{"title":"Alkylation (Esterification) [Synthetic Reagents]","description":"\u003cp\u003e\u003cstrong\u003eAlkylation (Esterification) [Synthetic Reagents]\u003c\/strong\u003e — menghimpun reagen alkilasi yang mentransfer gugus alkil ke gugus fungsi seperti asam karboksilat, mencakup reagen asam (HCl-alkohol, BF3-alkohol) dan senyawa dialkil karbonat. Kategori ini berperan mengubah senyawa polar menjadi bentuk ester atau turunan alkil yang lebih mudah dianalisis maupun disintesis lebih lanjut.\u003c\/p\u003e\u003cp\u003eReagen dalam kategori Alkylation (Esterification) banyak dipakai untuk derivatisasi sampel sebelum analisis kromatografi gas (GC), mengubah asam lemak atau asam karboksilat menjadi metil ester (FAME) atau alkil ester lain agar volatilitas dan stabilitas termalnya meningkat. Reagen berbasis BF3-alkohol dan HCl-alkohol umum digunakan di laboratorium analisis lipid, pangan, dan petrokimia, sementara dialkil karbonat berfungsi sebagai agen alkilasi dalam sintesis organik.\u003c\/p\u003e\u003cp\u003eContoh produk dalam koleksi ini: \u003ca href=\"\/en\/products\/tci2510x004156728\"\u003eTCI X0041 7647-01-0 Hydrogen Chloride - Methanol Reagent (5-10%) [for Esterification]\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510c004013970\"\u003eTCI C0040 542-52-9 Dibutyl Carbonate\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510x003956727\"\u003eTCI X0039 7647-01-0 Hydrogen Chloride - Butanol Reagent (5-10%) [for Esterification] (1mL*10)\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510c004113972\"\u003eTCI C0041 105-58-8 Diethyl Carbonate\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510x003656726\"\u003eTCI X0036 373-57-9 Boron Trifluoride - Methanol Reagent (10-20%) [for Esterification] (1mL*10)\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510c005313987\"\u003eTCI C0053 616-38-6 Dimethyl Carbonate\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510x003556725\"\u003eTCI X0035 676-65-3 Boron Trifluoride - Isopropyl Alcohol Reagent (10-20%) [for Esterification] (1mL*10)\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510c160016244\"\u003eTCI C1600 3459-92-5 Dibenzyl Carbonate\u003c\/a\u003e.\u003c\/p\u003e\u003cp\u003ePemilihan reagen perlu memperhatikan jenis pelarut alkohol (metanol, butanol, isopropanol), konsentrasi reagen aktif, serta kemasan ampul siap pakai untuk menjaga konsistensi hasil derivatisasi. Seluruh produk merupakan produk asli Tokyo Chemical Industry (TCI) Jepang, dengan kemurnian, kemasan, dan kondisi penyimpanan tercantum pada halaman masing-masing item.\u003c\/p\u003e\u003cp\u003eKategori lain yang sejajar di bawah GC Derivatization Reagents, sering dipakai bersamaan dalam satu alur kerja laboratorium:\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-trimethylsilylation-gc-derivatization-reagents\"\u003eTrimethylsilylation [GC Derivatization Reagents]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-esterification-alkylation-gc-derivatization-reagents\"\u003eEsterification, Alkylation [GC Derivatization Reagents]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-silylation-others-gc-derivatization-reagents\"\u003eSilylation (Others) [GC Derivatization Reagents]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-chiral-derivatization-for-optical-purity-determination-gc-derivatization-reagents\"\u003eChiral Derivatization for Optical Purity Determination [GC Derivatization Reagents]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-acylation-gc-derivatization-reagents\"\u003eAcylation [GC Derivatization Reagents]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-gc-derivatization-reagents-others\"\u003eGC Derivatization Reagents (Others)\u003c\/a\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eKoleksi ini masih terbagi menjadi 1 kelompok yang lebih spesifik:\u003c\/p\u003e\u003cul\u003e\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-alkyl-transfer-synthetic-reagents\"\u003eAlkyl Transfer [Synthetic Reagents]\u003c\/a\u003e\u003c\/li\u003e\u003c\/ul\u003e\u003cp\u003eKembali ke \u003ca href=\"\/en\/collections\/tci-l3-gc-derivatization-reagents\"\u003eGC Derivatization Reagents\u003c\/a\u003e. Untuk pengadaan volume besar, kemasan khusus, atau grade tertentu, hubungi tim AMI Scientific — distributor resmi TCI Japan di Indonesia — untuk pengecekan ketersediaan dan lead time langsung ke Jepang.\u003c\/p\u003e","products":[{"product_id":"tci2510c223116927","title":"TCI C2231 3570-58-9 2-Chloroethyl Methanesulfonate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C2231 2-Chloroethyl Methanesulfonate is a non-heterocyclic building block belonging to the mesylate ester family, widely applied as a two-ended alkylating reagent in organic synthesis. Its molecular structure carries a mesylate group serving as an excellent leaving group at one end and a chlorine atom at the other, giving researchers two reactive sites with clearly differentiated levels of reactivity. This configuration is particularly useful for introducing a two-carbon bridge into a target molecule in stepwise fashion, then closing it through a cyclization reaction. The compact size of the molecule makes it an economical choice from an atom-economy standpoint in synthetic design.\u003c\/p\u003e\n\u003cp\u003eThe principal advantage of a mesylate over aromatic sulfonates lies in its lower molecular weight, so the mass of reagent required per mole is smaller and the methanesulfonate by-product is more easily separated during the purification stage. The mesylate group is also far more readily displaced than chloride or bromide, which means nucleophilic substitution can proceed at low temperature with a weak base, making it suitable for substrates that are sensitive to harsh conditions. The reactivity difference between the mesylate end and the chloride end allows reactions to be directed selectively to one site before the second site is engaged.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this building block is typically found in university organic chemistry research groups, pharmaceutical and medicinal chemistry programmes, and industrial R\u0026amp;D units engaged in intermediate preparation. It is handled in fume hoods on a research and pilot scale, where the ability to run substitution steps under mild conditions is valued in facilities that do not always have access to specialised low-temperature or inert-atmosphere equipment. Its role as a compact bifunctional linker makes it a practical stock item for multi-step synthesis work.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eStepwise alkylation of nucleophiles, where the highly labile mesylate end reacts first under mild conditions while the chloride end remains available for a later, separate transformation.\u003c\/li\u003e\n\u003cli\u003eIntroduction of two-carbon bridges into target molecules, allowing researchers to extend a scaffold by a short ethylene linker before closing the structure through a subsequent cyclization step.\u003c\/li\u003e\n\u003cli\u003eRing-closing and cyclization chemistry, in which the two differentiated reactive ends are engaged in sequence so that intramolecular bond formation completes the desired ring system.\u003c\/li\u003e\n\u003cli\u003ePreparation of synthetic intermediates in medicinal and pharmaceutical chemistry research, where mild substitution conditions protect sensitive functional groups elsewhere in the substrate molecule.\u003c\/li\u003e\n\u003cli\u003eBifunctional linker chemistry for joining two distinct nucleophilic partners, exploiting the clear reactivity gap between the mesylate and chloride termini to control the order of coupling.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI (Tokyo Chemical Industry)\u003c\/li\u003e\n\u003cli\u003eCAS number: 3570-58-9\u003c\/li\u003e\n\u003cli\u003eChemical name: 2-Chloroethyl Methanesulfonate\u003c\/li\u003e\n\u003cli\u003eCatalogue code: C2231\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in standard TCI research-scale packaging; please confirm the size options when ordering\u003c\/li\u003e\n\u003cli\u003eStorage: keep in the original tightly closed container under the conditions stated on the manufacturer's label and safety data sheet\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the container tightly closed in a cool, dry, well-ventilated area away from heat, ignition sources, moisture, and incompatible materials such as strong bases and strong oxidising agents, following the conditions specified on the manufacturer's label and safety data sheet. Keep the material in its original supplier container, or in a chemically compatible, clearly labelled vessel if transfer is necessary. Handle only inside a functioning fume hood, wearing safety glasses, chemical-resistant gloves, and a laboratory coat. As an alkylating agent, this compound should be treated with particular care: avoid skin contact, eye contact, and inhalation of vapours, minimise the quantity handled on the open bench, and consult the safety data sheet before use, spill clean-up, or waste disposal.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086113190106,"sku":"TCI2510C223116927","price":3761000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2231.jpg?v=1767097961"},{"product_id":"tci2510d129421008","title":"TCI D1294 1188-33-6 N,N-Dimethylformamide Diethyl Acetal [for Esterification]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D1294 N,N-Dimethylformamide Diethyl Acetal [for Esterification] is an organic synthesis reagent from the formamide acetal family, formulated specifically for esterification work. The reagent supplies an ethyl group, allowing carboxylic acids to be converted into their corresponding ethyl esters without a strong acid catalyst and without prolonged reflux in an excess of alcohol. As a non-heterocyclic building block, it holds an important position in both synthesis and analytical laboratories, because it shortens the working sequence and reduces the risk of damaging other sensitive functional groups present on the target molecule.\u003c\/p\u003e\n\u003cp\u003eThe principal advantage of this reagent lies in its mild, essentially neutral reaction conditions. Substrates carrying acid-labile groups, additional ester linkages, or stereogenic centres can therefore be processed with a lower risk of racemisation and decomposition than would be expected under classical acid-catalysed esterification. Beyond esterification, the formamide acetal framework is also able to react with active methylene compounds to form enaminone derivatives, although the product's primary intended use is genuinely directed towards esterification reactions. It is supplied as a moisture-sensitive liquid, so the best results are obtained only when the reagent is handled and stored correctly.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent is typically used in university and institutional research groups working on organic synthesis, in medicinal and natural-product chemistry projects where sensitive intermediates must be esterified, and in analytical laboratories that prepare ester derivatives prior to instrumental measurement. Because it removes the need for strongly acidic conditions and extended reflux, it fits well into routine bench workflows where sample quantities are limited and functional-group integrity has to be preserved.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eEthyl ester preparation from carboxylic acids: supplies the ethyl group directly, so conversion proceeds without a strong acid catalyst or a large excess of ethanol under prolonged reflux.\u003c\/li\u003e\n\u003cli\u003eEsterification of acid-sensitive substrates: the mild, nearly neutral conditions allow molecules bearing acid-labile protecting groups or additional ester linkages to be converted with reduced decomposition.\u003c\/li\u003e\n\u003cli\u003eDerivatisation of stereogenic compounds: because harsh acidic media are avoided, substrates containing stereogenic centres can be esterified with a lower risk of racemisation during the reaction.\u003c\/li\u003e\n\u003cli\u003eEnaminone synthesis from active methylene compounds: the formamide acetal framework reacts with active methylene substrates to build enaminone derivatives useful as intermediates in further synthetic sequences.\u003c\/li\u003e\n\u003cli\u003eSample derivatisation in analytical laboratories: forming ester derivatives shortens the preparation sequence and helps preserve other sensitive functional groups on the analyte before instrumental analysis.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 1188-33-6\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003eProduct designation: D1294, N,N-Dimethylformamide Diethyl Acetal [for Esterification]\u003c\/li\u003e\n\u003cli\u003ePhysical form: liquid, moisture sensitive\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in the pack sizes offered for this catalogue item\u003c\/li\u003e\n\u003cli\u003eStorage: keep tightly closed and protected from moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eBecause this reagent is a moisture-sensitive liquid, it should be stored in a tightly closed original container and protected from atmospheric humidity; best results are obtained only when the reagent is kept dry. Store in a cool, well-ventilated area away from heat, ignition sources, and incompatible materials, and keep the container closed when not in use. Dispense in a fume hood using dry glassware and dry syringes or cannulas, and minimise the time the container remains open. Wear safety glasses, chemical-resistant gloves, and a laboratory coat while handling. Return the container to storage promptly after use and follow the manufacturer's safety data sheet together with local laboratory waste-disposal procedures.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5mL","offer_id":48086433038554,"sku":"TCI2510D129421008","price":1010000.0,"currency_code":"IDR","in_stock":true},{"title":"25mL","offer_id":48086433071322,"sku":"TCI2510D129421009","price":2828000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D1294.jpg?v=1767102837"},{"product_id":"tci2510d130121014","title":"TCI D1301 6006-65-1 N,N-Dimethylformamide Dipropyl Acetal [for Esterification]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D1301 N,N-Dimethylformamide Dipropyl Acetal [for Esterification] is a member of the formamide acetal family carrying two propoxy groups, prepared specifically for esterification reactions in both synthesis and analytical laboratories. The reagent allows carboxylic acids to be converted directly into their propyl esters without a strong acid catalyst and without the need to add excess alcohol under prolonged reflux conditions. As a non-heterocyclic building block, it complements the dimethyl and diethyl variants within the same family of reagents, giving researchers a choice of ester alkyl group according to the demands of a particular analysis or synthetic target.\u003c\/p\u003e\n\u003cp\u003eThe distinguishing feature of this reagent lies in its propyl chain, which is longer than either the methyl or ethyl equivalent, producing ester derivatives with different polarity and different retention behaviour in chromatographic analysis. This difference is especially valuable when the peak of a methyl or ethyl derivative overlaps with components of the sample matrix, since the analyst can select propyl derivatisation instead to obtain better separation. The reaction conditions are mild and close to neutral, which preserves the integrity of other functional groups present in the molecule and reduces the risk of unwanted side reactions during derivatisation.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, reagents of this type are used in university synthesis groups, government research institutes, and analytical service laboratories that prepare samples for chromatographic determination. Because it works under gentle, near-neutral conditions and avoids the handling of strong acid catalysts, it fits well into routine sample-preparation workflows where a straightforward and reproducible derivatisation step is required before instrumental measurement, and where the choice of alkyl group must be adapted to the sample matrix at hand.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eDirect esterification of carboxylic acids: converts the acid group into the corresponding propyl ester in a single step, without a strong acid catalyst or a large excess of alcohol under long reflux.\u003c\/li\u003e\n\u003cli\u003eDerivatisation for chromatographic analysis: forms propyl ester derivatives with polarity and retention characteristics that differ from methyl and ethyl analogues, giving analysts an alternative when peaks overlap.\u003c\/li\u003e\n\u003cli\u003eResolution of matrix interference problems: when methyl or ethyl derivative peaks coincide with sample matrix components, switching to propyl derivatisation shifts retention and delivers better chromatographic separation.\u003c\/li\u003e\n\u003cli\u003eSynthesis of propyl esters on substrates with sensitive functionality: the mild, near-neutral reaction conditions preserve other functional groups on the molecule that acidic esterification methods could damage.\u003c\/li\u003e\n\u003cli\u003eBuilding block work in non-heterocyclic organic synthesis: serves alongside the dimethyl and diethyl acetal variants so researchers can select the ester alkyl group that matches their synthetic target.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 6006-65-1\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003eProduct code: D1301\u003c\/li\u003e\n\u003cli\u003eApplication grade: supplied as a reagent designated for esterification\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in the packaging options offered by the manufacturer for this catalogue item\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the reagent in its original tightly closed container, protected from moisture, in a cool and well-ventilated area away from direct sunlight and sources of ignition. Acetal reagents of this type are moisture-sensitive, so containers should be resealed promptly after use and, where practical, handled under a dry inert atmosphere. Dispense and transfer the material inside a fume hood using clean, dry glassware and dry syringes or cannulas. Laboratory personnel should wear safety goggles, chemical-resistant gloves, and a laboratory coat, and should avoid inhaling vapours or allowing contact with skin and eyes. Keep the reagent separate from strong acids and strong oxidising agents, and consult the manufacturer's safety data sheet before use and before disposal of residues.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5mL","offer_id":48086433267930,"sku":"TCI2510D130121014","price":986000.0,"currency_code":"IDR","in_stock":true},{"title":"25mL","offer_id":48086433300698,"sku":"TCI2510D130121015","price":2828000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D1301.jpg?v=1767102850"},{"product_id":"tci2510d130221016","title":"TCI D1302 18503-90-7 N,N-Dimethylformamide Dibutyl Acetal [for Esterification]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eN,N-Dimethylformamide Dibutyl Acetal (DMFDBA), with CAS number 18503-90-7, is a chemical compound widely utilized in laboratory settings for esterification reactions. As a key building block in organic synthesis, it plays a vital role in the formation of esters from carboxylic acids. Its stability and reactivity make it a versatile reagent for creating complex molecular structures. This compound is particularly favored for its ability to participate in both esterification and other organic transformations, making it an essential component in synthetic chemistry workflows.\u003c\/p\u003e\n\u003cp\u003eDMFDBA is known for its excellent solubility in organic solvents, which facilitates mixing and reaction processes in laboratory experiments. Its chemical properties allow it to react efficiently with a variety of acids and alcohols, enhancing its utility in esterification reactions. The compound’s stability under various reaction conditions ensures consistent results, making it a reliable choice for researchers. Additionally, its dual role as both a reagent and a solvent increases its flexibility in different experimental setups, contributing to its widespread use in chemical laboratories.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, DMFDBA is commonly used in organic chemistry research, compound development, and industrial chemical production. It supports academic institutions and research centers in advancing chemical knowledge and innovation. Its availability and effectiveness make it a standard material in both educational and industrial chemical applications within the country.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis for esterification reactions due to its reactivity with carboxylic acids and alcohols.\u003c\/li\u003e\n\u003cli\u003eDevelopment of new chemical compounds in research laboratories requiring reliable reagents for complex molecular structures.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical production where DMFDBA is used as a building block for ester formation processes.\u003c\/li\u003e\n\u003cli\u003eEducational institutions for teaching and conducting experiments in organic chemistry courses.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research for the synthesis of ester-based compounds used in drug development.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 18503-90-7\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory supply formats\u003c\/li\u003e\n\u003cli\u003ePhysical form: Liquid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct sunlight and incompatible materials\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eDMFDBA should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to keep it in a tightly sealed container to prevent evaporation and contamination. Due to its chemical nature, it should be stored separately from strong oxidizing agents and acids to avoid potential reactions. Proper ventilation is essential when handling this compound to minimize inhalation risks. Laboratory personnel should wear appropriate personal protective equipment, such as gloves and safety goggles, when working with DMFDBA to ensure safe handling and reduce exposure risks. Regular monitoring of storage conditions is advised to maintain the compound's integrity and ensure compliance with safety standards.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5mL","offer_id":48086433333466,"sku":"TCI2510D130221016","price":1313000.0,"currency_code":"IDR","in_stock":true},{"title":"25mL","offer_id":48086433366234,"sku":"TCI2510D130221017","price":4115000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D1302.jpg?v=1767102854"},{"product_id":"tci2510d130321018","title":"TCI D1303 36805-97-7 N,N-Dimethylformamide Di-tert-butyl Acetal [for Esterification]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eN,N-Dimethylformamide Di-tert-butyl Acetal is a chemical compound widely used in laboratory settings for its role in esterification reactions. As a key building block in organic synthesis, it enables the formation of esters through efficient and controlled chemical processes. This compound is particularly valued for its ability to react with various carboxylic acids, making it a versatile reagent in synthetic chemistry. Its stability and reactivity make it a reliable choice for researchers working on complex molecular structures.\u003c\/p\u003e\n\u003cp\u003eThe compound's chemical properties, including its stability and reactivity, make it a preferred choice for laboratory applications. It is known for its ability to undergo esterification efficiently, which is crucial in the synthesis of ester compounds with diverse industrial and pharmaceutical applications. Its non-heterocyclic nature allows it to be used in a wide range of chemical reactions without interfering with other functional groups. This makes it a go-to material for chemists seeking reliable and consistent results.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, N,N-Dimethylformamide Di-tert-butyl Acetal is commonly used in organic chemistry research. It is a staple in both academic and industrial settings, where its reliability and efficiency are highly appreciated. Its availability in liquid form and ease of use further contribute to its popularity among researchers. Its non-volatile nature also ensures safety during handling and storage, making it a trusted reagent in controlled laboratory environments.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis for esterification reactions due to its efficient and stable chemical properties.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research for the development of ester-based compounds with therapeutic applications.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemistry applications where ester compounds are required for product formulation.\u003c\/li\u003e\n\u003cli\u003eAcademic research in chemical laboratories for teaching and experimental purposes.\u003c\/li\u003e\n\u003cli\u003ePolymer science for the synthesis of ester-functionalized polymers with specific properties.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 36805-97-7\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities\u003c\/li\u003e\n\u003cli\u003ePhysical form: Liquid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry place away from direct sunlight to maintain its stability and reactivity. It is recommended to use airtight containers to prevent exposure to moisture and air, which could affect its performance. Due to its chemical nature, it should be handled in a well-ventilated area, and appropriate personal protective equipment should be worn. While it is relatively stable under normal storage conditions, it should not be exposed to extreme temperatures or incompatible substances. Proper labeling and safe storage practices are essential to ensure the safety of laboratory personnel and the integrity of the compound.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5mL","offer_id":48086433431770,"sku":"TCI2510D130321018","price":3660000.0,"currency_code":"IDR","in_stock":true},{"title":"25mL","offer_id":48086433464538,"sku":"TCI2510D130321019","price":12745000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D1303.jpg?v=1767102858"},{"product_id":"tci2510d133221062","title":"TCI D1332 4637-24-5 N,N-Dimethylformamide Dimethyl Acetal [for Esterification] (0.5mL*10)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D1332 N,N-Dimethylformamide Dimethyl Acetal [for Esterification] is a methylating reagent supplied in a specially prepared format of ten glass ampoules, each containing 0.5 mL. Widely known by the abbreviation DMF-DMA, this reagent converts carboxylic acids into their corresponding methyl esters quickly and cleanly, without requiring a strong acid catalyst or an excess of solvent. In the laboratory it plays an essential role during sample preparation prior to gas chromatographic analysis, because free carboxylic acids tend to produce broadened, asymmetric peaks on the column.\u003c\/p\u003e\n\u003cp\u003eThe qualities that make analysts choose this reagent lie in its single-dose ampoule packaging and the purity maintained specifically for esterification work. Each ampoule holds a pre-measured quantity, so the analyst does not need to open a large bulk container repeatedly, and the risk of quality deterioration through contact with atmospheric moisture is kept to a minimum. The methylation reaction proceeds at moderate temperature within a short time and generates volatile by-products, which therefore do not interfere with chromatographic injection.\u003c\/p\u003e\n\u003cp\u003eBeyond esterification, DMF-DMA is also widely used as an enaminone-forming reagent and as a one-carbon unit source in synthetic chemistry. In Indonesian laboratories this combination of roles suits analytical services, university research groups, and quality control units that prepare acidic samples for gas chromatography while also running small-scale building block synthesis. The ten-ampoule set allows a single delivery to cover several separate work sessions.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMethyl ester preparation from carboxylic acids: the reagent performs the conversion rapidly and cleanly without a strong acid catalyst or excess solvent, simplifying the workflow.\u003c\/li\u003e\n\u003cli\u003eSample derivatisation before gas chromatography: free carboxylic acids give broad, asymmetric peaks, so converting them to methyl esters improves peak shape on the column.\u003c\/li\u003e\n\u003cli\u003eRoutine analytical sample preparation: each pre-measured ampoule removes the need to repeatedly open a bulk container, which keeps handling consistent between analytical batches.\u003c\/li\u003e\n\u003cli\u003eEnaminone formation in synthetic chemistry: DMF-DMA is widely employed as an enaminone-forming reagent, making this pack useful for building block work beyond esterification.\u003c\/li\u003e\n\u003cli\u003eOne-carbon unit introduction: the reagent serves as a source of a single carbon unit, supporting synthetic routes that require this fragment in non-heterocyclic building block chemistry.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 4637-24-5\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack size: 0.5 mL × 10 ampoules per set\u003c\/li\u003e\n\u003cli\u003eGrade note: supplied as a reagent for esterification\u003c\/li\u003e\n\u003cli\u003eStorage: keep ampoules sealed and protected from moisture until use\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the ampoules in their original packaging in a cool, dry place away from direct sunlight and sources of heat, keeping each unit sealed until the moment of use so that contact with atmospheric moisture is avoided. Because the material is sensitive to water vapour, the single-dose ampoule format should be used as intended: open one ampoule per working session rather than transferring the contents into a larger shared container. Handle the reagent in a fume hood with appropriate gloves, safety glasses, and a laboratory coat, and open glass ampoules carefully to avoid cuts. Prepare and transfer the reagent using clean, dry glassware, and dispose of residues and empty ampoules through the laboratory's chemical waste procedure.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1set","offer_id":48086435168474,"sku":"TCI2510D133221062","price":1970000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D1332.jpg?v=1767102920"},{"product_id":"tci2510d159521401","title":"TCI D1595 4909-78-8 N,N-Dimethylformamide Dineopentyl Acetal [for Esterification]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eN,N-Dimethylformamide Dineopentyl Acetal (DMF-DIPA) is a chemical compound widely used in laboratory settings for its role in esterification reactions. As a key reagent, it serves as a versatile source of ester groups that can react with various substrates to form new organic compounds. This compound is particularly valuable in synthetic chemistry due to its ability to act both as a solvent and a reactive component, streamlining the synthesis process without the need for additional reagents. Its application spans multiple areas of organic chemistry, making it an essential material for researchers and chemists working in both academic and industrial environments.\u003c\/p\u003e\n\u003cp\u003eDMF-DIPA is preferred for its chemical stability under controlled conditions and its reactivity in a wide range of chemical environments. It possesses a high boiling point, which allows it to be used in reactions requiring elevated temperatures. Its ability to participate in esterification reactions makes it a reliable choice for producing ester derivatives. Additionally, its dual functionality as a solvent and reagent enhances its utility in complex synthesis pathways. These properties make DMF-DIPA a go-to compound in Indonesian laboratories where efficiency and reliability are paramount.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, DMF-DIPA is commonly used in organic chemistry research, especially in the pharmaceutical and chemical industries. It plays a crucial role in the synthesis of complex organic molecules, contributing to the development of new drugs and materials. Its availability and effectiveness make it a staple in many research facilities across Indonesia, supporting both academic and industrial chemical innovation.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eEsterification Reactions: DMF-DIPA is ideal for esterification due to its ability to provide ester groups, facilitating the formation of ester derivatives in organic synthesis.\u003c\/li\u003e\n\u003cli\u003eOrganic Synthesis: It is widely used in the synthesis of complex organic compounds, acting as both a solvent and reactive component to enhance reaction efficiency.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical Research: Its role in producing ester derivatives makes it valuable in drug development and compound modification processes.\u003c\/li\u003e\n\u003cli\u003eIndustrial Chemistry: DMF-DIPA supports the production of various chemical products by enabling efficient and reliable esterification pathways.\u003c\/li\u003e\n\u003cli\u003eAnalytical Chemistry: It is used as a solvent in analytical procedures to dissolve and process organic compounds for further analysis.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 4909-78-8\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory supply\u003c\/li\u003e\n\u003cli\u003ePhysical form: Liquid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from heat and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eDMF-DIPA should be stored in a cool, dry environment, away from heat and direct sunlight to maintain its chemical stability. It is recommended to use sealed containers made of materials compatible with organic solvents, such as glass or high-density polyethylene. Due to its reactivity, it should be handled in a well-ventilated area, and appropriate personal protective equipment should be worn. Avoid exposure to oxygen and heat to prevent degradation. Proper storage ensures the compound remains effective for its intended applications in laboratory settings.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5mL","offer_id":48086449520858,"sku":"TCI2510D159521401","price":1086000.0,"currency_code":"IDR","in_stock":true},{"title":"25mL","offer_id":48086449553626,"sku":"TCI2510D159521402","price":3181000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D1595.jpg?v=1767103306"},{"product_id":"tci2510d207122115","title":"TCI D2071 4637-24-5 N,N-Dimethylformamide Dimethyl Acetal [for Esterification]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D2071 N,N-Dimethylformamide Dimethyl Acetal, commonly abbreviated as DMF-DMA, is a versatile liquid reagent prepared specifically for esterification work. In the laboratory it acts as a mild methylating agent that rapidly converts carboxylic acids into their methyl esters without requiring strong mineral acids or hazardous diazomethane. This role is particularly important during sample preparation prior to gas chromatographic analysis, because many organic acids are insufficiently volatile and are difficult to separate cleanly until they have been converted into their more readily analysed ester derivatives.\u003c\/p\u003e\n\u003cp\u003eThe properties that make this reagent a preferred choice are its selective reactivity and its comparatively gentle reaction conditions. The aminal acetal group in its structure readily releases methanol and forms a reactive intermediate species, so esterification can proceed under moderate heating with by-products that are easily evaporated away. DMF-DMA is also well known as an enaminone-forming reagent and as a one-carbon source for heterocyclic synthesis, including pyrazoles, pyrimidines, and isoxazoles, so a single bottle can support several different kinds of work at once.\u003c\/p\u003e\n\u003cp\u003eBecause it is supplied in liquid form, the reagent is straightforward to measure and to add directly to a reaction mixture or to a derivatisation vial. In Indonesian laboratories this suits routine analytical service work, teaching and research laboratories in organic synthesis, and quality control settings where organic acid content is determined by gas chromatography. Its dual usefulness in both derivatisation and synthetic chemistry makes it a practical item to keep on hand where a single reagent inventory has to serve mixed workloads.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMethyl ester derivatisation for gas chromatography — converts poorly volatile organic acids into methyl esters that elute and separate far more cleanly, improving peak shape and quantitation in routine GC analysis.\u003c\/li\u003e\n\u003cli\u003eMild esterification of carboxylic acids — provides a route to methyl esters without strong mineral acid catalysts or hazardous diazomethane, which simplifies both the procedure and the safety controls required.\u003c\/li\u003e\n\u003cli\u003eEnaminone formation in organic synthesis — reacts with activated methyl and methylene compounds to give enaminone intermediates that serve as flexible platforms for further ring-forming chemistry.\u003c\/li\u003e\n\u003cli\u003eHeterocyclic building block chemistry — acts as a one-carbon source in the construction of pyrazoles, pyrimidines, and isoxazoles, supporting medicinal and materials-oriented synthetic programmes.\u003c\/li\u003e\n\u003cli\u003eTeaching and research laboratory synthesis exercises — its moderate reaction conditions and easily evaporated by-products make reaction workup and product isolation more manageable for students and researchers alike.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 4637-24-5\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003eProduct code: D2071\u003c\/li\u003e\n\u003cli\u003ePhysical form: liquid reagent, specified for esterification use\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in the standard TCI catalogue pack sizes for this item; please confirm the required size when ordering\u003c\/li\u003e\n\u003cli\u003eStorage: keep tightly closed in a cool, dry, well-ventilated area away from moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the reagent in its original tightly closed container in a cool, dry, and well-ventilated chemical store, away from heat sources, ignition sources, and direct sunlight. Because the acetal group releases methanol on reaction, keep the container sealed against atmospheric moisture and reclose it promptly after each withdrawal; amber glass or the supplier's original glass packaging is appropriate. Handle and dispense in a fume hood, wearing safety glasses, chemically resistant gloves, and a laboratory coat. Use clean, dry glassware and dry syringes or pipettes when transferring, avoid contact with strong acids and oxidising agents, and consult the manufacturer's safety data sheet before first use and before disposal of residues.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mL","offer_id":48086491660506,"sku":"TCI2510D207122115","price":1768000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D2071.jpg?v=1767104141"},{"product_id":"tci2510d458725220","title":"TCI D4587 54648-79-2 N,N'-Diisopropyl-O-methylisourea","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eN,N'-Diisopropyl-O-methylisourea (DMIM), also known as TCI D4587 with CAS number 54648-79-2, is a synthetic reagent widely used in organic chemistry laboratories. This compound plays a crucial role in the formation of C-X bonds, particularly in carbon-carbon bond formation reactions. Its versatility makes it a valuable tool for chemists engaged in synthetic reactions, enabling the synthesis of complex organic molecules. DMIM is commonly used in substitution and replacement reactions, depending on the reaction conditions applied. Its presence in laboratory settings supports the development of new compounds and the modification of molecular structures.\u003c\/p\u003e\n\u003cp\u003eDMIM is valued for its chemical stability under specific conditions, although it is highly sensitive to moisture and air exposure. This sensitivity necessitates careful handling and storage to maintain its reactivity. The presence of the isourea group in its molecular structure contributes to its reactivity, making it suitable for various synthetic applications. Its chemical properties allow it to participate in a wide range of reactions, making it a preferred choice for researchers in both academic and industrial settings.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, DMIM is extensively used in organic chemistry research by universities and research institutions. It is particularly relevant in the development of synthetic compounds, including pharmaceutical applications. Its role in facilitating chemical reactions makes it an essential component in the synthesis of new materials and drug compounds. The compound's utility in laboratory settings underscores its importance in advancing chemical research in Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis applications benefit from DMIM's ability to facilitate C-X bond formation, supporting the creation of complex molecular structures.\u003c\/li\u003e\n\u003cli\u003eIt is ideal for substitution reactions where the isourea group enhances reactivity and selectivity under controlled conditions.\u003c\/li\u003e\n\u003cli\u003eDMIM is commonly used in the development of pharmaceutical compounds, aiding in the synthesis of drug molecules through targeted chemical modifications.\u003c\/li\u003e\n\u003cli\u003eResearch institutions rely on DMIM for molecular structure modification, enabling the design of new compounds with desired properties.\u003c\/li\u003e\n\u003cli\u003eIts role in carbon-carbon bond formation makes it a key reagent in the synthesis of polymers and specialty chemicals.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 54648-79-2\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Synthetic Reagents \u0026gt; C-X(Non-Halogen) Bond Formation [Synthetic Reagents]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified in the provided data\u003c\/li\u003e\n\u003cli\u003ePhysical form: Not specified in the provided data\u003c\/li\u003e\n\u003cli\u003eStorage note: Should be stored in a sealed container, away from heat and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eDMIM should be stored in a sealed container to prevent exposure to moisture and air, which can degrade its chemical properties. It is recommended to keep the material in a cool, dry place away from direct heat sources to maintain its stability. Laboratory personnel should handle DMIM with care, using appropriate personal protective equipment such as gloves and safety goggles to avoid skin contact or inhalation. Due to its sensitivity, it is essential to ensure that the storage area is well-ventilated and free from potential contaminants. Proper labeling and secure storage are necessary to prevent accidental exposure and ensure safe handling in laboratory environments.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5mL","offer_id":48086698492122,"sku":"TCI2510D458725220","price":3636000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D4587.jpg?v=1768818147"},{"product_id":"tci2510e105828941","title":"TCI E1058 60683-30-9 O-Ethyl-N,N'-diisopropylisourea","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI E1058 60683-30-9 O-Ethyl-N,N'-diisopropylisourea is a synthetic reagent widely used in laboratory settings for its role in organic synthesis. This compound is specifically designed for reactions involving the formation of C-X bonds, where X is not a halogen. Its chemical structure includes an isourea group and an ethyl group, making it a versatile reagent in the creation of complex organic molecules. It is commonly employed in substitution reactions and bond-forming processes, contributing to the development of new chemical compounds.\u003c\/p\u003e\n\u003cp\u003eThe compound's preference in laboratory applications stems from its stability under controlled conditions and its ability to act as an electron donor in specific chemical reactions. This property enhances reaction rates and improves the efficiency of synthetic processes. Its sensitivity to moisture and high temperatures necessitates careful handling, but its reactivity and effectiveness make it a valuable tool in organic chemistry. The compound's role in accelerating reactions and improving yields makes it a preferred choice for researchers working on complex synthesis projects.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, O-Ethyl-N,N'-diisopropylisourea is frequently used in chemical research, especially in the synthesis of organic compounds. Its application spans various experimental setups, including those requiring high reactivity and precise chemical transformations. Researchers rely on this reagent for its consistent performance and reliability in synthetic processes, making it an essential component in many laboratory workflows.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic Synthesis: This reagent is ideal for organic synthesis due to its ability to participate in bond-forming reactions and facilitate the creation of complex molecular structures.\u003c\/li\u003e\n\u003cli\u003eSubstitution Reactions: Its role in substitution reactions makes it suitable for modifying existing molecules by replacing functional groups with desired substituents.\u003c\/li\u003e\n\u003cli\u003eC-X Bond Formation: It is specifically used in reactions that involve the formation of C-X bonds without halogen atoms, aligning with its classification in synthetic reagents.\u003c\/li\u003e\n\u003cli\u003eResearch and Development: Its reactivity and effectiveness make it a preferred choice for R\u0026amp;D in chemical laboratories aiming to develop new compounds.\u003c\/li\u003e\n\u003cli\u003eAnalytical Chemistry: It is used in analytical procedures where precise chemical transformations are required for the identification and characterization of compounds.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 60683-30-9\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Synthetic Reagents \u0026gt; C-X(Non-Halogen) Bond Formation [Synthetic Reagents]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified in the provided data\u003c\/li\u003e\n\u003cli\u003ePhysical form: Not specified in the provided data\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and high temperatures\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its stability and prevent degradation. It is recommended to use airtight containers to protect it from moisture and humidity, which can affect its chemical integrity. Due to its sensitivity to high temperatures, it should be kept away from heat sources and direct sunlight. Laboratory personnel should handle the compound with appropriate personal protective equipment to ensure safety during use and storage. Proper labeling of storage containers is essential to prevent accidental exposure and ensure safe handling in the laboratory setting.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5mL","offer_id":48086920724698,"sku":"TCI2510E105828941","price":2121000.0,"currency_code":"IDR","in_stock":true}]},{"product_id":"tci2510h128234074","title":"TCI H1282 16156-50-6 Hexyl Methanesulfonate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eHexyl methanesulfonate is the mesylate ester of hexanol, a compound formed by joining a six-carbon alkyl chain to a methanesulfonate group. In organic chemistry, the mesylate group is recognised as one of the best leaving groups available, which makes this compound function in practice as a ready-to-use alkylating reagent. In the laboratory, it is employed to attach a hexyl chain to a wide range of nucleophiles such as amines, thiols, phenols, and carboxylate anions, without the need to prepare a halide derivative in-house — derivatives that are often less reactive or less stable.\u003c\/p\u003e\n\u003cp\u003eThe main reason for choosing a mesylate over an alkyl halide is its higher reactivity and more predictable behaviour. The methanesulfonate anion is an exceptionally stable conjugate base, so nucleophilic substitution proceeds efficiently under relatively mild conditions and at temperatures that need not be high. The hexyl chain itself is long enough to impart meaningful lipophilic character to the product, yet still short enough that solubility in common organic solvents remains good. This combination makes it a practical choice for both quaternisation work and surface modification.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent fits naturally into synthetic work where a defined six-carbon chain must be introduced reliably and reproducibly. Research groups working on organic synthesis, materials modification, and the preparation of functionalised intermediates value a reagent that behaves consistently from batch to batch, since it removes one variable from multi-step routes and allows the alkylation step to be carried out under conditions that are straightforward to control with standard laboratory equipment.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eN-Alkylation of amines — the excellent leaving-group character of the mesylate allows hexyl chains to be attached to primary and secondary amines efficiently under mild conditions.\u003c\/li\u003e\n\u003cli\u003eQuaternisation of tertiary amines and nitrogen heterocycles — the reagent converts neutral nitrogen centres into quaternary ammonium species carrying a lipophilic six-carbon tail.\u003c\/li\u003e\n\u003cli\u003eS-Alkylation of thiols — thiolate anions react readily with this mesylate, giving hexyl thioethers without recourse to less stable or less reactive alkyl halide reagents.\u003c\/li\u003e\n\u003cli\u003eO-Alkylation of phenols and carboxylate anions — the stable methanesulfonate conjugate base supports clean substitution, making it useful for preparing hexyl ethers and esters.\u003c\/li\u003e\n\u003cli\u003eSurface and materials modification — the hexyl chain imparts meaningful lipophilic character to modified substrates while retaining good solubility in common organic solvents.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eProduct code: H1282\u003c\/li\u003e\n\u003cli\u003eCAS number: 16156-50-6\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in the pack sizes listed on this product page\u003c\/li\u003e\n\u003cli\u003eStorage: store according to the conditions stated on the manufacturer's label and safety data sheet\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the container tightly closed in a cool, dry, and well-ventilated area, away from heat sources, direct sunlight, and incompatible materials, following the conditions stated on the manufacturer's label and safety data sheet. Keep the material in its original container or in a chemically compatible, clearly labelled vessel, and reseal it promptly after each use to limit exposure to moisture and air. As an alkylating reagent, it should be handled in a fume hood using appropriate personal protective equipment, including safety glasses, chemical-resistant gloves, and a laboratory coat. Avoid contact with skin and eyes and avoid inhalation of vapours. Dispose of residues and contaminated materials in accordance with institutional chemical waste procedures and applicable local regulations.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48087267705050,"sku":"TCI2510H128234074","price":3358000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48087267737818,"sku":"TCI2510H128234075","price":10322000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510H1282.jpg?v=1767117725"},{"product_id":"tci2510i005534997","title":"TCI I0055 542-69-8 1-Iodobutane (stabilized with Copper chip)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI I0055 1-Iodobutane (stabilized with Copper chip) is a straight-chain, four-carbon haloalkane reagent that occupies an important position as a butylating agent in organic synthesis laboratories. The compound belongs to the non-heterocyclic building block class, meaning it serves as a basic starting material used to install the n-butyl group onto the framework of target molecules through nucleophilic substitution reactions. On the researcher's bench, a reagent of this kind acts as the bridge between simple starting materials and more complex molecules, whether for methodology research, the development of functional materials, or the preparation of reference compounds that are not commercially available in finished form.\u003c\/p\u003e\n\u003cp\u003eThe characteristic that makes 1-iodobutane a frequent choice lies in its carbon–iodine bond, which is relatively weak compared with other carbon–halogen bonds, so that the iodide ion functions as an excellent leaving group. As a consequence, alkylation reactions often proceed under milder conditions, with shorter reaction times and lower temperatures than would be required using the corresponding bromide or chloride analogues. This product is supplied as a liquid stabilized with a copper chip, a stabilizer that serves to bind and suppress the free iodine formed during storage, helping the reagent remain usable over a longer working period.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, reagents of this type are typically used in university organic chemistry research groups, government research institutes, and industrial development units that carry out small-scale synthesis. They appear in postgraduate research programmes, in the preparation of intermediates for further study, and in teaching laboratories that demonstrate substitution chemistry. Because the material is handled in modest quantities, it is commonly ordered as a bench reagent and drawn upon across multiple experiments rather than consumed in a single run.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eNucleophilic substitution studies: the excellent iodide leaving group makes this reagent a dependable substrate for demonstrating and investigating SN2 reaction behaviour under controlled laboratory conditions.\u003c\/li\u003e\n\u003cli\u003eN-butylation of nucleophiles: the reagent transfers an n-butyl group to amines, alcohols, thiols, and other nucleophilic centres, allowing chemists to build substituted derivatives from simpler precursors.\u003c\/li\u003e\n\u003cli\u003eSynthesis of non-heterocyclic building blocks: as a straight-chain alkyl halide, it extends carbon frameworks and supplies the four-carbon unit needed to assemble more elaborate target structures.\u003c\/li\u003e\n\u003cli\u003ePreparation of reference and comparison compounds: laboratories use it to make n-butyl-substituted standards that are not available commercially in finished form for analytical comparison.\u003c\/li\u003e\n\u003cli\u003eMethodology and functional materials research: milder alkylation conditions let researchers test new synthetic routes or modify materials without exposing sensitive substrates to elevated temperatures.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 542-69-8\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePhysical form: liquid, stabilized with a copper chip\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in the standard TCI catalogue pack sizes; please confirm the required size when ordering\u003c\/li\u003e\n\u003cli\u003eStorage note: keep in the tightly closed original container, protected from light, in a cool and well-ventilated place\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the reagent in its original tightly closed container in a cool, dry, and well-ventilated area away from direct sunlight, since light exposure encourages the formation of free iodine. Do not remove the copper chip, as it serves as the stabilizer for the material. Use amber glass or the supplier's original packaging rather than transferring the liquid into unsuitable containers. Handle the reagent inside a fume hood while wearing chemical-resistant gloves, safety goggles, and a laboratory coat. Keep it away from strong oxidizing agents and heat sources, close the container immediately after dispensing, and dispose of residues and contaminated materials through the laboratory's chemical waste procedure.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48087350804698,"sku":"TCI2510I005534997","price":531000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48087350837466,"sku":"TCI2510I005534998","price":4039000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510I0055.jpg?v=1769142656"},{"product_id":"tci2510i005835002","title":"TCI I0058 75-03-6 Iodoethane (stabilized with Copper chip)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eIodoethane is a chemical compound widely used in organic reactions for the synthesis of complex molecules. It serves as a key building block in the formation of carbon-iodine bonds, which are essential in nucleophilic substitution and alkylation reactions. This compound plays a crucial role in laboratory settings, where it is used as a precursor for the production of various compounds with applications in pharmaceuticals, materials science, and organic chemistry. Its ability to participate in multiple reaction types makes it an indispensable tool for chemists working on synthetic pathways.\u003c\/p\u003e\n\u003cp\u003eIodoethane is known for its chemical stability, although it remains highly reactive under certain conditions. The addition of a copper chip stabilizes the compound, enhancing its safety during handling and use. This stabilization makes it a preferred choice for laboratories seeking reliable and safe reagents. Its reactivity and utility in a wide range of chemical processes make it a versatile material for both research and educational purposes.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Iodoethane is commonly used in organic chemistry research, particularly in higher education institutions and research centers. It is frequently employed in experiments requiring substitution reactions, where its reactivity and stability contribute to successful outcomes. Its presence in these settings highlights its importance as a fundamental reagent in both academic and industrial chemical applications.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis experiments where carbon-iodine bond formation is essential for creating complex molecular structures.\u003c\/li\u003e\n\u003cli\u003eNucleophilic substitution reactions that require a reactive iodide source for efficient reaction pathways.\u003c\/li\u003e\n\u003cli\u003eAlkylation processes in the development of pharmaceutical compounds and specialty chemicals.\u003c\/li\u003e\n\u003cli\u003eEducational laboratory settings for teaching fundamental organic chemistry concepts and reaction mechanisms.\u003c\/li\u003e\n\u003cli\u003eResearch applications in material science for the synthesis of polymers and functional materials.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 75-03-6\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Liquid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dark place away from heat and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eIodoethane should be stored in a cool, dark environment to maintain its stability and prevent degradation. It is recommended to use sealed containers made of materials compatible with its chemical properties, such as glass or stainless steel. Due to its volatility and potential toxicity, proper ventilation is essential in the laboratory. Personal protective equipment, including gloves and safety goggles, should be worn during handling. Avoid exposure to open flames or high temperatures, as the compound is flammable. Regular monitoring of storage conditions ensures the safety and effectiveness of the material in experimental use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48087351099610,"sku":"TCI2510I005835002","price":505000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48087351132378,"sku":"TCI2510I005835003","price":1062000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48087351165146,"sku":"TCI2510I005835004","price":3863000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510I0058.jpg?v=1769056466"},{"product_id":"tci2510i006835021","title":"TCI I0068 107-08-4 1-Iodopropane (stabilized with Copper chip)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1-Iodopropane is a chemical compound widely used as a foundational reagent in various laboratory applications. It serves as a key building block in organic synthesis, particularly in reactions involving nucleophilic substitution and elimination. Its simple molecular structure allows for high reactivity under different experimental conditions, making it a versatile tool for chemists. This compound is commonly found in both academic and industrial research settings, where it plays a crucial role in the development of complex organic molecules.\u003c\/p\u003e\n\u003cp\u003eThe properties of 1-Iodopropane make it a preferred choice for laboratory use. The presence of iodine in its molecular chain provides strong reactivity and the ability to participate in a wide range of chemical reactions. Additionally, the stabilization with a copper chip enhances its stability, reducing the risk of decomposition during storage and use. This makes it more reliable for long-term applications, especially in environments where consistent performance is essential. Its compatibility with various reagents and solvents further contributes to its popularity among researchers.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 1-Iodopropane is extensively used in both educational and research contexts. It is an essential component in university chemistry curricula and research institutions, particularly in organic synthesis experiments. Its role in teaching and practical applications ensures that it remains a vital resource for students and professionals alike. The compound’s reliability and effectiveness make it a standard item in many laboratory setups across Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis experiments benefit from 1-Iodopropane due to its reactivity and role in forming alkyl halides and esters.\u003c\/li\u003e\n\u003cli\u003eNucleophilic substitution reactions often utilize this compound because of its iodine content, which facilitates reaction mechanisms.\u003c\/li\u003e\n\u003cli\u003eElimination reactions in laboratory settings frequently involve 1-Iodopropane due to its ability to participate in such processes.\u003c\/li\u003e\n\u003cli\u003eTeaching laboratories use this compound to demonstrate fundamental chemical reactions and molecular structures.\u003c\/li\u003e\n\u003cli\u003eResearch institutions rely on 1-Iodopropane for the development of complex organic compounds and heterocyclic structures.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 107-08-4\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities\u003c\/li\u003e\n\u003cli\u003ePhysical form: Liquid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and incompatible materials\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003e1-Iodopropane should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to keep the compound in a sealed container made of materials compatible with its chemical properties, such as glass or high-density polyethylene. Due to its reactivity, it should be handled in a well-ventilated area, preferably under a fume hood, to minimize exposure. Avoid contact with incompatible substances like strong oxidizing agents or bases. Always wear appropriate personal protective equipment, including gloves and safety goggles, when handling this compound. Regular monitoring of storage conditions ensures the stability and safety of the material in the laboratory setting.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48087351820506,"sku":"TCI2510I006835021","price":733000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48087351853274,"sku":"TCI2510I006835022","price":1970000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48087351886042,"sku":"TCI2510I006835023","price":5856000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510I0068.jpg?v=1769142658"},{"product_id":"tci2510i006935024","title":"TCI I0069 75-30-9 2-Iodopropane (stabilized with Copper chip)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2-Iodopropane (stabilized with Copper chip) is a chemical compound widely used in laboratory settings for its reactivity and versatility. As a building block in organic chemistry, it plays a crucial role in the synthesis of various organic compounds. Its simple molecular structure allows it to participate in multiple chemical reactions, making it an essential tool for researchers. This compound is particularly valuable in reactions that require high reactivity and the ability to form complex molecules through functional group transformations.\u003c\/p\u003e\n\u003cp\u003eThe reactivity of 2-iodopropane is attributed to the presence of iodine, a highly electronegative halogen atom. This property makes it ideal for nucleophilic substitution and alkylation reactions. The inclusion of a copper chip as a stabilizer enhances its safety by reducing the risk of decomposition and uncontrolled reactions. This stabilization ensures that the compound remains stable during storage and use, making it a reliable choice for laboratory applications.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 2-Iodopropane is commonly used in organic chemistry research, especially in universities and research institutions. Its role in synthesizing complex molecules and its stability under controlled conditions make it a preferred material for both academic and industrial research. The compound's ability to react with various functional groups supports its use in a wide range of chemical processes and experimental designs.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis reactions benefit from 2-Iodopropane due to its reactivity and ability to form complex molecules through nucleophilic substitution.\u003c\/li\u003e\n\u003cli\u003eAlkylation processes often utilize this compound as a versatile reagent for introducing alkyl groups into organic frameworks.\u003c\/li\u003e\n\u003cli\u003eResearch in functional group transformations relies on 2-Iodopropane for its capacity to participate in diverse chemical mechanisms.\u003c\/li\u003e\n\u003cli\u003eStability under controlled conditions makes it suitable for long-term storage and repeated use in experimental setups.\u003c\/li\u003e\n\u003cli\u003eIt is commonly used in academic settings for teaching and research in organic chemistry, supporting both theoretical and practical learning.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 75-30-9\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities\u003c\/li\u003e\n\u003cli\u003ePhysical form: Liquid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003e2-Iodopropane should be stored in a cool, dry place away from direct sunlight to maintain its stability. It is recommended to use sealed containers to prevent exposure to air and moisture. Due to its reactivity, it should be handled in a well-ventilated area, preferably under a fume hood. The presence of a copper chip as a stabilizer reduces the risk of decomposition, but care should still be taken to avoid contact with incompatible substances. Proper personal protective equipment, such as gloves and safety goggles, should be worn during handling to ensure laboratory safety.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48087351918810,"sku":"TCI2510I006935024","price":733000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48087351951578,"sku":"TCI2510I006935025","price":1616000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48087351984346,"sku":"TCI2510I006935026","price":4721000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510I0069.jpg?v=1768360884"},{"product_id":"tci2510i106236408","title":"TCI I1062 16156-53-9 Isobutyl Methanesulfonate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eIsobutyl Methanesulfonate (IMS) is a chemical compound widely utilized in organic synthesis reactions within laboratory settings. As a key building block, IMS plays a crucial role in facilitating various chemical transformations, particularly in substitution and nucleophilic reactions. Its structural characteristics allow it to act as an effective electrophilic reagent, making it a versatile component in synthetic pathways. IMS is commonly used as a starting material for the synthesis of complex organic molecules that require specific reactivity. Its stability under controlled conditions makes it a reliable reagent for laboratory applications.\u003c\/p\u003e\n\u003cp\u003eIMS is preferred due to its consistent chemical properties and stability in laboratory environments. It exhibits good solubility in organic solvents such as ethyl acetate and ethanol, which simplifies mixing and reaction processes. The compound’s ability to function as an electron donor enhances its reactivity in polar environments, making it suitable for a range of synthetic procedures. Its predictable behavior and compatibility with various reaction conditions contribute to its popularity among chemists.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, IMS is extensively used in chemical research, particularly in the development of new compounds and molecular modifications. It is a common reagent in both educational and applied research settings, supporting both teaching and experimental work. Many research institutions and universities rely on IMS for its reliability and effectiveness in various chemical processes.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis reactions benefit from IMS due to its reactivity and stability, enabling efficient chemical transformations.\u003c\/li\u003e\n\u003cli\u003eMolecular modification projects utilize IMS to create complex structures with controlled reactivity and functional groups.\u003c\/li\u003e\n\u003cli\u003eEducational laboratories use IMS to demonstrate nucleophilic and substitution reactions, providing hands-on learning experiences.\u003c\/li\u003e\n\u003cli\u003eIndustrial research applications incorporate IMS for its consistent performance in large-scale chemical processes.\u003c\/li\u003e\n\u003cli\u003eAnalytical chemistry experiments rely on IMS for its solubility and reactivity in polar solvents, aiding in compound characterization.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 16156-53-9\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various sizes as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Liquid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eIMS should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to use airtight containers made of glass or polyethylene to prevent contamination and maintain chemical integrity. As a reactive compound, IMS should be handled with appropriate personal protective equipment, including gloves and safety goggles. It is important to ensure proper ventilation in the workspace to minimize exposure. IMS is not flammable but should be kept away from incompatible materials. Regular monitoring of storage conditions ensures the compound remains stable and suitable for laboratory use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087438033114,"sku":"TCI2510I106236408","price":986000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48087438065882,"sku":"TCI2510I106236409","price":3005000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510I1062.jpg?v=1767120733"},{"product_id":"tci2510m060738357","title":"TCI M0607 62-50-0 Ethyl Methanesulfonate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eEthyl Methanesulfonate (EMS) is a chemical compound widely used in laboratory applications, particularly in the synthesis of organic compounds. As a versatile building block, EMS plays a crucial role in various chemical reactions, especially in the formation of heterocyclic compounds and complex functional groups. Its simple molecular structure allows for efficient participation in substitution and replacement reactions, making it a valuable reagent in synthetic chemistry. Due to its reactivity, EMS is often employed in reactions that require precise functional group modifications.\u003c\/p\u003e\n\u003cp\u003eEMS is known for its high reactivity, especially towards bases and polar compounds. This reactivity makes it a preferred choice for chemists seeking efficient and effective synthetic pathways. Its ability to undergo nucleophilic substitution reactions under controlled conditions ensures its utility in a wide range of chemical transformations. Additionally, EMS is a strong alkylating agent, which contributes to its effectiveness in modifying molecular structures. These properties make it a reliable and powerful reagent in organic synthesis.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, EMS is commonly used in organic chemistry research, particularly in the synthesis of compounds requiring methyl substitution or complex chemical reactions. It is also utilized in molecular modification studies, where its reactivity and versatility are highly valued. Due to its role in creating structurally diverse compounds, EMS remains an essential component in many experimental setups within the chemical research community in Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis where EMS is used for methyl substitution reactions due to its strong alkylating properties.\u003c\/li\u003e\n\u003cli\u003eHeterocyclic compound formation as EMS facilitates the construction of complex ring structures through substitution.\u003c\/li\u003e\n\u003cli\u003eFunctional group modification in chemical reactions where precise structural changes are required.\u003c\/li\u003e\n\u003cli\u003eResearch in molecular modification studies due to its reactivity and ability to participate in various chemical transformations.\u003c\/li\u003e\n\u003cli\u003eDevelopment of new chemical compounds in synthetic chemistry applications requiring efficient reagents.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 62-50-0\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory supply\u003c\/li\u003e\n\u003cli\u003ePhysical form: Liquid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eEthyl Methanesulfonate should be stored in a cool, dry place, away from moisture and direct sunlight. It is recommended to use sealed containers made of materials resistant to chemical corrosion, such as glass or high-density polyethylene. Due to its corrosive and irritating properties, proper personal protective equipment, including gloves and safety goggles, should be worn when handling EMS. It is essential to ensure good ventilation in the laboratory to prevent inhalation of vapors. EMS should be kept in a secure location, away from incompatible substances like strong bases or oxidizing agents. Always follow standard laboratory safety protocols to minimize exposure and ensure safe handling.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48087549903066,"sku":"TCI2510M060738357","price":1944000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48087549935834,"sku":"TCI2510M060738358","price":5276000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510M0607.jpg?v=1767123325"},{"product_id":"tci2510m064138403","title":"TCI M0641 21124-13-0 1-Methyl-3-p-tolyltriazene [for Esterification]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1-Methyl-3-p-tolyltriazene is a chemical compound widely used in laboratory settings for its role in esterification reactions. This compound serves as a key building block in organic synthesis, enabling the creation of complex molecular structures. Its unique chemical properties make it an essential reagent for chemists working on various synthetic pathways. Due to its reactivity, it is particularly valuable in reactions requiring substitution or functional group modification. Its presence in the chemical toolkit of Indonesian laboratories underscores its importance in both academic and industrial research.\u003c\/p\u003e\n\u003cp\u003eThe compound's reactivity and structural versatility make it a preferred choice for synthetic chemists. Its triazene group allows for participation in multiple chemical reactions, offering flexibility in reaction design. While it exhibits stability under certain conditions, it is sensitive to moisture and UV light, which necessitates careful handling and storage. These properties make it ideal for applications where controlled chemical transformations are required, ensuring reliable results in experimental procedures.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 1-Methyl-3-p-tolyltriazene is commonly used in organic chemistry research, especially in the development of new compounds and molecular modifications. Its role in esterification processes is critical for producing esters and related derivatives. Researchers in Indonesia rely on this compound for its ability to facilitate complex chemical transformations, supporting both educational and applied research initiatives.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis applications benefit from its reactivity and structural versatility, allowing for the creation of complex molecules.\u003c\/li\u003e\n\u003cli\u003eEsterification processes utilize its ability to participate in substitution reactions, enhancing the efficiency of chemical transformations.\u003c\/li\u003e\n\u003cli\u003eResearch in molecular modification leverages its triazene group for targeted chemical modifications and functional group introduction.\u003c\/li\u003e\n\u003cli\u003eChemical reaction optimization relies on its stability under controlled conditions, ensuring consistent results in experimental setups.\u003c\/li\u003e\n\u003cli\u003eAcademic and industrial research projects use it as a key reagent in developing new compounds and exploring synthetic pathways.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 21124-13-0\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified in the provided data\u003c\/li\u003e\n\u003cli\u003ePhysical form: Not specified in the provided data\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and UV light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to use sealed containers to prevent exposure to moisture and UV light, which can affect its reactivity. Due to its sensitivity, it should be handled with care, using appropriate personal protective equipment. Proper storage conditions are essential to ensure its effectiveness in laboratory applications. Laboratory staff should be trained in safe handling procedures to minimize risks associated with its reactivity. Regular monitoring of storage conditions is advised to maintain the integrity of the compound.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087552000218,"sku":"TCI2510M064138403","price":1162000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48087552032986,"sku":"TCI2510M064138404","price":11232000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510M0641.jpg?v=1767123401"},{"product_id":"tci2510m119339178","title":"TCI M1193 25236-64-0 2,2,2-Trifluoroethyl Methanesulfonate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2,2,2-Trifluoroethyl Methanesulfonate is a fluorinated building block widely used in organic chemistry for the synthesis of complex compounds. This reagent plays a crucial role in laboratory settings, particularly in reactions involving substitution or nucleophilic mechanisms. Its electrophilic nature makes it a valuable tool in the formation of fluorinated compounds, which are essential in pharmaceutical and material science applications. Due to its molecular stability and high reactivity, it is a preferred choice for researchers aiming to achieve precise control over molecular structures during synthesis.\u003c\/p\u003e\n\u003cp\u003eThe compound's unique properties, including its polar nature and ability to form bonds with various functional groups, make it highly versatile in chemical reactions. The presence of fluorine atoms in its molecular structure enhances its reactivity and selectivity, allowing it to participate in a wide range of synthetic pathways. These characteristics make it an indispensable reagent for chemists working on fluorinated compound development, especially in research environments where precision and efficiency are paramount.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 2,2,2-Trifluoroethyl Methanesulfonate is commonly used in scientific research and chemical product development. It is a key component in studies related to fluorinated compound synthesis, supporting both academic and industrial research initiatives. Its availability in the local market ensures that researchers have access to this essential reagent for their experiments and innovations.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eFluorinated Compound Synthesis: This reagent is ideal for creating fluorinated compounds due to its reactivity and ability to form stable bonds with functional groups.\u003c\/li\u003e\n\u003cli\u003eOrganic Reaction Research: Its electrophilic nature makes it suitable for substitution and nucleophilic reactions, providing versatility in synthetic pathways.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical Development: It is used in the synthesis of drug molecules where fluorine atoms are required for enhanced biological activity and stability.\u003c\/li\u003e\n\u003cli\u003eMaterial Science Studies: The compound is employed in the creation of advanced materials with specific chemical and physical properties.\u003c\/li\u003e\n\u003cli\u003eAcademic Research: It supports teaching and research in chemistry, particularly in courses and projects involving fluorinated building blocks.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 25236-64-0\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Fluorinated Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Liquid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and incompatible materials\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to use airtight containers made of materials compatible with its chemical properties, such as glass or high-density polyethylene. Due to its reactivity, it should be handled with care, using appropriate personal protective equipment. Avoid contact with moisture and incompatible substances to prevent unwanted reactions. Proper labeling and storage conditions are essential to maintain its stability and ensure safe handling in laboratory settings.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48087591813338,"sku":"TCI2510M119339178","price":1289000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48087591846106,"sku":"TCI2510M119339179","price":3636000.0,"currency_code":"IDR","in_stock":true}]},{"product_id":"tci2510m144639535","title":"TCI M1446 16427-44-4 2-Methoxyethyl Methanesulfonate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2-Methoxyethyl Methanesulfonate is a chemical compound widely used as a building block in organic synthesis. It serves as a versatile reagent in laboratory settings, particularly in reactions where methanesulfonate groups are required for substitution or functionalization. Its role in the laboratory is critical for the development of complex molecules, especially in esterification and substitution reactions. This compound is commonly employed in synthetic pathways to introduce specific functional groups into target molecules, making it an essential tool for chemists working on molecular design and modification.\u003c\/p\u003e\n\u003cp\u003eThe compound is known for its reactivity and solubility in organic solvents, which makes it a preferred choice for a variety of chemical processes. Its ability to participate in multiple reaction types, such as nucleophilic substitution and esterification, enhances its utility in synthetic chemistry. Additionally, its stability under controlled conditions allows for predictable outcomes in laboratory experiments. These properties make it a reliable and efficient reagent for researchers aiming to achieve high yields and purity in their chemical syntheses.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 2-Methoxyethyl Methanesulfonate is extensively used in organic chemistry research. It plays a key role in the synthesis of new compounds, modification of existing molecules, and the development of chemical materials. Its widespread application in both academic and industrial research settings highlights its importance in advancing chemical innovation and scientific discovery within the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic Synthesis: Ideal for creating complex molecules through esterification and substitution reactions.\u003c\/li\u003e\n\u003cli\u003eFunctional Group Modification: Used to introduce methanesulfonate groups into target compounds for further chemical transformations.\u003c\/li\u003e\n\u003cli\u003eEsterification Reactions: Facilitates the formation of ester bonds, essential in the synthesis of various organic compounds.\u003c\/li\u003e\n\u003cli\u003eResearch and Development: Applied in the development of new chemical materials and pharmaceutical intermediates.\u003c\/li\u003e\n\u003cli\u003eAnalytical Chemistry: Serves as a reagent in analytical procedures requiring precise chemical interactions and reactions.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS Number: 16427-44-4\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack Sizes: Available in various quantities as per standard laboratory supply formats\u003c\/li\u003e\n\u003cli\u003ePhysical Form: Liquid\u003c\/li\u003e\n\u003cli\u003eStorage Note: Store in a cool, dry place away from direct light and heat\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry place, away from direct light and heat to maintain its stability and reactivity. It is recommended to use sealed containers made of materials compatible with organic solvents to prevent contamination and evaporation. Due to its reactive nature, it should be handled with appropriate personal protective equipment, including gloves and safety goggles. Proper ventilation is essential when working with this compound to minimize exposure. It is important to avoid contact with incompatible substances and to follow standard laboratory safety protocols to ensure safe handling and use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48087610786010,"sku":"TCI2510M144639535","price":2247000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48087610818778,"sku":"TCI2510M144639536","price":5705000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510M1446.jpg?v=1767125008"},{"product_id":"tci2510m201640125","title":"TCI M2016 89238-99-3 4-Methoxybenzyl 2,2,2-Trichloroacetimidate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eThe TCI M2016 89238-99-3 4-Methoxybenzyl 2,2,2-Trichloroacetimidate is a synthetic reagent widely used in laboratory settings for the formation of C-X (non-halogen) bonds. This compound plays a crucial role in organic synthesis by acting as a versatile electrophilic reagent. It is commonly employed in substitution reactions and the construction of complex molecular structures. Its unique chemical structure allows it to participate in various reaction mechanisms, making it an essential tool for chemists working in both academic and industrial environments.\u003c\/p\u003e\n\u003cp\u003eOne of the key properties that make this reagent a preferred choice is its high reactivity and solubility in organic solvents such as ethyl acetate and chloroform. These characteristics facilitate efficient dissolution and reaction processes, ensuring consistent results in synthetic procedures. Additionally, the compound's stability under controlled conditions contributes to its reliability in laboratory applications. Its ability to function as a donor in nucleophilic substitution reactions further enhances its utility in a wide range of chemical transformations.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent is highly relevant for research in organic chemistry, pharmacology, and materials science. It is frequently used in the development of new compounds, drug synthesis, and the study of heterocyclic and aromatic structures. Many research institutions and universities in Indonesia rely on this compound for its precision and effectiveness in complex synthetic processes. Its availability through AMI Scientific ensures that Indonesian researchers have access to high-quality reagents for their scientific endeavors.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis for the formation of C-X bonds in complex molecule construction due to its electrophilic nature and reactivity.\u003c\/li\u003e\n\u003cli\u003eDrug development and pharmaceutical research as it supports the synthesis of aromatic and heterocyclic compounds.\u003c\/li\u003e\n\u003cli\u003eSN1 and SN2 reaction mechanisms where it acts as a good electrophilic substrate for nucleophilic attack.\u003c\/li\u003e\n\u003cli\u003eMaterial science applications in the creation of advanced polymers and functional materials through controlled chemical reactions.\u003c\/li\u003e\n\u003cli\u003eAcademic research in universities and research institutes for teaching and experimental purposes in synthetic chemistry.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 89238-99-3\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Synthetic Reagents \u0026gt; C-X(Non-Halogen) Bond Formation [Synthetic Reagents]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard chemical reagent packaging sizes\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid or liquid depending on formulation and supplier specifications\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis reagent should be stored in a cool, dry, and well-ventilated area away from direct sunlight and sources of heat. It is recommended to use airtight containers made of glass or high-density polyethylene to prevent contamination and maintain chemical integrity. Due to its reactivity, it should be handled with appropriate personal protective equipment such as gloves and safety goggles. Avoid exposure to moisture and incompatible substances to ensure safe storage. In laboratory settings, it is important to follow standard operating procedures for chemical handling to minimize risks and ensure compliance with safety regulations.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48087642144986,"sku":"TCI2510M201640125","price":2650000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48087642177754,"sku":"TCI2510M201640126","price":9338000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510M2016.jpg?v=1771058111"},{"product_id":"tci2510o006644361","title":"TCI O0066 122-51-0 Triethyl Orthoformate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTriethyl Orthoformate from TCI, product code O0066, is the ortho ester of formic acid. Its central carbon atom carries three ethoxy groups and one hydrogen. It is a versatile reagent in organic synthesis and does three main jobs. It is a one-carbon source at the formate oxidation level. It forms diethyl acetals and ketals. It also acts as a water scavenger in moisture-sensitive reactions. For these reasons, Triethyl Orthoformate is kept on hand in almost every synthetic organic chemistry laboratory. It is classed as a non-heterocyclic building block, yet it is widely used to build heterocyclic scaffolds.\u003c\/p\u003e\n\u003cp\u003eChemists choose this reagent because it reacts readily with nucleophiles under acid catalysis. Its by-products are only ethanol and ethyl formate, and both are easy to separate from the target product, so work-up stays simple. When it meets water, the compound consumes that water. In acetal formation, this shifts the equilibrium toward the product and improves conversion without extra drying steps. As a one-carbon source, it can close rings when heterocycles such as benzimidazoles, imidazoles, triazoles and quinazolinones are made from diamine or amino-amide precursors. Because it is a liquid, it is also easy to measure and dispense accurately.\u003c\/p\u003e\n\u003cp\u003eIn Indonesia, Triethyl Orthoformate is widely used in university organic chemistry laboratories, in medicinal chemistry research, and in the development of pharmaceutical and agrochemical active ingredients. Students and researchers use it for thesis work, synthesis practicals and multi-step routes where they need a dependable formylating or protecting reagent. Research groups making heterocyclic compounds for bioactivity screening use it as a standard one-carbon reagent. Industrial R\u0026amp;D teams use it when developing and optimizing synthetic routes, where consistent reagent quality helps results stay reproducible between batches.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAcetal and ketal protection: it converts aldehydes and ketones into diethyl acetals or ketals under acid catalysis, and its water-consuming action pushes the equilibrium toward the protected product.\u003c\/li\u003e\n\u003cli\u003eHeterocycle ring closure: it serves as a one-carbon source to cyclize diamine or amino-amide precursors into benzimidazoles, imidazoles, triazoles and quinazolinones, which are common scaffolds in medicinal chemistry.\u003c\/li\u003e\n\u003cli\u003eWater scavenging in moisture-sensitive reactions: it reacts with traces of water in the reaction mixture, which helps keep conditions dry for transformations that suffer when moisture is present.\u003c\/li\u003e\n\u003cli\u003eFormate-level one-carbon introduction: it delivers a single carbon at the formate oxidation level to nucleophiles, so chemists can build formyl-derived functional groups and intermediates in a controlled way.\u003c\/li\u003e\n\u003cli\u003eTeaching and research synthesis: its liquid form is easy to measure, and its easily separated by-products (ethanol and ethyl formate) make it practical for university practicals, thesis projects and route development work.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI (product code O0066)\u003c\/li\u003e\n\u003cli\u003eCAS number: 122-51-0\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in the pack sizes offered by TCI; please ask AMI Scientific for the options currently available\u003c\/li\u003e\n\u003cli\u003ePhysical form: liquid\u003c\/li\u003e\n\u003cli\u003eStorage note: moisture-sensitive; keep the container tightly closed in a cool, dry place\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eTriethyl Orthoformate reacts with water, so protect it from moisture at all times. Keep it in its original, tightly sealed container in a cool, dry, well-ventilated area, away from heat, open flames and other ignition sources. Store it away from acids and oxidizing agents. After each use, close the container quickly, and flush it with dry inert gas if possible to protect the remaining reagent. Handle it in a fume hood and wear suitable gloves, safety glasses and a laboratory coat. Avoid breathing vapors and avoid contact with skin and eyes. Always read the supplier's Safety Data Sheet before use. Dispose of waste according to institutional and local regulations.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mL","offer_id":48087883350234,"sku":"TCI2510O006644361","price":505000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48087883383002,"sku":"TCI2510O006644362","price":960000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510O0066.jpg?v=1767131293"},{"product_id":"tci2510o006844365","title":"TCI O0068 149-73-5 Trimethyl Orthoformate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTrimethyl Orthoformate from TCI, product code O0068, is the ortho ester of formic acid. Its central carbon atom carries three methoxy groups and one hydrogen atom. It is the methyl counterpart of triethyl orthoformate and one of the basic reagents in organic synthesis laboratories. Chemists use it to form dimethyl acetals and ketals, as a one-carbon source for closing heterocyclic rings, and to take up water in reactions that must stay anhydrous. Its range of uses makes it a regular item on the reagent shelf in research and teaching laboratories.\u003c\/p\u003e\n\u003cp\u003eChemists often choose this reagent over its ethyl analogue because it is smaller and because its by-products, methanol and methyl formate, have low boiling points and are easy to remove after the reaction. Dimethyl acetals made with it are generally easier to cleave than diethyl acetals, which suits temporary protection strategies where the carbonyl group must be recovered later. Combined with methanol and an acid catalyst, it converts ketones into dimethyl ketals very effectively. It is also used to prepare methyl esters and enol ethers. Because it is a liquid, it can be measured out conveniently by volume.\u003c\/p\u003e\n\u003cp\u003eIn Indonesia, Trimethyl Orthoformate is widely needed by organic chemistry, medicinal chemistry, and process development laboratories at universities and in the pharmaceutical industry. It is often used to synthesise drug intermediates, where protecting carbonyl groups and building heterocyclic frameworks are routine steps. Academic research groups use it for multistep synthesis projects and student research. Industrial process chemists value its easily removed by-products when they scale reactions from the bench toward pilot production.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eDimethyl acetal and ketal formation: with methanol and an acid catalyst, the reagent converts aldehydes and ketones into dimethyl acetals and ketals efficiently, which helps protect carbonyl groups during multistep synthesis.\u003c\/li\u003e\n\u003cli\u003eTemporary carbonyl protection: dimethyl acetals from this reagent are generally easier to cleave than diethyl acetals, so they suit strategies where the carbonyl must be recovered under mild conditions.\u003c\/li\u003e\n\u003cli\u003eHeterocyclic ring closure: the orthoformate carbon acts as a one-carbon source for closing heterocyclic rings, which makes it a useful building block when constructing heterocyclic frameworks for medicinal chemistry.\u003c\/li\u003e\n\u003cli\u003eWater scavenging in anhydrous reactions: the reagent reacts with water, so it can remove moisture from reactions that must stay dry and help push equilibria toward the desired product.\u003c\/li\u003e\n\u003cli\u003ePreparation of methyl esters and enol ethers: it is used to make methyl esters and enol ethers, and its volatile by-products, methanol and methyl formate, are easy to remove during workup.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI (product code O0068)\u003c\/li\u003e\n\u003cli\u003eCAS number: 149-73-5\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: please see the product listing for available pack sizes\u003c\/li\u003e\n\u003cli\u003ePhysical form: liquid\u003c\/li\u003e\n\u003cli\u003eStorage: keep tightly closed, dry, and away from moisture; follow the TCI label and Safety Data Sheet\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore Trimethyl Orthoformate in its original tightly sealed container in a cool, dry, well-ventilated area, away from heat and ignition sources. Because the reagent reacts with water, keep the container closed when not in use so moisture does not degrade it. Transfer it with dry glassware and syringes, and consider working under an inert atmosphere for moisture-sensitive reactions. Handle it in a fume hood, and wear safety glasses, chemical-resistant gloves, and a lab coat. Always follow the storage conditions, hazard information, and disposal instructions in the TCI Safety Data Sheet and product label.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mL","offer_id":48087883514074,"sku":"TCI2510O006844365","price":455000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48087883546842,"sku":"TCI2510O006844366","price":986000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510O0068.jpg?v=1767131302"},{"product_id":"tci2510o021544568","title":"TCI O0215 4447-60-3 Triisopropyl Orthoformate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTriisopropyl Orthoformate from TCI (product code O0215) is an orthoester of formic acid: a compound with a single central carbon atom bonded to three isopropoxy groups. Orthoesters are versatile reagents in organic synthesis, used mainly to form acetals and ketals, in formylation reactions, and to scavenge water in moisture-sensitive reactions. In the laboratory, this material works both as an activated one-carbon source and as a way to shift reaction equilibria toward the desired product, which makes it a useful reagent for synthetic chemists.\u003c\/p\u003e\n\u003cp\u003eChemists choose this reagent because its isopropoxy groups are bulkier than the methoxy or ethoxy groups of smaller orthoformates, so it can react differently and more selectively when a synthesis calls for it. Orthoformates react with water to form a formate ester and an alcohol. This lets them bind the water released during acetalization and drive the reaction to completion. With amines, orthoformates can form formamidines or take part in heterocycle synthesis, for example of benzimidazoles. The reagent is sensitive to acid and moisture, so it must be handled correctly to stay effective.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent is relevant to research groups in organic synthesis and medicinal chemistry, and to teams developing synthetic routes to target compounds. University chemistry departments, pharmaceutical research units and industrial R\u0026amp;D laboratories may use it for protecting carbonyl groups, building heterocyclic scaffolds and carrying out water-sensitive transformations. Because the material comes from TCI, a well-known reagent brand, it is a consistent choice for teams that need reproducible results in routine and exploratory synthesis work.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAcetal and ketal formation: the orthoester supplies the alkoxy groups and consumes the water released, pushing carbonyl protection reactions toward completion under mild acid catalysis.\u003c\/li\u003e\n\u003cli\u003eWater scavenging in moisture-sensitive reactions: because orthoformates react with water to form a formate ester and an alcohol, the reagent helps keep reaction mixtures dry and shifts equilibria toward products.\u003c\/li\u003e\n\u003cli\u003eFormylation reactions: as an activated one-carbon source, triisopropyl orthoformate can add a formyl-equivalent carbon to suitable substrates in multistep organic synthesis routes.\u003c\/li\u003e\n\u003cli\u003eFormamidine synthesis: reaction with amines can give formamidines, which are useful intermediates and functional groups in synthetic and medicinal chemistry research programs.\u003c\/li\u003e\n\u003cli\u003eHeterocycle construction, such as benzimidazoles: the orthoformate provides the single carbon needed to close the ring when it reacts with suitable diamine precursors in heterocyclic synthesis.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI (product code O0215)\u003c\/li\u003e\n\u003cli\u003eCAS number: 4447-60-3\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in the pack sizes offered by TCI for this product code; please check the product page for current options\u003c\/li\u003e\n\u003cli\u003ePhysical form: liquid\u003c\/li\u003e\n\u003cli\u003eStorage note: sensitive to moisture and acid; keep the container tightly sealed in a cool, dry place\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore Triisopropyl Orthoformate in its original, tightly closed container in a cool, dry, well-ventilated area, away from moisture, acids and sources of ignition. Because the reagent reacts with water, reseal the container promptly after each use. Where possible, keep it under an inert atmosphere such as dry nitrogen or argon to preserve its reactivity. Use clean, dry glassware and syringes when dispensing it. Handle the material in a fume hood and wear appropriate personal protective equipment, including safety glasses, chemical-resistant gloves and a laboratory coat. Keep it separate from strong acids and oxidizing agents. Always read the supplier's Safety Data Sheet before use and follow your institution's chemical safety and waste disposal procedures.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mL","offer_id":48087893999834,"sku":"TCI2510O021544568","price":1162000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510O0215.jpg?v=1767131591"},{"product_id":"tci2510o026944637","title":"TCI O0269 588-43-2 Tributyl Orthoformate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTributyl Orthoformate (TCI O0269), with CAS number 588-43-2, is a chemical compound widely used in organic laboratory settings. As an ester of formic acid, it plays a crucial role in various organic reactions, particularly in substitution and replacement reactions. Its simple molecular structure makes it a versatile building block for the synthesis of more complex compounds. This compound is especially valuable in the development of heterocyclic and complex molecular structures, where stability and reactivity are key factors. Its presence in laboratory research supports the advancement of chemical synthesis techniques and the exploration of new chemical pathways.\u003c\/p\u003e\n\u003cp\u003eTributyl Orthoformate is known for its chemical stability under specific conditions, which enhances its usability and storage convenience. It is a colorless liquid with a distinct odor, making it easily identifiable in laboratory environments. Its non-reactive nature in certain conditions makes it a preferred choice for reactions requiring high stability. This property ensures that it remains a reliable reagent in a wide range of synthetic processes. Additionally, its availability in various packaging options makes it a practical choice for researchers working in different laboratory settings.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Tributyl Orthoformate is commonly used in organic chemistry research, especially by academic institutions and research organizations. Its role in the synthesis of complex molecules and heterocyclic compounds makes it an essential component of many research projects. The compound’s reliability and availability contribute to its widespread use in both educational and industrial research environments.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis reactions where stability and reactivity are crucial for the formation of complex molecules.\u003c\/li\u003e\n\u003cli\u003ePreparation of heterocyclic compounds due to its role as a building block in the synthesis of such structures.\u003c\/li\u003e\n\u003cli\u003eSubstitution and replacement reactions where Tributyl Orthoformate acts as a reagent with controlled reactivity.\u003c\/li\u003e\n\u003cli\u003eResearch in chemical engineering and pharmaceutical development that requires reliable and stable chemical intermediates.\u003c\/li\u003e\n\u003cli\u003eEducational purposes in academic laboratories for teaching and demonstrating organic chemistry techniques.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 588-43-2\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various sizes as per supplier offerings\u003c\/li\u003e\n\u003cli\u003ePhysical form: Colorless liquid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eTributyl Orthoformate should be stored in a cool, dry location, away from direct sunlight and sources of heat. It is recommended to use sealed containers made of materials compatible with its chemical properties, such as glass or high-density polyethylene. Due to its liquid form, it should be kept in properly labeled containers to prevent spills and contamination. In laboratory settings, it is important to ensure good ventilation and avoid exposure to incompatible substances. Regular inspection of storage containers is advised to maintain the integrity of the compound and ensure safe handling. Proper storage conditions help preserve its chemical stability and ensure its effectiveness in laboratory applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mL","offer_id":48087898357978,"sku":"TCI2510O026944637","price":3787000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510O0269.jpg?v=1767131678"},{"product_id":"tci2510t013650853","title":"TCI T0136 75-57-0 Tetramethylammonium Chloride","description":"\u003cp\u003e\u003cstrong\u003eTetramethylammonium Chloride\u003c\/strong\u003e (CAS 75-57-0) is a high-quality chemical from TCI, supplied as \u003cstrong\u003eReagent Grade \/ for Synthesis\u003c\/strong\u003e.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eApplication:\u003c\/strong\u003e Synthesis reagent for a wide range of organic chemistry transformations in laboratory and industrial 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Indonesia.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48088291803354,"sku":"TCI2510T013650853","price":455000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48088291836122,"sku":"TCI2510T013650854","price":1718000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510T0136.jpg?v=1768363097"},{"product_id":"tci2510t026851049","title":"TCI T0268 80-40-0 Ethyl p-Toluenesulfonate","description":"\u003cp\u003e\u003cstrong\u003eEthyl p-Toluenesulfonate\u003c\/strong\u003e (CAS 80-40-0) is a high-quality chemical from TCI, supplied as \u003cstrong\u003eGC Grade \/ for Synthesis\u003c\/strong\u003e.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eApplication:\u003c\/strong\u003e Synthesis reagent for a wide range of organic chemistry transformations in laboratory and industrial 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Indonesia.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48088302518490,"sku":"TCI2510T026851049","price":531000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48088302551258,"sku":"TCI2510T026851050","price":2752000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510T0268.jpg?v=1767139721"},{"product_id":"tci2510t026951051","title":"TCI T0269 80-48-8 Methyl p-Toluenesulfonate","description":"\u003cp\u003e\u003cstrong\u003eMethyl p-Toluenesulfonate\u003c\/strong\u003e (CAS 80-48-8) is a high-quality chemical from TCI, supplied as \u003cstrong\u003eGC Grade \/ for Synthesis\u003c\/strong\u003e.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eApplication:\u003c\/strong\u003e Synthesis reagent for a wide range of organic chemistry transformations in laboratory and industrial 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Indonesia.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48088302649562,"sku":"TCI2510T026951051","price":481000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48088302682330,"sku":"TCI2510T026951052","price":1541000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510T0269.jpg?v=1767139725"},{"product_id":"tci2510t067651578","title":"TCI T0676 75-59-2 Tetramethylammonium Hydroxide (10% in Methanol)","description":"\u003cp\u003e\u003cstrong\u003eTetramethylammonium Hydroxide (10% in Methanol)\u003c\/strong\u003e (CAS 75-59-2) is a high-quality chemical from TCI, supplied as \u003cstrong\u003eReagent Grade\u003c\/strong\u003e.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eApplication:\u003c\/strong\u003e Synthesis reagent for a wide range of organic chemistry transformations in laboratory and industrial 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Indonesia.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mL","offer_id":48275462652122,"sku":"TCI2510T067651578","price":481000.0,"currency_code":"IDR","in_stock":true},{"title":"100mL","offer_id":48275462684890,"sku":"TCI2510T067651579","price":1162000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510T0676.jpg?v=1768206334"},{"product_id":"tci2510t072651634","title":"TCI T0726 599-91-7 Propyl p-Toluenesulfonate","description":"\u003cp\u003e\u003cstrong\u003ePropyl p-Toluenesulfonate\u003c\/strong\u003e (CAS 599-91-7) is a high-quality chemical from TCI, supplied as \u003cstrong\u003eGC Grade \/ for Synthesis\u003c\/strong\u003e.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eApplication:\u003c\/strong\u003e Synthesis reagent for a wide range of organic chemistry transformations in laboratory and industrial 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Indonesia.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mL","offer_id":48088340398298,"sku":"TCI2510T072651634","price":1465000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48088340431066,"sku":"TCI2510T072651635","price":9742000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510T0726.jpg?v=1767140449"},{"product_id":"tci2510t072751636","title":"TCI T0727 778-28-9 Butyl p-Toluenesulfonate","description":"\u003cp\u003e\u003cstrong\u003eButyl p-Toluenesulfonate\u003c\/strong\u003e (CAS 778-28-9) is a high-quality chemical from TCI, supplied as \u003cstrong\u003eGC Grade \/ for Synthesis\u003c\/strong\u003e.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eApplication:\u003c\/strong\u003e Synthesis reagent for a wide range of organic chemistry transformations in laboratory and industrial 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