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HS Code |
119164 |
| Iupac Name | (2S)-bornane-10,2-sultam |
| Molecular Formula | C10H17NO2S |
| Molar Mass | 215.31 g/mol |
| Cas Number | 76357-60-9 |
| Appearance | White to off-white solid |
| Melting Point | 174-178 °C |
| Solubility In Water | Slightly soluble |
| Boiling Point | Decomposes before boiling |
| Chirality | S-configuration at position 2 |
| Smiles | C1CC2CC(C1)C3(C2)NS(=O)(=O)C3 |
| Inchi | InChI=1S/C10H17NO2S/c1-2-8-5-10(7(8)6-1)9(3-4-10)11-14(12,13)9/h7-9,11H,1-6H2/t7-,8-,9-,10+/m0/s1 |
| Storage Temperature | Store at room temperature |
As an accredited (2S)-Bornane-10,2-Sultam factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | White, sealed glass bottle containing 25 grams of (2S)-Bornane-10,2-Sultam. Clearly labeled with product name, CAS number, and hazard symbols. |
| Shipping | (2S)-Bornane-10,2-Sultam is shipped in tightly sealed containers, protected from moisture, heat, and direct sunlight. It is handled in compliance with local and international regulations for laboratory chemicals. Appropriate hazard labeling and documentation are provided to ensure safe and secure delivery to the destination. Handle with care during transportation. |
| Storage | (2S)-Bornane-10,2-sultam should be stored in a tightly sealed container, protected from moisture and direct sunlight. Keep it at room temperature in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Ensure storage in accordance with local chemical safety regulations and maintain clear labeling to avoid accidental misuse. |
Applications of (2S)-Bornane-10,2-Sultam in Industrial Manufacturing(2S)-Bornane-10,2-Sultam is a critical chiral auxiliary in asymmetric synthesis across several high-value industrial sectors. As a direct manufacturer, we support customers with validated material traceability and fully controlled production parameters, enabling reliable downstream integration in each demanding field below. 1. Chiral Synthesis in Active Pharmaceutical Ingredients (APIs)Pharmaceutical manufacturers utilize this sultam extensively for stereocontrolled construction of enantiomerically pure intermediates in API production. Its capacity to induce chirality delivers consistent batch-to-batch selectivity, crucial for regulatory approval. We supply material with documented impurity profiles, supporting use in commercial-scale enantioselective alkylation, aldol condensation, and other key transformation steps, particularly in β-lactam and macrolide synthesis for cardiovascular, oncology, and CNS therapeutics. Industry compliance standards
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2. Agrochemical Chiral Intermediate Manufacturing(2S)-Bornane-10,2-Sultam is widely applied by crop protection chemical manufacturers for enantioselective synthesis of insecticides, fungicides, and herbicides that require precise isomeric purity for biological performance. Chiral switching in patent-expired products also drives adoption, as downstream formulators rely on our material’s consistent chirality induction and low trace metals content for industrial-scale batch reproducibility. Industry compliance standards
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3. Fine Chemical Stereoselective Intermediate ProductionManufacturers in the fine chemicals sector deploy (2S)-Bornane-10,2-Sultam for differential synthesis of stereochemically complex molecules. Its predictable asymmetric induction is particularly suited to fragrance intermediates, specialty monomers, and complex building blocks demanded by flavors and specialty performance chemicals. QC data supports scale-up for both custom orders and standard catalog products. Industry compliance standards
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4. Research-Scale Stereocontrolled Library SynthesisAcademic and commercial R&D laboratories rely on our sultam for rapid assembly of stereochemically diverse molecule libraries, vital in lead discovery and structure-activity relationship studies. High-purity product and accompanying batch analyses enable predictable outcomes in small-scale, exploratory asymmetric syntheses as well as method development for new synthetic pathways. Industry compliance standards
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For over two decades, we have focused on optimizing chiral auxiliaries and fine chemicals for researchers who demand predictability and efficiency in challenging transformations. (2S)-Bornane-10,2-Sultam stands out in our portfolio, not just because of the molecule’s history in organic chemistry, but for how it consistently performs in the hands of professionals trying to deliver asymmetric syntheses at laboratory and commercial scales.
Chemists walk a tightrope every day: balancing reliable yields, reproducibility, process simplicity, and regulatory compliance is a reality in both discovery labs and pilot plants. In asymmetric synthesis, the pressure intensifies—costly building blocks and long routes amplify the impact of each auxiliary. We designed our (2S)-Bornane-10,2-Sultam offering to meet that kind of day-to-day scrutiny, specifically in enantioselective alkylations, aldol reactions, α-alkylations, and other transformations where outcome determines project timelines and costs.
We have tested and refined our production to reach an assay above 99% while controlling impurities found in off-the-shelf material. By overseeing every step from raw camphor derivative to sultam formation and isolation, we have direct oversight over enantiomeric purity and physical profile. This attention shows in the consistency of batch-to-batch performance and solubility—two details customers bring up most often in technical support calls. One reason research organizations and process chemists continue to purchase directly from us is the trust built through years of hassle-free laboratory and pilot-plant operations.
We produce both standard and custom specifications of (2S)-Bornane-10,2-Sultam, targeting not just the common chiral auxiliary applications but also enabling users to scale processes confidently, knowing material from different lots will not deviate in spectral profile or manipulation requirements. Most commercial products derived by our partners get their chiral purity from a stage using this sultam, so we track stability and storage recommendations as part of our standard support. Moisture content and physical form (from crystalline powder to larger granules) matter in scaling, especially where process transfer is involved.
Alternatives to (2S)-Bornane-10,2-Sultam exist, such as camphorsultam analogues, Evans’ auxiliaries, and proline derivatives, yet few combine the unique steric and electronic control embodied by this molecule. The rigidity and non-reactive camphor skeleton direct selectivity and create crystal-clear separation in many asymmetric transformations. Some competitors offer material from resellers; these often come with batch variability or documentation gaps. Large manufacturers prioritize high throughput, but we stay close to the practical struggles of synthetic chemists—customers have told us that our product lets them trim purification time and material wastage because the enantioselectivity is so direct and the recovery step predictable.
Many users remember the headaches triggered by auxiliary removal and recycling. Our version remains easy to recover and purify, recovering much of its value per cycle. Technical experts in our operation traced impurities and volatile byproducts at the microgram level, because in our work, an undetected impurity can cascade into final product issues or lost yields several steps down the line. We spend additional cycles on recrystallization and filtration, specifically to address points often missed in high-volume production of sultams.
Not all projects follow textbook pathways. We regularly receive requests for bespoke particle sizes, moisture content limits, or variants with slightly tweaked substitution patterns. Process development chemists often seek a tighter melting point range or ask for trace residual solvent documentation compatible with regional pharmacopoeias. As the producer, we can adjust production runs accordingly and provide representative lots for internal evaluation before formal orders. This flexibility lets groups validate our material in pilot vessels and automated synthesizers.
For customers optimizing cost, the consistent recovery yield on (2S)-Bornane-10,2-Sultam stands out. The recovered auxiliary typically keeps its assay close to the original, and our data packages include common recovery conditions and spectral standards, so facilities without advanced analytical support avoid common pitfalls. Since we control the entire workflow from acquisition of the chiral starting material to final QA, extra purification is not dumped on the customer. This model gives our users tighter cost projections and less inventory risk, especially in projects where uncertainty in chiral source costs threaten timelines.
The batch feedback loop started on day one. Our plant chemists, technical sales staff, and QA engineers built a standardized post-sale reporting process. Users would receive follow-up calls, not just to ask about shipment arrival but to learn how the material handled in their glassware, what results they saw after auxiliary removal, and if any adjustment in physical form could save them hours of downstream processing. Based on this data, we modified drying conditions, storage documentation, and even particle size output. Facilities that handle parallel syntheses in automated systems asked for larger average grain size to avoid clumping, so we retooled filtration and drying to deliver that.
Small discovery labs in pharma outreach programs demanded ampoule-sealed micro-batches to extend shelf life; in response, we began packaging options that trade off cost for certainty where supply chain disruptions threaten tight scheduling. International clients requested certain spectral documents and additional stability data to satisfy regulators early in development programs. Our team supports those requests, and this has led to smoother project audits and faster development timelines for our customers.
Synthetic groups depend on predictable stereochemical outcomes—many processes must be repeated for validation, patent filings, or scale-up. The specific three-dimensional locking provided by (2S)-Bornane-10,2-Sultam means results seen in earlier stages carry over in kilogram or multi-kilogram production. This auxiliary enforces diastereoselectivity, allowing easy separation later, whether by chromatography or crystallization, without investing additional time troubleshooting mother liquors or spectra for side-products.
We set our analytical support to predict the key questions that synthetic teams will face: what trace solvents remain, is there racemization in projected reaction profiles, and do residual metals persist from catalyst traces used upstream? Spectra and analytical results for every lot come directly from the same laboratories that produce the product, so readings reflect reality, not marketing hopes. In a world with growing scrutiny on reproducibility and documentation, this direct data visibility helps groups build process documentation without pulling their own staff into endless verification cycles.
Chiral auxiliary strategies can frustrate even the most seasoned chemists, especially when process economy matters—to strip out cost, the auxiliary must always be recyclable, both chemically and in a workflow sense. We have received countless queries about how to simplify the recovery step. By tracking not only the main synthesis but the practical handling, storage, and separation, our team identified bottlenecks unique to large batch recycling. We recommend straightforward procedures to avoid hydrolysis and oxidation during auxiliary removal and post-process storage. This comes straight from iterative improvements logged by our pilot and commercial customers.
Not all users run into the same issues. Small molecule pharma often needs single-digit gram runs for preclinical validation, while agrochemical programs might handle tens of kilograms for early field trials. Both classes of users benefit when we tune drying, compaction, and recommend common solvents for easy integration into multi-step protocols. Direct feedback from dozens of research groups convinced us to provide quick-turn technical response, often with data from our own plant replicating the customer's steps—so problem-solving can happen in real time.
Markets for chiral precursors and specialty auxiliaries have moved rapidly, with more regulatory input and sustainability expectations now than at any point in our professional careers. As the original manufacturer, we see supply chain risk every day. Securing feedstock purity, scaling up without ecological trade-offs, and addressing local compliance are ongoing challenges. Our raw material sourcing emphasizes traceable, non-conflict camphor derivatives. All processing solvents are recycled where possible, and waste streams are kept to a minimum, with third-party audits supporting our internal data.
Our certification processes give end users more confidence, especially now that pharmaceutical and fine chemical sectors require transparent supply chain documentation from every external supplier. We share our processes openly—visitors and auditors regularly verify process controls, documentation of impurity testing, and protocols for lot tracking. Many customers build their own audits based on our data sets, which helps them address questions from regulatory bodies without extra process mapping.
We have built this business by partnering directly with synthetic teams. From academic research groups developing new methodologies, through process chemistry teams scaling up validated protocols, to industrial manufacturers running pilot plants—our work responds to these needs, not to marketing trends. Senior chemists in our production unit have run the same types of reactions as our customers, and their understanding shapes our approach: clean baseline, genuine transparency in technical data, and immediate attention to reported issues.
Process teams want to avoid unexpected costs and reams of paperwork. We address these priorities with direct communication and material designed to outperform general market versions. Our production line evolved based on these end-use requirements, with technical leads from both sides of the transaction collaborating to solve issues long before a batch goes out the door.
One recent customer optimizing a kilogram-scale stereo-selective alkylation in a new synthetic route came to us after battling inconsistent results with a generic camphorsultam supplier. They reported months of yield and purity swings, along with increased time needed to separate side-products. Once our (2S)-Bornane-10,2-Sultam entered their workflow, yield stability returned, and they saw sharper NMR signals with minimal baseline drift. This let them lock down their process conditions and support a regulatory filing that would have otherwise stalled.
In another case, a research group scaling up an asymmetric aldol developed an unexpected racemization problem during auxiliary cleavage. After running our QC assays and consulting on storage recommendations, the group minimized exposure to air and improved basic workup—a simple fix, yet one often overlooked. Their issue resolved, allowing them to recover auxiliary across multiple batches without reinvestment. These real project cycles shape the feedback that heads straight into our day-to-day technical improvements.
With the rising cost of failure in pharmaceutical and specialty material syntheses, there isn’t much margin for experimentation with unreliable suppliers or unknown auxiliary lots. By working with a manufacturer who focuses on practical outcomes, labs gain steady access to a tool that enables crucial asymmetric transformations and supports economical material recovery. Researchers running gram-scale exploratory reactions or kilogram-scale validation know their results won’t swing with each order.
Teams working on patent-critical or GMP-building stages can access real lot-to-lot documentation tracing, analytical support within hours, and recommendations based on documented experience, not generic advisories. This focus on practical deliverables takes the unpredictability out of auxiliary selection and use—chemists know exactly what to expect from the material and how to manage its lifecycle for maximum process value.
Every year brings sharper scrutiny on reliability, sustainability, and cost discipline. Most discovery chemistry groups see reduced budgets but rising standards. In response, we have streamlined our production, closed feedback loops, and invested in analytical and regulatory compliance systems. Our goal is to maintain the flexibility and responsiveness we started with while supporting larger, more demanding programs as the field evolves.
For synthetic chemists and process teams, (2S)-Bornane-10,2-Sultam represents a tested, reliable chiral auxiliary—one with a transparent supply chain, rigorous analytical backup, and technical support grounded in real chemical manufacturing. Our entire team’s experience flows through every lot, document, and advisory note because we understand the stakes involved in every asymmetric step you run.