|
HS Code |
550967 |
| Chemical Name | (S)-4-Benzyl-1,3-Thiazolidine-2-Thione |
| Cas Number | 35795-44-7 |
| Molecular Formula | C10H11NS2 |
| Molecular Weight | 209.33 g/mol |
| Appearance | Off-white to light yellow solid |
| Melting Point | 92-95 °C |
| Optical Rotation | [α]D20 +70° (c=1, CHCl3) |
| Solubility | Soluble in organic solvents (e.g., DMSO, CHCl3) |
| Smiles | C1C(SC(N1)=S)CC2=CC=CC=C2 |
| Inchi | InChI=1S/C10H11NS2/c12-10-11-8(6-7-13-10)5-9-3-1-2-4-9/h1-4,8H,5-7H2,(H,11,12)/t8-/m0/s1 |
| Purity | Typically ≥98% |
| Storage Conditions | Store at 2-8°C, protected from light and moisture |
| Chirality | S-enantiomer |
| Uses | Used as a chiral building block in organic synthesis |
As an accredited (S)-4-Benzyl-1,3-Thiazolidine-2-Thione factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 10 grams, sealed with a screw cap; labeled with chemical name, molecular formula, CAS number, and hazard warnings. |
| Shipping | The chemical (S)-4-Benzyl-1,3-Thiazolidine-2-Thione is shipped in secure, tightly sealed containers to prevent contamination and degradation. Packaging complies with all relevant safety and regulatory standards for hazardous materials. The product is transported under ambient conditions unless otherwise specified, and accompanied by appropriate documentation for safe and legal handling during transit. |
| Storage | (S)-4-Benzyl-1,3-thiazolidine-2-thione should be stored in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Avoid exposure to strong oxidizing agents and extreme temperatures. Store at room temperature or as specified by the supplier, and ensure proper chemical labeling and compatibility with neighboring substances to prevent contamination or hazardous reactions. |
Applications of (S)-4-Benzyl-1,3-Thiazolidine-2-Thione in Industrial ManufacturingWe specialize in manufacturing (S)-4-Benzyl-1,3-Thiazolidine-2-Thione, a chiral intermediate widely used in precise chemical synthesis. Below, we outline real-world industrial applications, technical integration, compositional guidelines, relevant compliance requirements, and typical end products across several specialized sectors. 1. Chiral Pharmaceutical Intermediate for Antidiabetic APIsMajor API manufacturers select this material for stereospecific synthesis of several thiazolidinedione-based antidiabetic drugs, including (S)-Pioglitazone and (S)-Rosiglitazone, owing to its well-defined chiral center and reactivity profile. The compound serves as a protected synthon during early-stage API building block assembly, facilitating establishment of the S-configuration in downstream syntheses. Downstream users introduce it post-aldol condensation or during the ligation sequence, followed by selective deprotection. Quality and purity must meet stringent pharmaceutical standards, with analytical controls at each batch. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Precursor for Custom Sulfur-Containing Agrochemical SynthesisLeading agrochemical producers use this molecule as a sulfur donor in synthesizing herbicidal and fungicidal agents, especially in products containing sulfur-heterocycles. The defined configuration aids in tuning biological selectivity for chiral agrochemicals. Technicians control the feed amount precisely, as improper levels may lead to impurity build-up or incomplete cyclization. Feed-in is generally at the sulfur incorporation or cyclization stage, with close temperature and pH monitoring to protect stereochemistry and purity. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Building Block in Stereoselective Peptidomimetic SynthesisSpecialty peptide and peptidomimetic manufacturers incorporate this compound to build sulfur-bridged amino acid analogs with rigidified 3D structures. Its chiral center supports enantioselective peptide backbone construction, influencing bioactivity and metabolic profile of the final molecule. It is added during the backbone extension segment, where coupling conditions, solvent selection, and protection strategies determine the integration rate. QC tests for residual reagents and byproducts prior to subsequent elongation cycles. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Intermediate for Custom Organic Electronic Material SynthesisAdvanced materials manufacturers leverage this compound for synthesizing sulfur- and nitrogen-rich monomers used in organic semiconductors and conductive polymers. Its chemical configuration enables precise control of electronic properties by affecting π-conjugation in the polymer backbone. Integration requires strict anhydrous and oxygen-free conditions to prevent premature oxidation. Technicians meter in the material during the monomerization reaction, followed by direct in-line polymerization. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
5. Synthon for Custom Organic Sulfur Ligands in Metal CatalysisCatalyst manufacturers value this compound for preparing chiral sulfur ligands and auxiliaries, targeting enantioselective hydrogenation and cross-coupling reactions in fine chemical production. The molecule supplies both sulfur and a defined stereo anchor, leading to improved catalytic selectivity. Personnel must control feed addition to metal salt solutions, observe inert handling protocols, and validate ligand integrity by NMR and HPLC prior to catalyst formation. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
6. Chiral Auxiliary for Enantioselective Natural Product SynthesisSynthetic chemistry laboratories and pilot facilities deploy this intermediate as a chiral auxiliary in the total synthesis of complex natural products, particularly for constructing five-membered sulfur heterocycles with defined configuration. Its stability under a range of reagents and solvents allows for use in multistep sequences involving alkylations, reductions, and ring closures. Specialized technicians control reaction scale and auxiliary removal efficiency to meet experimental and pre-commercial trial needs. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
|
Competitive (S)-4-Benzyl-1,3-Thiazolidine-2-Thione prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: admin@sinochem-nanjing.com
Flexible payment, competitive price, premium service - Inquire now!
Manufacturing (S)-4-Benzyl-1,3-Thiazolidine-2-Thione stands out as a daily exercise in precision and accountability. After years shepherding this compound from raw material handling to sealed shipments, our team recognizes every variable—every reaction condition, purification step, and analytical signature. Each batch reflects not just a recipe, but the steep learning curve and hands-on knowledge accumulated along our production lines.
Our plant operates with purpose-built glass-lined reactors for the synthesis of (S)-4-Benzyl-1,3-Thiazolidine-2-Thione. We maintain batch records for every lot, indexing date, environmental conditions, and parameters. Crystalline product usually appears off-white to pale yellow, like an early-morning fog. Each production run targets distinct chirality—our capabilities focus on the (S)-enantiomer, given the sharp difference in downstream application compared to racemic or (R)-series analogues.
Typical purities exceed 98% by HPLC, with enantiomeric excess at least 99%. Our in-house HPLC methods, validated for resolution and repeatability, cut down ambiguous results. Water content stays under 0.5% by Karl Fischer titration. Shelf stability runs over 24 months sealed under nitrogen at ambient temperature; we track this through long term retention samples tested at 6, 12, and 24 months using the same equipment as initial QC.
We often receive requests for bulk, but also smaller scale pilot lots for research and pharmaceutical development. Whether for 10-gram vials or multi-kilo drums, we fill each with material tracked step-by-step back to the synthesis day.
Any skilled chemist running thiazolidine intermediates understands that reaction control means more than following process instructions. Thioamide synthesis requires tight hold on temperature, nitrogen sparging, and reaction time. Cutting corners means spending nights rerunning product, or losing time to a potent rotten-egg odor that escapes even good scrubbers.
Working with benzyl isothiocyanate, we source material with strict impurity control, checking GC traces batch-to-batch. Each step, from mixing with (S)-cysteine to work-up, carries lessons. Water can introduce racemization risks. Overheating can generate by-products that complicate crystallization. My colleagues take pride in making adjustments on the fly to keep batches on target—sometimes lowering agitation, sometimes extending dry time in our vacuum ovens. These choices lift yields and boost reproducibility.
Our personnel perform in-process checks with FT-IR and TLC, confirming little left over from the reactants. The strong C=S stretch is obvious on spectra, and the characteristic melting point falls within a narrow 124-127°C window for a good batch. Dust control remains a hands-on effort, since thiazolidines like this pick up static fast and tumble out as fine powders. Operators wear gloves, not just for safety, but also for better dexterity at the weighing stations.
Compared to commodity intermediates, the (S)-4-Benzyl-1,3-Thiazolidine-2-Thione offers pronounced impact on several process chemistries, especially for chiral pharmaceuticals and certain agrochemical agents. The clear benefit shows itself during asymmetric synthesis, as the S-configuration lets chemists tune downstream transformations without risking racemic drift.
Generic versions might deliver variable purities or uncertain chiral ratios. Years spent troubleshooting problems from off-spec batches or material shipped in inappropriate packaging led us to tighten every parameter—particle size distribution, packaging materials, dessicant loads. Racemic mixes sometimes cost less but burden customers with separation steps. We make only the optically pure (S)-series, answering customers who need confidence in each molecule’s configuration.
Some suppliers blend their lots or deliver amorphous powders prone to caking. Our facility maintains rigorous control over drying and grinding—those steady, practiced hands matter. Even the drum liners are anti-static, minimizing risk of product loss on opening. If you’ve ever had to chisel a caked block of thiazolidine out of a barrel, you know what these measures prevent.
(S)-4-Benzyl-1,3-Thiazolidine-2-Thione typically enters the pharmaceutical pipeline as a building block for chiral drugs, or as a resolving agent for amino acid derivatives. Our best customers run these chemistries on kilo scales, and every production hiccup ripples down to scheduling or regulatory reviews. In pharma, an out-of-spec batch means days lost, extended validation, and rerun documentation.
We always run parallel samples through literature-validated procedures to judge yield and reactivity, simulating customer use cases. These screening reactions reveal batch-by-batch consistency not just in purity but in true chemical performance. In some hands, the thiazolidine acts as a masked cysteine equivalent; in others, it mediates new sulfur-carbon bond formations. Tracking the downstream implications becomes second nature after working closely with industrial partners during process scale-up.
Our direct experience reveals the pitfalls behind “good enough” sourcing. Once, a batch from a new upstream material showed a subtle difference in crystallization habit, nearly sending product through customer QC—but not quite. Extra time spent verifying each shipment through in-depth NMR and chiral HPLC is time well spent. Our staff invests the effort because we have seen the havoc caused by irregularities.
We grew out of a background managing fine organic intermediates, watching the supply side for trends—price swings, pollution control issues, shifting sources of cysteine or benzyl isothiocyanate. Direct sourcing lets us backtrace any unusual event to a specific batch of raw material, not a faceless broker overseas. All our key vendors go through periodic audits for both environmental compliance and documentation.
Controlling every factor behind the finished thiazolidine meant overhauling solvent recovery and waste management operations. Years ago, we dumped too much aqueous and organic waste offsite. Reinvestment in recovery units produced solvent purity high enough for reuse, trimming raw material costs and lowering environmental burden. This helps us keep costs down without cutting corners, an advantage reflected on every quote.
Our operators come to appreciate every strange odor and color shift in a batch—sometimes it signals new risks, sometimes just a different solubility profile from a fresh lot of cysteine. If a reaction takes too long, they know to check pH, and whether the storage drum sat exposed to air too long in the humid season. These details carve the difference between “produced” and “carefully made.”
Packing (S)-4-Benzyl-1,3-Thiazolidine-2-Thione takes more than shoveling crystals into a drum. We run every filled package through secondary screening—sampling from the top, middle, and bottom layers of the drummed material—to confirm consistency. Each drum or bottle receives a nitrogen flush, heat-sealed foil liner, and then weather-resistant secondary containment. These steps sound modest, but every one came from hard lessons with hydration, powder compaction, or contamination from prior packaging.
We track exported batches through a digital system, linking drum numbers to manufacturing and QC certificates. Problems rarely start on the dock; they more often appear months later when a user opens a drum exposed to temperature swings or warehouse humidity. Using multiple barrier layers holds moisture out, but our experience shows that dry warehouse conditions and FIFO (first-in, first-out) stock rotation go further.
On the transportation side, our in-house logistics team knows how to handle these shipments with minimal vibration and temperature fluctuation. We have switched couriers and shipments chains in humid seasons, remembering difficult summers when an entire container faced port delays and condensation issues. Frequent communication with storage partners reduces these headaches for customers down the line, sparing reprocessing or disposal.
People often ask about the difference between our thiazolidine and other thioamide-based intermediates. From daily contact with customers, we see distinct improvements—yield, reaction selectivity, and purification. Our (S)-enantiomer does not introduce the same levels of side-products or duplicate reaction steps required by less pure, non-chiral materials.
In scale-up work, cheaper sources create headaches with inconsistent melting points, variable solubility, and color issues that make in-line QA difficult. Some competitors accept off-white or even gray to beige powders, which rustle up purification headaches later. We check every container for color and clarity, and our operators take personal pride in each lot’s tidy crystalline profile. These are not just aesthetic preferences—they speak to underlying purity and strict process discipline.
We have responded to customer feedback by continually refining our process. Years ago, a spike in demand led to batch loss—stress on the system revealed the limits of previous equipment setups. We responded with process mapping, investment in better temperature controls, new real-time analytics, and more cross-training for staff. As a result, we cut batch failure rates in half and reduced waste. Our experience proves that every detail, from operator training to instrument calibration, counts toward trustworthy supply.
Running a thiazolidine intermediate plant requires more than chemical know-how. Regulations tighten on waste, air emissions, and documentation. We have adopted newer digital tracking systems and batch histories, helping us trace every product drum back to its start. Years spent interacting with environmental authorities shaped our workflow and raw material movement.
One key risk comes from feedstock chain interruptions. Cysteine and benzyl isothiocyanate, especially in pandemic times, suffer from sourcing volatility. We keep a rolling stock buffer and work closely with multiple upstream partners, even running our own periodic QC on incoming material. This way, we sidestep delays or unforeseen contaminations that so often stall competitors.
We have also faced headwinds from evolving safety and exposure limits for isothiocyanates. Ventilation upgrades and engineering controls anchor every process update. Operators join periodic safety drills, and each incident sparks a plant-wide review. From direct experience, any gap in risk control multiplies costs, so staying ahead of regulation is memory, not just a requirement.
Walking through the plant, seeing rows of labeled drums and gleaming reactors, the importance of quality resonates every day. Communication with customers drives continued innovation in our process—whether it is adapting to new regulatory filings, supporting scalability studies, or troubleshooting a reaction outlier in a pharma pilot plant. Our plant’s history runs parallel to the markets we serve, growing together in technical depth and real-world feedback.
Our operators keep their focus, from raw feed in the tank farm straight to the shipping dock. They understand every minor adjustment in temperature or filtration relays through to a successful customer outcome. Manager and operators alike share an ethos built over repeated success and learning from the moments that fall short. Every drum of (S)-4-Benzyl-1,3-Thiazolidine-2-Thione carries not just material, but the persistent effort to refine, document, and deliver against ever-higher expectations.
We carry the benefits of direct manufacturing not just in product quality, but in the way our knowledge shortens troubleshooting, helps partners react to new research, and adapts to rapid changes in chemical markets. Our plant lives in the details—raw material receipts, batch cards, HPLC traces, operator notes. These stories live on in each shipment that leaves our doors.
Producing (S)-4-Benzyl-1,3-Thiazolidine-2-Thione in-house brings with it a deeper sense of trust, efficiency, and accountability that no trading intermediary can rival. Each lot tells a story, written daily on the production floor and delivered in every drum that finds its way to your laboratory or plant. This experience, built from real production, ensures our product lines match both technical specification and customer expectation, batch after careful batch.