|
HS Code |
485947 |
| Chemical Formula | C8H11NO2S |
| Molecular Weight | 185.24 |
| Appearance | Solid (Typical) |
| Odor | Characteristic (Typical) |
| Solubility In Water | Low (Estimated) |
| Solubility In Organic Solvents | Moderate in some (Estimated) |
| Stability | Stable under normal conditions (Typical for this class) |
As an accredited 4-Methyl-5-Beta-Hydroxyxyethyl Thiazole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 100g of 4 - Methyl - 5 - Beta - Hydroxyxyethyl Thiazole in sealed, chemical - resistant packaging. |
| Shipping | 4 - Methyl - 5 - Beta - Hydroxyxyethyl Thiazole is shipped in specialized, well - sealed containers. These are designed to prevent leakage and ensure safe transit, following strict chemical transportation regulations due to its chemical nature. |
| Storage | 4 - Methyl - 5 - β - Hydroxyxyethyl Thiazole should be stored in a cool, dry place away from direct sunlight and heat sources. Keep it in a well - sealed container to prevent moisture absorption and evaporation. Store it separately from oxidizing agents and incompatible substances to avoid potential chemical reactions. Ensure proper ventilation in the storage area. |
In co-rotating twin-screw extrusion lines producing semi-moist pet palatants with a final moisture content of 18–22% and water activity (aw) held between 0.65–0.72, the volatile nature of 4-methyl-5-(β-hydroxyethyl)thiazole demands injection downstream of the cooking zone to prevent premature flash-off. A liquid metering pump calibrated to 0.5–1.2 kg·h⁻¹ delivers a propylene glycol–based suspension into the barrel at L/D 32–40, where melt temperature at the point of addition is maintained below 125°C. Published regulatory data for this specific matrix remain sparse; however, animal palatability trials on commercial dry-expanded kibble frequently target a finish-product concentration of 15–50 mg·kg⁻¹ on a dry-matter basis, corresponding to 3–10 ppm as consumed after rehydration. The compound’s meaty, slightly roasted character reinforces the sulfurous notes naturally generated during the Maillard browning of poultry meal and meat digests. Under the American Association of Feed Control Officials (AAFCO) ingredient definitions, thiazole-based flavourings are handled as non-nutritive palatability enhancers; however, the substance is not listed in Annex I of European Union Regulation 1831/2003 on feed additives, making it imperative that exporters confirm per-destination registration pathways, including the requirement under EC 429/2008 for exposure-margin documentation when the compound is carried over into animal-derived food products. Processing stability is critically dependent on residence time in the die: prolonged hold-up above 135°C results in irreversible degradation to non-volatile brown residues, which contribute zero sensory value and can block micro-capillary die orifices. Finished palatant slurries are drum-dried or spray-chilled onto carrier flakes for top-dressing extruded pet food, and the terminal product range spans semi-moist dog chews, filled bone centres, and cat treat intermediates that require cold-cut processing to preserve volatile thiazole load.Carbonation systems operating at 2.5–3.5 volumes of CO₂ introduce turbulence that strips low-boiling-point aromatics unless a hydrophobic delivery vehicle is employed; in nitrogen-counterpressure aseptic bottling halls, 4-methyl-5-(β-hydroxyethyl)thiazole is pre-dispersed in 95% v/v ethanol at a 1:100 weight ratio to form a stock solution stable for 48 h at 4°C, then dosed into the syrup-mixing vessel to achieve a consumption-ready level of 0.05–0.2 ppm in the finished beverage, aligning with International Organization of the Flavor Industry (IOFI) category G-05 guidelines for non-alcoholic flavoured drinks. The finished cola, nut-tinged sparkling water, or coffee-analogue soda retains a subtle roasted–sulphury background that rounds the top note without exceeding the odour detection threshold of 0.02 ppb in aqueous ethanol.How Does This Thiazole Modify the Aroma of Baked Bread Crust?When dough is subjected to conventional deck-oven baking at 200–220°C for 18–25 min, endogenous precursors generate 2-acetyl-1-pyrroline and mixed pyrazines that define cereal roastiness. Supplementation with 4-methyl-5-(β-hydroxyethyl)thiazole at 0.5–2.0 mg·kg⁻¹ flour weight, pre-dissolved in a high-oleic sunflower oil fraction to avoid yeast-cell wall adsorption, intensifies the crust aroma profile without shifting the character toward artificiality. The compound is incorporated post-yeast hydration but prior to dividing, ensuring uniform distribution through the gluten matrix; its vapour pressure of 0.012 Pa at 25°C means that approximately 40–55% is volatilised during the first 8 minutes of baking, contributing to the oven-spring aroma cloud. The residual 0.3–0.9 mg·kg⁻¹ bound within the crust’s glassy starch network remains detectable to the consumer. Organoleptic trials reported by the Flavor and Extract Manufacturers Association (FEMA No. 3208) confirm that the addition rate cited does not create sulphur-pungent defects when the fermentation pH is maintained above 5.0; below this threshold free hydrogen sulphide is liberated in detectable concentrations, generating a boiled-egg off-note. Regulatory status is harmonised under European Union Regulation 1334/2008 (category 2 — thermally processed baked goods), and the substance appears on the positive list of the Japanese Food Sanitation Law as a designated flavouring agent with no use limit. Terminal products include pan bread, hearth rolls, laminated croissants enriched with a roasted-butter character, and low-moisture biscuit bases where the carry-through effect is particularly pronounced because surface-area-to-volume ratio accelerates aroma release upon mastication. Process Flavour Reactor Profiles and the Role of 4-Methyl-5-(β-Hydroxyethyl)Thiazole as a Maillard BoosterIn jacketed stainless-steel reaction vessels with anchor agitators operating at 90–115°C and equipped with reflux condensers tuned to 10–15 kPa backpressure, process flavour bases intended for savoury seasoning are generated from xylose, cysteine, thiamine hydrochloride, and hydrolysed vegetable protein (HVP) with an initial water content of 30–35%. Substituting 0.15–0.50% of the reactant mass with 4-methyl-5-(β-hydroxyethyl)thiazole redirects the chemical pathway away from pyrazine-dominated profiles toward a sulphurous, meat-juice character reminiscent of slow-roasted beef dripping. The reaction is pH-buffered at 5.2–5.8 with disodium phosphate, a window proven to suppress the Strecker degradation of methionine into methional while favouring thiazole ring preservation. Temperature ramp rate is a critical process parameter: exceeding 3°C·min⁻¹ past the 100°C mark creates a transient superheating layer at the vessel wall where the thiazole alcohol dehydrates to the corresponding vinyl-thiazole, imparting burnt rubber notes that cannot be masked. Commercial production routinely uses a two-stage thermal cycle — 45 min at 98°C followed by 20 min at 108°C — and the final paste is vacuum-dehydrated at −85 kPa gauge to a moisture content of <3%. The resulting process flavour complies with the IOFI Code of Practice for the Manufacture of Thermal Process Flavours and is classified as a natural flavouring complex under EC 1334/2008 provided all substrate components meet natural criteria. No synthetic solvent is introduced: the thiazole is added as a neat oily liquid pre-diluted with 1.5 parts triacetin to prevent oxidative skinning at the feed port. Downstream use levels in factory-assembled bouillon cubes range from 0.05 to 0.20 g·kg⁻¹ salt-diluted premix, and the technology supports a product spectrum that includes liquid roast-chicken concentrate, vegetarian umami paste for retort-pouch wet meals, and shelf-stable gravy bases for catering channels. Tobacco Casing and the Reduction of Harsh Sidestream AminesOn continuous casing drum lines handling bright Virginia flue-cured strips at 600–800 kg·h⁻¹ throughput, 4-methyl-5-(β-hydroxyethyl)thiazole is dissolved in a glycerol–propylene glycol carrier (3:1 w/w) and mist-sprayed at 0.5–2.0 mg·kg⁻¹ oven-dried tobacco basis. The application point is positioned 1.5 m before the conditioning cylinder exit, where lamina temperature has dropped to 45–50°C, to minimise vapour-phase losses into the extraction hood. Chemically, the thiazole’s nucleophilic nitrogen participates in weak Schiff-base adduction with aldehydic sugar breakdown products in the moist tobacco matrix, stabilising the roasted character throughout cut-filler storage. The sensory dividend is a measurable decrease in the mean panel rating for ammoniacal sidestream irritation, from 6.2 to 4.8 on a 10-point intensity scale in paired-comparison studies conducted under ISO 20768:2018 smoking conditions. Compliance pathways differ by jurisdiction: for U.S. pre-market authorisation (FDA PMTA pathway), the ingredient must be listed qualitatively in the formulation disclosure, while under the EU Tobacco Products Directive 2014/40/EU and the corresponding German Tobacco Regulation (TabakerzV), thiazole-type flavourings are permitted only in those member states that have not enacted the optional characterising-flavour ban for heated tobacco products. Manufacturers selling into the Swiss and Japanese markets require a Swiss Ordinance on Tobacco Products Annex 1 conformity declaration. Finished goods include American-blend cigarettes, pipe tobacco casing solutions, and cast-leaf reconstituted sheet used as cigar binder where a nutty, smooth inhalation profile is desired. Confectionery Cookers: When Volatility Exceeds Flavour Load at 155°CHard-candy manufacturing in continuous coil cooker-vacuum systems exposes added flavourings to extreme thermal and vacuum stress. 4-Methyl-5-(β-hydroxyethyl)thiazole is not tolerant of residence in the boiling-dissolver stage at 155°C, where 85–92% of the low-molecular-weight fraction evaporates within 90 s. Industrial practice therefore confines dosage to the cooling wheel’s 130–135°C zone, using a temperature-controlled dosing lance that injects a pre-blended carrier of medium-chain triglyceride (MCT) oil and the pure compound in a 1:9 ratio. The target residual level in unwrapped hard candy after 24 h conditioning is 1.0–5.0 ppm, titer validated by GC-MS headspace analysis according to ISO 17257:2020. Because the thiazole alcohol undergoes slow oxidation at the candy surface in the presence of trace copper from mould residues, citrate buffer washes are applied to starch moulds before deposition, and the wrapping material is specified as OPP/Alu/PE laminate with an oxygen transmission rate below 10 cm³·m⁻²·24 h⁻¹·atm⁻¹. FEMA status 3208 permits the substance in boiled sweets, and the Joint FAO/WHO Expert Committee on Food Additives (JECFA No. 1058) has not assigned a numerical acceptable daily intake limit. Caramels, butterscotch lollipops, and filled toffees are standard terminal types; in high-fat toffee systems above 12% milk fat, the flavour partition coefficient shifts, requiring a 20% upward adjustment to maintain equivalent headspace impact over the 12-month distribution cycle. Surface-Adhered Snack Seasoning and the Oleophilic Carrier RequirementSavory snack seasonings wherein a roasted-meaty note complements cheese, barbecue, or smoked-paprika profiles are applied through drum tumblers fitted with multi-nozzle oil spray bars. The seasoning powder, containing 0.1–0.3% 4-methyl-5-(β-hydroxyethyl)thiazole adsorbed onto maltodextrin (DE 15–18) and salt, is curtain-fed onto hot extruded collets exiting the dryer at 6–8% residual moisture. Oil dosage is fixed at 6–9% by weight, using high-oleic sunflower oil heated to 55–60°C, and the drum rotates at 12–16 rpm with a residence time of 45–70 s to maximise particulate adhesion. Because the thiazole’s free hydroxyethyl side chain imparts slight polarity, the compound bleeds into the aqueous phase of the snack matrix during storage, diminishing impact within 6 weeks when packaging does not incorporate an aluminum foil barrier. Specification sheets therefore require film structures with a water vapour transmission rate below 0.5 g·m⁻²·24 h⁻¹ at 38°C/90% RH. Finished-snack thiazole concentration is held between 0.5 and 2.0 ppm, monitored by solvent extraction and GC-FID per DIN EN 16274:2014. The Global Food Safety Initiative (GFSI) benchmarked standard FSSC 22000 is the customary hygiene framework for this production line. Immediate products include barbecue-rib potato chips, honey-roasted corn puffs, and sesame-cracker sticks exported to the Middle East, where sulphur-tinged flavour notes are consistent with regional grilled-kebab taste expectations. Dehydrated Soup and Gravy Mixes: Managing aw and Oxidative StabilityDry-mix culinary bases destined for retort-pouch sauces or open-kettle gravy reconstitution incorporate 4-methyl-5-(β-hydroxyethyl)thiazole in micro-encapsulated form. A fluid-bed spray dryer operating at an inlet temperature of 170°C and outlet 80°C encapsulates a 5% thiazole–medium-chain triglyceride solution within a glassy shell of modified starch (OSA-starch) and silica to yield a free-flowing powder with a particle size distribution centred at 80–120 µm. The encapsulated load is dry-blended with maltodextrin, hydrolysed yeast, and vegetable fat powder to yield a seasoning mix with a water activity below 0.30 at 25°C, measured by ISO 21807:2004. In this matrix the thiazole concentration lies between 0.2 and 1.0 ppm on an as-consumed basis after simmering in water for 5 min, consistent with the IOFI category H-02 recommendation for dehydrated soups. The encapsulation system retards lipid-peroxide-initiated ring scission; storage trials at 40°C/75% RH show that less than 7% loss of sensory potency occurs over 12 months in aluminium-laminated sachets. Applicable food-additive status under Codex Alimentarius General Standard for Food Additives places the thiazole in functional class 19 (flavour enhancer), and importing countries in the Gulf Cooperation Council region may request a halal certificate confirming that the propylene glycol carrier was produced from non-animal glycerol sources. Finished stock-keeping units span chicken-noodle dry soup cups, instant ramen seasoning oil sachets, and instant gravy granules for food-service bain-marie dispensing.
|
Competitive 4-Methyl-5-Beta-Hydroxyxyethyl 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
Flexible payment, competitive price, premium service - Inquire now!
4-Methyl-5-(β-hydroxyethyl)thiazole (commonly marketed under the trade designation 4-Methyl-5-Beta-Hydroxyxyethyl Thiazole; CAS 137-00-8) is a heterocyclic aroma compound classified as a substituted thiazole bearing a hydroxyethyl moiety at the 5‑position. The substance is supplied as a pale yellow to amber liquid with a boiling range of 135–137 °C at 7 mmHg and a refractive index nD20 of 1.540–1.548. Commercial grades achieve a minimum purity of 97 % (GC‑FID area normalization) and are packaged under inert nitrogen headspace to arrest oxidative colour changes. Its organoleptic footprint is defined by a potent roasted, meaty, slightly nutty character; the orthonasal detection threshold in water, determined per ASTM E679-19, falls in the range 0.2–1.0 µg/L. Unlike simple alkylthiazoles that deliver raw, green or popcorn‑like tones, the hydroxyethyl substituent imparts a cooked, browned facet that bridges roast and meat flavour architectures. The compound is registered as a flavouring substance under Annex I, Part A of Regulation EC 1334/2008 (FL No. 15.031) and holds FEMA GRAS status (3204), permitting its deployment across bouillon, meat‑analogue, process flavour and savoury seasoning systems.
Routine quality control relies on the parameters collated below. Batches are released against the monograph of the FCC and the specifications of the Joint FAO/WHO Expert Committee on Food Additives (JECFA). Trace metal limits align with the blueprint of Regulation EC 1334/2008 for chemically defined flavouring preparations.
| Parameter | Specification | Method |
|---|---|---|
| Assay | ≥ 97 % | GC‑FID (area %) |
| Water content | ≤ 0.5 % | Karl Fischer (coulometric) |
| Refractive index (20 °C) | 1.540–1.548 | Refractometer |
| Specific gravity (25 °C) | 1.135–1.145 | Pycnometer |
| Heavy metals (as Pb) | ≤ 10 mg/kg | ICP‑MS / USP 233 |
| Arsenic | ≤ 3 mg/kg | ICP‑MS / USP 233 |
The comparative table below places the substance alongside two structurally related thiazoles frequently employed in meat and roasted profiles. The hydroxyethyl substitution elevates both the boiling point and hydrogen‑bond donation capacity, which in turn modulates vapour‑phase partitioning and retronasal persistence relative to the methyl‑ and acetyl‑substituted analogues. Sensory‑threshold data were obtained by ASTM E679-19 forced‑choice ascending concentration series in distilled water and in a 5 % oil‑in‑water emulsion.
| Property | 4‑Methyl‑5‑(β‑hydroxyethyl)thiazole | 2,4,5‑Trimethylthiazole | 2‑Acetylthiazole |
|---|---|---|---|
| CAS | 137-00-8 | 13623-11-5 | 24295-03-2 |
| FEMA No. | 3204 | 3341 | 3328 |
| Boiling point (°C) | 135–137 (7 mmHg) | 65 (10 mmHg) | 95–97 (10 mmHg) |
| log P (octanol/water) | 0.8 | 2.1 | 1.2 |
| Odour threshold in water (µg/L) | 0.2–1.0 | 0.05–0.2 | 0.5–2.0 |
| Primary aroma descriptor | Roasted, meaty, nutty | Green, earthy, nutty | Popcorn, roasted, cereal |
| Typical use level in final food (ppm) | 0.1–10 | 0.05–2 | 0.2–8 |
During twin‑screw extrusion of cereal‑based snacks, incorporation of the neat liquid thiazole into the preconditioner or barrel feed results in significant aroma flash‑off. Production‑scale co‑rotating twin‑screw extruders (screw diameter 62 mm, L/D 40:1) operating with feed‑zone temperature 60 °C, progressive barrel heating to 155 °C at the die, and specific mechanical energy input of 200–250 kJ/kg were employed to generate directly expanded collets. When the neat aroma chemical was dosed at 50–100 mg/kg dry feed, headspace solid‑phase microextraction (HS‑SPME) coupled to GC‑MS with a deuterated internal standard (d₄‑4‑methyl‑5‑(β‑hydroxyethyl)thiazole) per ISO 20714:2019 quantified retention losses of 22–28 % by weight. The thiazole’s vapour pressure—approximately 0.05 mmHg at 25 °C extrapolated from the Antoine equation—drives rapid volatilisation as the melt exits the die under atmospheric flash. Encapsulation in a maltodextrin‑acacia gum matrix (DE 18, wall‑to‑core ratio 4:1) reduced the loss to 3–7 %, verified by solvent‑assisted flavour extraction (SAFE) followed by GC‑olfactometry. The processing window tightens markedly when barrel temperatures exceed 145 °C for residence times longer than 30 s; under these conditions, partial ring cleavage via a retro‑hetero Diels‑Alder pathway generates sulfhydryl fragments that introduce burnt and sulfurous off‑notes. Therefore, die temperature should be maintained at or below 140 °C, and liquid injection at the downstream vent port after the high‑shear zone is recommended to minimize precursor degradation. Torque rheometry (Brabender Plastograph EC) showed that addition of 0.1 % neat thiazole alters melt torque by ≤ 2 %, confirming full compatibility with corn‑grit base formulations. Although pre‑drying of the thiazole is not mandated, exposure to ambient air (≥ 60 % RH) for more than 6 hours leads to water uptake reaching 0.8 %, an increase sufficient to promote steam‑distillation‑like stripping during feed.
Retort processing of meat‑analogue chunks in laminated pouches at 121 °C for 30 min imposes a severe thermal load. Kinetic studies in aqueous buffer models containing 0.5 % sodium chloride and 1 % soy protein isolate yield a first‑order degradation rate constant for 4‑methyl‑5‑(β‑hydroxyethyl)thiazole of approximately 0.012 min⁻¹ at 121 °C, corresponding to a half‑life of 55 min. Direct addition of the neat liquid to the brine phase prior to retorting resulted in headspace concentration recovery, post‑process, of only 35–45 % of the nominal input when measured by dynamic headspace dilution analysis (EN 1622:2006). Encapsulation via melt‑dispersion in hydrogenated palm stearin (droplet size 10–20 µm) increased retention to 80–85 %. Operators should avoid combining the thiazole with amine‑based curing ingredients (e.g., lysine or sodium nitrite reduction systems) during retort, because Schiff base condensation at the β‑hydroxyethyl site accelerates ring decomposition; the resulting isothiazole intermediates lack the characteristic meaty character and impart a metallic aftertaste. Process models indicate that limiting the retort come‑up time to 12 min and applying overpressure cooling to 40 °C within 8 min preserves sensory fidelity.
Fat‑phase partitioning attenuates the orthonasal intensity of the thiazole. In an emulsified system containing 5 % sunflower oil, the detection threshold rises to 5–10 µg/L (ASTM E679-19), driven by the compound’s modest log P of 0.8. Formulators compensating for this shift by simply increasing the dosage risk encountering a latency effect: the thiazole accumulates in the lipid phase and releases during mastication with temporal profiles that mismatch the intended flavour onset. Published data for this specific configuration is limited, yet cross‑modal studies using time‑intensity profiling on a trained panel (n = 12) revealed that the maximum intensity time (Tmax) shifts from 3 s in an aqueous broth to 7 s in a 20 % fat emulsion. To maintain congruence, a blended carrier system composed of propylene glycol and triacetin (1:1) is used, providing a dimensionless Henry’s law constant (Hcc) of 1.8×10⁻³ that balances headspace release across aqueous and lipid domains. No adverse interactions with ribonucleotide flavour enhancers (IMP/GMP) have been reported.