|
HS Code |
456762 |
| Cas Number | 111-87-5 |
| Iupac Name | Octan-1-ol |
| Molecular Formula | C8H18O |
| Molecular Weight | 130.23 g/mol |
| Appearance | Colorless liquid |
| Odor | Mild, fragrant odor |
| Boiling Point | 195-199 °C |
| Melting Point | -16 °C |
| Density | 0.83 g/cm³ at 20 °C |
| Solubility In Water | 0.54 g/L at 25 °C |
| Flash Point | 81 °C |
| Refractive Index | 1.429 at 20 °C |
As an accredited Octanol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Octanol is packaged in a 500 mL amber glass bottle, tightly sealed, labeled with hazard warnings and chemical identification for laboratory use. |
| Shipping | Octanol is shipped in tightly sealed containers, such as drums or intermediate bulk containers, to prevent leakage and contamination. It must be stored in a cool, well-ventilated area away from heat, ignition sources, and incompatible materials. Shipping should comply with international regulations, including proper labeling as a flammable liquid (UN 1993). |
| Storage | Octanol should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from heat, ignition sources, and incompatible substances such as strong oxidizing agents. Keep it out of direct sunlight and separate from food and feed. Appropriate labeling and secondary containment are recommended to prevent leaks or spills. Use non-sparking tools and explosion-proof equipment if necessary. |
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Purity 99%: Octanol purity 99% is used in plasticizer manufacturing, where it ensures high product flexibility and durability. Viscosity grade 12 cP: Octanol viscosity grade 12 cP is used in solvent formulations, where it enhances solubility and uniform mixing. Molecular weight 130.23 g/mol: Octanol molecular weight 130.23 g/mol is used in pharmaceutical intermediates, where it promotes targeted synthesis with consistent yield. Boiling point 195°C: Octanol boiling point 195°C is used in flavor and fragrance production, where it improves volatility and aroma dispersion. Melting point -16°C: Octanol melting point -16°C is used in surfactant preparation, where it maintains stability in low-temperature applications. Stability temperature 150°C: Octanol stability temperature 150°C is used in coatings manufacturing, where it allows for high-temperature processing without decomposition. Density 0.83 g/cm3: Octanol density 0.83 g/cm3 is used in extraction processes, where it facilitates phase separation and efficient recovery. Water content ≤0.1%: Octanol water content ≤0.1% is used in lubricant blending, where it minimizes emulsification and ensures product clarity. |
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Step into any laboratory or industrial plant dealing with chemicals, and odds are strong you'll spot a drum or bottle labeled Octanol. This isn’t just another solvent sitting around for occasional use. Octanol fills a wide range of roles because its structure — an eight-carbon alcohol — provides the backbone for reactions and products across multiple industries. Among the various forms, n-Octanol remains the workhorse. Its relatively unbranched nature and reliable properties give it broad appeal, from manufacturing to research and even flavor and fragrance design.
Plenty of alcohols exist, but only a handful move into both factories and research labs with the kind of purpose and consistency seen with Octanol. It boils at a point high enough to avoid quick evaporation but low enough for gentle distillation, making recovery and reuse straightforward. Octanol dissolves both polar and nonpolar molecules, which comes in handy — in simple language, it can blend oily and watery substances better than plenty of shorter-chain alcohols like ethanol or longer, waxier types such as decanol. This sweet spot between volatility, solubility, and molecular heft marks a big reason for its popularity.
My first run-in with Octanol came during my early days in a biochemistry lab. We needed to separate out molecules based on their tendency to sit in water or oil. Octanol, with its partly water-loving, partly oil-loving structure, let us draw out compounds that either wouldn’t budge from water or would never leave oil. This property forms the heart of the so-called "octanol-water partition coefficient," a test that helps drug companies predict whether a new medicine reaches its target inside the human body or gets stuck at the cell’s edge.
Having navigated more than my share of synthetic routes, I’ve also used Octanol for esterification reactions — where it pairs with acids to build flavors and fragrances. Walk into a shop selling fresh soaps or cosmetics, and you’ll probably smell the clean, slightly fatty note of esters that started off as Octanol. The consistency matters too: a well-sealed drum of Octanol keeps its composition steady over time, which means you won’t find yourself recalibrating equipment or patching up processes mid-batch.
Octanol typically refers to n-Octanol (1-octanol), though occasionally branched forms like 2-octanol enter the scene. The unbranched type brings a linear, predictable structure that reacts with precision, while branched varieties behave slightly differently due to changes in how the molecules ‘fit together’ during reactions. This might sound minor but can cause real headaches for chemists chasing high yields or specific scents. For my synthesis runs, sticking to n-Octanol — with its established boiling point, density, and purity grade — kept troubleshooting to a minimum. A boiling point around 195°C means I could distill it without risking thermal damage to sensitive compounds.
In terms of purity, high-end applications in pharmaceuticals and analytical testing rely on Octanol hitting at least 99% purity. Anything less introduces noise into measurements or byproducts into syntheses. Industrial grades sometimes relax on purity to fit bulk applications, where absolute cleanliness isn’t so critical, such as adding flexibility to plasticizers or blending into lubricants for machines.
Talk to anyone developing flavors or crafting innovations in plastics, and Octanol’s name comes up because it bridges the gap between ‘science’ and ‘taste or feel’. In the flavor industry, the fruity and mild waxy profile lends itself to many esters. These esters then sneak into candies, sodas, and condiments. I once worked with a company that used Octanol-based esters to mimic the peel of certain citrus fruits — a surprising amount of testing came down to which batch of Octanol offered the most consistent aroma after reaction.
On the biomedical side, Octanol’s use in partitioning studies affects early-stage drug development. In my own experience, a reliable batch of Octanol helped nail down absorption properties of experimental compounds, saving time and resources as projects moved from petri dish to early animal studies.
Industrial roles can’t be ignored either. Plenty of plastics improve durability and flexibility because Octanol-based additives mix seamlessly with polymer chains. Lubricants and hydraulic fluids grow more stable thanks to its side chains, which provide flexibility under shifting temperatures and pressures.
A chunk of chemistry depends on more than just formulae. Experienced lab techs and chemical plant foremen trust Octanol for its reliability during separation, extraction, and synthesis. Try running parallel reactions with benzyl alcohol, pentanol, or decanol. Each comes with its quirks: benzyl alcohol loves water too much for some separations, while longer alcohols like decanol become so greasy that blending evenly takes extra muscle or sonication. Octanol manages to thread the needle, providing enough oil-loving character for flavor chemistry without drifting into near-insolubility.
In partition testing — an area I’ve visited regularly — switching from Octanol to another alcohol scrambles results and erodes confidence in cross-lab comparisons. The n-octanol/water system is now so embedded in medicinal chemistry, even new AI-driven drug companies reference data generated on this exact platform.
So, what genuinely distinguishes Octanol from close cousins? For one, the linear model (n-Octanol) holds up during polymerization and blending better than most branched alternatives. That helps both in labs and in scaling to industrial levels. Octanol doesn’t just sit on the shelf as a quiet reactant; it resists rapid evaporation, reducing inhalation risk, and offers a balance between odor profile and chemical reactivity. Those responsible for worker safety lean toward Octanol because managed ventilation and routine precautions keep exposures down, especially compared to more volatile, lower-boiling alcohols.
A key point learned through practical use: Octanol’s moderate toxicity gives it a clear edge over shorter-chain alcohols, which present much higher volatility hazards, and over some long-chain types that can accumulate in fat tissue. Environmental studies have mapped out Octanol’s breakdown in water and soil, finding it degrades efficiently, with less persistence or bioaccumulation compared to high-molecular-weight alternatives — a reason industrial operations dealing with waste and emissions frequently prefer it.
Industry data reveals that annual global demand for Octanol exceeds hundreds of thousands of metric tons, driven mostly by its essential use in plasticizer production (e.g., dioctyl phthalate or DOP). Roughly 60% of global Octanol output transforms into plasticizer components, where performance and reliability underpin the infrastructure around us: cables, flooring, insulation, and medical-grade flexible tubing. Compared to 2-ethylhexanol, another common plasticizer precursor, n-Octanol’s more predictable reactivity leads to less batch-to-batch variation and smoother certification for large contracts.
Safety profiles reinforce its practical value. Although Octanol can cause irritation if mishandled, it’s much less dangerous than methanol or ethylene glycol, chemicals known for severe systemic toxicity. Regulatory authorities in major economies classify it below stricter hazard thresholds, provided users follow outlined exposure guidelines and storage norms. I’ve seen plants where introducing Octanol improved chemical hygiene by replacing more harmful solvents, lowering insurance costs and incident rates alike.
Even with a solid track record, Octanol brings its share of problems — especially at scale. Its faint sweetness makes it attractive to taste panels, but ingestion carries risks. Accidental spills sometimes spread beyond intended boundaries due to its sluggish evaporation and mild surfactant properties. In the past, I’ve overseen cleanups where routine containment failed, demanding extra training for quick absorption and disposal.
Another challenge sits at the production end. Much of the world’s Octanol comes as a byproduct from petroleum or through catalytic processes involving high pressures and temperatures. These routes eat plenty of energy and leave behind smaller, less-useful alcohols that need recovery or treatment. Innovative companies now invest in bio-based alternatives, extracting Octanol from renewable sources (such as castor bean oil or engineered microbes), trying to slash the carbon footprint. Scaling these methods up without sacrificing purity or consistency remains a hurdle, but progress grows year by year.
Shifting to green chemistry introduces further wrinkles: I’ve seen pilot projects switching from fossil-derived to biosourced Octanol hit unexpected wall when subtle impurities derail pharmaceutical synthesis or flavor compounding. Better analytics and purification techniques offer a road forward, though investment and tight collaboration with end users are necessary to overcome issues before full certification arrives.
Waste and emissions management continually draws scrutiny. With global attention shifting to sustainability, chemical operations using Octanol can cut overall impact by designing closed-loop systems to capture spills, filter air emissions, and recover byproducts. In several settings I’ve visited, real progress followed only when operators combined rigorous staff training with investments in scrubbers, absorbent stations, and clear labeling.
Improving worker and environmental safety means balancing tradition with innovation. In my own line, adopting sealed-transfer systems and standardized labeling greatly reduced mix-ups and risk. Newer sensor arrays spot leaks early — sometimes before nose or eye detects a thing. Fast-cleanup kits and on-call teams respond to spills within minutes, translating to less downtime and fewer regulatory headaches.
On the sourcing side, strategic partnerships between producers and end users drive forward advances in bio-based Octanol, sharing data on impurity profiles and helping tweak fermentation or extraction conditions. I’ve witnessed these industry-academic collaborations speed up learning cycles for scaling up, as answers flow back not only to chemical manufacturers but also to clinicians, flavor chemists, and materials scientists who must trust the final product.
For those actively working with Octanol — from process engineers to research chemists — continued education stays vital. Annual refreshers on handling, coupled with regular updates on regulations, help keep teams aligned with best practices. In my experience, low staff turnover in well-trained teams keeps safety incidents rare and product consistency high.
Digital quality-control systems now help monitor batches, flagging outliers in real time and allowing for corrections before end use. Early warning on batch purity or trace contamination saves time, slashes waste, and lets operations move from ‘fixing problems’ to ‘preventing them.’ The use of AI-driven predictions based on historical Octanol behavior will only increase, helping match client demands with available supplies better than the old “order and wait” cycles.
Anyone adapting to changing standards in sustainability faces down both cost and technical headwinds. Advance planning, coupled with transparent reporting, reassures regulatory stakeholders and end clients. In the chemical sector’s future, those companies backing public sharing of impurity data and progress on emissions stand to lead, not lag, as supply chains and certification standards grow tougher.
Octanol won’t lose its place soon, given its adaptability and the widening range of uses in science, industry, and everyday products. The bridge between small-scale discovery — whether in a university lab or flavor house — and industrial scaling depends on trust built over years of safe, reliable use. From my own years working with Octanol, seeing both stumbling blocks and successes, it’s clear that a balanced approach keeps the wheels turning. Keeping both eyes open to new advances while respecting what works underpins ongoing success with this chemical tool.
Businesses and researchers relying on Octanol can build on years of cross-discipline trust and shared experience. Combining practical knowledge, transparent safety culture, and a willingness to evolve creates long-term benefits. Investments in better handling, safer workspaces, and greener production methods can deliver genuine progress, inside the lab and out on the production floor.
Octanol’s versatility — not only as a chemical but as a catalyst for practical change — keeps it woven into modern manufacturing. Experienced users know that’s not just good chemistry; it’s good business and good science, forged in the spaces where real-world problems meet creative solutions. As industries change and standards rise, Octanol’s future remains tied to the willingness of its users to adapt, improve, and lead.