{"title":"Benzothiophenes [Small Molecule Semiconductor Building Blocks]","description":"\u003cp\u003e\u003cstrong\u003eBenzothiophenes [Small Molecule Semiconductor Building Blocks]\u003c\/strong\u003e — mencakup senyawa aromatik berinti benzotiofena dan dibenzotiofena, termasuk turunan terhalogenasi, terboronasi, dan tergugus alkoksi maupun alkiltimah, yang menampilkan sistem elektron terkonjugasi kaya sulfur. Golongan ini menjadi unit pembangun inti bagi molekul semikonduktor organik.\u003c\/p\u003e\u003cp\u003eBenzothiophenes dipakai peneliti elektronik organik sebagai blok bangun pada sintesis material semikonduktor melalui reaksi kopling silang, misalnya untuk menyusun oligomer dan polimer terkonjugasi yang dipakai pada sel surya organik dan transistor film tipis. Turunan terboronasi dan terstanilasi berperan sebagai mitra reaksi dalam kopling Suzuki atau Stille untuk memperpanjang sistem konjugasi molekul.\u003c\/p\u003e\u003cp\u003eContoh produk dalam koleksi ini: \u003ca href=\"\/en\/products\/tci2510t385055557\"\u003eTCI T3850 2195419-19-1 10-(Triethylsilyl)benzo[lmn]thieno[2,3-f][3,8]phenanthroline-1,3,6,8(2H,7H)-tetraone\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b552312174\"\u003eTCI B5523 17347-32-9 6-Bromobenzo[b]thiophene\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510t323654800\"\u003eTCI T3236 912824-84-1 4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)dibenzothiophene\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b555112210\"\u003eTCI B5551 248-70-4 Benzo[b]benzo[4,5]thieno[2,3-d]thiophene\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b549012140\"\u003eTCI B5490 1160823-78-8 4,8-Bis[(2-ethylhexyl)oxy]-2,6-bis(trimethylstannyl)benzo[1,2-b:4,5-b']dithiophene\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b558912258\"\u003eTCI B5589 7342-82-7 3-Bromobenzo[b]thiophene\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b548512134\"\u003eTCI B5485 1352642-35-3 4,8-Bis[5-(2-ethylhexyl)thiophen-2-yl]benzo[1,2-b:4,5-b']dithiophene\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b575212484\"\u003eTCI B5752 1448185-87-2 N-([1,1'-Biphenyl]-4-yl)dibenzo[b,d]thiophen-4-amine\u003c\/a\u003e.\u003c\/p\u003e\u003cp\u003ePerhatikan jenis gugus fungsi reaktif (halogen, boronat, atau trimetilstanil) yang menentukan kompatibilitas dengan reaksi kopling tertentu, serta kemurnian yang memengaruhi konsistensi sifat elektronik material akhir. 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 Small Molecule Semiconductor Building Blocks, sering dipakai bersamaan dalam satu alur kerja laboratorium:\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-carbazoles-small-molecule-semiconductor-building-blocks\"\u003eCarbazoles [Small Molecule Semiconductor Building Blocks]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-fluorenes-fluorenones-small-molecule-semiconductor-building-blocks\"\u003eFluorenes, Fluorenones [Small Molecule Semiconductor Building Blocks]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-thiophenes-small-molecule-semiconductor-building-blocks\"\u003eThiophenes [Small Molecule Semiconductor Building Blocks]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-anthracenes-anthraquinones-small-molecule-semiconductor-building-blocks\"\u003eAnthracenes, Anthraquinones [Small Molecule Semiconductor Building Blocks]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-small-molecule-semiconductor-building-blocks-others\"\u003eSmall Molecule Semiconductor Building Blocks (Others)\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-secondary-arylamines-small-molecule-semiconductor-building-blocks\"\u003eSecondary Arylamines [Small Molecule Semiconductor Building Blocks]\u003c\/a\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eKembali ke \u003ca href=\"\/en\/collections\/tci-l3-small-molecule-semiconductor-building-blocks\"\u003eSmall Molecule Semiconductor Building Blocks\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":"tci2510b552312174","title":"TCI B5523 17347-32-9 6-Bromobenzo[b]thiophene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e6-Bromobenzo[b]thiophene (CAS 17347-32-9) is a brominated heteroaromatic compound widely used as a synthetic building block in organic chemistry laboratories. It serves as a key substrate in transition-metal-catalyzed cross-coupling reactions for constructing benzo[b]thiophene-based molecules. Its main applications include pharmaceutical and agrochemical research, as well as the development of functional organic materials.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085885223130,"sku":"TCI2510B552312174","price":3598000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5523.jpg?v=1767092466"},{"product_id":"tci2510b555112210","title":"TCI B5551 248-70-4 Benzo[b]benzo[4,5]thieno[2,3-d]thiophene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBenzo[b]benzo[4,5]thieno[2,3-d]thiophene is a high-purity fused thiophene-based organic semiconductor widely utilized in advanced electronic materials research. It exhibits excellent charge carrier mobility, making it a preferred active-layer material for organic field-effect transistors (OFETs) and flexible electronic devices. This compound is also commonly employed in printed logic circuits and organic sensor development due to its rigid, planar molecular structure that enables high-quality crystalline thin-film formation.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48085886599386,"sku":"TCI2510B555112210","price":957000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48085886632154,"sku":"TCI2510B555112211","price":3345000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5551.jpg?v=1768815817"},{"product_id":"tci2510b558912258","title":"TCI B5589 7342-82-7 3-Bromobenzo[b]thiophene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e3-Bromobenzo[b]thiophene (CAS 7342-82-7) is a heterocyclic building block featuring a bromine substituent at the 3-position of the benzothiophene core, making it a highly versatile intermediate for cross-coupling reactions such as Suzuki-Miyaura, Heck, and Sonogashira couplings. This compound is widely employed in medicinal chemistry research for synthesizing bioactive molecules, as the benzothiophene scaffold is prevalent in anti-inflammatory, antimicrobial, and anticancer agents. It also finds application in the development of functional organic materials, including organic semiconductors, OLED components, and sulfur-based chemical sensors.\u003c\/p\u003e\n\u003cp\u003e---\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48085889450202,"sku":"TCI2510B558912258","price":1771000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085889482970,"sku":"TCI2510B558912259","price":6156000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5589_fdda2eaf-0144-46a0-ad3e-4a869471c649.jpg?v=1767862516"},{"product_id":"tci2510b575212484","title":"TCI B5752 1448185-87-2 N-([1,1'-Biphenyl]-4-yl)dibenzo[b,d]thiophen-4-amine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B5752 N-([1,1'-Biphenyl]-4-yl)dibenzo[b,d]thiophen-4-amine is a small molecule semiconductor building block designed for organic electronics research. Featuring a dibenzothiophene core coupled with a biphenyl-amine moiety, this compound offers excellent charge transport characteristics and thermal stability suitable for device fabrication. It serves as a key precursor in the development of hole-transport materials and emissive layers for OLEDs, OFETs, and organic photovoltaic applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48085900820698,"sku":"TCI2510B575212484","price":2475000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48085900853466,"sku":"TCI2510B575212485","price":9557000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5752.jpg?v=1768815881"},{"product_id":"tci2510b582112570","title":"TCI B5821 171364-86-6 2-(Benzo[b]thiophen-3-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B5821, with the CAS number 171364-86-6, is a highly specialized organoboron compound known as 2-(Benzo[b]thiophen-3-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane. This reagent plays a crucial role in the field of organometallic chemistry, particularly in synthetic processes that require precise and efficient chemical transformations. It is widely used in laboratories for its ability to participate in various coupling reactions, making it an essential tool for chemists working on complex molecule synthesis. Its unique structure combines a benzo[b]thiophen-3-yl group with a tetramethyl-dioxaborolane core, enabling it to interact effectively with transition metals in catalytic systems.\u003c\/p\u003e\n\u003cp\u003eThe compound is valued for its stability under controlled laboratory conditions and its reactivity in a variety of chemical environments. These properties make it a preferred choice for researchers aiming to achieve high yields and consistent results in synthetic reactions. Its compatibility with a range of catalysts and its ability to undergo selective transformations contribute to its widespread use in advanced chemical applications. Additionally, the compound's versatility allows it to be adapted to different synthetic strategies, enhancing its utility in both academic and industrial research settings.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent is commonly used in organic chemistry research, especially in pharmaceutical development, material science, and environmental chemistry. Its reliability and effectiveness in promoting efficient chemical reactions make it a vital component in the toolkit of chemists working on innovative projects. Its application in these fields underscores its importance in advancing scientific discovery and technological development in Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis for creating complex molecular structures due to its reactivity in coupling reactions.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research for developing new drugs through efficient synthetic pathways involving organoboron reagents.\u003c\/li\u003e\n\u003cli\u003eMaterial science applications in the production of advanced polymers and functional materials.\u003c\/li\u003e\n\u003cli\u003eEnvironmental chemistry studies for the synthesis of compounds used in pollution control and remediation.\u003c\/li\u003e\n\u003cli\u003eCatalytic processes in industrial settings where transition metal-based reactions are required for high efficiency.\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: 171364-86-6\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron [Organometallic Reagents]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory reagent packaging\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid or liquid, depending on the specific formulation and packaging\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, 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 with moisture and air, it should be handled in a fume hood when possible, and appropriate personal protective equipment should be worn. Regular monitoring of storage conditions is essential to ensure the compound remains stable and effective for laboratory use. Always follow standard safety protocols to minimize exposure and ensure safe handling in a controlled environment.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085905047770,"sku":"TCI2510B582112570","price":4470000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5821.jpg?v=1768204445"},{"product_id":"tci2510b586112624","title":"TCI B5861 65642-94-6 1-Bromodibenzothiophene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1-Bromodibenzothiophene (CAS 65642-94-6) is a brominated dibenzothiophene derivative widely used as a heterocyclic building block in organic synthesis, particularly in cross-coupling reactions to construct complex molecular architectures. This compound plays a key role in materials science research, including the development of organic semiconductors, OLED emitters, and organic field-effect transistors (OFETs). It is also employed in medicinal chemistry as a core scaffold for exploring novel sulfur-containing pharmaceutical candidates.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085907079386,"sku":"TCI2510B586112624","price":4610000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5861.jpg?v=1767092857"},{"product_id":"tci2510b594012713","title":"TCI B5940 189097-35-6 5-Bromobenzo[b]naphtho[1,2-d]thiophene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B5940 5-Bromobenzo[b]naphtho[1,2-d]thiophene is a brominated heterocyclic building block designed for advanced organic synthesis in research laboratories. This compound serves as a versatile intermediate for coupling reactions and the construction of complex molecular architectures. Its fused naphthothiophene core with strategic bromo substitution makes it particularly valuable for materials science research, including organic semiconductors and optoelectronic materials, as well as medicinal chemistry applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085910683866,"sku":"TCI2510B594012713","price":3824000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085910716634,"sku":"TCI2510B594012714","price":13183000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5940_db32dcbc-a1c3-483c-8a96-afb7b367078f.jpg?v=1767863919"},{"product_id":"tci2510b624713078","title":"TCI B6247 1398397-58-4 2-Bromo[1]benzothieno[3,2-b][1]benzothiophene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2-Bromo[1]benzothieno[3,2-b][1]benzothiophene is a brominated benzothienobenzothiophene (BTBT) derivative that serves as a versatile building block for synthesizing small-molecule organic semiconductors. The bromine substituent enables further functionalization via cross-coupling reactions, such as Suzuki-Miyaura or Stille coupling, to access advanced π-conjugated materials. These resulting materials are widely employed in the fabrication of organic field-effect transistors (OFETs), organic photovoltaics (OPVs), and flexible printed electronic devices.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48085926248666,"sku":"TCI2510B624713078","price":6943000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6247.jpg?v=1769144643"},{"product_id":"tci2510c245717228","title":"TCI C2457 19404-18-3 5-Chloro-3-methylbenzo[b]thiophene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e5-Chloro-3-methylbenzo[b]thiophene is an organic compound widely used in scientific research related to chemistry and materials science. It plays a crucial role in the study of molecular structures and electronic properties, particularly in the development of semiconductor materials. As a fundamental building block in the synthesis of complex compounds, this compound is essential for laboratories requiring precision and accuracy in chemical experiments. Its unique chemical structure, featuring a thiophene ring with sulfur atoms, contributes to its reactivity and versatility in various synthetic pathways.\u003c\/p\u003e\n\u003cp\u003eThis compound is preferred due to its complex heterocyclic structure and the presence of chlorine and methyl groups at specific positions. These functional groups influence the stability and reactivity of the molecule, making it ideal for substitution and functionalization reactions. Its specific chemical properties allow for precise control over molecular structures in synthesis processes, which is vital for the creation of advanced materials. The presence of sulfur further enhances its utility in reactions involving electron transfer and redox processes.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 5-Chloro-3-methylbenzo[b]thiophene is commonly used in material research, especially in organic chemistry and semiconductor technology. Local researchers utilize this compound to develop new materials with applications in electrochemistry and electronic devices. Its role in advancing scientific innovation makes it a valuable resource for both academic and industrial research settings.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis research benefits from this compound due to its reactivity and structural versatility in creating complex molecules.\u003c\/li\u003e\n\u003cli\u003eSemiconductor material development utilizes its electronic properties for designing advanced electronic components.\u003c\/li\u003e\n\u003cli\u003eElectrochemical studies leverage its redox behavior for investigating electron transfer mechanisms in new materials.\u003c\/li\u003e\n\u003cli\u003eMaterial characterization experiments rely on its unique molecular structure for analyzing chemical interactions and stability.\u003c\/li\u003e\n\u003cli\u003eFunctionalization reactions use its substitutable groups for modifying molecular properties in targeted applications.\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: 19404-18-3\u003c\/li\u003e\n\u003cli\u003eCategory: Materials Science \u0026gt; Material Building Blocks \u0026gt; Small Molecule Semiconductor 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: Solid, crystalline appearance\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture\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 light and moisture to maintain its chemical integrity. It is recommended to use airtight containers made of materials that are chemically inert, such as glass or high-density polyethylene, to prevent contamination and degradation. In laboratory settings, it is important to handle the compound with appropriate personal protective equipment, including gloves and safety goggles, to ensure safety during handling and experimentation. Proper ventilation should be maintained when working with this compound to minimize exposure to vapors. Regular monitoring of storage conditions is advised to ensure optimal preservation and usability of the material.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086127182042,"sku":"TCI2510C245717228","price":2671000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086127214810,"sku":"TCI2510C245717229","price":8545000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2457.jpg?v=1769180396"},{"product_id":"tci2510d014819480","title":"TCI D0148 132-65-0 Dibenzothiophene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eDibenzothiophene is a chemical compound classified under the heterocyclic category and is commonly used as a building block in the synthesis of complex compounds. This compound is widely utilized in laboratory settings for its unique reactivity and structural versatility. Its molecular structure consists of two aromatic rings connected by a single sulfur atom, which imparts specific chemical behavior and makes it a valuable reagent in organic chemistry. Due to its ability to participate in various chemical reactions, it is a key component in the development of new pharmaceuticals, advanced materials, and other specialized chemical products.\u003c\/p\u003e\n\u003cp\u003eOne of the main reasons for its popularity is its chemical stability under certain conditions, combined with its reactivity in the presence of heat or catalysts. This dual nature allows it to be used in a wide range of synthetic pathways. Additionally, its solubility in organic solvents makes it highly convenient for use in laboratory experiments. The compound’s complex molecular structure also makes it an essential material for the synthesis of other heterocyclic compounds, further enhancing its utility in chemical research.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Dibenzothiophene is frequently used in research involving substitution reactions and aromatic chemistry. Its role in the development of new compounds and its compatibility with various experimental setups make it a preferred choice for chemists working in both academic and industrial settings. Its properties and applications align well with the needs of modern chemical research in Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSynthesis of Heterocyclic Compounds: Dibenzothiophene is ideal for creating complex heterocyclic structures due to its unique sulfur-containing ring system.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical Research: It is used in the development of new drugs because of its ability to participate in various chemical reactions.\u003c\/li\u003e\n\u003cli\u003eOrganic Chemistry Experiments: Its reactivity and solubility make it a versatile reagent for a wide range of synthetic reactions.\u003c\/li\u003e\n\u003cli\u003eMaterial Science Studies: It is employed in the creation of advanced materials due to its structural properties and chemical stability.\u003c\/li\u003e\n\u003cli\u003eAromatic Reaction Studies: Its role in substitution and aromatic reactions makes it a key component in studying reaction mechanisms.\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: 132-65-0\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier guidelines\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\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\u003eDibenzothiophene 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 exposure to moisture and air. Due to its reactivity under certain conditions, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. It is important to store it separately from strong oxidizing agents and incompatible substances to avoid any potential chemical reactions. Regular inspection of storage conditions is advised to ensure the compound remains in optimal condition for laboratory use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086349480154,"sku":"TCI2510D014819480","price":704000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086349512922,"sku":"TCI2510D014819481","price":2250000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D0148.jpg?v=1767100932"},{"product_id":"tci2510d222322331","title":"TCI D2223 1207-15-4 2,8-Dimethyldibenzothiophene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D2223 2,8-Dimethyldibenzothiophene is a sulfur-containing heterocyclic compound built on a dibenzothiophene skeleton carrying two methyl groups at the 2 and 8 positions. The dibenzothiophene framework is widely recognised in laboratory work as the representative aromatic sulfur species that is difficult to remove from petroleum fractions, which is why its derivatives are routinely employed as model compounds and comparison standards. The presence of methyl groups on both sides of the ring system brings this molecule even closer to the profile of the real sulfur compounds found in diesel fuel and crude oil.\u003c\/p\u003e\n\u003cp\u003eThe properties that make this compound a preferred choice are its high stability and its clearly defined substitution pattern. The fused aromatic rings make it a stable solid that does not readily decompose during storage or analysis, so it is well suited for use as a long-term reference material. The sulfur atom in the thiophene position is less reactive than that of ordinary thiols or sulfides, and this is precisely the reason the compound is used to test the robustness of desulfurisation catalysts. In addition, its extended conjugated framework gives it luminescence and ultraviolet absorption characteristics that are of interest in organic electronic materials research.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is typically used where a well-defined aromatic sulfur reference is needed rather than a general-purpose reagent. It supports petroleum and fuel-related research groups working on desulfurisation, analytical laboratories that need a consistent comparison compound for sulfur determination, and materials chemistry groups exploring heterocyclic building blocks. As a heterocyclic building block, it also serves synthesis work in university and institutional research laboratories where reproducible starting materials matter.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eHydrodesulfurisation catalyst evaluation — the hindered, low-reactivity thiophenic sulfur makes it a demanding test substrate that reveals the true performance limits of a desulfurisation catalyst.\u003c\/li\u003e\n\u003cli\u003eModel compound studies for petroleum fractions — its methyl substitution pattern mimics the refractory sulfur species actually present in diesel fuel and crude oil samples.\u003c\/li\u003e\n\u003cli\u003eReference and comparison standard in sulfur analysis — the defined substitution pattern and stable solid form give consistent, reproducible results across repeated analytical runs.\u003c\/li\u003e\n\u003cli\u003eOrganic electronic materials research — the extended conjugated aromatic framework provides luminescence and ultraviolet absorption behaviour useful when screening heterocyclic cores for device applications.\u003c\/li\u003e\n\u003cli\u003eHeterocyclic synthesis building block — the stable dibenzothiophene skeleton with fixed 2,8-substitution serves as a reliable starting point for constructing more complex sulfur heterocycles.\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: 1207-15-4\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003eChemical name: 2,8-Dimethyldibenzothiophene\u003c\/li\u003e\n\u003cli\u003ePhysical form: solid\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in standard TCI catalogue pack sizes; please confirm the required size when ordering\u003c\/li\u003e\n\u003cli\u003eStorage: store in a closed container in a cool, dry, well-ventilated area\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the material in its original tightly closed container in a cool, dry and well-ventilated place, away from direct sunlight, heat sources and incompatible substances such as strong oxidising agents. Amber glass or the supplier's original packaging is suitable for keeping the solid protected from light and moisture. Handle the compound in a fume hood and use appropriate personal protective equipment, including safety goggles, gloves and a laboratory coat, and avoid generating or inhaling dust when weighing out portions. Keep the container closed when not in use, return it promptly to its designated storage location, and dispose of residues and contaminated materials in accordance with the applicable chemical waste procedures at your institution. Always consult the manufacturer's Safety Data Sheet before first use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48086505357530,"sku":"TCI2510D222322331","price":4386000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D2223.jpg?v=1767104429"},{"product_id":"tci2510d224522368","title":"TCI D2245 31574-87-5 2,8-Dibromodibenzothiophene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2,8-Dibromodibenzothiophene is a chemical compound widely used in scientific research within the fields of materials science and organic chemistry. As a building block for advanced materials, it plays a crucial role in the synthesis of complex compounds that find applications in semiconductor development, polymer engineering, and composite materials. Its unique molecular structure enables it to be a foundational element in creating materials with specific functional properties. This compound is particularly valued for its versatility in laboratory settings where precise chemical reactions are required.\u003c\/p\u003e\n\u003cp\u003eThe compound's aromatic structure and bromine substituents contribute to its chemical stability while allowing for controlled reactivity under specific conditions. These characteristics make it a preferred choice for researchers aiming to manipulate molecular structures with precision. Its ability to participate in various synthetic pathways enhances its utility in developing new materials with tailored properties. The compound’s chemical profile also makes it suitable for studies focused on reactivity and stability in organic systems.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 2,8-Dibromodibenzothiophene is commonly used in research related to semiconductor materials and polymers. Local research institutions leverage this compound to advance technologies in electrochemistry and innovative material development. Its availability in the local market supports ongoing scientific endeavors, ensuring that researchers have access to essential materials for their work.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSemiconductor material development: This compound is used to synthesize advanced semiconductor materials due to its structural versatility and chemical reactivity.\u003c\/li\u003e\n\u003cli\u003ePolymer synthesis: It serves as a building block for creating specialized polymers with unique electronic and mechanical properties.\u003c\/li\u003e\n\u003cli\u003eComposite material research: Its chemical stability allows it to be integrated into composite formulations for enhanced performance.\u003c\/li\u003e\n\u003cli\u003eOrganic reactivity studies: The compound's bromine groups make it ideal for investigating reaction mechanisms and stability under different conditions.\u003c\/li\u003e\n\u003cli\u003eElectrochemical applications: It is utilized in the development of electrochemical systems due to its ability to participate in controlled redox 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: 31574-87-5\u003c\/li\u003e\n\u003cli\u003eCategory: Materials Science \u0026gt; Material Building Blocks \u0026gt; Polymer\/Macromolecule Semiconductor 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: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct sunlight and moisture\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 moisture to maintain its chemical stability. It is recommended to use airtight containers made of materials that are chemically inert, such as glass or high-density polyethylene, to prevent contamination and degradation. Due to its bromine content, it should be handled with care, ensuring proper ventilation in the laboratory to minimize exposure. Standard laboratory safety protocols should be followed, including the use of personal protective equipment when handling or disposing of the compound. Proper labeling and storage conditions are essential to ensure the compound remains safe and effective for research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086506701018,"sku":"TCI2510D224522368","price":873000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086506733786,"sku":"TCI2510D224522369","price":2896000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086506766554,"sku":"TCI2510D224522370","price":8966000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D2245.jpg?v=1768817611"},{"product_id":"tci2510d395424393","title":"TCI D3954 909280-97-3 2,6-Dibromobenzo[1,2-b:4,5-b']dithiophene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2,6-Dibromobenzo[1,2-b:4,5-b']dithiophene is a semiconductor building block based on the benzodithiophene framework, a fused aromatic system that combines one benzene ring with two thiophene rings in a symmetrical arrangement. The two bromine atoms at the 2 and 6 positions make it a bifunctional monomer that is ready for use in cross-coupling reactions to construct conjugated polymers and oligomers. In materials science laboratories, this unit ranks among the most widely used electron-donor units in the design of active materials for organic solar cells and organic transistors, largely because its framework is exceptionally flat and rigid.\u003c\/p\u003e\n\u003cp\u003eThe characteristic that drives its selection is the planar fused geometry, which promotes regular intermolecular pi-stacking in the solid state. That tightly packed arrangement increases orbital overlap, so charge-carrier mobility within thin films is improved. The sulfur content of the two thiophene rings also contributes interchain interactions that stabilize film morphology. The high molecular symmetry ensures that the resulting polymers have a regular repeating structure free of regioisomeric defects, while the carbon-bromine bonds at the alpha positions of the thiophene rings are highly reactive toward cross-coupling chemistry.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this building block is typically encountered in university and institutional research groups working on organic electronics, conjugated polymer synthesis, and thin-film device fabrication. It is normally used at small synthetic scale on a Schlenk line or in an inert-atmosphere setup, where the monomer is coupled with complementary comonomers and the resulting material is characterized and then processed into thin films for device evaluation.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eConjugated polymer synthesis: the two alpha-positioned bromine atoms act as reactive handles for cross-coupling polymerization, allowing controlled chain growth with complementary comonomers.\u003c\/li\u003e\n\u003cli\u003eOrganic solar cell active layers: the benzodithiophene unit serves as a strong electron-donor segment, and its rigid planar core supports the ordered morphology such devices depend on.\u003c\/li\u003e\n\u003cli\u003eOrganic transistor semiconductor materials: regular pi-stacking and enlarged orbital overlap in the solid state translate into improved charge-carrier mobility across the deposited thin-film channel.\u003c\/li\u003e\n\u003cli\u003eOligomer and model compound preparation: the bifunctional, highly symmetric structure lets researchers build well-defined conjugated oligomers without introducing regioisomeric defects into the sequence.\u003c\/li\u003e\n\u003cli\u003eStructure-property relationship studies: the fused framework and thiophene sulfur atoms provide a fixed reference unit for investigating how backbone planarity influences film morphology and electronic behaviour.\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: D3954\u003c\/li\u003e\n\u003cli\u003eCAS number: 909280-97-3\u003c\/li\u003e\n\u003cli\u003eChemical name: 2,6-Dibromobenzo[1,2-b:4,5-b']dithiophene\u003c\/li\u003e\n\u003cli\u003eCategory: Materials Science \u0026gt; Material Building Blocks \u0026gt; Polymer\/Macromolecule Semiconductor Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in standard TCI research-scale packaging; please confirm the pack size when ordering\u003c\/li\u003e\n\u003cli\u003eStorage: keep in the original tightly closed container as indicated on the manufacturer's label\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the material in its original tightly closed container in a cool, dry, well-ventilated area away from direct sunlight, heat sources, and incompatible chemicals, following the storage conditions stated on the manufacturer's label and safety data sheet. Amber glass or the supplied original packaging is suitable, and transferring under an inert atmosphere is advisable when the compound will be used in moisture- or air-sensitive coupling reactions. Handle it inside a fume hood using safety glasses, gloves, and a laboratory coat, avoid generating dust during weighing, and keep containers clearly labelled. Collect residues and contaminated consumables as chemical waste for disposal through the established laboratory waste route.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086647767258,"sku":"TCI2510D395424393","price":6690000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086647800026,"sku":"TCI2510D395424394","price":21894000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D3954.jpg?v=1768817982"},{"product_id":"tci2510d405724534","title":"TCI D4057 108847-20-7 Dibenzothiophene-4-boronic Acid (contains varying amounts of Anhydride)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D4057 Dibenzothiophene-4-boronic Acid (CAS 108847-20-7) is an organoboron reagent that carries a boronic acid group at the 4-position of the dibenzothiophene framework. As is common for aromatic boronic acids, this product contains varying amounts of the boroxine anhydride formed by natural intermolecular dehydration. In synthetic laboratories, the compound serves as the nucleophilic partner in Suzuki-Miyaura cross-coupling reactions, the most reliable method for forming carbon-carbon bonds between two aromatic fragments. With this reagent, a dibenzothiophene unit can be attached directly and efficiently onto a target molecular scaffold.\u003c\/p\u003e\n\u003cp\u003eThe property that makes this reagent widely chosen is the character of the dibenzothiophene unit itself. Its rigid, electron-rich tricyclic framework provides high thermal stability, a large triplet energy, and good hole-transporting behaviour, which is why it has become a favoured motif in the design of organic light-emitting diode materials. The 4-position, located adjacent to the sulfur atom, gives a distinctive substitution geometry that influences molecular shape and solid-state packing. It should be noted that the presence of the anhydride causes the effective molecular weight to vary, so stoichiometric calculations should account for this.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent is typically used in university and institutional research groups working on organic synthesis, functional materials, and optoelectronics, as well as in industrial R\u0026amp;D units developing new molecular scaffolds. It is normally handled in gram or sub-gram quantities on the bench, weighed out for coupling reactions under inert atmosphere, and stored alongside other moisture-sensitive organometallic reagents in a controlled chemical store.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSuzuki-Miyaura cross-coupling: acts as the nucleophilic boron partner that transfers the dibenzothiophene fragment to an aryl halide, forming a robust biaryl carbon-carbon bond under palladium catalysis.\u003c\/li\u003e\n\u003cli\u003eOLED material synthesis: introduces a dibenzothiophene unit whose high triplet energy and thermal stability make it a preferred building block for host and charge-transport materials.\u003c\/li\u003e\n\u003cli\u003eHole-transport layer development: the electron-rich tricyclic core imparts good hole-transporting character, so the reagent is useful when constructing molecules intended for hole-transporting functions.\u003c\/li\u003e\n\u003cli\u003eFunctional aromatic scaffold construction: allows direct, efficient attachment of a rigid sulfur-containing tricycle onto larger conjugated frameworks without multi-step protection or functional group manipulation.\u003c\/li\u003e\n\u003cli\u003eStructure-property studies: substitution at the 4-position adjacent to sulfur gives distinctive geometry, letting researchers examine how substitution pattern affects molecular shape and solid-state packing.\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: 108847-20-7\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron [Organometallic Reagents]\u003c\/li\u003e\n\u003cli\u003eComposition note: contains varying amounts of the corresponding boroxine anhydride\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in standard TCI catalogue pack sizes; please confirm the required size when ordering\u003c\/li\u003e\n\u003cli\u003eStorage note: keep tightly closed in a cool, dry place, protected 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, well-ventilated chemical store, away from moisture and sources of ignition. Aromatic boronic acids absorb water and undergo further dehydration to the boroxine on standing, so the container should be closed promptly after each use and, where practicable, kept under an inert atmosphere. Weigh the solid in a fume hood using clean, dry spatulas and glassware. Wear a laboratory coat, safety glasses, and chemically resistant gloves. Because the anhydride content varies, verify stoichiometry before use and consult the manufacturer's safety data sheet for full handling guidance.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086653501658,"sku":"TCI2510D405724534","price":1659000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086653534426,"sku":"TCI2510D405724535","price":5312000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D4057.jpg?v=1769141943"},{"product_id":"tci2510d415324665","title":"TCI D4153 1016-05-3 Dibenzothiophene 5,5-Dioxide","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D4153 Dibenzothiophene 5,5-Dioxide is a heterocyclic compound built on a dibenzothiophene skeleton in which the sulfur atom has been fully oxidized to a sulfone group. It is classified as a heterocyclic building block because its flat tricyclic framework frequently serves as the core of functional molecules. In the laboratory, this material is used both as a synthetic starting material and as a reference compound in sulfur chemistry studies, particularly research that examines how organosulfur compounds behave during oxidation, adsorption, or subsequent catalytic reactions.\u003c\/p\u003e\n\u003cp\u003eThe property that makes it a preferred choice is the sulfone group, which is strongly electron-withdrawing while remaining thermally and chemically stable. This combination lowers the electron density across both benzene rings, making the framework robust toward harsh reaction conditions while still allowing functionalization through aromatic substitution or directed coupling reactions. Because it acts as a rigid, planar electron acceptor, the compound is also of interest for optoelectronic materials research that requires acceptor units with high rigidity. That same stability is what makes the material convenient to handle and store.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is typically encountered in university and institutional research settings working on organosulfur chemistry, catalysis, and functional organic materials. It serves as a well-defined reference substance when comparing oxidation states of sulfur-containing aromatics, and as a starting scaffold when researchers construct larger heterocyclic targets. Its stability under ordinary bench conditions makes it practical for laboratories that store building blocks over extended project periods.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis starting material — the rigid tricyclic core provides a defined scaffold that can be elaborated through aromatic substitution or directed coupling into larger functional molecules.\u003c\/li\u003e\n\u003cli\u003eSulfur chemistry reference compound — representing the fully oxidized sulfone state, it serves as a benchmark when researchers compare oxidation levels of organosulfur aromatics.\u003c\/li\u003e\n\u003cli\u003eOxidation behaviour studies — because the sulfur is already fully oxidized to the sulfone, it acts as a defined endpoint for investigations into organosulfur oxidation pathways.\u003c\/li\u003e\n\u003cli\u003eAdsorption and catalytic reaction research — its chemical robustness allows it to be carried through demanding catalytic and adsorption experiments without degradation of the core framework.\u003c\/li\u003e\n\u003cli\u003eOptoelectronic materials research — the planar, rigid, electron-accepting sulfone framework suits work that requires acceptor units with high structural rigidity and thermal stability.\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: 1016-05-3\u003c\/li\u003e\n\u003cli\u003eProduct code: D4153\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in standard TCI catalogue pack sizes; please confirm the size required when ordering\u003c\/li\u003e\n\u003cli\u003eStorage: store in a closed container 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\u003eStore the compound in its original tightly closed container, kept in a cool, dry and well-ventilated area away from direct sunlight, moisture and strong oxidizing agents. Amber glass or the supplier's original packaging is suitable for keeping the solid protected from light and humidity. Handle in a fume hood using gloves, safety glasses and a laboratory coat, and avoid generating or inhaling dust when weighing the solid. Keep containers clearly labelled, reseal them promptly after use, and consult the manufacturer's safety data sheet before handling or disposal.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086658351322,"sku":"TCI2510D415324665","price":1462000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086658384090,"sku":"TCI2510D415324666","price":5004000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D4153.jpg?v=1767107156"},{"product_id":"tci2510d505225869","title":"TCI D5052 83834-12-2 3,7-Dibromodibenzothiophene 5,5-Dioxide","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e3,7-Dibromodibenzothiophene 5,5-Dioxide is a chemical compound widely used in scientific research, particularly in the field of materials science. This compound plays a crucial role in the development of advanced materials due to its unique molecular structure. It serves as a building block for the synthesis of complex organic compounds, making it an essential tool for researchers working on polymer and semiconductor applications. Its presence in laboratory settings enables the creation of innovative materials with tailored properties, supporting both academic and industrial research.\u003c\/p\u003e\n\u003cp\u003eThe compound is valued for its chemical stability and specificity, which make it a preferred choice in laboratory environments. Its ability to form bonds with various functional groups allows for precise chemical modifications, enhancing its versatility in synthetic processes. The compound's stability under normal laboratory conditions ensures consistent results and minimizes the risk of degradation during storage and use. These properties make it a reliable and efficient material for a wide range of chemical experiments and material development projects.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 3,7-Dibromodibenzothiophene 5,5-Dioxide is commonly used in material science research, especially in the development of polymers and semiconductors. It is a key component in the synthesis of advanced materials, contributing to the growth of scientific innovation in the region. Many research institutions in Indonesia rely on this compound for its reliability and effectiveness in experimental processes.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePolymer synthesis for creating high-performance materials with tailored properties.\u003c\/li\u003e\n\u003cli\u003eSemiconductor research to develop new electronic components and devices.\u003c\/li\u003e\n\u003cli\u003eOrganic chemistry experiments requiring precise molecular modifications.\u003c\/li\u003e\n\u003cli\u003eMaterial characterization studies to analyze structural and functional properties.\u003c\/li\u003e\n\u003cli\u003eAdvanced chemical synthesis for the production of complex organic 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: 83834-12-2\u003c\/li\u003e\n\u003cli\u003eCategory: Materials Science \u0026gt; Material Building Blocks \u0026gt; Polymer\/Macromolecule Semiconductor Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture\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 moisture to maintain its chemical stability. It is recommended to use airtight containers to prevent exposure to air and humidity, which could affect its integrity. Due to its chemical nature, it should be handled with appropriate personal protective equipment, including gloves and safety goggles, to ensure laboratory safety. Proper ventilation is essential when working with this material to minimize inhalation risks. Regular inspection of storage conditions is advised to ensure long-term stability and usability in research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48086742073562,"sku":"TCI2510D505225869","price":2082000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D5052.jpg?v=1769180688"},{"product_id":"tci2510d552126442","title":"TCI D5521 7428-91-3 Dibenzo[b,d]thiophen-2-amine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eDibenzo[b,d]thiophen-2-amine is a chemical compound widely used in scientific research, particularly in the field of materials science. As a small molecule semiconductor building block, it plays a crucial role in the development of advanced materials. Its complex molecular structure enables it to participate in various chemical reactions, making it a valuable tool for researchers aiming to modify material properties. In the laboratory, this compound is often employed as a foundational element for creating new materials with enhanced performance and stability.\u003c\/p\u003e\n\u003cp\u003eThe unique chemical properties of Dibenzo[b,d]thiophen-2-amine make it a preferred choice for material scientists. It exhibits chemical stability and the ability to form bonds with a variety of other molecules, which is essential for creating functional materials. Its molecular structure allows for controlled reactivity, ensuring consistent results in experimental settings. These characteristics make it ideal for applications requiring precision and reliability in material synthesis and modification.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Dibenzo[b,d]thiophen-2-amine is commonly used in material science and technology research. It is an essential component in the development of semiconductors and construction materials, contributing to the advancement of scientific innovation. Its versatility and chemical properties support a wide range of experimental needs, making it a reliable resource for researchers in the field.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSemiconductor material development: This compound is ideal for creating advanced semiconductor materials due to its molecular structure and chemical stability.\u003c\/li\u003e\n\u003cli\u003eMaterial synthesis and modification: Its ability to bond with other molecules makes it suitable for modifying material properties in various research contexts.\u003c\/li\u003e\n\u003cli\u003eResearch in material construction: It is used in the development of construction materials that require enhanced performance and durability.\u003c\/li\u003e\n\u003cli\u003eChemical reaction studies: Its controlled reactivity supports precise chemical reactions necessary for material innovation.\u003c\/li\u003e\n\u003cli\u003eNanotechnology applications: The compound's molecular complexity enables its use in nanoscale material synthesis and functionalization.\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: 7428-91-3\u003c\/li\u003e\n\u003cli\u003eCategory: Materials Science \u0026gt; Material Building Blocks \u0026gt; Small Molecule Semiconductor Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities as per supplier guidelines\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid (as per standard product description)\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\u003eDibenzo[b,d]thiophen-2-amine should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep the compound in a sealed container to prevent exposure to moisture and air. Suitable storage containers include glass or high-density polyethylene (HDPE) bottles to ensure chemical integrity. Laboratory personnel should handle the compound with care, using appropriate personal protective equipment such as gloves and safety goggles. It is important to avoid inhalation of vapors and skin contact during handling. Proper labeling and storage conditions help ensure the safety and effectiveness of the compound in research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48086763733210,"sku":"TCI2510D552126442","price":1322000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48086763765978,"sku":"TCI2510D552126443","price":4582000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D5521.jpg?v=1769142113"},{"product_id":"tci2510d560426565","title":"TCI D5604 6287-82-7 2,3-Dibromobenzo[b]thiophene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2,3-Dibromobenzo[b]thiophene is a heterocyclic compound widely used in chemical reactions for the synthesis of complex molecules. As a building block in organic chemistry, it serves as a versatile intermediate in various synthetic pathways. Its unique structure, featuring two bromine atoms at positions 2 and 3, enhances its reactivity and makes it a valuable tool for structural modification. In laboratory settings, this compound is essential for researchers aiming to develop new pharmaceuticals, polymers, and industrial chemicals. Its ability to undergo substitution and other chemical reactions makes it a key player in synthetic chemistry.\u003c\/p\u003e\n\u003cp\u003eThe compound’s chemical properties make it a preferred choice for synthetic chemists. The presence of bromine atoms allows it to participate in electrophilic substitution and radical reactions, offering multiple synthetic pathways. Its stability under controlled conditions ensures predictable outcomes in laboratory experiments, while its reactivity under specific conditions enables the creation of diverse molecular structures. These characteristics make it an ideal candidate for advanced chemical research and development. The compound’s versatility supports a wide range of applications, from drug discovery to material science.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 2,3-Dibromobenzo[b]thiophene is extensively used in organic chemistry and pharmacology research. It is a common reagent in academic and industrial settings, supporting the development of new compounds with potential therapeutic or industrial applications. Many research institutions and universities rely on this compound for its reliability and effectiveness in chemical synthesis. Its role in molecular modification makes it an essential component of modern chemical research in Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis applications benefit from this compound's reactivity and structural versatility, enabling the creation of complex molecules in pharmaceutical and polymer research.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research utilizes its electrophilic substitution potential to develop new drug compounds with targeted biological activities.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical production relies on its stability and reactivity for the synthesis of specialty chemicals and materials.\u003c\/li\u003e\n\u003cli\u003eMaterial science experiments use its heterocyclic structure to design new polymers and functional materials with unique properties.\u003c\/li\u003e\n\u003cli\u003eAcademic research in chemistry and pharmacology employs it as a key building block for exploring molecular modifications and reaction mechanisms.\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: 6287-82-7\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard chemical supply practices\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid, typically in crystalline or powder form\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 keep it in a sealed container to prevent moisture absorption and contamination. Due to its reactivity, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. It is important to store it separately from strong oxidizing agents and incompatible substances to avoid potential chemical reactions. In laboratory settings, it should be kept in a well-ventilated area to ensure safe handling and minimize exposure risks. Proper storage and handling procedures are essential to maintain its chemical integrity and ensure safe use in research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086768058586,"sku":"TCI2510D560426565","price":1913000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086768091354,"sku":"TCI2510D560426566","price":6634000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D5604.jpg?v=1767108964"},{"product_id":"tci2510d592326915","title":"TCI D5923 1242077-24-2 2,6-Dibromobenzo[1,2-b:5,4-b']dithiophene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D5923 with CAS number 1242077-24-2 is 2,6-Dibromobenzo[1,2-b:5,4-b']dithiophene, a brominated monomer belonging to the group of material building blocks for small molecule semiconductors. Its core structure is a benzodithiophene, that is, a benzene ring fused with two thiophene rings to form a flat and rigid conjugated system. In the laboratory, this compound serves as a donor unit or core unit that is assembled into conjugated polymers as well as small molecule semiconductors through transition metal-catalysed coupling reactions, making it an important base material in organic electronics and organic photovoltaics research.\u003c\/p\u003e\n\u003cp\u003eThe property that makes it a preferred choice is the presence of two bromine atoms at positions 2 and 6, which act as symmetrical reactive groups for polymerisation as well as for directed functionalisation. The opposing positions of the bromine atoms allow chain growth to proceed in a linear fashion, so that conjugation along the polymer backbone is maintained. Bromine atoms on a thiophene ring are also very well suited to Suzuki–Miyaura, Stille and Sonogashira reactions as well as direct arylation, giving researchers a wide choice of synthetic methods. The sulfur-rich benzodithiophene core contributes further to the electronic character of the resulting material.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this monomer is typically used in university and institutional research groups working on organic electronics, conjugated polymer synthesis and organic photovoltaic devices. It is handled on the bench scale during multi-step synthesis campaigns, where it is coupled with complementary comonomers to build semiconducting backbones. Because it is supplied as a defined TCI building block, it fits research workflows in which the identity and reactivity of the starting monomer must be consistent from batch to batch.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eConjugated polymer synthesis: the two symmetrical bromine handles allow step-growth polymerisation with complementary comonomers, producing linear semiconducting backbones with conjugation preserved along the chain.\u003c\/li\u003e\n\u003cli\u003eOrganic photovoltaic material development: the flat, rigid, sulfur-rich benzodithiophene core is used as a donor or core unit when constructing polymers and small molecules for organic solar cell research.\u003c\/li\u003e\n\u003cli\u003eSuzuki–Miyaura and Stille cross-coupling: aryl bromide positions on the thiophene rings react readily under transition metal catalysis, making this monomer a routine partner in palladium-catalysed coupling work.\u003c\/li\u003e\n\u003cli\u003eSonogashira coupling and alkyne extension: the bromine substituents permit attachment of alkynyl groups, letting researchers extend conjugation and tune the electronic structure of the resulting semiconductor.\u003c\/li\u003e\n\u003cli\u003eSmall molecule semiconductor building: the compound acts as a rigid central core for directed functionalisation, allowing symmetric small molecule semiconductors to be assembled around a single planar conjugated unit.\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: 1242077-24-2\u003c\/li\u003e\n\u003cli\u003eChemical name: 2,6-Dibromobenzo[1,2-b:5,4-b']dithiophene\u003c\/li\u003e\n\u003cli\u003eCategory: Materials Science \u0026gt; Material Building Blocks \u0026gt; Small Molecule Semiconductor Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in standard research-scale catalogue pack sizes; please confirm the required size when ordering\u003c\/li\u003e\n\u003cli\u003eStorage note: store in a cool, dark and well-closed container as recommended for brominated semiconductor building blocks\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, dark and dry place, away from heat, direct sunlight, moisture and incompatible chemicals. Keep the material in its original amber or opaque glass container, or transfer it to a tightly sealed glass vial; for extended storage, an inert atmosphere is advisable to protect the monomer from moisture and air. Handle in a well-ventilated fume hood using safety glasses, nitrile gloves and a laboratory coat, and avoid inhalation of dust and contact with skin or eyes. Use clean, dry spatulas when weighing to prevent contamination that could affect subsequent coupling reactions, and collect chemical waste according to institutional laboratory waste procedures.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"500mg","offer_id":48086783918298,"sku":"TCI2510D592326915","price":6184000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D5923.jpg?v=1769180715"},{"product_id":"tci2510d603227049","title":"TCI D6032 108847-24-1 Dibenzo[b,d]thiophen-3-ylboronic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eDibenzo[b,d]thiophen-3-ylboronic Acid is a chemical compound widely used in laboratory settings as a building block for the synthesis of complex heterocyclic compounds. This versatile reagent plays a crucial role in organic chemistry, particularly in the development of molecules with specific biological functions. Its unique structure, featuring boron and sulfur atoms, contributes to its reactivity and stability, making it an essential component in various chemical reactions. Researchers rely on this compound to create new substances with tailored chemical and biological properties, supporting advancements in pharmaceutical and material sciences.\u003c\/p\u003e\n\u003cp\u003eThe compound's reactivity and functional group make it a preferred choice for synthetic chemists. Its ability to participate in coupling reactions, substitution processes, and interactions with diverse reagents enhances its utility in laboratory applications. The presence of boronic acid functionality allows for efficient cross-coupling reactions, which are fundamental in the synthesis of complex organic molecules. These properties make it a valuable tool for scientists aiming to design and develop novel compounds with specific functionalities.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Dibenzo[b,d]thiophen-3-ylboronic Acid is commonly used in research related to organic chemistry, pharmacology, and materials science. It is particularly favored in academic and industrial settings where the synthesis of bioactive compounds and advanced materials is required. Its role in drug discovery and the development of new chemical materials underscores its importance in the scientific community.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of heterocyclic compounds due to its reactive boronic acid group and sulfur-containing structure.\u003c\/li\u003e\n\u003cli\u003eDevelopment of bioactive molecules in pharmacological research for drug discovery and therapeutic applications.\u003c\/li\u003e\n\u003cli\u003eCreation of advanced materials in material science through cross-coupling reactions and functional group modifications.\u003c\/li\u003e\n\u003cli\u003eSupport for synthetic pathways in academic and industrial laboratories requiring complex molecule construction.\u003c\/li\u003e\n\u003cli\u003eUse in chemical research for studying reactivity and stability of functional groups in various reaction conditions.\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: 108847-24-1\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder\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\u003eDibenzo[b,d]thiophen-3-ylboronic Acid should be stored in a cool, dry environment to maintain its chemical integrity and prevent degradation. It is recommended to use airtight containers to protect the compound from moisture and air exposure. Due to its reactivity, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. The compound is best stored in a well-ventilated area to minimize any potential risks associated with its chemical properties. Proper labeling and storage conditions are essential to ensure safe handling and long-term stability in laboratory settings.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48086788604122,"sku":"TCI2510D603227049","price":1181000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48086788636890,"sku":"TCI2510D603227050","price":4049000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D6032.jpg?v=1767109607"},{"product_id":"tci2510d608727117","title":"TCI D6087 1207-12-1 4,6-Dimethyldibenzo[b,d]thiophene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e4,6-Dimethyldibenzo[b,d]thiophene is a heterocyclic compound widely used in chemical reactions for the synthesis of complex molecules. As a building block in organic chemistry, it plays a crucial role in the development of new compounds with specific structural and functional properties. Its presence in substitution and ring-opening reactions makes it a versatile tool for creating aromatic and heterocyclic structures. This compound is particularly valuable in laboratory settings where the construction of intricate molecular frameworks is required.\u003c\/p\u003e\n\u003cp\u003eThe compound’s stable molecular structure and reactivity make it a preferred choice for researchers. It exhibits good reactivity and the ability to form bonds with various functional groups, which enhances its utility in synthetic pathways. These characteristics allow it to be integrated into a wide range of chemical processes, making it indispensable in both academic and industrial research. Its compatibility with different reaction conditions further broadens its application scope.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 4,6-Dimethyldibenzo[b,d]thiophene is commonly used in scientific research, especially in the fields of organic chemistry and pharmaceutical development. Many research institutions and universities rely on this compound for experiments requiring stable and reactive chemical building blocks. Its availability in the local market supports efficient research operations without the need for imports.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis research utilizes this compound to construct complex molecular frameworks due to its reactivity and structural versatility.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical development benefits from its role in creating heterocyclic structures essential for drug molecule design.\u003c\/li\u003e\n\u003cli\u003eAnalytical chemistry applications leverage its stability for use in reference standards and reaction intermediates.\u003c\/li\u003e\n\u003cli\u003ePolymer science experiments incorporate it as a building block for synthesizing functionalized materials with specific properties.\u003c\/li\u003e\n\u003cli\u003eEnvironmental chemistry studies use it as a model compound for studying reaction mechanisms and environmental fate of heterocyclic substances.\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: 1207-12-1\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities to meet research needs\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture\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 moisture to maintain its stability. It is recommended to use airtight containers made of glass or high-density polyethylene to prevent contamination and degradation. Due to its chemical nature, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to ensure laboratory safety. Avoid exposure to incompatible substances, and ensure proper ventilation in the workspace. Regular monitoring of storage conditions is advised to maintain the integrity of the material for research use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086790897882,"sku":"TCI2510D608727117","price":2615000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086790930650,"sku":"TCI2510D608727118","price":9106000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D6087.jpg?v=1767109697"},{"product_id":"tci2510h162834531","title":"TCI H1628 63676-22-2 2-(4-Hydroxyphenyl)benzo[b]thiophene-6-ol","description":"\u003cp\u003e\u003cstrong\u003e2-(4-Hydroxyphenyl)benzo[b]thiophene-6-ol\u003c\/strong\u003e (CAS 63676-22-2) 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 Five-membered heterocyclic compound used as a building block in pharmaceutical, agrochemical, and functional-material synthesis.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eSpecifications:\u003c\/strong\u003e\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003eMolecular formula: C14H10O2S\u003c\/li\u003e\n\u003cli\u003eCAS number: 63676-22-2\u003c\/li\u003e\n\u003cli\u003ePurity: \u0026gt;98.0%(GC)\u003c\/li\u003e\n\u003cli\u003eTCI product code: H1628\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eAvailable from \u003cstrong\u003eAMI Scientific\u003c\/strong\u003e, the authorised TCI distributor in Indonesia. \u003cstrong\u003eContact us for pricing and stock availability\u003c\/strong\u003e — we ship throughout 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