Anhui Liwei Chemical Co., Limited
Products

4-(Hydroxymethyl)-2-Nitrophenol


    • Product Name 4-(Hydroxymethyl)-2-Nitrophenol
    • Alias 4-(Hydroxymethyl)-2-nitroresorcinol
    • Einecs 629-022-9
    • 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

    271485

    Chemical Name 4-(Hydroxymethyl)-2-Nitrophenol
    Molecular Formula C7H7NO4
    Molecular Weight 169.14 g/mol
    Cas Number 4318-56-3
    Appearance Yellow solid
    Melting Point 123-125°C
    Solubility In Water Moderate
    Boiling Point Decomposes before boiling
    Density 1.49 g/cm³ (estimated)
    Smiles C1=CC(=C(C=C1CO)[N+](=O)[O-])O
    Inchi InChI=1S/C7H7NO4/c9-4-5-1-2-6(8(11)12)7(10)3-5/h1-3,9-10H,4H2
    Pka 7.7 (phenolic OH, estimated)

    As an accredited 4-(Hydroxymethyl)-2-Nitrophenol 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-(Hydroxymethyl)-2-Nitrophenol, tightly sealed, with hazard and safety labeling displayed.
    Shipping 4-(Hydroxymethyl)-2-Nitrophenol is shipped in tightly sealed containers to prevent contamination and moisture absorption. It should be packaged according to relevant chemical safety regulations, labeled clearly, and protected from light and heat. Transport must comply with local, national, and international regulations for hazardous materials, ensuring safe and secure delivery.
    Storage 4-(Hydroxymethyl)-2-nitrophenol should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizing or reducing agents. Protect from moisture and sources of ignition. Proper chemical labeling is required, and access should be limited to trained personnel. Store at recommended temperatures, typically between 2–8 °C.
    Free Quote

    Competitive 4-(Hydroxymethyl)-2-Nitrophenol prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615380400285 or mail to sales2@liwei-chem.com.

    We will respond to you as soon as possible.

    Tel: +8615380400285

    Email: sales2@liwei-chem.com

    Get Free Quote of Anhui Liwei Chemical Co., Limited

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    4-(Hydroxymethyl)-2-Nitrophenol: Precision in Chemical Synthesis

    Introduction to 4-(Hydroxymethyl)-2-Nitrophenol

    In the field of chemical manufacturing, the details of a product often define its value to both researchers and industrial users. Over the years, we have worked to deliver specialty chemicals that meet tight quality demands, and 4-(Hydroxymethyl)-2-Nitrophenol holds a particular place in our catalog. The molecule offers a specific blend of reactivity and control, aimed at users requiring selective functionality in both research and scaled production environments. 4-(Hydroxymethyl)-2-Nitrophenol—often sought for its dual hydroxymethyl and nitro groups arranged on the phenol backbone—stands as an example of careful process design, from raw material selection through to drying and packaging.

    Our team produces this compound under carefully monitored reaction conditions because both its purity and its performance depend on tight process controls. This gives our clients reproducibility in their reactions without unexpected byproducts that can stall synthesis or compromise downstream results. We have seen that the choice of starting materials, attention to temperature, and control over pH all play roles in shaping the final product profile. This hands-on manufacturing approach means our material supports areas like dye synthesis, fragrance R&D, and pharmaceutical intermediate development where a stable, well-characterized input is a necessity.

    Physical and Chemical Overview

    Given the molecular structure—bearing both an electron-donating hydroxymethyl group and a nitro group—our 4-(Hydroxymethyl)-2-Nitrophenol exhibits patterns of reactivity that make it more than just a basic chemical intermediate. The nitro group, in particular, sets the stage for downstream reductions, condensations, or couplings that feed into more complex synthetic routes. At the same time, the phenolic hydroxyl offers another vector for derivatization or functionalization. During batch QA, our analytical team checks parameters such as melting point, assay, moisture content, and residual solvents. The crystalline form is important, as it affects both solubility and stability on storage.

    What truly sets our batches apart come from our willingness to sample each lot individually and adjust process steps as required, rather than imposing a one-size-fits-all cycle. Working with this molecule, small differences in time or the sequence of reagent additions shape the impurity profile. Some customers require fluorometric purity for sensitive applications, others look for lot-to-lot assurance over longer time spans; our lab’s data system tracks every batch forward and backward, allowing us to confirm product lineage and spot trends before final release.

    From Batch to Application: Reliability in Performance

    Across many years in the specialty chemicals market, we have found that most of our industrial and academic users don’t simply look for purity figures—they value a clear understanding of what else might be present, and what routine differences in synthesis may mean for their experimental or production needs. In large-scale coupling reactions—such as those crafting azo dyes or pharmaceutical precursors—unknown contaminants frequently delay process qualification, so we favor transparency in every stage from input selection to analytical reporting.

    For users focused on analytical chemistry or fine organic synthesis, water content and trace inorganic residues present recurring concerns. We have designed drying and purification steps to keep moisture below low ppm levels, and we regularly analyze trace metals to anticipate their role as possible reaction poisons. Feedback from users drives incremental process upgrades, and several of our older approaches have shifted due to what we learn from customers who push the material’s boundaries in their own labs.

    Comparing 4-(Hydroxymethyl)-2-Nitrophenol to Similar Phenolic Compounds

    The market offers a wide range of nitrophenols and phenolic derivatives, each with their own functional signatures. In our observation, the addition of the hydroxymethyl group at the para position to nitro (and ortho to phenol) gives this product a degree of selectivity that plain 2-nitrophenol or even 4-nitrophenol can’t match. For processes demanding site-specific derivatization or a leaving group that balances stability against reactivity, our product’s configuration saves work in downstream synthetic planning.

    Clients often ask about using more standard nitrophenol isomers or related compounds with different substituents. While simple nitrophenols remain useful for broader classes of reactions or as colorimetric indicators, they lack the dual-handed reactivity that comes from our molecule’s unique backbone. Our practical comparison work shows that reaction yields and isolation efficiency shift substantially based on the substitution pattern, especially if future transformations involve nucleophilic aromatic substitution or nitro reduction.

    Another point of difference lies in environmental and handling considerations. 4-(Hydroxymethyl)-2-Nitrophenol shares phenolic behavior in terms of moderate toxicity and oxidative sensitivity, though the nitro substituent does introduce additional storage needs as a precaution against heat and light exposure. Our quality control staff recommends dark, cool, dry storage in tightly sealed containers, a procedure shaped by decades of experience handling thousands of kilos in every season.

    End Uses: Research, Industry, and Innovation

    Batches of our 4-(Hydroxymethyl)-2-Nitrophenol often travel into pathways as varied as pigment chemistry, specialty resins, and advanced pharmaceuticals manufacturing. Academic partners use the product in enzyme assay development and mechanistic studies where the combination of a phenolic oxygen and neighboring electron-withdrawing nitro group helps model real-world biochemical processes. One research group, for example, leveraged our material as a synthetic anchor to install uncommon linkers on protein surfaces, which in turn supported drug conjugation studies now published in peer-reviewed journals.

    In industrial settings, some of the largest demand comes from dye and pigment formulation. The precise spatial separation in the molecule supports azo coupling much more cleanly than non-hydroxymethyl relatives, giving brighter colors and better batch uniformity. This product finds use in controlled oxidative conditions for creating polymeric colorants with enhanced fade resistance or solubility profiles, key to textile and plastic coloration. We also supply our product to electronic material developers, who use it as a starting point for specialty photoresists and charge transport materials where tight control over contaminant ions determines device yield.

    Pharmaceutical users turn to 4-(Hydroxymethyl)-2-Nitrophenol as an intermediate towards more sophisticated heterocyclic systems, and the unique substitution pattern streamlines transformations otherwise hampered by less accessible functional groups. Synthesis of certain CNS-active agents or metabolic probes relies on its structure to avoid lengthy protection-deprotection steps. Our support chemists regularly work with clients to troubleshoot routes involving this compound, sharing impurity profile data and insights from lab-scale pilot work.

    Manufacturing: Detail-Driven at Every Step

    Working at scale with specialty chemicals teaches that consistent results only come from consistency at every stage: from raw material traceability to analytical method validation. In our plant, each reactor batch logs the origin, lot, and storage regime for incoming phenol derivatives, acids, and reducing agents. Staff chemists control pH and agitation schedules with real-world context, guided by previous runs as much as by lab notebooks. By investing in dry, filtered nitrogen blanketing through critical reaction steps, we keep out ambient moisture and oxygen, maximizing product yield while minimizing side reactions.

    Post-synthesis, our purification focus doesn’t end with a single recrystallization. We screen for trace carbonyls and reduced byproducts using LC-MS and GC analyses. Packaging is performed under low-humidity conditions, and every drum or flask carries traceability back to a single batch-run document. That traceability lets our support team pull out batch trends at any point—helping customers identify sources of variability or failure, whether in a research-grade pilot or a multi-ton manufacturing campaign.

    From a manufacturer’s perspective, these process and quality investments reflect the way customer expectations have shifted over the last 15 years. Where once an assay and melting point sufficed, our clients today expect to know everything from the trace metal fingerprint to the history of each environmental parameter during synthesis. Our operations are structured to make this possible—building in time for documentation, review, and process adjustment before each shipment leaves the facility.

    Quality Control: Lessons from Real-World Feedback

    Our approach to QA has evolved with each year in production, shaped in large part by customer troubleshooting sessions and growing regulatory scrutiny. Many of our process improvements can be traced to actual use cases where a problem in downstream chemistry pointed directly to a nuance in our own production. For example, during scale-up for a client’s colorant manufacturing, we found that a slightly modified temperature ramp improved the shelf life and color stability of their end product—an insight that now shapes every lot we produce.

    Our internal standards are always informed by what the most demanding end uses require, rather than by minimum compliance. Most QA samples undergo at least two orthogonal analyses against certified reference standards, and our team maintains profiles of all common degradation products so that reporting is complete. We share COAs that track analytical results over time, not just one-off spot tests. As a direct manufacturer, our ability to resolve unexpected concerns quickly depends on detailed records and having in-house expertise to interpret odd results, not just pass or fail based on thresholds.

    The lessons gained from frequent and open customer communication guide our continual refinement efforts. When an academic partner brought attention to a possible trace contaminant interfering with enzyme-labeled assays, the project sparked a detailed route revision—ultimately tightening both our own batch definition and our residual analysis suite. Production-level improvements are not theoretical to us—they show up in higher yields and reduced failures for end users, and so we see this feedback loop as essential, not optional.

    Packaging, Storage, and Logistics: Minimizing Risk Across Borders

    With global shipping routines shaped by climate variations and lead time pressures, our logistical operation extends the care we take in synthesis and analysis. We use specialty HDPE and glass containers designed for chemical compatibility, filling and sealing under local negative pressure to keep out dust and airborne moisture. For clients in humidity-prone regions or with slow inventory turnover, we offer desiccant-pack options and vacuum-sealed liners based on documented feedback about long-term stability.

    Several international clients highlight issues that stem from local storage failures—a problem that our tech support works to address by sharing real-world shelf-life data and performance monitoring protocols. Our shipments include full documentation on recommended handling steps, informed not just by regulatory needs but by reports drawn from customers in climates ranging from desert to monsoon. Each delivery aims to offer material ready for immediate use, whether the shipment lands in a university lab or a multi-ton plant feed system. Over the years, building customer trust through attention to these logistical details has become integral to our way of working.

    Regulatory and Safety Considerations From the Factory Floor

    Handling 4-(Hydroxymethyl)-2-Nitrophenol safely starts long before material leaves the plant. All our warehouse and production technicians receive specialized training focused on the unique chemical risks—combining lessons learned from routine practice with up-to-date industry standards. The nitro group requires care with respect to heat and reducing environments, so each storage and processing area includes systems for spill management, containment, and rapid temperature control. Regular site safety walkthroughs and monitored mitigation plans keep daily handling risk low.

    Our compliance records stretch back to the earliest product introductions. We maintain updated data on regional chemical regulations, hazard labelling, and environmental impact, tracking shifts in UN transport codes and site-specific exposure limits as they are issued. Direct communication channels between plant chemists and in-house regulatory staff allow us to catch issues before they delay a customer’s process. On-site first-aid and fire response procedures, along with regular staff drills, help keep incidents rare. Lessons from any event, no matter how minor, feed into updated protocols and wider training. For every batch delivered, our customers benefit from both the long-term safety history of our plant and the way we integrate the latest regulatory changes into ongoing work.

    Continuous Improvement: Saving Customer Time and Trouble

    Manufacturing chemicals for advanced applications is often a lesson in humility. Unexpected outcomes in downstream processes point the way to meaningful upgrades on our end. Each criticism or support call marks a point for evaluation and improvement; over time, this approach saves us and our clients both time and resources. By establishing supply partnerships grounded in open, detailed dialogue, we have improved buffer selection, dried packaging routines, and analytical targets. These changes grow from real operating experience rather than generic policy.

    Production chemists set concrete goals based on client requests, not abstract industry trends. For some, this has meant introducing extra filtration or tighter assay windows; for others, it has involved flexible batch sizing and fast-track release logistics. The technical backbone of our operation relies as much on trust and shared learning as on instruments and SOPs. This collaborative culture sets our approach apart from bulk commodity operations, and, as a direct result, shapes the product reliability and technical support that customers report back to us as most valuable.

    Product Evolution and Future Directions

    Our continuing work with 4-(Hydroxymethyl)-2-Nitrophenol points to the importance of product stability and predictability as market requirements evolve. Sectors like electronic materials and pharma intermediates demand not just high-purity material, but documentation and lot traceability that allows full transparency over years of business. We have adapted our documentation procedures so clients can trace a given batch back to every critical control point in its manufacture. This traceability covers everything from supplier certificates to internal QA checklists.

    Looking forward, feedback from advanced formulation houses and research organizations continues to drive our innovation. Together with our R&D teams, we have piloted secure sample retention programs and batch-matched documentation packets, tailored for clients running stability or registration studies. While our foundation lies in reliable, high-purity chemicals, the integration of informatics, process analytics, and rapid-response technical support offers a complete ecosystem for end-users. Whether in synthetic chemistry, formulations, or regulatory documentation, our experience as original producers gives us the tools to support growing market complexity without sacrificing individualized attention.

    Final Thoughts: Why Source from the Manufacturer

    Much of what gives value to 4-(Hydroxymethyl)-2-Nitrophenol has less to do with its raw chemical structure, and more to do with the way it’s produced, supported, and documented from day one. Manufacturers hold unique insight into the life history of each batch, tracking process excursions and subtle seasonal shifts that affect outcome. Each kilogram shipped comes backed not just by paperwork, but by a team of hands-on chemists and QA professionals who draw on decades of problem-solving.

    Clients who choose direct sourcing enjoy real-time updates, defect management, and dialog with those responsible for every process decision and test report. From the initial order to repeat shipments, those direct relationships turn our experience into practical productivity for every project. Over years—in lab, pilot, and full industrial settings—we have watched our material translate into fewer delays, improved processes, and deeper customer satisfaction.

    In summary, working with a chemical manufacturer means gaining all the benefits of experience: in synthesis, logistics, compliance, and collaboration. 4-(Hydroxymethyl)-2-Nitrophenol, treated with care and attention at each stage, will continue to serve as a reliable cornerstone for researchers and industry users who value not just a chemical, but an ongoing partnership founded in technical depth and a commitment to continuous improvement.