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(±)-Linalool

    • Product Name (±)-Linalool
    • Alias alpha-Linalool
    • Einecs 201-134-4
    • 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

    240554

    Chemical Name (±)-Linalool
    CAS Number 78-70-6
    Molecular Formula C10H18O
    Molar Mass 154.25 g/mol
    Appearance Colorless to pale yellow liquid
    Odor Floral, lavender-like
    Boiling Point 198-199°C
    Density 0.858-0.863 g/cm³ (20°C)
    Refractive Index 1.462-1.465 (20°C)
    Flash Point 76°C (closed cup)
    Solubility in Water Insoluble
    Specific Rotation ±0° (racemic mixture)
    Vapor Pressure 0.16 mm Hg (25°C)

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

    Packing & Storage
    Packing (±)-Linalool, 100 mL, is packaged in a sealed amber glass bottle with a secure screw cap and clear labeling.
    Shipping (±)-Linalool is typically shipped in tightly sealed containers, protected from light, heat, and moisture. It should be handled as a flammable liquid, complying with relevant transport regulations (such as DOT, IATA, IMDG). Proper labeling, documentation, and packaging are required to ensure safety during transit. Store and transport upright.
    Storage (±)-Linalool should be stored in a cool, dry, and well-ventilated area, away from heat sources, open flames, and direct sunlight. Keep the container tightly closed when not in use and store it separately from strong oxidizers and acids. Ensure proper labeling and avoid prolonged exposure to air to prevent oxidation and degradation of the compound.
    Application of (±)-Linalool

    Applications of (±)-Linalool in Industrial Manufacturing

    (±)-Linalool is an essential monoterpene alcohol widely used in industrial manufacturing, primarily as a fragrance, flavoring substance, and intermediate in synthesis processes. As a direct manufacturer, we supply this material to industries with established regulatory frameworks and well-defined downstream applications. The scenarios below showcase authentic, compliant, and process-focused uses of (±)-Linalool across major sectors.

    1. Fine Fragrance Compounding for Perfume Manufacturing

    Fine fragrance producers rely on (±)-Linalool as a character-defining aroma ingredient for floral, citrus, and fresh olfactive profiles, particularly within Eau de Parfum and Eau de Toilette formulations. The addition rate depends on desired scent intensity and regulatory limits for skin contact, mandating close quality control on purity and enantiomeric ratios. Our material is used during the concentrate blending phase, where precision dosing ensures compliance with IFRA guidelines. Downstream producers integrate (±)-Linalool in the creation of designer fragrances, mass-market perfume products, and high-volume personal care scents.

    Industry compliance standards

    • International Fragrance Association (IFRA) Standards, latest Amendment
    • European Cosmetics Regulation (EC) No 1223/2009
    • REACH Registration and Notification
    • Allergenic Labeling per EU Regulation 648/2004 (Detergents Regulation)

    Typical usage ratio

    • 0.5%–4% of total concentrate; restricted by IFRA Category-specific limits; optimization based on scent profile and allergen thresholds

    Downstream process integration

    • Added to alcohol-soluble concentrate during bulk blending; homogeneity checked before dilution and filling

    Final product types

    • Eau de Parfum sprays
    • Eau de Toilette sprays
    • Fine fragrance mists
    • Luxury scented oils

    2. Flavor Formulation for Food and Beverage Industry

    Global flavor houses utilize naturally derived and synthetic (±)-Linalool for formulating citrus, floral, and spicy flavor accords in food and beverage products. Critical for recreating natural orange, coriander, and lavender notes, (±)-Linalool is dosed carefully according to food safety regulations and regional additive limits. The compound is introduced at blending or emulsion preparation stages in flavor houses, which then supply the compounded flavor to beverage, confectionery, and dairy processors.

    Industry compliance standards

    • US FDA 21 CFR §172.515 (Flavoring Substances and Adjuvants)
    • EU Regulation (EC) No 1334/2008 on flavorings
    • JECFA/FEMA GRAS Status (FEMA No. 2635)
    • China GB 2760 Food Additive Use Standard

    Typical usage ratio

    • 0.001%–0.05% in finished food or beverage product; precise proportioning based on product matrix and regional legal limits

    Downstream process integration

    • Integrated into aqueous or oil phase during technical flavor compounding; emulsified for water-based beverages; standardized in bulk tanks for accuracy

    Final product types

    • Non-alcoholic beverages (orange soda, cola, citrus-flavored drinks)
    • Confectionery flavorings (chewing gum, hard candies)
    • Dairy preparations (fruit yogurts, flavored milk)
    • Processed baked goods (aromatic bread, cakes)

    3. Botanical-Based Cleaning Products and Detergents

    Manufacturers of environmentally friendly and plant-based household cleaners employ (±)-Linalool as a primary scent active, valued for its fresh herbal and floral top notes. Suitable for use in surfactant-based formulations, (±)-Linalool is introduced at the fragrance solubilization step, ensuring consistent dispersion throughout the matrix. It enhances product differentiation for laundry detergents, surface sprays, and dishwashing liquids intended for the mass market, while also having to comply with consumer safety and labeling requirements for allergenic substances.

    Industry compliance standards

    • EU Detergents Regulation (EC) No 648/2004 for surfactants and fragrance allergens
    • IFRA Standards for household applications
    • US EPA Safer Choice Standard (when seeking certification)
    • REACH SVHC Communication (if applicable)

    Typical usage ratio

    • 0.02%–0.15% of total detergent mass; precise dosing guided by scent strength and allergen labeling rules

    Downstream process integration

    • Blended into premixed surfactant solution before final dilution; emulsified for uniform aroma distribution; monitored by QC for stability

    Final product types

    • Plant-based laundry detergents
    • Multi-purpose household cleaners
    • Dishwashing liquids
    • Air-freshening cleaning sprays

    4. Antimicrobial Additives in Industrial Personal Care Products

    Formulators in the personal care sector select (±)-Linalool for antimicrobial and deodorizing properties when developing deodorants, antibacterial soaps, and specialized hygiene products. Its performance as a natural scent additive with mild antimicrobial effect is harnessed in rinse-off and leave-on products, especially in brands focused on botanical actives. The raw material is added at the aqueous or oil blending phase of bulk manufacturing, depending on intended release profile and product base. Careful dose control is required to balance efficacy claims with consumer tolerance and compliance to cosmetics regulations.

    Industry compliance standards

    • EU Cosmetic Regulation (EC) No 1223/2009 (Annex III for restricted substances)
    • FDA Title 21 CFR 700 Subpart B (Cosmetic Product Requirements)
    • ISO 22716:2007 Cosmetics — Good Manufacturing Practices (GMP)
    • Allergen Disclosure per EU 1223/2009 Annex III

    Typical usage ratio

    • 0.03%–0.2% of formulation mass; determined by antimicrobial efficacy, sensory profile, and dermal tolerance limits in finished product testing

    Downstream process integration

    • Introduced during bulk mixing or before homogenization; solubilized either in oil phase or pre-emulsified as required by formulation

    Final product types

    • Roll-on and stick deodorants
    • Antimicrobial hand washes
    • Botanical body washes
    • Deodorizing foot creams

    5. Insect Repellent Actives for Consumer and Agricultural Products

    The agrochemical and consumer protection industry incorporates (±)-Linalool in insect repellent preparations for personal care and household use, leveraging its volatility and low mammalian toxicity. Its regulatory status allows integration into biocidal products in specific regions. Producers add this active during premixing or microencapsulation stages to control release, packaging repellent sprays, candles, or evaporative devices. The accurate tracking of (±)-Linalool content ensures consistent efficacy and adherence to concentration limits set by pesticide regulations.

    Industry compliance standards

    • US EPA FIFRA Biopesticide Rules (where registered as a minimum risk pesticide)
    • EU Biocidal Products Regulation (EU BPR, Regulation (EU) No 528/2012)
    • Australian APVMA Approvals (where formulated as a repellent)
    • WHOPES Guidelines for efficacy and safety of repellents

    Typical usage ratio

    • 1%–5% of the total product formulation; adjustments based on intended target species and regulated application thresholds

    Downstream process integration

    • Premixed into spray concentrate; microencapsulated for controlled release in air or on skin surfaces; added during bulk blending prior to packaging

    Final product types

    • Personal insect repellent lotions
    • Mosquito repellent candles
    • Room spray repellents
    • Protective agricultural sprays (in selected markets)

    6. Synthesis Intermediate for Vitamin E and Fragrance Ingredients

    Bulk chemical and pharmaceutical manufacturers employ (±)-Linalool as a chiral intermediate in the synthesis of high-value chemicals, notably Vitamin E (tocopherol) and specialty fragrance molecules such as linalyl acetate and tetrahydrolinalool. The material is first purified to suitable specifications, then subjected to selective catalytic processes or transformation via Grignard or hydrogenation pathways. These operations take place in dedicated synthesis facilities with flow- or batch-based inline quality controls. The derived compounds serve as critical inputs for vitamin premixes and tailored fragrance bases.

    Industry compliance standards

    • USP–NF and European Pharmacopoeia (for downstream Vitamin E)
    • ISO 9001:2015 Quality Management for fine chemical synthesis
    • ICH Q7 GMP for Active Pharmaceutical Ingredients (defining batch traceability and purity standards)
    • REACH compliance for intermediates

    Typical usage ratio

    • Feedstock input calculated by stoichiometric requirement, typically 1–1.2 molar equivalents; actual amount determined by process yield and purity targets

    Downstream process integration

    • Charged into synthesis reactors as a primary or co-feedstock; monitored for conversion to target molecule; product isolated and purified downstream

    Final product types

    • Natural and synthetic Vitamin E (DL-α-tocopherol)
    • Linalyl acetate (fragrance ester)
    • Tetrahydrolinalool (for perfumery bases)
    • Other C10 fragrance intermediates
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    Certification & Compliance
    More Introduction

    (±)-Linalool: From Process to Practical Application

    Introduction to (±)-Linalool Production

    Our plant produces (±)-linalool using established processes designed for efficiency, high yield, and reliability. Working on this production floor, I've seen how minute changes in parameters—temperature, catalyst choice, solvent ratios—can shift purity outcomes. That's why each batch is tested with rigorous controls, using gas chromatography and spectrometry to confirm both composition and impurity profile. (±)-Linalool has the empirical formula C10H18O, and what often surprises those outside the industry is how a terpene alcohol like this, clear and barely tinted, can carry such a range of floral, citrus, and spicy nuances that perfumers and product developers chase.

    Our Experience with Specifications

    From daily sample runs and feedback across QA meetings, I know our output remains above 97% assay, with water content under 0.3% by Karl Fischer titration. Color readings most days fall beneath 20 APHA, and careful storage under nitrogen keeps oxidation at bay so the product reaches full shelf life. Years ago, clients would ask for “linalool,” no matter the isomer or aroma character; today, buyers pay close attention to chiral composition and typical impurity residues—realities that never go away as regulations tighten, especially for applications in fine fragrance and food.

    User Contexts: What Sets (±)-Linalool Apart

    Standing on the production line, I remind new technicians that each drop of (±)-linalool starts as raw hydrocarbon feed. Hydrogenations, fractional distillations, and meticulous quality checks transform those raw materials into something both stable and versatile. Customers blend this material into perfumes, deodorants, household cleaners, laundry liquids, and even sauces and confectionery. Chemists behind flavor and fragrance development seek the gripping middle ground—(±)-linalool’s mild sweetness that isn’t overwhelming, plus its ability to soften sharper notes like limes, lemon, or lavandin, and form bridges between head and heart notes in a scent.

    In regular review meetings, application chemists share feedback on how (±)-linalool delivers better solubility in polar and non-polar environments compared to similar terpenoids. Safety managers highlight low toxicity at standard usage levels, referencing internal safety audits and IFRA guidelines. Stability testing shows good hold even in alkaline cleaning formulas, something alfa-terpineol or citral don’t always match.

    Comparing (±)-Linalool to Natural and Enantiomerically Pure Grades

    As a manufacturer, I'm asked whether our (±)-linalool matches the natural material found in lavender or coriander. Natural linalool, most often, leans toward the (–)-linalool enantiomer; some essential oils carry as much as 93% of that isomer, while our racemic mixture represents a 50:50 blend of (+)- and (–)-linalool. For cost efficiency and consistent properties, synthetically derived racemic linalool makes sense. Its aroma mimics both floral and woody undertones, but skilled perfumers tell us they detect subtle differences in top note diffusion and drydown—subtleties that determine whether they order natural isolates or stick to the racemic product.

    Enantiopure grades, produced via asymmetric synthesis or chromatographic resolution, command higher prices and see more demand in projects where regulatory labeling or allergen avoidance become marketing points. The (±)-form, by contrast, finds its way mostly into functional uses: air care, non-luxury fragrances, personal care, and industrial scents. In food and beverage, the strictest customers still ask for natural or botanically derived linalool; others, who develop flavor formulations for beverages, chewing gum, or frostings trust our grade for its reliable character and neutral impact on color and viscosity.

    Production Processes and Quality Practices

    Sourcing raw materials, selecting catalysts, and designing reaction trains—these are decisions we make every season in response to both raw material volatility and energy costs. Crude turpentine distillate sometimes carries unpredictable side products; adjusting feed specs and distillation sequences allows us to stay inside tolerance ranges. By keeping reaction times optimized and working with established partners for supply, daily production stays within target yield. Process safety audits, using HAZOP and root cause analysis, drive our ongoing investments in process containment, vapor handling, and final purification.

    Our QA teams pull multiple samples from each lot. They use headspace GC to quantify minor terpene impurities—alpha-terpineol, geraniol, nerol, limonene—because international flavor and fragrance buyers demand predictable profiles, especially if the product ends up in a region like the EU or Japan. If there’s a spike in acidity, redistillation handles the worst of it, but ongoing investments focus on preventing contamination upstream. We store finished (±)-linalool in lined, inert tanks to avoid aldehyde formation, sending off multiple test shipments for accelerated shelf life analysis each quarter.

    Meeting Customer Demands Through Practical Adjustments

    Over the years, customer audits have grown tenser and more precise—not just in documentation, but through in-person inspections and direct site walkthroughs. I remember a large multinational’s team visiting our facility; they wanted digital logs of every pressure gauge, every setpoint for vacuum distillation runs, every trace of solvent recycled and scrubbed from the exhaust. Providing this level of transparency secured us a key global contract, especially as we demonstrated repeat stability, traceability, and consistent odor panels across shipping batches.

    Customers sometimes seek tailored impurity specs—lower alpha-terpineol, or absence of certain monoterpene residues. With continuous distillation, column tweaking, and real-time process analyzers, our supervisors maintain tight control over cut points and recycle streams, reducing off-spec generation and supporting waste minimization. We accept that every process improvement, whether in energy use, feedstock conversion, or effluent management, delivers both savings and a cleaner, safer work environment.

    Regulatory Realities and Best Practices

    Our compliance group tracks REACH registrations, IFRA standards, and country-specific tonnage banding. End users—especially those adding (±)-linalool to skincare, wash-off products, or ingestible goods—rely on our documentation package, including up-to-date safety data, toxicology, and allergen certifications. Over the years, we've responded to new labeling demands about potential allergens (linalool is one), and each specification revision prompts a backward review of all analytical data. Updates from IFRA, flavor safety authorities, or the US and Chinese agencies drive periodic changes to specification sheets. We document each step, maintain secure batch logs, and provide full audit trails for every large shipment.

    There’s a distinct change over time in what buyers care about: yesterday’s focus was solely on major byproducts and storage stability. Now, attention turns to trace chiral purity, batch traceability back to raw material origin, and evidence of process safety for every step. We support this evolution with transparent dialogue, routine external audits, and frequent update briefings with technical and regulatory staff from our largest customers. Bringing in third-party inspectors or participating in industry-wide performance benchmarking helps reinforce trust, internally and out in the marketplace.

    Operational Insights from Manufacturing

    Running (±)-linalool plants means handling intermittent maintenance shutdowns and upgrades while keeping supply steady. A mid-winter incident long ago taught us about the risks of heat exchanger fouling; a minor drop in jacket temperature caused product discoloration, and even after purification, sensitive instruments sniffed out the shift. Now a preventive schedule targets cleaning and inspection at regular intervals. Small actions—like double-sealing transfer hoses or setting up vapor recovery on tanker loading lines—add reliability and prevent both losses and odor complaints.

    Operators share feedback in daily huddles: If vacuum holds weak, even for half a run, residual aldehydes sneak through and end up affecting odor profiles. Close coordination with maintenance and automation teams supports quick-turnaround fixes, limiting waste and holding true to customer contract timelines. Facility modernization, continuous training, and in-house troubleshooting bring direct rewards—each year, fewer off-spec lots exit the plant, and waste streams decrease.

    End Applications and Industry Shifts

    Every year brings a new spin on how (±)-linalool gets used. Ten years ago, formulators mixed this material primarily into soap, detergent, and low-cost spray fragrances. Now, the same molecule pops up in savory snack seasonings, health drinks, and even pet care products. Marketing teams from major cosmetic brands ask about microplastic alternatives and natural equivalence, pushing us to clarify both synthetic origin and the evidence supporting safe, residue-free use.

    Some end users craft complex blends with dozens of components; others appreciate (±)-linalool for its ability to shift a fragrance from harsh or medicinal to soft and inviting. Fewer major recalls occur now thanks to advances in supply chain traceability and batch documentation. In our feedback from downstream brands, the subtle hints of coriander or lavender that (±)-linalool delivers anchor many fresh and clean fragrance launches. Household goods formulators report reduced air care volatilization losses compared to other monoterpenes, improving efficiency and lowering costs.

    Sustainability and Process Improvements

    We've changed how (±)-linalool gets made since resource scarcity and the need for greener footprints took center stage. Efficient energy use, solvent recovery, and support for feedstock suppliers who farm more sustainably now shape annual strategy. Recovering residual linalool from side streams instead of treating everything as waste means less landfill and more responsible product stewardship. Tracking and reporting environmental KPIs as part of customer service sharpens team focus and improves both compliance and company reputation.

    Continuous process improvement affects both bottom line and environmental profile. Whether we’re optimizing energy consumption, reworking end-of-run distillation cuts to extract more value, or finding alternative packaging with lower weight, all changes reflect conversations with buyers who want measurable, dependable improvements. For customers who ask about carbon footprint and origin, transparency in sourcing and reporting, plus a willingness to share and improve, strengthens our market position.

    Research, Innovation, and Ongoing Challenges

    Technical teams investigate new extraction and synthesis routes for (±)-linalool, aiming for higher yield and fewer byproducts. Ongoing research with university partners, pilot runs for new catalysts, or bio-based reactor strains could one day scale up for industrial venturing. Analytical methods evolve too: lower detection limits, better chiral purity measurements, and on-line QC provide more actionable data for process optimization and final shipment release.

    Scale alone no longer sets manufacturers apart—customers now look for proven process expertise, quick adaptation to spec changes, and solid relationships along the value chain. We invest in continuous education, send staff to international conferences, and foster a culture of open technical exchange.. These investments give us early warning on any new industry trend, allow quick pivots during regulatory changes, and support real-world troubleshooting without delays.

    The Future of (±)-Linalool Manufacturing

    Looking ahead, I see tightening quality criteria, rising sustainability demands, and swift changes in how customers approach both supply and compliance. Manufacturers capable of tracking and reducing every critical impurity, owning each test along the route from raw material to outgoing drum, and communicating with end users in plain language will set the pace. Automation, data-driven prediction of process yields, and real-time global traceability are on our roadmap.

    At the production level, creating high-quality (±)-linalool involves skilled staff cross-trained to handle both synthesis and high-volume logistics. Success comes as much from ongoing incremental improvements as from single breakthrough innovations. Safety, sustainability, and customer requirements guide investment, while internal feedback loops push for better practices and quick response to unexpected feedstock variation or process upsets.

    Our plant produces (±)-linalool not only in response to market need, but through the ongoing commitment to quality, reliability, and adaptability. Each batch shipped represents years of hard-won experience, lessons learned from process trials, regulatory adaptation, and direct conversations with chemists, buyers, and fellow manufacturers across the specialty chemical world.