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1,2,3,4-Tetrahydronaphthalene

    • Product Name 1,2,3,4-Tetrahydronaphthalene
    • Alias Tetralin
    • Einecs 202-371-1
    • 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
    Specifications

    HS Code

    214614

    Cas Number 119-64-2
    Molecular Formula C10H12
    Molar Mass 132.20 g/mol
    Appearance Colorless liquid
    Melting Point -35 °C
    Boiling Point 207 °C
    Density 0.963 g/cm³ at 20 °C
    Refractive Index 1.536 at 20 °C
    Flash Point 81 °C (closed cup)
    Solubility In Water Insoluble
    Vapor Pressure 0.3 mmHg at 25 °C

    As an accredited 1,2,3,4-Tetrahydronaphthalene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 500 mL amber glass bottle, tightly sealed with a screw cap, labeled "1,2,3,4-Tetrahydronaphthalene," with hazard warnings.
    Shipping 1,2,3,4-Tetrahydronaphthalene should be shipped in tightly sealed containers, away from heat, sparks, and open flame. It must be handled as a flammable liquid, following relevant regulations (such as UN 2301, Class 3). Proper labeling, ventilation, and use of compatible packaging materials are essential to ensure safe and compliant transportation.
    Storage 1,2,3,4-Tetrahydronaphthalene should be stored in a tightly closed container in a cool, dry, well-ventilated area away from sources of ignition, heat, and strong oxidizing agents. Protect from direct sunlight and moisture. Proper labeling and secondary containment are recommended to prevent leaks or spills. Handle under a fume hood and use appropriate personal protective equipment when accessing the chemical.
    Application of 1,2,3,4-Tetrahydronaphthalene

    Purity 99%: 1,2,3,4-Tetrahydronaphthalene with purity 99% is used in pharmaceutical intermediate synthesis, where it ensures high reaction yield and product consistency.

    Boiling Point 207°C: 1,2,3,4-Tetrahydronaphthalene with a boiling point of 207°C is used in heat transfer fluid systems, where it provides stable thermal conductivity.

    Molecular Weight 132.2 g/mol: 1,2,3,4-Tetrahydronaphthalene with molecular weight 132.2 g/mol is used in organic synthesis, where it allows for predictable stoichiometric calculations.

    Stability Temperature up to 150°C: 1,2,3,4-Tetrahydronaphthalene stable up to 150°C is used in polymerization processes, where it maintains chemical integrity under reaction conditions.

    Low Viscosity Grade: 1,2,3,4-Tetrahydronaphthalene with low viscosity grade is used in lubricant formulations, where it enhances fluidity and reduces mechanical wear.

    Hydrogen Content 8.41%: 1,2,3,4-Tetrahydronaphthalene with hydrogen content 8.41% is used in hydrogen donor solvents, where it improves reduction capabilities in catalytic reactions.

    Density 0.97 g/cm³: 1,2,3,4-Tetrahydronaphthalene with a density of 0.97 g/cm³ is used in chemical separation processes, where it aids phase discrimination and material handling.

    Melting Point -35°C: 1,2,3,4-Tetrahydronaphthalene with a melting point of -35°C is used in low-temperature applications, where it provides liquid phase stability in cryogenic conditions.

    UV Absorbance 254 nm: 1,2,3,4-Tetrahydronaphthalene with UV absorbance at 254 nm is used in analytical chemistry, where it enables detection and quantification of aromatic compounds.

    High Flash Point 120°C: 1,2,3,4-Tetrahydronaphthalene with a flash point of 120°C is used in industrial solvent systems, where it enhances operational safety and reduces flammability risk.

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    Certification & Compliance
    More Introduction

    1,2,3,4-Tetrahydronaphthalene: A Closer Look at a Versatile Liquid Aromatic

    Why 1,2,3,4-Tetrahydronaphthalene Catches Attention

    A drum of 1,2,3,4-tetrahydronaphthalene, for most people, might just look like a clear, oily liquid on a warehouse shelf. For folks working in chemical plants, research labs, or specialty manufacturing, 1,2,3,4-tetrahydronaphthalene isn’t faceless at all. It goes by the name tetralin, and over the years, I’ve worked with it in organic synthesis, seen it used as a hydrogen donor, and come across it as a cleaner in some tough industrial settings. Its molecular structure – basically a naphthalene ring that’s taken up hydrogen atoms to leave it partially saturated – leaves it stable and yet reactive at the same time. That odd dual nature lets it turn up in more places than some might expect.

    Understanding What Sets Tetralin Apart

    Most people familiar with industrial chemicals have seen aromatic hydrocarbons: naphthalene, benzene, toluene. Tetralin steps out from that familiar crowd, largely because of what that partial hydrogenation does. Where naphthalene is a solid whitish chunk you might recognize from mothballs, tetralin pours easily even in winter. It holds onto some of naphthalene’s aromaticity, but with less volatility and less tendency to crystallize or sublimate. Boiling at around 207°C, with a faint, sweetish odor, it doesn’t bounce up into the air too fast. For workers used to benzene’s sharp smell and high vapor pressure, tetralin is much less overpowering.

    People worry about toxicity with aromatics, and rightly so. Tetralin doesn’t erase those concerns, but data show lower acute toxicity by inhalation and skin contact, compared to benzene or pure naphthalene. Anyone spending long days handling chemicals develops respect for exposure limits and personal safety. In my experience, tetralin rarely gives headaches or dizziness, provided the space is well ventilated. I have always worn gloves and goggles, and I encourage others to do the same, but compared to more notorious aromatics, the risk profile of tetralin is a touch milder.

    Technical Notes: Physical and Chemical Characteristics

    Industrial users and researchers look first at properties like purity, boiling point, molecular weight, and compatibility with other reagents before picking a solvent. The standard technical-grade tetralin arrives at purities over 98%, often around 99%. This high degree of purity is essential for laboratory work, where even slight contaminants introduce confounding factors during synthesis or analysis. Tetralin dissolves a broad range of organic compounds, including some copolymers and resins that resist other fluids. Those who have struggled to get stubborn residues off glassware appreciate tetralin’s solvency. On that front, tetralin outperforms mineral spirits or kerosene every time.

    Tetralin stays liquid under cold storage and doesn’t gum up precision equipment. Its relatively high boiling point helps where high-temperature reactions demand a solvent that won’t vanish before a reaction completes. In my early days in a university organic lab, tetralin allowed us to run reflux reactions at over 200°C, which was out of reach for most affordable solvents. I’ve seen factory lines use it in cleaning baths for removing sticky residues from polymer extruders, and in the field of electrical transformer maintenance, some engineers swear by tetralin as a flushing agent for oil-insulated equipment.

    Practical Uses in Industry and Labor

    A walk around any chemical plant or industrial site will show that every solvent has its fans. Tetralin gets a lot of mileage as a hydrogen-donor solvent in transfer hydrogenation. By offering up hydrogen atoms during processing, it enables reactions that otherwise would stall or demand more expensive setups. For example, the reduction of coal tar, petrochemicals, or even some specialty organics can proceed more gently using tetralin as the hydrogen shuttle.

    It also has fans in the plastics and resin industries. Certain resins only dissolve in fluids that can break the surface tension and interact with their molecular structure. Tetralin has just the right polarity for stubborn polymers. I recall an old colleague describing how switching from toluene to tetralin improved yields in preparing specific polystyrene block copolymers, while keeping equipment easier to clean at the end of a shift.

    Some people point to its role in laboratory analysis. Tetralin’s relatively mild odor and lower volatility make it easier to work with during longer procedures. Students in organic chemistry sometimes use tetralin in teaching labs – it won’t cover the entire bench in vapor, so you can concentrate without tearing up or coughing. For specialized chromatography, it helps in dissolving lipophilic samples that resist lighter solvents.

    Not all uses involve synthetic chemistry or cleaning. In transformer oil research, tetralin helps test and evaluate the breakdown products in aging insulation oils. This matters to utilities, because transformer oil failures cost millions and can threaten worker safety. Special test protocols have long relied on tetralin’s solvent power – it gets into the nooks and crannies of aged insulation materials without attacking the copper or steel inside transformers. It also washes out residues that less polar solvents won’t touch.

    Where Tetralin Stands Out Among Aromatics

    Solvents are not all made equal, and the industry has plenty of options. Toluene, xylene, and naphthalene all have their loyal followings. But tetralin draws attention because of where it fits in the middle: more stable and less volatile than toluene or benzene, less prone to solidify or sublimate than naphthalene. For industrial users dealing with large ambient temperature swings, this reduces headaches. Tanks don’t form large crystals, and internal pipes don’t clog up.

    Price-wise, tetralin sits above toluene, but often below more exotic reagents. Many plants use toluene by the tanker for routine cleaning and processing, only bringing out tetralin for specific jobs where nothing else works quite as well. That makes sense, given that its manufacturing involves extra steps and raw materials compared to the simple cracking of petroleum products like toluene or xylene.

    Tetralin’s lower vapor pressure has practical safety consequences. Those who run plant storage yards know that less vapor given off means lower fire risk, easier vapor control, and a more comfortable working environment on hot days. Workers get fewer complaints about odor and fewer headaches during long jobs. From my years on shift, I’ve noticed maintenance crews much prefer cleaning extruders with tetralin versus naphthalene slurries, which stink up everything and leave sticky cakes inside tanks.

    It also doesn’t punch above its weight when it comes to environmental risk. Volatile aromatic hydrocarbons tend to evaporate rapidly and form problematic smog precursors. By staying put, tetralin cuts down on those stray fumes. Still, anything that can dissolve tough resins will have some aquatic and soil toxicity if spilled, so safe handling and spill controls remain essential. Having managed a few spill cleanups, I can say tetralin’s slow evaporation buys crucial time for containment, compared to flashier solvents.

    Challenges and Room for Progress

    No chemical is perfect, and tetralin brings its own set of issues. Sourcing high-purity tetralin sometimes turns into a bottleneck for smaller labs, especially if they order infrequently or through multiple wholesalers. Pricing fluctuates along with demand from the plastics and chemicals market. During market surges in the plastics sector, prices can climb faster than the budgets set by research labs or mid-sized manufacturers. The volatility in the global chemicals market requires buyers to build strong relationships with reputable suppliers and to monitor trends in feedstock costs.

    There’s also pressure from regulators to reduce reliance on aromatic hydrocarbons across the board. Some agencies look particularly closely at long-term exposure risks, environmental persistence, and the fate of such chemicals in wastewater. While tetralin shows a lower acute risk profile and is more stable than many close cousins, it’s not considered benign. Many facilities have invested in vapor recovery, improved ventilation, and employee training. In my time managing compliance for a specialty chemicals line, we updated ventilation and leak detection after one lab worker noticed the repeated low-level odor of tetralin. Subsequent air testing showed our controls reduced actual exposure below the regulated threshold, but that regular monitoring made a difference in worker confidence and safety.

    Waste disposal offers another challenge. Tetralin’s chemical stability means it doesn’t easily break down, so it requires incineration or specialized treatment to avoid moving into water systems. Some innovative recyclers have experimented with reclaiming spent tetralin from used cleaning baths, but contamination often pushes up the costs. For smaller users, group disposal via chemical waste programs can cut costs and minimize risk, and I’ve found it worthwhile to join such partnerships whenever possible.

    Looking Forward: Sustainable Use and Industry Innovation

    Innovation moves fast, and the pressure for sustainable chemistry keeps growing. Some companies now look for “greener” alternatives, such as esters, glycol ethers, or new proprietary solvents. Nevertheless, when it comes to balancing solvency, stability at high temperatures, and availability, tetralin stays competitive. Engineers have begun to investigate how to fine-tune hydrogenation processes using less tetralin, or to blend it with co-solvents that reduce overall aromatic content in emissions. Universities have documented new uses for tetralin in advanced materials, like liquid-phase exfoliation for nanomaterials and as a medium for controlled-particle syntheses.

    For process engineers, the key is matching the solvent to the task. Tetralin isn’t always the first pick, but for certain resins, specific hydrogenation reactions, or jobs involving difficult residues, it solves problems that shut down operations with other chemicals. I once spoke with a senior operator at a midwestern plastics plant who swore by tetralin during resin flushes at the end of production runs. He told me that switching to less effective solvents only passed the cleanup headache on to the night shift, who would spend hours scraping out hardened residues. Tetralin, on the other hand, shortened the cleanup, cut down on mechanical wear, and kept output on schedule.

    A lot of effort goes into minimizing worker exposure and environmental hazards. In newer facilities, vapor containment, closed transfer systems, and solvent recycling all play their part. Safety data, regular hygiene surveys, and strong onsite training blunt the risks. I remember a project where we converted all drum-transfer pumps to sealed systems with reinforced gaskets after a near-miss spill episode. Not only did the change prevent vapor leaks, but it also kept controls cleaner and extended equipment life.

    Training matters, too. A solvent is only as safe as its handler’s habits. For many years, taking time to coach new workers on personal protective equipment, spill control, and the quirks of each solvent paid off in accident-free records and lower insurance costs. I’ve made it my business to always review safety bulletins with my teams, because seasoned hands sometimes slip into risky routines when pressure is high.

    While the future may lean toward niche replacements or blended solvents, tetralin’s balance of performance and reliability secures its role. It’s a kind of workhorse – not the star of the show, maybe, but dependable in a wide range of industrial and lab contexts. Its chemistry remains studied and well-documented, offering strong assurance that new users have good data to rely on.

    Supporting Facts and Regulatory Context

    The facts add up: tetralin’s relatively modest vapor pressure, lower acute toxicity compared to other aromatics, and high solvency for challenging hydrocarbons are documented in leading chemical databases. Regulations continue to evolve, though, and staying up-to-date keeps operations on the right side of local laws. Agencies in the US, EU, and Asia generally set occupational exposure limits for tetralin similar to or stricter than those for naphthalene, but less restrictive than benzene or toluene. Any company or lab storing tetralin ought to consult updated guidance regularly.

    Environmental persistence is a key concern raised by both governments and citizen organizations. Although tetralin slowly degrades in the environment, it can build up in soil and water systems after large or repeated spills. Good stewardship practices – containment, prompt cleanup, and professional waste disposal – make a difference. Over a decade in compliance roles, I’ve seen that cutting corners only leads to fines, lost community trust, and, sometimes, permanent bans on certain operations. Regular third-party audits and adopting best practices from larger players makes sense, especially for small outfits.

    Tetralin production demands energy and petrochemical feedstocks, so the shift in global energy markets affects both its availability and carbon footprint. Some researchers have explored using biobased sources for similar aromatic structures, but so far, few routes match the price and consistency offered by classic petrochemicals.

    Opportunities for Smarter Handling and Reduced Impact

    People with long experience handling solvents know there’s always room to tighten up procedures. Several practical steps can cut risks and costs:

    I’ve helped install vapor monitoring systems and set up recycling lines in a midsize facility – improvements recouped their costs in a few years by shrinking both purchase orders and hazardous waste fees. Site visits to other companies always offer ideas, and open discussions with everyone from janitorial staff to process engineers often surfaces minor problems before they get big and expensive.

    On the prevention side, spill drills and regular reviews of chemical inventory keep the team sharp and responsive. I once walked into a storeroom after a minor earthquake and found a tetralin drum had toppled, wedged against a support column. Only habits drilled from regular training – keeping the area uncluttered and heavy drums stacked lowest – kept the event from turning into a major incident. It bears repeating that the simplest solutions sometimes prove the best.

    Critical Takeaways for Those Considering Tetralin

    Any decision to use 1,2,3,4-tetrahydronaphthalene should hinge on a mix of chemical compatibility, safety considerations, budget, and worker preference. For many years, its spot in the toolbox has come not from being the cheapest or the most benign, but from being the solvent that gets hard jobs done where others fall short. Today’s attention to environmental, health, and regulatory factors does not diminish the value of a proven, well-documented material – it just adds another layer of responsibility.

    Tetralin stands out among aromatic solvents because it hits a sweet spot between chemical performance and manageable handling. It takes regular practice and close attention to use it wisely, whether in cleaning, synthesis, or special analyses. Users should respect its potential, invest in training and containment, and watch market and regulatory shifts. In my experience, the companies and labs that thrive and avoid trouble are always the ones that make these steps part of their culture, not just a compliance tick-box.

    In the end, 1,2,3,4-tetrahydronaphthalene is more than just another liquid in a drum – it’s a tool shaped by decades of practice, each year bringing a sharper sense of its strengths, limits, and safe ways forward. The key lies in steady stewardship, a bit of innovation, and ongoing attention to getting it right for workers, customers, and the wider community.