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3'-Aminoacetanilide Hydrochloride

    • Product Name 3'-Aminoacetanilide Hydrochloride
    • Alias m-Aminoacetanilide Hydrochloride
    • Einecs 629-543-6
    • 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
    VTB
    Specifications

    HS Code

    786584

    Product Name 3'-Aminoacetanilide Hydrochloride
    Synonyms 3-Acetylaminoaniline hydrochloride
    Cas Number 2368-51-4
    Molecular Formula C8H10ClN2O
    Molecular Weight 186.63 g/mol
    Appearance White to off-white solid
    Melting Point 215-218°C (decomp.)
    Solubility Soluble in water
    Purity Typically ≥98%
    Storage Conditions Store at room temperature, keep tightly closed

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

    Packing & Storage
    Packing The 25g quantity of 3'-Aminoacetanilide Hydrochloride comes in a tightly sealed amber glass bottle with a tamper-evident label.
    Shipping 3'-Aminoacetanilide Hydrochloride is typically shipped in a tightly sealed container, protected from moisture and light. It should be packed in compliance with local and international regulations for chemical transport, including appropriate hazard labeling. Shipping is conducted under ambient conditions, with clear documentation for safe handling and emergency procedures.
    Storage 3'-Aminoacetanilide Hydrochloride should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from moisture and incompatible substances such as strong oxidizers. Protect it from direct sunlight and sources of ignition. Store at room temperature, preferably between 15-25°C, and ensure proper labeling to avoid accidental misuse.
    Application of 3'-Aminoacetanilide Hydrochloride

    Applications of 3'-Aminoacetanilide Hydrochloride in Industrial Manufacturing

    As a direct manufacturer, we supply 3'-Aminoacetanilide Hydrochloride to multiple advanced industrial sectors. Our strict quality controls and established supply channels enable end users to incorporate this intermediate into specialty synthesis workflows and regulated production environments.

    1. Pharmaceutical Intermediate Synthesis

    Pharmaceutical manufacturers use 3'-Aminoacetanilide Hydrochloride as a building block in producing specific active pharmaceutical ingredients (APIs). In this scenario, process teams introduce this intermediate at the coupling or amidation step, often preceding the key heterocyclic ring-forming stages of generics and patented molecules. Its use supports specific purity demands set by regulatory submissions, including low residual solvent profiles and tight control of related substances during scale-up and validation runs. Formulators optimize the loading percentage based on molecular weight comparisons and target yield, balancing excess with purification overhead.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU EudraLex Volume 4 GMP
    • US FDA 21 CFR Part 211
    • Relevant region-specific Drug Master Files (DMF) requirements

    Typical usage ratio

    • 20% to 45% molar ratio in intermediate coupling reactions, with the range adjusted by route efficiency and reaction scale

    Downstream process integration

    • Feed into batch reactors before condensation steps
    • In-situ neutralization or salt-split hydrolysis, followed by filtration and concentration
    • API isolation through solvent exchange or crystallization post-coupling

    Final product types

    • Anti-inflammatory drug intermediates
    • Analgesic and antipyretic agent precursors
    • Heterocyclic active substances
    • Custom fine chemical intermediates for clinical trial materials

    2. Dye and Pigment Manufacturing

    Textile and specialty dye manufacturers adopt 3'-Aminoacetanilide Hydrochloride for the diazotization and subsequent coupling steps in the production of high-fastness azo dyes. This precursor enables tailored chromophore development for applications in synthetic fiber, wool, and technical textile coloration. Production engineers account for color index targets and fastness specifications when determining batch charge quantities, ensuring minimal batch-to-batch variance in shade intensity and stability. Material purity and moisture content are closely monitored, as these directly impact reaction kinetics and filterability in downstream processing.

    Industry compliance standards

    • OEKO-TEX Standard 100 for textile chemical inputs
    • ISO 9001:2015 for pigment and dye quality management
    • ZDHC Manufacturing Restricted Substances List (MRSL)
    • REACH Annex XVII Restrictions for azo compounds

    Typical usage ratio

    • 12% to 35% of the total amine inputs per batch; precise level based on desired diazo component structure and absorption requirement

    Downstream process integration

    • Charging to diazotization vessel under cooled acidic conditions
    • Combining with coupling partners for pigment formation
    • Salt filtration, washing, and spray drying prior to delivery

    Final product types

    • Azo textile dyes for polyester, nylon, and cotton fabrics
    • Disperse dye classes for synthetic fiber blends
    • Engineering colorants for plastics and coatings
    • High-stability pigments for printing inks

    3. Agrochemical Active Ingredient Manufacturing

    The agrochemical industry incorporates 3'-Aminoacetanilide Hydrochloride as an intermediate in the synthesis of certain herbicide and insecticide actives. This input is specifically dosed in the aromatic amination and acylation stages during the creation of substituted aromatic ureas and triazines, supporting product registration and toxicology standards. Engineers adapt process parameters to maximize conversion while minimizing isomer impurity formation, as required under registration dossiers and final formulation QA—especially in multipurpose plants handling both crop protection and microbicide actives.

    Industry compliance standards

    • FAO/WHO Specification and Evaluation of Agricultural Pesticides
    • Global GAP for agrochemical supply chain integrity
    • ISO 17025 for analytical testing in finished product QC
    • Local regulatory approval (e.g., EPA in the United States, China ICAMA)

    Typical usage ratio

    • 18% to 38% on a molar equivalency basis relative to other aromatic amines, varied by the synthetic pathway and product registration specification

    Downstream process integration

    • Charged into reactor vessel during initial amination step
    • Followed by conversion to isocyanate or triazine intermediate
    • Final technical grade active isolation and granulation

    Final product types

    • Aromatic urea herbicides
    • Selective triazine-based crop protection agents
    • Precursor compounds for microbicides and fungicides
    • Technical concentrates for agrochemical formulation plants

    4. Specialty Polymer Modifier Production

    Specialty polymer and resin producers use 3'-Aminoacetanilide Hydrochloride to introduce amino functionality during polymerization of engineered resins, including polyamides and ketone-cured systems. The compound’s controlled reactivity supports process design for adhesion and crosslinking modification, influencing the mechanical and thermal properties required in electronic encapsulants, automotive coatings, and anti-static films. Process engineers fine-tune dosing relative to chain length and desired functional group density, measuring impact on final resin dispersibility, cure kinetics, and color stability.

    Industry compliance standards

    • ISO 14001:2015 for environmental management in polymer processing
    • ASTM D638 for polymer tensile testing
    • RoHS Directive (2011/65/EU) for electronics applications
    • REACH Registration requirements for chemical monomers

    Typical usage ratio

    • 0.5% to 5% w/w as a functional comonomer or chain-end modifier; ratio based on required amine group concentration for end-use

    Downstream process integration

    • Polymerization kettle addition during pre-polymer or oligomer formation
    • Secondary functionalization or curing with hardener additives
    • Extrusion or casting into finished resin shapes

    Final product types

    • Functionalized polyamides for engineering parts
    • Antistatic films and coatings for electronics
    • Modified thermosetting resins for adhesives and encapsulants
    • Paint additives for automotive and industrial finishes
    Free Quote

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    Certification & Compliance
    More Introduction

    3'-Aminoacetanilide Hydrochloride: Shaping Precision in Advanced Synthesis

    Experienced Hands Meet Genuine Chemistry

    Every bell rings in the chemical world for a reason: advances don’t show up out of nowhere, and steady hands behind the reactor matter. Our long days and short nights in the lab aren’t spent staring at spreadsheets or catalogues—our work happens stacked around reactors, glassware, and sample vials, sweating the small stuff. 3'-Aminoacetanilide Hydrochloride didn’t roll out as the result of a trend; it took patient steps, constant QC checks, and hard questions about what users face at the bench and on the production floor.

    Making 3'-Aminoacetanilide Hydrochloride Reliable Batch After Batch

    We’ve handled 3'-Aminoacetanilide Hydrochloride for years. From first handling raw anilines in their pure state to monitoring crystallization curves overnight, we saw how tweaks—even a one-degree shift in temperature—could impact color, solubility, or purity. Every kilogram means discipline, blending technical know-how with steady hands. We focus on water content, opted for robust hydrochloride formation conditions, and spent months firing small test runs before scaling up batch production.

    Not all amidoaniline salts tell the same story. Some appear clean but hide stubborn side-products. Ours has gone through columns, extra washes, and a battery of dissolution and loss-on-drying tests, not because brochures expect it, but because any chemist running a synthesis wants starting materials that behave as advertised.

    Model and In-House Specifications

    We label the current batch under model designation 3AA-HCL22, reflecting the year we finalized our synthesis pathway overhaul. It didn’t matter how the competition designated theirs—we focused on key points that actual users bring up after real bench time. Central checks include appearance (free-flowing crystalline powder), purity (NMR, HPLC at >99.5% on dry basis), and specific chloride content measured by argentometric titration.

    Moisture can spell disaster in multi-step synthesis. Instead of just aiming for standard values, we track Karl Fischer data down to parts per thousand, knowing that even trace water may throw off regioselectivity or yield in sensitive coupling reactions. The hydrochloride salt format means better handling: storage stability jumps up, and dosing becomes much more exact for folks running weight-based additions.

    Everyday Synthesis Challenges: Why This Product Emerged

    We didn’t set out to make another intermediate for the sake of a catalogue boost. Our partners designing dyes, agricultural products, and even a few teams in pharma synthesis all shared the same complaints: the base-free amines shift color, absorb water from the air, and tend to degrade by the time they arrive in a drum. We noticed how the hydrochloride salt kept its pale look, moved smoothly during material handling, and arrived at the lab bench as crisp as it left our warehouse—a difference you only earn with hands-on experience.

    In dyes, the meta-amino functionalization that 3'-Aminoacetanilide brings opens the door to unique azo couplings and direct dye frameworks. Competing products, often stored above 25°C or sampled without proper seal, lose snap and invite degradation. We’ve kept cold-chain options available—not because a spec sheet dictated it, but because we’ve seen too many delayed runs blamed on inferior starting material.

    Real Bench Outcomes—How Chemists Use It

    We talk with chemists who look past sales patter. They want to know if a new batch dissolves at the same rate, if the salt comes off the spoon in a single pour, or if a reaction stalls. The hydrochloride version allows accurate solution-phase dosing, with far better batch homogeneity. The amide linkage, resistant to hydrolysis under mild conditions, enables extended reactivity. We’ve watched several groups use our material for direct aromatic substitutions: whether adding nitro groups, running Sandmeyer chemistry, or coupling onto heterocyclic scaffolds, they reported cleaner isolation and less baseline noise in their analytical traces.

    There’s nothing magic in a chemical that simply arrives clean—except that it does. Out-of-spec batches might foam, clump, or even generate odors; our approach prevents these problems by grooming mother liquors, controlling filter cake dryness, and storing acidified product in light-proof containers. We’ve turned back hundreds of kilos because they didn’t meet the standards we check batch by batch. Clients often call because the product “just worked”—not for lack of pack-in paperwork, but because getting the chemistry right means fewer headaches later.

    Differences From Other Aniline Derivatives

    Several analogues crowd the specialty market: basic 3-Acetamidoaniline, para-isomers, free base acetanilides, and plain aniline hydrochloride. Each brings its quirks to synthesis. The 3'-Aminoacetanilide spine offers a key site for meta-direction, letting synthetic chemists access regions otherwise blocked off with ortho or para isomers. The hydrochloride variant racks up benefits: it resists oxidation better, resists atmospheric moisture, and stores easily for long-term projects. Acetanilide bases, while inexpensive, rarely hold up under the same scrutiny, developing browning or uneven melting after a few weeks open in the lab.

    Free base amidoanilines tend toward oiling or “caking up” on long shelf storage, which leads to weighing inaccuracies and troublesome transfers in glovebox work. Our hydrochloride holds its powder form, cuts static issues, and measures accurately—even in small-scale, glovebox, or preparative chromatography routines. These small details make the difference on the ground.

    Volume Scale, Batch Consistency, and Industrial Thinking

    We run full-scale facilities—reactors large enough to take on pilot plant requests, but tight enough in process control to still serve smaller labs. Each batch run gets retained samples, multiple spot purity checks, and real-world testing in common solvent systems. Users report minimal “dead material” loss in charge-dissolve cycles. Our controlled granulation gives a finished product that tips cleanly from bags or drums without leaving behind stubborn residue, making automated lines and manual scales equally reliable.

    Down to the kilogram, our focus remains on reproducibility. Quarterly, we test legacy batches kept under varied storage conditions. We find little yellowing or off-odor, even after months of warehouse life. This type of data matters more to us than glossy certificates alone; it translates to trusted syntheses for high-value targets, where a failed batch costs serious time and money. We run stability trials and regularly stress our product with extended freeze-thaw and humidity cycling, because over the years, we’ve seen how unpredictable things can get from factory to lab bench.

    Regulatory, Analytical, and Practical Perspective

    Handling a substance that slots into the broader framework of intermediate chemicals means living up to tight compliance. We register every process change and track every analytical result, keeping open records for select clients needing audit trails. Every batch comes through a series of identification and confirmation runs: NMR (proton and carbon), FTIR for amide and aromatic character, and GC-MS for residual solvent and starting material checks.

    Beyond the papers, users see the benefit in cleaner baselines during high-performance tasks, whether those involve condensation reactions, dye-forming azo coupling, or stepwise pharmaceutical lead optimization. Batch-to-batch consistency shows itself in stable melting points, sharply defined TLC spots, and a satisfying lack of off-products, which we’ve learned to value during countless scale-up and purification runs.

    Integrated Partner Approach—Not Just a Box-Shipper

    Chemistry manufacturing stops being routine if you listen to what people in the field go through. Our direct conversations with end-users set our targets: delivery schedules aren’t just set by opening hours, and packaging means more than just weight and volume. Those crimped foil bags and acid-verified plastic drums took years to perfect, safeguarding against both light and errant humidity spikes.

    Technical guidance doesn’t end after delivery. Our teams often troubleshoot side reactions, stepping in when an unfamiliar impurity or reaction stall pops up. It’s not rare for a scientist to call us at late hours because a critical coupling or diazotization failed with material from another source, only to see specs matched and process rescued with our hydrochloride lot. Our responsibility extends further than just shipment.

    Solvent Interaction and Suitability for Various Syntheis Environments

    We repeatedly examine how the product behaves in different system setups. End-users who work in DMF or DMSO for high-polarity couplings cannot afford batch-to-batch variability. Our hydrochloride salt dissolves predictably, granting easy access to both low- and high-ionic strength regimes. For those in aqueous, buffered, or partially organic conditions, we’ve tested shelf stability, absence of precipitate formation, and the ability to recover the amide intact after reaction.

    Some intermediates break down or undergo hydrolysis in less than perfect storage or handling. Through hundreds of experiments, our material maintained its integrity—avoiding common pitfalls such as discoloration or loss of reactivity, which plague the free base and even the technical para isomers. These differences appear small but directly impact the bottom line during scale-ups and process transfers.

    Challenges We’ve Faced—and How They Shaped Product Design

    Not every production run succeeded the first time. Some lots failed at the filtration stage, or carried traces of parent aniline derivatives that clouded up end-user reactions. A few years back, a supplier’s raw material quality dip forced us to invest in extra pre-cleaning and double-chlorination, driving costs up, but necessary for batch integrity. During one hot summer, a shipment stored too long on the dock exposed the risk of cakes forming in untreated drums; continuous investment in moisture-barrier packaging came from that single error.

    We’ve also seen pressure build from tighter regulatory scrutiny, with downstream users expecting full traceability and restrictions on residual solvents. We responded not with compliance out of obligation, but by integrating solvent stripping into our protocol and updating cleaning-in-place rigs, to keep residuals below detection limits. These changes weren’t just for show; regular internal audits turned up issues that only careful, experienced hands could catch before users ever noticed them.

    Sustainable Choices: Long-Term Supply and Environmental Responsibility

    We learned early that reliable manufacturing asks for more than just fast output: consistent upstream supply, clean sourcing of hydrochloric acid, and safe disposal of by-products shape the ground reality of production. Each drum of hydrochloride salt we ship comes from phasing out old solvent-intensive methods, with a clear log of waste minimization and proper neutralization of mother liquors. We also invest in energy efficiency during each stage, keeping the environmental impact low while keeping purity high.

    Long-term partners bring up practical concerns—secure, recurring supply through volatile markets, and predictable delivery. We lock in key raw materials well in advance, maintaining buffer stock and alternate sourcing routes to avoid delays. Security of supply has become just as important as specification, with users relying on steady shipments to maintain their own production schedules.

    Practical Experience on the Floor

    Many years in production reveal that measurement and description only carry weight when outcomes match up. Users talk more about whether they lost time weighing sticky powders, whether a product caked up after a few weeks, or if a key step failed unexpectedly. Our 3'-Aminoacetanilide Hydrochloride stands out not because of abstract claims, but due to the absence of problems: no errant melting, minimal dusting, and resilience against the small but crucial hassles that break workflows.

    We respond to feedback not by writing boilerplate responses, but by revisiting process flows, retraining operators, and double-checking equipment settings—nothing replaces understanding the rhythms of a live plant. The real dividend shows up in site satisfaction, fewer complaints, and smoother troubleshooting upstream of the next step, whether that's dye formulation or route scouting in drug development.

    Why 3'-Aminoacetanilide Hydrochloride Works In Unique Applications

    We’re trusted by manufacturers who push beyond routine syntheses—those working in specialty dyes, agricultural intermediates, and experimental APIs. These teams often need custom functionalities from their backbone chemicals, whether for specific meta substitutions, designing pH-responsive dyes, or prototyping small-molecule scaffolds for SAR studies. The hydrochloride format—consistent, stable, and robust—remains their choice because the alternatives so frequently fail during real-world runs.

    Competitors often focus on minimum spec hits—a melting point range or chromatogram matching the master card. In practice, getting reliable salt formation, staying colorless weeks after the drum is cracked, and minimal foaming in reaction vessels become defining. In head-to-head trials, users found our hydrochloride version gave purer downstream product, easier washing of intermediates, and higher overall conversion, whether scaling to pilot or staying at bench-top.

    Wrapping Experience into Every Batch

    Mass manufacturing should not overwrite attention to detail. We push every lot past the expected endpoints. Adhering to routine only makes sense when you’ve seen how deviation causes setbacks long after the first test run, whether it’s an unexpected ghost peak in the chromatogram or a lost day reworking a failed reaction. Every year, as new application areas emerge—environmental chemistry, materials science, or niche pharma leads—we adapt our analytical and process tools accordingly.

    Our approach is not set by forms or checklists. It’s shaped by late-night clean ups, failed runs, and the satisfaction of seeing someone else’s chemistry succeed without drama. 3'-Aminoacetanilide Hydrochloride may be a small part of a larger pathway, but its reliability, stability, and real-world performance keep it trusted across complex, diverse fields.

    Moving Forward With Real Value

    Our ultimate job is to clear the way for others’ breakthroughs. By eliminating variability at the material level and upcycling every lesson learned from production to delivery, every drum that goes out the door becomes a quiet contributor in someone else’s discovery. We don’t see this as just shipping a product—it’s collaboration born out of years in the trenches, hundreds of conversations, and the discipline to do right by fellow chemists and engineers.

    Anyone can match a set of specifications; genuine benefit comes from standing behind each batch until the last gram is used. For us, the story of 3'-Aminoacetanilide Hydrochloride means doing things right every time, building dependable partnerships, and seeing the best work happen because, upstream, the chemistry genuinely works.