|
HS Code |
345204 |
| Chemical Name | S-Allyl Cysteine |
| Molecular Formula | C6H11NO2S |
| Molar Mass | 161.22 g/mol |
| Appearance | White crystalline powder |
| Solubility In Water | Highly soluble |
| Melting Point | 104-106°C |
| Source | Aged garlic extract |
| Chemical Class | Organosulfur compound |
| Cas Number | 21593-77-1 |
| Odor | Odorless |
| Ph Value | Approximately neutral in solution |
| Stability | Stable under normal conditions |
| Storage Conditions | Store in a cool, dry place |
| Optical Activity | Levorotatory |
| Boiling Point | Decomposes before boiling |
As an accredited S- Allyl Cysteine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The S-Allyl Cysteine is packaged in a sealed amber glass bottle containing 10 grams, clearly labeled with product and hazard information. |
| Shipping | S-Allyl Cysteine is shipped in tightly sealed, chemical-resistant containers to ensure stability and prevent contamination. The packaging complies with international safety regulations for hazardous materials. It is protected from heat, moisture, and direct sunlight during transit, and accompanied by a safety data sheet (SDS) for proper handling upon delivery. |
| Storage | S-allyl cysteine should be stored in a tightly sealed container, protected from light and moisture, at 2-8°C (refrigerator). Store in a well-ventilated area, away from incompatible substances such as strong oxidizing agents. Ensure proper labeling and avoid prolonged exposure to air to maintain stability and prevent degradation. Always follow local regulations and safety guidelines when handling and storing this compound. |
|
Purity 98%: S- Allyl Cysteine with purity 98% is used in pharmaceutical formulations, where it enhances antioxidant activity and ensures high bioavailability. Molecular weight 161.24 g/mol: S- Allyl Cysteine with a molecular weight of 161.24 g/mol is used in nutraceutical supplements, where it supports precise dosage control and standardized efficacy. Water solubility 100 mg/mL: S- Allyl Cysteine with water solubility 100 mg/mL is used in beverage fortification, where it ensures rapid and homogeneous dissolution for improved product quality. Stability temperature up to 60°C: S- Allyl Cysteine with stability temperature up to 60°C is used in functional food manufacturing, where it maintains bioactivity during heat processing. Particle size <50 µm: S- Allyl Cysteine with particle size less than 50 µm is used in tablet production, where it provides uniform blending and consistent tablet integrity. Melting point 110–112°C: S- Allyl Cysteine with a melting point of 110–112°C is used in solid dosage forms, where it ensures stable formulation and controlled release profiles. Optical purity >99%: S- Allyl Cysteine with optical purity over 99% is used in enantiomer-specific therapeutic applications, where it minimizes side effects and maximizes pharmacological benefits. Odorless grade: S- Allyl Cysteine with odorless grade is used in oral care products, where it prevents undesirable flavors and improves consumer acceptance. Low heavy metals <10 ppm: S- Allyl Cysteine with low heavy metal content below 10 ppm is used in clinical research studies, where it ensures safety for human trials and compliance with regulatory standards. Microbial limit <100 CFU/g: S- Allyl Cysteine with microbial limit under 100 CFU/g is used in parenteral nutrition formulations, where it reduces contamination risk and maintains sterility. |
Competitive S- Allyl Cysteine prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please contact us at +8615365186327 or mail to admin@ascent-chem.com.
We will respond to you as soon as possible.
Tel: +8615365186327
Email: admin@ascent-chem.com
Flexible payment, competitive price, premium service - Inquire now!
Working on the production floor, the value of S-Allyl Cysteine isn't just in its chemical profile—it has everything to do with how it supports human health, practical formulation, and manufacturing consistency. Our team transforms raw materials through carefully managed biological processes that optimize purity and safety. Experience in the plant has shown how details in fermentation, crystallization, and filtration can decide whether a batch meets stringent pharma benchmarks or falls short of customer needs. In our hands, S-Allyl Cysteine (commonly called SAC) delivers a difference you can measure, both analytically and by customer feedback on solubility, color, and odor.
The SAC we produce is offered in a crystalline white powder form. Our typical specification maintains a purity standard that consistently reaches above 98%, confirmed by HPLC and related analytic techniques. Over years in production, strict in-process controls have helped us tighten variability between batches, giving formulation chemists peace of mind when relying on downstream performance. Particle size, bulk density, and loss on drying are not afterthoughts. Controls in this area help prevent clumping during weighing or formulation, something our early customers flagged as a real headache with competitors’ products. Every time the team improves sifting or drying, the benefits show up directly in mixing trials and feedback from laboratories.
S-allyl cysteine occupies a unique niche among organosulfur compounds due to its origins in garlic (Allium sativum) and its acknowledged bioactivity. As a manufacturer, we’ve tracked peer-reviewed research showing antioxidant and possible neuroprotective roles for SAC. Professionals in dietary supplement development often ask about the stability profile of our SAC during tableting or encapsulation. Comparison to related compounds like allicin or diallyl sulfide shows SAC stands out for its stability during formulation and storage. Garlic extracts suffer oxidation issues; SAC, whether alone or in blends, has proven to resist breakdown, especially under ambient conditions. This difference doesn’t just matter on paper. Finished product shelf life, consistent dosing, and organoleptic acceptance improve noticeably when SAC is chosen as the lead active ingredient.
Market trust has roots in manufacturing transparency. Our operation controls every step, from sourcing the biological starter material to finished, packed SAC. This gives us more than traceability—it brings direct knowledge about how to problem-solve. For instance, customers have brought us technical puzzles: issues like off-odors in finished food supplements, or dark spots in powder blends. Digging into these hiccups, we pinpointed upstream fermentation conditions as culprits, and tuned our processes to eliminate such outcomes. Traders and distributors rarely have the ability to do this kind of root-cause analysis. Being directly involved from start to finish means a customer’s challenge can become a new site standard within days or weeks, not years.
To outsiders, all garlic derivatives may seem roughly the same. On the production side, we see dramatic chemical, sensory, and application-driven contrasts. Take allicin and SAC: Allicin, although highly visible in popular literature, decomposes rapidly and presents unpleasant volatility during processing. Diallyl disulfide and other compounds exist in garlic extracts, but most lack the water solubility and handling safety that come standard with pure SAC. Another common misperception involves “aged garlic extracts,” which are mixtures with variable composition and lower purity, where consistency batch-to-batch can be poor. Pure, isolated SAC removes uncertainty. R&D teams benefit not just from a stably dosed active, but from the peace of mind that comes with analytic documentation. Every year, industry panel discussions highlight supplement mislabeling issues; the majority stem from insufficient traceability or lack of carefully isolated actives. By focusing on S-Allyl Cysteine in a consistent, tested form, our process offers a solution that addresses both efficacy targets and regulatory risks.
Scaling up production for S-Allyl Cysteine did not rest on switching a few dials. We invested time in modifying our fermentation parameters, as yields can fluctuate based on strain behavior, pH control, and feedstock composition. Early runs revealed that minor contaminating sulfur compounds affected both safety and aroma—something that laboratory-scale trials rarely predict. Years of incremental improvements now allow us to offer a product almost odorless, without the harsh sensory footprint of some competing grades. This matters for both direct ingestion and for applications in functional foods, where end-users demand uniform, clean flavor notes. Every critical control point was built to answer complaints we once heard: “Can you make this taste less like burnt onions?” Now, through a combination of physical separation and analytical checkpoints, we can.
Constant documentation builds trust with partners. Our facility documents each batch with certificates reporting assay, impurity profile, moisture, and heavy metal screening. Regulatory compliance isn’t a paperwork exercise: we faced rigorous audits from global nutraceutical customers who required full transparency on method, raw material handling, and storage. On several occasions, international partners needed analytical data to pass customs clearance or meet local standards, such as those in Europe or North America. Because testing begins long before packaging, and extends to real-time batch release, we remove much of the guesswork that plagues lesser-documented materials. Raw data from HPLC, microbiological, and elemental screens inform each shipment. If new regulatory demands arise—perhaps tighter limits on trace elements or stricter specifications for residual solvents—our analytic support adapts to ensure continuity.
Product development teams rely on feedback loops to guide improvements. Our SAC routinely sees use in dietary supplement tablets, liquid formulations, powdered drink blends, and functional foods. The main reason: its clean taste, water solubility, and one-step blending process. In one case, a customer formulating a functional beverage needed reassurance about long-term clarity and taste. Our technical lab collaborated to assess long-term solution stability, ultimately helping reformulate their product line with predictably excellent results. Feedback from supplement manufacturers confirms that granulation and compressibility arm formulators with a flexible active. This isn’t theoretical—production runs with our SAC avoid the sticking, capping, or discoloration issues that often come from lower purity or impure mixtures. We built our processes to address those real headaches, having seen the full chain from process hiccup to unhappy customer.
Pure SAC distinguishes itself from the garlic-derived powders or generic aged extracts on the market. The latter are hard to standardize, often carry strong odors, and frequently introduce inconsistent bioactive levels. Customers comment on dustiness, clumping, and unpredictable taste—problems directly linked to inconsistent production and mixing of multiple actives. By isolating S-Allyl Cysteine, we address issues at the molecule level, delivering a chemically defined, odor-neutral, and highly soluble alternative. Years of feedback from formulators—whether in sports nutrition or over-the-counter medicine—repeatedly show higher batch yields, reduced waste, and better customer acceptance whenever switching from generic garlic mixtures to our pure SAC.
Commitment to sustainability is not confined to marketing brochures. Source material selection began with tests on hundreds of garlic cultivars—not all provide the right precursor concentrations for efficient fermentation. By mapping out supply chains and investing in local agricultural partnerships, we have improved both the consistency and traceability of our inputs. In some regions, competitors struggle to guarantee pesticide-free, non-GMO garlic sources, which eventually shows up as volatility in final product quality. Our sourcing teams monitor crop conditions, work directly with growers, and insist on laboratory prequalification before any material reaches the plant. Not every customer notices these decisions, but those with strict organic, kosher, or allergen-control needs consistently return because shortcuts never enter the daily routine.
Scaling up S-Allyl Cysteine production called for investments in both upstream fermentation and downstream purification. Initial pilot lines suffered from bottle-necking in filtration steps, compromising yields. By implementing novel filter media and optimizing temperature control, we boosted throughput while maintaining purity—and avoided introducing further processing aids or additives. Over time, introducing automation in process control reduced error-prone manual handling. Critical sensors track key control points, including pH, temperature, and pressure, so deviations trigger rapid action from on-site technicians. These investments result in time savings, lower batch failures, and a quantifiable jump in output stability. The proof is in lower complaint rates from end users, smoother in-plant blending operations, and happier technical teams.
A constant concern among supplement brands involves the shelf life and storage conditions of actives. Our field experience has shown that S-Allyl Cysteine, once properly dried and sealed, offers excellent long-term stability at room temperature. Guidance to customers focuses on moisture control and avoidance of light, with double-layer packaging used for extra protection in humid environments. The lack of reactive sulfur maintains both potency and mild aroma, a property not always present in less pure materials. Cases where customers mixed SAC with hydroscopic carriers led to useful lessons in process transfer—recommending desiccants, improved blending techniques, and minimizing residence time in open air environments. These improvements, always fed back into our protocol, come from real use cases rather than theoretical shelf life projections.
S-Allyl Cysteine finds growing appeal in functional beverages, protein-fortified products, and even savory foods targeted at wellness seekers. Culinary technologists appreciate its discreet flavor impact, particularly in recipes where a strong garlic taste cannot be tolerated. Protein bars and rehydration mixes have sometimes revealed formulation surprises: clumping and sandiness. Adjustments by our team—tweaking granulation and adjusting hydration levels—resolved these issues, and internal trials validate that the active maintains its properties throughout baking, extrusion, and freeze-drying. By working with both traditional supplement brands and innovative food startups, our line keeps pace with the next wave of consumer needs, always led by conversations between our process engineers, QA teams, and the people out in the field creating new products.
Feedback from supplement and food technologists drives our approach to ongoing process improvements. Common requests include finer control over particle size, documentation on possible allergens, and assistance with regulatory dossiers. Through iterative adjustments, we’ve reduced fines (dusty particles), improved ease of pouring in automated lines, and added third-party allergen and GMO status documentation to each outgoing batch. One complaint that stood out involved the potential for product caking during ocean shipments to the tropics. Answeing directly, we changed both packaging format and recommended logistics partners, preventing losses and logistical delays.
Increasingly, suppliers are asked to meet regulations from around the world at the same time. Our plant has hosted technical teams from nutraceutical multinationals, independent auditors, and even government panels, all demanding transparency across each lot we make. From certifications for good manufacturing practice to successfully passing audits for allergen control, we learned to keep complete audit trails. No process gets documented only for local rules—all must survive the most stringent international checks. Data integrity, chain of custody on materials, and full disclosure of process steps keep us on the safe side, even as regulations evolve. Relationships with partners remain strong when issues are caught early, nonconformances are reported proactively, and all feedback loops are kept in motion. Compliance, in our world, is more than a certificate—it’s a habit of mind.
Every exhibition booth, every virtual seminar, brings questions from technical users and product managers. What makes your S-Allyl Cysteine different? Was it tested for specific allergens? How does it behave in low pH drinks? These aren’t generic. Each is rooted in someone’s daily production challenges. Our answers only carry weight because we have spent years production-side, seeing how theoretical risks play out in real manufacturing. If a beverage formulator worries about sedimentation, we supply stability data. A supplement brand facing label claims gets support on analytical method validation. Our approach grows from sharing real-world experience, not just pointing at a data sheet.
Every batch of S-Allyl Cysteine we ship reflects thousands of decisions—from which garlic lot to buy, to how many hours to hold a tank in fermentation, to what documentation accompanies final packaging. Customers value our material not simply for purity, but for promises kept and problem-solving that draws on years of chemical manufacturing know-how. Issues aren’t viewed as mysteries; they’re tackled by looking back through data, forward to better processes, and always sideways—to the customer’s reality. In a market crowded with generic actives and shaky supply chains, direct manufacturing experience stands out as both insurance and a guarantee for tomorrow’s innovators. As consumer, regulatory, and technical demands rise, our task remains the same: keep S-Allyl Cysteine predictable, support partners’ new ideas, and never lose sight of practical chemistry’s impact on health, product quality, and trust.