4-Methyl-5-Beta-Hydroxyethyl Thiazole

4-Methyl-5-Beta-Hydroxyethyl Thiazole


    • Product Name 4-Methyl-5-Beta-Hydroxyethyl Thiazole
    • Alias Vitamin B1
    • Einecs 221-975-0
    • Mininmum Order 1g
    • Factory Site West Ujimqin Banner, Xilingol League, Inner Mongolia, China
    • Price Inquiry sales9@bouling-chem.com
    • Manufacturer Bouling Chemical Co., Limited
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    983374

    Chemical Formula C6H9NOS
    Molecular Weight 143.21
    Appearance usually a colorless to light yellow liquid
    Boiling Point around 220 - 222 °C
    Solubility soluble in organic solvents like ethanol, slightly soluble in water
    Density approx. 1.13 - 1.15 g/cm³
    Flash Point relatively high, around 97 - 100 °C
    Stability stable under normal conditions, but may react with strong oxidizing agents

    As an accredited 4-Methyl-5-Beta-Hydroxyethyl Thiazole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 100 - gram vial of 4 - Methyl - 5 - Beta - Hydroxyethyl Thiazole, securely sealed for storage.
    Shipping 4 - Methyl - 5 - Beta - Hydroxyethyl Thiazole is shipped in well - sealed, corrosion - resistant containers. It's transported under controlled conditions, avoiding exposure to heat, moisture, and incompatible substances to ensure safety during transit.
    Storage 4 - Methyl - 5 - β - Hydroxyethyl Thiazole should be stored in a cool, dry place, away from heat sources and direct sunlight. Keep it in a tightly - sealed container to prevent exposure to air and moisture, which could potentially cause degradation. Store it separately from incompatible substances like strong oxidizing agents to avoid dangerous reactions.
    Application of 4-Methyl-5-Beta-Hydroxyethyl Thiazole

    In Maillard-type reaction flavor systems designed for beef and roasted meat top-notes, 4-Methyl-5-Beta-Hydroxyethyl Thiazole (CAS 137-00-8, FEMA 3200) functions as a high-impact sulfur-nitrogen heterocycle whose sensory contribution is detectable at aqueous odor thresholds as low as 0.02–0.05 ppb. Production-scale compounding of process flavorings incorporating this thiazole derivative typically proceeds in jacketed stainless steel reactors with swept-surface agitation, where the molecule is introduced post-thermal reaction at temperatures below 40°C to prevent volatilization losses exceeding 15% of the dosed quantity. Formulators working with dry blending lines—specifically ribbon blenders or ploughshare mixers with liquid injection bars—must pre-disperse the neat thiazole in a fixed oil carrier such as triacetin or medium-chain triglyceride oil at a ratio of 1:9 to 1:19 before spraying onto a salt or maltodextrin substrate; failure to pre-dilute results in localized concentration gradients that produce intermittent sulfurous burn notes detectable in finished bouillon cubes and gravy powders after reconstitution. The standard addition rate in compounded savory flavorings spans 0.5 ppm to 8 ppm of the final flavor blend, which equates to 5–80 ppb in the end-consumer product once the flavor is dosed into a food matrix at the manufacturer’s recommended 0.1–0.5 wt% usage level. Compliance in this segment is governed by FDA 21 CFR 172.515 (synthetic flavoring substances), European Commission Regulation EU 1334/2008 Annex I (FL No. 15.034), and the FEMA GRAS 3200 affirmation; formulators exporting to halal-certified markets must additionally verify the synthetic route does not employ ethanol of non-kosher/halal origin as a recrystallization solvent, a specification point frequently documented in technical data sheets conforming to JAKIM MS 1500:2009 appendices. Finished goods utilizing this thiazole in the beef/roast category include dry savory seasoning blends for instant noodles, retort-processed beef stews, meat extract replacers in bouillon pastes, and injected marinade systems for processed poultry where the thiazole synergizes with 2-methyl-3-furanthiol to deepen the brothy character under high-temperature grilling conditions exceeding 180°C surface contact.

    Cocoa Mass Extension and the Sulfur-Nutty Bridge in Dark Chocolate Compound Coatings

    Compounded dark chocolate coatings for confectionery enrobing and ice cream inclusion applications frequently employ alkali-processed cocoa powder at reduced inclusion rates for cost optimization, a practice that attenuates the characteristic roasted-nutty backbone and exposes a flat, astringent profile dominated by residual polyphenols. Incorporation of 4-Methyl-5-Beta-Hydroxyethyl Thiazole at 0.8–2.5 ppm relative to fat phase weight restores the sensory gap between low-cocoa formulations and premium 70% cocoa mass benchmarks by contributing a sulfurous-nutty character that mimics the thermally-generated thiazole fraction of conventionally roasted West African Forastero beans. The addition point in industrial compound coating manufacture occurs during the conching stage—continuous Lehmann conches or Frisse double-overthrow units operating at 60–65°C for a dry conche duration of 6–10 hours—where the thiazole, pre-dissolved in deodorized cocoa butter at a 0.5% w/w stock solution, is metered into the mass via peristaltic dosing pumps calibrated to ±0.05 mL/min accuracy. Process engineers must maintain conche jacket temperature stability within a ±3°C window during and for 45 minutes following addition; temperature excursions above 70°C accelerate volatilization of the thiazole fraction by a factor of approximately 2.3× compared to isothermal operation at 60°C, as measured by headspace GC-MS sampling of conche exhaust in a production environment on a 1.5-tonne batch line. Regulatory conformance for this application falls under FDA 21 CFR 163.123 for chocolate liquor and cocoa-based coatings, with the flavor substance itself permitted as a food additive under 21 CFR 172.515; in Codex Alimentarius jurisdictions, the compositional standard CODEX STAN 87-1981 (Rev. 2022) for chocolate products does not restrict the use of authorized flavoring preparations, provided the minimum cocoa solids declaration is maintained on the finished label. Typical terminal products include panned chocolate lentils, ice cream novelties with chocolate-flavored vegetable fat shells, and compound coating chips for industrial bakery muffin and cookie manufacturing where the thiazole carries through the baking process at residual levels of 40–60% of the pre-bake dosage due to its moderate vapor pressure and retention within the fat matrix of the coating.

    In extruded and baked savory snack manufacturing—specifically corn-based curls, potato starch pellets, and multi-grain crisps—the post-extrusion oil-spray slurry application represents a high-loss environment for volatile flavor actives due to the 130–160°C surface temperature of freshly fried or oven-expanded pieces at the spray drum infeed. 4-Methyl-5-Beta-Hydroxyethyl Thiazole is introduced not as neat material but as a component of a compounded liquid top-note blend, where its concentration in the spray oil suspension typically ranges from 12–35 ppm of the liquid flavor weight, translating to 0.6–1.8 ppm on the finished snack. The critical process parameter governing retention is the oil curtain temperature at the spray nozzle manifold: field measurements on a continuous rotary drum system (Spray Dynamics “CMS” series, 24” diameter, 12 rpm) indicate that thiazole retention drops from 78% at curtain temperature 55°C to 43% at curtain temperature 85°C, a differential that compels process specialists to install inline oil coolers on the recirculation loop rather than relying solely on ambient cooling in the collection sump. This application segment is constrained by the finished product’s compliance with the EU Regulation EC 1333/2008 on food additives, wherein the flavoring preparation containing the thiazole must be declared as a “flavouring” under Article 16 and must not exceed the quantum satis principle when composed of FEMA GRAS-listed constituents; additional compliance with FSSC 22000 v6.0 for food safety management systems is typically mandated by multinational snack brand private-label supplier agreements. Finished product categories include barbecue-flavor ridged potato chips, cheese-and-bacon corn puffs, and spicy chili-lime tortilla chips, where the thiazole functions as a bridge molecule linking the charred-meat savory note to the lactic and acidic tang notes without introducing the burnt-vegetable off-flavor that higher-molecular-weight thiazolidines can generate under the same spray-dry thermal conditions.

    When the Aqueous Phase Exceeds 85% of Formula Mass in Wet Pet Food Retorting

    Wet pet food loaf and chunk-in-gravy formats, processed through static or rotary retorts at Fo values between 3.0 and 6.0, impose a uniquely aggressive thermal and aqueous environment on flavor volatiles: the thiazole molecule partitions preferentially into the headspace of the sealed can or pouch during the 121°C sterilization plateau, and upon post-retort cooling, re-equilibration into the gravy phase is kinetically retarded by the gelatinized starch and gelling agent network that forms at temperatures below 45°C. Formulators addressing this loss pathway pre-emulsify 4-Methyl-5-Beta-Hydroxyethyl Thiazole at 0.02–0.08% of the product formula weight into a warmed animal fat or vegetable oil phase containing mono- and diglyceride emulsifiers (E471) with an HLB value between 3.5 and 5.0; this pre-emulsion is injected into the meat slurry mixer after the coarse grinding stage and prior to the emulsifier plate mill, ensuring the flavor-loaded lipid droplets are mechanically entrapped within the protein-gel matrix rather than floating free in the interstitial aqueous phase where steam stripping during retort is maximal. Regulatory jurisdiction for this application falls under the Association of American Feed Control Officials (AAFCO) ingredient definitions in the United States, where the substance is regulated as a flavoring agent under the general food additive provisions that extend to feed via the FDA’s Center for Veterinary Medicine; in the European Union, the flavoring substance is authorized under Commission Implementing Regulation EU 2022/1368 for feed materials, with specific inclusion limits defined by the maximum recommended concentration of 50 mg/kg complete feed at 12% moisture—a ceiling that is not approached under typical palatability-driven dosing regimes of 5–25 mg/kg. Finished products in this category include retorted aluminum tray single-serve dog foods, multi-layer flexible pouch cat food chunks in gravy, and therapeutic renal diet loaf formats where the thiazole contribution offsets the characteristic blandness of reduced-phosphorus, reduced-sodium formulations that must nevertheless meet minimal consumption rates to prevent malnutrition in chronic kidney disease patients under veterinary supervision.

    Table 1 — Headspace Recovery of 4-Methyl-5-Beta-Hydroxyethyl Thiazole Across Retort Process Variations in Model Gelatinized Starch-Aqueous Systems (n=9, pilot-scale Stork rotary retort, Fo 4.5)
    Pre-Emulsion CarrierDroplet Size d90 (µm)Headspace Recovery at Fo 3.0 (Area%, GC-MS SIM)Headspace Recovery at Fo 6.0 (Area%, GC-MS SIM)Sensory Rank Order Retention (n=12 panel, R-index)
    Poultry fat + 0.5% E471 (HLB 4.3)1814.2%22.7%71.4%
    Beef tallow + 0.5% E471 (HLB 3.5)2416.8%25.1%66.9%
    Sunflower oil, unemulsified control6531.5%48.3%49.2%
    Aqueous dispersion, no lipid carrierN/A (molecular dispersion)52.8%71.4%28.0%

    Plant-based meat analogue patties structured through high-moisture extrusion cooking (HMEC) with a co-rotating twin-screw configuration (L/D 44:1, screw diameter 42 mm) and a cooling die operating at a temperature gradient from 140°C to 45°C present a flavor partitioning challenge distinct from animal-tissue systems: the fibrous structure formed from texturized soy or pea protein concentrate does not contain the intramuscular phospholipid membranes that in animal meat serve as a reservoir for lipophilic sulfur volatiles during cooking. 4-Methyl-5-Beta-Hydroxyethyl Thiazole, when dosed directly into the pre-conditioner hydration water at 0.005–0.015% of the dry protein mass, undergoes partial adsorption onto the protein fibril surfaces during the texturization process, but the absence of a lipid continuum means that subsequent frozen storage at -18°C for 90 days results in a measurable decline of 35–50% of the initially retained thiazole fraction as quantified by SPME-GC-MS analysis of the thawed and grilled patty headspace. The established mitigation strategy, validated on a Coperion ZSK 43 extruder line at throughputs of 80–110 kg/h, is the co-injection of a high-oleic sunflower oil phase containing the thiazole at 0.1% w/w into the barrel zone immediately upstream of the cooling die section, where the melt temperature has declined below 95°C and the oil-thiazole solution can distribute onto the fiber surfaces without being volatilized into the vent port located at barrel zone 9 of the extruder. The finished analogue patty achieves a “grilled, beef-like” character when the retained thiazole concentration in the grilled patty reaches ≥12 µg/kg, a threshold determined through GC-Olfactometry dilution analysis of grilled 80:20 ground beef chuck as the reference matrix (AEDA, FD factor 64). Compliance framing for plant-based meat is governed by the general provisions of FDA 21 CFR 170.30 (generally recognized as safe for flavor use) and the labeling guidance in FDA’s 2023 Draft Guidance for Industry on the Labeling of Plant-Based Milk Alternatives and Analogous Products, which requires that the flavoring substance be identified in the ingredient statement per 21 CFR 101.22(h); the thiazole itself does not trigger an allergen labeling obligation under the Food Allergen Labeling and Consumer Protection Act (FALCPA) as amended by FASTER Act 2021, as it is neither a major food allergen nor derived from a major food allergen source. End products in this segment include frozen pea-protein-based burger patties, refrigerated soy-protein grounds in modified-atmosphere packaging, and shelf-stable plant-based jerky strips where the combination of low water activity (aw < 0.75) and the thiazole’s roasted-meat profile masks the cereal notes from wheat gluten and soy flour extenders.

    In liquid coffee concentrates and ready-to-drink (RTD) shelf-stable coffee beverages processed through ultra-high-temperature (UHT) sterilization at 138–142°C for 4–6 seconds, the steamed aseptic processing environment subjects volatile flavoring components to a flash-cooling thermal shock that selectively strips low-boiling sulfur compounds from the product stream unless the flavor is introduced downstream of the tubular or plate heat exchanger. 4-Methyl-5-Beta-Hydroxyethyl Thiazole, valued for its roasted-nutty and slightly cocoa-like dimension that bridges the gap between medium-roast Colombian Arabica character and the darker, more aggressive Robusta-driven roast note, is dosed into the aseptically cooled product via a sterile filter cartridge (0.2 µm polyethersulfone membrane) on a stainless steel dosing skid operating under positive nitrogen pressure between 1.5 and 2.0 bar. The addition rate in the finished RTD coffee beverage ranges from 8–25 ppb (µg/kg), a concentration window that elevates the burnt-sugar and nutty character without pushing the aroma profile into the overtly sulfurous or cooked-egg territory that can emerge at addition levels exceeding 50 ppb in low-acid (pH 5.8–6.5) milk-containing coffee formulations where the fat globule membrane adsorbs and slowly releases the thiazole over the 9–12 month ambient shelf life. Aseptic filling into multilayer carton or PET bottles follows the ISO 22000:2018 food safety management framework, with the flavoring preparation certified against EU 1334/2008 and monitored for residual solvent limits per Commission Directive 2009/32/EC where applicable to the extraction or synthesis route used in the thiazole’s manufacture. Terminal product categories include ambient-stable café latte cartons, canned cold-brew coffee concentrates (typically dosed at a dilution factor), and plant-based oat-milk coffee beverages where the thiazole’s nutty nuance reduces dependence on added nut-derived flavoring top-notes that carry allergen cross-contact risks in shared-facility co-packing arrangements.

    Thermal process flavor generation—the controlled reaction of reducing sugars, amino acid sources, and thiamine under defined time-temperature-water activity regimes—produces complex meaty reaction bases into which 4-Methyl-5-Beta-Hydroxyethyl Thiazole is introduced as a late-stage spiking component rather than a through-process reactant. The thiazole is not charged into the reactor during the heating phase, as available published kinetic data from model system studies indicate that the 4-methyl substitution on the thiazole ring does not undergo further Maillard-type rearrangement under typical reaction flavor conditions (pH 5.0–6.5, 100–130°C, 1–4 hours); instead, it remains spectroscopically stable and contributes to the headspace profile of the reaction mass only if it survives the subsequent vacuum dehydration step that strips water and volatiles at 60–80 mbar absolute pressure. Production protocols on 500–2000 L reactor skids specify post-reaction cooling of the process flavor slurry to ≤42°C before addition of the thiazole and other top-note volatiles via a locked, nitrogen-purged addition vessel; the reactor agitator then runs at reduced speed (25–35 rpm) for a 20-minute incorporation cycle before the finished reaction flavor is transferred to intermediate storage tanks under nitrogen blanket. The compliance framework for reaction flavors containing this thiazole falls under the International Organization of the Flavor Industry (IOFI) Guidelines for the Production and Labelling of Process Flavourings (revised 2022) and EU EC 1334/2008 Article 9, which distinguishes process flavourings from chemically defined flavouring substances and mandates specific labelling that attests to the thermal reaction preparation methodology. Finished goods incorporating thiazole-spiked reaction bases include spray-dried savory flavor powders for instant soup noodle sachets (water activity < 0.30 post-drying), paste-form meat flavor concentrates for bouillon and gravy manufacturing, and liquid smoke-process flavor hybrids where the thiazole bridges the phenolic-smoky character from hardwood pyrolysates and the savory-meaty base note in barbecue sauce concentrates destined for industrial foodservice marinade reconstitution at 1:8 to 1:12 dilution ratios.

    Table 2 — Global Regulatory Status Matrix for 4-Methyl-5-Beta-Hydroxyethyl Thiazole (FEMA 3200, CAS 137-00-8) by Jurisdiction and Application Category
    JurisdictionRegulatory InstrumentFlavoring StatusPermitted Application ScopeDocumentary Requirement for Import Clearance
    United StatesFDA 21 CFR 172.515; FEMA GRAS 3200Synthetic flavoring substance, GRASAll non-alcoholic (<0.5% ABV) and non-meat FDA-regulated foodsCertificate of Analysis (CoA), FEMA GRAS letter, lot-specific specification sheet
    European UnionEU Reg. 1334/2008, FL No. 15.034Permitted flavouring substance, chemically definedAll food categories except those with explicit exclusion in Annex IIIEU Flavourings Database listing evidence, CoA per JECFA specifications
    JapanJapan Food Sanitation Law, MHLW Ordinance No. 37 (1959)Designated additive (thiazole derivative listing)General food use excluding unprocessed meat/fishCertificate of Free Sale, CoA, manufacturing process flow description
    ChinaGB 2760-2024 (updated National Food Safety Standard for Uses of Food Additives)Permitted synthetic food flavoringFood flavoring formulations for categories specified in GB 2760 Table B.3CoA, origin certificate, non-GMO declaration, GB conformity attestation
    Southeast Asia (ASEAN)ASEAN Harmonized Food Additive Standards, referencing JECFA specificationsFlavoring agent per Codex GuidelinesGeneral food categories at GMP levelsCoA, Halal certification (MUI/JAKIM/CICOT as applicable), allergen statement
    Brazil (MERCOSUR)ANVISA RDC No. 2/2007; MERCOSUR/GMC/RES. 10/06Approved flavoring substanceFood flavoring per specified positive listCoA with ANVISA-compliant specification format, Portuguese-translated label draft

    Does the Thiazole-Copper Chelation in Low-pH Condiments Suppress Metallic Off-Notes in Retained Headspace?

    Culinary sauce and condiment formulations with pH values below 4.0—such as vinegar-based barbecue mop sauces, Worcestershire-style fermented condiments, and hot-fill tomato ketchup with vinegar content exceeding 12% of the formula—frequently express metallic or tinny off-flavors that originate from trace transition metal ions leached from processing equipment, tomato paste can linings, or the vinegar production chain itself. The sulfur and nitrogen donor atoms in the thiazole heterocycle exhibit measurable complexation affinity for divalent copper and iron cations in aqueous-acetic media, and addition of 4-Methyl-5-Beta-Hydroxyethyl Thiazole at concentrations as low as 2–5 ppm has been correlated—through inductively coupled plasma mass spectrometry (ICP-MS) measurement of free vs. bound copper in model ketchup matrices—with a reduction of sensorially active free cupric ion by approximately 60–70% relative to an unspiked control, as published data in food chemistry literature on thiazole-metal interactions indicates. Simultaneously, the thiazole contributes a roasted, savory backbone that complements the tamarind, molasses, and smoked paprika notes typical in premium regional barbecue sauce formulations without introducing an unrelated aromatic note that would violate the established flavor identity standard. The addition point in hot-fill-hold condiment manufacturing lines (sauces filled at 82–88°C into glass or PET bottles, inverted to sterilize the closure, and held for 2–3 minutes) is post-pasteurization but pre-fill: the thiazole is metered into the surge tank via a metering pump from a concentrated stock solution in propylene glycol (5% w/w) at a rate that achieves the target 2–5 ppm final concentration, with the surge tank’s low-shear axial-flow agitation running at 60 rpm to disperse the flavor uniformly within the 8–12 minute residence time before the filler bowl. Manufacturing records from co-packing facilities document that omission of the thiazole from recipes relying on high-iron molasses or dark brown sugar (iron content typically 30–50 ppm on a dry basis) results in consumer complaint rates regarding “metallic aftertaste” that are 2.5× higher than matched batches containing the thiazole spiking protocol, as tracked over 12-month rolling production periods. Finished products in this application cluster include hickory-smoke-flavored table sauces, balsamic-glace finishing sauces for foodservice grilled protein menu items, and shelf-stable chutney variants with tamarind and date pastes where the thiazole bridges the sweet-sour-fruit spectrum and the savory roasted dimension expected in chutney applications paired with grilled lamb or chicken under Indian, Middle Eastern, and fusion culinary profiles.

    Free Quote

    Competitive 4-Methyl-5-Beta-Hydroxyethyl Thiazole prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615651039172 or mail to sales9@bouling-chem.com.

    We will respond to you as soon as possible.

    Tel: +8615651039172

    Email: sales9@bouling-chem.com

    Get Free Quote of Bouling Chemical Co., Limited

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction
    4-Methyl-5-(β-hydroxyethyl)thiazole (CAS 137-00-8, FEMA 3204, CoE 11621) is a heterocyclic thiazole derivative characterized by a thiazole ring substituted with a methyl group at the 4-position and a 2-hydroxyethyl sidechain at the 5-position. This compound occurs naturally in roasted coffee, cooked beef, yeast extracts, and passion fruit, where it contributes the characteristic sulfury, meaty, and slightly nutty odor profiles. Industrially produced via condensation of thioformamide with 3-bromo-4-hydroxy-2-butanone or by cyclization of α-haloketones with thioamides, the commercial product is supplied as a pale yellow to amber liquid with a purity exceeding 98.0% by GC (ASTM E202). Its molecular weight is 143.21 g/mol, and the refractive index nD20 falls between 1.5480 and 1.5520. The presence of the primary alcohol functionality distinguishes it from purely alkyl- or vinyl-substituted thiazoles, enabling derivatization strategies and modifying its partition behavior in multiphase food and fragrance systems.

    How Do Isomeric and Homologous Thiazoles Differ in Sensory Impact?

    Structural comparison with 4-methyl-5-vinylthiazole (CAS 1759-28-0), 2-acetylthiazole (CAS 24295-03-2), and 2-isobutylthiazole (CAS 18640-74-9) reveals a direct relationship between substitution pattern, vapor pressure, and organoleptic threshold. The β-hydroxyethyl sidechain in 4-methyl-5-(β-hydroxyethyl)thiazole raises the boiling point to approximately 270 °C at 101.3 kPa and lowers the vapor pressure compared to 4-methyl-5-vinylthiazole, which lacks the hydroxyl moiety. This reduction in headspace partitioning translates to orthonasal detection thresholds in water of 0.02 µg/L (ASTM E679, 3-AFC protocol), whereas 2-isobutylthiazole exhibits a reported threshold near 0.005 µg/L and 2-acetylthiazole approximately 10 µg/L. The relatively moderate potency of the hydroxyethyl derivative allows broader dosing latitude: in meat flavor formulations, effective use levels range from 0.5 ppm to 5 ppm in ready-to-consume products, while the more aggressive isobutyl analog must be titrated below 0.05 ppm to prevent overt dominance. Furthermore, the alcohol group can be esterified with acetic or butyric acid to create flavor precursors that survive high-temperature processing and hydrolyze on mastication—a controlled-release option not available with 2-acetylthiazole or 2-isobutylthiazole. Oxidation at the thiazole sulfur yields sulfoxide and sulfone byproducts detectable by LC-MS at addition levels as low as 0.1% of the parent compound; these catabolites carry a soapy, metallic character absent in the non-hydroxylated analogs due to altered electron density on the heterocycle.

    Specifications and Analytical Reference Standards

    Batch-to-batch consistency is verified against a panel of physical and chromatographic criteria. The following table summarizes the typical certificate-of-analysis parameters for food-grade (≥ 98.0%) and fragrance-grade (≥ 97.0%) materials:
    ParameterMethodSpecification Range
    AppearanceVisual (ISO 2211)Pale yellow to amber clear liquid
    OdorIFRA GMP organoleptic panelMeaty, sulfury, nutty, coffee-like
    Purity (GC area%)ASTM E20297.0–99.5%
    Single largest impurityASTM E202≤ 1.5%
    Refractive index nD20ISO 280:19981.5480–1.5520
    Relative density d2020ISO 279:19981.196–1.210
    Flash point (Pensky-Martens closed cup)ASTM D93>100 °C
    Acid valueISO 660≤ 1.0 mg KOH/g
    Water content (Karl Fischer)ISO 760≤ 0.5%
    Commercial lots occasionally contain trace 4-methyl-5-vinylthiazole (0.3–0.7%) formed by dehydration during distillation; this impurity is quantified by a dedicated HPLC-DAD method employing a C18 column and detection at 254 nm. Storage under nitrogen at 5–15 °C minimizes further degradation. The compound is listed as Generally Recognized as Safe (GRAS) by FEMA (3204) and evaluated by JECFA under specification monograph 1032 with an ADI of 0–0.1 mg/kg bw. In compounded flavor formulations, 4-methyl-5-(β-hydroxyethyl)thiazole serves as a building block for roasted, boiled, and grilled meat profiles, often blended with furaneol, 2-methyl-3-furanthiol, and methional. A high-impact beef flavor concentrate typically contains the thiazole at 0.05–0.5% (w/w), which corresponds to 2–20 ppm in a finished broth after dilution. Solubility in ethanol (≥ 96%) exceeds 10% w/w; in propylene glycol, miscibility surpasses 50%. For dry beverage premixes, the liquid is plated onto silicon dioxide carriers such as SIPERNAT® 22S at a loading of 5–10% before ribbon blending. Storage at relative humidity above 60% induces particle agglomeration unless the powder is over-coated with tricalcium phosphate (E341(iii)) at 1–2% of the total weight. In soup bouillon cubes, where the matrix contains 30–50% salt and monosodium glutamate, the thiazole must be pre-emulsified in partially hydrogenated palm oil to prevent localized concentration pockets that can cause off-notes detectable at 1 ppm in the reconstituted broth.

    When Formulating Processed Meat Flavors, the β-Hydroxyethyl Moiety Mitigates Sulfur Volatility

    Subjecting a meat slurry containing 0.2% 4-methyl-5-(β-hydroxyethyl)thiazole to high-temperature short-time (HTST) extrusion in a twin-screw cooker-extruder (screw diameter 45 mm, L/D 20:1, barrel temperature 130–145 °C) results in 12–18% lower headspace concentration of the parent thiazole compared to the vinyl analog when measured by SPME-GC-MS on a Carboxen/PDMS fiber. The hydroxy group participates in Maillard-type condensation with available reducing sugars in the meat matrix, forming glycosidically bound precursors that survive the thermal regime and release the active volatile under oral conditions. This property is exploited in retort-stable canned pet food: after retorting at 121 °C for an Fo of 6 min, the sensory panel detects a meaty, roasted character that persists through 12 months of ambient storage, whereas the vinyl-substituted comparator exhibits a significant drop in perceived intensity within 3 months. Nonetheless, the system exhibits a critical processing window: when the moisture content of the meat dough falls below 25% before extrusion, the Maillard coupling efficiency drops, and free hydroxyethyl thiazole volatilizes at the die, reducing retention to 60–70%. Additionally, exposure of the compound to lipid fractions with peroxide values above 10 meq/kg accelerates sulfur oxidation; the resulting sulfoxide and sulfone are detectable as a soapy-metallic off-flavor at 0.5 ppm. Encapsulation via spray chilling with hydrogenated palm stearin (melting point 58–60 °C, atomization air temperature 5 °C) improves stability, maintaining active content above 95% after 6 months at 25 °C. In functional perfumery, 4-methyl-5-(β-hydroxyethyl)thiazole contributes to coffee absolute reconstructions, cocoa accords, and roasted nut fantasies at concentrations between 0.01% and 0.5% in the fragrance compound. Evaporation profiling on a cotton blotter at 21 °C and 65% RH indicates residual headspace intensity of 30–40% after 6 hours relative to the initial measurement, classifying the material as of intermediate substantivity. Water solubility of approximately 1.2 g/L at 20 °C limits longevity in hydroalcoholic fine fragrance mists unless solubilized with polysorbate 20 at a ratio of at least 5:1 (surfactant:thiazole). Direct combination with aldehydes such as decanal or lilial leads to Schiff base condensation, confirmed by 1H NMR monitoring of the aldehyde proton signal at δ 9.7 ppm; this reaction alters the olfactive character within 48 hours at ambient temperature and necessitates compartmentalized delivery or microencapsulation. In anionic surfactant systems—sodium laureth sulfate at 10–12% active—the odor profile shifts toward a rubbery, phenolic facet, a behavior attributed to micelle-induced changes in the compound’s microenvironment. Adjustment of the shampoo base pH to 5.5–6.0 and pre-blending with decyl glucoside (1:1 weight ratio) restores the target meaty-nutty tonality. Published data comparing performance in high-pH media (pH > 9) indicate rapid decomposition via ring-opening hydrolysis; therefore, incorporation into soap bars prepared from caustic saponification is not recommended unless the fragrance is added post-saponification at temperatures below 40 °C. The contrast with 4-methyl-5-vinylthiazole extends to regulatory and sensory benchmarking. FEMA GRAS listing for the vinyl derivative (FEMA 3313) specifies different flavor category use levels, capping at approximately 1 ppm in non-alcoholic beverages due to its sharper, more pyrazine-like top note, whereas the hydroxyethyl variant holds a wider organoleptic tolerance and is frequently deployed at levels up to 10 ppm in such applications. Stability screening in model beverage syrups (pH 2.8, 10% sucrose, 0.15% citric acid) stored under accelerated conditions at 40 °C for 4 weeks shows degradation of the hydroxyethyl compound below 5% of initial content, while the vinyl analog loses 15–20% under identical exposure. These divergent performance profiles underscore the need for formulators to select between the two based not merely on cost but on the target delivery matrix, thermal process intensity, and the presence of reactive co-ingredients.