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4-(1-Adamantyl)Phenol

    • Product Name 4-(1-Adamantyl)Phenol
    • Alias 4-Hydroxyphenyladamantane
    • Einecs 402-110-5
    • 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
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    Specifications

    HS Code

    184694

    Compound Name 4-(1-Adamantyl)phenol
    Chemical Formula C16H20O
    Cas Number 700-58-3
    Appearance White to off-white crystalline powder
    Melting Point 163-165°C
    Boiling Point N/A (decomposes)
    Solubility In Water Insoluble
    Density 1.13 g/cm3
    Purity Typically ≥98%
    Storage Conditions Store in a cool, dry place
    Synonyms 4-Adamantylphenol; 4-(Adamantan-1-yl)phenol
    Smiles C1C2CC3CC1CC(C2)C3C4=CC=C(C=C4)O
    Refractive Index N/A
    Logp Approx. 4.6

    As an accredited 4-(1-Adamantyl)Phenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 100 g of 4-(1-Adamantyl)phenol packaged in a sealed amber glass bottle with a tamper-evident cap and hazard labeling.
    Shipping 4-(1-Adamantyl)Phenol is shipped in tightly sealed containers, compliant with chemical safety regulations. It should be transported at ambient temperature, shielded from direct sunlight and moisture. Proper labeling, documentation, and handling precautions are essential to ensure safe delivery. Follow applicable local, national, and international shipping regulations for hazardous laboratory chemicals.
    Storage Store **4-(1-Adamantyl)phenol** in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizers and acids. Protect from direct sunlight and moisture. Clearly label the container, and ensure it is kept in a chemical storage cabinet designed for organic compounds to minimize contamination and exposure.
    Application of 4-(1-Adamantyl)Phenol

    Applications of 4-(1-Adamantyl)Phenol in Industrial Manufacturing

    We manufacture 4-(1-Adamantyl)Phenol for advanced material synthesis and specialty production chains. Below, we describe real-world industrial application scenarios detailing usage within distinct downstream sectors, relevant compliance environments, integration points in the workflows, and resulting finished products.

    1. High-Performance Polymer Antioxidants

    This compound acts as a key intermediate in synthesizing hindered phenol antioxidants for premium polymer stabilization. Producers incorporate it to extend the thermal and oxidative life of engineering thermoplastics, including polyolefins, polycarbonates, and polyesters. Industrial users select grades based on residual purity and trace metal content to ensure compatibilities across high-temperature molding and extrusion lines.

    Industry compliance standards

    • EN 2002-1: Polymer Additives—Antioxidants Specification
    • ISO 9001:2015—Quality Management for Polymer Additive Manufacturing
    • EU REACH (Regulation EC No. 1907/2006) for polymer stabilizers
    • FDA 21 CFR 177.1520 (for additive components in food contact polyolefins as applicable)

    Typical usage ratio

    • Utilized at 0.05%–0.2% by weight in thermoplastics; final ratio depends on resin type, processing conditions, and service temperature of the end-use product

    Downstream process integration

    • Introduced during the compounding phase in twin-screw extrusion lines; premixed or dosed directly with resin pellets and carrier oil prior to pelletization

    Final product types

    • Automotive interior parts
    • Food-grade containers
    • Electrical insulation films
    • High-durability household appliances

    2. Liquid Crystal Display (LCD) Monomer Synthesis

    Downstream manufacturers employ this raw material to synthesize specialty aromatic monomers for use in advanced liquid crystal compounds. Its adamantyl backbone provides enhanced stability and molecular alignment in thin-film transistor manufacturing. Users apply tight impurity controls and specific particle size distributions to prevent phase defects in final panel manufacturing.

    Industry compliance standards

    • IEC 61249-2-40: LCD material chemical purity
    • ISO 14644-1: Cleanroom process controls for electronic materials
    • RoHS Directive 2011/65/EU—Restriction of Hazardous Substances
    • JPCA-ES-01: Japan Electronics Packaging Standard

    Typical usage ratio

    • Used at 2–8 mol% in precursor mixes; adjusted based on desired birefringence and viscosity profile of the liquid crystal system

    Downstream process integration

    • Introduced during the intermediate monomer alkylation or arylation stage, then purified and blended prior to liquid crystal formulation

    Final product types

    • Thin-film transistor LCD panels
    • Display modules for smartphones
    • TFT monitors and industrial screens
    • Medical diagnostic imaging displays

    3. Advanced Epoxy Resin Systems

    Producers use this compound to engineer epoxy curing agents for reinforced composites and adhesives. It improves glass transition temperature and enhances long-term hydrolytic resistance. Only high-purity lots with specific melting point and minimal water residue meet the demand for electronics-grade and aerospace-grade resin systems.

    Industry compliance standards

    • ASTM D1763—Epoxy Resins and Modifiers for Composites
    • JIS K6930—Thermosetting Resins Quality Standard
    • UL94—Flammability Testing for Polymer Materials
    • ISO 9001:2015 for aerospace composite raw material traceability

    Typical usage ratio

    • Present at 1–6 phr (parts per hundred resin) as a co-curing additive, depending on formulation rheology and mechanical performance targets

    Downstream process integration

    • Mixed into base resin and hardener solution, followed by degassing and thermal curing; added before degassing step to optimize wetting and crosslinking density

    Final product types

    • Aircraft structural panels
    • Wind turbine blade laminates
    • High-strength electronic encapsulants
    • Industrial adhesive formulations for metal bonding

    4. Photoresist Formulation for Semiconductor Fabrication

    Fab operators and specialty chemical formulators select this material as a component for designing advanced positive photoresists. Its robust aromatic framework promotes thermal pattern retention and minimizes line roughness during photolithographic etching. Only products with low metal content and controlled ionic contamination meet precision requirements for next-generation semiconductor nodes.

    Industry compliance standards

    • SEMI C1—Specifications for Photoresist Materials
    • ISO 14001—Environmental Management in Chemical Production
    • SEMATECH Material Purity Guidelines
    • IEC 62474—Material Declaration for Electrical and Electronic Products

    Typical usage ratio

    • Applied at 0.5–2% by weight of total photoresist liquid composition; final ratio varies with pattern resolution requirements and process chemistry

    Downstream process integration

    • Dissolved during the photoresist formulation step prior to filtration and can-filling; incorporated before spin coating on wafers for polymer backbone enhancement

    Final product types

    • Patterned silicon wafers (logic and memory chips)
    • Photomask blanks
    • Printed circuit board substrates
    • Microelectromechanical device platforms

    5. Specialty Surface Coatings for Chemical Equipment

    Chemical process equipment manufacturers utilize this intermediate to develop phenolic-based coatings for corrosion protection and chemical resistance. The adamantyl group imparts enhanced thermal stability and solvent non-permeability, which is critical in high-acidity or high-alkalinity environments. Quality assurance teams specify minimal organic volatiles and residual monomers to comply with coating performance audits.

    Industry compliance standards

    • ISO 12944—Corrosion Protection by Protective Paint Systems
    • ASTM D5144—Phenolic Resin Coating Standard
    • EU Directive 2010/75/EU—VOC Emissions Regulations
    • API RP 583—Corrosion Under Insulation Standards for Oil & Gas

    Typical usage ratio

    • Employed at 3–10% by weight in resin mixes; dosing tailored for substrate geometry and anticipated temperature excursions

    Downstream process integration

    • Added during the high-shear mixing of primary binder resins; followed by dispersion, solvent thinning, and application by spray or dip-coating in plant-scale batch operations

    Final product types

    • Storage tank internal linings
    • Pump housings and chemical piping
    • Heat exchanger protective coatings
    • Industrial reactor and scrubber linings

    6. Selective Ligand Synthesis for Catalytic Systems

    Chemical synthesis specialists incorporate this raw material to build adamantyl-substituted phenolic ligands. These serve as chelating agents in homogeneous catalysis, improving activity and selectivity in fine chemical production. Trace metal analysis and ligand purity validation ensure reliability in hydrogenation and cross-coupling process steps.

    Industry compliance standards

    • IUPAC—Compendium of Analytical Methods for Organometallic Complex Characterization
    • ISO 17025—Analytical Laboratory Competency for Specialty Chemical Manufacturing
    • OECD Good Laboratory Practice (GLP) Guidelines
    • EU REACH Registration for Organometallic Ligands

    Typical usage ratio

    • Ligand forms at 0.1–1 molar ratio with catalytic metal centers; adjusted based on activity and substrate selectivity requirements

    Downstream process integration

    • Engaged during ligand synthesis through O-alkylation, then complexed with transition metal for in situ catalytic runs in batch or continuous flow reactors

    Final product types

    • Pharmaceutical intermediates
    • Agrochemical actives
    • Fine specialty chemicals
    • Polymer-grade monomeric units
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    Certification & Compliance
    More Introduction

    4-(1-Adamantyl)Phenol: Precision Chemistry for Demanding Processes

    Understanding 4-(1-Adamantyl)Phenol from the Manufacturer’s Lens

    4-(1-Adamantyl)Phenol doesn’t get much attention outside technical circles, yet for those who deal with specialty syntheses or develop advanced materials, it stands out for reliability and chemical stability. We spent years examining routes for selective phenol functionalization, only to find that the adamantyl group—attached at the para position—yields properties unique compared to standard phenolic compounds. This chemical offers more than just a reactive aromatic ring; it brings the dense, almost diamond-like stability of adamantane, which influences solubility, melting points, and downstream compatibility for a host of specialty applications.

    The Product at a Glance

    At our site, each kilogram comes off the reactor with a focus on purity and batch consistency. The product typically appears as a crystalline solid, off-white to pale yellow, depending on trace impurities, with melting points hovering near 175°C. We run each batch through rigorous HPLC and NMR characterization. Our standards demand no less than 99% purity, as trace organic residues compromise downstream outcomes in polymers or advanced resins. By overseeing synthesis from raw materials to packaging, we ensure the product stays free from halogenated byproducts, which often complicate waste management for our customers.

    Applications Driven by End-User Needs

    People bring us new use cases every year, but the core market remains in specialty polymer development and pharmaceutical intermediates. Research labs favor 4-(1-Adamantyl)Phenol for its rigid cage structure, useful when engineers seek to increase thermal stability or impart hydrophobicity in end formulations. In epoxide or urethane systems, this structure resists unwanted crosslinking or degradation. We learned early on that, compared to p-tert-butylphenol or plain phenol, the adamantyl derivative yields materials that maintain their physical properties under heat or stress conditions that quickly break down less bulky analogues.

    Comparing with Other Phenolic Compounds

    For perspective, commercial phenols with linear or branched alkyl substituents, like tert-butylphenol, fail to approach the steric bulk or rigidity that the adamantyl group provides. Our chemists observed that, in certain resins and coatings, the adamantyl core almost acts like a built-in plasticizer, controlling flexibility without introducing low molecular weight additives that easily migrate. Physical testing backs this up; glass transition temperatures climb, and solvent resistance improves. In pharmaceutical synthesis, the cage structure can prevent metabolic degradation, prolonging the activity or stability of lead compounds. We listen to customer feedback and lab data—the conclusion always points to the adamantyl moiety delivering real-world performance gains.

    Production and Quality Commitments

    Control starts at raw material selection. Adamantane itself presents sourcing headaches, but we built relationships with the right upstream suppliers and keep tight reins on specifications. Our reactors run processes with carefully tuned acid catalysis to ensure para-selectivity. After synthesis, we refine and recrystallize until we reach our target purity. Some product ends up in R&D work, other lots spin off toward high-volume production. No matter the end use, we rely on gas chromatography-mass spectrometry and high-resolution NMR to catch any stray isomers or contaminants.

    We’re equally invested in the logistics. The product never travels in metal drums that can shed particles or react with trace moisture. Instead, each batch goes straight into fluoropolymer-lined containers. Uniform labeling and batch documentation travel with the shipment, giving customers traceability down to operator-level procedures. Our QC lab logs every anomaly, following through on corrective actions instead of stashing problematic lots.

    Supporting Research and Industrial Clients

    Research teams appreciate more than just a steady supply of material. We invite feedback on custom particle sizing or alternate forms, such as micronized powders for polymer compounding or melt-processable pellets for automated reactors. For one client, we tailored granule size to solve dusting issues common with fine crystalline materials. Technical support doesn’t mean scripted answers from a call center. Our chemists answer questions about reactivity, storage, and compatibility based on first-hand process experience. If a scale-up batch deviates from usual melting behavior, we track down root causes, from residual solvents to unforeseen side reactions during customer processing.

    Environmental and Handling Considerations

    4-(1-Adamantyl)Phenol won’t volatilize like lighter phenols, and it holds up well under dry storage. We recommend keeping containers closed and away from direct sunlight to guard against trace oxidation, especially over extended warehouse dwell. Our own staff process material in full containment, using local exhaust and dust control, even though acute toxicity runs low compared to other substituted phenols. Waste handling remains straightforward; non-halogenated waste can often run through DBOF incinerators in compliant jurisdictions. We monitor research into more sustainable synthetic routes, with an eye toward reducing solvent loads and waste byproducts with every campaign.

    Technological and Regulatory Trends Shaping the Field

    Recent years brought heightened scrutiny over residual volatile organics in finished plastics and composites. End-users, especially in electrical and electronics, want assurance that outgassing from phenolic intermediates won’t taint performance in tightly controlled assemblies. Our lab data shows 4-(1-Adamantyl)Phenol delivers lower total organic volatiles compared to its alkylphenol cousins—a fact increasingly cited by large OEM customers. On the regulatory front, REACH and similar frameworks push for detailed declarations of impurities. We document everything above 0.1% and submit updated dossiers with each annual production cycle, keeping customers ahead of audits and certification requirements.

    New R&D projects focus on pushing boundaries of polymer thermal resistance and hydrophobicity, areas where this compound plays a valuable supporting role. Teams developing adhesives or conformal coatings incorporate small amounts to boost resistance without impacting viscosity or cure profiles. In some cases, the rigid adamantyl backbone enables new architectures in star-shaped polymers or dendrimers, which find use in filtration materials and biomedical devices. Our technical team collaborates with researchers exploring these frontiers, sharing insights on what works—and what fails—in the real world.

    Comparisons That Matter on the Production Floor

    Working alongside R&D chemists and production engineers, we compared polymer samples where one batch used traditional branched alkylphenols and another incorporated 4-(1-Adamantyl)Phenol. Mechanical testing and accelerated aging studies revealed fewer micro-cracks, improved retention of mechanical properties, and reduced discoloration under UV exposure in the adamantyl group samples. Customers bring these observations to their own QC teams, who report similar trends during internal evaluations.

    Critically, 4-(1-Adamantyl)Phenol exhibits less tendency toward oxidative yellowing—a common headache for formulators running high-performance resins in optical applications or consumer products with demanding color specs. Direct substitution of standard alkylphenols with this molecule yields clear cost-per-performance advantages, especially as the price differential narrows due to maturation of synthetic routes.

    Chemical Handling and Storage: What Works

    Our facility uses stainless steel and fluoropolymer-lined tanks exclusively during storage and transfer. We learned from early incidents that even trace metal catalysis accelerates degradation in bulk, so our SOPs strictly limit any contact with unapproved surfaces. Every drum ships with a full COA, not a generic sheet, allowing our customers to check actual batch-specific data before use. We recommend storing the material below 30°C and away from sources of high humidity.

    We found a sweet spot in packaging: dense, double-bagged liners inside rigid fiber drums, which block out moisture and reduce static. Customers adopting this practice reported dramatic reductions in caking, leaching, and dust formation—problems that plagued early adopters using single-layer bags or generic containers.

    Collaborative Problem-Solving and Product Development

    Sometimes our clients approach us with unique challenges—formulation problems other suppliers struggled to resolve. A polymer company needed enhanced thermal performance beyond what linear alkylphenols ever delivered. After evaluating several candidates, they settled on 4-(1-Adamantyl)Phenol for its backbone rigidity. Working jointly, we adjusted dosing and testing until the resin achieved a higher resistance to softening and warping at service temperatures above 200°C. The product far outperformed alternatives, extending the final product’s lifespan without tradeoffs in processability.

    Other applications require exacting particle sizes or tailor-made blends. For a large electronics manufacturer, we customized a blend of 4-(1-Adamantyl)Phenol with minor co-monomers to achieve specific dielectric properties. The project required constant dialogue and on-site support, as every processing line poses unique blending and thermal history demands.

    Field Data: Resilience and Reliability

    Field feedback validates our observations time and again. A surface coatings company reported that their commercial clearcoat, with a portion of standard alkylphenol replaced by 4-(1-Adamantyl)Phenol, retained gloss and hardness after accelerated weathering cycles that dulled competing formulations. OEMs in automotive and electronics see fewer warranty claims and longer service intervals as a direct outcome of stable, unreactive phenolic intermediates.

    In pharmaceutical synthesis, customers mention improved yields and fewer downstream purification headaches, mainly due to the adamantyl ring resisting acid- or base-catalyzed rearrangement. Medicinal chemists like the option to add metabolic resilience to active structures without introducing excessive steric hindrance that would block key interactions with biological targets.

    Building Lasting Trust with Production Partners

    Over the years, the best partnerships formed where technical and supply chain teams could rely on unfiltered access to our chemists and plant engineers. We share formulation successes, but also process failures and lessons learned—like how improper solvent selection during phenolylation led to lower yields and difficult purifications. These shared insights help customers avoid costly missteps, and foster a working relationship built on data and trust, not marketing spin.

    Continuous Process Improvements and the Path Forward

    With specialty chemicals, standing still means falling behind. Our R&D group constantly refines synthetic techniques to boost yield and shrink the footprint of process waste. We invest in inline monitoring tools that flag deviations before batches leave the pilot plant. Regular reviews of industry literature uncover new computational methods predicting reactivity and product stability—tools we now use to shorten development cycles for customer pilot projects.

    As demand for higher-performing materials intensifies, finding routes to reduce costs without sacrificing quality remains a guiding principle. We keep a close eye on supply chain risks, learning from past interruptions to pre-qualify alternate raw material sources and shipping lanes. The goal: provide 4-(1-Adamantyl)Phenol with the consistency and responsiveness today’s customers expect, from kilogram pilot runs to multi-metric ton campaigns.

    Using Science and Real-World Experience to Serve the Market

    Decades in the chemical industry taught us that there aren’t shortcuts to earning customer loyalty, especially in high-value specialty materials. We rely on data—melting points, purity assays, field test results—and the honest sharing of process wins and pitfalls. 4-(1-Adamantyl)Phenol may seem niche, but for those pushing the envelope in advanced polymers, coatings, and pharmaceutical intermediates, its impact reaches far beyond the lab bench. Whether your need centers on performance, consistency, or regulatory compliance, we stand ready to discuss technical particulars and help solve production challenges—drawing not only on experience but a commitment to best-in-class chemistry.