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HS Code |
834054 |
| Product Name | Boc-L-4-Chlorophe |
| Chemical Name | N-Boc-4-chloro-L-phenylalanine |
| Cas Number | 161902-46-5 |
| Molecular Formula | C14H18ClNO4 |
| Molecular Weight | 299.75 |
| Appearance | White to off-white solid |
| Purity | ≥98% |
| Storage Temperature | 2-8°C |
| Solubility | Soluble in DMSO, methanol |
| Melting Point | 95-98°C |
| Synonyms | tert-Butoxycarbonyl-4-chloro-L-phenylalanine |
As an accredited Boc-L-4-Chlorophe factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical `Boc-L-4-Chlorophe` is packaged in a 25g amber glass bottle with a tamper-evident cap and detailed labeling. |
| Shipping | Boc-L-4-Chlorophe is shipped as a solid, securely sealed in a chemical-resistant container. It is packed according to all applicable chemical safety regulations, with cushioning to prevent breakage and exposure. The package is clearly labeled with hazard information and shipped via a certified carrier specializing in laboratory chemical transport. |
| Storage | Boc-L-4-Chlorophe should be stored in a cool, dry, and well-ventilated area, away from sources of heat and ignition. Keep the container tightly closed, protected from moisture and direct sunlight. Store at 2-8°C (refrigerated) for optimal stability. Avoid contact with incompatible substances such as strong oxidizers and acids. Follow standard chemical storage protocols and ensure appropriate labeling. |
Applications of Boc-L-4-Chlorophe in Industrial ManufacturingBoc-L-4-Chlorophe, as an important amino acid derivative, plays a critical role in several downstream sectors with demanding regulatory and technical requirements. We supply this raw material to industrial partners who incorporate it into active pharmaceutical intermediates, peptide synthesis, specialty chemical production, and advanced research reagents. Below, we detail its specific applications, processing integration points, required compliance standards, formulation parameters, and resultant end products. 1. Peptide-Based Active Pharmaceutical Ingredient (API) SynthesisPharmaceutical manufacturers use Boc-L-4-Chlorophe as a protected building block during solid-phase peptide synthesis (SPPS) stages for APIs containing chlorinated phenylalanine residues. Its reliable coupling and deprotection characteristics are essential for process control, chain elongation fidelity, and compliance with global quality standards. End users favor this material for producing custom and generic peptide APIs indicated for metabolic, oncological, and cardiovascular therapy areas. Industry compliance standards
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2. Small Molecule Drug Intermediate ManufacturingChemical process development teams select Boc-L-4-Chlorophe for its role as a chiral intermediate in the multi-step synthesis of specialty heterocycles, enzyme inhibitors, and halogenated small molecules with pharmaceutical relevance. Reliable supply and strict quality control ensure final synthetic intermediates fulfill regulatory submission requirements and downstream scalability. Industry compliance standards
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3. Specialty Peptidomimetic and Diagnostic Oligomer ProductionManufacturers of diagnostic kits and specialty biochemical reagents incorporate Boc-L-4-Chlorophe to construct modified peptides, oligomers, and peptidomimetics that require precise halogenated residue positioning for binding affinity, stability, or signal labeling. This application supports advanced molecular diagnostics and research tool markets. Industry compliance standards
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4. Research-Grade Analytical Reagent SynthesisReagent suppliers and scientific institutions use Boc-L-4-Chlorophe as a precursor for custom analytical standards, reference peptides, and isotopically labeled compounds. Strict traceability and analytical purity support advanced academic and industrial research protocols where halogenated amino acids serve as analytical tools, calibrators, or method validation materials. Industry compliance standards
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Boc-L-4-Chlorophe stands out in our lineup for its reliable protection of amino groups in peptide synthesis. As a manufacturer, real-world production issues and customer feedback shape the way we refine this product. Over the years, our process moved from small-batch synthesis to a dedicated workflow that ensures each lot meets critical demands for purity and consistency. For chemists who work deep in the weeds of peptide research or API development, this material solves practical bottlenecks that don’t get solved by generic precursors.
Our offering: Boc-L-4-Chlorophenylalanine, model identifier L-4-Cl-Phe-Boc, appears as a white to off-white powder. Batch purity hits above 98% on a dry basis, as confirmed by HPLC and NMR. Moisture content typically measures below 0.5%. This purity doesn’t just tick quality control boxes—it translates into cleaner downstream reactions and less trouble with side products. We keep particle size within a specified range, not because it looks good on paper, but because clumping in your flask or poor dissolution slows lab work down. Each kilogram packs tight into double PE bags inside fiber drums, shipped with the kind of handling you’d use for your own bench stock.
This building block gets chosen for one major reason: the combination of a Boc-protected amino group with a chloro-substituted aromatic ring. For solid-phase peptide synthesis (SPPS), Boc protection often gives a robust shield that stands up to TFA cleavage at just the right point in the process. Our product finds its way into complex projects—from early-stage discovery to full-scale pilot runs. Think about cyclopeptide assembly, or designing peptidomimetics with special functional handles. The chloride at the para position isn’t just a curiosity. It allows specific sites for later halogenation or cross-coupling reactions.
Some chemists stick with the Fmoc series for all their needs. We keep both on hand, but in our experience, Boc provides distinct benefits when working with sequences sensitive to base or moisture. Deprotection by acid makes the workflow more predictable in certain routes. Clients often ask why one would bother with Boc at all, but in practice, not all syntheses run best under base-labile conditions. During scale-up, acidolysis does not always cause racemization or rearrangements that base can trigger. In those cases, Boc-L-4-Chlorophe fits perfectly.
Manufacturing this compound isn’t a matter of buying bulk starting materials and pushing a button. Beginning with enantiopure L-4-chlorophenylalanine, every step in our route goes through hands-on optimization. On-site process chemists tested dozens of Boc-protection approaches until side-product profiles dropped into single-digit percentages. Our HPLC trace for each lot lines up over months of production cycles. This kind of repeatable outcome stems not from one magic step, but from coordinated adjustments—solvent swaps, reagent ratios, temperature holds.
Batch-to-batch variability sinks more projects than anyone likes to admit. You can’t have a mid-synthesis shift in melting point or residue melting onto glassware. Customers working with 10+ residues per peptide tell us the same story: each step depends on the last, so the protection group must disappear cleanly—no trace. The Boc group on our L-4-Chlorophe removes on cue, without unexpected byproducts that can bleed through purification steps. We monitor for t-butyl cations, dipeptide formation, and minute racemization signals—in real time, not just as part of last-minute release testing.
Academics and industry labs alike care about trace metals and unintentional contaminants. As production chemists, we see how even low ppm levels of copper or iron—often introduced in raw L-4-chlorophenylalanine or via solvents—cause headaches in complex peptide assemblies. Metal content analysis forms a standard checkpoint, with documented reductions via improved glassware selection and extra scrubbing of reactor surfaces. Any glycine, alanine, or diastereomeric impurities get flagged before packaging. After years of talking with principal investigators, we learned that a subpar batch doesn’t only waste materials—it sometimes invalidates weeks of synthetic effort.
Solubility issues and the little details get big in scale-up. Material that cakes, throws off fine dust, or clumps under humidity won’t run through splitters or feed automatically into reaction vessels. We don’t skimp on blending or vacuum drying, because as former bench chemists ourselves, we value chemical that measures out by scoop or pipette, not a hammer.
Products like Fmoc-L-4-chlorophenylalanine offer alternative protection strategies, yet their lability profiles and compatibility with certain reagents limit usage in acid- or base-sensitive sequences. Fmoc chemistry excels in parallel, automated syntheses with demand for rapid base-mediated deprotection. Boc, in contrast, dominates where acidolysis steps can be tightly controlled, and product sensitivity to base matters.
From the ground up, the parameters we watch for Boc-L-4-Chlorophe differ fundamentally from those on standard L-4-chlorophenylalanine. Not all Boc-protected amino acids resist hydrolysis or oxidation at the same rate. We tinker with antioxidant additives and oxygen-barrier packaging, especially in hot, humid climates. At gram scale, users report visibly higher performance—the compound dissolves swiftly in DMF or DCM, filters cleanly, and doesn’t introduce haze or particulates in SPPS.
The chloride on the aromatic ring has a job: ready for further cross-coupling or halogen exchange post-synthesis. Other substitutions, such as methyl or fluorine, don’t always serve the same synthetic strategy. Our clients in API R&D appreciate that we deliver precise positional substitution, as off-target substitutions haunt analytical and scale-up results. Feedback cycles with custom peptide houses led us to push for tighter controls on chiral purity and improved documentation. We draw on concrete case histories—one client flagged a problem where a competitor's lot gave lower yield and more byproducts; our material, from a verified route, solved the bottleneck by sidestepping unexpected acidolysis fragility.
In contract research labs, organic chemists depend on reliable Boc building blocks for non-standard peptides. Novel peptidomimetic frameworks or targeted cancer therapy candidates often need a halogenated phenylalanine early in the sequence—this makes downstream radiolabeling or probe conjugation easier. We receive regular requests for large lots, destined for clinical trial materials, where every variable has to be under tight control.
During a recent project with a European pharmaceutical firm, our Boc-L-4-Chlorophe fed directly into solid-phase peptide synthesis of a macrocyclic scaffold used in diagnostic imaging. The purity and chemical stability allowed the research team to run multiple coupling-deprotection cycles with virtually no detectable side-reactions. Their lead chemist later reported yields above target and complete removal of protection without residual color or odor, which sped their purification process significantly.
We support academic projects, too. One research group in Asia used our material while developing new analogues for neurological targets. Side-product suppression and straightforward cleavage conditions mattered for their limited resources. Our technical support staff walked their PI through best practices for storage: airtight containers with desiccant until ready to dissolve. Real feedback shapes how we tweak packaging, ensuring less lost material to atmospheric moisture.
Every batch of Boc-L-4-Chlorophe turns into a running dialogue with process engineers. We build lead times for raw material sourcing because disruptions upstream (not always visible to the lab chemist) can send ripples through the whole supply chain. Back in 2020, we encountered solvent shortages that delayed key steps. We had to retool the purification protocol—switching supplier partners midway—to keep our carbon footprint down and our output steady.
Working with direct end-users—even at small volume—gives us real information about bottlenecks in logistics and changing regulatory compliance. In the past, bulk shipments carried without secondary containers risked moisture uptake before arrival. Chemists complained of sticky, partially hydrolyzed material. Since upgrading the packaging line to sealed PE drum liners, drop-off in quality complaints followed almost overnight.
Our production teams adapted vigorously during pandemic-related restrictions, focusing on batch record traceability, new training for line staff, and regular environmental monitoring. Technology upgrades for real-time impurity tracking allowed us to move faster, reducing isolation time and boosting lot turnover without lowering quality checks.
Let’s get specific about process. Boc-L-4-Chlorophe synthesis demands tight stoichiometry; excess Boc2O leads to t-butyl ester byproducts, but too little leaves mixed residues. Automated pumps, temperature-controlled jacketed reactors, and constant pH monitoring have become standard in our plant. Our team rotates through cleaning cycles and uncapping reactors only under nitrogen, which keeps the batch from picking up airborne contaminants. Chemists in the plant report any deviation, so adjustments happen before costly mistakes reach shipments.
End-users sometimes share wish lists for even better performance or easier dissolution. Some prefer finer powders to weigh out faster; others want granules for automated dosing. Maintaining consistency means balancing these needs—just slamming the mill at the end won’t guarantee the right dissolution. Milling, sieving, and drying settings pull from years of plant-floor experience. Direct dialogue with peptide manufacturers highlights what works and what gets in the way.
Understanding how this product holds up in transit shapes our packing approach, too. Hot shipping lanes risk slow decomposition or caking. Customers running mass spectrometry analyses demand certificates stating lot analysis—including details about storage temperatures and contamination thresholds—as a standard inclusion with each container. We learned not to cut corners on documentation after one large shipment sat on a dock in tropical heat; the loss in stability drove a change in shipping and labeling practices across our whole range.
Regulators demand more traceability with each passing year. We stay ahead by documenting every reagent and batch process step. Regulatory submissions grow heavier, but our habituated attention to process documentation pays off in both external audits and real user confidence. Recent changes in hazardous goods classification for intermediate compounds pressed us to refine storage labeling, update SDS documentation, and retrain shipping partners. Rather than treat compliance as a paperwork exercise, our senior chemists walk the floor to ensure labeling actually reflects in-practice handling.
On-site, responsible waste management turns theory into practice. Each purification generates contaminated solvent and solid residues; we invested in upgraded scrubbing systems and increased volume in our effluent treatment plant. Downstream recovery and incineration cut emissions, keeping discharge within statutory limits. Periodic, unscheduled external audits keep us sharp—internal standards for impurity ppm rarely get close to maximum allowed levels. Such detailed controls give end-users confidence, making their own regulatory filings easier.
Global demand for specialized amino acids continues to grow as custom peptide synthesis ramps up in biotech and pharmaceutical R&D. We hear from customers who want higher-purity materials, better documentation, and advice on protocol tweaks. Their needs push us toward tighter product release standards and more transparent supply chain documentation. Even small improvements in lot consistency or speed of fulfillment ripple across project timelines for new therapeutic entities or diagnostic test development.
Increasingly, researchers value technical support almost as much as the product itself. We leverage not just formal analytics, but the daily notes taken by line chemists and plant managers. This “tribal knowledge” has trimmed downtime, improved output, and prevented costly product loss events not just with Boc-L-4-Chlorophe but across our specialty amino acid portfolio.
Boc-L-4-Chlorophe showcases the close link between chemical manufacturing and real-world research. Each gram produced reflects direct experience—we don’t take shortcuts, because customers using this product for peptide synthesis or advanced materials can’t afford inconsistencies. Every improvement, from process upgrades to better packaging, starts as feedback from the bench and flows straight into plant practice. Drawing on honest dialogue with researchers and an experienced technical team, we choose what works—not just what the textbook suggests. Years on both the plant floor and in the lab prove that quality materials aren’t the product of one-time successes but keep evolving through a cycle of open communication, constant monitoring, and willingness to dig deep into the details. We aim for reliability batch after batch, so your syntheses stay on track from idea to outcome.