|
HS Code |
346899 |
| Product Name | Trans-4-Hydroxy-D-Proline |
| Cas Number | 4295-08-5 |
| Molecular Formula | C5H9NO3 |
| Molecular Weight | 131.13 g/mol |
| Appearance | White to off-white crystalline powder |
| Melting Point | 208-211°C (dec.) |
| Solubility | Soluble in water |
| Optical Rotation | [α]D20 = +52° to +56° (c=1, H2O) |
| Purity | ≥98% |
| Boiling Point | Decomposes before boiling |
| Storage Temperature | 2-8°C |
| Synonyms | D-Trans-4-Hydroxyproline |
| Smiles | OC1CC(NC1)C(=O)O |
| Inchi | InChI=1S/C5H9NO3/c7-3-1-4(6-2-3)5(8)9/h3-4,6-7H,1-2H2,(H,8,9)/t3-,4+/m1/s1 |
As an accredited Trans-4-Hydroxy-D-Proline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Trans-4-Hydroxy-D-Proline is packaged in a 1-gram amber glass vial, tightly sealed, with clear labeling and safety instructions. |
| Shipping | Trans-4-Hydroxy-D-Proline is shipped in tightly sealed containers to protect from moisture and light. It is handled as a non-hazardous chemical and typically sent at ambient temperature. Proper labeling and documentation accompany the shipment, following standard regulations for laboratory reagents to ensure safe transport and delivery. |
| Storage | Trans-4-Hydroxy-D-Proline should be stored in a tightly closed container, protected from light, moisture, and air. It is best kept at 2-8°C (refrigerated) in a dry, well-ventilated area away from incompatible substances. Ensure the storage area is cool and avoid exposure to sources of heat, strong oxidizers, and direct sunlight to maintain chemical stability and purity. |
Applications of Trans-4-Hydroxy-D-Proline in Industrial ManufacturingAs a specialized manufacturer of trans-4-hydroxy-D-proline, we support global downstream sectors with tailored-grade input material and technical guidance. Our experience spans several advanced formulation and synthesis pathways, driving rigorous compliance and dependable supply for high-value end products. Below, we present in-depth application scenarios based on real industrial usage. 1. Chiral Building Block in Pharmaceutical API SynthesisPharmaceutical manufacturers use trans-4-hydroxy-D-proline as a chiral intermediate in the synthesis of small-molecule drugs, notably for creating specific stereochemistry in peptidomimetic APIs and antiviral compounds. In these routes, careful control of purity, isomeric ratio, and trace impurity levels is critical. Process chemists integrate the material at the key step where enantiopure backbone construction directly impacts API pharmacological profile and regulatory acceptability. Close batch-to-batch uniformity underlies qualification for cGMP manufacturing and DMF (Drug Master File) support. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Amino Acid Derivative for Peptide Coupling and Oligopeptide ProductionPeptide and oligopeptide manufacturers rely on trans-4-hydroxy-D-proline to introduce hydroxyproline residues with precise stereochemical configuration during SPPS (solid-phase peptide synthesis) or solution-phase protocols. Hydroxyproline’s rigid structure is essential for mimicking collagen-like protein segments and facilitating folding or biological activity in synthetic peptides for diagnostics, research, or as pharma starting material. The input material must deliver low racemization levels and fully traceable QC documentation for seamless integration into peptide lines subject to regulatory audit. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Custom Synthesis of Collagen Analogs in Biomedical EngineeringBiomedical engineering firms use trans-4-hydroxy-D-proline in the bespoke synthesis of collagen-mimetic molecules and scaffolds for tissue engineering, wound healing, and regenerative medicine implants. This amino acid introduces defined hydroxylation crucial for triple-helix formation and mechanical properties in engineered matrices. The qualification process mandates full traceability of the chiral input and monitoring of hydroxyproline content to ensure sterility, biocompatibility, and performance under ISO 13485 systems. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Reference Standard and Analytical Reagent for Stereochemical Quality ControlAnalytical laboratories and pharmaceutical QC departments require high-purity trans-4-hydroxy-D-proline as a reference standard for chiral purity assessment, amino acid analysis, and development of quantitative LC-MS/MS and HPLC protocols. Laboratories apply this material to validate API or peptide batch quality, determine hydroxyproline residue content in biomaterials, and calibrate analytical instruments within regulatory submission protocols. Lot consistency, strict documentation, and qualification for laboratory use are required for acceptance in regulated environments. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
|
Competitive Trans-4-Hydroxy-D-Proline prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: admin@sinochem-nanjing.com
Flexible payment, competitive price, premium service - Inquire now!
Working in the chemical field for years, every step from raw materials to final quality checks has taught us how crucial it is to deliver a dependable product that researchers and manufacturers count on. Trans-4-Hydroxy-D-Proline stands out as one of those compounds that rewards attention to detail at every single phase of production. Our team invests heavily in maintaining consistency, purity, and clear parameters so that scientists are never left second-guessing the contents of a bottle.
With the CAS number 4295-08-9 and molecular formula C5H9NO3, this product has served as a cornerstone across multiple fields, from peptide synthesis to pharmaceutical R&D. Unlike its cis isomer, trans-4-hydroxy-D-proline supports ring conformations compatible with a wide range of peptide backbones, increasing its versatility in research applications. The D-isomer, specifically, enables the exploration of novel peptide structures, as natural proteins overwhelmingly rely on L-amino acids. By pushing past well-trodden ground, chemists unlock new reactivity and biological properties, all made possible by this precise chemical scaffold.
Lab work and pilot-scale runs never capture the full challenge of reliable, bulk-scale manufacturing. Each batch unlocks new lessons, often teaching the importance of temperature control, reagent sourcing, and solvent purification. All these steps become visible in the repeatability of analysis data. We've encountered and resolved issues like unexpected stereochemical inversions or drops in purity during crystallization, which can spell the difference between go and no-go for a synthetic route.
Trans-4-Hydroxy-D-Proline from our reactors consistently meets or exceeds 99 percent HPLC purity. Every shipment comes with full analytical documentation—NMR, MS, IR—paralleling demands from pharmaceutical partners and academic research groups. Some might see documentation as paperwork. For us, it mirrors our regular batch scrutiny, because discrepancies—even small ones—in these files can lead to hours of troubleshooting and lost resources down the line.
The difference between D- and L-amino acids creates a fundamental fork in the road for biological testing. Proteases, for instance, struggle to cleave peptides built from D-isomers, turning D-variants into tools for tuning half-life or resisting enzymatic degradation. Synthetic chemists repeatedly stress the difficulty of obtaining D-isomers at scale and purity high enough to make new analogues, especially hydroxy-D-prolines, where the hydroxyl group needs careful handling to maintain the desired 4-position and trans geometry.
L-isomers (such as trans-4-hydroxy-L-proline) show up more frequently in natural molecules like collagen, but D-forms allow designers to challenge typical biological interactions, giving rise to protease-resistant scaffolds, or tailored inhibitors in drug design. Having that stereocontrol opens up applications that stretch from vaccine adjuvant design to stable bioconjugates for diagnostic imaging. Our experience comes not just from the manufacturing end, but through years of close collaboration with clients who return to us once they see how tightly controlled stereochemistry makes or breaks their results.
Chemists value trans-4-hydroxy-D-proline for roles in peptide synthesis, especially where backbone modifications influence secondary structure or binding affinity. For research into enzyme inhibitors, swapping in a D-proline can block natural enzyme processing. Medicinal chemists create cyclic peptides and mimics that stay intact in harsh biological media. Sometimes just a single stereochemistry shift at proline enhances selectivity or bioavailability. Working with contract synthesis teams, we find many they rely on our batches to test libraries of new drug candidates—having a stable, pure starting material prevents failed syntheses downstream.
In academic labs, research groups utilize our hydroxy-D-proline for structural biology projects. It acts as a probe in folding studies, or as a structural motif in supramolecular chemistry. Solid-phase synthesis operations often need kilogram quantities each month, putting supply reliability at the center of ongoing projects. We take client requests seriously and are transparent about lead times for large orders or requests for supplementary analytical data. This open line helps teams plan research timelines with fewer surprises.
Trans-4-hydroxy-D-proline shares many similarities with its L-isomer, but its behavior diverges in biological systems. Collagen’s triple helix, for instance, depends almost entirely on the L-form. D-forms, on the other hand, enable engineers to build protease-stable scaffolds. Some customers arrive after discovering the limitations of racemic hydroxyproline they sourced elsewhere. Racemic forms muddy experimental results, and separating isomers at the bench siphons valuable time from core projects.
Cis-4-hydroxy-D-proline and related analogs introduce their own challenges. Their synthesis often struggles with lower yields and extra purification, leading to wider batch-to-batch variation. Researchers running comparative studies see different chemical reactivity and stability between cis and trans compounds, as well as between D- and L- isomers.
As one result, those working in structure-activity relationship (SAR) studies or advanced synthetic methods frequently request trans-4-hydroxy-D-proline by name, as it allows for clear interpretations and robust synthetic outcomes. Attempts to substitute in the L-form when the D- was called for have led to costly restarts; project leaders often share such lessons with us, underlining the direct productivity gains from picking the right isomer upfront.
Behind each bottle lies a documented process honed by years of feedback. Our lot records extend from raw amino acid sourcing, through hydroxylation, cyclization, resolution, and multiple recrystallization stages. All steps align with analytical control checkpoints—TLC, chiral HPLC, and final full spectrum analysis.
We survey each batch for moisture content and residual solvents, since trace contamination can derail downstream chemistry, especially when prepping for scale-up or GMP conversion. Over the years, we’ve responded to custom requests for heavy metal assays or particle size analysis, integrating feedback into our process. Direct dialogue with scientists using our trans-4-hydroxy-D-proline has identified subtle analytical requirements, such as quantitating potential epimerization side-products or providing advanced chiral purity profiles.
Shipping and storage follow well-tested protocols to avoid deterioration. Simple changes, such as adjusting container size and selecting container materials with low water permeability, have sharply reduced reported shelf-life issues.
Chemical manufacturing depends on more than reactors and paperwork. Reliable supply of starting materials underpins everything we do. Raw D-proline, each reagent, and solvent is sourced through vetted suppliers—partnerships that sometimes take years to develop. If a reagent purity slips, it impacts stereoselectivity and yield. We’ve seen supply chain snags: a temporary shortage at a solvent plant can ripple down, delaying large scale batch production.
We stay engaged with global and regional sourcing channels, tracking shifts in availability which might impact lead times or pricing. Coordinating with logistics providers knowledgeable in handling sensitive, moisture-prone materials minimizes customs delays and preserves product condition. We have found that such groundwork removes headaches for researchers waiting on critical shipments, especially during periods of high demand or regional disruptions.
Discussions with chemists and technical staff about real-world pain points in peptide synthesis—low coupling efficiency, reagent incompatibility, solubility breakdowns—inform our ongoing product refinements. Rather than treating clients as silent recipients, we trade observations about challenging coupling steps or solvent choices in routine correspondence. This feedback informs not only our quality control, but the ongoing evolution of synthesis and purification protocols.
Formulating internal FAQs and technical bulletins based on these exchanges, we answer questions ranging from scalable coupling conditions to best storage practices. This has led to the design of batch packaging that matches client workflows, whether that's single-use ampules for sensitive work or larger jars for batch processing. Each innovation comes from accumulated feedback and the understanding built over years of close chemical collaboration.
Mistakes and surprises have shaped our manufacturing more than anything else. A single batch that fails to meet purity specifications—perhaps because of batch crossover or minor contamination—forces a hard look at every upstream step. Sometimes feedback from a disappointed customer leads to a change in standard operating procedures; for example, refining our documentation of solvent lots and expiration dates. These improvements take hold not just in paper records but in work habits and team mindset.
We make our analytics, release criteria, and processing details open to audit by regular clients. The willingness to open our records speeds trouble-shooting when a downstream process hits a snag and gives everyone on the project team confidence in what's inside the bottle.
All large-scale chemistry brings with it responsibility for safe handling, reduction, and treatment of waste streams. Years ago, hydroxy-D-proline batches produced more aqueous and organic waste than our current approach, but ongoing investments in solvent recovery and waste minimization now reduce total output per kilogram of production by over half compared to earlier processes.
Adhering to strict waste-handling and community safety rules has sometimes meant increased costs, but it also paves the way for long-term operation in compliance with both local and international frameworks. It is not only the right thing to do—it’s built into customer trust and the daily health of our production team.
Emerging applications in peptide-based therapeutics and drug-delivery platforms continue to drive demand for specialized non-standard amino acids like trans-4-hydroxy-D-proline. More collaborative projects push us toward even higher standards of purity—beyond 99%, seeking additional verification by chiral SFC or advanced HPLC-MS. Clients working in structure-based drug design and high-throughput screening are increasingly looking for isomerically pure building blocks to keep pace with rapid compound library development.
Our in-house R&D works alongside researchers developing new peptide scaffolds or conjugates, helping to address unanticipated solubility or reactivity challenges. We keep an eye on trends such as green chemistry, exploring catalytic and enzymatic methods that might decrease environmental impact or increase stereoselectivity further.
Producing trans-4-hydroxy-D-proline in quantity and to high specifications has pushed us to improve at practically every level. With every development, we discover new challenges and deepen our understanding of raw material sourcing, process control, logistics, and technical support. Our relationships with chemists, project managers, and technical staff across the globe give shape and meaning to the work.
The end result—a stable, high-purity compound with critical stereocontrol—makes research into new therapies, materials, and diagnostics a smoother process. Each batch marks a collective achievement built on conversations, feedback, and years of small refinements. Manufacturing chemicals isn’t just about mixing ingredients and bottling the result. It includes the combined experience of people working to help others carry out new science and solve old problems.
Producing trans-4-hydroxy-D-proline means managing dozens of variables, from seasonal changes affecting raw material condition to maintaining uninterrupted cold-chain logistics for sensitive shipments. It takes more than following a standard route from route selection to final bottling. We insist on tight monitoring of each reaction, not just because customers demand high purity, but because our own troubleshooting over the years has taught us exactly where small lapses lead to outsized impacts. Each improvement and process tweak arises from a real situation—a problematic shipment or a research group finding an off-spec result—that gets traced, analyzed, and built into the next round.
For those working in discovery, protecting the reliability of their building blocks saves time, money, and morale. Our focus on clear communication, rigorous record-keeping, and willingness to listen has made us a front-line partner instead of just a materials supplier. The field keeps moving, and new demands keep us learning every day.
We commit to keeping an open channel with every scientist or manufacturer placing their research in our hands. No batch of trans-4-hydroxy-D-proline leaves our facility without full documentation, and we welcome questions about route history, impurity profiles, or process changes.
With a product this specialized, even small improvements matter—whether that's a switch to a greener solvent, an optimization that increases yield marginally, or a new specification requested for a specific trial. Over time, this continuous evolution creates value: not just in the molecules packaged and shipped worldwide, but in the professional trust and shared mission with every team we work with.