|
HS Code |
435250 |
| Name | (R)-3-(1-Hydroxypropyl)phenol |
| Molecular Formula | C9H12O2 |
| Molecular Weight | 152.19 g/mol |
| Cas Number | 131755-22-5 |
| Appearance | White to off-white solid |
| Smiles | CC(O)CC1=CC=CC(=C1)O |
| Optical Rotation | [α]D20 +22° (c=1, MeOH) |
| Melting Point | 70-74°C |
| Solubility | Soluble in methanol, ethanol, DMSO |
| Boiling Point | No data available |
| Purity | Typically >98% |
| Storage Temperature | 2-8°C |
| Inchi Key | IKDUCUBAZGSGIV-SSDOTTSWSA-N |
As an accredited (R)-3-(1-Hydroxypropyl)Phenol 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 (R)-3-(1-Hydroxypropyl)phenol, sealed with a screw cap and tamper-evident label. |
| Shipping | (R)-3-(1-Hydroxypropyl)phenol is shipped in tightly sealed containers, protected from moisture and light. It is packed according to standard chemical regulations, with appropriate hazard labeling and documentation. Transport is typically via ground or air freight, ensuring temperature control and compliance with safety guidelines to prevent contamination or degradation of the product. |
| Storage | (R)-3-(1-Hydroxypropyl)phenol should be stored in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep away from incompatible substances such as strong oxidizers and acids. Recommended storage temperature is 2–8°C (refrigerator). Always ensure proper labeling and follow laboratory safety protocols while handling and storing this compound. |
Competitive (R)-3-(1-Hydroxypropyl)Phenol prices that fit your budget—flexible terms and customized quotes for every order.
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Every day in our factory, (R)-3-(1-Hydroxypropyl)phenol plays a straightforward role in the world of chemical synthesis. Our team has focused on refining its production because hands-on results matter, especially in the fields of pharmaceuticals and advanced materials. The compound stands out for its precise chiral structure, with the (R)- configuration shaping how it behaves in reactions. Chemists know that the smallest shift in arrangement can change activity, so we have made a commitment to high-precision synthesis and repeatable quality across our lots.
Our model for (R)-3-(1-Hydroxypropyl)phenol meets the needs of both research and commercial operations. Batch records sit above ninety-nine percent chemical purity, and we keep an eye out for both organic and inorganic impurities that may creep in during manufacturing. The physical appearance is clear: a white to nearly white crystalline solid that holds its melting point just as the textbooks and literature describe. In production, we monitor temperature control and raw material handling—temperature swings during condensation can spoil stereochemistry, and this is never left to chance here. This attention helps us keep isomer content tightly in line with specifications and supports consistent performance in downstream applications.
Customers from medical research and chemical engineering ask for (R)-3-(1-Hydroxypropyl)phenol because this enantiomer brings unique properties into play. If you’ve worked with chiral intermediates before, you understand that the wrong isomer can double development time or cut yield in half. The (R)- group lends selectivity for synthesizing certain drugs and fine chemicals—think beta-adrenergic receptor ligands and other complex molecular targets—where racemic mixtures fall short. Applications push beyond the classic pharmaceutical setting too: some researchers employ this compound as a building block in chiral catalysis and specialty monomers, where consistent stereochemistry translates to more efficient downstream reactions.
We see in our testing that the (R) form’s melting range and solubility in common solvents allow fast integration into existing processes. Whether you’re doing hydrogenation, coupling, or ring-opening, you want a material that dissolves right, reacts as expected, and cleans up crisply. Our team has spent months tweaking solvent selection and drying methods to cut byproduct formation—there’s no shortcut here, and that hard work turns up in the final product’s analytical data. NMR, HPLC, and optical rotation all line up batch after batch, and we don’t shy away from sharing technical details when needed.
Running a chemical facility means you face daily challenges—raw material swings, scale-up surprises, and regulatory twists. Our approach to (R)-3-(1-Hydroxypropyl)phenol keeps things practical. We source precursors from established partners with transparent quality records. Any deviation in supply chain gets flagged immediately, because we’ve seen how a bad starting batch can echo through reactions and ruin the week’s work. Automated controls help us maintain batch sizes from the gram scale for process development up to multi-kilogram runs for pilot campaigns. If any deviation occurs—a shift in temperature ramp or unplanned downtime—our analysts spot it early and isolate off-spec batches before they can reach the next stage.
We focus a lot on minimizing waste by keeping reactions to high yield and low byproduct. Less solvent means easier post-processing and safer working conditions for our staff. In recent years, we added in-line spectroscopy to directly monitor reaction progress, which cut down on quality holds and reprocessing cycles. Every refinement in the process stacks up to a more dependable supply and lets us get product out the door with shorter lead times—something our regulars depend on, especially as project timelines tighten.
End users often share what they value most: material that does what the literature says, time and again, without extra troubleshooting. For example, a customer working on a new chiral pharmaceutical intermediate found their conversion yields leapt from sixty to above ninety percent after switching to our (R)-3-(1-Hydroxypropyl)phenol. The feedback pointed to better consistency in melting behavior and improved filtration after the main reaction. That validation matters to us. It signals that our production attention isn’t just theoretical—it turns into safer, smoother, and more cost-effective results in R&D labs around the world.
The chemical landscape includes plenty of phenols and substituted derivatives, but (R)-3-(1-Hydroxypropyl)phenol carves out a role where chirality transforms results. Simple 3-(1-hydroxypropyl)phenol, sold without specific chiral configuration, can’t offer the same selectivity demanded by enantioselective synthesis. We have compared competing samples and seen the effect when a racemate blunts reaction rates or introduces unwanted byproducts. In our own work developing new catalysts, we found that process time goes up and clean-up becomes harder without the pure (R) isomer.
The primary alcohol at the 1-position on the propyl side chain gives this compound more versatility than some related hydroxyphenyl compounds, such as plain hydroxypropylphenol or those with substitution elsewhere on the aromatic ring. That placement means reactivity patterns in oxidation, esterification, or protection group strategies open up a wider set of options for creative chemists. Our technical team keeps hands-on data ready for the most common transformations, so project chemists don’t waste cycles re-optimizing work the field already solved. There’s no confusion about solubility or compatibility, either—the compound readily dissolves in polar protic and aprotic solvents we see across synthesis labs.
Another key difference comes from the ease of purification. The clear difference in melting point helps crystallization and filtration, getting chemists to pure product with fewer steps. Compared to phenolic products with more complex or hindered side chains, (R)-3-(1-Hydroxypropyl)phenol stands out for consistent handling and storage. Shelf life holds steady even under standard warehouse conditions, which customers appreciate during lulls in large-scale runs or long validation cycles. We steer clear of unnecessary stabilizers or formulation changes, trusting in robust synthesis and packaging methods to maintain quality.
Quality in specialty chemicals must be more than a document on file—we prove it on the line. Our lab validates each lot with a mix of chromatographic, spectroscopic, and enantiomeric purity checks. Optical rotation, a classic but reliable method, gets run beside NMR and HPLC to make sure the chiral configuration stays true. For a product like (R)-3-(1-Hydroxypropyl)phenol, where end uses involve regulated substances, there’s no shortcut. Our regulatory specialists check each lot for compliance with local and global expectations. This includes managing cross-contamination risks and tracing raw material certifications back to the source. We prefer fixing issues face-to-face with our operations team, not patching after the fact with paperwork.
Partnership with customers and researchers also keeps us sharp. Many requests come in for analytical support and guidance—whether on solvent compatibility, optimal storage temperature, or batch application strategies. Our technical support team, many with years on the plant floor themselves, step in to answer questions based on real runs, not just theory. This practical approach has solved a range of hurdles, from stubborn emulsions during coupling reactions to tricky isolation after crystallization. That daily dialogue means our process doesn’t stand still, and what we learn gets built into every batch moving forward.
Shipping and logistics get as much attention as production. Specialty chemicals need predictable, careful packaging to arrive ready for use, not degraded by moisture or heat. We take time to match pack sizes, from small glass vials for R&D to robust drums for production. Our supply chain team tracks every shipment through customs and carrier routes. Years of experience taught us to never underestimate the value of early communication—catching regulatory roadblocks or customs delays ahead of time makes a big difference in keeping projects on track. Our rapid feedback loop here cuts down customer downtime and lets teams plan with confidence.
While producing (R)-3-(1-Hydroxypropyl)phenol, our facility learned a few lessons that newcomers overlook. One is temperature control during hydrogenation and crystallization—slow ramps and vigilant monitoring make or break enantiomeric excess. Early on, we saw how even a ten-minute delay in temperature adjustment could increase byproduct levels. Feedback from chemists helped us deploy digital controls and backup checks during nights and weekends, putting an extra barrier between us and out-of-spec product.
Water control during synthesis and storage plays another major role. This compound’s primary alcohol group loves to pick up moisture, which can affect both measured purity and downstream reactions. We moved to vacuum drying and nitrogen blanketing earlier in the process. These steps add work but result in product that’s ready for sensitive reactions right out of the package. No customer wants to find the right compound but need to re-dry before every use, so this investment pays off in return business and smoother technical support calls.
Dealing with waste streams and byproducts keeps our environmental compliance record clean. Onsite solvent recovery and waste neutralization bring us in step with modern regulations and community expectations. Instead of treating waste as a burden, our process engineers look for ways to reclaim solvent and minimize the use of harsh reagents where possible. Our customers in regulated markets—especially pharmaceuticals and food-related chemicals—regularly audit our site for these procedures. Having transparent records and real-world testing makes audits run smoother and gives peace of mind to our downstream partners.
No batch process sits still for long—new customer requirements and tighter regulations mean we keep evolving. We track new literature and technology, adapting reaction conditions as needed and working with equipment vendors to update systems. Being based on the production side, we sometimes see the gap between “what works on paper” and “what works for two hundred liters in steel reactors.” For (R)-3-(1-Hydroxypropyl)phenol, we refined our crystallization profile several times since the early days. Each adjustment cut cycle times or improved yield, giving our team a hands-on feel for efficiency.
We have open lines between plant staff, lab analysts, and sales—so feedback circulates fast. If a lab customer suggests a change in solvent for better compatibility, we look at integrating it upstream where it makes sense for bulk runs. This culture of continuous improvement isn’t just management talk—it’s built into each shift and every trial batch. By the time a product leaves our plant, it’s been through dozens of pairs of hands, each focused on doing their job right.
Industry moves fast, and the push towards greener chemistry never lets up. We’re experimenting with more sustainable solvents and catalytic systems in both R&D and production. As these upgrades prove themselves, they move to main line production—a win-win for both performance and the environment. Customers tell us they notice the difference—not in a brochure, but in lower impurities, easier handling, or a smoother customs clearance.
Our day-to-day work gives us a close perspective on why customers stay loyal. (R)-3-(1-Hydroxypropyl)phenol, produced with care and repeatable methods, gives chemists the freedom to take risks in their research, knowing their starting material won’t let them down. The actual science—stereoselectivity, reactivity, and process fit—backs up the business piece of the puzzle. Supply security, clear communication, and hands-on troubleshooting fill in the rest of the story.
In our own facility, practical experience with this compound shows up in both lab notebooks and shipping logs. Careful route design, steady quality control, and willingness to work directly with users make all the difference. We’ve invested in the people, the process, and the technology to keep pace with new challenges and support innovation at the bench scale and beyond.
Manufacturing (R)-3-(1-Hydroxypropyl)phenol has brought more than technical expertise to our shop floor—it’s taught us about problem-solving, teamwork, and listening to real user feedback. Every clean batch and satisfied customer points to the value of staying hands-on and detail oriented. The world keeps finding new uses for high-purity chiral phenolic intermediates, and we stay ready to meet those needs with grounded, practical experience. Quality starts with chemistry, but it endures because people care enough to do the job right, every time.