Usage Patterns Shape Our Output

    Some customers want a reactive intermediate for esterification. For others, D(+)-2-Octanol serves as a starting block for chiral surfactants or flavor molecules. Usage pattern matters; formulations aimed at the cosmetic industry demand reduced odor and near-zero color, often pushing our process engineers to squeeze yet another level of purification out of the process. We tune hydrogenation and distillation parameters to match new requirements when partners declare application changes. In custom projects, we’ve observed increased demand for food-grade or USP-compliant grades, and refocused analytical support accordingly, pulling from project files where similar requests cropped up before.

    Frequently, pharma scale-up teams reach out mid-project, asking for parallel test lots with altered impurity limits. Our modular manufacturing line accommodates experimental and scale-up orders, with precise split-batch control. This approach means R&D teams can move from 1 kg evaluation up to full-scale runs without waiting for new plant qualification. It’s a learning process for both sides, but hard lessons in managing tight optical purity have taught us that early technical engagement always beats surprises during validation.

    Supporting Claims with Data and Experience

    Few metrics matter more than reproducibility. Our internal QA data, spanning five years, tells us D(+)-2-Octanol consistently leaves the facility with >99% GC purity, backed by enantiomeric excess (ee) certifications that set customer minds at ease. Complaint rates stay low: under 0.2% per annum, largely linked to shipping or drum damage rather than chemical quality. Final batch release relies on independent verification – documented by both our in-house and third-party labs.

    Our hands-on approach finds roots in the tradition of chemical craftsmanship, but it is anchored in current global regulations. Each shipment includes batch records with certificate-of-analysis, and digital access to chromatograms when users check conformity claims. This accountability comes from hard-won feedback: years ago, a poorly documented batch led to a difficult conversation with a key European partner. We haven’t forgotten the lesson, so now documentation travels with the product every time.

    Challenges in Aligning with Evolving Market Needs

    Managing D(+)-2-Octanol production demands continuous awareness of global trends. Environmental and safety initiatives reshape the way customers think about solvents and reagents. Restrictions on CMR (carcinogenic, mutagenic, and reprotoxic) agents influence customer selection as they look for greener alternatives. Our team watches regulatory developments closely – most recently in Europe – ensuring no proposed mutation in environmental rules surprises us or our buyers. Sourcing raw inputs with available traceability ensures that our end product stays on side with new rules, while minimizing batch recalls or compliance stress.

    Supply chain fragility, highlighted during recent global disruptions, taught us multiple lessons. We diversified sourcing for key intermediates to prevent shortages and invested in on-site quality control labs. Every incoming raw lot receives identity and purity checks before entering production, insulating downstream users from price and quality swings. Production staff carry out extra checks for materials imported under changing customs regimes, guaranteeing each ingredient matches the product’s safety data sheet and long-term storage requirements.

    Potential Solutions to Recurring Industry Problems

    Long-term partnerships emerge when users see actual solutions to their challenges. Often, chemical makers and users share a goal – reliable material with minimal noise in downstream results. Early technical engagement cuts down on costly raw material deviation. That’s why our technical sales and application chemists spend time understanding the intended reactions and storage protocols, recommending tailored features such as dry packaging or aggressive inertization for sensitive applications.

    Ongoing research into greener production supports both sustainability and product differentiation. Our site trialed biocatalytic approaches, seeking improved yields and less hazardous waste. While these routes present learning curves and regulatory questions, results so far suggest bioprocesses can match traditional synthetic routes for key quality metrics while leveraging renewable feedstocks. We plan further pilot-scale investigations with user feedback guiding final adoption. Any developments transferring from lab to plant will proceed only alongside side-by-side testing data with users who know their own end-product specifications best.

    We also learned from feedback that easier access to application support – real-time troubleshooting, fast provision of technical documentation, and open sharing on impurity profiles – allows our customers to adapt as regulations shift. Investing in dedicated technical support lines and digital documentation platforms cuts waiting times and makes audits smoother. Users have commented that this support defines, rather than simply supplements, the product experience.

    Small Details Make a Big Difference

    Handling and storage often make or break product performance. We follow clear routines: store D(+)-2-Octanol away from high heat and ensure drums remain tightly sheltered from sunlight. This routine emerges from seeing degraded stock sabotage multi-thousand-euro syntheses. Strict adherence avoids unplanned downtime, customer complaints, and regulatory fines on both sides of the supply chain.

    Freight options can affect both timeline and quality. Air freight reduces lead times for research batches, avoiding prolonged exposure during summer transit. In contrast, sea bulk exports demand additional stabilization measures, which we provide through inert lining and regular container monitoring. Each logistics adjustment comes from long-term tracking of which incidents prompt customer dissatisfaction. These records inform new transport protocols whenever feedback indicates a possible weak link.

    Comparing D(+)-2-Octanol to Other Secondary Alcohols

    D(+)-2-Octanol distances itself from other medium-chain alcohols in practical style. C8 alcohols like n-octanol or racemic mixtures lack the optical activity required in chiral syntheses. Even with similar boiling points and volatility, their applications diverge when selectivity counts. Highly regulated industries – pharmaceuticals, agrochemicals, and flavors – look beyond basic alcohol content and focus on repeatable chiral influence and low off-odor. Our D(+)-2-Octanol delivers those metrics, keeping downstream processes predictable.

    Technicians who switch from mixed 2-octanol sources to D(+) grades often report higher product yields and easier compliance documentation, with fewer issues in final product testing. The subtle differences in optical purity matter when writing patents or facing inspection. Over the years, we’ve fielded calls from clients whose suppliers delivered only generic grades, resulting in repeated syntheses and delayed market launches. Investing in the right chiral building block pays long-term dividends.

    The Human Side: Our Team’s Reflections on Customer Success

    Talk to any operator, engineer, or applications chemist in our plant and you’ll hear the same message: a product succeeds or fails not just on its purity, but on how well it solves the user’s problem. Successful D(+)-2-Octanol projects often come down to collaboration. We clarify project needs early, discuss intended scale, and forecast growth. This transparency lets us align production schedules with customer demand, avoiding sudden shortages or conflicting orders.

    Production pride grows from seeing products we made form the backbone of customer innovation. One story stands out: a longtime partner chose our D(+)-2-Octanol during a critical drug development phase. They credited reliable optical activity and documentation support for passing a major regulatory audit with no findings – a rare and constructive moment for both teams. Such experiences reinforce a core belief: partnership, not just supply, anchors our work.

    Continuous Improvement and Looking Ahead

    No chemical plant ever completes its journey on the first try. We review every customer request, audit finding, and support ticket, then roll lessons learned into improved SOPs and in-line analytics. Each gain in enantiomeric excess, analytical accuracy, and packaging innovation helps users achieve success. We challenge our team to develop cleaner, faster, and more resilient production, matched by transparent reporting with an open channel to our technical specialists.

    With greater demand for precision and environmental responsibility in specialty alcohols, our company expects D(+)-2-Octanol’s role to grow. We follow new analytical technologies, invest in automation, and support continuous operator training to raise industry standards. Success in D(+)-2-Octanol production means meeting both current needs and staying ahead of future expectations. For each partner developing medicines, fragrances, or essential intermediates, we offer more than a product: we deliver experience, support, and an unwavering focus on quality you can measure and trust.