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HS Code |
388595 |
| Iupac Name | (1R,2R,8aS)-decahydro-1-(3-hydroxy-3-methyl-4-pentenyl)-2,5,5,8a-tetramethyl-2-naphthol |
| Molecular Formula | C20H34O2 |
| Molar Mass | 306.48 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Density | 0.96 g/cm³ (approximate) |
| Solubility In Water | Insoluble |
| Logp | Approximately 4.7 |
| Refractive Index | 1.494 (approximate) |
| Cas Number | 515-03-7 |
| Synonyms | Ambroxide, Ambroxan |
| Odor | Sweet, woody, ambergris-like scent |
| Flash Point | Above 110°C |
| Stability | Stable under normal conditions |
As an accredited (1R,2R,8AS)-DECAHYDRO-1-(3-HYDROXY-3-METHYL-4-PENTENYL)-2,5,5,8A-TETRAMETHYL-2-NAPHTHOL factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 25 grams, sealed with PTFE-lined cap; features chemical name, CAS number, hazard labels, and batch information. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for (1R,2R,8aS)-Decahydro... ensures safe, efficient bulk chemical packaging and transportation, preventing contamination and loss. |
| Shipping | This chemical, (1R,2R,8aS)-Decahydro-1-(3-hydroxy-3-methyl-4-pentenyl)-2,5,5,8a-tetramethyl-2-naphthol, should be shipped in tightly sealed containers, protected from moisture and light. Ship at room temperature, using appropriate hazardous material packaging, and following relevant DOT/IATA regulations for chemical transport. Include Material Safety Data Sheet (MSDS) with shipment. |
| Storage | Store **(1R,2R,8aS)-Decahydro-1-(3-hydroxy-3-methyl-4-pentenyl)-2,5,5,8a-tetramethyl-2-naphthol** in a tightly sealed container, protected from light, heat, and moisture. Keep at a cool, dry place, preferably refrigerated (2–8°C). Ensure adequate ventilation and avoid exposure to strong oxidizers or acids. Clearly label containers and follow all safety protocols for handling organic chemicals. |
| Shelf Life | Shelf life: Store in a cool, dry place, protected from light and air; typically stable for 2 years under recommended conditions. |
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Purity 98%: (1R,2R,8AS)-DECAHYDRO-1-(3-HYDROXY-3-METHYL-4-PENTENYL)-2,5,5,8A-TETRAMETHYL-2-NAPHTHOL with a purity of 98% is used in pharmaceutical intermediate synthesis, where high purity ensures optimal yield and product consistency. Molecular Weight 304.5 g/mol: (1R,2R,8AS)-DECAHYDRO-1-(3-HYDROXY-3-METHYL-4-PENTENYL)-2,5,5,8A-TETRAMETHYL-2-NAPHTHOL at 304.5 g/mol is employed in specialty organic chemistry, where precise molecular weight facilitates accurate formulation and dosage control. Melting Point 156°C: (1R,2R,8AS)-DECAHYDRO-1-(3-HYDROXY-3-METHYL-4-PENTENYL)-2,5,5,8A-TETRAMETHYL-2-NAPHTHOL with a melting point of 156°C is used in thermal processing for advanced materials, where defined phase transition supports controlled manufacturing processes. Stability Temperature 120°C: (1R,2R,8AS)-DECAHYDRO-1-(3-HYDROXY-3-METHYL-4-PENTENYL)-2,5,5,8A-TETRAMETHYL-2-NAPHTHOL with a stability temperature of 120°C is applied in formulations for cosmetics, where thermal stability ensures product shelf-life and efficacy. Viscosity Grade Low: (1R,2R,8AS)-DECAHYDRO-1-(3-HYDROXY-3-METHYL-4-PENTENYL)-2,5,5,8A-TETRAMETHYL-2-NAPHTHOL of low viscosity grade is utilized in coating formulations, where low viscosity enables smooth application and uniform surface coverage. |
Competitive (1R,2R,8AS)-DECAHYDRO-1-(3-HYDROXY-3-METHYL-4-PENTENYL)-2,5,5,8A-TETRAMETHYL-2-NAPHTHOL prices that fit your budget—flexible terms and customized quotes for every order.
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Manufacturing specialty chemicals demands hands-on experience, deep technical knowledge, and an ability to adapt to changing needs. Over the years, our chemists have focused on creating (1R,2R,8aS)-Decahydro-1-(3-hydroxy-3-methyl-4-pentenyl)-2,5,5,8a-tetramethyl-2-naphthol, also known by some practitioners as an advanced naphthol derivative, to address challenges raised by clients who require both high performance and reliable quality. Because we control every step of the process, from synthesis to final drying, we have seen firsthand how crucial each parameter is to the finished product’s behavior.
The backbone of this molecule is a fused naphthalenic ring system bearing four methyl groups and a unique allylic side chain with a tertiary alcohol. With a molecular formula C17H30O2, it presents a hefty, yet manageable structure with well-defined stereochemistry. Our standard offering typically arrives as a highly pure, white to off-white crystalline solid, depending on the hydration state as it leaves the final purification step. Given the rugged process conditions sometimes required for related compounds, this product stands out for its resistance to unwanted isomerization or decomposition, even during warm-weather shipments.
Most research and industrial teams look for compounds with both molecular complexity and practical reactivity. The four methyl groups and the pentenyl alcohol moiety make this compound especially useful as a building block in the synthesis of complex fragrances, pharmaceuticals, and flavor compounds that demand a chiral, non-aromatic core. Our team has engaged with several formulation scientists who appreciate the persistent olfactory notes made possible by the rigidity and steric shielding in this structure; even minor changes to the methyl or hydroxyl placement can push the profile into a different chemical class altogether.
The combination of secondary and tertiary centers creates opportunities for regioselective and stereoselective functionalizations. In our process, we rely on catalyst systems that have shown consistent selectivity for the (1R,2R,8aS) configuration, avoiding the waste and downstream complications of isomeric mixtures. This results in higher yields where every percentage point matters, especially for high-value end uses.
It’s easy to underestimate the difference between research-scale synthesis and plant-scale runs. On a few grams, it’s tempting to gloss over exotherms or subtle color changes after distillation. At the multi-kilogram scale, even slight deviations can mean off-spec product or worse, uncontrolled side reactions. With this naphthol, our early trial batches underscored the importance of drying—residual solvent can not only reduce yield but encourage the formation of oxidized byproducts. Our reactors, built for both glass-lined and stainless steel applications, handle the full batch spectrum, but regular calibration and real-time analysis proved indispensable for each critical stage.
We also learned that standard gas-phase oxidation, a common method with simpler naphthols, wouldn’t yield the right selectivity here. Suitably inert atmospheres provide protection during the key bond-forming steps, so oxygen ingress is strictly controlled from start to finish. Our instrumentation gives us confirmation with every batch: GC-MS and chiral HPLC analysis before and after each synthetic transformation, not just as a last-minute box-check before shipping. This insistence on hands-on validation ensures minimal variability between lots—a must for both research and scale-up applications where consistency leads to time savings down the line.
Researchers and procurement teams often wonder what sets this naphthol apart from similar-looking compounds. The industry offers a range of monocyclic or bicyclic naphthol analogues, many with one or two methyl substitutions. The unique 3-hydroxy-3-methyl-4-pentenyl extension gives our molecule a pronounced difference in both reactivity and downstream application flexibility. Most competitors bring straight-chain substitutions or aromatic side chains to the table, which miss the blend of lipophilicity and potential for hydrogen bonding found here.
In practice, teams working with simpler mono-substituted naphthols report problems with poor solubility in both polar and non-polar solvents, a headache for anyone trying to prepare masterbatches for polymer or resin modification. Our product, thanks to the pentenyl alcohol and multiple methyl groups, delivers solubility and compatibility with a broad range of solvents, from high-boiling ethers to mid-range ketones, while also retaining enough polarity for emulsification—critical for fragrance encapsulation and slowly-releasing pharmaceutical matrices.
The chiral purity also distinguishes this molecule from commodity-grade naphthols, which often arrive as racemic mixtures. Many downstream syntheses lose selectivity and lose yield when starting with unresolved material. We have worked closely with chiral catalyst providers to refine both the selectivity and the throughput for this structure, which now meets the needs of customers in the fine chemicals and life sciences sectors who need reproducibility from kilo-lab to commercial scale.
Once the product reaches the client, performance often turns on subtleties not captured by standard property tables. For example, flavor formulators have commented that the controlled release profile achieved with this naphthol derivative supports both short- and long-lasting olfactory notes, crucial for consumer-facing formulations. The molecular rigidity, teamed with the three-dimensional substitution pattern, gives higher volatility resistance, which several clients in the fragrance sector have leveraged to develop products that offer extended shelf life in warm and humid retail environments.
In pharmaceutical applications, the molecule offers unique opportunities as a chiral scaffold. Medicinal chemists we collaborate with have noted the ease of derivatization at the terminal alcohol while maintaining the configuration at the fused ring junctions. This saves steps in the lead optimization phase and reduces time spent rerunning unsuccessful reactions, translating into faster project turnover. Pharmacokinetics teams have reported improved stability in both plasma and simulated gastric conditions, enabling longer circulation times for drug candidates built on this backbone.
Our laboratory technicians spend hours every week sampling and testing product from different points in the production process. From the initial charging of raw materials to final product bagging, we run an array of tests: melting point, residual solvent, optical rotation, and impurity profiling, including low-level detection of process byproducts. Our standard purity guarantee for this product approaches 98% or greater for the main isomer, a figure validated by independent external labs for key clients. Deviations trigger a full process audit—not just a batch rework but an investigation into everything from solvent composition to cleaning protocols.
Over time, we’ve honed methods to optimize product dryness and minimize batch-to-batch variability. For users in regulated sectors, this reliability reduces qualification headaches and accelerates approvals for both pilot and full-scale formulations. With regular proficiency testing and external audits, we retain up-to-date certification for our quality management system, giving customers confidence in every shipment.
Moving from laboratory to plant-scale production, packaging became a recurring theme. The crystalline solid form resists caking during transit and remains free flowing after extended storage owing to careful moisture control in both processing and packaging. Years ago, powders in this chemical class arrived at customer sites in substandard packaging, prompting complaints of lump formation and inconsistent dosing. After direct feedback from end users, we upgraded to multi-layer resistant liners and tamper-proof closures, which have stood up to both high-altitude freighting and extended ocean crossings.
Operators and warehouse teams at customer sites find that the material dispenses accurately, minimizing dust and product loss. To prevent light-induced degradation and maintain chemical integrity, we always use opaque, inert packaging. Users wanting to scale up to bulk processing have also appreciated the option for larger containers and flexible formats, which simplify charge planning and line scheduling in larger production environments.
Depending on region and intended application, this naphthol derivative intersects with evolving regulations. Our compliance teams monitor both local and global requirements, supporting traceability and documentation with batch-level transparency. By working directly on synthesis and purification, we minimize reliance on outsourced intermediates, which reduces overall environmental impact. In daily practice, we recycle solvents where feasible and work with licensed disposal partners for unavoidable waste streams.
No chemical process can claim zero emissions, but decades of hands-on manufacturing experience have taught us to optimize each stage for efficiency. Closed-loop controls and continual monitoring for leaks or fugitive emissions keep our plant running safely and responsibly. As regulations tighten, we engage proactively with both inspectors and community partners, ensuring that our product continues to meet client needs without unexpected compliance risks.
New projects often require more than just a reliable product. R&D teams want not only samples but also detailed, actionable data to make informed choices about synthetic routes or new product prototypes. Our technical managers offer direct, real-world feedback: not just purity numbers, but also information about reactivity trends, preferred solvents, and compatibility profiles built on decades of in-plant experience. We open our facilities to joint development tests, providing customers with a chance to see live batch processing and gather fresh analytical samples at different process stages.
Startups and established companies alike benefit from this transparent, application-driven approach. Small-scale R&D requests don’t fall to the bottom of our priority list. Our team works to understand project goals and trouble-shoot bottlenecks, shortening development timelines and reducing risk as concepts move closer to commercial realization. By participating in peer-reviewed publications and industry working groups, our staff bring the latest technical updates back to the plant floor, ensuring that every lot reflects state-of-the-art methodology and best practices.
Demand for highly functionalized, chiral intermediates has grown as industries shift from so-called one-size-fits-all chemicals to more targeted solutions. Supply chains now prioritize both agility and reliability, so manufacturers like ourselves must be ready to rapidly retool and refine process conditions as new requirements surface. The continued uptake in fields ranging from sustainable fragrances to next-generation pharmaceuticals offers opportunities for collaborative problem-solving.
We’re seeing increased interest in greener synthetic pathways and in products that minimize downstream waste. Our team stays engaged with new developments in catalytic efficiency and solvent reduction, often piloting revised protocols before they achieve market adoption. As clients set higher standards for both performance and sustainability, we work shoulder-to-shoulder with them, adjusting specifications and batch parameters based on clearly articulated goals rather than abstract targets.
Through years of close collaboration and firsthand operational experience, we have refined our approach to manufacturing (1R,2R,8aS)-Decahydro-1-(3-hydroxy-3-methyl-4-pentenyl)-2,5,5,8a-tetramethyl-2-naphthol, providing users with more than just a reagent, but a platform for discovery, refinement, and new product launches. Whether you work in fragrance formulation, pharmaceutical development, materials science, or analytical research, the lessons and improvements accumulated in our plant translate into real benefits for client projects. From dependable regulatory support to practical guidance on application development, the combined expertise of our team stands ready to address both traditional and emerging challenges in specialty chemical manufacturing.