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4-Nitroquinoline N-Oxide

    • Product Name 4-Nitroquinoline N-Oxide
    • Alias 4NQO
    • Einecs 208-950-7
    • 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

    377471

    Chemical Name 4-Nitroquinoline N-Oxide
    Cas Number 56-57-5
    Molecular Formula C9H6N2O3
    Molecular Weight 190.16 g/mol
    Appearance Yellow crystalline powder
    Melting Point 180-188°C
    Solubility Soluble in ethanol, DMSO, slightly soluble in water
    Density 1.51 g/cm³
    Purity Typically ≥98%
    Storage Conditions Store at 2-8°C, keep dry and away from light

    As an accredited 4-Nitroquinoline N-Oxide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle with screw cap, labeled: "4-Nitroquinoline N-Oxide, 5 grams, CAS 56-57-5, for laboratory use only."
    Shipping **4-Nitroquinoline N-Oxide** should be shipped in tightly sealed containers, protected from light and moisture. It requires appropriate hazard labeling due to its toxic and possible mutagenic properties. Transport using secondary containment, following all relevant regulations for hazardous chemicals. Ensure handling by trained personnel and provide relevant safety documentation.
    Storage 4-Nitroquinoline N-Oxide should be stored in a tightly closed container, away from light, heat, and moisture, in a cool, dry, and well-ventilated area. It should be isolated from incompatible materials, such as strong acids or bases and oxidizing agents. Storage must comply with institutional and legal requirements for hazardous chemicals, with clear labeling and access restricted to trained personnel.
    Application of 4-Nitroquinoline N-Oxide

    Applications of 4-Nitroquinoline N-Oxide in Industrial Manufacturing

    As a specialized chemical manufacturer, we support global industrial partners who require high-quality 4-Nitroquinoline N-Oxide for niche synthesis, specialty material research, and advanced downstream formulations. Below are the primary application scenarios with technical details and practical manufacturing perspectives.

    1. DNA Damage Research in Laboratory Reagents

    Research material suppliers and pharmaceutical R&D centers use 4-Nitroquinoline N-Oxide as a model DNA-damaging agent. It acts as a mutagen in cell-based and molecular assays, simulating oxidative DNA lesions. Laboratories utilize this compound to investigate DNA repair pathways and evaluate genotoxicity, critically informing protocol design for molecular biology and toxicology research.

    Industry compliance standards

    • ISO 9001:2015 (Quality management for reagent manufacture)
    • OECD Test Guideline 471 (Bacterial Reverse Mutation Test)
    • NIH Guidelines for Recombinant DNA Research
    • GLP (Good Laboratory Practice) compliance for contract research applications

    Typical usage ratio

    • 1–50 μM concentration in in vitro cell assay systems
    • 0.1–10 mg/kg body weight when applied in animal studies; trial-dependent and adjusted by protocol

    Downstream process integration

    • Added as a standardized mutagen during assay setup in laboratory workflow
    • Included in positive control groups for DNA damage or repair evaluation panels

    Final product types

    • Research reference kits for DNA damage studies
    • Ready-to-use mutagen solutions for genetic toxicology
    • Positive control vials for biological assay manufacturers
    • Contract research reagent supplies for CROs

    2. Synthesis of Heterocyclic Pharmaceutical Intermediates

    API manufacturers utilize 4-Nitroquinoline N-Oxide as a starting reactant or intermediate for synthesizing complex heterocyclic scaffolds. Its reactive quinoline core enables regioselective modifications in multi-step routes such as nitration, reduction, amination, or ring closure. These steps serve targeted synthesis of kinase inhibitors and antineoplastic agents in process development and commercial API manufacture.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • United States Pharmacopeia (USP) standards for intermediate synthesis
    • European Pharmacopeia (Ph. Eur.) regulations for impurity profiling
    • EDQM Certificate of Suitability (CEP) requirements for APIs containing synthetic intermediates

    Typical usage ratio

    • Varies from 0.1–5 molar equivalents based on synthetic step and process optimization
    • Adjusted according to desired yield and downstream purification needs

    Downstream process integration

    • Serves as the initial or secondary building block in multi-step API synthesis
    • Subjected to controlled reduction, substitution, or cyclization for target active structure assembly

    Final product types

    • Heterocyclic drug intermediates
    • Kinase inhibitor cores
    • Antitumor agent intermediates
    • Quinoline-derivative scaffolds for investigational new drugs

    3. Industrial Dye and Pigment Synthesis

    Specialty chemical producers incorporate 4-Nitroquinoline N-Oxide in the development of advanced pigments and colorants. It operates as a functional group introducer allowing the incorporation of nitro-quinoline motifs into dye structures. This results in pigments with improved photostability and colorfastness needed for high-durability coatings and specialty inks.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006 compliance for pigment ingredients
    • ISO 14001:2015 (Environmental management for dye synthesis)
    • ASTM D4303 (Lightfastness of pigments used in coatings)
    • OEKO-TEX Standard 100 for textile applications

    Typical usage ratio

    • 0.5–2 molar equivalents in pigment precursor reactions
    • Adjusted based on desired chromophore intensity and downstream analytical purity

    Downstream process integration

    • Introduced during the azo-coupling or ring functionalization step in pigment synthesis
    • Subjected to final purification to control colorant grade and consistency

    Final product types

    • Specialty printing inks
    • Industrial dye concentrates
    • High-performance pigment dispersions
    • Functional colorants for coatings

    4. Chemical Carcinogenesis Assays for Safety Evaluation

    Chemical producers and toxicology service providers use 4-Nitroquinoline N-Oxide to simulate carcinogenic exposures in controlled laboratory studies. Application includes standard carcinogenesis bioassays in rodents and mechanistic studies in tissue cultures to evaluate cancer risk for new compound registration and regulatory submissions.

    Industry compliance standards

    • OECD Guidelines for the Testing of Chemicals (TG 451, Carcinogenicity Studies)
    • GLP (Good Laboratory Practice) for toxicity laboratories
    • ISO/IEC 17025 (Testing laboratory accreditation including chemical safety assessments)
    • IARC Monographs (International Agency for Research on Cancer recommendations for carcinogen use)

    Typical usage ratio

    • 0.1–20 mg/kg body weight in animal models, protocol-specific
    • Concentration adjustments for in vitro models according to cell sensitivity and time exposure

    Downstream process integration

    • Administered as a known chemical carcinogen for positive control arms in chronic exposure studies
    • Supplied as a standard mutagen for regulatory submission packages on substance evaluation

    Final product types

    • Certified laboratory assay kits for carcinogenicity testing
    • Validated toxicology testing panels
    • Research reference substances for safety assessment labs
    • Positive control reagents for regulatory compliance

    5. Genotoxicity Reference Agent for Food Safety Assessment

    National reference laboratories, food additive producers, and third-party testing services deploy 4-Nitroquinoline N-Oxide as a standardized positive control in food mutagenicity assays. Its application helps validate Ames tests and mixed-function oxidase systems that detect genotoxic contaminants, as required by global food safety authorities.

    Industry compliance standards

    • Codex Alimentarius General Standard for Food Additives (GSFA)
    • OECD Test Guideline 471 and 487 for mutagenicity and genotoxicity
    • ISO 17034 for reference material producers
    • FSSC 22000 (Food Safety System Certification)

    Typical usage ratio

    • 0.5–5 μg/plate in Ames tests
    • Slightly higher concentrations in metabolic activation systems, customized for matrix

    Downstream process integration

    • Introduced as a reference mutation inducer during positive control test setup
    • Dosed into food simulant matrices for trace-level detection tool validation

    Final product types

    • Genotoxicity testing kits for food industry
    • Reference chemical standards for laboratory quality systems
    • Positive control products for third-party safety assessment
    • Ames test panels certified for regulatory submissions
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    Certification & Compliance
    More Introduction

    Our Experience with 4-Nitroquinoline N-Oxide: A Closer Look at a Powerful Research Compound

    Introduction

    After years of hands-on production, 4-Nitroquinoline N-Oxide (4NQO) stands out in our synthesis lineup. Known in the lab as an efficient mutagen, its structure, C9H6N2O3, offers a unique nitro-quinoline backbone. Plenty of customers come through our doors looking for a compound that delivers reliable results in genotoxicity and DNA damage studies. I have watched the demand for quality 4NQO grow, especially where researchers want cleaner results, tighter reproducibility, and the reassurance that each lot remains consistent from batch to batch.

    Chemists who visit our facility often comment on the purity differences between our output and lower-tier products. Years in chemical synthesis have shown us that purity drives experimental clarity. Even minor variations in byproduct concentration impact cell-based assays or mutagenesis screens. Our typical 4NQO specification includes an assay ≥ 98% by HPLC, moisture less than 1%, and batch-to-batch identity checks by NMR and FTIR. Laboratories carrying out sensitive molecular biology research rely on us to catch even the subtlest impurities.

    Applications and Real-World Observations

    Nearly all requests for 4NQO require robust, reliable performance in mutagenesis protocols. Both academic teams and private labs reach out for this compound when modeling DNA damage, screening for cellular repair mechanisms, or testing anti-mutagenesis strategies in cancer research. The underlying reason lies in the nitro group position and the oxide functionality, which induce single and double-stranded DNA breaks with a level of consistency not found in some related agents.

    During collaborations on animal studies, it has become clear that many scientists select 4NQO over classic mutagens like ethyl methanesulfonate or formaldehyde. This preference comes largely from 4NQO's direct DNA interaction and well-mapped bioactivity profile. Investigators tracking tumorigenesis report fewer confounding reactions or metabolic byproducts, so their data stays clean and interpretable. We’ve visited customer labs to run side-by-side comparisons, and the reproducibility from our batches tends to exceed the expectations of researchers struggling with non-standardized material.

    We’ve supported clients probing oxidative DNA lesions who depend on the precise oxidative profile offered by our 4NQO. Unlike broad-spectrum oxidizers, this compound forms stable DNA adducts that can then be quantified and tracked through molecular assays. In our own QC lab, daily experience proves the value of trace impurity monitoring. A poorly controlled process leaves researchers guessing at the source of ambiguous results. That’s why our technicians take pride in managing both synthesis conditions and packaging to seal in purity.

    Comparisons and Lessons Learned from the Field

    While working directly in chloroquinoline derivatives, we often hear researchers ask about differences between 4NQO and alternatives such as 2-Acetylaminofluorene or benzo[a]pyrene. Many such molecules require metabolic activation, which introduces variability depending on cell type or enzymatic activity in animal models. Our own in-house side-by-side assessments demonstrate that 4NQO’s genotoxic effects do not depend on a host’s metabolic system, which reduces the noise in genotoxicity and DNA repair studies.

    For those who have wrestled with batch inconsistency or strange background effects linked to secondary byproducts, the difference is clear. Over the years we’ve fine-tuned column purification and crystallization steps, reducing the presence of minor quinoline nitroso analogs and reaction residues. Our chief process engineer has shared stories about early days, when we would troubleshoot inconsistent results by questioning water content and glassware history. Today, that attention persists, but guided by automated moisture analysis and carefully tracked raw materials.

    Unlike many other DNA-reactive agents, 4NQO produces a class of stable monoadducts, giving clarity when mapping mutational outcomes. In our ongoing customer feedback log, research teams routinely note a sharper dose-response curve when using our material. Attempts to replicate this with less refined sources fall short, particularly in complex cellular or animal contexts. We hear this from both seasoned researchers and early-career scientists, who notice how our product streamlines their troubleshooting process and increases the accuracy of dose calibration.

    Sourcing, Handling, and Stability

    Drawing from our own experience, the journey from raw input to packaged product shapes the ultimate utility of this compound. While 4NQO is light-sensitive and degrades if exposed to ambient humidity, we mitigate this with amber glass vials, inert gas purging, and vacuum sealing as soon as the final checks clear our in-process QC. Our storage rooms keep environmental conditions stable, and we log batch histories with dedicated software so product provenance remains transparent for every customer.

    On several occasions, customers who previously sourced material from a general laboratory supplier approached us after facing rapid degradation or unclear shelf-life curves. The difference isn’t theoretical—our hands-on storage trials show that small deviations in moisture control or packaging material directly impact stability and subsequent biological activity. The team in charge of packaging can cite dozens of stories about early experiments into different seals and vial types. Their insight led to the current setup, which reduces degradation over time and keeps lab results consistent, even after travel through complex shipping chains.

    Lab users report little waste, and sample return rates drop off after institutions switch to our production. We encourage teams to report back on shelf life under varied storage practices, and at user conferences we host open discussions. These ongoing conversations influence our own practices and validate that attention to stability translates directly to better experimental science.

    Dealing with Safety and Regulatory Demands

    Years ago, regulations for hazardous chemicals became more detailed. As production chemists, we respond by maintaining strict inventory, training, and disposal processes inside our facility. Handling 4NQO means every worker in the plant understands its risks, and that hazardous waste systems remain tight. Anyone wanting to order 4NQO from us gets documentation outlining these risks, not just stock safety data but field-learned tips for minimizing laboratory exposure.

    For larger users, regulatory documentation can slow research timelines. We stay in regular contact with institutional safety officers and respond quickly to custom reporting needs or regulatory reviews. We even invite some customers’ EHS teams to audit our safety workflows directly. Through these relationships, the broader research community benefits from streamlined access and evolving control strategies. Not once have we compromised on safety for faster output; every kilogram leaves our doors with full traceability and safe-handling guidance.

    Rare contamination incidents get documented and shared across industry meetings—everyone in the chemical synthesis world learns from each other’s slip-ups, and we regularly meet with regulatory consultants to discuss new restrictions or updated compliance procedures. These ongoing conversations feed into both our own process updates and help other manufacturers bring safer practices into place. The number of inquiries around new hazard statements, disposal channels, and end-of-life protocols keeps rising, and we address those directly through our established internal procedures.

    Batch Size, Customization, and Research Partnerships

    Across the years, requests for both small and medium-scale batches have increased. Individual university groups or private sector R&D projects often call for special lot sizes, special packaging, or additional purity documentation. As manufacturers, we are in a position to customize from the reaction vessel up, adjusting reaction times, purification criteria, or even isomer controls if a research application calls for stricter side-product exclusions.

    Several collaborations began this way: a research group with a challenging repair pathway model needed lower detection limits for nitroquinoline traces in treated samples. We brought them into our facility to review their analytical requirements and then adjusted the final purification cuts to deliver a product with impurity profiles tight enough for their methods. Since then, that process improvement stands as the new standard for all our runs.

    One pharmaceutical partner needed bundled analytical data mapped to each lot plus split-vial packaging for multi-center trials. Our experience as the direct manufacturer made this request ordinary instead of a logistical challenge, because major changes can be implemented by a quick meeting on the factory floor, not layers of middlemen or third-party brokers.

    Improving Access, Sharing Knowledge

    Not all users arrive at 4NQO with clear expectations, especially younger scientists or those new to mutagenic compound handling. We host training days and video walk-throughs to pass along lessons learned about weighing, solution preparation, storage, and disposal. In collaborations with universities, we’ve provided seminars on DNA lesion chemistry as well as hands-on technique improvement. Open feedback channels lead to new troubleshooting guides, and both victories and hurdles reported by our customer base guide our ongoing batch validation strategies.

    As makers, we also gather application notes from the field. Recent years show growing interest in labeling experiments or as a controlled positive for DNA damage checkpoint assays. Several partners have shared datasets from high-throughput screens, showing that even subtle differences in product composition ripple out into hundreds of readouts. Nothing is more satisfying than seeing published work cite the batch number and purity data we provided as foundational to their results.

    Quality, Reliability, and Trust

    Many in our team have spent years in the industry, watching the pendulum swing between price-driven commoditization and a return to trust in manufacturer relationships. It has become clear over time that researchers, regulators, and industrial partners want long-term consistency. No one benefits from chasing the lowest price only to face wasted experiments and ambiguous conclusions. The best science comes from starting with trusted material, and our philosophy focuses less on maximizing output and more on meeting both spoken and unspoken requirements from the global research community.

    We invest in analytical upgrades—routine HPLC, NMR, GC-MS checks, and trace residual analysis. These investments have paid off many times over, both in reduced customer complaints and in ongoing positive feedback. You don’t just ship a product and forget—the real world answers come later, when scientists call to talk about the smallest changes in color, melting point, or reactivity. Our job doesn’t end at the loading dock.

    A Living Product and Evolving Research Directions

    Chemistry rarely stands still. Over the past few years, 4NQO’s research footprint has expanded far beyond classical mutagenesis. DNA adductomics, advanced sequencing methods, and biomarker development now depend on tight reproducibility and trace-level impurity control. We work with customers looking for downstream compatibility, as well as those expanding into combination assays with repair inhibitors or antioxidant modulation. The feedback from these cutting-edge uses loops back through our production chain, motivating us to tighten controls or offer specialized lots as needs change.

    We’re asked more and more about green chemistry improvements—ways to reduce waste or swap out solvents for less hazardous alternatives. Some pilot batches now use alternative oxidants with less environmental impact, and every change is tested for product comparability before broader rollout. Building a sustainable process means collaborating closely with both our raw material suppliers and downstream users, who in many cases hold the key knowledge on future experimental directions.

    What Sets Our 4-Nitroquinoline N-Oxide Apart?

    Over years in direct synthesis, key differentiators have emerged. We employ true traceability: every lot is fully mapped from raw material shipment through to final packaging and shipping. Robust identity checks using both traditional and advanced spectroscopy reveal impurities before they can affect experiments. And our knowledge base, built through both in-house study and customer partnerships, guides continual process improvement.

    Customers who try our 4NQO after lower-cost alternatives often remark on the reliability it brings to their DNA damage or mutagenesis workflows. In many research areas, it only takes a few false starts with imported or distributor-grade chemical feeds to learn that hands-on synthesis, robust QC, and responsive technical support make a profound difference.

    We draw our pride from these many success stories. Each batch reflects decades of incremental improvement, countless conversations with real users, and a constant commitment to pushing world-class science ever forward. Whether for foundational mutagenesis studies or the next wave of biological innovation, reliable chemical building blocks remain as critical as the people wielding them. In this journey, we see ourselves as both makers and partners to a global research community working at the frontiers of understanding.