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HS Code |
845430 |
| Product Name | 3'-Amino-2'-Hydroxyacetophenone Hydrochloride |
| Cas Number | 34610-51-2 |
| Molecular Formula | C8H10ClNO2 |
| Molecular Weight | 187.62 g/mol |
| Appearance | Light yellow to brown powder |
| Melting Point | 200-205°C (dec.) |
| Solubility | Soluble in water |
| Purity | Typically ≥98% |
| Storage Temperature | 2-8°C |
| Synonyms | 2-Hydroxy-3-aminoacetophenone hydrochloride |
| Smiles | CC(=O)C1=C(N)C=CC(=C1)O.Cl |
| Inchikey | FWXOXMGDJYNHSU-UHFFFAOYSA-N |
As an accredited 3'-Amino-2'-Hydroxyacetophenone Hydrochloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The product is packaged in a 5g amber glass bottle, securely sealed, and labeled with chemical name, quantity, and safety information. |
| Shipping | **Shipping Description:** 3'-Amino-2'-Hydroxyacetophenone Hydrochloride is shipped in sealed, labeled containers with proper hazard identification. It is protected from moisture, light, and extreme temperatures. Handling follows safety guidelines for chemicals, and it is transported according to local and international regulations for chemical substances. Ensure secondary containment to prevent leaks during transit. |
| Storage | 3'-Amino-2'-Hydroxyacetophenone Hydrochloride should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizing agents. Protect it from light and moisture. Store at room temperature, preferably between 15°C and 25°C, and ensure the storage area is appropriately labeled and secure from unauthorized access. |
Applications of 3'-Amino-2'-Hydroxyacetophenone Hydrochloride in Industrial ManufacturingAs an original manufacturer specializing in aromatic intermediates, we supply 3'-Amino-2'-Hydroxyacetophenone Hydrochloride for a select range of industrial uses. The following sections outline primary downstream applications, with detailed information on compliance, formulation, integration, and finished goods produced with this specialty raw material. 1. Pharmaceutical API Synthesis (Cephalosporin Side Chain Intermediate)Major pharmaceutical companies use this compound as a key intermediate in the synthesis of advanced cephalosporin antibiotics. The molecule’s functional groups allow selective acylation and condensation in semi-synthetic API production. Manufacturers require high-purity material for upstream side chain modification steps, directly impacting product yield and impurity profiles according to pharmaceutical development standards. Industry compliance standards
Typical usage ratio
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2. Manufacturing of Specialty Azo Dyes for Textile PrintingDye manufacturers utilize this intermediate for the targeted synthesis of high-performance azo dyes. Its amino and hydroxy functional groups enable controlled diazotization and coupling processes to generate chromophores with improved fastness. End-users in the textile industry specify batch purity and process suitability for consistent color quality in digital or rotary textile printing applications. Industry compliance standards
Typical usage ratio
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3. Fine Chemical Production: Agrochemical IntermediateAgrochemical formulators deploy this compound as a building block in the design of selective herbicides and fungicides. Its ortho-hydroxy and para-amino positions offer routes for further substitution, applicable to phenoxyacetic acid and acetanilide derivative synthesis. Product selection focuses on impurity controls and reactivity, as end formulations must comply with global crop protection standards. Industry compliance standards
Typical usage ratio
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4. Synthesis of Fluorescent Markers for Biomedical ResearchLife sciences companies process this specialty intermediate to create custom fluorescent probe molecules. Its electron-rich core enables functionalization through etherification or diazo coupling, supporting the design of highly sensitive analytical markers. Strict quality specifications apply, as marker performance influences detection sensitivity and specificity in research assays. Industry compliance standards
Typical usage ratio
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5. Advanced Material Research: Precursors for Polymeric Resin ModificationPolymer and advanced material enterprises investigate this specialty hydrochloride as a reactive precursor for resin modification. Its functional groups allow covalent incorporation into epoxy and phenolic resin matrices, adjusting crosslinking density and introducing targeted hydrophilicity. Precise process control is essential to deliver reliable resin batch qualities for electronics and coatings markets. Industry compliance standards
Typical usage ratio
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At our facility, we have worked with many fine chemicals, but 3'-Amino-2'-Hydroxyacetophenone Hydrochloride stands out as a key intermediate with a particular relevance in specialty synthesis. Our history with this compound goes back years, and those years have provided a clear perspective on what sets it apart both in daily operations and in practical usage.
3'-Amino-2'-Hydroxyacetophenone Hydrochloride has earned respect among researchers for its unique reactivity. The molecule carries both an amino group and a hydroxy group in precise positions on the acetophenone core, which creates interesting opportunities for further transformation. The hydrochloride form improves the handling of the compound, minimizing dust and improving material flow across the production floor. Merely glancing at the raw crystals, you notice the distinction from acetophenone precursors that lack such functional intensification.
From a process chemistry standpoint, the modification steps leading to the hydrochloride salt demand constant vigilance over moisture levels. Too much humidity and the powder may cake; too little and static builds—less trivial concerns in bulk manufacturing than they might seem in a laboratory notebook. Routine analysis confirms the hydrochloride’s stability in proper packaging, giving researchers confidence their material stores well until used.
Our lot records document that subtle differences in the synthesis or purification step produce batches that look identical but handle differently in downstream reactions. With time, we’ve built protocols that spot these minor variations early, reducing surprises at the bench or during scale-up. While the amino and hydroxy groups both add complexity, they also provide reaction points. As such, 3'-Amino-2'-Hydroxyacetophenone Hydrochloride often finds a place in pharmaceuticals and dyes, where selectivity can make or break a project.
Not long ago, a client reported a drop in expected conversion during amide coupling. Working through the batch history, we discovered a trace of residual solvent—not enough to flag on a simple assay, enough to impact a sensitive reaction. This sort of issue inspires ongoing investment in equipment and staff training, not just end-testing but throughout plant operations. Familiarity with the quirks of ingredients like this hydrochloride helps avoid headaches later down the line.
Our typical 3'-Amino-2'-Hydroxyacetophenone Hydrochloride batches come as a light yellowish crystalline powder. Chemical purity is measured with HPLC, and residual solvents are tracked by GC-MS. Particle size distribution matters too; finer powders blend more rapidly, but tend to absorb atmospheric moisture faster. Each of these details matters because downstream users depend on predictable results from each container.
Package design also shapes handling. Larger containers tend to experience more compaction, so we use medium-sized drums lined with moisture barriers. Forklifts may speed up movement, but staff are trained to keep drums upright and shaded from excess heat. We have automated much of the weighing process, reducing direct operator contact and maintaining a cleaner transfer.
Our experience shows that chemists gravitate toward this hydrochloride variant when they want a reliable path to more complex molecules. Some prefer the base, 3'-Amino-2'-Hydroxyacetophenone free form, but the salt improves aqueous solubility significantly. This becomes a clear advantage in multi-step or high-throughput operations; less time is spent dissolving or dispersing the material, more time is spent synthesizing what really matters.
Compared with similar building blocks, the presence of both the amino and hydroxy group—especially at these positions—widens the palette of what can be constructed. With only an amino or only a hydroxy group, one loses either the nucleophilicity or the dimensional control needed for many aromatic substitutions. For example, as a precursor for quinoline or benzoxazine derivatives, this compound saves extra steps. Less time spent tweaking conditions, more time pushing boundaries.
On our floor, one often underestimated variable involves the way moisture interacts with this salt. Early batches sometimes clumped or developed a characteristic odor over prolonged storage. Those lessons shaped today’s approach: every bag is filled under controlled humidity, with regular monitoring and batch-leveled packing. Colleagues in R&D now report far fewer issues when opening material stored for months.
The different physical forms that can arise during the drying stage make repeatability a pressing challenge. Slight shifts in oven temperatures or airflow lead to different crystal habits—affecting everything from scoopability to homogeneity in blends. Production leads now calibrate dryers closely and log inspection notes daily, not just weekly. This investment in feedback loops goes beyond compliance; it reflects the pride and stubbornness of our plant team in delivering what’s promised.
Would-be alternatives include simple acetophenones, or derivatives such as 4'-amino-2'-hydroxyacetophenone. While each has its place, ours offers a balance of functional sites without cramming too many groups onto the aromatic ring, which can lead to unforeseen impurities or drop-offs in yield. We have seen customers try to substitute cheaper mono-functional analogs, only to report more purification steps, lower selectivity, or harsher conditions needed in their syntheses.
Within hydrochloride salts, not all are created equal. Some compounds show high hygroscopicity, quickly absorbing atmospheric moisture and turning syrupy. Through careful crystallization, our product resists that fate, holding its powdered integrity well under reasonable storage. That’s been a quiet win for shipping and long-term storage, and it means fewer surprises for those further down the chain.
A particularly telling comparison involves the interplay of reactivity and stability. Free base forms tend to oxidize or discolour faster, especially if handled in the open air. By contrast, this hydrochloride salt holds up far better across a broader range of transportation and storage environments. For projects with timelines of several months or shipments that cross varying climates, this difference can be worth days—and unnecessary headaches.
Pharmaceutical process engineers and dye formulators have both pulled us aside in the past to discuss the single biggest draw: selective transformations. The positioning of the functional groups reduces off-path reactivity, increasing the speed and clarity of downstream separations. This translates into more consistent pilot runs and less time spent on despised column purifications. In exploratory synthesis, teams gravitate toward reagents that perform without constant troubleshooting, and our field calls reflect this trend.
Another key lesson involves regulatory compliance. As a manufacturer, we don’t control what others claim—but our own material is tracked batch by batch in line with evolving safety regulations. Reliable supply chains hinge on more than just specification sheets; thorough records, transparent QA, and responsive support combine to keep project managers at ease. Even minor changes to raw material sources or process adjustments are communicated promptly, reflecting long-standing relationships with clients who value stability and transparency above all else.
Every time we trial small changes—whether in reactant grade, apparatus configuration, or packaging type—the feedback comes within days, often hours. Minor tweaks in crystallization rates can noticeably adjust particle size, while solvent switching affects both filterability and residual content. We listen to complaints and compliments, seeing them as opportunities to address root causes. More than a few process changes have started with an offhand observation from an operator at the filter table or a loading bay crew member spotting unusual caking. That experience—human eyes and judgement—keeps material quality aligned with real-world use, not just theoretical specs.
Scale brings new challenges. In laboratory glassware, most organic salts behave; in a hundred-kilogram reactor, color formation or subtle exotherms sometimes catch even veterans off guard. We’ve set up simulation runs and installed better in-line monitors, not only to detect but to prevent such hiccups. At scale, a few extra hours confirming batch completion can save days of rework if problems slip by. Compounds like 3'-Amino-2'-Hydroxyacetophenone Hydrochloride, built on layered chemistry, demand this sort of grounded approach.
As global interest in sustainable manufacturing rises, so does scrutiny over how intermediates like this are produced and handled. Byproducts, especially chlorinated waste, require diligent neutralization and recycling or disposal. Years ago, more lenient waste discharge allowed shortcuts, but today’s standards set a higher bar. We monitor effluent chemistry rigorously, with regular audits and upgrades to scrubber systems and waste stream separation, not just to meet standards but to stay ahead. No one wants to see their work undone by regulatory crackdowns upstream.
Personal safety at our facility is consistently reviewed. Our staff know that hydrochloride dust can irritate and gloves are never optional. Dust control, regular aspiration, and enclosed transfer lines limit exposure, and staff training revisits these practices quarterly. Even so, we hear of avoidable accidents at less conscientious plants. It pays to invest up front: healthy teams and stable production go hand in hand.
Our experience with supply disruptions has led us to diversify supplier networks for essentials like acetophenone and ammonia derivatives. Coordination with vendors, not just on price but consistency and contaminants, heads off later complaints and production pauses. We test every new lot, regardless of prior certifications, using our own acceptance criteria before even considering tank or reactor filling. Some raw materials respond surprisingly to slight storage differences; cold chain oversight in winter, humidity control in summer, each play a role in lot-to-lot stability.
Batch documentation is exhaustive. We track starting stoichiometry, reaction completion times, color formation, and mother liquor composition—all as built-in forms, not afterthoughts. These records have rescued teams from recurring problems, forming a kind of institutional memory for troubleshooting complex projects. Over the years, juniors have learned to value these logs as much as the managers do.
One seldom-discussed aspect is the close collaboration between manufacturing, client technical teams, and regulatory reviewers. Calls span topics from solubility issues to secondary reaction pathways exposed only at pilot scale. We have learned not to dismiss small requests or queries, as each conversation uncovers a potential for improvement. Sometimes a standard product meets a novel use—our support engineers thrive on these challenges, using field feedback to refine in-plant conditions or recommend new handling protocols.
Over time, mutual trust grows. Where end-users share issues openly, we adjust processes for clarity and reproducibility, supporting both scientific progress and schedule integrity. No finish line exists: today’s tweak becomes tomorrow’s standard as pharmaceutical and specialty chemical demands evolve.
We approach each production campaign for 3'-Amino-2'-Hydroxyacetophenone Hydrochloride with a mixture of anticipation and hard-earned caution. Market conditions shift, new applications emerge, and regulatory frameworks evolve—each brings opportunities as well as risks. Our ongoing investment in process improvement, contaminant reduction, and transparency positions our offering as reliable and practical. The lessons from the plant floor, distilled into daily routines and long-term infrastructure, give our customers materials they can trust.
Other intermediates come and go in the market, but the need for robust, predictable building blocks remains. Every drum that leaves our doors reflects more than numbers on a specification sheet. It speaks to the experience, mistakes, and improvements of chemical production teams determined to give researchers and formulators their best shot at successful, creative chemistry—without the repeated distraction of unreliable starting points.