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1-Naphthalenemethanol

    • Product Name 1-Naphthalenemethanol
    • Alias 1-Naphthalenecarbinol
    • Einecs 202-221-0
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    217869

    Chemical Name 1-Naphthalenemethanol
    Cas Number 703-19-9
    Molecular Formula C11H10O
    Molecular Weight 158.20 g/mol
    Appearance White to off-white solid
    Melting Point 72-76 °C
    Boiling Point 315 °C
    Density 1.16 g/cm3
    Solubility In Water Slightly soluble
    Smiles C1=CC=C2C(=C1)C=CC=C2CO

    As an accredited 1-Naphthalenemethanol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 1-Naphthalenemethanol is packaged in a sealed 100g amber glass bottle with a secure screw cap and clear hazard labeling.
    Shipping 1-Naphthalenemethanol is shipped in tightly sealed containers, protected from light and moisture, and stored in a cool, dry, and well-ventilated area. Proper labeling is required, and the chemical should be handled according to local regulations. Transportation typically follows standard procedures for organic chemicals, ensuring safety and compliance with hazardous material guidelines.
    Storage 1-Naphthalenemethanol should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Protect it from light and moisture. Properly label the storage area, and avoid prolonged exposure to air. Keep away from heat and direct sunlight to maintain stability and prevent decomposition.
    Application of 1-Naphthalenemethanol

    Applications of 1-Naphthalenemethanol in Industrial Manufacturing

    1-Naphthalenemethanol serves as a key specialty intermediate in multiple precision manufacturing segments, especially where fine chemical synthesis and targeted molecule construction are prioritized. As the direct producer, we support large-scale customers with reliable supply, batch consistency, and technical guidance to ensure exact integration into complex production lines.

    1. Pharmaceutical Intermediate Synthesis

    Pharmaceutical manufacturers directly employ 1-naphthalenemethanol in multi-step organic syntheses, especially for the preparation of naphthalene-based active pharmaceutical ingredients and advanced intermediates. This alcohol acts primarily as a protected functional group or as a Grignard reaction partner for further derivatization, often in the production of APIs like nebivolol and other beta-blockers. Strict compliance controls raw material traceability, impurity profile, and residual solvent levels to support DMF filings and quality assurance under international regulatory oversight.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 210/211 (US FDA)
    • EU EudraLex Volume 4 GMP Guidelines
    • Ph. Eur. and USP specifications for related intermediates

    Typical usage ratio

    • Varies between 0.5–1.2 mole equivalents relative to substrate, based on multi-step reaction design and targeted impurity limits

    Downstream process integration

    • Charged at the first or second synthesis stage for functional group construction, protection, or side-chain modification
    • Subjected to catalytic hydrogenation, oxidation, or alkylation before conversion to API scaffold

    Final product types

    • Nebivolol intermediates
    • Custom naphthylamines and aminoalcohols
    • CNS and cardiovascular small molecule APIs
    • High-purity reference standards for analytical use

    2. Agrochemical Active Ingredient Manufacturing

    Crop protection chemical companies process 1-naphthalenemethanol as a strategic building block for selective herbicides and fungicides. Its regulated aromatic moiety enables design of active compounds resistant to photodegradation in field use. Formulation scientists control integration to meet toxicity, degradability, and soil residence requirements, adhering to multi-region registration demands for agricultural markets.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice
    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS)
    • REACH Regulation (EC) No 1907/2006
    • US EPA 40 CFR Part 158 Pesticide Data Requirements

    Typical usage ratio

    • Applied at 1.0–1.5 mole equivalents for core coupling reactions or side-chain attachment on naphthalene backbones

    Downstream process integration

    • Introduced in the early-phase synthesis of naphthalene-derived agrochemical scaffolds
    • Enter coupling, esterification, and formulation stages, followed by formulation into concentrated technicals

    Final product types

    • Naphthyl-based herbicide actives
    • Fungicide technical concentrates
    • Seed treatment raw actives
    • Bespoke pesticide intermediates for further downstream derivatization

    3. Dyes and Organic Pigment Manufacturing

    Dye producers integrate 1-naphthalenemethanol as a precursor for vibrant azo and anthraquinone pigment molecules. Its controlled aromatic group allows for coupling reactions that impart required chromatic strength, migration resistance, and UV stability for both textile and plastics coloration. Batch QC ensures regulated trace impurity profiles for export and global textile safety compliance.

    Industry compliance standards

    • OEKO-TEX Standard 100 (for dyestuffs used in textiles)
    • EN 71-3 (Safety of Toys: migration of certain elements)
    • ISO 105 Series (Textile color fastness testing)
    • ZDHC Manufacturing Restricted Substances List (MRSL)

    Typical usage ratio

    • Utilized within 0.8–1.1 molar equivalents in controlled diazo coupling reactions; adjusted by shade and solvent selection

    Downstream process integration

    • Fed into azo- and anthraquinone-based pigment synthesis lines
    • Processed through diazonium salt formation and subsequent coupling onto naphthalenic core

    Final product types

    • Reactive textile dyestuffs
    • Organic pigments for plastics and inks
    • High-performance color dispersions
    • Special effect industrial coatings

    4. Specialty Polymer and Resin Modification

    Technical polymer manufacturers use 1-naphthalenemethanol as a functional monomer or chain modifier in the synthesis of high-performance urethanes and polyesters. Its aromatic structure introduces controlled rigidity, enhancing heat resistance and mechanical stability. Applications focus on electronics encapsulation, performance adhesives, and specialty coatings where tailored reactivity and surface characteristics are critical for final performance.

    Industry compliance standards

    • ISO 9001 Quality Management Systems
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances)
    • REACH SVHC (Substances of Very High Concern) notification requirements
    • UL 94 (Flammability testing of plastic materials)

    Typical usage ratio

    • Blended at 3–8 wt% in step-growth polymerizations, depending on target glass transition temperature and modulus requirements

    Downstream process integration

    • Dosed during initial polycondensation or co-polymer formulation stages
    • Enters as a chain extender or structural modifier to fine-tune molecular architecture

    Final product types

    • Heat-resistant polyurethane resins
    • Modified polyester for specialty films
    • High-gloss, durable coating intermediates
    • Low-migration encapsulants for electronics

    5. Fragrance and Flavor Ingredient Precursor

    Fine chemical houses employ 1-naphthalenemethanol in the targeted manufacturing of fragrance intermediates. Through catalytic oxidation and subsequent esterification, it enables construction of naphthyl-containing musky notes and fixative substances, demanded by regulatory-compliant formulations for personal care and home fragrance. Strict attention to byproduct profile, trace solvents, and allergen labeling supports international distribution.

    Industry compliance standards

    • IFRA (International Fragrance Association) Standards
    • EU Regulation (EC) No 1223/2009 on Cosmetic Products
    • US FDA 21 CFR Parts 172, 174, 182 (relevant for indirect food contact)
    • GMP for Cosmetics ISO 22716

    Typical usage ratio

    • Converted at 0.9–1.1 eq in intermediate steps; downstream usage rates adjusted to IFRA limits for finished hydrocarbons

    Downstream process integration

    • Undergoes initial oxidation to naphthaldehyde derivatives
    • Further reacted to esters or ketones incorporated in fragrance bases

    Final product types

    • Naphthyl-based fragrance fixatives
    • Base notes for fine perfumes and colognes
    • Aroma chemicals in personal care
    • Specialty home fragrance blends

    6. Photoinitiator and UV Absorber Synthesis

    Manufacturers in electronics and coatings industries utilize 1-naphthalenemethanol for producing advanced photoinitiators and UV absorbers. Its distinct substitution site facilitates synthesis of benzoin and benzil-type photoinitiators with strong absorption properties for use in UV-curable inks, coatings, and adhesives. Product consistency and ultra-low trace metal content are essential for high-value added electronics and functional film applications.

    Industry compliance standards

    • IEC 61249 Halogen Free Standard (for electronic materials)
    • ISO 14001 Environmental Management
    • Restriction of Halogens and RoHS Requirements in Electronics Manufacturing
    • ISO 2768 General Tolerances for industrial processing consistency

    Typical usage ratio

    • Used at 1.0 eq in photoinitiator batch steps, with downstream formulation concentrations typically 0.5–2% by weight in UV-curable systems

    Downstream process integration

    • Processed via benzoin condensation or acylation with aromatic acids
    • Blended into photoinitiator masterbatches before final formulating

    Final product types

    • High-efficiency photoinitiator powders
    • UV absorber additives for plastics and films
    • Light-stabilizing agents in performance coatings
    • UV-cured electronics adhesives
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    Certification & Compliance
    More Introduction

    1-Naphthalenemethanol: Our Experience in Production and Industry Use

    As a long-standing chemical manufacturer, we've spent years refining the synthesis of specialty aromatic compounds, and 1-naphthalenemethanol stands out as one of our most robust and dependable products. There's no need to dress this compound up as anything other than what it is—a workhorse for organic synthesis, valued for its reliability, structure, and the flexibility it brings to chemical design. Our clients trust us to deliver material that isn’t just high in purity but also delivers seamless results in real-world laboratories and industrial applications.

    The Distinct Backbone of 1-Naphthalenemethanol

    At its core, 1-naphthalenemethanol offers a simple but powerful structure—one that opens doors for further functionalization and complex molecule construction. Chemists keep coming back to this compound for good reason. It pairs a naphthalene ring with a methanol functional group, which means the molecule melds aromaticity with a reactive alcohol position. Throughout the history of synthetic chemistry, that fusion has served as a launching point for a variety of transformations. We’ve seen it behave predictably in Grignard reactions, reductive aminations, and as a substrate for etherification or esterification, supporting both high-throughput screening environments and precision synthesis in new pharmaceutical development.

    Our process begins with naphthalene and makes use of trusted reagents and controlled conditions. The finished product is not just about hitting a chemical benchmark for purity—it’s about making sure every flask, drum, or IBC that leaves our plant meets the same standard every single time. Chemists in the field notice differences in color, odor, and reactivity when manufacturers cut corners on process controls or raw material sourcing. We check each batch using NMR, GC, and Karl Fischer titration—if the data does not fall in line with what’s needed, it does not ship. This care comes from decades of client feedback, R&D, and putting ourselves in the customer’s shoes.

    Specifications and Quality Benchmarks

    Demand for 1-naphthalenemethanol crept upward in both research and bulk production over the past decade. This calls for suppliers to pay close attention to aspects that laboratories and industry customers watch for: purity, moisture range, and freedom from metal or halide residues. Purity tells only part of the story—it’s easy to hit 98 percent by conventional recrystallization and distillation. Pushing above 99 percent, on the other hand, takes more than method. Certain byproducts are difficult to separate, such as naphthalene impurities, methyl-naphthalene isomers, or benzylic alcohols. These often leave subtle traces that can trip up a reaction or cause product development teams weeks of troubleshooting.

    Quality to us comes down to a tight profile. The odor should be subtly aromatic with none of the sharp notes found in lower grades. Hue matters, too; a slight yellow tinge can indicate partial oxidation or carryover from incomplete purification. In practice, customers have pointed out these seemingly cosmetic issues can translate to downstream complications, causing color changes in formulations or unwanted reactivity in API synthesis. We maintain not only GC-area purity above 99.0 percent but also closely check optical clarity and residual solvent levels. Our water content specification does not stray beyond 0.1 percent by Karl Fischer titration—essential for water-sensitive transformations or storing material over extended periods.

    Key Usage Areas in Modern Chemistry

    Every year, our technical support team fields questions from organizations across the chemical value chain. Fine chemical manufacturers reach out looking to build complex intermediates. Academic researchers request analytical support for using 1-naphthalenemethanol in new reaction methodologies. Even clients in specialty polymers or material science appreciate the compound’s capacity as a building block for functionalized aromatic materials.

    What differentiates this alcohol from generic benzyl alcohol or naphthols comes down to structure. As a primary alcohol tethered to a naphthalene core, it acts as a unique scaffold—less reactive than benzylic derivatives but more versatile than simple naphthols for controlled functional group transformations. Phosphoramidite ligands, chiral auxiliaries, and fluorescent probes often use this backbone as a key element. In polymer and coatings research, substituting 1-naphthalenemethanol for other aromatic alcohols allows formulation chemists to fine-tune mechanical strength, glass transition temperatures, and even UV-absorption profiles. Our own R&D teams have published case studies highlighting the shifts in reactivity and stability with this molecule versus more common phenyl-based alcohols.

    In pharmaceutical and agrochemical sectors, the need for custom syntheses is relentless. Medicinal chemists have cited the use of 1-naphthalenemethanol as a protected or masked alcohol moiety, later manipulated into aldehydes, acids, or halides. Its aromatic system serves as an anchor point for introducing halogens or aliphatic groups that influence pharmacokinetic properties. Given the structural similarity to many bioactive molecules, small changes in the substituent pattern can have an outsized impact on target affinity or metabolic stability. Our client base often requests characterization support, needing detailed spectral data to correlate structure with activity in new analogs.

    Real-World Production Challenges and Solutions

    Running a fine chemicals plant rarely follows a straight path. Each stage of scale-up for 1-naphthalenemethanol brought its own set of issues. Early on, yields fluctuated as temperature control drifted or minor crudes developed unexpected byproducts. With each batch, our process engineers tracked everything from stirrer speed to solvent batch number. When a product recall at a customer’s site traced back to residual catalyst, we invested in new filtration and purification train stages. We learned the value of redundancy—not just analytical double-checks but also backups for every essential input.

    Solvent selection became a critical factor. Dimethylformamide, dioxane, and toluene respond differently under process conditions. Choosing the wrong solvent leaves residual traces that can show up months later in finished goods. We moved toward greener alternatives when possible but always prioritized batch reproducibility. Each change meant a revalidation—a time-consuming but necessary effort. The finished product’s stability in various packaging types came up during overseas shipments. A polymer lining change in steel drums produced subtle contaminants detected by sophisticated end-users, driving us to implement a pharmaceutical-standard container regime.

    Contamination control remains a high priority. Plants handling multiple aromatic compounds risk cross-contamination from reused lines or improper washing. Our rule: every batch of 1-naphthalenemethanol must be processed and drawn through lines dedicated to that batch alone, followed by validated cleaning. Unannounced audits by several leading customers taught us that documentation—how, not just what—plays a role in building trust.

    Understanding Differences From Related Aromatic Alcohols

    Anyone evaluating alternatives to 1-naphthalenemethanol needs to look beyond price or stated purity. Benzyl alcohol, for example, is widely available and more reactive in some contexts, but it brings its own set of drawbacks. Its volatility and lower boiling point can complicate reaction workups or long-term storage. Meanwhile, 2-naphthalenemethanol offers a shifted substitution pattern. On paper, only the position changes, but that relocation on the ring shifts electronic properties. Process developers who tried swapping these isomers in their syntheses remarked on differences in reactivity with oxidants, selectivity in substitution, and even solubility when building up larger molecules.

    Naphthols, another family member, hold a hydroxy group directly on the aromatic ring rather than as a pendant benzylic alcohol. That difference dramatically increases acidity and changes interactions with metal catalysts. We’ve collaborated with customers who started with naphthols, seeking to produce ethers or esters, only to find issues with selectivity or stability not present when using 1-naphthalenemethanol. This alcohol offers more predictable behavior in cross-coupling, hydrogenation, or step-growth polymerization.

    Some clients inquire about using 1-naphthalenemethanol for custom ligand synthesis or advanced material science. Others want a direct comparison with benzyl alcohol-based systems. In fluorescence and imaging probes, the naphthalene backbone opens the door to enhanced aromatic stacking or emission characteristics that aren’t easily achieved with simpler benzylic systems. When desk chemists try to swap out the alcohol or backbone, the changes in photophysical or mechanical performance can invalidate months of prior work.

    Packaging, Shelf-Life, and End-Use Considerations

    We package 1-naphthalenemethanol with the end-user’s needs in mind. Small R&D teams order in glass or high-density polyethylene bottles fitted with PTFE-lined caps to preserve purity during long bench storage. Larger industrial batches ship in drums and intermediate bulk containers that pass compatibility and purity leach testing before filling. For high-sensitivity applications, we offer inert-gas blanketing to prevent slow oxidation or hydrolysis, particularly during warmer months or in humid environments. Ensuring a tight seal and proper labeling eliminates the risk of mix-ups as material makes its way from dock to bench.

    Shelf stability matters, especially for clients juggling multiple projects or keeping stock for extended periods. This aromatic alcohol maintains its integrity as long as exposure to light, air, and heat stays minimal. We provide guidance on best storage practices, based on accelerated aging data and real-life user feedback. When users reported slight color shifts after repeated bottle openings, we looked closer at capping and lid design, advising them on how to minimize oxygen intrusion.

    Some industrial customers ask about traceability. Our plant operates under a batch-record system—a file follows each kilogram from raw material intake to finished lot. This system makes sure labs and production managers alike can retrace every step in the product’s journey. We provide full lot certificates with spectral data, detailed impurity profiles, and stability information. This transparency helps clients pass audits or troubleshooting reviews if downstream product quality raises questions.

    The Road Ahead: Continuous Improvement and Collaboration

    Few chemical compounds occupy the middle ground between simplicity and function like 1-naphthalenemethanol. As our customer base diversifies, the requests for greater customization grow. Some ask for higher purity or special drying. Others require new container sizes or stricter impurity cutoffs for regulatory compliance. We respond by going back over our process analytics, sampling procedures, and purification protocols.

    Every year, we invest in plant upgrades and staff training. We automated much of our analytical regime to catch shifts in impurity patterns before they impact large batches. We reward cross-functional teams—process engineers, analytical chemists, logistics coordinators—for catching minor deviations and proposing fixes that work at scale. Our openness to new methodology, within the safe zone of proven chemistry, ensures we bring a stable product to the table every time.

    At the same time, we keep a constant line of communication with clients. Many improvements came from things end-users pointed out, not in spreadsheets, but in day-to-day usage. For example, a pharmaceutical partner taught us to check for trace nitrosamine precursors, which were unregulated in the past but now fall under heavy scrutiny. That feedback loop makes us less reactive and more proactive in designing monitoring schemes or packaging improvements.

    Our technical service chemists travel to customer sites, often working side-by-side with plant or R&D staff. This boots-on-the-ground approach reveals pain points in real time—seal failures, unexpected crystallization, or difficulty in pumping material during winter months. Each observation feeds back into product development or logistics upgrades, shrinking the gap between what a user expects and what the industry delivers.

    Regulatory and Environmental Footprint

    The chemical sector faces an increasing number of regulatory hurdles at both the regional and global levels. Production of aromatic alcohols falls within these scopes, so we built risk management into our normal operating procedures. We track the evolving lists of restricted impurities, hazardous constituents, and shipping constraints. Outreach with local authorities and participation in industry consortia keeps us ahead of new compliance burdens.

    Waste minimization forms the basis of good chemical manufacturing these days. We keep solvent recoveries high and emissions low by reusing and purifying process streams as much as feasible. For 1-naphthalenemethanol, our in-plant recycling systems divert more than half of traditionally wasted solvent back into the production loop, while spent reactants go into energy recovery or feedstock generation. Continuous improvement here isn’t just about saving on costs; it’s about reducing the environmental signature of what we ship.

    Some downstream users want information on life-cycle impacts for regulatory filings or their own sustainability reports. Our data team compiles cradle-to-gate analysis for energy, water, and material usage, which we share upon request. This transparency enables more sustainable supply chains and can simplify environmental product declarations.

    A Partnership Built on Real-World Chemistry

    Anyone can supply chemicals. Delivering consistent, transparent, and technically supported product takes effort and investment over years. We understand that 1-naphthalenemethanol isn’t just another SKU on a list. Each drum or bottle represents a link in the research or production chain of countless industries—a bridge between known chemistry and future applications. Years of day-in, day-out interaction with chemists, process engineers, and formulators taught us that reliability, clear communication, and acute attention to the details underpin long-term partnerships.

    We remain committed to producing high-quality aromatic alcohols, supported by continuous learning and honest dialogue. Products like 1-naphthalenemethanol might look simple in structure, but the expectations and possibilities stretch far beyond the beaker or flask. As industries evolve and standards rise, we expect the same of ourselves and our materials. With each batch, shipment, and customer visit, we re-commit to the values that have sustained our business—technical rigor, responsiveness, and a willingness to grow alongside our clients’ ambitions.