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6-Aminocoumarin Hydrochloride

    • Product Name 6-Aminocoumarin Hydrochloride
    • Alias 6-Amino-2H-1-benzopyran-2-one hydrochloride
    • Einecs 686-391-7
    • 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

    185785

    Product Name 6-Aminocoumarin Hydrochloride
    Cas Number 91447-34-4
    Molecular Formula C9H8ClNO2
    Molecular Weight 197.62 g/mol
    Appearance Yellow to orange powder
    Purity Typically ≥98%
    Melting Point Approx. 235-238°C (decomp.)
    Storage Temperature 2-8°C (refrigerated)
    Solubility Soluble in water, organic solvents (e.g., DMSO)
    Application Fluorescent dye, chemical intermediate
    Synonyms 6-Amino-2H-1-benzopyran-2-one hydrochloride
    Inchi Key QWHTRQYKJWZXAN-UHFFFAOYSA-N
    Smiles C1=CC2=C(C=C1)C(=O)OC2N.Cl

    As an accredited 6-Aminocoumarin Hydrochloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 6-Aminocoumarin Hydrochloride, 5g: Supplied in a sealed amber glass bottle with tamper-evident cap, labeled with safety information.
    Shipping 6-Aminocoumarin Hydrochloride is shipped in tightly sealed containers to protect from moisture and light. Packaging complies with chemical safety regulations, and the product is labeled according to hazard and handling guidelines. Transport is typically via ground or air, following standard protocols for non-flammable, non-hazardous chemicals, with safety documentation included.
    Storage 6-Aminocoumarin Hydrochloride should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry place at room temperature, typically between 2–8°C (refrigerated is preferred). Ensure the storage area is well-ventilated and designated for chemicals. Avoid exposure to excessive heat, direct sunlight, and incompatible substances such as strong oxidizers.
    Application of 6-Aminocoumarin Hydrochloride

    Applications of 6-Aminocoumarin Hydrochloride in Industrial Manufacturing

    6-Aminocoumarin Hydrochloride serves a critical role in multiple high-value industrial sectors, where its selective fluorescence and reactive amino functionality are leveraged to develop specialized formulations and complex finished goods. With precise compliance, clear formulation guidance, and reliable integration into modern downstream manufacturing, our material supports the development of advanced products across multiple regulated application environments.

    1. Fluorescent Labeling in Life Science Reagents

    In the production of biochemical analysis kits and molecular diagnostics, manufacturers incorporate 6-Aminocoumarin Hydrochloride as a fluorescent probe, where its stability and high quantum yield support sensitive assays and imaging solutions. Its controlled reactivity enables efficient covalent binding with peptides, oligonucleotides, and antibody fragments during synthetic labeling steps, ensuring reproducibility and lot-to-lot consistency. Lifescience firms implement stringent batch quality control and validated processing workflows to meet international diagnostic reagent certifications.

    Industry compliance standards

    • ISO 13485:2016 (Medical Devices—Quality Management Systems)
    • IVDR (EU 2017/746—In Vitro Diagnostic Regulation)
    • USP/Ph. Eur./JP monograph criteria for reagent materials
    • CLSI EP05/EP06 precision and linearity requirements

    Typical usage ratio

    • 0.01–0.05 mg/mL in final labeling reactions; concentration optimized based on fluorophore brightness and quenching minimization needs relative to target biomolecule load.

    Downstream process integration

    • Enters peptide or DNA labeling steps post-synthesis via carbodiimide or NHS-ester crosslinking; incorporated under mild aqueous or pH-buffered conditions, followed by HPLC or SEC purification of labeled conjugates.

    Final product types

    • Fluorescently labeled antibodies and proteins
    • Molecular beacon probes
    • In vitro diagnostic detection kits
    • Cell imaging reagents

    2. Fluorescent Security Inks for Anti-Counterfeiting

    Security ink manufacturers formulate anti-counterfeiting coatings by introducing 6-Aminocoumarin Hydrochloride as a non-obvious, traceable library component, providing unique emission profiles under UV or specific-wavelength excitation. Its tailored solubility and fine particle dispersion allow stable integration into solvent-based or water-based ink systems, where it provides enduring luminescence for government-issued documents and secure brand packaging. Blending operations include emission spectrum calibration and migration stability validation to conform with regulatory authentication standards.

    Industry compliance standards

    • ISO 14298:2021 (Management of security printing processes)
    • OECD Mutual Acceptance of Data (for migration/safety studies)
    • RoHS Directive 2011/65/EU (for non-toxic additive content)
    • Confidential national banknote authentication standards

    Typical usage ratio

    • 0.1–1.0% w/w relative to total ink formulation; dosage fine-tuned based on substrate absorption properties and required detection threshold under security lamp conditions.

    Downstream process integration

    • Dispersed into resin binder or carrier solvent using high-shear mixing; incorporated before final pigment addition and filtration steps to prevent cross-contamination and preserve fluorescence intensity.

    Final product types

    • Banknote security threads and fibers
    • Passports and ID card coatings
    • High-security product packaging labels
    • Legal stamp and certificate markings

    3. Photoluminescent Polymer Compounds

    Compounders and plastics processors utilize 6-Aminocoumarin Hydrochloride as a specialized additive during masterbatch production to impart controlled photoluminescence in engineering polymers. Its high chemical purity ensures predictable color tuning in thermoplastics and thermosets, supporting targeted emission for electronics housings, instrument bezels, and specialty consumer goods. Raw material integration requires careful control of melt processing temperatures to prevent dye degradation, while downstream quality checks ensure batchwise spectral uniformity within specification limits.

    Industry compliance standards

    • REACH Regulation (EC 1907/2006)—Preregistration and SVHC compliance
    • EN 71-3:2019 (Toy Safety—Migration of chemical elements, if used in toys or consumer goods)
    • UL 94 (flammability rating for finished plastics)
    • RoHS 2011/65/EU Annex II restricted substance content

    Typical usage ratio

    • 0.05–0.20% w/w relative to total polymer weight; adjusted for final part thickness and target luminance criteria defined in product standards sheets.

    Downstream process integration

    • Introduced into twin screw extruder feed hoppers in masterbatch blending; pigment is premixed with carrier resin pellets before extrusion and pelletization. Compounders monitor temperature profiles to control photostability.

    Final product types

    • Luminescent wiring insulation
    • Glow-in-the-dark molded plastic parts
    • Electronic indicator cover plates
    • Photoluminescent signage substrates

    4. Fluorescent Tracing Agents for Environmental Monitoring

    Environmental solution providers rely on 6-Aminocoumarin Hydrochloride as a fluorescent marker in water flow and pollutant migration studies, where its high photostability and low detection limits allow accurate tracing in complex matrices. Process engineers add the marker to targeted sources during site evaluations, then capture and analyze samples to identify migration pathways or dilution curves. Integrating this tracing agent into large-scale monitoring programs requires full documentation for non-toxicological risk and traceability.

    Industry compliance standards

    • OECD 301/302 Biodegradability Guidelines (environmental fate)
    • EPA Method 445.0 (Determination of Chlorophyll and Pheophytin by Fluorescence)
    • Guidelines for Environmental Trace Substances (ISO 17025 laboratory protocols)
    • REACH/TSCA notification for use in monitoring reagents

    Typical usage ratio

    • 1–10 mg/L in tracer release solution; value determined by anticipated sample volume and site-specific dilution factors, with adjustment after pilot trial studies.

    Downstream process integration

    • Dissolved in tracer solution before controlled field release; environmental technicians collect time-sequenced samples from monitoring wells or river points, analyzing by fluorometry to map movement and dispersion.

    Final product types

    • Groundwater tracer kits
    • Pipeline leak detection solutions
    • Environmental monitoring study reagents
    • Hydrological process simulant kits
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    Certification & Compliance
    More Introduction

    6-Aminocoumarin Hydrochloride: A Closer Look from the Manufacturer’s Bench

    Bringing 6-Aminocoumarin Hydrochloride to a consistent, high-purity state sparks its own set of challenges and rewards. In our facility, we watch over every stage, right down to the last filtration. Those who work with organic luminescent dyes or design specialty reagents in pharmaceutical labs probably know what’s at stake. Tiny fluctuations in purity change fluorescence outputs, and small tweaks in crystal formation show up in every downstream application. This compound is not just another coumarin derivative—it is a niche building block, requiring careful attention from raw material sourcing to the final dry product.

    From Synthesis to Ready-for-Use: Inside Our Process

    We produce 6-Aminocoumarin Hydrochloride under controlled conditions, using validated routes that minimize side reactions and cut down on impurities, particularly unwanted isomers and over-chlorinated byproducts. Most synthetic steps favor high selectivity by balancing temperature, pH, and stoichiometry. We avoid pathway shortcuts that might look efficient but end up cluttering the final product with tars or insoluble residues.

    After initial synthesis, we clarify the solution several times before beginning any crystallization. Filtration here goes beyond routine lab work; we operate using calibrated micron-grade filters—caught too many times with blocked filter presses to ever ignore this detail. Solvents get recovered, dried, and analyzed for trace contaminants. At each purification stage, analysts from our own QC lab run thin-layer chromatography, NMR, and HPLC. Batches that fail even by a small margin never hit the packaging room.

    Crystalline Form and Handling Properties

    The hydrochloride salt of 6-Aminocoumarin forms small, pale yellow to off-white crystals, easy to distinguish from the deeper yellow tones of non-salt coumarins or the sometimes oily residues left by certain esterified variants. The choice to supply the hydrochloride over the free base doesn’t just come down to tradition—it’s all about stability. The salt form proves much less hydrophobic, dissolving reliably in polar solvents and water-containing systems. This helps in cell-imaging applications, where rapid dissolution speeds up workflows and makes final concentrations more predictable.

    Powders stay free-flowing with minimal tendency toward caking. Moisture content stays strictly below 0.5% due to our vacuum drying setup, which avoids residual solvent peaks in spectral scans. We pack the product in opaque, sealed glass to prevent breakdown when exposed to ambient light. Our own shipping crew has learned not to cut corners here; a single batch left in clear plastic on a sunny dock can degrade by the time it hits customs. It’s an expensive lesson—one we don’t repeat.

    Analytical Purity and Batch Consistency

    We set purity thresholds noticeably tighter than generic standards. Most external assays require about 98% HPLC purity; we guarantee no less than 99.2%, often reaching up to 99.6% without sacrificing yield. Each run gets graphed against a reference standard archived from the best-performing batch of the year. If a production shift sees a dip, we pull the lot for retesting rather than adjust the paperwork—a habit rooted in past mishaps where a false reading misled researchers at a partner university.

    Water content stays under control with Carl Fisher titration, and chloride levels confirm appropriate salt formation. Residual solvents—especially methanol and dichloromethane—don’t just show up on a compliance form: they matter for every downstream kinetic study. Our experience in project follow-up revealed that even sub-ppb traces can cause odd assay results or trigger regulatory flags for partners in North America and Europe. We keep a library of impurity spectra to reference in joint troubleshooting, knowing a stubborn, recurrent impurity might trace all the way back to a supply chain hiccup.

    Applications and Use Cases from the Field

    Research facilities and development labs use 6-Aminocoumarin Hydrochloride as a starting point for synthesizing new functional dyes, fluorescent tracers, and some niche pharmaceutical intermediates. Its electron-rich amino group is receptive for substitution, acylation, or further coupling. Very few amino-coumarin derivatives offer such a combination of modifiable function and robust fluorescence. Our direct involvement with scale-up projects for photonic and biochemical applications has given us insight into how a small change in batch purity or particle size distribution may skew spectral properties. Every trade-off encountered while producing larger lots—trade-offs between reaction kinetics, final purification, and crystal morphology—shows up in end-user reproducibility studies.

    In fluorometric assays, we have supplied researchers frustrated by autoquenching or spectral overlap due to minute contaminants. Most competitors may not bother about a faint, tailing impurity, yet in our discussions with end-users, these outliers cause unexpected data spikes. Labs using microplate readers, confocal setups, or custom-imaging solutions benefit from our checks on spectral stability. We work with technical leads to fine-tune solubility (hydration levels, choice of counterion, and phase distribution) and avoid unpredictable results in multiplexed or multistage experiments.

    Universities investigating enzyme pathways or cell permeability rely on the compound’s sharp absorption and emission bands, as well as its resilience against photobleaching. Free bases or other salts sometimes underperform under long-term lamp exposure; hydrochloride holds up better for repeat scans. Our ability to custom-mill batches and adjust particle size—sometimes as fine as a few microns—came about in response to challenging requests from a collaborative project in protein-binding studies. Pushing too far in one direction led to clumping; balancing flowability and surface area gets us the sweet spot for most protocols.

    Comparisons With Other Coumarin-Based Compounds

    Across the coumarin spectrum, differences in substitution pattern and salt form shape solubility, reactivity, and optical profiles. The free-base form of 6-aminocoumarin resists dissolution in neutral buffer systems and tends to stick to glassware in small-scale preps, wasting precious material. Other salts—acetates, sulfates, phosphates—each bring their own issues in terms of hydrolytic stability or unwanted IR peaks. Hydrochloride stands up to routine buffer changes, and its fluorescence remains sharp, with emissions in the upper 400-nanometer range.

    Structurally similar compounds may show broader or blue-shifted emission, or undergo partial degradation, delivering unreliable analytics. Substitution at other ring positions, especially with halogens or dialkylamino groups, can increase hydrophobicity or shift spectra, which might work for some engineering projects but pose problems for biochemistry or cell-imaging work. Several customers reached out after abandoning attempts to use methylated or ethylated analogs due to poor water solubility. Their feedback guided us to keep pushing for purity and uniformity in the hydrochloride variant, rather than joining every trend in designer coumarin chemistry.

    The big divide between our offering and a few widely available alternatives lies not in price but in performance and reliability. Lower-purity product—especially from non-specialist traders—often carries side-products from incomplete reactions or cross-contamination in shared reactors. Over time, we learned that even high-grade products from generic suppliers lose stability or darken during storage, especially when repackaged. Our post-shipment monitoring has demonstrated our packaged material maintains color, fluorescence, and response for extended periods without fading or precipitating. Small adjustments in drying and bulk-packing processes, overlooked by most, keep the product at spec after months in a warehouse.

    Quality Control and Assurance: Hands-On Accountability

    Control over every detail—down to the batch number and drying conditions—keeps us accountable and fosters trust with clients. We track each lot from the moment raw materials come through our gates. Staff log every process parameter, and supervisors personally check critical stages. This makes the difference in product consistency and allows robust traceability in case a batch ever needs investigation.

    We have set up side-by-side rechecks, comparing new batches with our established reference lots. Any drift from expected performance in application tests brings us back to the process bench, rather than writing off the result as “within tolerance.” For quality-conscious R&D labs, especially those operating under GLP or seeking publication, our focus on reproducibility makes a real impact, saving lost time and frustration.

    Some of our QC protocols grew out of facing setbacks—occasional missed targets, spectral mismatches, or an unexpected impurity reveal more about a process than a run of flawless results. Openness about these learning moments forms the basis for our continuous improvements. Gradual refinements in filtration, buffer selection, or crystallization scheduling have come from hands-on experience, not just from literature or supplier copy.

    Packing, Shipping, and Storage: Practical Experience Translated to Practice

    Shipping a sensitive powder means more than just checking paperwork. Early on, we shipped in semi-transparent containers by mistake, bleaching the brilliant color before arrival. Delays at customs warehouses with high humidity or poor air conditioning risked clumping, even when the rest of the paperwork passed with flying colors. Now, we ship in darkness-resistant, sealed glass ampoules, with each container purged under nitrogen before sealing. Moisture-absorbing packets keep everything dry.

    We keep storage instructions grounded: product should stay sealed until use, away from major sources of heat or direct sunlight. Our final lots maintain stability at room temperature for extended periods, outlasting most equivalent alternatives sold as “off-the-shelf reagent grade” by bulk traders. On customer request, we recently piloted smaller packaging units for rapid turnaround in multi-site academic studies, minimizing risk of cross-contamination and waste. These changes, drawn from years of feedback, aim to bring reliability from our plant to every lab bench.

    Regulatory, Compliance, and Documentation: Not Just a Checkbox

    Our compliance goes beyond basic certificates. We provide complete batch documentation, including analytical spectra, impurity breakdowns, solvent trace analysis, and a copy of every lot’s moisture and chloride assay. Auditors and procurement specialists often ask pointed questions—for good reason, given the stakes involved with novel research and downstream drug development. We’ve responded by opening our lab doors to partner audits and providing real-time, on-demand analytical detail. Feedback comes straight back to our production tweaks, avoiding lapses and keeping standards moving forward.

    Where documentation from brokers or resellers often trails weeks behind delivery, our own paperwork runs in parallel with each lot, handed over at the moment of shipment. For clients working across government or regulated pharma sectors, traceability makes all the difference when submitting grant applications, securing patents, or passing critical compliance checks. Our team stays ready to walk through any lot data, answering technical reviews with real numbers and case histories from past production runs—not canned responses.

    Why Direct Source Makes the Difference

    Producing in-house gives full visibility into process control and product history. You get answers straight from those who design and tweak the procedures, not third-party marketers reciting specs. Our technical team investigates every reported batch deviation or complaint, drawing on years of lab experience. This hands-on approach means issues rarely recur; root causes get identified and corrected, whether the culprit is a change in a raw material supplier, a subtle pH shift, or a new tank seal.

    We do not rely on a rotating cast of intermediaries or anonymous overseas suppliers. That lets us fine-tune process parameters, listen to real user feedback, and invest in incremental improvements based on observed needs instead of marketing trends. Having walked through many international production audits and joint research projects, our staff engage directly with chemists worldwide. This transparency has become essential, especially as clients raise the bar for data-driven vendor selection.

    Continuous Evolution: Listening and Learning

    No production process is static, and this one is no exception. Techniques that seemed optimal years ago—specific solvent ratios, filtration methods, batch drying times—have shifted as better data emerges from routine analysis and customer feedback. Several refinements took root after discovering subtle shifts in melting point or dissolving speed during accelerated stability tests. Collaborations with downstream users—especially those running compound libraries or automated synthesis platforms—provided new insight into how even small grain size distribution changes affect automation.

    Our R&D staff keeps up with published literature and connects those findings to actionable process changes. Some optimizations call for investment in new equipment or scheduling; others simply require better staff training on the shop floor. Everyone involved, from chemical engineers to logistics, shares knowledge about what works and what needs fresh thinking. That culture of open critique and responsiveness sets us apart, enabling us to adapt more quickly than larger, siloed competitors.

    Looking Ahead: Meeting the Next Generation of Research Goals

    Applications for 6-Aminocoumarin Hydrochloride continue to broaden, especially as fluorescence, tracer, and labeling technologies evolve. We are seeing requests from synthetic biology labs, advanced imaging groups, environmental monitoring R&D, and more. Each new field brings specific demands—some want even tighter ranges on fluorescent lifetime; others need ultra-narrow size fractions or custom packing. We work hard to keep pace, investing in lab-scale and pilot plant upgrades to remain flexible.

    Staying close to our users, from research scientists to plant engineers, keeps us grounded. They let us know when their applications shift, and we respond by tuning our product. By embracing the technical and logistical challenges of a specialized chemical like 6-Aminocoumarin Hydrochloride, we support those on the scientific front lines, helping ideas become discoveries. The trust built on honest feedback and open conversation is just as important as meeting any formal specification: it drives us to improve batch after batch, supporting the progress of every user who depends on reliable, consistent, and high-quality specialty chemicals.