|
HS Code |
977510 |
| Iupac Name | 2-[(1R)-1-methylpropyl]phenol |
| Molecular Formula | C10H14O |
| Molecular Weight | 150.22 g/mol |
| Cas Number | 3228-02-2 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 235-237 °C |
| Density | 0.967 g/cm³ (at 20 °C) |
| Refractive Index | 1.514 (at 20 °C) |
| Solubility In Water | Slightly soluble |
| Flash Point | 108 °C |
| Smiles | CC(C)Cc1ccccc1O |
As an accredited 2-[(1R)-1-Methylpropyl]Phenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 100 mL amber glass bottle with a secure screw cap, labeled "2-[(1R)-1-Methylpropyl]Phenol, 98% purity, Handle with care." |
| Shipping | 2-[(1R)-1-Methylpropyl]Phenol should be shipped in tightly sealed containers, clearly labeled, and protected from light, moisture, and incompatible substances. Transport in compliance with relevant local, national, and international regulations for hazardous chemicals. Ensure secondary containment, use appropriate cushioning to prevent breakage, and include safety documentation and handling instructions with the shipment. |
| Storage | 2-[(1R)-1-Methylpropyl]phenol should be stored in a cool, dry, well-ventilated area away from sources of ignition and incompatible materials such as strong oxidizers and acids. The container should be tightly closed, clearly labeled, and protected from light. Use appropriate chemical storage cabinets if possible. Ensure access is restricted to trained personnel and spill containment measures are in place. |
Competitive 2-[(1R)-1-Methylpropyl]Phenol prices that fit your budget—flexible terms and customized quotes for every order.
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The world of fine chemicals doesn’t tolerate uncertainty. Batch-to-batch consistency, confidence in purity, and a documented performance record form the backbone of stable supply chains. At the bench and in the plant, every gram counts and every impurity risks sidetracking a project. That’s why our team commits every stage of production to the details that matter: feedstock tracing, reaction monitoring, controlled isolation, and careful packaging.
2-[(1R)-1-Methylpropyl]Phenol runs in a lane of its own among alkylated phenols. Chemists know that a small change at the alkyl group can reshape reactivity and solubility, so this molecule typically draws attention where selective bioactivity or chemical resistance is required. The main structure stems from a clean phenol backbone, substituted precisely at the 2-position with a (1R)-1-methylpropyl group. As chemists, we know that enantiopurity is not a minor detail—it draws the line between full activity and defeat in both catalytic and biological systems.
From day one, our team has leaned on in-house expertise to standardize product lines without losing necessary flexibility. The model of 2-[(1R)-1-Methylpropyl]Phenol we built responds to the needs of specialty polymer chemists, pharmaceutical intermediates developers, fragrance formulators, and agrochemical researchers who demand purity, chirality, and repeatable reactivity. We keep a focus on total phenolic content, moisture, color, and enantiomeric excess, because our customers routinely call for reliable analytical support. GC, chiral HPLC, and NMR spectra form the backbone of our COA, and we retain every lot record for traceability.
We never leave our end users wondering about shelf life, storage, or compatibility with packaging; the practical aspects have always mattered. Sensitive organics like 2-[(1R)-1-Methylpropyl]Phenol need more than just a sealed bottle, so we use low-permeability glass and nitrogen-purge storage from the production floor right through shipping. Our fill lines are dedicated to avoid contamination from other phenolic products—so the color remains crystal clear, with no hint of oxidative discoloration at point-of-use.
This compound has found solid ground in three major arenas: synthesis of biologically active compounds, as a building block for performance polymers, and as a specialty intermediate in fragrance chemistry. Medicinal chemists gravitate toward the (1R) enantiomer to drive selectivity in targets ranging from anti-inflammatory agents to anti-microbial scaffolds. In these fields, the purity and defined optical configuration of our product close the gap between theory and application, saving months of purification headaches that a racemic batch would introduce.
Performance in materials science cannot be understated. The steric bulk and defined placement of the (1R)-1-methylpropyl group make this phenol a precise tool for crafting high-molecular-weight polymers with unique solubility profiles and resistance to environmental stress. Those running pilot lines see fewer side-products and waste streams, translating to real savings on scale. And for fragrance chemists, trace impurities show up easily in finished blends—so a starting chemical like this, manufactured up to food-grade benchmarks in an ISO-certified plant, brings much-needed reassurance.
Every application slot for 2-[(1R)-1-Methylpropyl]Phenol circles back to the reliability of its stereochemistry. The wrong enantiomer—wrong by as little as a few percent—can bring an entire discovery program or manufacturing route to a standstill. We’ve invested in continuous monitoring and thorough documentation not because it’s required by regulation, but because high-stakes innovation leaves no room for mismatched starting materials.
Synthetic experience is not a commodity in the niche world of enantiopure phenols. The scale-up strategy for this molecule didn’t come from a generic manual, it grew from systematic stress-testing at every stage—solvent selection, stoichiometry optimization, and temperature profiles that lock down side reactions. The phenol’s peculiar reactivity sometimes invites side-chain migration or ring oxidation during workup, and we’ve burned through plenty of pilot runs separating minor impurities at process development scale.
Personnel safety and environmental compliance drive our plant operations. Our suites carry state-of-the-art ventilation, and operators train to handle phenolic vapors and residues with the strictest protocols. Industrial hygiene audits and effluent monitoring keep us aware of every step’s environmental impact. Waste streams run through multi-stage treatments: neutralization, adsorption, and carbon filtration. We recycle solvents wherever possible, not simply to save cost, but because stewardship of precious resources runs through our company from top to bottom.
The broader family of alkylphenols and substituted phenols covers wide ground, but not every candidate can fit the needs of chiral synthesis, pharmaceutical development, or advanced materials research. Some chemists reach for simpler branched alkylphenols to ease solubility issues, or because they cost less at bulk scale. But cost-saving doesn’t make much sense if it means introducing trace byproducts that stop downstream reactions or skew biological screens.
Molecules lacking clear stereochemistry, such as their racemic counterparts, leave too much to chance. As a manufacturer, we know analytical labs down the supply chain cannot always rescue what gets lost at the source. They rely instead on the robust work already done here: enforcing enantiopurity through asymmetric synthesis, continual in-process controls, and final confirmation with reference standards.
Competing products sometimes come in with higher assay numbers on paper but falter on storage stability, color, or odor. Experience has taught us that nothing replaces proper handling and the discipline of single-use lines for specialty products. We have seen customers struggle with alternative grades that show early yellowing or a faint off-note after a few months on the shelf. That’s why our quality metrics include accelerated stability studies, real cold-chain logistics, and persistent customer feedback loops. Problems that hit the end user as unknown impurities often originate upstream, where attention to detail might slip.
One current talking point in specialty chemicals is digitalization and trackability. As the team overseeing every batch, we’ve driven implementation of full electronic batch records not for show, but to answer questions from customers in regulated sectors. Years ago, a shipment occasionally raised hard-to-track questions—Did this lot contain batch-to-batch deviation? Was a particular impurity profile consistent with the supplier’s claim? Automation of records and QR-linked COAs slashed our response time, closing the loop quickly and building trust.
Packaging is another challenge that deserves real-world attention. Many in our field overlook the tricky balance of minimizing leachables while delivering containers robust enough for international shipping. Early on, we faced feedback on glass particulate and seal failures when moving material across climates. Custom packing protocols, triple-sealed closures, and in-process optical inspection now sit square in our standard operating procedures. These changes raised our cost base slightly, but virtually eliminated post-fulfillment complaints from critical users in pharma and fine fragrance sectors.
Clients have also educated us on the importance of responsive technical support. Some R&D teams want deep insight into impurity profiles before committing to scale-up. Others send raw HPLC files for peer review, trusting our analytical chemists to pinpoint potential hurdles. As a manufacturer, we welcome this transparency; it sharpens our own process control and tightens downstream integration for everyone involved.
Technical dialogue rarely flows in a single direction. Our product development pipeline grows alongside our customers’ needs—not through generic feedback forms, but from hours spent on collaborative troubleshooting. In the last few years, the trend has moved closer to end-to-end traceability and direct plant access. Analytical raw data, real-time QC metrics, and written deviations all flow directly to customers under NDA.
It’s not uncommon for a product as specialized as 2-[(1R)-1-Methylpropyl]Phenol to become a bellwether for how a supplier handles tighter regulatory scrutiny or tighter campaign targeting. One failed batch in a reactor can set back drug development or new materials for months. Our investment in traceable workflows, on-call PhD technical managers, and post-market surveillance has allowed customers to come back project after project. They want more than a drum with a label—they want partners in scale-up and risk reduction.
We’ve taken hard lessons from supply disruptions caused by unpredictable shutdowns—material shortages, global events, regulatory shifts. Being a direct manufacturer brings the responsibility to buffer customers against the worst of these shocks. By holding critical raw materials in inventory, cultivating secondary routes as backup, and keeping every batch under internal audit, we have kept supply lines open when others falter. Feedback from longtime customers often centers not just on what’s in the bottle, but on the service surrounding every order: proactive status reports, advance COA sharing, and alerting end-users to possible changes in process.
Living and working in chemical manufacturing for decades, we know that no specification document or batch record alone guarantees quality. It’s the vigilance of operators keeping eyes on monitors at three in the morning, and the process engineers who break routine to investigate an odd result on an in-process check. It shows in the small details: unused lines double-checked for backflow, containers triple-labelled for in-plant movement, secondary containment re-inspected after every cleaning cycle.
Mistakes in production or packaging waste more than just material—they risk a customer’s breakthrough or an entire product launch. That’s why we value a learning culture, where deviations are openly discussed, near misses become training tools, and every operator is empowered to pull the cord if there’s a hint of nonconformance. For us, manufacturing 2-[(1R)-1-Methylpropyl]Phenol—a molecule that seems simple on paper—demands a high-trust environment and accountability at every step.
Innovation rarely stands still. Our R&D team works closely with global partners exploring new arenas—greener synthesis, biotransformations, and functionalized derivatives. Next-generation phenolic platforms call for even tighter control over contamination, chirality, and reactivity. We’re not waiting for regulations to tighten or for synthetic chemistry to paint us into a corner. Instead, continuous investment in new reactors, inline monitoring, and analytical technologies already runs in parallel with scale-up programs.
On the sustainability front, our plant upgrades target waste minimization and improved energy efficiency. Advances in catalysis, lower-impact solvents, and solventless routes are coming into pilot around specialty phenols. Finished product is only as green as its process footprint, and our team scrutinizes inputs and outputs with a critical eye—sharing lifecycle data with key accounts so environmental metrics become shared, not hidden.
2-[(1R)-1-Methylpropyl]Phenol does more than fill a space on a catalog page. Its function in synthesis, pharmaceuticals, advanced polymers, and emerging technologies depends on rock-solid manufacturing practices and serious attention to the needs of working chemists. Drawing from our lived experience on the production floor—overcoming setbacks, celebrating tight spec wins, and partnering with leaders in innovation—we have built more than just a product line. We have built a practice around openness, reliability, and authentic support for those creating the next big discovery.
As the field continues to evolve, standards rise, and expectations shift, we carry forward not just tools and procedures, but real collaboration and trust. From plant engineer to shipping manager to technical support chemist, each person in our manufacturing network stands behind every bottle and every batch of 2-[(1R)-1-Methylpropyl]Phenol that leaves our site.
