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5,6,7,8-Tetrahydronaphthalene-1-Carboxylic Acid

    • Product Name 5,6,7,8-Tetrahydronaphthalene-1-Carboxylic Acid
    • Alias Tetralin-1-carboxylic acid
    • Einecs 211-801-2
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    426602

    Chemical Name 5,6,7,8-Tetrahydronaphthalene-1-carboxylic acid
    Molecular Formula C11H12O2
    Molecular Weight 176.21 g/mol
    Cas Number 14160-63-3
    Appearance White to off-white solid
    Melting Point 122-126°C
    Boiling Point 369.1°C at 760 mmHg
    Solubility Slightly soluble in water, soluble in organic solvents
    Pubchem Cid 195046
    Density 1.162 g/cm³
    Smiles C1CCC2=C(C1)C(=CC=C2)C(=O)O
    Inchi InChI=1S/C11H12O2/c12-11(13)9-4-2-1-3-8-7-10(9)5-6-8/h4,7-8H,1-3,5-6H2,(H,12,13)
    Synonyms 1-Carboxy-5,6,7,8-tetrahydronaphthalene
    Storage Temperature Room temperature
    Refractive Index 1.563 (estimated)

    As an accredited 5,6,7,8-Tetrahydronaphthalene-1-Carboxylic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 50g amber glass bottle with a secure screw cap, labeled "5,6,7,8-Tetrahydronaphthalene-1-Carboxylic Acid," including safety and handling information.
    Shipping 5,6,7,8-Tetrahydronaphthalene-1-Carboxylic Acid is securely packaged in airtight, chemical-resistant containers to prevent contamination or leakage during transit. Shipping complies with relevant regulations, typically via ground or air transport, ensuring safe and prompt delivery. Accompanying documentation includes Safety Data Sheets and labeling according to international chemical shipping standards.
    Storage 5,6,7,8-Tetrahydronaphthalene-1-carboxylic acid should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers or bases. Proper labeling and chemical hazard identification are recommended. Always follow local regulations and institutional safety protocols for storage and handling.
    Application of 5,6,7,8-Tetrahydronaphthalene-1-Carboxylic Acid

    Applications of 5,6,7,8-Tetrahydronaphthalene-1-Carboxylic Acid in Industrial Manufacturing

    5,6,7,8-Tetrahydronaphthalene-1-Carboxylic Acid serves as a specialty intermediate in multiple industrial sectors that demand high-purity performance and traceable compliance. As the direct manufacturer, we supply this chemical for downstream use across fine chemicals, agrochemicals, pharmaceutical intermediates, specialty coatings, and polymer modification, ensuring full process traceability and batch-specific technical support for each application.

    1. Synthesis of Pharmaceutical Intermediates

    This compound acts as a key precursor in synthesizing advanced intermediates for cardiovascular and anti-inflammatory drug APIs. Downstream processors employ it in multi-step reactions, such as halogenation, amidation, and esterification, which determine the final stereochemistry and purity profiles of target molecules. Our production meets the stringent molecular purity and lot-to-lot consistency required for cGMP synthesis pathways.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211 (Current Good Manufacturing Practice for Finished Pharmaceuticals)
    • European Pharmacopoeia (Ph. Eur. 10.0) compliance for starting materials
    • DMF referencing available for regulated markets

    Typical usage ratio

    • 20–50% molar input in first-step intermediate synthesis
    • Ratio adjusted based on downstream API target and desired yield versus byproduct control
    • Adapted to support scale-up from kilo-lab to full plant volumes

    Downstream process integration

    • Charged into API synthetic route as the primary carboxylic acid source during the initial coupling or activation step
    • Used in batch and continuous flow reactor systems
    • Integrated with in-process QC, including HPLC and NMR monitoring

    Final product types

    • Intermediate blocks for antihypertensive drugs
    • Chiral building blocks for anti-inflammatory APIs
    • Bulk intermediates exported for final API assembly

    2. Agrochemical Intermediate Manufacturing

    Used as a structural intermediate in the manufacture of selected herbicides and fungicides, this raw material enables precise control of aromatic ring saturation and functional group positioning. Agrochemical clients require consistent reactivity profile across bulk lots for controlled synthesis of crop protection agents, meeting all applicable environmental and safety standards.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for Chemical Production
    • Regulation (EC) No 1107/2009 concerning the placing of plant protection products on the market
    • FAO/WHO specifications for pesticide technical material input
    • REACH Annex II Safety Data Sheet (SDS) and GHS classification

    Typical usage ratio

    • 15–35% by weight in active ingredient synthesis
    • Exact ratio determined by active molecule design and process yield optimization
    • Ratio adjusted for batch or continuous production

    Downstream process integration

    • Fed as an intermediate in closed-reactor alkylation and ring-modification processes
    • Participates in condensation or cyclization under controlled thermal conditions
    • Production integrated with full traceability and audit documentation

    Final product types

    • Precursor for broadleaf-selective herbicides
    • Key intermediate for triazole fungicides
    • Custom pesticide intermediate blocks for contract synthesis clients

    3. High-Performance Polymer Modification

    In specialty polymer plants, this compound functions as a chain-modifying monomer or comonomer offering enhanced UV stability and adjusted glass transition characteristics. Processors value batch purity and low-volatility profile for integration into custom polymer grades used in engineering plastics and advanced construction materials, particularly where aromatic core modifications determine the final polymer's mechanical and thermal performance.

    Industry compliance standards

    • ISO 14001:2015 Environmental Management in Polymer Manufacturing
    • ASTM D638/D790 for mechanical property testing of plastics
    • RoHS Directive 2011/65/EU on restricted substances in consumer goods
    • Full MSDS and Certificate of Analysis per shipment

    Typical usage ratio

    • 2–7% (w/w) blend with backbone monomers, depending on target polymer grade
    • Higher ratios up to 12% for specialty copolymers requiring improved performance profile

    Downstream process integration

    • Intake via direct feed into polymerization reactor alongside other monomers
    • Undergoes in-situ reaction to incorporate aromatic ring structure
    • Monitored through real-time FTIR and DSC analysis

    Final product types

    • UV-resistant ABS and polycarbonate plastics for electronics housing
    • Modified engineering thermoplastics in auto parts
    • High-durability building composite panels

    4. Advanced Industrial Coating Ingredients

    This raw material is adopted by formulators of high-performance coatings for corrosion resistance and chemical shielding, especially where specialized aromatic carboxylic components impart flexibility and sustained barrier properties. Users demand detailed batch analyses for paint and resin compatibility tests, ensuring consistent response in multi-component formulations for marine and heavy-industrial sectors.

    Industry compliance standards

    • ISO 12944 for corrosion protection of steel structures by protective paint systems
    • ASTM D4214 for coating appearance and aging
    • Directive 2004/42/EC (VOC content for coatings)
    • Detailed batch traceability for all supplied lots

    Typical usage ratio

    • 3–10% by resin weight in multi-component coatings
    • Adjusted to optimize final viscosity, adhesion, and *in situ* crosslinking speed
    • Development-grade formulations may require up to 15% to test performance margins

    Downstream process integration

    • Introduced during the resin blending stage prior to solvent adjustment
    • Blended with epoxy or polyurethane bases as a reactive component
    • Subjected to accelerated weathering and salt spray tests for QC verification

    Final product types

    • Heavy-duty marine anticorrosive coatings
    • Chemical storage tank linings
    • Industrial maintenance enamels
    Free Quote

    Competitive 5,6,7,8-Tetrahydronaphthalene-1-Carboxylic Acid prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to sales7@sinochem-nanjing.com.

    We will respond to you as soon as possible.

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    Certification & Compliance
    More Introduction

    5,6,7,8-Tetrahydronaphthalene-1-Carboxylic Acid: Product Insights from the Manufacturer

    A Closer Look at 5,6,7,8-Tetrahydronaphthalene-1-Carboxylic Acid

    As a chemical manufacturer, years of working with aromatic carboxylic acids demonstrate the value subtle molecular differences can bring to research and industry. 5,6,7,8-Tetrahydronaphthalene-1-carboxylic acid, or THNA-1-CA, stands out for its unique combination of aromatic stability and the partial saturation of its naphthalene ring. The substituted carboxylic acid group invites a range of chemical transformations that our partners in both pharmaceutical development and specialty chemicals appreciate for its reliability and reactivity.

    THNA-1-CA arises naturally as a logical extension of the naphthalene carboxylic acid family. The presence of saturated carbons in the 5,6,7,8 positions gives the structure increased solubility in several organic solvents, which lines up with practical needs in bench-scale and pilot-scale synthesis. Compared to completely aromatic relatives, this compound behaves with a softer, more manageable aromatic ring system, often translating to less oxidative sensitivity during complex syntheses.

    Our Manufacturing Practice and Product Assurance

    Regular manufacturing batches display purity exceeding 98%, with the pale solid form a mark of high-quality isolation. Over the years, we have refined our hydrogenation and carboxylation steps to keep impurities minimal and batch differences nearly negligible. Thin-layer chromatography, HPLC, and NMR spectrometry checks are standard with each production run, as our clients—especially those scaling up in medicinal chemistry—prefer consistent, transparent records for critical reactions.

    Working directly with the raw materials and the synthesis itself builds a deep understanding of each batch’s behavior. It’s not just reactivity that counts. Factors like melting point (typically in the 145 to 151 degree Celsius range) and resistance to degradation set this carboxylic acid apart from less robust analogs. We avoid off-odors and yellowing by strict exclusion of oxygen and moisture—showing clear improvements in flow chemistry and larger-scale preparations, where batch homogeneity matters more than ever.

    End Uses: Bridging Research and Industry

    In the years of working with scientists and process engineers, we see THNA-1-CA put to use as an intermediate that bridges traditional fused aromatic systems with partially hydrogenated motifs. Medicinal chemistry programs often look to this structure when designing frameworks with improved pharmacokinetics, since the partially saturated ring can reduce oxidative metabolism compared to fully aromatic naphthalene compounds. In polymers and specialty resins, the tetrahydro substitution bestows greater flexibility to the resulting backbone, enhancing toughness without sacrificing chemical compatibility.

    Some past collaborations involved using THNA-1-CA in Suzuki and Heck couplings. The ability to survive a range of palladium catalysts while presenting an activated carboxylic acid group accelerates route scouting for diverse heterocycles. Peptide synthesis programs report smoother derivatizations with this acid, noting lower side-product formation where more aromatic rings could otherwise interfere. These real-world experiences build confidence in the chemical’s reliability far more than any listing or technical sheet can deliver.

    The Real Differences: Saturated Versus Aromatic Acids

    Working with a range of aromatic carboxylic acids gives us a unique vantage point to observe subtle yet crucial performance differences. Classic naphthalene-1-carboxylic acid, for instance, packs a full set of aromatic electrons, making it quite rigid and sometimes more prone to undesired side-reactions under strongly basic or oxidative conditions. THNA-1-CA provides a middle ground: the hydrogenated positions add a level of conformational flexibility that becomes essential in catalyst-laden environments, or where the acid must endure extended thermal stress.

    Researchers in our partner labs have highlighted the contrast during preparative reactions. THNA-1-CA tends to form fewer colored byproducts under heating, and its partially saturated core resists electrophilic attack better than simple benzoic acids. This opens up options for those seeking to modify the acid moiety without scrambling the core skeleton. Another key difference comes in the form of solubility: the tetrahydro motif slightly raises the compound’s affinity for certain polar aprotic solvents, making purification by crystallization more straightforward in scale-ups.

    Hands-On Handling Experience

    Decades of producing and packaging THNA-1-CA for a global client base have taught us where challenges arise. The pure acid form stores without caking in airtight polymer containers under dry nitrogen. Even under these conditions, we recommend keeping it at room temperature, away from any strong oxidants, for longest shelf life. Early on, we learned to avoid glass ampoules for long-haul shipping, as the compound’s moderate reactivity could cause etching in the presence of trace moisture.

    In process applications, users appreciate the granulated solid for its easy dissolution in N,N-dimethylformamide (DMF), dimethyl sulfoxide (DMSO), and other specialty media. We find that it dissolves at roughly 10-15 grams per 100 mL of DMF at room temperature, streamlining reagent preparation, especially in automated reactors or multi-step flows. This attribute places it ahead of some other carboxylic acids that require special handling to break up agglomerates or dissolve completely.

    Reducing Production Wastes and Improving Purity

    In any fine chemical manufacturing process, cutting down on byproduct streams and boosting crystallization efficiency spells cost savings and environmental responsibility. During the past decade, we worked to reduce hydrogenation catalyst residues below regulatory thresholds, validating each batch by ICP-OES. Process intensification efforts—such as recycling wash solvents and deploying more selective catalysts—cut both metal waste and organic residues, while keeping the acid’s purity above the 98% mark.

    Our hands-on experience with post-reaction filtration informed us about optimizing parameters: for this tetrahydro compound, filtrate pH and flow rates dictate yield more than particle aggregation, which complicates production of less-saturated naphthalenic acids. Recrystallization from toluene or ethyl acetate remains the best route for isolating pure material on kilo scales, delivering solid that free-flows and packs densely for shipping, yet remains easy to re-dissolve during downstream processing.

    Practical Challenges and Lessons Learned

    THNA-1-CA gives industrial synthetic chemists a solution to some of the bottlenecks with more stubborn aromatic acids. Early batches sometimes suffered trace coloration, traced back to microimpurities in hydrogen sources and solvent lots. Over time, switching to high-purity hydrogen and distilling solvents in-house all but eliminated yellowing. In one instance, a customer’s high-throughput screen flagged a drop in yield that correlated with shipping delays in summer months. We responded by reviewing packaging—adding secondary barrier bags and ice packs—which fixed the shelf stability concerns and secured the client’s trust. Real-world feedback like this drives changes and strengthens product reliability.

    Some project leads have attempted to substitute THNA-1-CA with closely related analogs, only to discover differences in product selectivity, especially in chiral amide coupling sequences. Peer experience suggests that the partial saturation delivers needed flexibility to intermediate and transition state conformations, sparing downstream steps from avoidable yield loss or excess impurities.

    End-User Insights: Opportunities and Limitations

    THNA-1-CA’s partial hydrogenation and carboxylate placement create opportunities in asymmetric synthesis. The acid’s scaffold allows for easy transformation into a suite of amides, esters, and other derivatives, offering medicinal chemists a reliable source for rapidly building drug-like molecules. In agrochemical discovery work, we found the compound’s lower aromaticity lessens photo-instability under illuminated greenhouse trials, hinting at uses beyond pharmaceuticals and into advanced material science.

    Synthetic polymer researchers sometimes seek greater rigidity, and in these situations, a fully aromatic acid might offer more cross-link density. For flexibility and tailored backbone electronics, THNA-1-CA steps in. When formulating polymers for optoelectronic or soft-materials applications, this acid’s combination of chemical reactivity and molecular mobility helps ensure finished products resist yellowing, surface cracking, or unwanted phase separation.

    As with any specialized compound, the wrong application reduces value. Strong oxidizers—such as those used in certain analytical digestions—can attack the tetrahydro part of the molecule more readily than an all-aromatic acid. Users in these fields benefit from honest conversations with process chemists who know the compound both from the lab bench and kilo-plant, making sure each batch finds its most reliable use.

    Comparing Supply Chain and Sourcing Decisions

    Our years as a direct manufacturer, dealing daily with raw supplies and finished product shipments, offer another perspective that traders and resellers rarely mention. Consistency comes not just from paperwork, but from oversight—source material traceability, batch record retention, and careful maintenance of storage conditions. Every batch of THNA-1-CA passes through the same hands, lab, and analytical tools, shrinking the risk of variation that plagues bulk commodity purchases.

    Periodically, we benchmark our product against that from other global suppliers. The cost-per-gram tells only part of the story. It’s the repeat synthesis runs—where yield stays predictably high from week to week—and downstream transformations that avoid surprise impurities. This reliability means less rework, less lost time, and steadier research progress. Many of our clients have replaced multi-source purchases with single, direct relationships, citing improved lab productivity and process scaling.

    Supporting Responsible Use and Future Development

    Regulatory expectations around purity and trace impurities have grown stricter in recent years. As a manufacturer, these shifts mean upfront investments in validated cleaning procedures, metal content testing, and comprehensive batch archiving. Rather than viewing these as burdens, we treat them as safeguards for our clients downstream. Each approved batch reflects conversations with the regulatory teams of pharmaceutical firms, who often require confirmation that potential impurities derive only from known process reagents and are not introduced by poor-quality raw materials.

    Looking forward, we continue to improve environmental sustainability in THNA-1-CA production. Opportunities exist in solvent recycling, energy-efficient hydrogenation, and closed-system isolation. We actively partner with academic and industrial researchers focused on greener carboxylation and ring hydrogenation routes, pooling experience to cut carbon footprints without sacrificing product integrity. These efforts align with both our values and the increasing expectations of customers throughout the chemical supply chain.

    Partnering with Chemists: Insights That Drive Innovation

    Chemical manufacturing is not just a matter of filling drums and barrels. Working with THNA-1-CA from the ground up, we think alongside the chemists who carry out late-stage derivatization, pilot-scale process optimization, or full-scale production. Regular feedback cycles—delivered through phone calls, detailed reports, and site visits—build a shared knowledge base.

    In some cases, customers unearthed novel reaction pathways or solutions to common bottlenecks using THNA-1-CA, reporting back so we could test their findings in our own facilities. Insights shared between manufacturer and user create a feedback loop; improved reaction selectivity or material performance in the field leads us to refine our purification or packaging, often resulting in enhanced batch reproducibility and more detailed certificate records.

    A deeper understanding of reaction mechanisms and physical property trends supports not only our business but the progress of our partners’ research. While the formal literature covers much, authentic in-plant experience leaves us in a position to offer practical advice rooted in every ton produced and every day spent testing what others overlook.

    Ongoing Commitment to Consistent Supply and User Satisfaction

    Material shortages and unexpected demand spikes sometimes challenge the market. Because we manufacture our own THNA-1-CA, with direct oversight from synthesis to shipment, clients avoid many of the uncertainties that come with brokered or batch-mixed lots. Keeping safety stocks, adjusting batch sizes, and offering timely shipping updates has proven more valuable than the lowest possible price alone. Repeat orders and long-term partnerships stem from a shared goal: keeping research timelines on track, avoiding downtime, and reducing administrative headaches.

    By staying connected to both the process chemistry and the business realities of our clients, we adapt batch sizes, packaging, and specification focus. End-user requirements evolve, and it is our responsibility to track analytical needs—such as stricter residue reporting or special packaging for storage-limited sites—responding with flexibility and integrity based on years of firsthand experience.

    Closing Thoughts: Recognizing the Value in Every Molecule

    5,6,7,8-Tetrahydronaphthalene-1-carboxylic acid reflects the idea that careful molecular design and precision in production add measurable value to both the chemical and its end uses. For synthetic chemists, process engineers, and research managers, buying direct from an experienced manufacturer means more than technical data—it means insight, reliability, and a steady source of ideas about how to make workflow smoother and science stronger.

    Our confidence in THNA-1-CA does not spring from marketing headlines, but from decades of hands-on work, supplier partnerships, and continuous improvement in both chemistry and service. The chemical’s unique blend of rigidity and flexibility, its clean profile and robust handling characteristics, and the lessons learned from every synthesis define not just the product, but the people committed to delivering it.