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HS Code |
733833 |
| Productname | Boc-(R)-3-Amino-4-(4-Chloro-Phenyl)-Butyric Acid |
| Synonyms | tert-Butoxycarbonyl-(R)-3-amino-4-(4-chlorophenyl)butanoic acid |
| Molecularformula | C15H20ClNO4 |
| Molecularweight | 313.78 g/mol |
| Appearance | White to off-white solid |
| Purity | Typically ≥98% |
| Solubility | Soluble in organic solvents like DMSO, DMF |
| Storagetemperature | 2-8°C |
| Opticalactivity | (R)-configuration, chiral |
| Protectinggroup | Boc (tert-Butoxycarbonyl) |
| Chemicalclass | Amino acid derivative |
| Smiles | CC(C)(C)OC(=O)N[C@@H](CC1=CC=C(C=C1)Cl)C(=O)O |
| Usage | For chemical synthesis and peptide chemistry |
As an accredited Boc-(R)-3-Amino-4-(4-Chloro-Phenyl)-Butyric Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The packaging contains 10 grams of Boc-(R)-3-Amino-4-(4-Chloro-Phenyl)-Butyric Acid in a sealed amber glass bottle, clearly labeled. |
| Shipping | Boc-(R)-3-Amino-4-(4-Chloro-Phenyl)-Butyric Acid is shipped in sealed, chemical-resistant containers to ensure stability and prevent contamination. The package includes safety labeling and documentation in compliance with relevant regulatory guidelines. Temperature and handling requirements are followed to maintain product integrity during transit, typically shipped by certified chemical carriers. |
| Storage | **Boc-(R)-3-Amino-4-(4-Chloro-Phenyl)-Butyric Acid** should be stored in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Ideally, keep it at 2–8°C (refrigerator conditions). Avoid excessive heat, freezing, and exposure to air. Ensure proper labeling and follow all relevant safety and handling guidelines for organic chemicals. |
Applications of Boc-(R)-3-Amino-4-(4-Chloro-Phenyl)-Butyric Acid in Industrial ManufacturingBoc-(R)-3-Amino-4-(4-Chloro-Phenyl)-Butyric Acid plays a key role in the synthesis of specialty compounds within the pharmaceutical and fine chemical industry. As a specialized manufacturer, we provide this chiral intermediate for critical steps in multiple downstream applications, supporting advanced process controls and strict regulatory requirements. 1. Chiral Intermediate for Sartan Antihypertensive APIsPharmaceutical manufacturers routinely incorporate this intermediate into the key synthesis pathway for certain sartan-class antihypertensive drugs. The (R)-configuration provides precise stereochemistry for forming targeted final actives, ensuring reliable molecular integrity for each API batch. The Boc group confers temporary protection during peptide coupling and downstream derivatization, facilitating consistent scaling from pilot to commercial production. Integration into validated routes speeds up regulatory submission and guarantees batch traceability under cGMP frameworks. Industry compliance standards
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2. Protected Chiral Building Block in Peptide Drug SynthesisFine peptide pharmaceutical producers use this material as a chiral protected amino acid derivative in selective peptide elongation processes. Its Boc group stability under mild acid conditions enables precise chain extension without risk of racemization. Post-assembly, the intermediate supports straightforward deprotection and facilitates purification during HPLC or preparative chromatography, contributing to consistently high purity yields for regulatory submissions. Industry compliance standards
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3. Key Intermediate for CNS Active Compound SynthesisThis material functions as a specific intermediate in the synthesis of investigational compounds targeting central nervous system (CNS) receptors. Its chiral nature allows developers to build molecular fragments that retain target selectivity and metabolic stability. Process chemists value its particulate control in continuous or batchwise preparation, ensuring downstream coupling reactions demonstrate high enantiospecificity and chemical consistency required in clinical candidate preparation. Industry compliance standards
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4. Intermediate for Chiral Ligand Synthesis in Asymmetric CatalysisProducers of chiral ligands for industrial asymmetric catalysis select this compound to construct custom ligand frameworks for enantioselective synthesis. The rigid chiral center and the Boc-protection facilitate controlled reaction conditions and reproducible ligand configurations. After incorporation, the material allows for efficient downstream conversion to ligand scaffolds, which are applied in metal-catalyzed hydrogenation and carbon-carbon bond forming processes on kilogram-to-multiton scale. Industry compliance standards
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The work we do at the manufacturing floor never really stops, especially on days when our reactors are full of Boc-(R)-3-Amino-4-(4-Chloro-Phenyl)-Butyric Acid. Watching that complex sequence of raw materials turn into a molecule that serves a real role in research and pharmaceutical development reminds us why we sweat the details. From selecting the right protective group, like tert-butoxycarbonyl, to that final purification run, every choice matters. Chemists always look for compounds that deliver both chiral purity and chemical stability, but this one answers calls for both.
Some years back, most amino acid derivatives hadn’t yet been tailored so specifically to suit today’s asymmetric synthesis requirements. Researchers worked with what was on hand or modified starting materials themselves, which increased uncertainty in yield and purity batch to batch. By keeping tight rein on our own process, from sourcing to the last quality-control step, we anchor the final product’s value in the way we create it. Each run must hit strict specs for enantiomeric excess – drifting even half a percentage point changes everything for downstream chemistry.
People think supplying chemical building blocks is about mixing A and B. It’s easy to mistake all white powders as interchangeable until you work a reaction with a poor-quality lot. Boc-(R)-3-Amino-4-(4-Chloro-Phenyl)-Butyric Acid isn’t forgiving of shortcuts. Over years of producing it, we’ve learned the enemy of reliability lurks in overlooked water content, minor temperature fluctuations, or an extra day on the shelf. We design our process to avoid that: constant monitoring, strict environmental controls, and no guesswork at packaging. Customers often come back to us after using lower-purity material elsewhere. Reactions stall; side products creep up and waste time they can’t spare.
To keep every batch consistent, we follow channels of synthesis that deliver both the optical rotation our clients specify and purity levels their chromatography confirms. Each batch record shows our hands have checked and double-checked at each step. Not all manufacturing approaches are equal. We've seen how small variations in supplier practices ripple outward—customers find themselves troubleshooting failures they never expected, chasing hidden contaminants. Our controlled method for Boc protection means decomposition and racemization never have a foothold. That’s not something a middleman can guarantee, only a maker who knows the lot from start to finish.
On paper, Boc-(R)-3-Amino-4-(4-Chloro-Phenyl)-Butyric Acid typically comes with a given CAS number, molecular formula, and molar mass, but the story behind this compound unfolds during scale-up production. We work against a clear reference for chiral purity, confirmed each time by polarimetry and HPLC with chiral columns. Most buyers ask for at least 98% chemical purity, and our standard process pushes beyond, meeting benchmarks for strict research demands. Less obvious is how moisture content—sometimes ignored—kills yield in sensitive couplings. By packaging under controlled humidity, we solve this before the customer ever opens the container.
Grain size also plays a role. We keep particle size within a manageable range so the compound handles easily in research and pilot plant settings. Over-milled batches tend to clump; under-milled material disperses poorly. Sometimes a technician calls to ask why last week’s batch worked and this one doesn’t—often the answer lies in these fine details. For us, specifications sit as the outcome of careful process, not just numbers on a certificate.
Scientists working on new pharmaceuticals or specialty chemicals favor Boc-(R)-3-Amino-4-(4-Chloro-Phenyl)-Butyric Acid for its clean, reliable introduction of a chiral center protected with a Boc group. They use it to construct more elaborate molecules via peptide bond formation, Suzuki couplings, or custom syntheses where enantioselectivity means the difference between a hit and an inactive line in a data table. We've seen entire projects hinge on the reliability of building blocks like this. Flaws in optical purity or contaminant profiles throw off the big picture: yields fall, purification headaches multiply, and regulatory filings run into delays.
In development programs we’ve supported for small-molecule therapeutics, this compound finds its value in bringing a protected amine function to more advanced scaffolds. The 4-chlorophenyl ring adds leverage for future diversification, making downstream modifications possible. The acid function activates confidently during peptide coupling, while Boc protection resists undesired reactions under a wide range of conditions but comes off easily with mild acid. Our chemists tailor this aspect, balancing stability in storage against reactivity in the lab.
Most amino acid derivatives aren’t interchangeable in synthetic routes, and Boc-(R)-3-Amino-4-(4-Chloro-Phenyl)-Butyric Acid stands out for a mixture of reasons rooted in its actual structure. The (R) configuration matters for chiral drug development; the 4-chloro substituent enables further cross-coupling or direct substitution chemistry; the Boc protecting group’s robust nature shields the amine during activation or coupling steps in solid- and solution-phase approaches. It sidesteps pitfalls that come from using raw amino acids, which stain yields and seed unnecessary by-products during scale-up.
Alternatives like Fmoc-protected versions are out there, but the Boc group’s hydrolytic profile suits slightly harsher or catalyst-driven methods—this comes up in process development for customers who want broad flexibility. We talk through real-world applications every week with researchers whose work goes down if their compound base falls apart between synthesis steps. Unlike unprotected analogs, this product arrives ready to lock into diverse coupling conditions, freeing up time otherwise spent running test reactions or investigating mystery by-products.
The manufacturing side brings authority on process repeatability, which underpins trust. We draw on routine audits, in-house checks, and that steady rhythm of making batch after batch without guessing. Sourcing only from foreign third parties means losing that certainty. As the manufacturer, we resolve raw material inconsistencies at source, retest each precursor, and adjust process parameters based on patterns we spot over hundreds of syntheses. When impurities pop up in starting materials, our chemists trouble-shoot and resolve with tweaks well ahead of time—not by the time the final product fails QC. Problems caught early don’t snowball for our customers.
This reality grew clearer as global supply chains ran into disruptions that forced buyers to choose between uncertain timelines and unverified quality. Our investment in process control—down to regular calibration of every scale and temperature probe—ensures our Boc-(R)-3-Amino-4-(4-Chloro-Phenyl)-Butyric Acid won’t throw surprises. We’ve seen how generic or resold material often arrives off-spec: moisture creeping up, lots mixed from multiple origins, or incomplete HPLC purity. The difference flows down to the research itself—either results move forward, or teams stall rearranging experiments and budgets.
The world expects more from chemical producers with every passing year, both in technical merit and responsible stewardship. Our direct experience in synthesizing Boc-(R)-3-Amino-4-(4-Chloro-Phenyl)-Butyric Acid means less waste, as we tune recipes to maximize yield and minimize unnecessary solvents and by-products. We introduced in-line recovery systems after noticing that classic workups sacrificed too much solvent and increased the cost of disposal. Cleaner processes save on cost and reduce the environmental load—no abstract metric, just measurable savings by the end of each month.
Our approach to operator health and safety means each batch reflects not only product quality, but also adherence to safe handling procedures at every scale. Knowing the compound’s reactivity profile inside out saves time, but it also ensures our staff faces minimal risk. We document and improve steps each time we see opportunities for better containment or safer conditions. Regulatory compliance isn’t a checkbox for us—it emerges from a culture shaped by experience and lesson, where people know not to take shortcuts.
On the ground, production doesn’t always roll out smoothly. Some days, variations in solvent quality force adjustments to crystallization conditions. Sometimes the chiral catalyst loses potency, cutting into enantioselectivity. We keep redundant controls, so a single off-spec reagent never sinks a batch. Extra analytical runs, cross-checks, and an open line between synthesis and QC teams keep the chain strong from start to finish. These aren’t just process safeguards—each problem solved here keeps a researcher from losing weeks on a failed reaction later.
Demand cycles don’t always follow forecasts. One month, custom synthesis requests spike; another, we face slowdowns in raw material shipments from overseas. By holding core inventory and locking in key suppliers through direct partnerships, we weather market swings without passing uncertainty onto research partners or production teams down the supply chain. Our process design flexes to produce regular lots or scale up on short notice without quality dips. That flexibility only comes from mastering the compound’s quirks in real-world production, not just theoretical routes in a catalog.
We often talk directly with customers working out synthesis plans for new targets. Our technical team understands where Boc-(R)-3-Amino-4-(4-Chloro-Phenyl)-Butyric Acid fits and points out risks or advantages others miss because we’ve run the reactions ourselves, seen by-products run on our own TLC plates, and fixed problems at bench scale long before considering formal scale-up. A deep familiarity with the molecule helps us share more than just stock answers. If a researcher wants to modify the protection strategy, swap out the aromatic group, or couple under non-standard conditions, we have grounded insights on what usually works—and, just as importantly, what tends to go wrong.
Long-running projects depend on traceability. Every lot we ship comes with detailed documentation, including impurity profiles and enantiomeric excess data generated by our team, not copied or outsourced. If something goes wrong after shipping, we can trace the bottle back to its exact process date, raw material bin, and even equipment run. This lets us support post-purchase investigations without delay. The value of direct manufacture sits in these details. Genuine transparency supports ongoing research and protects both our relationships and our reputation.
Feedback from customers shapes how we evolve the production of Boc-(R)-3-Amino-4-(4-Chloro-Phenyl)-Butyric Acid. Questions about solubility or compatibility with specific coupling agents trigger small-batch trials and tweaks to our drying protocol or particle sizing. By keeping an open door (and line), we loop client insights back into process improvements. Sometimes we find ways to remove a persistent trace impurity; other times, we adjust packaging methods for better shelf life based on storage conditions at a major client site. We keep watch on trends in peptide synthesis, API precursor chemistry, and next-generation drug discovery so what we deliver fits both current needs and the likely curve ahead.
Process validation drives out ambiguity. We mark every new approach—be it a minor change in solvent or a switch in raw material supplier—with small-scale verification, risk assessment, and documented release criteria. These controls come from firsthand experience, not regulatory imposition. By the time a finished container leaves our plant, it’s already run the gauntlet of a team dedicated to keeping quality and reliability non-negotiable.
As research directions shift, we see more interest in tailoring molecular building blocks for new applications, novel coupling strategies, and rapid prototyping of potential drug candidates. Boc-(R)-3-Amino-4-(4-Chloro-Phenyl)-Butyric Acid evolves along with these demands, as chemists look for flexible, high-purity intermediates that cut down on avoidable troubleshooting. Our direct role as manufacturer pushes us to anticipate new technical requirements instead of just catching up to them. This means re-validating our route for higher throughput, integrating greener solvents when the chemistry supports it, and double-checking our analytics to suit more sensitive downstream applications.
Staying close to each synthesis run—never outsourcing critical steps—lets us adapt quickly. If a new research project wants custom packaging, an altered batch size, or a ready-to-use pre-solution, we’re able to design that with the confidence that comes from knowing our route and our equipment inside and out. This advantage keeps our product trusted among academic labs, pharmaceutical developers, and innovators whose projects drive the next breakthroughs in medicine and beyond.
To us, Boc-(R)-3-Amino-4-(4-Chloro-Phenyl)-Butyric Acid means more than a code or chemical name—it represents the cumulative experience packed into every kilogram. From the person who weighs the raw materials to the technician who inspects each final bottle, every step draws on years of lessons learned with hands-on chemistry. We see in this compound both the foundation for tomorrow’s therapies and the test of technical strength that underlies real-world manufacturing. By keeping each stage of production in sight, we offer not just a product but genuine support for the discoveries ahead.