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HS Code |
741971 |
| Chemical Name | 3-(2-Methyl-4-Nitro-1H-Imidazol-1-Yl)Propionitrile |
| Molecular Formula | C7H8N4O2 |
| Molecular Weight | 180.17 g/mol |
| Cas Number | 137507-94-3 |
| Appearance | Yellow solid |
| Melting Point | 98-102°C |
| Solubility | Soluble in DMSO, slightly soluble in water |
| Storage Conditions | Store at 2-8°C, keep container tightly closed |
| Pubchem Cid | 13036035 |
| Iupac Name | 3-(2-methyl-4-nitro-1H-imidazol-1-yl)propanenitrile |
| Smiles | Cc1nc([N+](=O)[O-])n(CC#N)c1 |
| Synonyms | 3-(2-Methyl-4-nitroimidazol-1-yl)propanenitrile |
As an accredited 3-(2-Methyl-4-Nitro-1H-Imidazol-1-Yl)Propionitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 25g of 3-(2-Methyl-4-Nitro-1H-Imidazol-1-Yl)Propionitrile is packaged in a sealed amber glass bottle with hazard labeling. |
| Shipping | 3-(2-Methyl-4-Nitro-1H-Imidazol-1-Yl)Propionitrile should be shipped in tightly sealed containers, protected from light, heat, and moisture. It must comply with all local, national, and international regulations for transportation of chemicals. Proper labeling and documentation are required, and handling should be restricted to trained personnel wearing appropriate protective equipment. |
| Storage | Store 3-(2-Methyl-4-nitro-1H-imidazol-1-yl)propionitrile in a cool, dry, and well-ventilated area, away from heat and sources of ignition. Keep the container tightly closed and protected from light and moisture. Store separately from incompatible materials such as strong oxidizing or reducing agents. Ensure that proper chemical labeling and safety precautions are in place to prevent accidental exposure or spills. |
Applications of 3-(2-Methyl-4-Nitro-1H-Imidazol-1-Yl)Propionitrile in Industrial Manufacturing3-(2-Methyl-4-Nitro-1H-Imidazol-1-Yl)Propionitrile finds precise, technically demanding uses within select high-value industrial sectors. The following application scenarios reflect our continued commitment to end-use traceability, material handling best practices, and deep integration with downstream process specifications. 1. Nitroimidazole-Based Active Pharmaceutical Ingredient (API) SynthesisIn the pharmaceutical sector, this compound serves as an essential intermediate for the synthesis of targeted nitroimidazole APIs used in anti-infective therapeutic classes. API manufacturers relying on controlled nitration, alkylation, and subsequent condensation pathways use it to increase the purity and yield of intermediates, ensuring efficient scale-up compliance for regulated medicine production. Industry compliance standards
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2. Radiosensitizer Intermediate for Oncology Drug DevelopmentLeading radiopharmaceutical manufacturers select this material as a starting intermediate in the synthesis of 2-nitroimidazole class radiosensitizers, which play a critical role in enhancing the therapeutic index of cancer radiation treatments by selectively targeting hypoxic tumor cells. Industry compliance standards
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3. DNA Probe and Fluorescent Label SynthesisBiotechnological production platforms deploy this material for the assembly of nitroimidazole-linked fluorescent probes and molecular labels, which are applied in hypoxia detection kits and advanced bioassays to assess cellular oxygenation status in research and diagnostic laboratories. Industry compliance standards
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4. Specialty Electronic Chemical Intermediate for Photoresist FormulationElectronics manufacturers use this compound as an intermediate in the synthesis of advanced photoactive additives for negative-tone photoresist materials. Its controlled reactivity supports pattern resolution improvements and enhances process stability in high-volume semiconductor wafer production environments. Industry compliance standards
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Experience in manufacturing 3-(2-Methyl-4-Nitro-1H-Imidazol-1-Yl)propionitrile has helped us see just how much care each batch deserves. This compound, often known by its abbreviated chemical designation or referenced as a functional imidazole nitrile, relies on tightly controlled synthetic methods. As a producer, meticulous management of reaction parameters—temperature, pressure, solvent selection, and timing—form the backbone of our process. That means technicians check more than purity and moisture content; every run receives attention to crystal habits, bulk density, and trace residues, since minor variations impact downstream performance.
Unlike bulk commodity chemicals, this substance serves specialty applications where subtle differences stop research or production runs in their tracks. Most often, customers come from the fields of fine chemicals, pharmaceuticals, or material science. With experience in scale-up and plant operations, we recognize the need for reproducible quality, because trial lots prepared with variable impurities or particle profiles rarely behave the same way in subsequent syntheses or formulations.
Tuning the specifications of 3-(2-Methyl-4-Nitro-1H-Imidazol-1-Yl)propionitrile goes beyond reaching minimum assay percentages. Workers in the lab see firsthand what happens if traces of side-products make it into customer hands—yields can drop, product isolation can turn messy, or unexpected color changes raise red flags in analytical reports. We invest in process refinement because partners demand traceable lots with stable properties, not just numbers on a certificate. It’s about confidence born from batches that behave exactly the same, run after run.
Part of what makes this compound distinct comes from the nitro-imidazole core functionalized with a propionitrile tail. Each synthetic stage brings its own risks for residual solvents or unreacted intermediates, so we build multi-step purification into our process. Crystallization protocols trim away color bodies, and proprietary filtration systems handle even ultra-fine particulates. Chromatographic analysis and NMR fingerprinting back up our outgoing QC, so what lands in customers’ hands matches their intended methodology without introducing unwanted variables.
Chemistry at scale is unforgiving. The lessons come from listening to the clink of failed crystallizations, the smell of anomalous plant runs, or headaches from separating closely related byproducts. For 3-(2-Methyl-4-Nitro-1H-Imidazol-1-Yl)propionitrile, repeated campaigns revealed sensitivity of the nitro group to high temperatures, and how one extra hour on a stirring bench could tip the balance toward impurity formation. Shop floor operators test each lot for color and texture changes, since subtle deviations often point to bigger issues upstream—maybe a drift in feedstock quality, or unnoticed buildup in a reactor jacket.
We learned to treat every synthetic batch of this compound as a diagnostic tool. By comparing viscosity, filterability, and drying profiles across runs and seasons, it became clear which deviations matter. This way, production isn’t just about output tonnage or analytic numbers, but grasping how real materials interact with both machines and people. A batch that optimizes for throughput instead of quality never goes out the door. Our commitment gets measured by how few complaints we get from collaborators—and how many return for ongoing projects because their method works with what we supply.
Researchers and developers consistently tell us that performance in downstream applications depends on the predictability of upstream materials. For 3-(2-Methyl-4-Nitro-1H-Imidazol-1-Yl)propionitrile, customers tend to work in selective reduction, derivatization, or heterocyclic modifications, and value a carefully managed impurity profile that keeps unwanted side reactions at bay. The compound’s distinctive structure offers a combination of reactivity and stability that supports further customization in both drug discovery and advanced materials.
In pharmaceutical research, this molecule serves as a precursor for novel imidazole derivatives and nitro-containing scaffolds. Here, researchers favor the nitrile group’s versatility—it can be transformed into carboxylic acids, amides, or other moieties through straightforward chemical routes. We’ve also supplied batches for macromolecular assembly where consistent particle size helps control final product morphology. It’s the reliability of each delivered kilogram that saves time during process development and validation.
Many compare imidazole derivatives in the lab based on apparent similarities in their substitution pattern or theoretical reactivity. Our experience says the substitution at the 2-methyl, 4-nitro positions and appending propionitrile make a significant difference in both physical handling and downstream use. For one, the presence of a nitro group imparts distinct polarity and influences solubility across organic and aqueous media, aiding in certain coupling or protection chemistries. The propionitrile extension opens alternate synthetic pathways that aren’t accessible with simple alkyl or halide substitutions.
From a practical perspective, batches of closely related substances—like 2-methyl-4-nitroimidazole or its ethyl or butyl nitrile cousins—often behave unpredictably if substituted for this product in existing syntheses. We have worked with chemists who switched to our precisely specified variant after seeing batch failures with generic or off-brand grades. It’s clear that margin for error narrows as methods scale beyond milligram testing, and early investments in process-specific materials prevent costly troubleshooting at late stages.
Those familiar with sensitive or regulated sectors know that documentation isn’t just paperwork—it’s often the start of real collaboration. Each lot comes with certificates linking back to production logs that trace feedstocks, operators, and every parameter adjustment. We carry out stability tests over time, so customers receive assurances not only about the initial batch but how it can be stored and deployed over a project’s lifetime. That attention to detail comes directly from years fielding customer questions, managing audits, and re-confirming practices in front of demanding clients.
Our reactors and drying units stay dedicated for these specialty runs, reducing risk of cross-contamination or accidental carryover. Multi-stage cleaning protocols and staff familiarization help keep the line between campaign products crystal clear. Foremen and supervisors train all new recruits on why a single speck of an unrelated nitro compound can disrupt high-stakes projects, so vigilance supports reliability.
Clients increasingly explore structure-activity relationships that drive drug discovery, smart materials, or even diagnostic imaging agents. This encourages us, as the maker of 3-(2-Methyl-4-Nitro-1H-Imidazol-1-Yl)propionitrile, to invest in workflow improvement, so future requirements don’t catch our plant unprepared. We regularly adjust reactor designs and testing protocols to anticipate scale-up trajectories or to match evolving regulatory standards for trace impurity content. Investments in better environmental and safety controls on the plant floor follow the lessons found in published and internal incident reports.
We’ve partnered with customers during process development, conducting joint troubleshooting or reworking small batches to meet exploratory requirements. If a research team needs particular solvent residuals minimized or a narrower particle size window, we can directly test optimizations in-house. We take pride in how flexible, onsite manufacturing supports rapid response, troubleshooting, and tailored iteration, which traders or bulk brokers rarely attempt on specialty intermediates.
Manufacturing of nitro compounds—especially functionalized imidazoles—means accountability for emissions, waste management, and occupational safety. We treat every run as a chance to reinforce containment, monitoring, and staff training. Nitrile intermediates can pose challenges with air and aqueous releases, so plant engineering focuses on closed systems, real-time leak detection, and minimization of hazardous waste streams. Byproducts and filtrates head for responsible treatment rather than disposal shortcuts.
Worker exposure receives active oversight, with personal protective equipment and air monitoring built into daily checklists. Engineering controls—local exhaust, sealed gloveboxes for powder transfers, and redundant spill containment—reduce the chance of accidental contact with nitro compounds. Each plant shutdown cycle includes a thorough review to confirm compliance with both local and international standards. Others may treat safety as a cost-center; we see it as an investment in uninterrupted, high-quality output and workforce stability.
Long-term customers ask deeper questions about sensory properties—color, odor, apparent flow—and shelf-life, because not every lab has access to dryboxes or inert-atmosphere storage. We’ve tailored packaging and labeling to guard against ambient humidity, while batch reserve samples undergo long-term tracking under controlled conditions. Some clients routinely check against retained samples, especially for method validation or regulatory submission, and our processes ensure those samples always match what they received in bulk.
Routine batch-to-batch consistency might sound like a goal any manufacturer can claim, but practice shows otherwise. Plant chemists cross-check results over extended periods to confirm that seasonal changes in raw materials, utilities, or ambient conditions don’t introduce unnoticed drift. Our customers value the stability built into every package, knowing it reflects the rigor demanded by years of customer feedback and process evolution.
If you’ve ever relied on a specialty chemical whose performance shifted between lots, you know the cost of interrupted research or product failures. That’s why investment in the root causes of inconsistency—feedstock qualification, operator training, process analytics—pays dividends for both sides of the partnership. As the people closest to the reactors, we hear early about pain points: solubility issues in solvents, tricky filterability, or sticky residues on production glassware.
Feedback from both large and small customers led us to tighten control over final drying steps and double-check for physical stability in storage. Once, a development partner flagged variable melting characteristics in year-old inventory; we responded by improving our inert packaging formats and testing at multiple temperature conditions. Adjustments like these don’t just help one customer, but strengthen every future delivery. It shows that solutions often come from open channels and a willingness to re-examine assumptions, not just the written SOP.
The science behind every kilogram of 3-(2-Methyl-4-Nitro-1H-Imidazol-1-Yl)propionitrile reaches beyond initial specifications sheets. Our work depends on plant operators checking every intermediate for subtle changes, QC chemists running advanced analytics to verify batch fingerprints, and customer-facing teams following lots from planning through follow-up. Success comes not from generic platitudes about “quality” but from ongoing vigilance and practical collaboration.
From the raw materials in bulk tanks straight to final customer applications, the focus remains on durability, matching customer process flows, and solving unique project hurdles. No two applications look exactly alike, so real-world adaptability means more than just reaching analytical targets. Getting it right batch after batch, year after year, proves the real value of deep manufacturing experience.