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HS Code |
864658 |
| Chemical Name | 1,2,3-Trichloro-2-Propanol |
| Cas Number | 96-18-4 |
| Molecular Formula | C3H5Cl3O |
| Molecular Weight | 163.43 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 174-176 °C |
| Melting Point | -33 °C |
| Density | 1.532 g/cm3 at 25 °C |
| Refractive Index | 1.474 |
| Flash Point | 80 °C (closed cup) |
| Solubility In Water | Miscible |
| Synonyms | Glycerol trichlorohydrin |
As an accredited 1,2,3-Trichloro-2-Propanol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 1,2,3-Trichloro-2-Propanol is packaged in a 500 mL amber glass bottle with a secure screw cap and safety labeling. |
| Shipping | **1,2,3-Trichloro-2-Propanol** should be shipped in tightly sealed containers, clearly labeled as a hazardous material. It must comply with all applicable local, national, and international transport regulations for toxic and potentially harmful chemicals, ensuring secondary containment to prevent leaks and exposure. Handle with protective equipment and avoid extreme temperatures or incompatible substances during transit. |
| Storage | 1,2,3-Trichloro-2-propanol should be stored in a tightly closed, clearly labeled container in a cool, dry, and well-ventilated area, away from direct sunlight. Keep separate from incompatible materials such as oxidizing agents and strong bases. Store at room temperature, in an area with spill containment. Access should be limited to trained personnel using proper protective equipment. |
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Purity 99%: 1,2,3-Trichloro-2-Propanol with 99% purity is used in pharmaceutical intermediate synthesis, where it ensures high product yield and reduced impurities. Viscosity grade 8 cP: 1,2,3-Trichloro-2-Propanol with viscosity grade 8 cP is used in resin formulation processes, where it enables uniform blending and improved dispersion. Molecular weight 163.4 g/mol: 1,2,3-Trichloro-2-Propanol of molecular weight 163.4 g/mol is utilized in agrochemical manufacturing, where it facilitates precise dosing and optimal compound stability. Melting point 49°C: 1,2,3-Trichloro-2-Propanol with a melting point of 49°C is applied in specialty polymer processing, where it allows controlled solidification and consistent material properties. Stability temperature up to 140°C: 1,2,3-Trichloro-2-Propanol with stability temperature up to 140°C is used in high-temperature reaction systems, where it provides chemical durability and sustained reaction efficiency. Particle size <20 microns: 1,2,3-Trichloro-2-Propanol with particle size under 20 microns is employed in coating additives, where it offers enhanced surface coverage and smooth application. Water solubility 18 g/L: 1,2,3-Trichloro-2-Propanol with water solubility of 18 g/L is used in aqueous formulation development, where it ensures homogeneous mixing and stable dispersions. |
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Having worked around chemical warehouses and research labs, I have seen how much the fine details of a single raw material impact a whole project. Among those niche chemicals, 1,2,3-Trichloro-2-Propanol stands out for anyone who relies on precision and consistency in synthesis or specialty processing. For folks less familiar, this compound with a clear structure and a bit of a sharp, distinctive odor seems straightforward on paper, yet its role in specialty organic synthesis continues to evolve alongside changing industry needs.
With a chemical formula of C3H5Cl3O, this halogenated alcohol balances three chlorine atoms with a propanol backbone—common enough to imagine, but surprisingly uncommon in the way it delivers results in both research and specialized industrial applications. Experienced chemists often recognize that odd number of chlorines and single hydroxyl group as giving it an edge during certain selective reactions, especially under controlled settings where predictability is everything.
Out in the market, most 1,2,3-Trichloro-2-Propanol is supplied in liquid form, usually arriving in tightly sealed glass or HDPE bottles—the same sort of rigid containment most folks use for storing solvents and reagents that are both reactive and valuable. The typical batches I’ve handled tend to hover near a high purity threshold, somewhere north of 98%. That’s mostly because even small slivers of contamination start to throw off yields and react unpredictably in multi-step syntheses, especially for fine chemicals and active pharmaceutical intermediates.
I remember watching senior chemists puzzling over synthetic routes, searching for intermediates just reactive enough to move things along without adding new headaches. 1,2,3-Trichloro-2-Propanol became a favorite tool in those labs. It tends to show up as an intermediate rather than an end-use product, acting as a building block for other chlorinated organic compounds. This might sound like a small role, but for drug discovery, custom reagents, or R&D involving halogenation, having access to a batch where every drop behaves exactly as calculated makes life easier and results more reliable.
There’s plenty of chatter about alternatives, but lab hands often return to this compound during the early stages of synthesis, especially when targeting molecules with extra chlorine atoms in precise spots. In real-world experiments, the difference becomes clear: using a similar compound, such as a dichloropropanol, rarely yields the same results. That extra chlorine matters for both reactivity and selectivity, saving time by cutting out extra reaction steps or rearrangements. The option to introduce the trichloro functionality right at the start shortens timelines and reduces waste, which hits close to home in grant-funded projects or lean manufacturing environments.
Anyone working directly with hazardous or reactive chemicals knows the importance of rigorous specifications. The purity and trace impurity profile make or break downstream reactions. 1,2,3-Trichloro-2-Propanol generally ships with a clear, colorless appearance—cloudiness often points to breakdown or poor storage. Most suppliers aim for minimal water content, since moisture can trigger unwanted reactions and reduce shelf life. The best batches I’ve seen pour clean and leave minimal residue, which helps during transfers as well as analytical tracking.
From a manufacturing standpoint, shelf life becomes a recurring topic—nobody wants a slow-degrading batch eating into productivity or safety. While basic storage in a cool, dry place prevents rapid deterioration, real-world situations sometimes cause trouble: one time, an overlooked shipment endured a muggy summer in a poorly ventilated storeroom. Weeks later, the compound lost its punch, failing to meet reactivity benchmarks until a fresh batch arrived. That experience stuck with the team, reinforcing how storage habits aren’t just about housekeeping—they protect both safety and investment.
There’s a tendency to treat chlorinated alcohols as interchangeable pieces in chemical catalogs, but those who spend time with these compounds notice crucial differences. Take 1,2,3-Trichloro-2-Propanol and stack it side by side with its close cousins—say, 1,2-dichloro-3-propanol or 2,3-dichloro-1-propanol. The change from di- to tri-chloro shifts both physical properties and the way chemical reactions play out. A test batch for a new synthesis will react faster or yield a cleaner product with one, while dragging or stalling with the other.
For developers scaling up pilot projects, those differences matter. Swapping in a similar molecule might cut procurement costs or sidestep a backorder, but more often, the move leads to headaches: unexpected byproducts, missed purity targets, or sluggish processing times. I’ve seen production lines recalibrated in response to these sorts of hiccups, burning through both money and morale. This reality has led many labs to standardize on 1,2,3-Trichloro-2-Propanol for runs that count. The upshot: a smooth path to regulatory approval and a track record that stands up during quality audits—often the make-or-break moment for new products.
Over the years, end users in both academia and specialty manufacturing have come to rely on 1,2,3-Trichloro-2-Propanol for its predictability. It is not the sort of chemical that has a starring role in mainstream products or grabs headlines, but for research teams and process engineers, its stability, known reactivity, and clean handling simplify life when margins for error are slim. Pull up data sheets or white papers from major institutions, and its name comes up where demanding applications call for repeatable performance.
Part of what drove me to trust this compound on projects involved years of dealing with inconsistent lots and troubleshooting reaction failures. More than once, I watched experienced chemists take samples straight to the chromatograph for confirmation, since only top-grade lots would make the cut. Once the right source and batch are in play, scales tip back in favor of minimal troubleshooting, with teams able to focus on downstream innovation rather than constant review of basic materials.
Chemistry does not live in a vacuum, and safety conversations never stop. Unlike commodity solvents, 1,2,3-Trichloro-2-Propanol requires thoughtful handling due to its reactivity profile and potential health impacts. Direct skin contact, inhalation, and improper storage all open doors to risks—anyone who’s spent time in safety training or managed incident logs knows small oversights can cost dearly. This is why seasoned staff respect the labeling and don proper gear even during routine use.
Compared to less chlorinated relatives, the potential hazards trend slightly higher. This raises the bar for safe working practices, especially in shared or academic environments where multiple research streams intersect. Safety data sheets from reputable institutions offer guidance, but the real learning happens through team culture: chemical fume hoods, regular inspection of storage containers, and a daily habit of reviewing procedures make a measurable difference.
Much is said about innovation in chemistry, but anyone in the trenches knows it’s the everyday reliability of starting materials that unlocks forward progress. Reliable 1,2,3-Trichloro-2-Propanol remains one of those rarely discussed yet deeply influential resources. During one student research project, repeated failures with generic reagents led the group to switch to a high-quality batch purchased through a vetted supplier. Not only did yields improve, but the overall mood shifted—less guesswork, fewer surprises, and a renewed sense of confidence in the success of experimental plans.
Supply chain disruptions sometimes put laboratory teams in the tough position of switching between suppliers. Some turn to local distributors, risking uneven purity and batch variation. Others hold out for consistent imports, valuing the investment in time and logistics for the peace of mind that comes with trusted performance. I have seen institutions initiate collaborative purchasing among multiple labs to guarantee access and lock down quality standards, especially when grant timelines and student deadlines converge.
While 1,2,3-Trichloro-2-Propanol handles its role well, every chemical comes with limits. Shelf life will always play a role, especially for users with sporadic projects and slow turnover. Roadblocks also pop up with regulatory compliance as standards shift or new research uncovers previously unknown risks associated with halogenated compounds. Many organizations encourage regular chemical hygiene reviews, including audits of storage and disposal practices, both to stay correct with the letter of the law and to ensure responsible stewardship for student researchers just getting their bearings.
Some labs have started to experiment with in-house purification or stabilization approaches to squeeze out more working life from each container, hoping to control budgets and avoid last-minute reordering. Others re-examine inventory management, leaning on barcode systems and digital logs to ensure no batch sits forgotten on the shelf until it degrades. While these strategies sound common sense, their adoption can cut waste and support safer workspaces—an outcome anyone who has sorted through expired stock can appreciate.
There was a time when disposal practices were barely discussed, but priorities shifted. Many chemists now recognize their role in minimizing environmental harm, especially with chlorinated compounds that resist easy degradation. 1,2,3-Trichloro-2-Propanol fits this picture, requiring special attention to waste disposal. The best teams lay down clear protocols for neutralizing and disposing of waste, sometimes building in regular checks with environmental engineers or outside consultants, keeping wastelogs up to date and partnering with approved disposal services.
University labs and smaller companies may face cost barriers in adopting advanced waste management, but shared investments in training and resources promote collective responsibility. Some regions provide take-back programs or group hazardous waste pickups, easing the burden on single labs. R&D managers who keep abreast of environmental standards also spot emerging trends, such as shifts in allowable emissions or updates to lists of controlled substances. That awareness lets them plan well ahead of regulatory deadlines, preventing costly last-minute scrambles and keeping reputations intact.
Once you see which processes stand or fall on the back of a reliable reagent, it’s not hard to appreciate the value of continued improvement in sourcing and handling. Conversations about green chemistry push R&D teams to think creatively: How can classic chlorinated intermediates like this one play a positive role in lower-emission and less wasteful workflows? Some institutions invest in routes that cut out byproducts or recycle used solvents, placing 1,2,3-Trichloro-2-Propanol in a central spot as a known quantity enabling more experiments to yield actionable data. This helps students and professional researchers hit publication and production goals while walking a bit lighter on the planet.
Advanced synthesis projects often call for specialized know-how when it comes to critical inputs. Here, building relationships with established suppliers—ones who invest in analytical capabilities for purity testing and transparent sourcing—pays dividends. These relationships free up time that would otherwise be spent retesting every shipment, letting teams focus on core tasks rather than plugging leaks in the supply chain.
There’s no sugarcoating the fact that operating with hazardous materials like 1,2,3-Trichloro-2-Propanol keeps everyone on their toes. Competence builds through repetition, sound mentorship, and learning from the mistakes of the past. Labs that last operate with a blend of vigilance and openness to process improvement: regular refresher trainings, open-book audits, and review of incident reports keep standards high.
The next phase for this compound—and countless others like it—involves integration into systems that value traceability and accountability just as much as price or theoretical yield. Labs that emphasize ongoing education and maintain both digital and physical records not only mitigate risk, but build a story of reliability that matters to funders, auditors, and, most importantly, the people whose hands touch each batch. When you walk into a lab where bottles of 1,2,3-Trichloro-2-Propanol are tagged, tracked, and securely stored, you know you’re in a place that takes both performance and responsibility seriously.
Reflecting on years spent alongside teams balancing creativity and safety, the lesson becomes clear: reliable supplies of chemicals like 1,2,3-Trichloro-2-Propanol set the table for real breakthroughs, from new drugs to more sustainable production methods. Careful sourcing, measured use, and attention to both regulatory guidance and local experience combine to minimize risks for both people and the environment. As organizations keep learning and adapting, leadership at every level—lab managers, procurement officers, student supervisors—can shape practices that support excellence and safeguard the community.
With a little extra planning and an ongoing commitment to improvement, the next wave of researchers can continue to rely on compounds like 1,2,3-Trichloro-2-Propanol as more than just reagents. These chemicals play their quiet part as the connective tissue of progress, helping teams reach further and safer in chemistry’s ever-expanding frontier.