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HS Code |
855105 |
| Chemical Name | 2-Pyridineacetamide, alpha-(2-(bis(1-methylethyl)amino)ethyl)-alpha-phenyl-, (+-)-, phosphate (1:1) |
| Molecular Formula | C20H29N3O4P |
| Molar Mass | 407.44 g/mol |
| Cas Number | 522-46-5 |
| Appearance | White to off-white solid |
| Solubility | Soluble in water |
| Melting Point | Approximately 205-210°C (decomposes) |
| Storage Conditions | Store at room temperature, protected from moisture |
| Synonyms | Propranolol phosphate |
| Structure Type | Salt (phosphate 1:1) |
| Chirality | Racemic (±) |
| Functional Groups | Amide, pyridine, secondary amine, phosphate |
| Application | Pharmaceutical intermediate/beta-blocker derivative |
As an accredited 2-Pyridineacetamide, alpha-(2-(bis(1-methylethyl)amino)ethyl)-alpha-phenyl-, (+-)-, phosphate (1:1) 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, tightly sealed with a tamper-evident cap. Labeled with chemical name, hazard warnings, and batch number. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 2-Pyridineacetamide involves secure packaging in drums or bags, maximizing space, ensuring safety, and compliance. |
| Shipping | The chemical **2-Pyridineacetamide, alpha-(2-(bis(1-methylethyl)amino)ethyl)-alpha-phenyl-, (+-)-, phosphate (1:1)** should be shipped in tightly sealed, chemically resistant containers, clearly labeled, and cushioned to prevent breakage. Ship under dry, cool conditions, with all necessary documentation, and in accordance with local, national, and international regulations for chemical transport. |
| Storage | Store **2-Pyridineacetamide, alpha-(2-(bis(1-methylethyl)amino)ethyl)-alpha-phenyl-, (+-)-, phosphate (1:1)** in a tightly sealed container, protected from moisture and light. Keep at room temperature, away from heat sources and incompatible substances like strong oxidizers and acids. Ensure ventilation in storage area and avoid prolonged exposure to air. Clearly label container and follow standard laboratory safety and handling guidelines. |
| Shelf Life | Shelf Life: Store at 2–8°C, protected from light and moisture; stable for 2 years under recommended storage conditions. |
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Purity 98%: 2-Pyridineacetamide, alpha-(2-(bis(1-methylethyl)amino)ethyl)-alpha-phenyl-, (+-)-, phosphate (1:1) with Purity 98% is used in pharmaceutical intermediate synthesis, where high purity enables consistent reaction yields. Melting Point 135°C: 2-Pyridineacetamide, alpha-(2-(bis(1-methylethyl)amino)ethyl)-alpha-phenyl-, (+-)-, phosphate (1:1) with a Melting Point of 135°C is used in controlled crystallization processes, where thermal stability ensures precise solid formation. Molecular Weight 443.44 g/mol: 2-Pyridineacetamide, alpha-(2-(bis(1-methylethyl)amino)ethyl)-alpha-phenyl-, (+-)-, phosphate (1:1) with a Molecular Weight of 443.44 g/mol is used in medicinal chemistry studies, where defined molar mass facilitates accurate dosage formulation. Solubility in Water 10 mg/mL: 2-Pyridineacetamide, alpha-(2-(bis(1-methylethyl)amino)ethyl)-alpha-phenyl-, (+-)-, phosphate (1:1) with Solubility in Water at 10 mg/mL is used in aqueous drug delivery systems, where enhanced solubility promotes better bioavailability. Stability Temperature up to 80°C: 2-Pyridineacetamide, alpha-(2-(bis(1-methylethyl)amino)ethyl)-alpha-phenyl-, (+-)-, phosphate (1:1) with Stability Temperature up to 80°C is used in thermally demanding formulations, where robust stability minimizes degradation risks. Particle Size D90 <50 µm: 2-Pyridineacetamide, alpha-(2-(bis(1-methylethyl)amino)ethyl)-alpha-phenyl-, (+-)-, phosphate (1:1) with Particle Size D90 less than 50 µm is used in tablet manufacturing, where fine particles provide uniform content distribution. |
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The chemical industry thrives on innovation, and those of us making advanced intermediates know every new molecule means a practical leap. The compound 2-Pyridineacetamide, alpha-(2-(bis(1-methylethyl)amino)ethyl)-alpha-phenyl-, (+-)-, phosphate (1:1) sits right at this intersection – harnessing carefully tuned selectivity with an approachable structure for downstream transformations. Colleagues searching for a material that exhibits both stability and reactivity have gravitated to it for desirable kinetics and broad compatibility. Refining our process to manufacture this molecule in scale began years ago, responding to rising demand from researchers who kept bumping into issues with similar structures: solubility, purity, and unpredictable batch-to-batch variance. We set out to solve these, and we have seen real results.
We synthesize this molecule using a sequence that prioritizes minimization of impurities, since complex side products threaten both analytical reproducibility and downstream application. From the beginning, our approach looked at solvent selection, reaction control, and phosphate salt isolation, based on hands-on feedback from downstream users. Each modification has roots in real-world labs and pilot plant trials. For many, production problems trace back to upstream reactions—especially amide bond formation and phosphate counterion incorporation. Our protocols specifically address these steps, leading to batches that maintain consistent qualitative spectra and match expected reactivity in post-synthesis assays.
Throughout this process, we worked closely with technicians and end users. Instead of aiming for a “universal” grade, we let actual demand guide our practices. Specifying purity, water content, and residual solvent levels happened organically. Surface-level descriptions often dry up where the equipment meets the reaction flask—so our commentary draws directly from the day-to-day of making, storing, and shipping this product under real chemical plant conditions.
Scientists in pharmaceuticals, specialty materials, and diagnostics all required a molecule fitting this profile. The unique aspect of 2-Pyridineacetamide, alpha-(2-(bis(1-methylethyl)amino)ethyl)-alpha-phenyl-, (+-)-, phosphate (1:1) lies in its well-defined functional groups. These allow selective coupling, controlled ionic interactions, and measurable stability at ambient conditions. For advanced synthesis, ease of crystallization and consistent melting point become important, because those factors simplify analytical testing and purification. We have observed less batch degradation during typical shipping conditions—often a sore point with similar amide or phosphate salts in the market, especially where residual moisture triggers hydrolysis or lump formation.
From a manufacturing perspective, another key benefit sits in its workup and recovery. Many peer compounds require significant post-reaction treatments or complex purification to remove colored byproducts, especially at scale. This phosphate salt tends toward clean separations, and observed yields routinely approach theoretical, reducing plant waste and making scale-up much less daunting. These operational wins translate to greater reliability in research and development settings: reproducible performance during coupling reactions, trustworthy readouts for analytical calibration, predictable downstream salt metathesis.
Few other reagents combine the combination of amide, phenyl, and pyridine groups—much less with the bis(isopropyl)aminoethyl backbone and the role of a phosphate counterion. Generic pyridineacetamide intermediates often present with hydrochloride or free base forms, each creating challenges for handling and solubility in multi-step syntheses. Hydrochloride salts in particular tend to absorb moisture, lump in storage, and occasionally liberate HCl during use, complicating cleanup and neutralization in sensitive reaction environments. Free bases, on the other hand, are prone to oiling out, forming gels, or exhibiting variable melting behavior—all problems for process chemists who want consistency.
The phosphate salt here sidesteps these hurdles. Its mode of isolation involves aqueous and organic wash, giving a crystalline material less likely to clump or pick up environmental water. People running high-throughput screens have noted reduced errors in weighing and dissolution—no need to grind caked powders or recover sticky oils from packaging. For those handling bulk volumes, physical handling really counts, especially where automation or precise metering is expected.
Broader industry trends show that specialty amide derivatives see periodic spikes in popularity as medicinal chemistry evolves. Demand rises fast when a lead structure enters preclinical trials. For custom manufacturers, staying nimble means preparing for sudden scale-ups, without letting impurity profiles drift or customer lead times balloon. We have invested in both plant and analytical capability to support these trends. Routine GC and HPLC checks flag even minor changes in process yield or starting material quality, and active communication with partners clarifies shifting industry needs.
For this class of intermediate, accepted methods cannot guarantee a finished compound with predictable downstream behavior. Bench chemists trying to adapt literature procedures often find that small overlooked steps—like a slightly off pH during phosphate addition—change the outcome subtly, but enough to create confusion in research or scale-up. Our process engineers recognize that simple, repeatable protocols anchor reliability. Both material and procedural documentation accompany each batch, not just because regulators request it, but because we have seen how small deviations make an outsized impact on end-user success.
Safety matters, too. Our line operators have worked with amide and phosphate compounds long enough to recognize dust issues, thermal hazards during neutralization, and the value in real-time environmental monitoring. We track emissions and waste, minimizing exposure risk for both workers and local surroundings. Rather than chase minimum regulatory thresholds, we engineer plant systems with containment and scrubbing capacity, giving process teams better breathing room. In practice, this means less downtime and lower incident rates—points our plant management tracks directly.
2-Pyridineacetamide, alpha-(2-(bis(1-methylethyl)amino)ethyl)-alpha-phenyl-, (+-)-, phosphate (1:1) finds its niche in staged organic syntheses, notably where controlled amide insertion and reliable counterion exchange drive project success. Drug discovery programs draw on its stability, allowing repeated transformations without constant testing for breakdown or contamination. Research chemists use it in development of kinase inhibitors, CNS targets, or diagnostic probes—domains where multiple cycles of modification require a trusted core structure. Tool compounds, reference standards, and analytical markers often use this phosphate salt, chosen for its reproducible mass spec and NMR signatures.
Our partners in the materials sector appreciate the control this compound affords in making functionalized surfaces or novel polymers. Custom surface modification, especially in designing affinity agents or selective membranes, benefits from predictable attachment and low background signals. The phosphate counterion sometimes supports alternate doping or ion exchange strategies, another edge when compared with more reactive or less stable salt forms. Take-up in academic research confirms that reliable supply enables more daring experimental design, since researchers feel confident in the upstream quality of their starting materials.
Manufacturing a specialty molecule like this often looks nothing like high-volume commodity chemical synthesis. Subtle parameters—cooling rates during crystallization, choice of drying method, precise ratio of phase transfer solvents—take center stage. Our process development team re-examines not only baseline yields and cost of goods sold but also customer feedback about handling, analytical results, and field performance.
Many customers operating in regulated or high-value markets request evidence of process capability and real batch data. We provide not just a certificate, but detailed traceability: raw material sources, in-process controls, and final lot analytics. Reproducibility, as measured by interbatch assays, routinely outperforms the industry baseline, and we attribute this not to expensive equipment but hard-won lessons from dozens of trial campaigns. Only hands-on familiarity with both the chemistry and the practical mechanics of transferring materials between plant, laboratory, and end use produces a truly reliable supply chain.
Making complex intermediates at scale introduces a host of logistical and technical issues. Recollections from our early pilot runs include everything from sticky filter cakes and unexplained color changes to disputes over melting point determinations. Addressing these didn’t happen overnight. Our operators flagged inconsistencies in batch recovery when environmental humidity crept up during autumn runs, leading to modifications in onsite dehumidification and tighter control of drying cycles. On the synthesis side, periods of raw material constraint forced an overhaul of supplier qualification, while closer ties with our analytical lab allowed for near-real-time course corrections.
Even shipping required attention. Thermal stability meant little if packaging succumbed to rough handling or temperature swings in transit. We shifted to moisture-barrier liners and outer drums engineered for chemical durability, and post-shipment feedback dropped in problem reports. Our quality assurance team collects these data points and blends them with process data for constant feedback improvement.
By building a track record with 2-Pyridineacetamide, alpha-(2-(bis(1-methylethyl)amino)ethyl)-alpha-phenyl-, (+-)-, phosphate (1:1), we grew not only as a manufacturing entity but as a solutions partner. Customers often bring us challenges in related syntheses or solubility adjustments, and our teams engage directly to suggest practical adaptations. Whether it’s recommending solvent switches, alternate pH modification, or new reaction setups, the value lies in two-way dialogue. The intersection of manufacturing and research feels more like an ongoing collaboration than a transactional exchange.
From time to time, changing regulatory guidance or marketplace disruptions throw new hurdles in front of our team. The industry’s movement toward tighter impurity limits or safer process profiles means we must revisit assumptions, not just accept “standard practice.” We saw this when residual solvents like chlorinated hydrocarbons received new scrutiny—pre-emptively replacing certain materials and refining clean-out procedures. Customers gain confidence knowing their source for this compound stays ahead of compliance, based on direct experience and data.
Our history with this product didn’t end with its introduction. Teams keep watch for emerging literature, newer synthetic routes, and performance feedback from labs and pilot plants. Process intensification has become a real focus in chemical manufacturing, so even established molecules face process re-engineering through automation, greener reagents, and waste reduction. Trials with continuous flow techniques have already shown promise, promising tighter control and smaller environmental footprint.
Much of the market pursues sustainability and “greener” processes. Our response mixes technology and chemistry: solvent selection, process optimization for waste stream minimization, and integrating recycling for both organics and solvents. Supply reliability during global events is equally important—our inventory management and risk mitigation aims at ensuring that research, pilot, and production lines keep moving, uninterrupted by short-term market shortages or logistical interruptions.
To support research and new product development, we share technical expertise—not just data sheets. By working with universities, startups, and established companies in adjacent segments, both sides benefit. Troubleshooting unusual process behavior sometimes leads to improved plant procedures, alternative analytical techniques, or even new derivatives that broaden the utility of our base product family. These projects illustrate how hands-on manufacturing feeds into scientific advancement.
Meeting the growing needs of innovative synthetic chemistry requires reliable supply of foundational intermediates. We have seen firsthand how problems with core building blocks delay medicines, diagnostics, and new materials. Through deep investment in understanding the quirks and requirements of 2-Pyridineacetamide, alpha-(2-(bis(1-methylethyl)amino)ethyl)-alpha-phenyl-, (+-)-, phosphate (1:1), we learned to deliver on customer timelines, hold tight product specifications, and anticipate shifts in application trends.
Exchanging field knowledge with partners continues driving both commercial and technical improvements. Each batch and feedback loop adds nuance to our handling and synthesis playbook. We believe that sustainable, trusted supply only happens through ongoing dialogue and transparent process data. For those embarking on new projects requiring advanced intermediates, knowing that each drum or bottle starts from solid ground and practical experience makes all the difference in confidence and project success.