|
HS Code |
289476 |
| Name | 2-Nitrophloroglucinol |
| Chemical Formula | C6H3N1O5 |
| Molecular Weight | 169.09 g/mol |
| Cas Number | 577-74-0 |
| Appearance | Yellow crystals |
| Melting Point | 150-152 °C |
| Boiling Point | Decomposes |
| Solubility In Water | Slightly soluble |
| Density | 1.712 g/cm³ |
| Pubchem Cid | 11201 |
| Synonyms | 2-Nitro-1,3,5-benzenetriol |
| Iupac Name | 2-nitrobenzene-1,3,5-triol |
As an accredited 2-Nitrophloroglucinol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of 2-Nitrophloroglucinol, securely sealed with a screw cap and hazard labeling. |
| Shipping | 2-Nitrophloroglucinol is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. Packaging complies with hazardous material regulations, and it is clearly labeled for safe handling. The chemical is transported under ambient conditions, following all relevant safety protocols to prevent spills, leaks, or accidental exposure during shipping. |
| Storage | 2-Nitrophloroglucinol should be stored in a tightly sealed, clearly labeled container in a cool, dry, and well-ventilated area away from heat, sparks, and open flames. Protect from sunlight, moisture, and incompatible substances such as strong oxidizers and reducing agents. Access should be restricted to trained personnel, and appropriate safety measures, including secondary containment, should be employed to prevent accidental release or exposure. |
Applications of 2-Nitrophloroglucinol in Industrial ManufacturingAs the direct manufacturer of 2-Nitrophloroglucinol, we supply this specialty intermediate to support key downstream chemical processes across the fine chemical and pharmaceutical sectors. Our involvement in both research partnerships and commercial supply helps ensure traceable raw material quality and process adaptability for industrial users seeking high-purity inputs. We focus on the principal end applications where 2-Nitrophloroglucinol contributes distinct molecular benefits in established production routes. 1. Pharmaceutical Intermediate Synthesis (Antibacterial API Production)Producers of antibacterial active pharmaceutical ingredients use 2-Nitrophloroglucinol as a core building block for the construction of substituted aromatic scaffolds, forming an integral part of multi-step synthesis routes for nitroaromatic drug candidates. Its established role in the generation of specific quinolone and related heterocyclic structures allows for flexibility in route selection while complying fully with mandatory trace impurity controls and precursor documentation. Quality control teams routinely validate batch-to-batch composition using reference standards traced to pharmacopeial monographs. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Agrochemical Intermediate ManufacturingIn the agrochemical sector, formulation chemists utilize 2-Nitrophloroglucinol as a precursor for designing selective herbicides and pesticide actives, capitalizing on its core aromatic nitro functionality. Specific downstream processes require careful control of substitution patterns on the benzene ring to achieve targeted bioactivity and environmental degradation profiles. Formulators must comply with residue standards, and production runs are regularly assessed under ISO and REACH guidelines for full traceability and quality assurance. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Dyes and Pigments Intermediate ProductionManufacturers of specialty dyes and pigments integrate 2-Nitrophloroglucinol as an intermediate to produce colorants with tailored absorption profiles, particularly for yellow, orange, and brown shades. Controlled nitration patterns enable the synthesis of pigments resistant to fading and solvent dissolution, and downstream blending often requires input material of high purity to maintain consistent batch colorimetric properties. Compliance with chemical inventory control and textile industry standards is mandatory. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Chemical Research Reagent ProductionProducers of analytical and specialty chemical reagents leverage 2-Nitrophloroglucinol for its high reactivity and defined substitution pattern in organic synthesis research kits and combinatorial chemistry libraries. Research-grade material must consistently meet stringent purity benchmarks, and custom packaging supports QC traceability from synthesis to laboratory use. Quality managers conduct batch approval using validated analytical methods compliant with recognized reagent standards. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
|
Competitive 2-Nitrophloroglucinol prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: admin@sinochem-nanjing.com
Flexible payment, competitive price, premium service - Inquire now!
Maintaining high purity and batch-to-batch consistency calls for real expertise. As a manufacturer, the process of synthesizing 2-Nitrophloroglucinol never runs on autopilot. Over the years, we’ve closely refined every step — from raw material sourcing through carefully timed nitration to final quality testing. Our direct experience with the quirks of this aromatic nitro compound sets our material apart.
2-Nitrophloroglucinol carries the chemical structure 1,3,5-trihydroxy-2-nitrobenzene. This molecular backbone offers a balance of reactivity and stability, making it a valued option for research and industrial synthesis. Our standard supply model focuses on powdered crystalline form, yellowish to brownish tones, backed by HPLC and GC assessments.
In our ongoing production, we keep working to reduce trace impurities, especially di-nitro byproducts and residual acids from the nitration step. Every run gets moisture content monitored, managed below 0.5%, and meets verified melting point data to avoid surprises during customer application. In lab and kilo scales, we’ve noticed slight shifts in crystal throughput when ambient humidity spikes, so we package the material under low moisture conditions and use tight-seal drums or bottles.
Many researchers approach us asking why this compound stands out. Its three hydroxy groups and one nitro substitution open up reactivity paths hard to replicate with other phenolic nitrobenzenes or simpler trihydroxybenzenes. We see strong uptake in fields requiring either an electron-rich ring for chelation studies or a stepping stone for more intricate heterocyclic compound synthesis.
Academics and R&D teams push for clean, single isomer preparations. The meta arrangement of hydroxyls allows unique substitution patterns, including O-alkylation, reduction, or diazotization. This trait steers interest toward advanced dye intermediates, photographic chemicals, and high-value pharmaceutical scaffolds. Down the line, 2-Nitrophloroglucinol becomes a launching pad for ligands, especially in metal ion sensing or template polymerizations. No other nitrophenol with this configuration tackles these synthetic routes as directly.
We sit close to the reactions and see the subtle differences that batch history introduces. Tuning the temperature and acid ratios in the nitration sets whether final purity edges toward 97% or gets closer to 99%. We don’t settle for hydrated fractions or visual checks; we invest in spectroscopic and chromatographic validation each time.
Handling safety takes top priority — for our teams as well as for downstream users. Nitroaromatics can decompose quickly if mixed with basic or oxidative agents or stored at high heat. We keep all our packaging climate-monitored before shipment. Over the years, we’ve tweaked drying, filtration, and neutralization steps to wring out trace acids. That way the delivered material won’t surprise you with unexpected color changes or reaction stalling, especially when you’re scaling up in batch reactors.
Our production is never outsourced. We control the full chain, right down to the selection of acids used in the nitration and the way we treat waste streams. That control means we can support small batch requests for pilot studies and rapidly pivot to larger quantities for established specialty chemistry lines.
We get a lot of questions about how 2-Nitrophloroglucinol compares to phloroglucinol, nitrophenol isomers, or other polyhydroxybenzene derivatives. No other molecule in this class matches the combination of ortho and meta effects from the nitro and hydroxy groups. Phloroglucinol alone won’t deliver the nitrated reactivity, and nitrophenol isomers usually lack the density of hydroxy substitution for advanced coupling and chelation work.
From our experience, 2-Nitrophloroglucinol provides unique pathways in both electrophilic and nucleophilic substitution, enabling access to compounds that 2,4,6-trinitrophenol or 4-nitrophloroglucinol can’t produce cleanly. In nitro photography research and oxidative dye development, this isomer’s selectivity has led customers to report higher yields and cleaner downstream separation compared to broader-spectrum nitrated phenols.
Solubility and stability profiles set it apart from related products, too. In polar organic solvents, dissolution completes swiftly without extended agitation, but in water, solubility drops rapidly. That trait makes it less suitable for some aqueous-heavy synthesis protocols, but in organic solvent-mediated routes, it becomes a reliable partner.
Questions about supply chain accountability have become more frequent. As the actual manufacturer, we take direct accountability for every drum, from the acids and solvents entering the plant to the finished lot in your hands. We track every batch in a digital system, storing QC data, spectra, and synthesis notes for every lot. This isn’t just about compliance, it’s about making sure every customer gets replicable results across projects and years.
We’ve seen how minor changes in raw materials — a shift in acid strength or a subtle impurity in the starting phenolic feedstock — ripple through to the end product. Our technical staff keeps regular batches of standard reference samples, making sure that each shipment maintains a tight specification band. Repeat customers often compare our certificate of analysis to in-house testing and find consistent results.
Every person on the plant floor knows the hazards associated with aromatic nitro compounds. Even the technicians at user sites have reached out to share their tips and feedback. Avoid moisture and strong base exposure; these conditions can trigger off-colors or even unintended exothermic reactions. Our standard advice for end-users: keep the containers sealed, store them cool and dry, and avoid direct sunlight.
We reinforce secondary containment around drums and bottles, and recommend ventilated storage with incompatible chemicals segregated. Even after material leaves our facility, our technical team responds directly to customer questions about shelf life, compatibility with new reagents, and best neutralization or waste handling practices. Building trust means sharing what works and what doesn’t from our own experience.
It’s always a thrill when research teams come back and share how a batch of 2-Nitrophloroglucinol pushed forward a synthesis nobody thought possible. From the early days in photographic chemistry to recent work in sensor development, users leverage the dense functionalization for forming azo, quinone, and complex metal-organic hybrids. The unusual substitution pattern supports regioselective coupling and ring closures—a result that’s hard to reproduce with more common building blocks.
Drug discovery projects sometimes use this compound as an intermediate for antitumor or anti-infective agents. Materials science projects see it as a potential chelating agent, letting them bind metals selectively. Environmental chemistry groups employ it for binding and detecting metal ions at ultra-low concentrations. We keep learning from customers pushing the boundaries and feed those insights back into process improvements.
Manufacturing a niche intermediate like 2-Nitrophloroglucinol isn’t just about kilos and consistency. We see our technical support as part of the product. We’ve walked users through scale-ups, handled troubleshooting for slow reactions, and even shared details about filtration or washing when weird color changes cropped up. If a lab finds unexpected spots on TLC or odd XRF readings in a metal complex, our chemists connect directly with yours to run down the cause.
Real-world synthetic challenges drive what we do. Years of hands-on testing have shown that reaction temperature and timing during nitration can make the difference between a single clean product and complicated mixtures. Substituent arrangements on the aromatic ring aren’t just theoretical — we’ve learned firsthand how they drive selectivity in downstream reactions and impact scale-up.
No chemical process stays static for long. In our workshop, we keep iterating, reviewing new catalytic systems and greener acid routes to improve safety and lower environmental impact. We audit effluent streams for nitro byproducts and manage acid neutralization in-house, aiming to reduce the ecological footprint of production with every campaign.
We collaborate with universities and research labs on pilot projects, adopting new analytical methods and feeding real-world user data back into QC protocols. These feedback loops lead to technical improvements and tighter product specs. We stay open about process tweaks and notify customers if a small change could affect reactivity, especially in highly sensitive synthesis chains. Transparency builds confidence for both R&D scientists and procurement managers.
Every shipment of 2-Nitrophloroglucinol reflects years of accumulated know-how — not just in the reactions, but in the people, process tweaks, and feedback from users. We listen to technical challenges from across the world and keep refining our approach. The unique combination of hydroxy and nitro substitution provides applications unmatched by related compounds, and the integrity of each batch matters as much to us as to the people running reactions at your bench.
If your work calls for a compound with high specificity, clean analytical traces, and a manufacturer standing behind the chemistry, you’re welcome to draw on our direct expertise. Every batch, drum, or sample tells part of our ongoing story in chemical manufacturing — and we look forward to supporting both routine and cutting-edge projects with the best material and solid technical partnership.