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HS Code |
731172 |
| Chemical Formula | C7H11NS |
| Molecular Weight | 141.23 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Odor | Nutty, earthy, and somewhat sulfurous odor |
| Boiling Point | 170 - 171 °C |
| Density | 0.987 g/cm³ at 25 °C |
| Solubility In Water | Insoluble |
| Solubility In Organic Solvents | Soluble in common organic solvents like ethanol, ether |
| Flash Point | 55 °C |
As an accredited 2-Isobutyl Thiazole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 100g of 2 - Isobutyl Thiazole packaged in a sealed, labeled chemical - grade bottle. |
| Shipping | 2 - Isobutyl Thiazole, a chemical, is shipped in carefully sealed containers. Packaging adheres to safety regulations. Shipment is via approved carriers, ensuring proper handling and protection during transit to prevent any leakage or damage. |
| Storage | 2 - Isobutyl Thiazole should be stored in a cool, well - ventilated area away from heat, sparks, and open flames. Keep it in a tightly sealed container to prevent leakage and exposure to air and moisture. Store it separately from oxidizing agents and incompatible substances. This helps maintain its chemical integrity and reduces the risk of hazardous reactions. |
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When low-acid tomato paste is recombined and thermally processed in a continuous tubular steriliser at 121 °C for an F₀ value of 8–12 min, the native cis-4-heptenal and 3-(methylthio)propanal fractions degrade rapidly, leaving a flat cooked-pulp character. In such systems, 2-isobutylthiazole is introduced not as a top-note scaffold but as a fidelity-restoration tool targeting the specific aroma gap created by Strecker aldehyde loss. The molecule’s vapour pressure of approximately 0.15 mmHg at 25 °C and its log P of 2.89 dictate that it partitions preferentially into the headspace of agitated tanks unless a dispersed oil-in-water emulsion carrier is used. Production lines running 8,000 L batch kettles with bottom-sweep agitation at 35 rpm achieve homogenous distribution only when the compound is pre-blended into a 5% w/w sunflower oil cut that is injected post-pasteurisation via a GEA Hilge positive-displacement pump into the recirculation loop. Compliance is verified against 21 CFR 172.515 (synthetic flavouring substances) and the Union List of flavourings under Regulation (EC) 1334/2008, where 2-isobutylthiazole is coded FL 14.014. The Joint FAO/WHO Expert Committee on Food Additives (JECFA) assessment No. 1315 indicates an ADI of “not specified,” confirming no safety concern at intended levels. For standard 28–30 °Brix ketchup and 12–14 °Brix tomato soup bases, the recommended addition rate spans 2–8 ppm in the finished product, with the tighter end of the range applied to soups subjected to extended hot-holding above 85 °C. Processors using APV Crepaco plate heat exchangers note that pre-heating the carrier oil above 70 °C triggers premature volatilisation; therefore, a cold-side injection point downstream of the final cooling section is mandatory. In retort pouch packaging of ready-to-eat tomato rice, spiking at 10 ppm compensates for an empirically observed 35–45% loss through the laminated aluminium foil barrier during the 12-month ambient shelf life at 40 °C, quantified by static headspace GC-MS using a DB-WAX column. Finished products range from industrial pizza sauce in 3 kg doypacks to aseptically filled tomato juice in 200 mL SIG Combibloc cartons, all requiring the absence of any exogenous aroma that could be flagged during the EU Positive List conformity audit. What Limits Flavour Fidelity in Low-Fat Chocolate Systems?Chocolate matrices with a fat phase below 28% and a non-fat cocoa solids content exceeding 45% undergo a kinetic redistribution of lipophilic aroma molecules during conching and tempering that magnifies harsh acetic and pyrazine notes while suppressing the creamy, nutty dimension that 2-isobutylthiazole contributes. In such formulations, the compound’s high lipid solubility (octanol-water partition coefficient cited above) drives it into the cocoa butter phase, where its vapour pressure above the chocolate melt is reduced by approximately 40–55% relative to a high-fat dark chocolate baseline, according to headspace dilution analysis performed with a GERSTEL MPS autosampler coupled to a time-of-flight mass spectrometer. To achieve consistent cocoa-nutty character, the material is incorporated not as a neat substance but as a co-crystallised powder with dextrose monohydrate at a loading of 0.1–0.3% flavour in carrier, which is then roller-refined to a particle size of 20–30 µm prior to conching. This spatial entrapment minimises volatilisation loss during the 55–70 °C conching phase lasting 6–18 hours. Addition equivalent to 0.5–1.5 ppm in the final chocolate mass is corroborated by FEMA typical maximum use data for chocolate products. Regulatory coverage is provided under FEMA 3134 and the Japan Food Chemical Research Foundation list as a permitted food flavouring, while adherence to EU 1334/2008 requires documentation of the absence of restricted chiral isomers. Processing equipment context matters: Buhler five-roll refiners set to 18–22 µm particle fineness exhibit a shear stress that can prematurely fracture co-crystallised particles, raising the free surface area and subsequent evaporative loss by 12–18%. Therefore, a split-addition protocol—60% of the dose before dry conching and 40% blended into the lecithin mix during the final liquid conching stage—is implemented on Aasted tempering lines to maintain uniformity. Terminal applications include single-origin Ecuadorian dark chocolate tablets with 75% cocoa mass and sugar-free couverture supplied to moulded praline manufacturers, where the compound’s stability under alkaline de-nibbing conditions must be verified via GC-Olfactometry on a sample taken from the continuous ball mill discharge. Roasted Nut Seasoning: Blooming Kinetics and Surface AdhesionOil-roasted peanut and almond products, processed in 220–260 °C forced-air roasters followed by immediate drum seasoning, present a transient hot-oil film on the kernel surface that acts as both a carrier and a stripping agent for volatile thiazoles. Applying 2-isobutylthiazole directly to the drum at this stage results in a measured chemical utilisation efficiency of only 25–30%, with the remainder exhausted through the perforated drum into thermal oxidiser units. A more effective strategy involves pre-dissolution in a flavour-stabilised high-oleic sunflower oil at a concentration of 0.5–1.0 g/kg, then spraying at a flow rate of 120–180 mL/min through 0.5 mm full-cone nozzles under a nitrogen pressure of 0.8 bar when the nut surface temperature has cooled to 110–120 °C. Surface adhesion shear tests using a TA.XTplus texture analyser equipped with an Ottawa cell confirm that 80% of the thiazole fraction adheres to the outer 200 µm of the nut epidermis within 45 seconds of spraying, after which endogenous triacylglycerol crystallisation enrobes the aroma and limits volatilisation. The addition rate targeted is 1.5–3 ppm on finished nut weight, adjusted downward by 20% when a subsequent enrobing chocolate layer is applied, as fat-phase migration dilutes the headspace concentration. Industrial batch sizes typical of Valley Cottage-type continuous enrobers exceed 2,000 kg/h, mandating real-time feedback control via an InProcess-LSP inline particle size analyser to prevent clumping that would invalidate ISO 22000 prerequisite programmes for foreign matter. Pertinent compliance data: listed in the association of Southeast Asian Nations (ASEAN) positive flavour list; compliance with JECFA 1315 purity criteria (≥98% assay by GC-FID); and permissible under the General Standard for Food Additives (GSFA, Codex STAN 192-1995) as a flavouring agent without numerical maxima for nut products. When the roasted nut is milled into a butter with a D₉₀ particle size of 25 µm, the shearing-induced temperature spike to 80 °C can accelerate thiazole oxidation in the presence of surface-active proteins; chelating agents such as 0.02% citric acid monohydrate must be formulated into the slurry to chelate pro-oxidant iron. Finished good formats encompass 40 g foil-laminated snack pouches, 15 kg bag-in-box pastes for confectionery filling, and seasoning blends for mixed nut jars. In coffee extraction plants handling 4–6 tonnes of green Robusta beans per batch, the aqueous extract drawn from percolation sets at 160–180 °C and 10–12 bar is subsequently concentrated to 40–45% solids in falling-film evaporators before being spray-dried in a Niro F-100 tower with an inlet temperature of 200–220 °C and an outlet of 90–100 °C. Under these conditions, the entire volatile organic fraction undergoes a mass transfer from the liquid droplet to the hot drying air within the first 1.5 seconds of flight, resulting in a surface-oil-deficient powder that exhibits only burnt-malt and furan-type notes upon reconstitution. 2-Isobutylthiazole, applied through a low-pressure homogeniser at 200 bar as a fine emulsion stabilised with modified starch (Capsul TA, octenylsuccinate starch, 10% in the emulsion) and sterile-filtered water, is dosed into the concentrate feed line at a rate that delivers 6–12 ppm on dry powder basis. The emulsion droplet size, verified by a Malvern Mastersizer 3000 to possess a D₅₀ of 2.5 µm, ensures that microcapsule wall integrity withstands the thermal shock of atomisation without bursting. Published recoveries using this configuration exceed 75% of the input charge, measured by stable isotope dilution assay. The regulatory dossier necessary for EU export of such spray-dried coffee flavours necessitates a detailed Certificate of Analysis confirming compliance with residual solvent limits under Directive 2009/32/EC and a declaration that the flavour is free from 4-methylimidazole and other processing contaminants referenced in Regulation (EU) 2019/133. Japan’s Food Sanitation Act specifications also apply when the coffee powder is blended with non-dairy creamer for vending machine sachets of 10 g each. Equipment-specific failure mode: build-up of thiazole-laden oil deposits on the cyclone walls of the drying chamber after 48 hours of continuous operation triggers cleaning cycles using 2% sodium hydroxide at 80 °C that can generate trace amine by-products with off-flavours. To mitigate this, a nitrogen blanket in the cyclone cone set to 0.5 m³/h is employed, and the tower is scheduled for intermediate water flushes every 36 hours. Finished consumer goods include instant low-acid coffee granules in 100 g glass jars with one-way valve bags and single-serve stick packs for the Japanese konbini market.
Minimising Headspace Loss During Tunnel Pasteurisation of Processed Cheese Spreads and Rellish BasesContinuous tunnel pasteurisers processing analogue cheese spreads in hermetically sealed polyethylene terephthalate cups (120 mm × 80 mm × 30 mm) at a belt speed of 1.2 m/min subject the product surface to cascading water zones stepped from 70 °C to 95 °C over a 32-minute cycle. The headspace volume of 22 mL inside the sealed cup acts as a steam-distillation chamber, stripping water-soluble and medium-volatility flavour molecules—including 2-isobutylthiazole added at 0.8–2.0 ppm in the pre-emulsified pasteurised cheese base—into the vapour phase. Destructive sampling every 2 minutes through the tunnel and subsequent GC-FID quantification on a DB-624 column reveals that 27–34% of the initial dose migrates from the food matrix to the headspace within the first 12 minutes, after which condensation onto the lid film re-deposits a fraction that is not recoverable by the consumer. Compensatory over-application is constrained by the 2 ppm ceiling imposed by the flavour supplier’s internal non-GMO project verification under the Non-GMO Project Standard, because the ethanol used in the liquid stock solution may be derived from fermentation sources requiring identity preservation. A process redesign adopted by a mid-sized Wisconsin co-packer eliminates the headspace flux by purge-injecting nitrogen into the cup with a residual oxygen level below 0.8% and then performing steam-assisted sealing within 1.5 seconds, which suppresses volatilisation irrespective of tunnel temperature. Under these modified conditions, recovery at the end of the 32-minute cycle rises to 89–93% of the input value. Regulatory oversight involves compliance with the FSSC 22000 prerequisite programme on chemical migration from lid sealants into the headspace condensate, requiring a written migration assessment report referencing Regulation (EU) 10/2011 for plastic food contact materials when the finished snack cup is exported to Germany. The relish-style line—a finely diced tomato-vegetable mixture with a pH of 3.8–4.1—poses an additional acid-catalysed hydrolysis risk for the thiazole ring if the product is held warm (> 60 °C) for more than 45 minutes prior to filling; a sequenced addition right before the filling hopper via a Prominent dosing pump, calibrated to deliver 1 mL of a 0.1% stock solution per 50 kg batch, is therefore enforced. Terminal formats range from 140 g polypropylene cups with aluminium foil lids for foodservice cheese dips to 250 g glass jars of tomato-capsicum relish placed on the ambient shelf-stable condiment aisle of Australasian supermarkets. When dry cereal-based snack pellets are expanded in a Clextral EV-32 twin-screw extruder with a 20:1 L/D ratio and a die temperature of 170 °C, the residence time of the flavour pre-blend inside the barrel is merely 3–8 seconds, during which partial degradation of 2-isobutylthiazole occurs not through simple thermal cracking but via a Maillard-type binding to available amino groups in the wheat gluten that forms the matrix. The bound thiazole remains undetectable by headspace analysis and fails to contribute to aroma until oral processing, which is undesirable for a dry, crisp snack intended for immediate perception upon opening a bag. To circumvent this, the flavour compound is applied post-extrusion in a seasoning drum, using a dry-blended carrier composed of 80% maltodextrin DE 10 and 20% salt (500 µm particle size), onto which the 2-isobutylthiazole has been pre-adsorbed at a loading of 0.08% by weight. This dry seasoning applied at 6–8% w/w on the extruded base yields a net concentration of 1.5–2.5 ppm in the finished snack. Sticking and dusting losses are minimised by spraying 0.3% of a medium-chain triglyceride oil mist simultaneously, which also improves adhesion; the amount of oil must remain below the threshold at which third-party organic certification under the USDA National Organic Program would be jeopardised due to non-organic carrier compliance. Normative references for the finished snack include CODEX STAN 192-1995 for flavouring agents and ISO 20938:2013 for testing the oxidative stability of the frying oil in which the pellet may have been pre-fried. Contamination risk associated with cross-batch carryover is significant in multi-product plants: validated cleaning protocols using 2.5% sodium bicarbonate solution at 75 °C for 20 minutes must be enforced before running a non-flavoured corn puff product, with final rinse water tested by solid-phase microextraction to ensure no detectable thiazole signal above the 0.05 ppb limit of quantitation. The commercial outcomes encompass barbecue-flavoured corn sticks sold in 55 g metallised flow-wrap packs and multi-grain hoops packed in 200 g stand-up flexible pouches with a PET/AL/PE laminate structure, where aroma scalping by the inner polyethylene sealant layer is a documented quality factor assessed by a 12-month sensory panel at elevated 38 °C storage.
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2-Isobutylthiazole (CAS 18640-74-9, C₇H₁₁NS, molecular mass 141.23 g/mol) is assigned FEMA GRAS designation 3134 and JECFA number 1034. The substance appears as a colourless to pale yellow mobile liquid with a boiling point of 180–182 °C at atmospheric pressure, a flash point of 58 °C (closed cup, ASTM D93), and a specific gravity of 0.990–0.998 at 20 °C (ASTM D4052). Refractive index measured at 20 °C falls between 1.490 and 1.498 (ISO 280:1998). Typical commercial assay by GC-FID (ASTM E202) is specified at ≥ 98.0%, with the predominant impurity profile consisting of positional isomers and trace alkylthiazole homologues. The substance is classified as a synthetic flavoring substance under 21 CFR 172.515 and is listed in the Union List of flavourings with FL-no. 15.026.
The organoleptic signature of 2-isobutylthiazole is dominated by a green, tomato-vine, earthy character with subtle grapefruit-peel undertones, a profile that distinguishes it sharply from oxygenated heterocycles. The thiazole ring, containing both sulfur and nitrogen in a 1,3 arrangement, raises the compound’s octanol/water partition coefficient (log P) to approximately 2.8, promoting rapid partitioning into the headspace of aqueous food matrices and a pronounced top-note impact. Orthonasal detection thresholds in water, determined by ASTM E679 forced-choice ascending concentration series using a trained panel, are reported in the range 0.002–0.005 µg/L. This positions 2-isobutylthiazole among the most potent green-vegetable character impact compounds, roughly one to two orders of magnitude lower in threshold than 2-acetylthiazole (popcorn, threshold ~ 10 µg/L in water) and comparable in potency to 2-isobutyl-3-methoxypyrazine, though the latter conveys a distinctly capsicum, bell-pepper, and galbanum profile rather than ripe tomato flesh and stem. Vapour pressure at 25 °C is estimated at 0.4 hPa, ensuring high headspace mobility without excessive flashing during thermal processing. The substitution of an isobutyl group at the 2-position lengthens the hydrophobic side chain relative to 2-methyl- or 2-ethylthiazole, shifting the aroma from roasted, alliaceous notes toward fresh, juicy vegetal nuances. The absence of an oxygen atom in the ring, contrasted with oxazole analogues, eliminates ethereal sweet notes and heightens the sulphuraceous, meat-ripe dimension when dosed above 1.0 µg/kg in aqueous systems.
| Property | 2-Isobutylthiazole | 2-Isobutyl-3-methoxypyrazine | 2-Acetylthiazole |
|---|---|---|---|
| FEMA No. | 3134 | 3132 | 3328 |
| log P | 2.8 | 1.7 | 0.8 |
| Threshold in water (µg/L) | 0.002–0.005 | 0.001–0.002 | 10–20 |
| Boiling point (°C) | 180–182 | — | 95–105 at 15 hPa |
| Primary odour descriptor | Tomato vine, green, earthy | Bell pepper, galbanum, earthy | Popcorn, roasted, cereal |
In tomato-based flavor formulations, 2-isobutylthiazole is incorporated as a high-impact top note to restore the fresh-picked character lost during thermal concentration of tomato paste. The compound is typically pre-diluted to 0.01–0.1% by weight in triacetin or propylene glycol (USP grade) before addition to a compounded flavor, owing to its extreme potency and the risk of localised olfactory fatigue among compounding staff. In finished food products, use levels measured by stable isotope dilution assay range from 0.05 µg/kg in clear tomato juice to 2.0 µg/kg in retorted tomato soup, where the loss of native 2-isobutylthiazole during sterilization at 121 °C for 30 min can exceed 70% of the initial fresh-fruit concentration. To compensate, flavour houses employ post-process top-noting: a buffered emulsion containing the thiazole is injected inline after the hold tube and before aseptic filling, a practice that requires the emulsion to remain kinetically stable at 4–8 °C for shelf-lives of 6–12 months. The presence of ascorbic acid at typical fortification levels (200–500 mg/kg) accelerates sulfhydryl oxidation by-products; therefore, encapsulation in modified starch (OSA-starch, E 1450) by spray drying at inlet temperatures of 180–190 °C is a standard mitigation, with retention efficiency verified by HPLC-UV at 254 nm after extraction.
The selection between 2-isobutylthiazole and 2-isobutyl-3-methoxypyrazine is governed by sensory target, regulatory constraints, and thermal processing severity. Pyrazines exhibit higher thermal stability owing to the fully aromatic 1,4-diazine ring, with decomposition onset above 200 °C in neutral pH. In contrast, the thiazole ring undergoes hydrolytic ring-opening at pH values below 3.0 when subjected to prolonged UHT conditions (140 °C for 4 s), forming trace amounts of 2-mercaptoketones that introduce catty, sulphidic off-notes detectable above 0.5 µg/kg. Consequently, manufacturers of shelf-stable acidic vegetable juices increasingly maintain dual stocks: 2-isobutyl-3-methoxypyrazine for products processed above 135 °C, and 2-isobutylthiazole for cold-pressed or mildly pasteurised (72 °C/15 s) formulations where the authentic vine-ripe character is prized. From a regulatory standpoint, 2-isobutyl-3-methoxypyrazine bears an EU FL-no. 14.006 and is also classified as a nature-identical flavouring substance; however, it carries a different labelling burden in certain clean-label programmes that exclude methoxy-substituted heterocycles. The thiazole, lacking a methoxy group, is sometimes favoured for “no artificial flavour” claims when declared as “natural tomato flavour” provided the product is sourced from a natural precursor via fermentation or enzymatic conversion. Cost-in-use on a per-kilogram-of-finished-product basis differs by a factor of approximately 3–5: 2-isobutylthiazole, despite a higher per-kilo raw material cost, requires a dosage 10–20 times lower to achieve equivalent green intensity, leading to a net reduction in flavour cost for high-volume applications such as bouillon cubes and dry soup mixes.
Regulatory compliance across jurisdictions is summarised in the matrix below. Each cell references the principal legislative instrument and the corresponding positive list number when applicable.
| Authority / Region | Reference | Status |
|---|---|---|
| US FDA | 21 CFR §172.515 | Synthetic flavouring substance; FEMA 3134 |
| EFSA / EU | Regulation (EC) No 1334/2008, FL-no. 15.026 | Evaluated, no safety concern at estimated dietary intake |
| JECFA | JECFA No. 1034 | Specification adopted; no ADI expressed |
| FSSAI (India) | FSSR 2011, Schedule 1 | Permitted flavouring substance |
| REACH (EU) | EC No. 242-468-8 | Registered exempt from authorisation |
Oxidative degradation of 2-isobutylthiazole in dry flavour carriers constitutes the primary constraint on shelf-life in powdered beverage premixes and seasoning blends. Neat liquid exposed to headspace oxygen at 40 °C shows a peroxide value exceeding 5 meq/kg within 72 h, correlating with a 30–40% reduction in GC peak area when sampled by SPME using a 50/30 µm DVB/CAR/PDMS fibre and analysed on a 30 m × 0.25 mm × 0.25 µm Stabilwax column. To counter this, encapsulation loads of 10–20% w/w flavour oil in a matrix of maltodextrin (DE 10–15) and gum arabic (E 414) with an inlet/outlet temperature profile of 190 °C/90 °C reduce headspace oxygen ingress such that less than 5% loss of 2-isobutylthiazole is observed after 12 months at 25 °C/60% RH in triple-laminated aluminium foil packaging (PET/Alu/PE, thickness ≥ 9 µm aluminium foil). Q10 values calculated from accelerated storage at 35 °C, 45 °C, and 55 °C cluster around 2.2, indicating that ambient shelf-life predictions derived from Arrhenius modelling align with real-time expiry dating within ±8%. In seasoning tablets compressed at 15–20 kN on a rotary press, migration of 2-isobutylthiazole into the adjacent effervescent layer containing citric acid/sodium bicarbonate can generate a detectable catty note within 3 months at 30 °C; industry practice segregates the thiazole-bearing granulate from the acidulant by an inert microcrystalline cellulose barrier layer compacted to a density of 0.8 g/cm³.
Analytical confirmation of identity and purity in finished goods relies on chiral-agnostic achiral GC methods, as no stereocentre exists in 2-isobutylthiazole. A validated protocol using a 5% phenyl–95% dimethylpolysiloxane column (30 m × 0.32 mm × 0.50 µm) with helium carrier at 1.5 mL/min and a temperature ramp from 50 °C (hold 2 min) to 240 °C at 8 °C/min resolves the target peak at a retention index of 1065 (linear alkane ladder C₇–C₃₀). Select ion monitoring (SIM) at m/z 99 (base peak), 141 (M⁺), and 71 distinguishes the compound from co-eluting 2-sec-butylthiazole, which exhibits a shifted retention index of 1045 and a characteristic fragment at m/z 86. Quantitative recovery from dry soup matrix using QuEChERS extraction (AOAC 2007.01) followed by dispersive SPE cleanup with PSA and C18 sorbents yields 85–92% recovery with RSD ≤ 8% at a fortification level of 0.5 µg/kg, sufficient to meet the measurement uncertainty requirements of ISO 17025-accredited flavour testing laboratories.