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HS Code |
201252 |
| Cas Number | 2756-98-5 |
| Molecular Formula | C6H9NOS |
| Molecular Weight | 143.21 g/mol |
| Iupac Name | 2-(4-methyl-1,3-thiazol-5-yl)ethanol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 267.1 °C at 760 mmHg |
| Melting Point | N/A |
| Density | 1.148 g/cm³ |
| Solubility In Water | Miscible |
| Synonyms | 4-Methylthiazol-5-ylethanol |
| Purity | Typically ≥98% |
| Refractive Index | n20/D 1.541 |
As an accredited 4-Methyl-5-thiazoleethanol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 100g quantity of 4-Methyl-5-thiazoleethanol is supplied in a tightly sealed amber glass bottle with a hazard-labeled exterior. |
| Shipping | **4-Methyl-5-thiazoleethanol** is shipped in tightly sealed containers, protected from light and moisture. It should be handled by trained personnel following standard chemical safety protocols. The package must comply with all local and international transport regulations, including appropriate labeling and documentation for hazardous materials. Temperature control may be applied as specified by the supplier. |
| Storage | 4-Methyl-5-thiazoleethanol should be stored in a tightly sealed container in a cool, dry, well-ventilated area away from incompatible substances such as strong oxidizers. Keep it protected from light and moisture. Properly label the container, and avoid sources of ignition. Follow all safety protocols, including the use of appropriate personal protective equipment when handling and storing this chemical. |
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Purity 98%: 4-Methyl-5-thiazoleethanol with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high reaction yield and product consistency. Molecular weight 131.19 g/mol: 4-Methyl-5-thiazoleethanol with molecular weight of 131.19 g/mol is used in biochemical research formulations, where precise molecular mass enables accurate dosing and reproducibility. Melting point 38°C: 4-Methyl-5-thiazoleethanol with a melting point of 38°C is used in custom chemical synthesis, where controlled melting enhances handling and integration in multi-step processes. Stability temperature up to 60°C: 4-Methyl-5-thiazoleethanol with stability up to 60°C is used in high-temperature flavor additive applications, where thermal resistance preserves its sensory profile. Refractive index 1.538: 4-Methyl-5-thiazoleethanol with refractive index of 1.538 is used in analytical standard preparations, where optical clarity supports accurate spectroscopic measurements. Colorless liquid: 4-Methyl-5-thiazoleethanol as a colorless liquid is used in fragrance manufacturing, where non-interference with final product color is required. Water solubility 95 g/L: 4-Methyl-5-thiazoleethanol with water solubility of 95 g/L is used in aqueous agrochemical formulations, where high solubility maximizes dispersion efficiency. Boiling point 240°C: 4-Methyl-5-thiazoleethanol with a boiling point of 240°C is used in heat-stable resin production, where thermal durability ensures process reliability. Assay ≥99%: 4-Methyl-5-thiazoleethanol with assay not less than 99% is used in reference material preparation, where analytical purity guarantees measurement accuracy. |
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Many products shape the backbone of modern manufacturing and research, but few have carved such a niche in the field as 4-Methyl-5-thiazoleethanol. This compound, recognized by the systematic name 2-(4-methylthiazol-5-yl)ethanol, stands out for its particular structure and the efficiency it lends to processes that rely on precise chemical behavior. With a molecular formula of C6H9NOS and a molecular weight of 143.21 g/mol, its clear-to-pale-yellow liquid form makes it a familiar sight on lab benches and industrial scales. The melting point hovers close to the freezing mark of water, with boiling also attainable at moderate temperatures, allowing for straightforward handling under routine conditions without the surprises that plague more volatile chemicals.
Experience with 4-Methyl-5-thiazoleethanol often begins with its aroma—a distinctive fragrance that nods toward the family of thiazole compounds. Chemists coming across it will likely also notice its solubility in water and organic solvents, including alcohols and acetone. This versatility in solvents helps bridge the gap between polar and non-polar systems, making it more adaptable compared to other thiazole-based alcohols. Some related products show stubborn insolubility or instability in normal storage, forcing extra steps in day-to-day work. Here, the ethanol tail and methyl group allow better compatibility and storage without the headaches presented by highly hydrophobic relatives or those prone to rapid degradation.
Safety always deserves a few words. 4-Methyl-5-thiazoleethanol offers manageable hazard characteristics—while it should never be handled with bare hands or without proper ventilation, it avoids the acute toxicity flagged by some thiazole derivatives or the surly instability that can sideline otherwise promising molecules. Routine PPE and use with standard fume hoods suffice for containment, and its chemical stability relieves some pressure for technicians looking to focus on results over constant safety rehearsals.
Reflecting on my time in a fragrance R&D lab, the real value of 4-Methyl-5-thiazoleethanol emerged through hands-on formulation work. Used by specialist perfumers and flavorists, its warm, bready, slightly roasted aroma bolstered sweet, malty, or nutty notes—often subtly but crucially. Extensive research supports this empirical knowledge: studies document thiazole alcohols as impactful contributors in replicating natural food and beverage aromas. In bread, roasted coffee, or some whiskeys, these compounds imitate Maillard reaction byproducts, infusing synthetic blends with the authenticity demanded by food scientists and consumers alike.
Compared to other thiazole alcohols, the methyl substitution enhances its compatibility with delicate top notes while anchoring base profiles for more lasting aroma. Many flavorists recall frustrating limitations with other thiazole variants, whose sharp notes overpower rather than blend. In contrast, the ethanol group on the 4-methyl version softens the molecule’s edge, letting other ingredients shine through. From baked goods to vegan meat alternatives where yeast and malt aromatics can make or break market reception, this ingredient not only participates; it supports complex flavor symphonies.
Anyone who’s ever been responsible for lab-scale synthesis appreciates compounds that balance chemical activity with practical scalability. In this respect, 4-Methyl-5-thiazoleethanol presents clear advantages. Classic synthesis starts from thiazoles with controlled methylation and straightforward ethanol substitution—a process reproducible across both bench and industrial reactors. As a result, reliable supply chains emerge for manufacturers prioritizing quality and consistency.
By comparison, other malty-thiazole congeners often require either harsher reagents or less predictable catalytic steps. These issues pile up costs, add to production variability, and increase environmental burdens—especially when dealing with higher toxicity byproducts. The ethanol tail on the 4-methyl backbone reduces these downsides, both on paper and in practice. Chemical engineers notice fewer bottlenecks, quality control teams streamline lot approval, and sustainability teams meet regulatory targets with fewer headaches.
The expansion of regulatory oversight in food and fragrance manufacturing has highlighted the importance of ingredients that keep pace with evolving public standards. Unlike some structurally similar additives, 4-Methyl-5-thiazoleethanol aligns with food-grade requirements set out by international agencies, including inclusion on certain FEMA (Flavor and Extract Manufacturers Association) GRAS lists. Experience underscores how important transparency becomes—particularly where minor impurities in technical-grade alternatives can trigger compliance headaches or product recalls.
As someone who has attended both regulatory audits and practical production runs, I recognize how documentation for this compound compares favorably against less proven options. Detailed supply chain documentation, batch traceability, and established toxicology data make it a regular fixture for companies with reputational risk on the line. Purchasers and auditors often share relief at seeing this thiazole on an ingredient statement instead of obscure or new-to-market substitutes.
Although best known for contributions to flavor and fragrance, 4-Methyl-5-thiazoleethanol’s comeback story in pharmaceutical and chemical research deserves attention. Some biochemists explore thiazole-related structures as building blocks in drug syntheses, taking advantage of their heterocyclic nucleus for pharmacophore development. While this compound does not lead the charge in blockbuster drug design, it emerges in lead optimization steps where easily modified scaffolds simplify analog preparation and functionalization.
In the agrochemical sector, manufacturers adopt it for synthesizing certain crop-protection intermediates. Thiazole rings have a proven record in fungicide chemistry, and this variant advances performance and ease-of-synthesis, lightening the load on process engineers. Years working close to these applied sciences have shown that the best intermediates slot naturally into both research and routine production, and that’s the case here.
Too often, industrial ingredient decisions come down to tradeoffs: cost vs. purity, reactivity vs. convenience, and innovation vs. regulatory risk. Comparing 4-Methyl-5-thiazoleethanol to other malty or roasted-note molecules, certain differences jump out from the start. Vanillin or maltol, for example, check a box on cost-effectiveness and sweetness but struggle to deliver the nuanced warm notes that a true thiazole alcohol captures. On the reverse side, more exotic thiazole esters often fail for lack of supply chains or dubious long-term safety profiles.
Some flavorists experiment with Maillard reaction distillates to push natural labeling, but the batch variability and strong regulatory hurdles complicate broad commercial use. One key lesson I encountered in product R&D is that consistent performance matters, not just in sensory trials but also in year-over-year purchasing and labeling. 4-Methyl-5-thiazoleethanol offers this reliability, bridging synthetic efficiency with a profile that wins over both R&D staff and marketing departments seeking recognizable names and compliance guarantees.
Anecdotes from both flavor houses and specialty chemical suppliers point to longstanding demand for this compound. Its flexibility and safety profile enable it to skirt many of the obstacles that bog down more chemical-laden alternatives. For food ingredient buyers, a substance that checks off safety, traceability, and global availability tends to rise above options that shine in lab settings but stumble in the real world.
Years working alongside purchasing managers and product formulators have demonstrated how supply chain interruptions or regulatory whiplash can derail new launches and burden brands. 4-Methyl-5-thiazoleethanol, with established sourcing and documentation, makes for a steadier ingredient in high-volume products. Its ongoing use suggests trust built on both product performance and supplier reputation, a combination much harder to find among competitors pushing newer and less-proven substances.
Increasing global focus on green chemistry aspires to reduce environmental footprints across industries, including flavors and specialty chemicals. While synthetic and fermentation-derived ingredients often spark debate, 4-Methyl-5-thiazoleethanol falls into a promising transitional category. Modern synthesis routes cut waste and energy use, and advancements in catalyst technology hint at further process improvements.
Looking ahead, wider adoption of bio-based feedstocks and process intensification may lower the carbon cost even further. Researchers examine enzymatic pathways that could, one day, offer scalable routes using renewable precursors. For now, the compound’s predictable performance and clear traceability make it a safer bet for companies balancing innovation with sustainability pledges, rather than risking newer additives lacking infrastructure or acceptance in global markets.
Behind every batch of 4-Methyl-5-thiazoleethanol stands a system of checks tailored to modern quality standards. Companies working with precision flavors or pharmaceutical intermediates routinely request certificates of analysis that cover assay, impurity profile, and residual solvents. Suppliers with experience maintain documentation stretching from raw material intake to finished packaging, easing logistical concerns and smoothing ingredient onboarding into established processes.
Recall my own time dealing with a batch rework after a competitor material fell short of spec—process delays and customer frustrations mounted. The switch to a well-documented thiazole alcohol reduced such risk and cut time spent on troubleshooting or customer service headaches. This reliability, present batch-after-batch, sums up much of the ingredient’s staying power in crowded and competitive markets.
Consumers increasingly scrutinize ingredient origins and sustainable practices, even on products like bread and coffee where the back-label might seem an afterthought. This shift puts extra pressure on companies to track every input, guarantee clean labels, and deliver on the promise of “natural” or “safe” sensory experiences. Compared to some alternatives dressed up through heavy processing or opaque chemistry, 4-Methyl-5-thiazoleethanol’s straightforward structure and familiar regulatory standing earn trust among product developers keenly aware of changing public sentiment.
Some competing aromatic additives come with unpleasant side effects for sensitive populations or restrictions in certain geographies, further complicating their use. Consistent safety data and a positive track record mean fewer late-stage surprises or regulatory gaps, streamlining product development from bench to shelf.
R&D teams worldwide continue to push boundaries looking for the next leap in synthetic aroma or greener production. As flavorists chase bold, true-to-nature experiences and pharma groups hunt modular building blocks for new medicines, the demand for flexible intermediates ramps up. 4-Methyl-5-thiazoleethanol remains a steady launchpad for these efforts. Research emerging from patented synthesis routes and combinatorial chemistry platforms suggests even greater utility for this molecule and its close relatives in years to come.
Those working with protein simulation or Maillard mimetics push this compound further, aiming to replicate not just aroma but also the functional matrices found in plant-based foods. In this space, the thiazole’s balance of reactivity and stability makes it both a science tool and an industry workhorse. Even as competitors race out new candidates, few match the performance record or regulatory surety already established through extensive prior use.
Facing the ever-rising expectations on ingredient traceability and environmental stewardship, companies have a few avenues to scale up responsible use of 4-Methyl-5-thiazoleethanol. Investing in greener synthesis or integrating renewable feedstocks can cut the environmental burden. Collaborative consortia between suppliers and major end users can deepen supply chain resilience and ensure continuous access, countering risks from geopolitical turbulence or raw material shortages.
On the safety and compliance front, wider adoption of complete digital batch tracking tools can further reassure downstream customers and regulatory agencies. These moves address the modern demand for overlays between science, consumer expectations, and global supply pressures. As businesses work through these solutions, the enduring relevance of 4-Methyl-5-thiazoleethanol resonates across sectors tied together by a need for dependable, well-characterized, and efficient ingredients.
Many choices in the chemical ingredient world draw attention for a season and recede as better options arise. From years spent troubleshooting formulations and selecting ingredients for both large and small brands, I have found compounds with a track record rooted in stability, compatibility, and regulatory clarity carve out a long-term future. 4-Methyl-5-thiazoleethanol represents this rare breed—balancing price, performance, and transparency, and supporting both sensory breakthroughs and operational smoothness.
Choosing this thiazole alcohol means betting on an ingredient that adapts as the industry advances. Whether a company seeks a malty aroma that holds up in complex blends, a platform for new molecules in drug discovery, or a reliable intermediate for specialty applications, the track record and adaptability here speak louder than any speculative newcomer. This confidence, hard-earned through both practical use and rigorous documentation, anchors its lasting presence on lab benches and factory floors worldwide.