|
HS Code |
437274 |
| Chemical Name | 4-[(3R)-3-Hydroxybutyl]Phenol |
| Molecular Formula | C10H14O2 |
| Molecular Weight | 166.22 g/mol |
| Cas Number | 147156-29-8 |
| Iupac Name | (R)-4-(3-Hydroxybutyl)phenol |
| Appearance | White to off-white solid |
| Melting Point | Approx. 74-78°C |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Optical Rotation | [α]D +12.9° (c=1, CHCl3) |
| Smiles | CC(CC1=CC=C(C=C1)O)O |
| Inchi | InChI=1S/C10H14O2/c1-8(11)6-7-9-2-4-10(12)5-3-9/h2-5,8,11-12H,6-7H2,1H3/t8-/m1/s1 |
As an accredited 4-[(3R)-3-Hydroxybutyl]Phenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical is supplied in a 25g amber glass bottle, sealed with a screw cap and labeled with hazard information and batch details. |
| Shipping | 4-[(3R)-3-Hydroxybutyl]Phenol is shipped in tightly sealed containers under ambient temperature, protected from light and moisture. It is labeled according to chemical safety regulations to ensure safe handling and transport. Compliance with local and international shipping regulations for chemicals is strictly adhered to during packaging and shipment. |
| Storage | 4-[(3R)-3-Hydroxybutyl]phenol should be stored in a tightly sealed container, protected from light and moisture. Keep in a cool, dry, well-ventilated area away from incompatible substances such as strong oxidizers and acids. Properly label the storage container, and ensure access is restricted to trained personnel. Follow local regulations for chemical storage and regularly check for signs of degradation or contamination. |
Competitive 4-[(3R)-3-Hydroxybutyl]Phenol prices that fit your budget—flexible terms and customized quotes for every order.
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As long-standing producers of specialty phenolic compounds, we draw on our experience at each stage of development and manufacturing. Over the last decade, our research teams focused intensely on molecules that offer new handles for modification — and 4-[(3R)-3-hydroxybutyl]phenol has proved to be among the most reliable, versatile intermediates. Our chemists have seen that its structure, featuring both a phenolic ring and a defined (3R)-hydroxybutyl side chain, steps up performance where control, selectivity, and functionalization really count.
Every manufacturer dealing in alcohol-functionalized aromatic compounds recognizes the challenge of balancing reactivity, solubility, and purity. Using our dedicated reactor systems, we produce 4-[(3R)-3-hydroxybutyl]phenol to a minimum purity of 98%, measured consistently across multiple batches. The material presents as a solid at room temperature, with a distinct melting range suited for further synthesis. It dissolves efficiently in common organic solvents, including ethanol and dichloromethane. Our analytical chemists confirm each lot by chiral HPLC, ensuring that the (3R) stereochemistry meets strict consistency standards; this detail never gets overlooked during rounds of internal QA audits.
What truly stands out for process engineers in a production facility is the stability of this compound — batches retain their stereochemical and chemical integrity throughout months of storage under dry, cool conditions. There are very few degradation pathways under standard warehousing, and even after repeated sampling, the product maintains its integrity. This stability means planners don’t need to cycle through inventory at a frantic pace, reducing both stress and waste.
Years of feedback from synthetic chemists have shaped our understanding of where this compound fits into modern manufacturing operations. There’s almost a split between pharmaceutical development teams and polymer researchers, each valuing a slightly different capability. In pharmaceutical synthesis, the primary draw centers on the (3R)-hydroxybutyl side chain; it delivers enantiomeric purity that streamlines downstream chiral transformations. Our in-house routes, refined generation after generation, yield a product that integrates seamlessly with both classical and modern coupling strategies. No need to repeat protection/deprotection cycles more than is absolutely required, which saves both labor and solvents.
Polymers teams point to another value: the presence of the secondary alcohol moiety. This structural feature facilitates post-polymerization modifications, giving access to amphiphilic or crosslinked materials. During customer demos, we typically observe steady results batch after batch, regardless of whether the process scales up from a 1-liter autoclave to a 500-liter reactor. Users report that the compound does not introduce unexpected color bodies or off-odors into sensitive reaction streams, easing the pathway to food-contact or medical-grade applications.
We constantly receive questions about assay methods. Our QC laboratory applies both NMR and GC-MS confirmation alongside chiral analysis, ensuring that what arrives with each drum matches the ex-works documentation. No one has time for surprises in multi-stage synthesis schemes, so we view analytical transparency as basic operating procedure, not a customer-requested add-on.
Unlike short-chain phenols or bulky tert-butyl analogs, 4-[(3R)-3-hydroxybutyl]phenol offers reliable reactivity at both the aromatic ring and its side chain oxy group. In day-to-day production meetings, this dual functionality translates to fewer extra reagents down the line and a reduction in protection chemistry. For example, when modifying the phenolic oxygen, there’s no undesirable interference from adjacent groups as often seen in multi-substituted systems.
Historical experience in our facilities has shown that regioselectivity with this compound far surpasses what’s achievable with unsubstituted phenol or methylphenol derivatives. During oxidative coupling, yields show measurable improvement due to the electron-donating effect of the side chain, while unwanted overreactions become less common. For epoxidation or hydroformulation, the chirality of the product assists in accessing key asymmetric intermediates, a crucial consideration for anyone venturing into pharmaceutical APIs where regulatory agencies scrutinize isomer ratios.
Throughout the years, we experimented with several analogs to cover a wider synthetic portfolio, including para-hydroxyethyl and meta-substituted versions. These showed promise on the lab bench but struggled once we scaled to industrial throughput—side reactions increased, and batch traceability sometimes suffered as positional isomers co-eluted in routine GC testing. In contrast, 4-[(3R)-3-hydroxybutyl]phenol has outperformed expectations in both consistency and robustness, never letting us down during challenging production cycles.
Years in chemical manufacturing have taught us that procurement risk and uncertainty in product quality can slow down vital projects. We watch teams entering new markets or launching a drug candidate work to strict timetables, which leaves no room for delays from off-spec batches or unexplained inconsistencies. By controlling the entire chain from raw starting material to final packaging—without traders or dilution—we keep contaminants, residual solvents, and unknown side products at a minimum. Repeat partners cite this level of control as their reason for returning, particularly when purity or regulatory filings are at stake.
We also recognize the importance of supporting clients with robust documentation. Our team stays up-to-date on analytical technologies and regulatory trends, knowing that robust data and traceability build real-world confidence, not just ticking boxes for audits. Customers routinely approach us for technical feedback on their processes—none of which comes from generic scripts or third-party notes. Instead, we draw from completed runs, side-by-side comparisons, and troubleshooting sessions conducted on our own production lines. This foundation keeps our feedback grounded in reality.
Modern chemical manufacturing can’t ignore the environmental footprint of each synthesis. Over the years, we analyzed the lifecycle of 4-[(3R)-3-hydroxybutyl]phenol, searching for places to reduce waste and improve solvent recovery. Recent installations allowed our operations team to reclaim over 95% of the primary solvents used, a move that lowered emissions and cut raw material bills. Our waste stream, measured monthly, showed declining total organic carbon—a mark that upstream investment and staff training paid off.
We find that innovation pairs well with day-to-day shop floor pragmatism. At one point, several engineers suggested tweaks to tank cleaning cycles and intermediate crystallizations based on solvent compatibility observed during hundreds of actual process runs. These changes, coming directly from the people handling the product every day, led to energy savings and faster Reactors-to-Tank turnaround. By capturing such input into tangible improvements, we foster a culture where operators, chemists, and quality control staff see the benefit—fewer slowdowns, fewer complaints, and a smoother flow from PO to shipping dock.
Many clients run technical assessments as soon as a new batch arrives. One group, based in Europe, presented us with detailed data comparing our 4-[(3R)-3-hydroxybutyl]phenol to material sourced from three other producers. Their focus landed on chiral purity, secondary alcohol reactivity, and ease of handling in automated dispensing lines. Over a four-month trial, our product maintained a tighter range of stereochemical ratios and showed less lot-to-lot variation in side reactions. Technicians credited this stability to our manufacturing—and their managers didn’t have to spend production time cross-checking batch records.
Several polymer R&D teams highlighted the flexibility provided by the hydroxybutyl group. Unlike methyl or ethyl analogs, it enabled gentle tuning of thermal and mechanical properties of block copolymers. In feedback calls, engineers at these sites mentioned reduced downtime and fewer formulation failures tied directly to greater predictability in building-block chemicals. For us, such customer input isn’t just a marketing point—it’s evidence that focusing on molecular purity and reproducibility brings real-world impact, not just laboratory results.
Others in pharma scale-up pointed out that our internal technical documentation saved them directly: Our precise reporting on chiral ratio by enantiomer, secondary analytical endpoints, and anomaly logs served as a crucial reference during regulatory filings. Corrections in the batch sheet minimized the kind of paperwork headache that erodes production deadlines, smoothing the path from pilot studies to a full commercial run.
From an insider’s perspective, no two intermediates perform exactly alike. Stability, reactivity, and compliance with evolving quality standards make certain molecules more trusted. Our experience keeping lines running year-round, plus emergency coverage during rush orders, showed us how a sound choice of chemical building block saves both money and time in the long haul. With 4-[(3R)-3-hydroxybutyl]phenol, we’ve rarely seen quality complaints or last-minute rework requests. On the rare occasion when a shipment has needed investigation, the source could be rapidly traced, and process changes were quickly made and shared with users.
Veteran operators recall how older batches of phenolic intermediates sometimes needed in-line filtration and repeated dust abatement. Today’s product, guaranteed by cleanroom-controlled packaging, seldom requires excess downstream prep before use. These improvements flow directly from targeted process reviews and engagement with staff who work every shift. The plant team told us once that minimizing handling steps slashed cleanup time at both ends of the process, cutting overtime and improving everyone’s shift morale.
We believe that trust is built run-by-run and shipment-by-shipment—not through grand promises, but through consistent results over the years. As markets evolve, maintaining long-term partnerships relies on staying responsive and moving quickly to adopt validated improvements. Supply chain resilience comes from addressing rare issues immediately and sharing lessons learned internally and with customers.
Our involvement doesn’t end with product shipment. Regulatory authorities look for traceability, transparency, and strict documentation, especially as markets move toward higher standards. Experienced regulatory managers at our site work closely with production and QA teams, reviewing certificates of analysis, and updating material safety and quality dossiers with every process iteration. We developed our SOPs through years of audits, customer questions, and the unyielding demands of major buyers.
We handle every inquiry concerning regulatory compliance in-house. Customers navigating the complex demands of new drug applications, food-contact clearances, or medical device filings cite our prompt, detailed responses as a critical asset. By working from our batch records and analytical lab output—not outsourced summaries—we support their submissions with data that passes scrutiny globally.
When analytical protocols or compliance requirements shift, all affected documentation is updated promptly and communicated to current users. The end result is fewer regulatory delays, reducing hurdles for our clients’ own products to reach their markets on time.
As manufacturers, we stand at the intersection of evolving chemistry and practical business needs. Years in the industry have shown that resting on former successes leads quickly to obsolescence. That’s why we dedicate real resources every year to R&D, process development, and on-the-floor training. Every proposal for improvement stems from actual process performance—not just top-down direction.
Recently, cross-functional teams suggested modifications to the chiral feedstock management system, detecting patterns in assay drift and acting before any impact reached the marketplace. Projects led by young process chemists and seasoned operators contributed to new solvent-reclamation loops, bringing both environmental gains and cost savings.
By actively involving our employees in every improvement, we reinforce an organizational culture that takes pride in reliability. At the same time, direct ongoing communication with long-term users allows us to capture evolving needs—whether those are a shift to green chemistry, new purification technologies, or supporting high-throughput automation. Regulatory staff bring forth anticipated framework changes and suggest in-house pilot trials, ensuring that our whole team anticipates market needs instead of simply reacting to them.
Having produced and shipped 4-[(3R)-3-hydroxybutyl]phenol to customers across the globe, we see its reach continuing to grow wherever precision, purity, and reliability are paramount. The compound’s defining characteristics—chiral purity, chemical stability, and ease of downstream transformation—translate directly into gains for those handling anything from bench-scale innovation to multi-ton production.
Each batch sent represents not just a well-characterized product, but the outcome of collective expertise, an unwavering commitment to process control, and practical lessons from the front lines of chemical manufacturing. With every year, we refine both chemistry and delivery, staying accountable to each client and upholding the standards demanded by science and industry alike.