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2'-Amino-3'-Hydroxyacetophenone

    • Product Name 2'-Amino-3'-Hydroxyacetophenone
    • Einecs 629-099-8
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    791883

    Chemical Name 2'-Amino-3'-Hydroxyacetophenone
    Cas Number 13682-22-9
    Molecular Formula C8H9NO2
    Molecular Weight 151.16 g/mol
    Appearance Light yellow to brown solid
    Melting Point 124-127 °C
    Boiling Point 327.9 °C at 760 mmHg
    Density 1.235 g/cm3
    Solubility Soluble in ethanol, methanol, slightly soluble in water
    Synonyms 2-Amino-3-hydroxyacetophenone
    Pubchem Cid 79566
    Iupac Name 1-(2-amino-3-hydroxyphenyl)ethan-1-one
    Smiles CC(=O)C1=C(C(=CC=C1)N)O
    Storage Condition Store at 2-8°C, protected from light and moisture
    Pka Approximately 9.5 (amino), 10.2 (hydroxy)
    Refractive Index 1.616

    As an accredited 2'-Amino-3'-Hydroxyacetophenone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 250g of 2'-Amino-3'-Hydroxyacetophenone is supplied in a sealed amber glass bottle with a tamper-evident screw cap.
    Shipping 2'-Amino-3'-Hydroxyacetophenone is shipped in a tightly sealed container with appropriate labeling, protected from light, moisture, and incompatible substances. The package follows standard chemical transport regulations, including hazard identification if applicable. Shipped at ambient temperature unless otherwise specified, with accompanying safety data and handling instructions for laboratory or industrial use.
    Storage **2'-Amino-3'-Hydroxyacetophenone** 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 oxidizing agents. Protect the chemical from light and moisture. Ensure proper laboratory labeling and restrict access to authorized personnel. Store at room temperature unless otherwise specified by the manufacturer.
    Application of 2'-Amino-3'-Hydroxyacetophenone

    Applications of 2'-Amino-3'-Hydroxyacetophenone in Industrial Manufacturing

    2'-Amino-3'-Hydroxyacetophenone enables advanced synthesis paths in industrial chemical production. As the original manufacturer, we address the unique needs of key sectors through consistent quality and technical support. Explore major downstream integration routes below.

    1. Pharmaceutical Intermediate for Cephalosporin Antibiotics

    This intermediate plays an essential role in the selective derivatization of the acetophenone core when manufacturing several semi-synthetic cephalosporin antibiotics. Downstream users rely on its aminophenol structure to introduce side chains required for specific antibacterial profiles. Key routes include nucleophilic substitution or condensation with protected β-lactam precursors under controlled temperature and pH. Manufacturers employ validated batch and continuous-flow synthesis under strict GMP controls to achieve pharmacopoeia compliance.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211 (Finished Pharmaceuticals)
    • European Pharmacopoeia Monograph 01/2023:0143
    • USP General Chapter <1092>: Pharmaceutical Impurities

    Typical usage ratio

    • Often 0.7–1.3 molar equivalents per β-lactam core, depending on cephalosporin side chain design; fine-tuned in pilot and scale-up stages for maximum conversion yield

    Downstream process integration

    • Charged directly into the functionalization stage reactor immediately after β-lactam core isolation
    • Participates in either aqueous or mixed solvent systems to optimize reactivity and minimize by-products
    • Consistent in-process controls monitor purity and residual solvent levels prior to final API isolation

    Final product types

    • Cefaclor oral capsules
    • Cefixime injectable powder
    • Cefprozil dry syrup formulations
    • Cefuroxime active pharmaceutical ingredient

    2. Building Block for Industrial Dye and Pigment Synthesis

    This raw material enables downstream synthesis of specialized azo and anthraquinone dyes through controlled diazotization and coupling steps. Dye manufacturers use its ortho-aminophenol moiety for high-affinity chromophore construction, particularly when targeting shades for technical textiles, inkjet inks, and specialty coatings. End users adjust the raw material feed ratio based on desired tinctorial strength, shade, and fastness properties, as well as substrate compatibility.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006
    • ISO 9001:2015-certified Quality Management Systems
    • OEKO-TEX Standard 100 for textile chemicals
    • Restriction of certain azo colorants per EU Directive 2002/61/EC

    Typical usage ratio

    • Typically 1.0–1.2 molar equivalents relative to diazonium salt for azo dye synthesis; adjusted down to 0.6–0.9 for blend pigment formulations or to tailor solubility profiles

    Downstream process integration

    • Added during initial colorant core assembly and diazotization stage under controlled alkaline or acidic reaction conditions
    • Critical for achieving homogeneous chromophore formation and color “lock-in” during pigment precipitation or milling
    • Feeds continuous or batch reactors with temperature and pH adjustment for product-specific shade development

    Final product types

    • Reactive and direct textile dyes
    • High-performance inkjet printing inks
    • UV-stable automotive pigments
    • Color masterbatches for engineering plastics

    3. Analytical Reagent Precursor for Chemical Test Kits

    The selective reactivity of this compound supports downstream production of advanced analytical reagents used in water and food safety test kits. Manufacturers functionalize its aminophenolic group to produce selective complexing agents and chromogenic substrates, which form colored or fluorometric end products on reaction with analytes such as trace heavy metals or ketones. Processing strictly controls trace impurities to avoid assay interference and ensures reagent stability throughout test kit shelf life.

    Industry compliance standards

    • EN ISO/IEC 17025 for chemical testing laboratories
    • EPA Method 200.8 for trace element analysis
    • ASTM D4327-21 for water quality nitrate analysis
    • Good Laboratory Practice (GLP) Principles as per OECD

    Typical usage ratio

    • Generally formulated at 0.02–0.1 wt% in liquid test reagent matrices, adjusted based on assay detection threshold and matrix compatibility

    Downstream process integration

    • Dissolved into the reagent matrix post-synthesis under inert atmosphere to prevent premature oxidation
    • Stabilized with chelating additives for enhanced shelf life and signal stability in field test kits
    • Homogenized prior to dispensing into single-use ampoules or multi-well cartridges

    Final product types

    • Colorimetric water test strips
    • Portable metal ion test kits
    • Food adulteration screening packs
    • Clinical urine analysis cartridges

    4. Precursor for Agrochemical Synthesis (Herbicide Safeners)

    Manufacturers in agrochemicals employ this intermediate to introduce aminophenol motifs into herbicide safener molecules. Specific coupling and cyclization reactions exploit the ortho-substituent pattern to deliver target selectivity in compounds that reduce phytotoxic risk to crops. Processes integrate this input at the midstream synthesis point, maintaining strict impurity profiles to meet downstream regulatory and field application requirements.

    Industry compliance standards

    • FAO/WHO Specification for Pesticides (FAO/WHO 2016)
    • US EPA 40 CFR Part 180 (Tolerances for Residues of Pesticide Chemicals)
    • ISO 17034:2016 for reference material producer quality
    • GLP (Good Laboratory Practice) for chemical synthesis

    Typical usage ratio

    • Ranges from 1.1–1.5 molar equivalents in condensation stage, guided by the desired product output and the nature of the target safener side chain

    Downstream process integration

    • Incorporated into batch or semi-batch reactors following initial alkylation or acylation reactions
    • Requires precise temperature ramping and controlled base addition to ensure selective cyclization and minimize by-products
    • Pilot scale up processes routinely monitor residual precursor and purity by HPLC or GC-MS

    Final product types

    • Maize herbicide safener active ingredients
    • Pre-mix formulation components for selective post-emergence protection
    • Granular and liquid crop protection blends
    • Seed coating additives for cereal crops
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    Certification & Compliance
    More Introduction

    2'-Amino-3'-Hydroxyacetophenone — Practical Insights from Our Manufacturing Bench

    Understanding 2'-Amino-3'-Hydroxyacetophenone

    Many years of daily work in chemical synthesis have shown us where certain specialty intermediates rise above others. 2'-Amino-3'-hydroxyacetophenone stands out as a workhorse in multiple research and industrial fields, especially for scientists pushing beyond the limits of standard acetophenone derivatives. This compound, recognized by chemists for its reliable performance and versatility, builds on the expectations placed on aromatic amines and phenolic ketones. Each unit we produce reflects deliberate choices in reaction control, purification, and packaging, shaped by what chemists in labs and factories actually encounter—not just what’s written on a data sheet.

    What Sets Our Manufacturing Apart

    Working hands-on with aromatic ketones, we know clean, reproducible batches matter more than anything else. Raw technical specs like melting point or molecular weight can’t tell you how a compound behaves in a real synthetic route. From the start, we select only benzene derivatives that meet tough criteria—not just for purity, but for their track record in further chemical transformations. Our facility relies on a series of carefully controlled steps designed to ensure high assay and to minimize impurities that could complicate reactions downstream. Solid-liquid separation, crystallization parameters, and washing techniques all get special attention. Experienced operators regularly check every lot, not just by instrumentation, but by watching how these crystals dissolve, react, and recrystallize. Years of nuanced tweaks go into each production batch before it reaches another chemist’s bench.

    Specifications That Impact Performance

    Each kilogram that leaves our plant demonstrates years of listening to end users, trialing improved process controls, and responding to the real-world variables often missing from spec sheets. We focus on consistent particle size, absence of foreign particulates, and a tight range of moisture content. Our delivered batches run with a typical assay above 99 percent for the target molecule, and side-products get chased down to parts-per-million levels. Residual solvents, if present, stay well below thresholds that might interfere in sensitive downstream steps. This level of control comes from frequent interaction with users—academic researchers, pharmaceutical developers, dye chemists—who depend on their intermediates to never add noise or residue to their complex workflows.

    Role in Synthesis and Research

    Chemists rely on 2'-amino-3'-hydroxyacetophenone as a truly adaptable intermediate. The molecule’s amine and phenolic groups provide two independent handles for selective transformations. One set of users takes advantage of the phenolic –OH to form ether or ester derivatives, while others leverage the –NH2 for building functionalized heterocycles or coupling reactions. In medicinal chemistry programs, this compound often serves as a starting block for exploratory SAR programs, feeding into the development of diverse lead compounds. Research into metal chelates, Schiff bases, and azo dye precursors benefits directly from its dual reactivity. Materials scientists appreciate its ability to introduce both electron-donating and withdrawing effects, helping adjust electronic properties for sensors or polymer-bound catalysts.

    Years spent tailoring batches for both established and exploratory projects have taught us which characteristics of 2'-amino-3'-hydroxyacetophenone make the biggest difference: solubility in polar and some nonpolar solvents, freedom from trace acids or bases, and matched reactivity lot-to-lot. Laboratories focusing on dye development or ligand design come back repeatedly for the stability and reliability they get from our processes.

    Practical Differences From Other Acetophenone Derivatives

    Direct experience with neighboring acetophenone products—the likes of 2'-hydroxyacetophenone, 3'-aminoacetophenone, or unsubstituted parent compounds—illustrates clear distinctions in how 2'-amino-3'-hydroxyacetophenone performs. Standard acetophenone lacks the combination of ortho-amino and meta-hydroxy functionality, which dramatically alters both reactivity and solubility. Substituting only a single group reduces options for selective protection or derivatization. For example, 2'-hydroxyacetophenone tends to act primarily as a phenolic donor, but offers fewer vectors for further elaboration in one synthetic sequence. Add both groups in our product, and you unlock bidentate ligand design, new heterocycle frameworks, and multipoint modification routes without tedious extra protection steps.

    Over the years, we have observed that 2'-amino-3'-hydroxyacetophenone participates in Schiff base formation more readily and yields cleaner products compared to ketones bearing fewer activating groups. Its symmetry and conjugation patterns also support dye formation with deeper color and greater stability—a feature appreciated by dye houses and research groups developing photoactive compounds. Unlike some o-aminophenols, our product resists browning and slow polymerization under standard storage, which keeps both shelf-life and batch-to-batch reproducibility high.

    User-Driven Adjustments: Listening and Adapting

    Manufacturing doesn’t stop at the reactor. Feedback from bench scientists drives frequent tweaks in isolation protocol, drying cycles, and packaging methods. A decade ago, several pharmaceutical partners reported issues with batch-to-batch moisture content. As a result, we implemented gravity-fed drying steps paired with closed-chamber moisture monitoring directly at the packing station, pushing lot uniformity to levels high enough for direct scale-up in syntheses without revalidation. Similar changes followed input from process scale-up teams: better handling for dust-free transfer, switch to antistatic liners, and dual-layer packs for export—to prevent pickup of atmospheric water or cross-contamination.

    Dye researchers and heterocycle specialists requested larger average crystal sizes to reduce clumping and speed up weighing in gloveboxes, while labs on the fine chemical synthesis end asked for ultrafine powder for faster dissolution. Because we never relied solely on spec sheets, adjustments came from real-world feedback, and every change has brought measurable benefits in our own and clients’ synthesis runs.

    Applications Across Sectors

    Aromatic ketone derivatives rarely stay confined to one sector. In pharma, 2'-amino-3'-hydroxyacetophenone starts life as a fragment for advanced heterocycle synthesis, then finds itself drafted into the design of kinase inhibitors, macrocycle libraries, and CNS-active leads. Each multi-step synthesis relies on clean, impurity-free intermediates, so we emphasize not only purity but also freedom from colored byproducts or odorants that can interfere with bioassays or stability testing. Years of consultation with drug discovery teams taught us how unforgiving downstream chemistry can be—one discolored lot wastes weeks of effort, so we tailor every step to eliminate these setbacks before they begin.

    Dyes and pigment industries look for new color bases with unique absorption patterns. Our product’s substitution pattern provides a foundation for deep hues and improved lightfastness. By working directly with dye development labs, we have supplied both fresh and stabilized older lots, and watched the evolution of azo and quinoid dyes with improved properties based on the starting material they chose. Polymers and coatings research groups target bidentate ligation and conjugation introduced through both the amine and hydroxy groups. In each arena, slight changes in impurity profile or crystal habit can spell the difference between a hit and a ruined run. That’s the reason we resist scaling shortcuts that might slip in trace contaminants—even under pressure for higher throughput.

    Day-to-Day Manufacturing Lessons

    Hands-on engagement teaches lessons unavailable from books or safety data sheets. Each ton of 2'-amino-3'-hydroxyacetophenone brings its own mix of variables: aging solvents, raw material lot variations, ambient temperature swings, or shifts in operator technique. The best technical teams don’t just monitor—they adapt, constantly improving filtration, washing, and drying routines. For instance, harsher purification aimed at squeezing out final traces of unwanted isomers can introduce fines or degrade crystal consistency. At the same time, too lenient a protocol leaves pockets of unreacted starting material. Our in-house chemists run side-by-side test reactions from each shift's material, often spotting issues long before advanced analytical instruments register a change.

    The most rewarding feedback comes in the form of cleaner postreaction extracts, faster filtrations, and higher yields for partners in both R&D and plant-scale use. Because of repetitive cycles of improvement in our methods, regular users have come to rely on familiar dissolution profiles, consistent visual appearance, and freedom from foul odor or haze—subtle but critical traits glossed over in surface-level product comparisons.

    Comparing with Market Alternatives

    Direct comparisons with rival products—either domestically or internationally sourced—usually come down to consistency and impurity profile. Cheaper products sometimes show up with hints of side-chain oxidation, residual halides, or blue-tinged discoloration, causing further trouble at the next synthetic step. In high-precision settings, even microscopic amounts of these unwanted impurities spell disaster for projects requiring reliable results.

    Bulk buyers chasing cost alone often learn the hard way that small compromises on quality turn into much larger losses downstream. Some batches from other sources clump under humid conditions, or develop an off-smell indicating ongoing oxidation. Our own long-term clients see the value in repeat performance—every lot matches the last, and every shipment runs through at least two rounds of in-house test syntheses before approval for delivery. This difference in quality translates into lower internal rejection rates, fewer delays in scale-up projects, and greater confidence in meeting both client and regulatory standards.

    Practical Safety and Handling Advice

    Production-scale experience makes practical handling advice second nature. 2'-Amino-3'-hydroxyacetophenone behaves predictably under normal lab and plant conditions, but its dual-reactive centers call for some attention to detail. Years of transferring, blending, and weighing have shown storage in cool, dry conditions prevents caking and formation of colored fines. Even at scale, the compound resists significant air or moisture degradation, but tightly sealed packaging keeps the product white and free-flowing for longer. Fume hoods or general-purpose extraction benches remain advisable due to the molecule’s slight aromatic odor and fine powdery nature—reducing risks of inhalation or cross-contamination. Staff quickly learn dry transfer and controlled scoop techniques prevent both spills and exposure.

    While the compound features no unusual hazards relative to other substituted aromatics, we coach every client on smooth, dust-free operation. Thanks to our repeated test batches and pilot runs, we continuously refine bulk material handling procedures—always balancing throughput and safety. These tips, compiled from years in the field, travel with each batch, helping prevent common pitfalls and supporting both productivity and safety.

    Supporting Innovation: Tailored for Scientists, Not Just Markets

    Millions of tons of generic acetophenones cross borders each year, but in research and high-value synthesis, only a handful of suppliers step up to the needs of innovation. Over the last decade, we watched many projects falter on ingredients sourced without detailed attention to side-product content, process reproducibility, or fine-tuned particle properties. That experience taught us to work alongside users—helping troubleshoot problem spots, recommending alternate routes, and keeping a sharp eye on trends in pharmaceuticals, materials science, and dye chemistry.

    2'-Amino-3'-hydroxyacetophenone continues to draw new interest from research circles. Novel catalysts, enzyme inhibitors, ligands, and colorfast dyes all benefit from starting materials that support invention and avoid introducing fresh challenges. Responding to project feedback, we developed both small- and large-scale production routes, always with an ear to challenges emerging in both academic literature and industrial pilot runs. Every change in our standard protocols—from solvent switchovers to purification upgrades—grew directly out of working side by side with those who use what we make.

    Future Possibilities and Responsive Manufacturing

    Manufacturers who pay close attention observe patterns that shape tomorrow’s products. A recent increase in requests for more finely tuned impurity panels signals a push toward even higher selectivity in both pharmaceutical and dye applications. By deploying newer analytical tracking and operator training, we consistently keep up with moving expectations. The shift toward greener chemistries means developing production timelines that minimize waste and energy use—without giving up the purity guarantees our clients demand.

    Every trial run, every complaint, every compliment pushes our production philosophy. Our team doesn’t see itself as just a provider of one compound among thousands; we see each batch as a continuing conversation with the scientific community. By integrating best practices learned over years—both from routine runs and unexpected surprises—we stay prepared to deliver not just another lot, but a real solution for those aiming to discover something new.

    Conclusion: Making a Difference with Reliable Chemistry

    The story behind each kilogram of 2'-amino-3'-hydroxyacetophenone says as much about modern synthesis as about our own company. Reliable chemicals serve as the backbone for both breakthrough research and dependable manufacturing. Every improvement in process design, every adjustment based on user experience, and every quality standard enforced on our production lines reflects our ongoing commitment to those relying on our product for success. As new fields of application open up, we remain dedicated to supplying the same trusted quality, helping to drive innovation across chemistry, materials science, and industrial technology.