Anhui Liwei Chemical Co., Limited
Products

4-(Benzyloxy)Iphenol


    • Product Name 4-(Benzyloxy)Iphenol
    • Alias 4-Benzyloxyphenol
    • Einecs 242-519-9
    • Mininmum Order 1 g
    • Factory Site Lingwu, Yinchuan, Ningxia, China
    • Price Inquiry sales2@liwei-chem.com
    • Manufacturer Anhui Liwei Chemical Co., Limited
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    662169

    Product Name 4-(Benzyloxy)phenol
    Cas Number 140-29-4
    Molecular Formula C13H12O2
    Molecular Weight 200.24 g/mol
    Appearance White to off-white crystalline powder
    Melting Point 120-124 °C
    Boiling Point 370.8 °C at 760 mmHg
    Density 1.17 g/cm³
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically ≥98%
    Synonyms p-Benzyloxyphenol, 4-Hydroxyphenyl benzyl ether
    Smiles C1=CC=C(C=C1)COC2=CC=C(C=C2)O
    Inchi InChI=1S/C13H12O2/c14-12-8-10-13(11-9-12)15-7-6-4-2-1-3-5-7/h1-12,14H

    As an accredited 4-(Benzyloxy)Iphenol 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 25 grams of 4-(Benzyloxy)phenol, tightly sealed, labeled with chemical name, CAS number, and hazard symbols.
    Shipping 4-(Benzyloxy)phenol is shipped in tightly sealed containers, protected from light and moisture. It is handled as a chemical reagent, following standard safety protocols. The package includes proper hazard labeling and documentation, ensuring compliance with local and international regulations for laboratory chemicals. Delivery is via regulated carriers specialized in hazardous materials.
    Storage 4-(Benzyloxy)phenol should be stored in a tightly sealed container, protected from light, moisture, and air. Store in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers or acids. Keep at room temperature and avoid excessive heat. Proper labeling and secondary containment are recommended to prevent accidental exposure or spillage.
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    Tel: +8615380400285

    Email: sales2@liwei-chem.com

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    Certification & Compliance
    More Introduction

    Introducing 4-(Benzyloxy)phenol: Building Blocks for Precision Synthesis

    From Our Factory Floor to Your Laboratory

    Working in chemical manufacturing introduces us to compounds that truly shape downstream industries. Fewer compounds illustrate this better than 4-(Benzyloxy)phenol. Day after day, production teams in our facility handle the technical dance of preparing this phenolic ether with care, discipline, and thorough monitoring. Chemists will immediately recognize the subtle interplay between the benzyloxy substituent and the phenol core, but from a manufacturing perspective, this molecule requires both expertise and attention on the shop floor. In our daily practice, we see that quality control begins with raw materials — any flaw in purity snowballs through the process, so both incoming benzyl chloride and hydroquinone reach our reactors only after strict checks for contaminants. Even small differences in batch purity can alter reactivity or downstream yield.

    Model and Batch Consistency: The Heart of Reliable Chemistry

    Our model for 4-(Benzyloxy)phenol targets a purity of 99% and above, with intentional focus on minimizing residual solvents and byproducts such as dibenzyl ethers or unreacted starting material. The spectroscopic fingerprint (NMR, IR) is confirmed internally for every batch, not just at the point of dispatch, because trace impurities impair the performance of this compound in pharmaceutical intermediates and specialty polymers. In practice, any deviation — even as small as a shift of a single proton in the spectrum — means an immediate review by our chemists. There is no substitute for real-world monitoring when manufacturing a molecule used as an intermediate in drug synthesis or advanced materials. By addressing quality control as early as possible, we reduce delays, cut down on rework cycles, and establish long-term relationships with customers who need certainty in every delivery.

    Why Do Chemists Choose 4-(Benzyloxy)phenol?

    In the commercial or academic environment, this compound serves as a versatile intermediate, particularly when pathways require a phenol group that must survive a series of synthetic transformations. The benzyl ether group offers protection; it resists acids and alkalis, making selective reactions at other positions possible. Later, gentle hydrogenolysis or treatment with specific reagents cleanly restores the free phenol. In our interaction with customers — from pharmaceutical R&D to technical materials labs — we hear about recurring frustration with phenol handling. Free phenols oxidize fast and form tars, yet when protected by a benzyl group, that risk drops sharply. For instance, we recently supported a peptide synthesis project where selective deprotection was key. Their route required a protected phenol that wouldn’t interfere with coupling steps in an aqueous phase. Our product provided the required stability and was easily deprotected by catalytic transfer hydrogenation, leading to a cleaner final product.

    Not All Benzyloxyphenols Are Created Equal

    Beyond the standard chemical literature, practical synthesis uncovers real differences. The position of substitution — para rather than ortho, for example — can change electronic and solubility properties. 4-(Benzyloxy)phenol, in particular, offers better processability in common organic solvents: dichloromethane, ethyl acetate, and ethanol. Subtle solubility advantages mean that extraction and purification go faster, with smaller volumes of solvent. Our manufacturing process intentionally avoids intermediates that might generate ortho isomers as impurities, relying on controlled temperature protocols and in-process chromatography checks. Colleagues in our lab have run parallel syntheses of both 2- and 4-(Benzyloxy)phenol — only the para isomer provides reliable film quality when used later in photoresist production, a difference visible under UV curing lamps. Nor does it end there. In colorant chemistry, the para isomer contributes to more predictable coupling steps with azo and sulfonate compounds, partly due to resonance stabilization that steers reactivity.

    Handling and Storage: Practical Realities

    Years in the chemical trade teach hard lessons. 4-(Benzyloxy)phenol, while more robust than free phenol, remains sensitive to air and light over long periods. Production shifts keep fresh material flowing, and our packing protocols ensure that moisture and oxygen don’t enter during transfer. Each kilo leaves our plant sealed in moisture-proof, UV-shielded drums, with batch numbers strictly tracked, because a single leaky container can jeopardize an entire synthetic campaign downstream. We hear back from customers who tried bulk storage at uncontrolled room temperatures, only to see color changes and losses in reactivity within weeks. In our daily work, this translates to advice that seems simple: keep the compound at consistent ambient conditions, avoid prolonged exposure to air, and rotate stock on a regular basis.

    Reliable Sourcing: Direct from Manufacturer Insights

    Many laboratories approach us after less successful experiences with intermediaries or repacked materials. These resellers sometimes reprocess, dilute, or relabel batches from multiple origins, raising the likelihood of cross-contamination or incorrect isomer ratios. We handle every batch from start to finish, and our staff chemists perform hands-on spectral analysis before shipping. Our customers find that predictable melting point range, absence of extraneous odors, and clear, pale color are strong indicators of fresh material. Missed steps in packaging or careless transport, often encountered with third-party distributors, promote decomposition. Every day, our plant operators face the reality that maintaining the chain from synthesis to storage directly determines delivered quality; it isn’t just paperwork, but clear evidence in the customer’s own flask.

    Applications That Reward Reliability

    Over the years, our main industrial partners have focused on pharmaceuticals, agrochemicals, specialty polymers, and advanced coatings. In drug synthesis, protecting groups make the difference between a workable sequence and a bottleneck. Benzyloxy protection stands up to hydrogenation, Grignard reactions, and even selective halogenation, but is ultimately easy to remove. A medicinal chemist in our network once compared an entire sequence using methyl-protected phenols instead of benzyloxy: yield dropped 20% by the fourth step, as conditions for deprotection damaged sensitive groups elsewhere. That comparison isn’t theoretical — production teams see the actual cost in hours lost on column purification and compound recovery. In coatings and photoresist manufacture, the reactivity of the 4-position is preferred due to well-documented light absorption profiles, providing greater control during photolithography. These outcomes don’t just live in the brochure; they show up in batch reports and pilot plant successes at the partner’s facility.

    Comparing with Alternatives: What Do You Gain?

    Every protection strategy in multi-step synthesis has its tradeoffs. Tosyl, methyl, and benzyl groups are often candidates. In real-world reactions, the benzyl group confers stability against acidic and basic reagents. We’ve watched a number of development chemists struggle with tosyl-protected phenols, which tend to generate unwanted byproducts under hydrogenation. Methyl-protected analogs resist deprotection, sometimes requiring harsh conditions that demolish the yield of precious material. The cost of equipment downtime and lost starting material starts adding up. It’s on the factory line that the clear advantage becomes evident — we see overall yields rise by 10-15% in sequential reactions compared to methyl or tosyl protection, measured across five years of pilot runs. That difference extends across solvent recovery and waste handling, resulting in tangible savings and consistency.

    Sustainability Is Not Just a Trend

    Modern chemists expect both technical performance and environmental responsibility. Over recent years, we’ve revamped synthetic protocols to minimize waste, replacing chlorinated solvents in purification steps with greener alternatives like ethyl acetate and carefully recycling spent materials. Waste streams containing benzyloxyphenol residues are treated on site using established oxidation methods, capturing volatile organics and preventing environmental discharge. Such measures only gain real impact when embedded in daily routines, supported by team training and process automation. Auditors and client representatives verify sustainability claims directly on our plant floor. Through years of investment, our output, waste management, and solvent recovery have all improved measurably. Our product has found use in pharmaceutical and materials science projects where regulatory compliance with REACH and region-specific guidelines is a mandatory starting point, not an afterthought.

    A Focus on People and Process

    A well-run chemical plant depends on more than equipment or access to raw materials. Real consistency comes from people. Every week, our production team, quality assurance staff, and logistics crew join in cross-check meetings, reviewing near-misses and updating standard operating procedures as new information accumulates. More than any certificate, the advice of an experienced technician who has seen phenol batch crystallization hundreds of times shapes the end result. Our partners rely on such details, often reaching out directly for insights about subtle hints of degradation or best practices for re-dissolving product in scale-up operations. We’ve even developed custom formulations for customers struggling with solubility in mixed aqueous-organic phases, drawing on decades of troubleshooting atypical solvent scenarios. This culture of direct, technical communication strengthens trust and delivers measurable results — shorter trouble-shooting cycles, fewer failed syntheses, higher yields at scale.

    Supporting Global Supply Chains, One Batch at a Time

    Worldwide supply chain disruptions have taught tough lessons about diversified sourcing and the value of a direct line to the original manufacturer. For specialty chemicals like 4-(Benzyloxy)phenol, delays or substitutions can derail research timelines, stalled pilot lines, or new product introductions. Our logistics team has adapted by working closely with freight professionals, customs agents, and downstream warehouses to ensure every consignment arrives on time and in the correct condition. Temperature loggers and humidity indicators accompany overseas shipments; these aren’t afterthoughts but a direct response to real-life customer feedback about product arrival status. By tracking every shipment, we anticipate issues — including customs holdups or transit delays — well before they become barriers. The value of this effort becomes real on the feedback calls we field each month, with stories of recovered time and preserved project budgets. Having products leave our facility in precisely the condition required by the end-user is no longer optional — it is mission critical.

    Future Directions and Ongoing Improvement

    The road ahead for specialty phenol derivatives isn’t clear-cut. New synthetic routes, recycling protocols, and green chemistry initiatives push producers like us to innovate constantly. Our R&D team works alongside partners in pharmaceutical process development and materials science to tweak reaction conditions, trial new catalysts, and test purification strategies that further reduce emissions and lower energy consumption. Every insight from these collaborations feeds back into routine manufacturing — for example, switching to more selective catalysts reduced waste byproducts by nearly 12% last year and improved throughput per reactor-hour. Our long-term partners benefit directly, as efficiencies at our plant translate to more competitive pricing and supply reliability downstream. We remain open to challenges that motivate further progress, whether adapting to tighter regulatory requirements, integrating digital batch-tracking systems, or developing new grades tailored for emerging applications in electronics or biocompatible materials.

    Learning by Doing: Lessons from Daily Production

    Process chemistry remains an ongoing experiment. Every shift uncovers variables — ambient humidity, tiny shifts in raw material quality, or subtle mixer speeds — that highlight the difference between a good batch and an exceptional one. Our operators routinely gather feedback, logging both anomalies and successes. One of our recent process trials concerned the effect of minor vacuum leaks during crystallization. On detection, we modified seal procedures and cut the occurrence of off-white, impure crystals significantly. It’s the details — checked every day, in real time, and discussed every week — that steadily improve output at every level. These details travel with every order of 4-(Benzyloxy)phenol we ship, a living record of practical experience and continuous improvement.

    Connecting Industry Needs with Chemical Expertise

    The ultimate test of a specialty chemical lies in its consistent, verified, and practical performance in sophisticated applications. From pharma intermediates to custom polymers, our output shapes discoveries and product launches around the world. The trust we have built through years of hands-on manufacturing and direct customer engagement stands behind every shipment. For those looking to solve synthetic challenges or improve reliability in their workflows, 4-(Benzyloxy)phenol delivers more than a specification on paper. It reflects an entire process chain built on genuine chemical expertise, day-to-day commitment, and a drive for better results across generations of chemists.