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HS Code |
302274 |
| Chemical Name | (S)-Tert-Leucinol |
| Cas Number | 10277-74-4 |
| Molecular Formula | C6H15NO |
| Molecular Weight | 117.19 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Specific Rotation | [α]D20 +18° to +22° (c=1, CHCl3) |
| Boiling Point | 188-189°C |
| Density | 0.856 g/mL at 25°C |
| Purity | Typically ≥98% |
| Smiles | CC(C)(C)[C@H](CO)N |
| Iupac Name | (2S)-2-amino-3,3-dimethylbutan-1-ol |
| Solubility | Soluble in water and most organic solvents |
| Storage Conditions | Store at 2-8°C, keep container tightly closed |
As an accredited (S)-Tert-Leucinol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | (S)-Tert-Leucinol is packaged in a 25g amber glass bottle with a secure screw cap and clear hazard labeling. |
| Shipping | (S)-Tert-Leucinol is typically shipped in a tightly sealed container, protected from moisture and direct sunlight. It is classified as a non-hazardous chemical for transport but should be handled with care. Standard shipping methods are used, and all shipments comply with relevant chemical transport regulations to ensure safety and integrity. |
| Storage | (S)-Tert-Leucinol should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances like strong oxidizers. Protect from moisture and direct sunlight. Store at room temperature, and avoid exposure to extreme temperatures. Ensure proper labeling and comply with local chemical storage regulations for safe handling and retention. |
Applications of (S)-Tert-Leucinol in Industrial ManufacturingAs a specialized manufacturer of (S)-Tert-Leucinol, we support industrial partners with high-purity material engineered for advanced synthesis and demanding regulatory environments. Our production serves key sectors where (S)-Tert-Leucinol is critical to enantioselective transformations and complex molecule construction. Below are focused application scenarios, each highlighting unique compliance, formulation, process, and product endpoints. 1. Asymmetric Synthesis of Pharmaceutical IntermediatesMajor pharmaceutical companies use our (S)-Tert-Leucinol in the asymmetric synthesis of active pharmaceutical ingredient (API) intermediates, especially in the manufacturing of chiral β-amino alcohols and β-amino acids. The raw material’s absolute configuration supports high stereoselectivity in reductive amination and chiral auxiliary strategies for blockbuster drugs and advanced intermediates. Manufacturing teams apply precise dosage according to reaction stoichiometry, closely monitoring for target enantiomeric excess and regulatory compliance as per ICH guidance and pharmacopeial standards. Industry compliance standards
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2. Chiral Ligand Synthesis for Metal CatalysisLarge-scale organometallic catalyst manufacturers select (S)-Tert-Leucinol as a precursory scaffold in the synthesis of oxazoline and diamine ligands. Its defined stereochemistry enables controlled assembly of P,N- and N,N-ligand architectures critical for high-yield asymmetric hydrogenation, transfer hydrogenation, and allylic substitution processes. Material QC ensures minimal racemization and trace impurity within ligand manufacturing campaigns compliant with export requirements and REACH documentation. Industry compliance standards
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3. Agrochemical Synthesis – Chiral Pesticide Active Ingredient ManufacturingProducers of advanced agrochemical actives employ (S)-Tert-Leucinol as a building block in the synthesis of enantio-enriched intermediates for chiral herbicides and fungicides. The raw material integrates into stereospecific alkylation and reductive amination pathways designed to minimize impurity profiles and support stewardship requirements for global agrochemical registration dossiers, particularly for crop protection products with strict MRL compliance. Industry compliance standards
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4. Fine Chemical Synthesis – Fragrance IntermediatesLeading fragrance compound manufacturers utilize (S)-Tert-Leucinol as a chiral source in the synthesis of specialty odorant intermediates. Its utility in the stereoselective synthesis of alcohols and amines enables the production of high-value fragrance ingredients that meet strict purity and olfactory performance criteria, especially for fine perfumery and flavor compounds. All batches undergo rigorous trace analysis to ensure compliance for IFRA and food-grade flavor standards. Industry compliance standards
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5. Laboratory Reagent for Chiral Analytical Method DevelopmentAnalytical standards manufacturers use (S)-Tert-Leucinol in the preparation of chiral derivatization reagents deployed for high-performance liquid chromatography (HPLC) and supercritical fluid chromatography (SFC) methods. These derivatized reagents enable contract labs and pharmaceutical QC units to validate stereochemical identity and quantification in both research and regulated environments where trace isomer differentiation is critical for release testing. Industry compliance standards
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The demand for high-purity chiral building blocks just keeps climbing every year. In the realm of fine chemicals, (S)-Tert-Leucinol shines as a backbone for producing enantiomerically pure active pharmaceutical ingredients and advanced intermediates. From the first trials of asymmetric synthesis that crossed our lab benches over a decade ago, we've seen first-hand how an amino alcohol such as (S)-Tert-Leucinol opens up efficient options for assembling molecules that cannot be built using achiral or racemic compounds. Its molecular structure carries a chiral center placed on the α-carbon, bringing reliable selectivity to asymmetric transformational pathways, especially where exact handness in synthesis spells the difference between success and wasted time.
Creating (S)-Tert-Leucinol with a high enantiomeric excess takes more than just following a set of instructions. Years of refining our proprietary catalytic hydrogenation process and regularly updating instrumentation have driven us toward repeatable batches that consistently hit rigorous chiral purity marks, often reaching ≥99% ee. This is not simply a number on a spec sheet—chemists who work with our product avoid costly purification steps and see genuine improvements in yield when running asymmetric reduction or dynamic kinetic resolution protocols. The material’s typical appearance—colorless to pale yellow liquid with nearly complete miscibility in common polar solvents—means direct integration into most synthetic schemes without laborious pre-processing or redissolving struggles.
Getting reproducible single-enantiomer output, especially in large volumes, presents a reality check for anyone with scale-up ambitions. We’ve recorded shifts in optical rotation tied to operational pressure and temperature, and spent hundreds of hours studying subtle changes caused by different grades of precursor ketone. Knowledge built through tracked data and hands-on troubleshooting ultimately cuts waste, which carries over to lower costs and fewer headaches for customers. Each batch faces full analytical review: chiral HPLC and GC, NMR, and Karl Fischer titration are routine, not extras. Direct conversations with project chemists keep us adapting in real time to evolving end-user requirements and regulatory shifts.
The difference between (S)-Tert-Leucinol and other chiral auxiliaries like (S)-Leucinol or (S)-Phenylglycinol boils down to field-tested behavior. Our product features a tert-butyl group on the β-carbon, creating marked steric hindrance not found in its straight-chain or smaller-branched relatives. This translates into sharper selectivity in catalytic and stoichiometric transformations, supporting a cleaner separation between product and byproduct under tight timelines. Pharmacological studies have uncovered unique biological profiles for molecules derived from chiral t-butyl structures—these fine points only show themselves after someone has invested the resources (and endured the headaches) of side-by-side screening during real development projects.
(S)-Tert-Leucinol stands up to challenging reaction conditions. Teams developing enantioselective hydrogenations, arylations, or aminations use its rugged chemical nature to run at higher temperatures or in stronger bases, then salvage more value per raw material kilogram. Compared to amino alcohols with bulkier or less-branched chains, our compound averages lower impurity formation, especially in multi-step syntheses where cumulative errors can cripple a project’s budget and timeline.
Seeing a molecule travel from lab discovery to commercial launch brings a level of satisfaction you only find after hundreds of hours on the production floor. (S)-Tert-Leucinol directly supports this pipeline for organizations building new APIs, agricultural actives, or fine chemical intermediates. Medicinal chemists value its role as a resolving agent, particularly during late-stage chiral fragment assembly in complex molecules with many sensitive groups. We have shipped multi-kilogram quantities to partners pursuing peptide mimetic candidates, oxazolidinone antibiotics, and CNS agents where the stereochemical fidelity of every atom is crucial for function.
Custom route design and process development often pivot on which chiral auxiliaries are available at scale. Many R&D chemists first learn about (S)-Tert-Leucinol during structure-based screening campaigns, where clear separation between enantiomeric pairs can simplify downstream regulatory submissions and intellectual property filings. For those working in scale-up or pilot-plant environments, consistent lot quality ensures that pilot batch data carries over to commercial runs without unexpected documentation headaches or batch rejections.
As a manufacturer dedicated to meeting global standards, we maintain robust documentation for (S)-Tert-Leucinol. Every batch ships with traceable data sets—including full NMR, IR, and optical rotation spectra—along with impurity profiling and solvent residual analysis. Our safety data sheets and environmental stewardship records address the increasing scrutiny of worldwide chemical users, while regular third-party audits and certifications help reinforce the reliability of our process controls.
Drug master file submission support and regulatory review packages grow out of thousands of hours of diligent recordkeeping and data collection during product release. Subcontracted analyses by well-accredited labs endorse the purity and composition established by our in-house team, making our supply a stable foundation for both clinical-stage and post-approval manufacturing.
Experience has shown that close dialogue with synthetic chemists leads to breakthroughs in both process efficiency and end-use success. One example involved scaling from 50 g to several hundred kilograms for a peptide intermediate, where a process originally producing high side-product levels became a reliable, cost-slashing solution after a series of feedback-driven changes to temperature control and reagent dosing intervals. Responding to feedback about undesirable residual odor, we tracked volatile byproduct sources and reworked venting and purification cycles, resulting in markedly improved downstream performance during the catalyst recycle stage.
Many challenges only come to light during regular use. Reproducibility in extraction after work-up, susceptibility to moisture in transport, and even compatibility with automation all represent concerns that only subside after working closely with research partners. Cupboards filled with competitor samples and our own historical runs provide ample evidence: what looks similar on paper can behave entirely differently in real synthesis.
Progress doesn’t happen by accident. Over the years, we’ve incorporated hydrogen transfer catalysts and dedicated reactors specifically optimized for sensitive chiral hydrogenations. Monitoring the interplay between catalyst age, substrate feed rates, and base selection has helped us sharpen the process, cutting cycle times and reducing waste while dialing in sharper optical purity. Early troubleshooting of agitation rates and heat transfer bottlenecks, plus some trial-and-error regarding solvent composition, steered us to today’s reliable performance.
Maintenance schedules for high-pressure reactors and sensor recalibrations play a less glamorous yet vital part in ongoing success. Small investments in updating analytical standards and data capture have fueled much of our progress from lab scale to commercial supply. Handling tough questions from quality assurance teams about trace impurities or scale-up reproducibility demands hard-won knowledge gained only through repetition, experimentation, and sometimes late nights in the plant.
Real partnership grows out of solving practical issues together. Research groups often send detailed feedback on ways (S)-Tert-Leucinol interacts with their unique synthetic steps. A cluster of users looking to minimize reaction times prompted us to re-examine distillation protocols; adopting a higher vacuum and more gradual temperature ramps cut color formation and trimmed cycle times. Major life science firms, biotech startups, and specialty ingredient makers have all benefited from our willingness to iterate on incoming raw materials, solvent choices, and agitation profiles.
A recent example saw a customer shifting to a continuous-flow manufacturing setup. After troubleshooting in tandem with their engineers, we refined particle size distribution and moisture content to keep their lines running clean without feed interruptions or filter clogs. Their feedback led to a new variant tailored for their reactor, extending shelf life under ambient conditions and removing a costly dehydration step.
Users weighing (S)-Tert-Leucinol against (R)- or racemic alternatives find clear contrasts in reactivity and selectivity. The strong electron-donating tert-butyl group produces a shielded transition state that slows down unwanted side reactions and side-chain racemization, keeping yields high in even the most rambunctious asymmetric reductions. Researchers comparing this compound to more basic options—such as (S)-Leucinol—notice improved purity and easier post-reaction separation, especially after multiple synthetic manipulations. The result is fewer surprises after scale-up and easier translation from flask to full-scale manufacturing.
In real projects, such as β-lactam or amino acid derivative synthesis, our (S)-Tert-Leucinol unlocks options not available with other amino alcohols. The extra electron cloud and steric profile support stereospecific interactions that prove crucial for complex, multi-site couplings, whereas less-hindered auxiliaries risk introducing epimers or forcing extensive downstream purification.
Working with organic building blocks every day, we see all sides—production risk, environmental control, exposure prevention, and regulatory inspection readiness. Proper ventilation, in-house air monitoring, and up-to-date worker safety instruction have kept accident rates driven down year after year. Product batches come with documentation on safe handling, storage, and compatible packaging, based on hard-earned lessons in real warehouse and shipping environments.
Waste minimization measures include solvent recycling wherever possible and close tracking of byproduct pathways for compliant offsite disposal. Investment in sealed vials and drums with inert-gas purges followed years of minor transport setbacks and customer reports about oxidative degradation. Our product reaches customers as fresh and consistent as it left our plant, giving chemists peace of mind during sensitive operations.
The landscape of chemistry changes fast, with new synthetic targets, evolving regulations, and technology leaps that challenge manufacturers daily. Our ability to supply (S)-Tert-Leucinol worldwide in both research and ton-scale manufacturing leverages decades of experience handling international freight, customs requirements, and diverse climate risks. Each order reflects lessons learned from hundreds of shipments: temperature-controlled containers, vacuum-sealed packaging, and timely documentation keep delays and disruptions at bay.
The knowledge we’ve gained from scaling production internationally—whether adapting to new environmental standards or working with customers to pass supplier audits—shapes each batch, each shipment, and each process tweak. Everyone down the line, from procurement to production, has contributed to a track record of consistent on-time delivery and reproducibility regardless of shipment size or destination.
(S)-Tert-Leucinol links multiple stages of chemical innovation, from discovery through scale-up to GMP-certified bulk volumes. Lab researchers depend on transparent data, tight material controls, and consistent communication at every step. Production teams use direct input from R&D to tweak operational parameters, quickly identifying emerging challenges such as scaling bottlenecks or changing impurity profiles. Customers working on tight project timelines have relied on our ability to adapt—whether that means holding reserve inventory, offering short-term special packaging, or supporting analytical testing to fit exacting criteria.
Long-term research incentives drive us to keep refining each process cycle. Recent investments in process automation, advanced analytics, and real-time monitoring have shortened lead times and improved environmental performance, giving end-users stronger confidence in the reliability and traceability of each batch.
Quality control is not a single step but an attitude built into every layer of production. Engaged chemists oversee every scale-up and packaging run, ensuring each lot meets the expectations that decades of customers have set. Analytical staff re-examine old standards and develop fresh validation protocols as new reaction types or regulatory guidance emerge. We approach quality as a shared goal—knowing that consistent, well-documented supply forms the backbone of every successful research or commercial production campaign involving (S)-Tert-Leucinol.
Our team values shared problem-solving. One recent example involved working with an overseas partner developing a new class of chiral ligands. Their custom requirements pushed our own process to new rigor, resulting in long-lasting improvements to scrap reduction, batch-to-batch uniformity, and analytical documentation. Both sides benefitted: their program advanced, and our staff carried forward new skills and insights.
The pace of discovery in synthetic chemistry continues to accelerate, with more pharmaceutical, agricultural, and specialty companies demanding flexible, scalable, and reliable sources of chiral auxiliaries. As new catalysts, process intensification methods, and flow chemistry options come online, we expect ongoing calls for (S)-Tert-Leucinol in ever-wider applications. Adapting to this changing landscape depends on open dialogue, technical curiosity, and an honest willingness to fix what does not work on the first try.
Drawing from field-proven experience, we will keep improving (S)-Tert-Leucinol’s cost efficiency, environmental profile, analytic transparency, and process compatibility. Each new collaboration teaches us something valuable, fuelling further investments in product tracking, waste reduction, and real-time customer support. By maintaining hands-on involvement throughout every stage, our team continues to set higher standards for reliability and partnership across the chiral chemicals sector.