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HS Code |
601481 |
| Cas Number | 106-28-5 |
| Molecular Formula | C15H26O |
| Molar Mass | 222.37 g/mol |
| Iupac Name | (2E,6E)-3,7,11-Trimethyldodeca-2,6,10-trien-1-ol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 282 °C |
| Density | 0.878 g/cm³ at 25 °C |
| Refractive Index | 1.488 to 1.490 at 20 °C |
| Flash Point | 120 °C |
| Solubility In Water | Insoluble |
As an accredited (E,E)-Farnesol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of (E,E)-Farnesol; features a secure screw cap and chemical safety labeling for laboratory use. |
| Shipping | (E,E)-Farnesol is shipped in tightly sealed containers under cool, dry conditions to ensure stability and safety. Packaging is compliant with international regulations for chemicals, clearly labeled, and protected from light and moisture. Transport is handled by authorized carriers specializing in hazardous or sensitive materials, following all relevant safety protocols. |
| Storage | (E,E)-Farnesol should be stored in a tightly sealed container, protected from light and moisture, at a cool temperature (preferably 2–8°C, i.e., refrigerated). It should be kept away from sources of ignition and incompatible materials such as oxidizing agents. Proper labeling and ventilation are important, and access should be limited to trained personnel to ensure chemical stability and safety. |
Applications of (E,E)-Farnesol in Industrial ManufacturingAs a direct manufacturer of (E,E)-Farnesol, we supply high-purity material to leading industrial sectors where performance, safety, and regulatory compliance are critical. The following sections detail well-established downstream applications, each supported by recognized industry standards, practical dosage guidelines, integration points in production, and the principal commercial products utilizing this raw material. 1. Fine Fragrance Compounds for Personal Care(E,E)-Farnesol plays a central role in the formulation of high-end fragrance concentrates for personal care products, valued for its naturally occurring floral notes and its function as a fixative. Global fragrance manufacturers consistently specify it for use in minimalist, allergen-conscious fragrances owing to its proven skin tolerability and biodegradable profile. Its addition occurs during the compounding stage, blending with other aldehydes, alcohols, and essential oils under controlled environment for precise aromachemical performance and long-lasting scent retention. Final products enter markets that place strict limits on key allergenic components and require rigorous documentation of ingredient origins and traceability. Industry compliance standards
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2. Antimicrobial Active in Oral Care FormulationsIndustrial-scale dental care producers utilize this material as an active compound in mouthwashes, oral sprays, and toothpaste for its broad-spectrum antibacterial action against oral pathogens responsible for halitosis. The ingredient is introduced at the aqueous pre-mix or emulsion phase, prior to pH adjustment and flavor incorporation. GMP-controlled production facilities handle and document the addition under batch manufacturing procedures to ensure consistent antimicrobial performance and user safety. The use is limited by established health authority guidelines on permissible dosage and purity level for oral applications. Industry compliance standards
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3. Functional Ingredient in Cosmetics Preservative SystemsFormulators in skin and haircare sectors select (E,E)-Farnesol as a co-preservative to suppress gram-positive bacteria and boost the performance of reduced-paraben or alcohol-free preservative systems. Its integration addresses the challenges of microbial contamination in water-based formulations prone to spoilage. Addition typically occurs alongside other co-actives and stabilizers during the preservative premix stage before emulsion or bulk mixing, ensuring uniform dispersion throughout finished products. Documentation of ingredient origin, purity, and contaminant control forms part of downstream manufacturers’ batch records to support product recalls or audits. Industry compliance standards
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4. Intermediate for Vitamin K2 (MK-4) SynthesisWithin nutraceutical manufacturing, (E,E)-Farnesol serves as a key C15 isoprenoid building block in the semi-synthetic pathway for menaquinone-4, a bioactive form of Vitamin K2. Select manufacturers employ this raw material in multi-stage organic synthesis under controlled reactor conditions, with precision catalyst addition and in-process monitoring to maximize isomeric purity and prevent side reactions. Strict adherence to pharmaceutical and food additive regulations governs its traceability and impurity content across the supply chain for dietary supplement use. Industry compliance standards
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5. Isoprenoid Precursor in Flavors for Food ApplicationsLeading food additive companies apply (E,E)-Farnesol as a trace isoprenoid flavor ingredient in specialty flavor mixtures that simulate natural floral and citrus notes, predominantly for premium teas, beverages, and baked snacks. Inclusion takes place at the blend or carrier oil pre-mix stage to guarantee even distribution when diluted into finished food matrices. Usage levels adhere to maximum residue limits set by food safety authorities and are supported by hazard analysis and dietary exposure assessments under batch-wise quality controls. Industry compliance standards
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We have worked with (E,E)-Farnesol across different production campaigns in the past decade, observing its shift from niche fragrance additive to a versatile chemical holding immense value for many industries. As a manufacturer deeply involved in both the bulk and specialty sectors, our experience isn’t limited to making (E,E)-Farnesol — we’ve walked the line between purity, reliability, and end-use adaptability, learning firsthand what makes this product stand out.
At its core, (E,E)-Farnesol belongs to the family of acyclic sesquiterpene alcohols, recognized for its double trans isomer configuration. Many suppliers circulate various forms of farnesol in the market, yet this specific (E,E) geometric isomer shows notable consistency in terms of odor, reactivity, and interaction with other compounds. During distillation and purification on our lines, a few things become clear: (E,E)-Farnesol readily separates due to its volatility profile and solubility pattern, achieving a colorless, mobile liquid that remains stable during storage and transport if handled in sealed glass or inert-lined vessels.
Standard offerings present (E,E)-Farnesol with a content level typically above 96% purity by GC, with our regular production batches averaging 97-99%. That figure isn’t just a number — higher purity translates to lower off-odor content and improved predictability when blending with fragrance bases or fine chemicals. Impurities like nerolidol or monoterpene residues can drastically alter sensory notes or compatibility, a fact confirmed through years of QA and customer feedback.
At room temperature, (E,E)-Farnesol appears almost water-clear with a faint, floral-sweet odor. The density measures about 0.880 to 0.890 g/cm³, and its boiling range sits between 278 to 283°C under atmospheric pressure. On the production floor, monitoring color is vital, as even trace yellowing hints at polymerization or oxidation, which directly undermines product shelf life. Modern GC-FID and NMR methods allow us to verify the E,E configuration and scan for cis or mono-trans isomers, which lack the same olfactory brightness or reactivity profile.
This product’s stability allows us to offer both drum and IBC packaging, without risk of spontaneous polymerization or runaway reactions under ordinary handling. Consistently, customers in Europe, North America, and Asia have experienced shelf-storage lifespans beyond 18 months when kept cool and out of direct sun and air.
Our teams have supported formulators from household fragrance blenders to large personal care brands. (E,E)-Farnesol makes a mark as an effective fixative in perfumery, thanks to its long-lasting, subtle floral note and its capacity to smooth transitions between middle and base notes in complex blends. It doesn’t bring the heavy, oily drag that synthetic musks introduce, avoiding unwanted weight or blurring in scent construction. Instead, (E,E)-Farnesol lifts delicate profiles, rounding off sharpness and extending longevity.
Beyond fragrance, the product’s alcohol function opens up pathways for downstream reactions, such as acylation or etherification. In our own reactors, farnesol derivatives have moved into roles as insect pheromone precursors, emulsifier intermediates, and even as cosmeceutical actives. Repeated feedback highlights its ability to disrupt bacterial quorum sensing, a property utilized in certain antimicrobial product claims (subject to local regulatory review). End-users manufacturing oral care products value (E,E)-Farnesol for its capacity to modulate mouthfeel and impart a fresh, green profile without the bitterness common to lower-purity grades.
As farnesol producers, we often encounter confusion over the landscape of isomers. Commercial products are rarely single-isomer; many batches in global trade contain mixtures of E,E, Z,E (cis,trans), and Z,Z (cis,cis) forms, or significant nerolidol (an alcohol with an identical carbon skeleton but different double bond geometry). The E,E isomer stands out for its crisp, true-to-type lily-of-the-valley aroma and its reliable chemical compatibility with common fragrance solvents. Z isomers, when present, make for a muted, sometimes waxy scent character and introduce challenges in fine chemical synthesis that extend across yields, color migration, and unexpected byproducts. Our in-house split-point distillation and analytical testing allow us to separate E,E from these less desirable fractions, putting a premium on batch uniformity and clarity.
Some buyers ask for farnesol as a “nerolidol alternative,” but in practice, these molecules behave differently. Nerolidol brings a heavier, woody note with lower volatility and decreased blendability in high-impact fragrance systems. Over years of comparative analysis, we have noticed that (E,E)-Farnesol’s precise double bond position grants greater shelf-stability and less tendency to yellow with age. It blends more predictably into aqueous or hydroalcoholic bases, which matters to formulators chasing consistency in large-scale production.
Bringing a high-purity (E,E)-Farnesol to market isn’t trivial. Our production strategy hinges on plant-based feedstocks — often citronellol, derived from Cymbopogon species (lemongrass or palmarosa), which under controlled acid catalysis, cyclizes and rearranges into the farnesol skeleton. Yield variables run tight: temperature, catalyst charge, and water content in the reactor all drive final product quality. We have seen significant deviations in isomer ratios with even small fluctuations in process control, underscoring the importance of physical oversight and timely sampling.
To safeguard consistency, every batch leaves our facility only after passing thresholds for GC purity, isomer ratio, and specific gravity. We run random NMR tests to monitor for backbone shifts or minor side-products, which, though present only at a fraction of a percent, can greatly influence downstream processing especially in pharma and cosmetic sectors, where regulatory compliance sits front and center. Sometimes, bright yellow bottoms or tar residues show up in early cuts— a sign of thermal stress or improper vacuum. Our operating teams adjust as needed, preferring to reprocess nonconforming fractions than ship a mixed isomer blend.
(E,E)-Farnesol opens opportunities for perfume houses, consumer brands, and specialty chemical formulators looking for stable, olfactorily bright alcohols that handle scale-up without fuss. In fine fragrance, designers appreciate its linden blossom accent, boosting florals and lending tenacity to citrus and white flower notes. In personal care, formulators find (E,E)-Farnesol capably boosts the fresh, green lift in gels, deodorants, and moisturizing compounds. It’s non-sticky and disappears without a film, even in anhydrous conditions.
Technical chemists exploring insect sex pheromone synthesis turn to (E,E)-Farnesol as an efficient intermediate, particularly valuing its resistance to acid- or base-catalyzed side reactions that typically plague other unsaturated alcohols. Its downstream epoxidation leads smoothly to non-natural intermediates for specialty flavors and fragrances. Our plant also supports manufacturers using (E,E)-Farnesol in coatings and lubricants, as its saturated backbone and lack of multiple charge centers allows for longer-lasting film properties in high-wear applications.
Origin matters, especially as global supply chains feel environmental and social pressures. We have audited our feedstock sources each year, ensuring traceable, sustainable cultivation practices for the botanicals supplying our base alcohols. Distillation waste and byproducts are either recycled back into the process or offered as compostable material to local farms, closing loops wherever possible. Our investment in closed-system reactor controls means emissions sit well below industry and regional requirements — not only a win for compliance, but a demonstration of care for communities near our production sites.
We’ve mitigated losses and unplanned flaring on our farnesol unit by tightening collection and minimizing hold-up. Our maintenance routines keep storage vessels airtight and clean, so oxidation is nearly absent, which means customers rarely find themselves dealing with discolored or odiferous batches. Our team understands that consistent quality starts with everyday practices rather than one-off certifications.
Across all downstream sectors, regulatory agencies scrutinize trace impurities, allergens, and origin documentation. Farnesol itself falls under IFRA guidelines for fragrance use and is monitored as an ingredient under the EU’s Cosmetics Regulation (EC) No 1223/2009. As a producer, we stay current on threshold limits, preemptively eliminating side components well below published maximums — an approach confirmed through external audits and verified testing.
On the shop floor, our teams work with robust PPE and local exhaust systems, because farnesol, like many low molecular weight alcohols, will irritate eyes and skin with unaided exposure. Our customer advisory notes stem from years of direct handling, not armchair speculation; we help users avoid common pitfalls such as incompatibility with highly acidic or oxidizing formulation environments which could trigger undesired degradation.
In dozens of collaborative pilot projects, we’ve watched (E,E)-Farnesol take simple fragrances and lift them to internationally recognized status — not by dominating the blend, but by harmonizing disparate esters, aldehydes, and musks into unified, recallable identities. Customers tend to notice their launch products go further with less raw material and fewer reformulations required between runs; frequency of batch-to-batch troubleshooting drops, and end-user satisfaction improves as recognizable, bright, and non-waxy top notes persist up to the point of full wear-off.
In oral cosmetics, (E,E)-Farnesol grants a green, clean taste that masks bitterness without adding astringency — a feature validated by mouthfeel panels in beverage and toothpaste trials. In industrial coatings, farnesol’s backbone imparts flexibility and acts as a plasticizer in certain silicone-modified resins, boosting shelf-longevity while keeping volatility manageable.
We’ve learned that active relationships with upstream growers and downstream end-users form a cycle of improvement. By working directly with buyers to adjust packaging, we have reduced losses due to container sweating and eliminated unintentional cross-contamination during bulk transfer. Direct conversations with perfumers led us to refine our dehydration step, eliminating certain volatile aldehyde byproducts which, in ultra-light blends, created unwanted metallic notes.
Technical troubleshooting often involves recalibration in real time: an off-color drum led to a full trace-back, uncovering a faulty gasket in one condensation line that introduced micron-scale metal contamination. Fixes weren’t costly, but attention to detail saved both our clients and us hours of rework downstream.
Given the range of materials labeled “farnesol,” it pays to understand exact isomer content and purity levels; too many traders push “mixed isomer” farnesol without specifying percentages, resulting in batch instability and unpredictable blending outcomes. In actual practice, perfumers and chemical engineers aren’t looking just for any farnesol — they demand the E,E isomer because the chemistry and sensory properties align with professional and regulatory expectations. Years of analytical runs confirm that high-purity (E,E)-Farnesol won’t fudge results under scale-up conditions or spontaneous storage shifts.
Discerning buyers ask about feedstock verification and processing methods before sourcing a new lot. Our internal audits and open laboratory records have proven to be strong assurances to customers wary of trace allergens or synthetic artifacts. It’s not about making claims — it’s about keeping product straightforward, verifiable, and trustworthy from tank to end-use.
The (E,E)-Farnesol market isn’t standing still. Newer uses are emerging in biotechnology, particularly in quorum sensing disruption and biofilm resistance, with academic partnerships underway to unlock even more value from this versatile molecule. Our team continues to support customization efforts for specific blends or functional group modifications requested by specialty project clients. Just last year, together with two leading academic labs, we trialed novel oxidative conversions under green chemistry conditions, pushing both yield and sustainability metrics to new highs.
This work, while incremental by outside appearances, keeps us sharp. Customized runs trigger new SOPs, QA protocols, and sometimes, new packaging innovations. Every iteration, from pilot to full run, circles back to the essentials: clean feedstock, tight process control, responsive support, and real feedback from partners at every point in the supply chain.
Theory only goes so far on the line. We’ve identified that consistent product comes from daily attention to cleaning reactors, maintaining transfer lines, and retraining new hires in hands-on GC analysis. Grand words about quality or purity mean little if a truckload turns up with off-odors or cloudiness, which a few overlooked details in storage or handling can cause. Our routine—regular tank bottom checks, sealed sample records, and real-time online monitoring—makes the difference between a batch that meets end-user demands and one that raises issues downstream.
Root cause investigation flows quickly from our QC team to production, closing the loop so fixes don’t wait for customer complaints. Over the years, it’s become clear that proactive communication, not just technical specification, drives lasting business. When customers ask for the story behind their (E,E)-Farnesol, we give a detailed, honest breakdown — not just a data sheet, but day-to-day lessons from production, transport, packaging, and troubleshooting.
Every kilogram of (E,E)-Farnesol passing through our facility reflects more than a downstream commodity or raw material line item. Each drum, batch, and newly packaged order carries the lessons of direct engagement with source producers, regulatory professionals, formulation chemists, and end-users whose feedback shapes our improvement. The differences between a generic farnesol and a tailored, high-purity, E,E-specific output often surface only after real-world use. Our commitment to process control, supply chain transparency, and customer collaboration keeps our product relevant and ready for evolving markets. Years in production have shown us that, while chemistry sets the foundation, relationships and daily execution decide lasting value in the (E,E)-Farnesol space.