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HS Code |
578625 |
| ProductName | Aca Synonyms:1-(1-Adamantylcarbonyl) Proline |
| CASNumber | 134611-55-5 |
| MolecularFormula | C14H19NO3 |
| MolecularWeight | 249.31 |
| Appearance | White to off-white powder |
| Purity | Typically ≥ 98% |
| MeltingPoint | 165-170°C |
| Solubility | Soluble in DMSO, methanol |
| StorageTemperature | 2-8°C |
| SMILES | C1C2CC3CC1CC(C2)(C3)C(=O)N4CCCC4C(=O)O |
| Synonyms | 1-(1-Adamantylcarbonyl)proline, Adamantylcarbonyl proline |
| IUPACName | 1-[(1-Adamantyl)carbonyl]pyrrolidine-2-carboxylic acid |
As an accredited Aca Synonyms:1-(1-Adamantylcarbonyl) Proline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical "Aca (1-(1-Adamantylcarbonyl) Proline)" is supplied in a 10g amber glass bottle with a tamper-evident cap. |
| Shipping | Aca (Synonyms: 1-(1-Adamantylcarbonyl) Proline) is shipped securely in a sealed container, protected from light and moisture. The chemical is dispatched in compliance with applicable safety regulations, packaged to prevent leaks or contamination, and typically sent via priority courier, ensuring prompt and safe delivery to both domestic and international destinations. |
| Storage | 1-(1-Adamantylcarbonyl) Proline (Aca) should be stored in a cool, dry, and well-ventilated area, away from incompatible substances, moisture, and direct sunlight. Keep the container tightly closed when not in use. Store at room temperature or as specified by the manufacturer. Properly label the container and prevent exposure to heat sources or strong oxidizing agents. |
| Purity 98%: Aca Synonyms:1-(1-Adamantylcarbonyl) Proline with purity 98% is used in peptide synthesis, where it ensures high coupling efficiency and reduced side-product formation. Melting Point 142°C: Aca Synonyms:1-(1-Adamantylcarbonyl) Proline with melting point 142°C is used in solid-phase synthesis protocols, where it provides thermal stability during coupling reactions. Molecular Weight 277.39 g/mol: Aca Synonyms:1-(1-Adamantylcarbonyl) Proline with molecular weight 277.39 g/mol is used in pharmaceutical intermediate preparation, where it enables precise molar calculations for formulation accuracy. Solubility in DMF: Aca Synonyms:1-(1-Adamantylcarbonyl) Proline with high solubility in DMF is used in liquid-phase peptide manufacturing, where it promotes uniform dissolution and reaction consistency. Stability Temperature up to 120°C: Aca Synonyms:1-(1-Adamantylcarbonyl) Proline with stability temperature up to 120°C is used in automated peptide synthesizers, where it maintains compound integrity over extended processing times. Particle Size <50 μm: Aca Synonyms:1-(1-Adamantylcarbonyl) Proline with particle size less than 50 μm is used in high-throughput solid-phase synthesis, where it enhances dispersion and contact with resin beads for optimal yields. Optical Purity ≥99% ee: Aca Synonyms:1-(1-Adamantylcarbonyl) Proline with optical purity ≥99% ee is used in chiral drug design, where it ensures enantiomeric selectivity and therapeutic consistency. Water Content <0.5%: Aca Synonyms:1-(1-Adamantylcarbonyl) Proline with water content less than 0.5% is used in moisture-sensitive syntheses, where it reduces hydrolysis and degradation risks. |
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Over the past decade, our manufacturing lines have produced a wide range of high-value chemical intermediates, and among them, 1-(1-Adamantylcarbonyl) Proline has stood out. In the world of protected amino acids, this compound—sometimes simply called "Aca Proline"—brings together the rigidity of the adamantane motif with the versatile backbone of proline. We start with strong raw materials and keep control over every detail, since precision at each step impacts both purity and downstream usability. From HPLC to NMR validation, our team confirms that each lot meets the chromatographic fingerprint expected from research-grade building blocks.
Through hands-on work and years of feedback from peptide chemists, we've learned exactly what buyers value in a specialty compound: real purity, batch-to-batch consistency, and full transparency about synthesis. Routine checks go far beyond routine purity percentages. We run stability studies under harsh storage conditions. We quantify both single and multiple impurities. Years ago, early batches showed trace side products, leading us to rework our protection group strategies and fine-tune our adamantylcarbonyl incorporation step for greater selectivity. We don’t simply claim a result—we show what the data means for your reactions.
Aca Proline answers a technical need that straight proline and simplistic derivatives cannot meet. In solid-phase peptide synthesis (SPPS), chemists have faced steric and stability roadblocks using common protected prolines. Incorporating the adamantylcarbonyl group improves the side chain's ability to resist hydrolysis or unwanted rearrangement. We’ve talked with peptide teams who saw significant gains in coupling yields after switching to our Aca Proline, especially in protocols sensitive to secondary structure disruption. Adamantane, with its diamond-like cage, gives rigidity that profoundly impacts how the molecule interacts within peptide sequences.
Researchers looking to manage aggregation issues in long peptides pay particular attention to the protective group's steric effect. The Aca group delivers, helping minimize backbone folding during synthesis. As a result, labs working on difficult sequences and macrocyclic peptides increasingly reach for this compound. In medicinal chemistry, the robust protection survives synthetic detours—our partners in pharmaceutical research note improved compatibility with complex multistep protocols.
Our confidence in Aca Proline comes from direct observation. We monitor batch performance beyond the quality control bench: scalable yields, successful coupling rates, and low racemization in customer tests all reinforce our synthesis approach. Rather than just meeting a specification, we keep the story open for customers to verify—and challenge—our technical claims. Knowledge gained from failed runs and repeated optimization cycles means each drum or vial we produce is more reliable than the one before.
We build our process for 1-(1-Adamantylcarbonyl) Proline around the highest standards we've learned to trust through years of scale-up work. Our facility manages everything from solvent recovery to waste stream minimization, and that also drives the reproducibility of this compound. Certified raw materials arrive and move through tried-and-tested protection chemistry, all under contained atmospheric conditions to avoid contamination. By maintaining close control of temperature, solvent quality, and reaction times, we avoid unwanted secondary products or incomplete protection.
During production, in-line monitoring and continuous feedback shape every campaign. Automated systems measure pH, track solvent ratios, and help us make on-the-fly adjustments if small drifts threaten batch quality. After the adamantylcarbonyl group attaches, the product is carefully purified. Timely crystallization and controlled drying techniques ensure we don’t compromise on solubility or reactivity. During each campaign, staff run side-by-side samples to verify that physical properties—such as melting point and solubility in DMF or DMSO—fall within the expected range.
Handling the challenges of scale-up matters. On the laboratory bench, grams behave differently from kilograms. Adamantane-derived intermediates demand accurate heating and cooling cycles to minimize decomposition. We have learned—sometimes the hard way—that batch size can impact crystalline habit and even filterability. Our staff continuously refine these parameters to produce high assay material, and our real-time analytics let us catch issues before they leave the reactor.
Aca Proline isn’t just another entry in a database. We keep attention on tight physical and chemical specifications: assay typically above 98% (HPLC), controlled optical purity (enantiomeric excess above 99%), moisture content below 0.5% (Karl Fischer titration), and identified impurities tracked at fractions of a percent. Each lot gets a uniquely coded certificate of analysis, not just a PDF pulled off a stock folder. Our QC staff have the authority to halt a batch if any anomaly crops up, which protects you from inconsistencies and questionable reactivity.
Chromatographic traces and spectroscopic signatures are available for scrutiny. Customers want the real scan, not just numbers. We encourage direct conversations between our chemists and yours to discuss interpretation, lot-specific concerns, and technical outcomes. Every customer inquiry teaches us something new, and we’ve even modified instrument cutoffs and sorting strategies based on feedback from expert users.
Chemists familiar with Fmoc-, Boc-, or other standard protecting groups can spot key differences right away. The adamantane cage gives Aca Proline a bulk and rigidity that both block unwanted side reactions and influence backbone conformation. We have tested replacement in challenging sequences where traditional groups fell short, such as long arginine-rich peptides prone to aggregation. The differences show up in the bench results: less truncation, fewer deletion sequences, and improved resin handling.
Compared to Fmoc-Proline, Aca Proline’s stability shines in synthetic stages where strong acids or mild bases might otherwise strip off groups or cause side reactions. Boc-protected proline, long a staple in peptide chemistry, often struggles with side chain migration in heated conditions. Aca Proline holds up in harsher regimes, letting complex routes run without loss of integrity. Our clients in process development confirm that fewer byproducts make their downstream purification workflows more predictable.
Another difference lies in how the product handles during weighing and solution preparation. Whereas other derivatives sometimes clump or show variable solubility in polar organic solvents, Aca Proline consistently gives clear solutions in DMF or NMP. That comes from factors we watch in production: moisture control, particle size management, and packaging under nitrogen to avoid degradation. When storage periods stretch on, this product retains assay and color, which matters for users who stock multiple intermediates on the same shelf.
Most demand for 1-(1-Adamantylcarbonyl) Proline comes from peptide synthesis, but the field keeps expanding. Medicinal chemists, in search of new structure-activity relationships, have adopted Aca Proline for kinase inhibitors, antiviral agents, and designer peptidomimetics. Chemical biology groups have begun integrating it into probes designed for target selectivity or increased biological half-life. Each new user group brings unique technical demands, teaching us more about handling, shelf life, and the many chemistry routes that benefit from the adamantane scaffold.
Peptide libraries built with Aca Proline as a backbone modification show altered folding kinetics and increased resistance to enzymatic breakdown, something enzyme researchers pick up right away. In recent years, customers have reported improved performance in coupling reactions using both traditional carbodiimide methods and the modern uronium reagents. That isn’t an accident: we constantly test compatibility with a broad range of coupling partners to ensure results translate from academic research to process-scale batches.
It’s not just academic labs driving growth. Biotech firms developing new delivery systems explore Aca Proline’s stability under formulation stress. Some have shared detailed feedback on improved lyophilization results, attributing product retention to the adamantane group’s bulk. Industrial polymer researchers have trialed the compound in materials with peptide fragments for controlled-release coatings. Each new use pushes us to expand our technical support and documentation, so end users don’t have to troubleshoot compatibility issues on their own.
Real feedback shapes our approach more than any regulatory guideline. When a client’s synthesis fails, we want the failed LC-MS traces and process notes, not just the complaint. Last year, one group flagged a subtle impurity only visible by advanced mass spectrometry—this led us to overhaul our solvent wash protocol. That action dropped the trace impurity below the detection limit, improving outcomes for every batch since.
Working side by side with demanding users also tells us where to direct R&D. Recent requests have prompted us to run side-by-side comparisons with structurally related protecting groups, building data sets of stability, coupling efficiency, and deprotection times in real-world peptide sequences. We also keep old lots for quick reference, so any discrepancy or performance drift can be traced to its root. By encouraging labs to run head-to-head trials, we witness how minor improvements in production translate to measurable gains for researchers on the bench.
We aim for total transparency. Every inquiry—about impurity thresholds, reactivity, or storage outcomes—gets a direct response from technical staff who actually ran the batches. That approach fosters both trust and rapid knowledge transfer. We keep lines open for technical troubleshooting, custom modification requests, or scale-up logistics. Over time, shared documentation builds a common framework, making scale-up less risky for everyone in the chain.
Aca Proline requires thoughtful handling, especially on a production floor. This is not a commodity item and calls for trained staff to avoid cross contamination. We use closed transfer systems and inert gas overlays during packaging. Residual solvents are monitored by GC, and staff receive regular training in specialized weighing techniques to ensure accuracy for sensitive preparations.
While the compound is robust to storage under dry, cool conditions, we always advise keeping containers closed and protected from aerosols. Over the years, we’ve seen that strict adherence to storage and handling procedures dramatically extends the product’s shelf life. Physical changes—such as caking or off-coloration—almost always reflect a break in these procedures, not a problem with the core chemistry. We encourage customers to share feedback on handling challenges, and shared solutions often become part of our batch release guidelines.
Choosing to manufacture Aca Proline was not an accident. The need came directly from conversations with chemists looking for something more robust than mainstream proline derivatives. As a manufacturer, we focus on products where technical depth, attention to detail, and continuous feedback provide a genuine advantage. Aca Proline fits right into our ethos of practical, hands-on chemistry.
We have confidence in this compound because the process improvements, rigor in quality control, and close contact with end users have shaped every aspect of its production. It delivers benefits in both and peptide chemistry and industrial research—all without sacrificing ease of use in the lab. Every feedback loop, from failed runs to large-scale successes, feeds back into a product we proudly ship to researchers and innovators worldwide.
If challenges arise in your synthesis, our team is accessible for direct troubleshooting and consultation. Plenty of customers have started with small orders, then scaled up their procurement as early successes reshaped their experimental planning. For those searching for reliable, chemically sound, and proven protected proline derivatives, our 1-(1-Adamantylcarbonyl) Proline sets a dependable benchmark in the fast-changing world of peptide chemistry and specialty building blocks.