|
HS Code |
255670 |
| Iupac Name | 2-nitro-3-phenylprop-2-enoic acid |
| Cas Number | 610-19-9 |
| Molecular Formula | C9H7NO4 |
| Molar Mass | 193.16 g/mol |
| Appearance | Yellow crystalline solid |
| Melting Point | 240-242 °C |
| Boiling Point | Decomposes before boiling |
| Solubility In Water | Slightly soluble |
| Density | 1.43 g/cm³ |
| Smiles | C1=CC=C(C=C1)C=CC(=O)O[N+](=O)[O-] |
| Pubchem Cid | 10307 |
| Inchi | InChI=1S/C9H7NO4/c11-9(12)6-7-4-2-1-3-5-8(7)10(13)14/h1-6H,(H,11,12) |
| Storage Conditions | Store at room temperature, in a cool, dry place |
As an accredited 2-Nitrocinnamic Acid 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-Nitrocinnamic Acid, labeled with chemical name, formula, hazard symbols, and handling instructions. |
| Shipping | **2-Nitrocinnamic Acid** is shipped in tightly sealed containers, protected from moisture, heat, and direct sunlight. It is classified as a hazardous material and must be transported following local and international regulations, with proper labeling and documentation. Ensure use of appropriate protective gear during handling to prevent exposure to skin and eyes. |
| Storage | 2-Nitrocinnamic acid should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of heat, moisture, and incompatible materials such as strong oxidizing agents and bases. It should be protected from light and handled with appropriate personal protective equipment to prevent inhalation, ingestion, and skin or eye contact. |
Applications of 2-Nitrocinnamic Acid in Industrial ManufacturingAs a direct manufacturer of fine chemical intermediates, we supply 2-Nitrocinnamic Acid to selected industrial sectors where its molecular structure supports dedicated synthesis and processing. Below, we detail verified downstream application scenarios, referencing exact compliance, blending ratios, integration stages, and typical end-use good types. 1. Pharmaceutical Intermediate for Non-Steroidal Anti-Inflammatory Drug (NSAID) SynthesisOur 2-Nitrocinnamic Acid serves as a critical starting material in the synthesis of certain NSAID active pharmaceutical ingredients, notably for specific arylacetic acid derivatives. Its nitro and cinnamic functionalities facilitate targeted nitration and reduction steps in multi-stage synthesis. Pharmaceutical companies employ this acid following controlled reduction procedures, closely monitored for impurity profiles to comply with stringent global drug regulatory requirements. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Intermediate for Specialty Dye ManufactureThe compound acts as a core intermediate in specialty azo and anthraquinone dye synthesis, supporting colorants with high color fastness for performance textiles. Dye manufacturers integrate the acid during diazotization and subsequent coupling with aromatic amines, creating high-purity pigments for demanding industrial textile and ink applications. Process traceability and strict limits on nitroaromatic contaminants are mandatory in this sector. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Fine Chemical Intermediate in Agrochemical SynthesisLeading crop protection manufacturers employ 2-Nitrocinnamic Acid as an intermediate for selective synthesis of pre-emergent herbicides and pest-resistant agents. The nitro and alkene substituents on the aromatic ring enable precise halogenation or further functionalization through Michael addition reactions, forming key building blocks for agrochemical active ingredients under strictly controlled synthesis environments. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Precursor in Liquid Crystal Compound Development2-Nitrocinnamic Acid features in the targeted synthesis of key mesogenic units for the electronics sector, specifically in manufacturing certain nematic or smectic liquid crystal materials for advanced display panels. The structural rigidity imparted by the cinnamoyl group and the electron-withdrawing nitro group provides the molecular anisotropy required for display quality, supporting further ester or ether linkage formation in downstream oligomerization steps. Manufacturers implement careful process control to minimize isomerization and polymerization side reactions. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
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As a manufacturer rooted in years of hands-on production, we view 2-nitrocinnamic acid not as a commodity but as an essential catalyst in the real world of chemistry and manufacturing. Production floors demand materials with reliability, clear physical identities, and versatility to drive value, and only a consistent process from raw material selection to finished product lets that potential shine. Our 2-nitrocinnamic acid, known by CAS number 619-34-3, answers that call with clarity and a solid batch history.
We shape every batch of 2-nitrocinnamic acid from the ground up, not as an isolated USP number but as a granular, slightly yellow crystalline solid with a melting point that lands around 240 to 243°C. Our teams run purification and drying stages carefully, targeting the tightest possible purity band, and most lots surpass 98%, established by HPLC and cross-checked via GC. That last 2 percent may matter to some—trace impurities like aldehydes or unreacted acids occur naturally, and controlling those gives formulation teams a cleaner canvas.
Moisture matters here, as even slight water content changes free-flowing crystals into sticky clumps. We keep water content under 0.5% by Karl Fischer, straight from the dryer, and bag under low humidity. The content of residual solvents never rises above the typical detection limits (0.2%), because—speaking candidly—solvents do nothing to help performance but plenty to interfere in downstream coupling and condensation steps.
Work in fine chemical manufacturing comes down to processes that either run or stop, so we always look at how a compound actually gets used. 2-nitrocinnamic acid rarely serves as a final molecule. Its main value shows up as an intermediate—something that makes the next step possible without introducing headaches along the way. In our experience, the cinnamic skeleton, with its conjugated double bonds and the ortho-nitro group, opens unique synthetic doors. Chemists tap this compound for two main types of downstream chemistry: reduction and cyclization.
In reduction work, the ortho-nitro group can selectively convert into an amine, introducing a functional handle for pharmaceuticals or dyes. That type of transformation forms the backbones of some anti-inflammatory agents or specific azo and anthraquinone dyes. Selectivity emerges from the position of that nitro group—it reacts in ways that meta- or para-nitro analogs simply can’t match, and the nature of our batches means side-products rarely cause trouble. Synthetic research on other nitrocinnamic acids bears this out, with ortho compounds delivering higher selectivity and less need for tedious post-reaction cleanup.
The product also finds life in cyclization, producing isoquinoline and quinoline derivatives. Strong demand comes from academic groups and process development labs who want predictable behavior under harsh conditions—straightforward melting, little decomposition, and no strangling odors or impurities to manipulate. Offering a stable, finely crystalline powder is about more than bright visuals: Optimal particle size lets the acid blend easily, reducing hot spots and local overheating, which can otherwise yellow or degrade a mixture.
Unlike some chemical catalog entries, every metric we share—acid value, melting point, impurity profile—connects directly to daily practice. We’ve seen batches tested in combinatorial catalyst screens, and inconsistent purity can mean runaway impurity signals. We’ve watched medicinal chemistry teams tweak reaction conditions, always looking for a substrate that gives sharp spots and clear lines on TLC plates, not a smear from cheap grades contaminated with starting cinnamic acid or nitrate byproducts.
Some might say “a nitrocinnamic acid is a nitrocinnamic acid,” but that misreads the impact small changes bring. Comparing 2-nitrocinnamic acid with its 3- or 4-substituted cousins, the ortho orientation changes both physical properties and chemistry. Paler yellow tone, slightly higher melting point, and markedly different reactivity—this is not a side note, it dramatically shifts how a research group handles their workflow. With our close control on nitro substitution, you won’t get mixed regioisomers hidden in the same bag, only a defined synthetic tool.
Manufacturers differ as well. Sourcing from trading houses or resellers can bring risk: relabeling batches from inconsistent origins, poorly tracked quality, or contamination carried from vendor blending. Strict internal controls and tracking, lot by lot, enables us to pinpoint deviations quickly. After years of running both single-kilogram and ton-scale lots, we know that deviations cost time and credibility—attributes that no one can afford to gamble with in a modern laboratory.
Granularity and ease of handling set this product apart from cheaper, less-refined acids. Large agglomerates can break glassware in automated systems. Fine, dust-like powders clog feeders and hamper transference. We’ve adjusted both sieve mesh size and agitation during crystallization to offer manageable grains encouraging flow without dust clouds. Warehouse staff notice the difference even before compounds reach the bench—bags stay easy to decant, and nothing cakes to the packaging.
One often-overlooked area is packaging. Our packaging team runs checks for static, humidity, and any breach of integrity during filling. HDPE bags inside sturdy drums hold each fresh lot. It’s not glamour work but it matters—nothing slows down a plant like opening a bag to find crystals stuck to the plastic or strange smells signaling off-gassing. Each label carries a batch number, tracking every gram to its reactor run—no generic “bulk” shipped loosely across seasons.
Traceability is worth more than a paper promise. We retain samples, post-shipment, long after lots have reached the customer. If a formulation chemist calls with a question on crystal form, flow behavior, or new analytical results, we pull reference material and run fresh checks—no need for speculation or guesswork. From the perspective of a manufacturing chemist, this kind of long memory prevents trouble at the source.
The standards for chemical supply have shifted beyond just purity and price. We source starting benzaldehyde and nitric acid from well-audited vendors—each with written records on supply chain transparency. In-house waste streams run through distillation and neutralization, with regular records provided to local authorities, not just filed and forgotten. Plant waste audits show a downward trend in total output, thanks to solvent reuse and repurposing neutralized residues into lower-value chemical processes.
Our commitment has grown in response to global expectations. End-users, whether in pharmaceuticals or dye intermediates, want to prove both origins and sustainability. For those with more stringent green chemistry needs, we’re piloting a process for 2-nitrocinnamic acid using less aggressive oxidants and lower total solvent load. The journey continues—compliance certificates alone don’t reassure unless proven by results and behavior.
Over decades in the chemical manufacturing world, lessons pile up. What fills a glossy catalog page may look uniform, but in practice, the differences in impurity levels, particle size, and even the dryness of a compound control whether plant equipment runs or stalls. At times, we’ve run lots at scale, then caught unexpected polymorphs or slow filtration clogging that didn’t show up in smaller test runs. Clear communication and tight process discipline fixed the issue—teaching us not to cut corners on batch records, retention samples, or in-line checks.
Our laboratory holds archives of supplied product stretching 15 years back, and those old bottles tell a story—shifts in color or consistency mirror process improvements and raw material changes over time. Every inquiry from a downstream user, whether about a subtle TLC impurity or a major process success, informs our next production cycle. Routine feedback loops with customers—sometimes on the other side of the world—feed back, not just spreadsheet order histories.
After raw production, our in-house analytical group takes over, running NMR, IR, and advanced chromatographic techniques to refine our process control. Discovering a minor isomer or residue early saves headaches for our downstream partners, whether they’re working on solid-supported reactions or complex metal-catalyzed couplings. We treat that feedback not as an optional extra but as the core of developing a higher-value, lower-risk product.
Product recalls or failed processes trace quickly to upstream weak points—off-grade material, outdated process steps, missed impurity control. Over the years, we’ve seen research projects grind to a stop because an alternate supply could not match physical or chemical identity. Customized specifications for purity, residual solvents, and moisture aren’t just about meeting a “technical spec”—they protect every step downstream, preserving time and funding that researchers can’t afford to waste.
In a competitive global market, the temptation to source from unverified agents grows. That short-term cost cut shows up as long-term disruption: missed delivery dates, inconsistent reactivity, and unforeseen plant downtime. Quality-driven customers have learned, often the hard way, that only a source accountable for every manufacturing step prevents these recurring headaches.
Chemists starting at bench scale focus on clarity and specificity. They need to understand melting point, reactivity range, and solvent compatibility. Pilot plant teams ask about bulk handling, dust suppression, and consistent performance as lots scale by a factor of 100 or more. Those details can slip through the cracks unless every operational step, from crystallization through packaging, adapts based on destination and use.
We listened to customer technical teams who flagged clogging in powder conveyors; we tuned particle size, making transport smoother on automated lines. When a downstream partner needed assurance on residual heavy metals for a tightly controlled API precursor step, we supplied ICP-OES analysis on every outgoing lot, not as a paid extra, but baked into our process. The feedback loop between manufacturing and application turns customer trouble into better process design—at the scale they need, whether 500 grams for exploration or 250 kilograms for full-scale synthesis.
Many can offer a spec sheet and a ready promise. Far fewer deliver a product story built on hands-on learning, mistakes corrected, and ongoing dialogue with those who trust each lot in their most sensitive work. For us, supplying 2-nitrocinnamic acid means owning that responsibility every day. A practical understanding of performance, from crystal behavior at elevated humidity to reactivity profiles in nuanced reduction chemistry, creates outcomes better than web catalog listings or one-size-fits-all pitches.
We see the compounds we make as vital links in chains stretching around the world—laboratories, manufacturing plants, research hubs—each driven by clear, direct, reliable supply. Our approach comes built from the real-life experiences of operators and chemists, shaped by batch histories, and informed by the questions that come up when a reaction fails or succeeds. We put practical, learned quality into every drum so that chemistry, not circumstance, shapes your results.