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1-(4-Hydroxyphenyl)-1-Butanone

    • Product Name 1-(4-Hydroxyphenyl)-1-Butanone
    • Einecs 240-530-0
    • 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
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    Specifications

    HS Code

    307411

    Chemical Name 1-(4-Hydroxyphenyl)-1-Butanone
    Molecular Formula C10H12O2
    Molecular Weight 164.20 g/mol
    Cas Number 5467-47-2
    Appearance White to off-white crystalline powder
    Melting Point 82-85°C
    Boiling Point 329.8°C at 760 mmHg
    Solubility Slightly soluble in water, soluble in organic solvents
    Density 1.108 g/cm3
    Smiles CCCC(=O)C1=CC=C(C=C1)O
    Pubchem Cid 10103
    Refractive Index 1.546

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

    Packing & Storage
    Packing Amber glass bottle containing 100 grams of 1-(4-Hydroxyphenyl)-1-Butanone, sealed with a screw cap and labeled for laboratory use.
    Shipping 1-(4-Hydroxyphenyl)-1-Butanone is shipped in tightly sealed containers to prevent contamination and moisture exposure. Standard chemical shipping protocols are followed, including appropriate labeling and documentation. The product is typically transported at ambient temperature, with precautions taken to avoid direct sunlight, excessive heat, and physical damage during transit.
    Storage 1-(4-Hydroxyphenyl)-1-butanone should be stored in a tightly sealed container, away from light, moisture, and incompatible substances such as strong oxidizers. Keep it in a cool, dry, and well-ventilated area, ideally at room temperature. Properly label the storage container and ensure that access is limited to trained personnel, following all relevant safety and chemical storage regulations.
    Application of 1-(4-Hydroxyphenyl)-1-Butanone

    Applications of 1-(4-Hydroxyphenyl)-1-Butanone in Industrial Manufacturing

    As the original manufacturer, we supply 1-(4-Hydroxyphenyl)-1-Butanone in large-scale, high-purity batches to support advanced industrial sectors where precision in formulation, regulatory compliance, and consistent quality are critical. Our material integrates directly into key downstream manufacturing stages across demanding industries. The following application scenarios detail exclusive, validated uses based on real market demand, with a focus on formulation standards, process integration, and final goods produced.

    1. Fragrance and Aroma Compound Synthesis

    Leading perfumery and flavor houses use our product as a foundational synthetic intermediate for creating musk and woody notes. Its phenolic and ketone structure ensures targeted reaction pathways for macrocyclic musk and complex aroma accord bases. QC teams in these plants check batch traceability under strict IFRA compliance for safe consumer exposure levels.

    Industry compliance standards

    • International Fragrance Association (IFRA) Standards
    • ISO 9235: Aromatic Natural Raw Materials & Derivatives
    • REACH Annex XVII (restrictions for fragrance substances)
    • EU CLP Regulation for safe labeling

    Typical usage ratio

    • Introduced at 0.2%–2.5% in aroma concentrate formulations. Labs adjust loading rate depending on product type: higher inclusion for base notes, lower for microencapsulated formulations due to release curve requirements.

    Downstream process integration

    • Charged into condensation or acylation reactors in the musk synthesis process step
    • Pre-blending occurs with fixatives prior to bulk mixing
    • Material undergoes solvent-based extraction followed by purification before final blending and QC.

    Final product types

    • Fine fragrance oils for perfume manufacturing
    • Flavoring agents for oral care products
    • Functional fragrances for home & personal care (candles, diffusers, air fresheners)
    • Microencapsulated aroma granules for detergents

    2. Pharmaceutical Intermediate for Nonsteroidal Drugs

    In pharmaceutical API (active pharmaceutical ingredient) synthesis, our material acts as a building block for specific NSAID (Nonsteroidal Anti-Inflammatory Drug) precursor molecules. Handling meets cGMP requirements with stringent in-process controls on trace impurities and heavy metal content. Our QC release documentation aligns precisely with regulatory audit requirements for beta-ketone intermediates.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP/NF Monographs (applicable for relevant APIs)
    • EDQM CEP (Certificate of Suitability) submission for EU market supply
    • FDA DMF (Drug Master File) referencing

    Typical usage ratio

    • Feeds into reaction streams at 0.5–1.0 molar equivalents as required for pharmaceutical intermediate assembly. Chemists fine-tune admit rate based on desired yield and side product minimization downstream.

    Downstream process integration

    • Dosed directly in batch or flow reactors for aldol condensation with aromatic aldehydes
    • Subjected to catalytic hydrogenation before final API crystallization step
    • QC performed on both intermediate and final synthesis run for purity and residual solvent control

    Final product types

    • Ketoprofen and derivative NSAID APIs
    • Pharmaceutical grade intermediates for anti-inflammatory therapy
    • Bulk API crystal forms for downstream tableting and encapsulation

    3. Polymer Additive in Specialty Coatings and Resins

    Specialty resin producers integrate this material as a polymerization aid for phenolic and ketonic crosslinking during resin curing. It enables targeted modification of molecular weight and rigidity in high-performance coatings for electronics and automotive parts. All supply meets rigorous hazardous materials traceability under downstream ISO and automotive standards.

    Industry compliance standards

    • ISO 9001 & ISO 14001 for quality and environmental management
    • RoHS Directive for electronic coatings
    • Automotive OEM technical specifications for chemical inputs (e.g., VW TL 226)
    • Toy Safety Directive 2009/48/EC for coatings in children’s products

    Typical usage ratio

    • Added at 0.3%–1.0% weight by weight of total resin solids. Adjustments account for end-use durability: automotive topcoats run higher, circuit board varnishes lower to control dielectric properties.

    Downstream process integration

    • Blended in during oligomer stage of resin synthesis, prior to crosslinking agent introduction
    • Dispersed with cosolvents to ensure complete reaction during thermal curing
    • Monitored for conversion rates with in-line FTIR or HPLC analytical checks

    Final product types

    • Protective automotive paints and clear coats
    • Electronic conformal coatings for PCB production
    • UV-cured industrial varnishes
    • Performance-enhanced thermoset molding resins

    4. Precursor in Fine Chemical Synthesis for UV Absorbers

    UV absorber manufacturers use our raw material as a starting compound for synthesizing benzophenone-based light stabilizers in polymers and coatings. Careful stoichiometric addition ensures efficient conversion with minimal by-products, especially when producing high-transparency stabilizers demanded by plastics and automotive glazing.

    Industry compliance standards

    • ISO 4582: Methods for exposure to laboratory light sources
    • FDA 21 CFR 177.1520 for polyolefin contact safety
    • EU Directive 2002/72/EC for plastics in food contact
    • REACH pre-registration for UV absorber substances

    Typical usage ratio

    • Integrated at 0.5%–2.0% of the UV stabilizer formulation mass; application chemists vary the charge depending on resin matrix polarity and transparency requirements in the end-product.

    Downstream process integration

    • Fed into condensation reactions under inert conditions; reacted with benzoyl chlorides or acid anhydrides
    • Purified via vacuum distillation before final blending
    • QC by HPLC/GC analysis to ensure conformance with optical absorbance specifications

    Final product types

    • UV stabilizer masterbatches for polymer producers
    • Light-resistant automotive and architectural plastics
    • Outdoor grade acrylic and polycarbonate films
    • High-clarity UV-absorbing coatings

    5. Intermediate for Synthesis of Agrochemical Actives

    Agrochemical formulators employ this substance as a key intermediate for synthesizing select herbicide and fungicide actives where controlled aromatic substitution is essential. Our manufacturing ensures traceability for every batch, meeting agrochemical regulatory filing requirements alongside robust stability and heavy metal controls to minimize environmental impact in field use.

    Industry compliance standards

    • FAO/WHO Specification for Pesticides
    • OECD Guidelines for the Testing of Chemicals
    • EPA 40 CFR Part 180 (residues in food)
    • Regulation (EC) No 1107/2009 - Authorization of Plant Protection Products

    Typical usage ratio

    • Added at 0.8–1.5 molar equivalents in the synthesis step, adjusted by downstream chemists based on required active yield and process efficiency optimization.

    Downstream process integration

    • Introduced during aromatic substitution in multi-step active ingredient manufacture
    • Used in batch synthesis, with inter-stage purification and solvent switches according to downstream process route
    • Monitored for conversion and impurity profile at each critical process control (CPC) point

    Final product types

    • Selective herbicide actives
    • Systemic fungicide intermediates
    • Technical agrochemical concentrates
    • Formulated crop protection end products
    Free Quote

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    Certification & Compliance
    More Introduction

    1-(4-Hydroxyphenyl)-1-Butanone: A Closer Look From the Manufacturer's Perspective

    Understanding the Value of 1-(4-Hydroxyphenyl)-1-Butanone

    From a manufacturer's standpoint, developing high-purity 1-(4-Hydroxyphenyl)-1-Butanone takes no shortcuts. We rely on deep process understanding and precise controls every step of the way, recognizing that even slight deviations during synthesis can alter physical and chemical properties. This compound carries a clean, light-colored crystalline structure, which we preserve through controlled reaction conditions and stringent purification. Through years of hands-on production experience, it has become clear that customers—especially those in the pharmaceutical fragrance and specialty chemicals spaces—expect both predictable performance and consistently reliable sourcing.

    Delivering this compound with a purity above 99% has become our benchmark. Our plant operators measure every batch for moisture, trace metals, and reaction by-products, so our shipments always align with detailed buyer specifications. Particle size and solubility characteristics draw attention too. We fine-tune crystallization to ensure complete dissolution in ethanol and ether, along with excellent processability in downstream syntheses. Our team has learned that some manufacturers using catalytic hydrogenation or high-purity oxidants require even tighter impurity profiles, pushing our purification methods further.

    Specifications That Matter in Real-World Settings

    The most common inquiry from new partners deals with physical consistency—crystal habit, melting behavior, and color clarity. Over time, we have built up robust analytical routines for every outgoing lot: melting point checks, spectroscopic fingerprints, and chromatography for trace organics. Field feedback has shown that small variations in these characteristics affect the performance of our clients’ end products, whether a cosmetic intermediate or a fragrance building block. Stability and low volatility remain critical, particularly for long-term storage or when product inventory moves between climate conditions. Our logistics team ensures packaging supports these requirements, eliminating the contamination risks that can quietly arise from poor container selection.

    We avoid standardizing batch specifications in ways that don’t reflect real manufacturing conditions. Each order goes through a review to match the buyer’s handling techniques and intended application. Some users ask for extra-dry, sieved product for high-vacuum distillations. Others run high-throughput reactors that benefit from immediate solubility and minimal dusting. We observe these practical differences daily, adjusting granulation or adding final dehumidification steps as needed. Our technical staff cross-references historical run data and customer feedback to close the loop from development to large-scale supply.

    Guidance for Proper Utilization

    We see a variety of uses for 1-(4-Hydroxyphenyl)-1-Butanone, often shaped by innovations from research labs and chemical engineers. In fragrance development, it acts as a key precursor, unlocking aromatic profiles not possible with less selectively substituted ketones. Quality-conscious perfumers seek this compound for its specific reactivity, enabling synthesis of complex molecules with reliable yields. Our experience shows that using a lesser-purified competitor product may compromise purity downstream, introducing off-notes or unwanted residuals. This issue affected a major customer who once sourced a lower-grade alternative—one batch of finished scent failed both instrumental and human panel tests. After switching back to our product, their rejection rate dropped, pointing to the subtle but real impact of purity and exact stereochemistry.

    In pharmaceutical research, the hydroxyl group on the aromatic ring opens up synthetic pathways for selective modifications—a feature scientists appreciate for intermediate preparation. Clients working on APIs (Active Pharmaceutical Ingredients) and advanced intermediates find our product fits seamlessly in multi-step syntheses, supporting high conversion rates and clean separations. One pharmaceutical process engineer commented to us on ease of handling, noting minimal dusting during large-scale transfer and clean filtration without recurrent clogging—direct benefits from our tight particle size range and moisture control. These refinements originate from production line experience, where we discovered that small differences in starting material quality can slow or complicate complex syntheses.

    Among specialty chemicals producers, 1-(4-Hydroxyphenyl)-1-Butanone stands out where unique functionalization is necessary. The compound brings together a reactive carbonyl and para-positioned hydroxyl group, opening possibilities for targeted condensation reactions or further functional group manipulation. In our own trials with catalytic alkylations, we observed strong selectivity compared with structurally similar precursors, saving time and reducing product isolation steps. These hands-on results underscore the value of tight process controls at manufacturing sources—a difference buyers notice only after experiencing smoother reactions and higher yields.

    Comparing to Related Products: Critical Differences and Lessons Learned

    Many new entrants to the market ask how this molecule differs from similar phenolic ketones or related chain lengths. As manufacturers, we note the unique handling and chemical reactivity of 1-(4-Hydroxyphenyl)-1-Butanone compared to, for example, 1-(4-Hydroxyphenyl)-2-Propanone or longer alkyl-chain analogues. Small changes in chain length or ring substitution noticeably alter melting points, solubility profiles, and compatibility with key reagents. In early process trials, our operators documented faster reaction start times and more reproducible outcomes with the butanone structure, which we traced to enhanced solubility and lower crystallization energy during processing. Buyers who switched from shorter-chain compounds reported less agglomeration and better recovery in continuous filtration steps.

    From a chemical reactivity perspective, the position of the hydroxyl group and length of the side chain influence selective reductions, condensations, and acylations. In one notable application, a customer in performance polymers tried a structurally similar ketone but achieved incomplete crosslinking. Swapping to our compound improved chain-end functionalization, which increased product stability under temperature cycling. These field experiences reinforce the importance of understanding even subtle structural differences at the molecular scale. For downstream applications demanding fine-tuned performance, substitution with readily available, less tailored phenolic ketones rarely delivers comparable results.

    Direct comparison data collected at our quality control laboratory indicates that impurities present in lower-grade materials—such as unreacted starting phenols or unwanted by-products from side-chain homologation—raise issues in both reactivity and color. For high-purity formulations, these contaminants may act as reaction inhibitors or generate undesired color bodies. Years ago, our facility invested in multilayer purification columns that have largely solved this issue for our primary customers, especially those in color-sensitive product lines.

    Meeting Industry and Regulatory Expectations

    Supplying 1-(4-Hydroxyphenyl)-1-Butanone is more than production volume and output rates. Our regulatory affairs team stays ahead by tracking evolving requirements both domestically and internationally. In the past, we managed a significant update to meet new REACH registration needs, investing in analytical transparency and demonstrating repeatability over years of production records. As manufacturers, we welcome audits and supply transparent chain-of-custody documentation, knowing that downstream users in health, flavor, and fragrance sectors face rising scrutiny.

    Several clients rely on us based on demonstrated compliance with environmental and worker-safety standards—a reflection of our long-held belief that responsible manufacturing strengthens the entire value chain. Within our own plant, closed loop solvent recovery and advanced filtration minimize waste and community impact, ensuring stable operations during supply chain disruptions. Our commitment goes beyond compliance; we actively share best practices during customer visits or technical exchanges, helping partner R&D teams streamline their own safety and environmental programs. Over time, this contributes to trust and recurring partnerships, which mean more than any short-term transactional deal.

    Solving Challenges By Drawing On Experience

    We have observed unique challenges in shipping and shelf life, especially in climates prone to high humidity. To solve issues like agglomeration or color change, we've iterated packaging methods—switching from conventional paper bags to advanced multilayer containers with moisture absorbers. Our technical staff developed a real-time environmental monitoring protocol within our warehouse, so we catch early signs of degradation before shipments leave our facility. Pharmaceutical clients with strict shelf-life requirements frequently request these innovations, finding fewer product returns and smoother regulatory review as a result.

    Chemical compatibility with other batch materials remains another area that benefits from production-side insight. Many of our customers conduct blend tests before scale-up, and we supply detailed data about storage and mixing behavior. We avoid mixing product from different lots unless full analytical reconciliation occurs, since we’ve learned firsthand that inter-lot differences (even minor) can cause unexpected reactions or performance drops. Manufacturing at scale means learning from lots that did not perform as expected, tracing root causes, and transparently communicating about corrective actions.

    Transportation represents a final but critical touchpoint between manufacturer and end user. In an early distribution arrangement, poor temperature control during overseas shipment affected color and crystallinity—prompting a complete overhaul of our logistical approach. Today, we work only with vetted logistics partners who maintain both temperature and humidity controls, along with precise chain-of-custody verification. Direct feedback from end users confirmed fewer failed incoming inspections and steadier performance across seasons.

    Looking Ahead: Innovation and Collaboration in Product Development

    As the demand for high-functionality specialty chemicals grows, we engage our R&D team to push the envelope on cleaner synthesis, energy-efficient production, and discovery of next-generation derivatives. Our chemists routinely conduct structure-activity mapping, screening altered butanone homologues for better reactivity or reduced toxicity. Working closely with university partners and customer research groups, we have taken part in developing proprietary downstream applications based directly on the performance of 1-(4-Hydroxyphenyl)-1-Butanone.

    New requests routinely shape our process. For instance, customers asked for green chemistry alternatives, seeking both lower energy consumption and reduced solvent loads. We responded by piloting continuous-flow synthesis routes and increased solvent recycling, which ultimately reduced our production footprint while preserving product quality. These ongoing collaborations lead us to invest further in plant automation, which boosts reproducibility and drops error rates—benefits that flow directly to the end user.

    Direct Experience: Building Trust Over Time

    Among legacy buyers, trust develops not just from batch-to-batch consistency, but also from transparent conversations about challenges and limitations. We always communicate openly about any procedural adjustments, proactive maintenance schedules, or raw material sourcing issues that could impact lead times or product profiles. Over the years, we have seen markets shift and regulatory pressures rise, but our long-term partners remain loyal due to a shared commitment to both technical excellence and ethical business practices. Several buyer accounts have remained active with us for over a decade, citing both consistent product quality and rapid technical response as chief factors.

    It is not uncommon for us to support end-user troubleshooting, sometimes visiting facilities to identify on-site issues linked to equipment design or off-spec handling. In one case, a customer faced repeated filtration blockages using competitor material. After switching to our batch, and with joint investigation, we traced the problem back to micro-scale impurities not addressed in the previous supplier’s process. Resolving these real-world challenges strengthens the supplier-customer relationship, building a foundation for ongoing success.

    Conclusion: Hands-On Manufacturing Insights Drive Real Results

    As a chemical manufacturer, our perspective on 1-(4-Hydroxyphenyl)-1-Butanone goes beyond simple batch records or data sheets. Each stage—from sourcing raw materials, calibrating reactors, to final quality assessments—carries real implications for downstream applications. Decades of direct involvement inform our approach, leading to continuous process enhancement, open customer collaboration, and deep technical understanding. This boots-on-the-ground experience serves both innovation and reliability, reinforcing the essential role of manufacturing know-how in specialty chemical supply. Buyers looking to achieve specific performance outcomes will find that direct engagement with the manufacturer—grounded in transparency, technical skill, and a shared commitment to quality—yields advantages not captured by generic marketplace descriptions.

    With industry demands evolving, we remain steadfast in adapting our methods while holding firm to the standards that our long-time partners expect. Every improvement, every challenge overcome, comes not just from process automation or equipment upgrades, but from people on the factory floor and technical staff dedicated to continuous learning. That remains the heart of our success in producing the highest quality 1-(4-Hydroxyphenyl)-1-Butanone available to the global marketplace.