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HS Code |
153783 |
| Product Name | Aminoacetonitrile Hydrochloride |
| Chemical Formula | C2H5ClN2 |
| Molecular Weight | 92.53 g/mol |
| Appearance | White to off-white crystalline powder |
| Melting Point | 143-146 °C |
| Solubility | Soluble in water |
| Cas Number | 6011-14-9 |
| Density | 1.20 g/cm³ (approximate) |
| Storage Temperature | 2-8 °C |
| Synonyms | 2-Aminoacetonitrile hydrochloride |
| Ph Value | 4.0-6.0 (10% solution in water) |
| Purity | Typically ≥98% |
| Application | Pharmaceutical intermediate |
| Hazard Statements | Harmful if swallowed, causes serious eye irritation |
| Boiling Point | Decomposes before boiling |
As an accredited Aminoacetonitrile Hydrochloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Aminoacetonitrile Hydrochloride is packaged in a 100-gram sealed amber glass bottle with a secure, tamper-evident screw cap. |
| Shipping | Aminoacetonitrile Hydrochloride is shipped in tightly sealed containers to prevent moisture absorption and contamination. Handle with care, using appropriate protective equipment. Store and transport at room temperature, away from incompatible substances. Comply with all relevant regulations regarding hazardous materials. Ensure clear labeling and provide safety data with the shipment for safe handling. |
| Storage | Aminoacetonitrile Hydrochloride should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from moisture, heat, and incompatible substances such as strong oxidizing agents. Keep it away from direct sunlight and sources of ignition. Proper labeling and secure storage are essential to prevent accidental exposure or contamination. Store according to local and institutional chemical safety regulations. |
Applications of Aminoacetonitrile Hydrochloride in Industrial ManufacturingAminoacetonitrile hydrochloride is an essential intermediate in multiple specialized chemical synthesis processes. Its role affects critical performance attributes, yield optimization, and regulatory compliance in downstream manufacturing for pharmaceutical, agrochemical, and fine chemical sectors. As a direct manufacturer, we strictly maintain traceability, batch consistency, and technical support for each application zone described below. 1. Pharmaceutical Active Pharmaceutical Ingredient (API) SynthesisAminoacetonitrile hydrochloride functions as a precursor in the synthesis of specific pharmaceutical APIs, including certain antineoplastic agents and anti-infectives. Its high purity and reliable reactivity allow for efficient condensation or cyclization stages, especially in routes requiring controlled nitrile conversion to amine or amidine functionalities. The raw material enters during regulated multi-step processes, demanding both chemical integrity and full trace documentation to the latest GMP directives. Industry compliance standards
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2. Agrochemical Active Ingredient SynthesisThis raw material supports the preparation of specific heterocyclic building blocks in agrochemical actives such as systemic fungicides and insecticides. Its high selectivity aids in routes demanding robust nitrile chemistry for subsequent catalytic hydrogenation or ring synthesis. Full validation per agro-REACH and GHS requirements is performed to enable large-scale production under integrated management systems. Industry compliance standards
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3. Specialty Fine Chemical Synthesis (Heterocycles)Manufacturers of fine chemicals utilize aminoacetonitrile hydrochloride in the creation of complex heterocycles such as imidazoles, triazoles, and guanidine derivatives. The specificity of the compound’s reactivity under defined anhydrous conditions facilitates synthesis not easily achievable with alternate nitrile sources. Regulatory scrutiny focuses on batch traceability and process emissions, especially for export-oriented production. Industry compliance standards
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4. Diagnostic and Analytical Reagent FormulationIn clinical diagnostics and laboratory reagent manufacturing, aminoacetonitrile hydrochloride serves as an intermediate to synthesize fluorescent tags or labeling reagents for biochemical assays. The strict demand for batch purity and absence of trace contaminants is critical due to its downstream application in sensitive clinical and environmental testing protocols. Manufacturers validate all lots against stringent QA/QC benchmarks and analytics. Industry compliance standards
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5. Intermediate for Veterinary Drug ManufactureVeterinary pharmaceutical producers employ aminoacetonitrile hydrochloride in synthesizing pyrazole-, triazole-, and pyridazine-based APIs for antiparasitic and antimicrobial formulations. The source purity and impurity profile management directly impact the downstream pharmacological safety, demanding validated analytical release and full process documentation. Industry compliance standards
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Producing aminoacetonitrile hydrochloride calls for careful attention to each part of the process, from sourcing starting materials all the way to applying the final quality checks before packaging. In practice, handling this compound means working closely with both organic synthesis and reliable purification methods. In our plant, we synthesize this chemical to meet the needs of pharmaceutical work, peptide intermediates, and custom research projects, not just for the bulk chemical trades. The model we produce, most often with the molecular formula C2H5N2Cl, typically comes as a white to slightly off-white crystalline powder, with a purity above 98%.
From the outset in the lab, it’s clear that this compound will demand strict environmental controls. The cyanide-containing function makes safety non-negotiable at every step, not just for regulatory compliance but for the health and safety of those operating the reactors and filtration systems. As manufacturers, we have seen many cases where overlooked humidity and temperature swings during isolation lead directly to product loss or unpredictable quality.
We settle on specifications based on common feedback from process chemists and pilot plant operators who use aminoacetonitrile hydrochloride as an intermediate. Clients often prefer particle sizes in the 40–60 mesh range for straightforward dissolution and filtration. Typical water content ranges under 0.5% help ensure shelf stability and handling ease. Bulk density matters less than with some ingredients, but consistency makes a difference during scaled-up procedures. In practice, trying to match a specification “on paper” means little unless the substance handles the same on every batch, so our benchmarks focus on actual user routines.
Purity standards stem from more than just reaching a percentage figure. Trace impurities—like formaldehyde, ammonia, or chloride levels—must actually stay well below levels that would interfere with key downstream reactions. Our facility uses both HPLC and titration to double-check results, since we have learned that relying solely on one method leaves blind spots. For example, a batch that looks fine on melting point alone may choke a reaction, and only careful impurity profiling reveals the problem.
This nitrate stands out as both a versatile intermediate and a specialty block for industrial processes. In the pharmaceutical world, its most recognized role is as a step toward the synthesis of amino acids and their derivatives. Laboratories employ aminoacetonitrile hydrochloride during Strecker amino acid synthesis, harnessing its reactivity for building alpha-amino acids with quick, cost-effective routes. Where the aim is to scale up production of non-proteinogenic amino acids, we see this substance bridge the gap between lab chemistry and industrial-scale amino acid manufacture.
We also supply peptide manufacturers who need a dependable supply of pure intermediates. Their feedstocks must meet tight purity and solubility standards to prevent downstream chromatographic headaches. Our interactions with these technical teams reveal that inconsistent supply chains directly stall R&D—securing a ready stock of this compound keeps their benches running on schedule.
Beyond pharmaceuticals, this compound becomes a useful building block in agricultural chemistry and specialty materials. Some of our long-standing customers develop custom agrochem intermediates starting with aminoacetonitrile hydrochloride. Their process development hinges on fine-tuning reagents at the molecular level; even tiny shifts in material quality can drive up costs, delay launches, or even threaten intellectual property claims if a batch fails to match a patent description. We have witnessed how critical robust documentation and traceability are in keeping product launches secure, especially in regulated markets.
People sometimes ask us: why manufacture aminoacetonitrile hydrochloride, and how does it actually compare to other common nitriles or even structurally similar chemicals? Experience over years in this factory has shown that direct comparisons often miss the detail that makes or breaks a customer process. Take acetonitrile, for instance, a simple, cheap solvent—while both contain a nitrile group, only aminoacetonitrile hydrochloride offers the amine functionality necessary for peptide coupling or amino acid building.
Other nitriles, like malononitrile or benzonitrile, don’t pull their weight when it comes to alpha-amino group introduction. The hydrochloride salt form also distinguishes this product. The salt boosts water solubility, making it a friend in aqueous workups or protocols needing organic-inorganic interchange. Compared to the free base, the hydrochloride tends to offer better thermal and chemical stability, which translates into less decomposition during shipment—something that matters to customers half a world away or operating in climates that swing between high humidity and dry cold.
In-house, we’ve set up parallel runs using the base and salt forms under identical storage and reaction conditions. The hydrochloride consistently holds its color and reactivity longer. Reject rates on client-side QC checks fall when samples come from the hydrochloride route. For both technical and commercial reasons, the hydrochloride salt emerges as a high-trust intermediate for cutting down purification steps and maximizing reaction success.
Producing aminoacetonitrile hydrochloride calls for specialized equipment and a focus on process safety uncommon even among other nitrile-manufacturing lines. The generation of hydrogen cyanide or other hazardous vapors can’t be ignored; we’ve installed dedicated scrubbers and in-process detection to keep emissions under strict control. Not every plant is ready to devote this kind of engineering attention to a low-tonnage intermediate, but missing these steps leads directly to environmental and cost liabilities. From our experience, quality and safety investment at the source plant trims down hidden costs for the entire supply chain.
While many other intermediates tolerate multi-purpose reactors or even outside tolling, aminoacetonitrile hydrochloride generates more discussion about cleaning validation and contamination risk between batches. Surfaces exposed to this compound require a strict cleaning-in-place protocol, verified with both analytical swabs and visual inspections. Thanks to this, downstream users see fewer QC fails and less unexplained impurity in their APIs and formulated goods.
Handling also shapes how the product moves from manufacturer to client. We regularly supply both bulk and smaller clinical-grade lots, but for both, caking and clumping become problems if packaging isn’t matched carefully to local climate and transit duration. Over the years, we have switched from simple plastic liners to high-barrier multi-layer bags with desiccant as a direct consequence of actual shipment failures and customer claims. There’s no substitute for iterative adjustment when packaging a chemical as reactive as this.
Year after year, customers remind us—sometimes pointedly—that consistent supply outweighs even price for intermediates which anchor high-value or tightly regulated syntheses. Shortages or shipment delays in this compound force entire manufacturing lines to halt. In the early years of our operation, we underestimated how dependent global clients can be on a single-source supply. A harsh winter delayed one large batch, causing missed production targets at several downstream pharmaceutical companies and costing them both time and market access.
This experience taught us to invest in robust inventory and backup raw material supplies, even if carrying the extra stock eats into working capital. Today, our warehouse tracks lot-by-lot inventories, shelf ages, and real-time demand. We share these supply details openly with key clients, building long-term relationships based on reliability, not just batch specs or one-off pricing.
We also see the value in doing more than routine quality control. While tech sheets tell part of the story, routine “spot checks” throughout the year—pulling random product lots and re-analysing for purity, trace metals, or unusual breakdown products—has caught a fair share of near-misses before product leaves our premises. One incident years ago involved a sudden spike in byproduct formation traced back to a supplier’s change in starting amine quality. Our close checks flagged the issue before any customer batches failed, saving a lot of frustration and cost both upstream and downstream.
As direct manufacturers, environmental impact hits close to home. Some nitrile syntheses shed toxic gases or heavy metals. Over time, pressure from internal teams and local regulations has driven us to retool the process, swap out problematic reagents, and upgrade emissions controls. Where possible, we have traded high-chloride waste processes for routes that minimize both chlorine and cyanide effluents. The goal isn’t just regulatory approval, but the safety and well-being of our plant crews and surrounding community.
Some of our effort shifts upstream to supplier selection. We now audit incoming raw material sources for both plant safety and eco-impact. Choosing a slightly more expensive feedstock becomes the obvious choice when the alternative is an entire wastewater treatment overhaul or cleanup event. In recent years, increasing customer demand for lower environmental footprint has driven us to collaborate more closely with green chemistry specialists—developing multi-step syntheses that cut the number of wasteful workups or hazardous isolation conditions. These changes never come about easily, but as on-the-floor operators, we see the results firsthand: fewer days lost to equipment downtime, safer air, and less complicated regulatory reporting.
End user demands in the fine chemical and biopharmaceutical sectors mean we hear growing requests for tailored particle sizes and batch certification to more exacting standards—sometimes way beyond what was normal practice just a few years ago. Changing industry trends—especially in peptide and amino acid drugs—have forced us to improve crystallization control and impurity quantitation. For example, just a decade ago, most buyers ignored sub-percent levels of side product; now, some need formal statements on each impurity over 0.05%, often with named structures. We meet this with expanded analytic capacity—NMR, LC-MS, and even qNMR when called for, with results directly shared with clients in the format they request.
Few intermediates punish poor shipping practice like aminoacetonitrile hydrochloride. Once, a shipment left in a port warehouse during a humid summer turned into a solid cake and lost value in one week. We have learned, sometimes at considerable expense, that packaging in multi-layer bags with high-quality desiccant extends the shelf life by months and cuts the frequency of customer complaints. Clear labeling of batch, storage, and dry handling instructions on every drum helps warehouse staff keep product in spec right up to the day it’s used. For overseas shipments, we organize humidity sensors in containers; the readings guide us on whether further packaging tweaks or faster air freight become necessary.
The chemical spot market sees many faddish booms and busts, but demand for certain pharmaceutical intermediates tends to grow steadily, regardless of trends. Aminoacetonitrile hydrochloride’s role in both existing generic drugs and novel research pathways lends stability to its market. While price volatility hits simple nitriles from time to time—often because of sudden solvent demand or regulatory shifts—the manufacturing complexity and real technical value of this compound keeps it in continuous demand, even at higher prices.
Feedback from buyers—at both start-ups and multinational pharma plants—regularly affirms that proven technical performance often outweighs marginal price differences. Delays or failed reactions due to questionable material end up costing more in lost time than can ever be saved on a price sheet. As direct suppliers, we keep technical support available well after the sales contract closes, helping customers troubleshoot applications in new syntheses and share practical handling tips based on our decades of experience.
Long-term experience reminds us that no process stays optimal forever. Regular feedback loops with customers inspire line-by-line reviews of both upstream synthesis and downstream packing. Sample batches sent out for pilot projects often come back with suggestions—finer materials to dissolve faster, batches dried to stricter moisture limits, or re-crystallisations to meet more stringent impurity specs. We prioritize these changes, knowing the reality on the shop floor sometimes means shifting production schedules or dedicating staff to handle customization—but the improved customer relationships and long-term business prove the worth of these efforts.
Alongside process and product upgrades, we invest in operator training—both to maintain safety and to improve product quality. Skilled handlers not only prevent accidents but also spot early warning signs that keep problematic batches from leaving the facility. We bring in external trainers on cyanide safety, quality management audits, and regulatory compliance. Regular operator feedback results in tweaks both large and small to the SOPs. It’s these “in the trenches” lessons—often missing from textbooks or technical marketing—that add up to a safer, cleaner, and more consistent product for end users.
Throughout the years, we have moved steadily toward full digital batch record-keeping. Transitioning from paper to electronic logs for every parameter during synthesis, blending, and packaging brought an immediate reduction in errors and faster root-cause tracking. Digital traceability lets us pull batch history when responding to customer questions or regulatory audits. Investments in integrated ERP and QC software also help us spot trends in yield, impurity, or customer satisfaction that manual logs would hide. In practice, data-driven oversight translates to higher product reliability and lower risk of the kind of hiccup that can cost both reputations and significant revenue.
Where some see only another white powder in a drum, direct experience with aminoacetonitrile hydrochloride reveals a product that sits at the intersection of safety, technical challenge, and reliable supply. Each day, our operators discover small but significant tweaks that make the difference between a smooth campaign and a costly, interruptive one. From raw material audits, through synthesis, purification, quality assurance, to logistics, every stage carries lessons in both what works now and what could work better tomorrow.
Through years of manufacturing this compound, we’ve gained an appreciation for the importance of consistency, responsiveness, and technical honesty, both inside our plants and with our customers. By combining these values with up-to-date equipment and a willingness to own our experiences—good and bad—we aim to provide more than just a chemical, but a reliable foundation for the world’s innovations in pharmaceuticals and beyond.