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HS Code |
164551 |
| Cas Number | 96-23-1 |
| Molecular Formula | C3H6Cl2O |
| Molecular Weight | 128.99 |
| Iupac Name | 1,3-dichloropropan-2-ol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point C | 174 |
| Melting Point C | -57 |
| Density G Per Cm3 | 1.36 |
| Solubility In Water | Miscible |
| Flash Point C | 71 |
| Refractive Index N20 | 1.462 |
| Odor | Pungent |
| Vapor Pressure Mmhg 20c | 1.1 |
As an accredited 1,3-Dichloro-2-Propanol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 1,3-Dichloro-2-Propanol is supplied in a 500 mL amber glass bottle with a secure cap, labeled with safety information. |
| Shipping | 1,3-Dichloro-2-Propanol should be shipped in tightly sealed containers, clearly labeled, and protected from heat and incompatible materials. Transport according to local, national, and international regulations for hazardous materials, specifically as a toxic and potentially environmentally hazardous substance. Ensure use of suitable secondary containment and emergency response equipment during transit. |
| Storage | 1,3-Dichloro-2-propanol should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Keep the container tightly closed and properly labeled. Store in a corrosive-resistant, chemical-resistant container, protected from moisture. Ensure access is limited to trained personnel, and use secondary containment to prevent accidental spills or leaks. |
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Purity 99%: 1,3-Dichloro-2-Propanol with purity 99% is used in pharmaceutical intermediate synthesis, where it ensures high-yield and reproducibility of target compounds. Stability Temperature 45°C: 1,3-Dichloro-2-Propanol with stability temperature 45°C is used in resin manufacturing processes, where it maintains chemical integrity during controlled heating. Molecular Weight 128.98 g/mol: 1,3-Dichloro-2-Propanol with molecular weight 128.98 g/mol is used in fine chemical formulation, where precise molecular mass enables accurate stoichiometry. Colorless Liquid: 1,3-Dichloro-2-Propanol as a colorless liquid is used in dye synthesis applications, where it prevents unwanted color contamination. Viscosity 2.1 mPa·s (20°C): 1,3-Dichloro-2-Propanol with viscosity 2.1 mPa·s at 20°C is used in coatings production, where it facilitates uniform blending and dispersion of components. Boiling Point 174°C: 1,3-Dichloro-2-Propanol with boiling point 174°C is used in solvent systems for specialty chemicals, where controlled evaporation rates are required. Water Miscibility: 1,3-Dichloro-2-Propanol with water miscibility is used in agrochemical formulations, where effective dilution and mixing are critical for application uniformity. Low Impurity Content: 1,3-Dichloro-2-Propanol with low impurity content is used in electronics-grade cleaning processes, where it minimizes the risk of residue and contamination. Density 1.398 g/cm³: 1,3-Dichloro-2-Propanol with density 1.398 g/cm³ is used in intermediate blending for plasticizers, where accurate volumetric measurement ensures consistent product quality. Assay ≥98%: 1,3-Dichloro-2-Propanol with assay ≥98% is used in laboratory reagent preparations, where reliable assay levels guarantee experimental reproducibility. |
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Not all chemical compounds turn heads outside of specialized industries, but 1,3-Dichloro-2-Propanol (commonly called 1,3-DCP) has a habit of doing just that. Much of its draw springs from its structure: two chlorine atoms tucked on either end of a simple three-carbon backbone, with a hydroxyl group nestled in the middle. This makes 1,3-DCP quite reactive—always a property that sparks interest for those involved with synthesis and research. Its molecular formula is C3H6Cl2O, and it presents itself as a colorless to light yellow liquid with a noticeable, sharp odor. Not hard to spot if you get close enough in a lab.
Where does 1,3-DCP fit into the landscape of industrial and laboratory chemicals? By experience, in research settings it tends to pop up during conversations about chemical intermediates, especially when people are sorting through routes to create more complex organic compounds. The dual chlorine atoms offer a pair of reactive sites, and the hydroxyl group in the middle makes it easy to imagine all sorts of downstream products. It’s never the end in itself, but serves as a reliable springboard.
Walking through storage areas or research sections, I can count on a few clear indicators when 1,3-DCP is around. A boiling point that hovers around 174°C means it doesn’t evaporate as quickly as more volatile chemicals, but you can smell it if the cap isn’t on tight. The density, about 1.33 g/cm³ at 20°C, makes it heavier than water, something that matters if you’re a chemist planning layering or separation work. Its solubility in water is limited, but in organic solvents like acetone, ether, and ethanol, it dissolves just fine, which is useful for multi-step synthesis.
It’s important to note that laboratory-grade 1,3-DCP typically arrives at high purities—frequently 98% or above—since impurities can throw off synthetic results and analytic work. Color sometimes gives away small traces of impurities, so a slightly yellow tint often signals heavier or less carefully processed material. The product is usually stored in tightly sealed, chemical-resistant containers, and you’ll catch a pungent, almost irritating aroma if you ever work with it directly.
Looking broadly, 1,3-Dichloro-2-Propanol functions as a building block, mostly for other chemicals. In organic synthesis, it plays a role in forming epoxides and glycidol derivatives, thanks to its convenient structure. Some chemists pursue it as a precursor to glycidyl ethers, which have ultimately found their way into various plasticizers, resins, and adhesives. Every time I circle back to polymer chemistry, the conversation ends up swinging around to the importance of reliable intermediates, and 1,3-DCP keeps coming up.
In a more historical sense, 1,3-DCP also made appearances as an intermediate in the production of certain pharmaceuticals and pesticides. Though the market now leans toward greener processes and less toxic alternatives, some legacy routes continue to rely on it for its directness and chemical efficiency. On rare occasions, analytical laboratories look for it as a marker in quality control, given its relation to certain contamination risks during chlorohydrin production.
Anyone handling 1,3-DCP learns quickly that this is not a chemical for casual work. There’s a reason experienced professionals stress ventilation and protective wear—prolonged exposure or careless spills carry significant health risks. Reports link 1,3-DCP to potential carcinogenicity, and it can cause irritation to skin, eyes, and the respiratory tract. I learned early never to underestimate that sharp, biting odor as a warning sign. Even at low concentrations, repeated exposures can bring trouble.
From an environmental perspective, 1,3-Dichloro-2-Propanol doesn’t break down readily. Wastewater from manufacturing or usage sites must be treated with care to avoid persistent chemical build-up that could harm local waterways or soil. Over years of tracking chemical life cycles, I’ve watched regulatory standards tighten, requiring more robust containment and recycling practices. Incineration under controlled conditions remains the preferred disposal method on an industrial scale. Labs increasingly devote resources to closed-loop processes to minimize escape of these chlorinated organics.
Given its reactivity, 1,3-DCP often gets compared with its cousin, 1,2-Dichloro-3-propanol (1,2-DCP), and even more so, with epichlorohydrin. The differences lie in structural arrangement and, as a result, in their subsequent chemical reactivity and end uses. 1,2-DCP, for example, places its chlorine atoms closer together, which gives rise to different reactivity profiles—something synthetic chemists like to exploit when planning their routes. Epichlorohydrin takes things further, introducing an epoxide ring into the mix, leading to major differences in the polymers and resins produced downstream.
From a regulatory perspective, both 1,2- and 1,3-DCP compounds have drawn concern as possible carcinogens, but 1,3-DCP’s usage has been less widespread historically, so fewer contamination issues have been recorded. Epichlorohydrin, meanwhile, dominates large-scale resin production, especially for epoxy resins, but has even tighter handling restrictions due to volatility and toxicity.
Over the last ten years, attention to safer, more sustainable routes to similar downstream products has shaped the way 1,3-DCP gets handled—or even chosen at all. I’ve seen more companies work hard to develop alternatives with lower toxicity profiles, both to satisfy regulatory agencies and to address growing consumer concern. That said, the unique reactivity of 1,3-DCP keeps it relevant for certain targeted syntheses, especially where no reliable alternative exists.
Chemical manufacturing keeps evolving. As laboratories invest in cleaner technologies and green chemistry initiatives, 1,3-DCP’s usage looks increasingly niche. Younger research teams put sharper focus on limiting waste, designing products that biodegrade more cleanly, and avoiding persistent organic pollutants altogether. Despite fewer large-scale projects showcasing 1,3-DCP, the compound maintains a foothold where specific reactivity or cost barriers make change impractical.
Classrooms and research facilities I’ve worked in stress the use of fume hoods and gloves every time 1,3-DCP hits the workbench. Proper ventilation sits front and center, along with standard-issue goggles and chemical-resistant aprons. It isn’t just about checking boxes—it’s about keeping people out of harm’s way. Safety data for 1,3-DCP leaves little room for compromise, given the repeated links to potential cancer risks and tissue irritation.
For facilities managing industrial quantities, closed-loop systems have proven most effective at reducing fugitive emissions. Electronic monitoring of air and wastewater delivers real-time warnings if limits approach concerning levels. Regular training of personnel, together with updated safety signage and documented handling protocols, make a clear difference in outcomes. Where possible, companies substitute less hazardous precursors in order to trim exposure at every stage, from delivery to disposal.
Waste management stands as a crucial piece of the puzzle. Incineration under temperature-controlled, oxygen-rich conditions minimizes the risk of forming harmful byproducts like dioxins or polychlorinated biphenyls. For academic work, research teams store and label containers with extreme care, ensuring accidental spills or mixing never reach common drains. During my own lab days, one misplaced bottle or lazy labeling would trigger a chain of emails and retraining, which feels frustrating in the moment, but clearly supports community safety.
Despite pushback from environmental groups, chemical research continues to find uses for intermediates like 1,3-DCP. The focus shifts toward controlled, small-scale synthesis, especially in designing specialty chemicals, pharmaceuticals, or fine-tuned agricultural products. Newer catalytic systems have started to cut down on waste and increase efficiency, allowing researchers to squeeze more value out of each batch while producing less residue.
Biotechnology has put forward a handful of promising biocatalytic routes to related compounds, sparking interest in repurposing or modifying 1,3-DCP as a starting point for more complex molecules. The shift from bulk to boutique gives room for creative uses while managing the risks associated with large-scale distribution. As techniques grow smarter and labs lean into automation and digital tracking, the safety margins improve and environmental releases become easier to spot and intercept.
For academic labs, the message comes through loud and clear: only use 1,3-DCP when no suitable alternative exists, and always double-check waste management steps. Outreach around the risks, as well as the ongoing development of replacement methods, reduces unnecessary exposure for those just starting out in chemistry. Teachers and mentors owe it to younger scientists to model safe, responsible chemical use—not out of obligation, but because best practices protect everyone.
Industry carries greater responsibilities. Investment in alternative synthesis routes and greener production lines, plus regular audits of current protocols, makes measurable strides toward both worker safety and regulatory compliance. Whether installing new air-scrubbing units or onboarding digital incident tracking systems, modern plants see both productivity and safety rise. Through professional networks, specialists now share strategies in real time, often speeding the adoption of better practices across the sector.
For anyone living near industrial sites, chemical names like 1,3-DCP carry weight—even if the processes run perfectly. Community awareness programs and clear, accurate communication about what’s being stored, made, or transported matter. I’ve joined town meetings where honest exchanges between scientists and residents replaced suspicion with understanding. Simple diagrams and direct answers—without deflecting difficult questions—make the difference in building trust.
Independent monitoring, either by local governments or in partnership with company outreach teams, provides regular updates to the public. Community air and water quality readings, posted online and explained in plain language, ease concerns and open the door for shared problem-solving whenever an issue appears. Publicly posted incident logs build accountability and sharpen a company’s attention to real-world impact, not just on-paper compliance.
Over years spent among labs and factory floors, it becomes clear that 1,3-Dichloro-2-Propanol sits at an intersection of need and responsibility. Its chemical properties fill a specific gap in certain syntheses, and for those reactions, its use is justifiable. At the same time, every step taken to minimize risks—be it through alternative processes, better engineering controls, or honest dialogue about hazards—brings the industry closer to serving both innovation and safety.
Students, researchers, and industrial leaders benefit from seeing where legacy chemicals like 1,3-DCP fit into workflow—and where newer, cleaner approaches deserve a shot. In the short term, careful handling and robust process checks protect communities and workers. Over longer time scales, research into novel syntheses promises to either phase out the riskier compounds or transform their usage into something as safe and dull as household vinegar. The story of 1,3-Dichloro-2-Propanol continues, shaped by those willing to keep an eye not just on profit or convenience, but on the bigger picture of health, safety, and shared progress.