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HS Code |
495981 |
| Product Name | L-(+)-Isoleucinol |
| Cas Number | 2637-76-9 |
| Molecular Formula | C6H15NO |
| Molecular Weight | 117.19 |
| Appearance | White solid |
| Purity | Typically ≥98% |
| Optical Rotation | [α]20/D +18° (c=2, H2O) |
| Melting Point | 58-61°C |
| Solubility | Soluble in water |
| Boiling Point | 223°C at 760 mmHg |
| Storage Temperature | 2-8°C |
| Synonyms | L-Isoleucinol, (S)-2-Amino-3-methylpentan-1-ol |
| Smiles | CC[C@H](C)[C@@H](CO)N |
| Inchikey | WSNCMKWTGZEKHM-LURJTMIESA-N |
| Ec Number | 220-098-2 |
As an accredited L-(+)-Isoleucinol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | L-(+)-Isoleucinol is supplied in a 5 g amber glass bottle with a screw cap, labeled with product details and safety information. |
| Shipping | L-(+)-Isoleucinol is shipped in tightly sealed, chemical-resistant containers to maintain stability and prevent contamination. The packaging ensures compliance with safety regulations for non-hazardous chemicals. Shipping is conducted via reliable couriers with tracking provided, and the material is typically dispatched at ambient temperature unless otherwise specified for sensitive applications. |
| Storage | L-(+)-Isoleucinol should be stored in a tightly sealed container, protected from light, moisture, and air. Keep it in a cool, dry place, ideally at 2-8°C (refrigerated) or as specified by the manufacturer. Store away from incompatible substances such as strong oxidizers. Ensure proper labeling and follow all relevant safety and chemical handling regulations. |
Applications of L-(+)-Isoleucinol in Industrial ManufacturingL-(+)-Isoleucinol is a high-purity amino alcohol widely utilized as an intermediate in several industrial sectors. Below we detail real downstream applications, highlighting regulatory requirements, technical usage, process stages, and finished-product categories tailored for specialized manufacturing lines. 1. Peptide Synthesis for Pharmaceutical APIsPharmaceutical manufacturers routinely incorporate L-(+)-Isoleucinol into solid-phase peptide synthesis (SPPS) for the production of custom peptide active pharmaceutical ingredients (APIs). Its use as a chiral building block simplifies side-chain modifications on hydrophobic peptides and improves enantiomeric purity at scale. Direct addition occurs during stepwise chain elongation on resin substrates, mainly in early N-terminus construction for bioactive peptides prescribed in metabolic disorder treatments. Industry compliance standards
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2. Chiral Auxiliaries in Agrochemical Intermediate SynthesisMajor agrochemical processors use L-(+)-Isoleucinol as a chiral auxiliary for the synthesis of selective herbicide and fungicide intermediates. The molecule’s stereochemistry supports asymmetric catalysis and resolution steps critical to achieving target isomer ratios in crop protection agents. Integration typically occurs before final condensation reactions, ensuring downstream intermediates meet required agro-toxicity specifications. Industry compliance standards
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3. Nutraceutical Ingredient FormulationNutraceutical contract manufacturers incorporate L-(+)-Isoleucinol as a specialized amino-derived functional ingredient, especially in sports nutrition, energy, and medical supplement products. Proper formulation enhances protein metabolism regulation or branched-chain amino acid (BCAA) balance. Entry into the ingredient blend occurs during dry mixing, followed by granulation or encapsulation, with quality controlled through amino acid profiling for compliance in dietary supplement applications. Industry compliance standards
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4. Stereoselective Catalyst Preparation for Fine ChemicalsFine chemical and specialty polymer manufacturers deploy L-(+)-Isoleucinol in stereoselective catalyst preparation, taking advantage of its chiral alcohol-amino moiety. This integration provides enhanced selectivity in hydrogenation and cross-coupling reactions. The raw material is first functionalized or derivatized with metals or ligands, forming catalytic complexes with increased turnover rates—and minimal racemization—which are later applied to homogenous catalysis processes in high-value fine chemical synthesis. Industry compliance standards
Typical usage ratio
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Over the years working in our laboratories, we have seen the demand for chiral building blocks grow as synthetic chemistry continues to push boundaries. L-(+)-Isoleucinol has become a regular fixture on our production line because of its specialized role in pharmaceutical development, flavor chemistry, and catalyst synthesis. As a manufacturer directly engaged in every batch, the importance of quality, transparency, and reproducibility remains central with every kilogram we release. Our team does not cut corners; we run every process with pride and caution, ensuring the final product serves customers in research and production without hiccups.
L-(+)-Isoleucinol, produced under controlled conditions at our facility, results from a well-established reduction of L-isoleucine derivatives. The chemical path matters; each stage of our synthesis is planned to preserve enantiomeric purity, which synthetic chemists count on for asymmetric reactions. This molecule is often used for its stereochemistry: (S)-2-amino-3-methyl-1-butanol. With a clear white to off-white solid, the substance has a clean profile that experienced chemists expect for sensitive reactions. Our analytical team validates the enantiopurity by chiral HPLC and checks the water content by Karl Fischer titration. Impurities never get a free pass here; monitoring ensures high standards batch after batch.
Every batch of L-(+)-Isoleucinol in our warehouse meets defined internal benchmarks. The product’s final form carries a purity exceeding 98%, a melting point range that speaks to its real crystallinity, and a residual solvent profile kept below the most current regulatory thresholds. We provide analytical data for each batch because we know chemists and production managers care as much about the fine points as we do.
Specifications are not just numbers in a table. Moisture content matters for reactivity; minor changes in water percentage can throw off downstream syntheses, especially in peptide coupling or reductive amination. By maintaining tight controls on residual solvents like methanol and isopropanol during work-up, we limit unwanted side-reactions down the line. These processes are not theoretical for us — operators adjust and test the reactor at every step, trained not just to follow a manual but to think through the chemistry as they run it.
We ship L-(+)-Isoleucinol to process chemists refining synthetic routes for chiral amines, medicinal chemists designing enzyme inhibitors, and research teams preparing asymmetric catalysts. Our product often finds its way into studies on β-amino alcohols, ligand design for transition metal catalysis, and as an intermediate in custom synthesis projects.
Some of our clients use it to build biologically active molecules based on the isoleucine backbone. Others draw on the compound’s amine and hydroxyl combination — with chirality locked in — for constructing scaffolds that resist racemization. Our own technicians use this compound as a standard in analytical methods development. Since each application leverages both the chemical core and physical handling properties of L-(+)-Isoleucinol, we respond quickly to requests for specialized quantities, particle sizes, or application-specific documentation.
Within the world of chiral amino alcohols, the subtle differences between isoleucinol and its isomers or analogues have significant consequences. Each backbone arrangement and stereochemistry play distinct roles in downstream chemistry. L-(+)-Isoleucinol offers a branched alkyl side chain, which distinguishes it from simpler amino alcohols such as L-alaninol or L-leucinol. This branching impacts solubility, physical stability, and the ability to form specific hydrogen-bonded networks in catalysis or crystal growth.
Racemic mixtures lack the selectivity our customers expect. Any time a process requires predictable activity or regulatory compliance — such as active pharmaceutical ingredients or food additives — purity and stereochemical integrity become non-negotiable. Our strict control prevents the d-(-) enantiomer from contaminating what must be an L-(+) product.
Compared to L-leucinol, which carries a more compact isobutyl side chain, L-(+)-Isoleucinol’s sec-butyl group lends itself to substrates where increased branching changes reactivity, rates of hydrogen abstraction, or selectivity in catalyzed reactions. A chemist optimizing a transition metal-catalyzed enantioselective reaction finds value in such differences; students of organic synthesis recognize these distinctions as the reason one variant outperforms another in tests, even if their paper structures look similar.
In our factory, every new batch embodies lessons learned from previous runs. Process engineers watch pH curves and temperature profiles, making adjustments based on patterns they have memorized from years of hands-on work. Aspects like color, smell, and granular structure announce problems before machines do. During a recent scale-up, we identified and resolved bottlenecks that had not appeared at lab scale — highlighting that bench chemistry does not always tell the full story once volumes rise.
Batch records document every decision, and customer feedback directly affects product refinement. Over time, this loop brings measurable improvements in reproducibility, reduction of off-spec material, and easier dissolving and filtering for clients. Validation isn’t outsourced; cross-checks between shifts and departments prevent the slippage that leads to inconsistent product or future troubleshooting headaches.
Our laboratory and production managers navigate complex regulatory environments in multiple countries. Not all regulatory frameworks treat amino alcohols with the same scrutiny. Expectations for trace metals, solvents, and identification methods differ from region to region. We invest the time and resources to collect the documentation needed for European, North American, and Asian filings, keeping the process clear for downstream users who require full transparency.
Supply chain interruptions — the kind that became common the past few years — rarely catch our team unprepared. We forward-source starting materials, both to secure raw inputs and to ensure each lot matches our internal standards. We have invested in new storage infrastructure so that chemical and physical stability persists from synthesis through delivery. Our experience tells us that a concrete floor and stable humidity matter almost as much as what goes on inside the flask.
We work closely with our logistics partners, making sure shipment is prompt and compliant with the latest transportation rules. During instances when regulatory conditions shift or shipping routes close without warning, we tap alternate suppliers without compromising traceability or purity. The priority remains clear: our customers receive the same L-(+)-Isoleucinol they have come to rely on, without underhanded substitutions or unexplained quality shifts.
Collaboration forms the backbone of our ongoing product improvement. Regular feedback with academic and industrial partners sparks incremental upgrades in both process and documentation. Once, a university lab discovered small inconsistencies in crystallinity, leading us to adjust our cooling profile for greater batch uniformity. This discovery did not come from a power-point presentation but from real-world results; students and postdocs running daily tests on our samples highlighted the issue before it could impact a commercial application.
Feedback does not go into a black box. Operators, chemists, and managers review results, debate the best corrective actions, and then implement what makes sense. This keeps documentation honest and up to date. We believe in sharing method validation results, impurity profiles, and test methods with anyone who needs them. For projects where quality and traceability dictate downstream registration, our detailed approach helps partners secure approvals quickly.
L-(+)-Isoleucinol stands apart from close relatives by virtue of its structural specificity. In applications requiring β-amino alcohol frameworks, the particular stereochemistry and side chain make a difference in selectivity and activity. Chemists working on kinase inhibitor synthesis often choose L-(+)-Isoleucinol over the L-alaninol variant because the larger side chain induces desired steric effects, leading to different binding properties. Structure–activity studies in medicinal chemistry reinforce the role of the sec-butyl group for potency and metabolic stability.
Peptide and peptidomimetic syntheses rely on the chiral fidelity of the intermediate. We have seen customers report batch failures when switching to off-the-shelf analogues from less rigorous sources. With L-leucinol or other amino alcohols, the difference in melting point, water content, or steric profile can alter the results — from solubility in key solvents to ease of handling in automated reactors. Our experience supports the claim that not all “chiral amino alcohols” are interchangeable; the cost of using an inferior variant can extend from lost time to failed product filings.
As a direct producer, providing substance is more than shipping drums and bottles. We maintain up-to-date documentation on genotoxic impurities, elemental analysis, and stability. Some requests come in for milligram quantities intended for basic research; others require kilos with certificates that can stand up to audit and regulatory review. We adjust package sizes, labels, and even forms of the product to suit downstream process needs — all rooted in feedback collected from the field.
During scale-up to multi-kilogram quantities, we have faced challenges with solubility and filtration that do not show up at gram scale. Addressing these, our technical staff revised the isolation procedure, optimizing both yield and physical appearance. This scale-up knowledge is part of every conversation we have with clients seeking to move from pilot to production. Failing to plan for these shifts has led others to costly do-overs; by keeping these lessons alive in our own operations, we aim to spare our partners wasted effort and time.
L-(+)-Isoleucinol anchors itself in the world of chiral intermediates due to its reliable performance and adaptability to diverse applications. Our hands-on approach to making, testing, and distributing this product stems from personal investment tied to every batch that leaves our factory. Trends in pharmaceutical manufacturing, flavor and fragrance synthesis, and next-generation catalyst research all push for higher quality and more tightly controlled products. The trust our clients place in us reflects not just product consistency, but our real understanding of how this molecule shapes the chemistry downstream.
As the market evolves, we continue to invest in analytical capabilities and process refinement. Chiral HPLC, mass spectrometry, and advanced purification setups are not just check-boxes — they allow us to catch rare impurities and outliers before they could impact customer research. For us, shipping a product goes hand-in-hand with accountability; lot histories stay on file for years, serving as a record for regulatory review or troubleshooting unexpected results.
Contaminated or substandard intermediates limit what innovative chemistry can achieve. Those of us who run production lines understand why robust supplier-client relationships matter in the long term. By paying attention to feedback and real-world usage, we keep the bar for L-(+)-Isoleucinol quality at the level expected by experts in the field.
As research expectations and regulatory frameworks continue to progress, customers increasingly look for both digital and human support. Our technical service team integrates customer feedback into the next round of improvements, and our documentation keeps pace with evolving regulations. On-site visits, tailored technical advice, and transparent sharing of test results round out a service model focused on real problem-solving, rooted in the daily work of producing and refining chemical building blocks.
Working shoulder to shoulder with process chemists, R&D leaders, and analytical labs teaches us the difference between theoretical quality and practical value. L-(+)-Isoleucinol remains a mainstay because we never lose sight of the human expertise required to keep quality consistent, applications broad, and the underlying chemistry sound. We stake our reputation on every batch because, in our experience, there’s no margin for error when science and industry rely on products like this to keep innovating.