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HS Code |
585252 |
| Product Name | O-Benzyl-DL-Serine |
| Cas Number | 15627-30-4 |
| Molecular Formula | C10H13NO3 |
| Molecular Weight | 195.22 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 109-113°C |
| Purity | Typically ≥98% |
| Solubility | Slightly soluble in water, soluble in organic solvents (e.g., ethanol, methanol, DMSO) |
| Storage Conditions | Store at 2-8°C, in a tightly closed container |
| Synonyms | DL-Serine, O-benzyl ether; Benzyloxy-DL-serine |
| Iupac Name | 2-Amino-3-(benzyloxy)propanoic acid |
| Smiles | C1=CC=CC=C1COC(C(C(=O)O)N) |
As an accredited O-Benzyl-DL-Serine 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 of O-Benzyl-DL-Serine, with a white screw cap and tamper-evident seal, labeled with hazard information. |
| Shipping | O-Benzyl-DL-Serine is shipped in compliance with safety regulations, packaged securely in sealed containers to prevent contamination or moisture exposure. It is typically transported at ambient temperature unless otherwise specified, with proper labeling and documentation. Shipment includes handling instructions and safety data to ensure safe delivery and storage upon arrival. |
| Storage | O-Benzyl-DL-Serine should be stored in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. It is advisable to keep it at room temperature, away from incompatible substances such as strong oxidizers. Proper labeling and storage in accordance with safety regulations are recommended to prevent contamination and degradation of the chemical. |
Applications of O-Benzyl-DL-Serine in Industrial ManufacturingAs a specialized manufacturer of O-Benzyl-DL-Serine, we supply this amino acid derivative directly to regulated industries where purity, batch consistency, and reliable scale-up are core requirements. Below, we detail the primary downstream application scenarios supported by this material, with explicit reference to relevant compliance, formulation, processing, and end-use criteria. 1. Peptide Synthesis for Pharmaceutical IntermediatesPharmaceutical peptide manufacturers use O-Benzyl-DL-Serine as a protected building block during solid-phase peptide synthesis (SPPS). The benzyl group provides temporary hydroxyl protection of the serine side chain, preventing unwanted reactions during elongation steps. After the main peptide chain assembly, downstream deprotection under catalytic hydrogenolysis yields the target peptide essential for active pharmaceutical ingredient (API) development, especially where serine residues occur within the sequence. Industry compliance standards
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2. Chiral Intermediate for Active Pharmaceutical Ingredient (API) SynthesisAPI manufacturers utilize O-Benzyl-DL-Serine as a synthetic intermediate for constructing small-molecule drugs requiring serinol or other aminodiol substructures. The benzyl-protected variant enables selective deprotection and functional group manipulation under mild conditions, ensuring downstream product purity. Applications focus on antiretroviral, cardiovascular, and CNS drug synthesis where interrupted serine analogues are key intermediates. Industry compliance standards
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3. Custom Building Block in Fine Chemical SynthesisChemical manufacturers focused on producing specialty esters, key starting materials, and custom intermediates select O-Benzyl-DL-Serine to provide a reactive protected serine unit. Its chemical stability during condensation, reduction, or substitution reactions makes it suitable for constructing complex organic frameworks, including protected aminodiols and functionalized amino acid esters for subsequent elaboration. Formulators value the selective removability of the benzyl group for multi-step synthesis planning. Industry compliance standards
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4. Protected Amino Acid Reagent for High-Purity Research ChemicalsResearch laboratories and specialty chemical producers use O-Benzyl-DL-Serine as a protected amino acid standard for analytical chemistry, purity benchmarking, and the manufacture of traceable standards. Its defined structure and controlled protection enable consistent reference material production, facilitating QC validation and analytical method development within life science and pharmaceutical R&D environments. Industry compliance standards
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5. Protecting Group Precursor for Advanced Bioconjugation ReactionsO-Benzyl-DL-Serine is applied in specialty bioconjugation workflows where regulated stepwise protection and deprotection of amino acid side chains is crucial. The benzyl-protected serine moiety supports construction of bioactive oligopeptides, modified proteins, and diagnostic reagents requiring precise spatial configuration during chemical modification. Biotech and diagnostics companies adopt stringent process controls to manage residual protecting group content post-processing. Industry compliance standards
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The chemical world often asks for specialty amino acid derivatives, but not every product on the market truly meets the needs of the bench chemist or process engineer. O-Benzyl-DL-Serine, which our reactor teams have been producing for years, stands out from the pack—both for its consistent quality and the know-how that goes into every batch.
We craft O-Benzyl-DL-Serine under tightly monitored conditions, with a focus on reproducibility and low impurity profiles that we’ve honed through continuous feedback from peptide labs and pharma partners. Each batch emerges as a fine white to off-white powder, ready to be integrated into peptide synthesis pipelines or intermediate steps where side-chain protection actually matters. The protection of the serine hydroxyl function by the benzyl group means that our compound resists the unwanted side reactions that plain DL-Serine so often suffers in solid-phase and liquid synthesis protocols.
Specifications get referenced plenty, but they don’t matter unless they translate into something useful at scale and in day-to-day lab work. Our O-Benzyl-DL-Serine consistently delivers purity exceeding 98% by HPLC, confirmed by both our in-process controls and final QC assays. Moisture content sits low, thanks to a vacuum drying step that came straight from feedback working with stickier alternatives. With a known molecular weight, exact melting range, and structurally validated by NMR and mass spec, the material responds predictably in analytical and preparative chemistries.
Back when our teams worked on the original process route, we learned quickly what customers were actually asking for: O-Benzyl-DL-Serine in a form that dissolves readily in organic solvents, with low tendency to cake in storage, and without residual by-products that complicate downstream reactions. That meant fine-tuning solvent systems during purification, and switching to high-grade benzyl chloride to avoid meta/para isomer traces that might trip up sensitive peptide syntheses.
Our product directly addresses pain points chemists report—unwanted deprotection under mild basic conditions, sticky residue in vessel cleanouts, and lot-to-lot variation in melting point. By continually testing process improvements on our pilot plant lines, we cut steps where no longer needed, trimmed solvent volumes, and refined purification to give the final compound a better handling profile than a lot of catalog alternatives. This makes a noticeable difference for users in pharma R&D, who routinely build libraries of protected amino acids for SAR studies, as well as for scale-up groups transitioning from grams to multi-kilos.
O-Benzyl-DL-Serine’s main difference from plain DL-Serine: that benzyl group, introduced via the sidechain hydroxyl. We do not use racemization-prone conditions at any stage, so the optical integrity of the DL mixture stays preserved. Some manufacturers take shortcuts—rougher benzylation methods can abandon unconverted starting material or generate over-benzylated byproducts, which show up as hazes or sticky residues. Our in-line monitoring during work-up catches those issues early, so the product in your flask matches the compound you expect on paper.
Compared with Fmoc- or Boc-protected serine derivatives, O-Benzyl-DL-Serine comes with better stability during certain coupling or activation conditions. For applications where Fmoc cleavage (or acid lability from Boc removal) complicates the downstream chemistry, O-Benzyl-DL-Serine provides an option that stands up to a wider variety of reaction parameters. Our technical teams have observed that, in peptide segments requiring robust protection but later global deprotection, the benzyl group’s established removability via hydrogenolysis provides both security and ease-of-removal. Chemists report fewer side products from O-Benzyl-DL-Serine when using palladium-catalyzed deprotection, especially when working with reactive substrates.
Manufacturing specialty amino acid derivatives means facing challenges that don't always show up in technical data sheets. In the early days, we speculated that offering higher purity O-Benzyl-DL-Serine would win over the entire customer base. Yet, real feedback forced us to adapt in other, less obvious ways. One big lesson was about trace water. Even 0.5% moisture, though in spec by old standards, caused unwanted ring opening in cyclization reactions at analytical labs. Our setup now includes in-line water testing and active moisture scrubbing to push moisture content much lower, giving downstream processes a smoother ride.
Another challenge centered on storage stability. Customers with low-throughput or infrequent use found that lesser products would yellow or clump up within weeks, which led to inconsistencies batch-to-batch at their sites. By switching up our packaging process—using moisture-barrier containers and integrating nitrogen blanketing at the final fill—we saw improved stability and less customer frustration. We take pride when repeat clients mention that our material still pours free and white months after opening.
Our technical staff doesn’t operate in an ivory tower. Direct communication with peptide chemists, process scale-up engineers, and university researchers drives our improvement cycle. More than a few times, a conversation about a stubborn solubility issue or an unexpected spiking impurity in customer test runs led to tweaks in our isolation and drying conditions. Sometimes that has meant investing in better glassware or switching to different solvent washes. Other times, we’ve run trial lots under customer-specific protocols to pinpoint bottlenecks and adapt our main production.
This on-the-ground feedback loop ensures a product that, once used, finds its way again into future synthesis routes and grant-funded research. We have seen more process innovations within the peptide sector over the past decade than in the previous twenty years combined, most of which require high-fidelity starting materials. By always tracking how our compound performs in these evolving environments—from new coupling agents to unusual solvents—we make strategic adjustments before issues snowball.
Scaling from grams to multi-kilogram lots comes with its own set of hurdles. Raw material sourcing, reactor design, and labor planning all shift as orders change from small research runs to production-scale campaigns. We've built in modular lines that let us pivot based on customer demand—if your workflow calls for half a kilo of O-Benzyl-DL-Serine in a rush, we're ready, and if your process needs bespoke analytical certificates or expanded impurity profiling, we produce the documentation fast because we know what goes into each tank and filter.
Our expanded purification suite and in-process analytical capability means we don’t wait for end-of-line testing to catch problems. We track every variable—temperature, pH, reagent concentration—across the hours-long synthesis and work-up. The same team troubleshoots and iterates across campaigns, so the lessons embedded in every previous batch show up in the next lot’s consistency. Customers ask us whether our O-Benzyl-DL-Serine meets specific thresholds on trace metals or organic by-products, and we can answer with lot-specific data, since we analyze it ourselves, on our own equipment, every time.
We’ve learned to approach each application with fresh eyes. In peptide synthesis, the conditions can vary by project—mild bases, strong acids, diverse solvents—and the choice of protecting group affects outcomes. O-Benzyl-DL-Serine meets a clear need for stability: the benzyl group won't budge under conditions that would strip Fmoc or Boc, and we've verified this by running side-by-side syntheses at both bench and pilot scale. Staff working in pharma pilot plants have praised our product for holding up through multiple transfer steps without decomposing or generating odd byproducts.
This durability finds a place beyond peptide synthesis, too. Researchers exploring non-ribosomal peptide analogues or even custom fuel cell membranes have told us that non-labile O-Benzyl protection extends utility into new types of organic synthesis—where serine’s open hydroxyl might react in unintended ways if left unprotected. We've supported projects ranging from biosensor development to specialty polymer precursors, mainly by providing consistent batches and troubleshooting solubility or reactivity issues together with customers.
Those seeking highly selective protection often compare O-Benzyl-DL-Serine to Fmoc-Ser(Bzl)-OH and Boc-Ser(Bzl)-OH. Our focus remains on straightforward O-Benzyl-DL-Serine without extra N-terminal protection, so you can adapt to specific coupling strategies or protection schemes. Our customers appreciate skipping the extra step of N-deprotection, especially in sequence assembly where time and yield matter.
Some workflows demand N-protection for immediate peptide chain formation, particularly for solid-phase synthesis. For these, we provide guidance on compatible downstream N-protection steps, drawn from our process experience. Our O-Benzyl-DL-Serine leaves your options open, supporting more flexible synthetic planning and fewer supply-chain headaches. In all cases, our ongoing technical support walks users through compatibility checks and test reactions whenever process changes demand it.
We see the market moving toward more elaborate protected amino acid libraries—tailored for novel peptide drugs, bioconjugation, or specialty materials. O-Benzyl-DL-Serine continues to anchor many of these new builds, both because of its straightforward synthesis and because of its lack of alternately-labile protecting groups. As regulatory scrutiny tightens in the pharma sector, we’ve strengthened our traceability protocols, from raw benzyl chloride sourcing to full spectra on each lot. This transparency now draws as much praise as the product's performance.
Long-term partnerships with academic and industrial groups have prompted us to innovate—for example, introducing particle size options or adding documentation for use in regulated environments. We also regularly test for new impurities linked to process evolution, since changes upstream can introduce unknowns that make a downstream synthesis unpredictable. With O-Benzyl-DL-Serine, you can count on a product that not only solves today’s problems but adapts as your chemistry grows in complexity.
Every kilo of O-Benzyl-DL-Serine carries a traceable production record. Our plant’s systems log actual operator notes, in-process observations, and yield numbers, not just batch numbers. If a downstream problem crops up, we reconstruct the conditions for that lot and adjust our process accordingly. Years of regulatory inspections and customer audits have shaped these habits, and open communication with our clients means issues don’t get swept aside. We see ourselves as partners in our customers’ research, not just as suppliers.
This attitude extends to how we handle batch fails. Once, we caught a rare cross-contamination with an aromatic impurity during a packaging line switchover run. The anomaly surfaced during a routine customer check, which mirrored our own in-plant tests. Rather than passing compromised material forward, we stopped, traced the root cause, cleaned down all lines, and refunded the affected lot. Our relationship with customers didn't suffer—in fact, that transparency built more confidence in the next batch.
We take pride in the fact that customers can plan years of research around our products and not worry about process breakdowns from poorly controlled synthesis routes. O-Benzyl-DL-Serine stands apart from many catalog sources because it comes from a facility with modernized process controls and staff that take ownership at each stage. Our plant management reviews every deviation, and recurring issues prompt immediate process or training upgrades.
We document and archive digital spectra, chromatograms, and yields for each batch, allowing repeat clients access to historical data as new project requirements arise. Some research partners working through regulatory approvals return to reference our historical QC data against their own long-term stability studies. Because transparency and reliability lie at the foundation of every kilo we ship, we adapt to tighter batch-to-batch tolerances as markets demand.
We don’t chase accolades or push buzzwords. Our O-Benzyl-DL-Serine reflects years of real-world partnerships and practical experience in the specialty reagent field. By addressing root causes of synthesis problems and listening to direct user feedback, we deliver a protected serine derivative that makes the busy life of a chemist or process engineer easier. Whether you’re bench scaling, operating process reactors, or guiding pharma R&D, you can count on a manufactured amino acid derivative that delivers under pressure, batch after batch.