{"title":"Thiophenes [Small Molecule Semiconductor Building Blocks]","description":"\u003cp\u003e\u003cstrong\u003eThiophenes [Small Molecule Semiconductor Building Blocks]\u003c\/strong\u003e — menghimpun senyawa heterosiklik beranggota lima dengan atom sulfur, mulai dari unit thiophene tunggal hingga struktur terthiophene dan tienotiofena terfusi, yang dilengkapi berbagai gugus fungsi reaktif seperti boronat, stanil, dan aldehida. Kategori ini berperan sebagai unit pembangun elektronik untuk perakitan molekul semikonduktor terkonjugasi.\u003c\/p\u003e\u003cp\u003eThiophenes dipakai peneliti material dan elektronika organik untuk menyusun molekul semikonduktor melalui reaksi kopling silang seperti Suzuki atau Stille, memanfaatkan gugus boronat dan trimetilstanil sebagai titik sambung antar unit aromatik. Turunan aldehida dan anhidrida dipakai untuk memperluas konjugasi pi atau menambahkan gugus fungsi pada sintesis material untuk sel surya organik dan transistor film tipis.\u003c\/p\u003e\u003cp\u003eContoh produk dalam koleksi ini: \u003ca href=\"\/en\/products\/tci2510t348555125\"\u003eTCI T3485 1040281-83-1 5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene-2-carboxaldehyde\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b555312212\"\u003eTCI B5553 934368-79-3 2-Bromo-5-(4-hexylphenyl)thiophene\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510t334354941\"\u003eTCI T3343 1073-31-0 3,4-Thiophenedicarboxaldehyde\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b569012399\"\u003eTCI B5690 178931-63-0 5,5''-Bis(trimethylstannyl)-2,2':5',2''-terthiophene\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510t334254939\"\u003eTCI T3342 6007-83-6 2,3-Thiophenedicarboxylic Anhydride\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b639513276\"\u003eTCI B6395 86134-26-1 2,5-Bis(trimethylstannyl)thiophene\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510t322154788\"\u003eTCI T3221 40985-58-8 Thieno[3,2-b]thiophene-2-carbonitrile\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510c271517570\"\u003eTCI C2715 25796-77-4 4H-Cyclopenta[1,2-b:5,4-b']dithiophen-4-one\u003c\/a\u003e.\u003c\/p\u003e\u003cp\u003ePerhatikan jenis gugus fungsi reaktif pada posisi cincin (boronat, halida, atau stanil) yang menentukan kompatibilitas dengan reaksi kopling tertentu, serta tingkat kemurnian yang berpengaruh pada kinerja 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-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\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-benzothiophenes-small-molecule-semiconductor-building-blocks\"\u003eBenzothiophenes [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":"tci2510b555312212","title":"TCI B5553 934368-79-3 2-Bromo-5-(4-hexylphenyl)thiophene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2-Bromo-5-(4-hexylphenyl)thiophene is a small-molecule semiconductor building block used in the synthesis of conjugated organic materials for electronic applications. Its bromo substituent enables efficient cross-coupling reactions such as Suzuki or Stille coupling, while the hexylphenyl moiety enhances solubility in common organic solvents for solution processing. This compound is widely utilized in research and development of organic field-effect transistors (OFETs), organic photovoltaics (OPVs), and other organic electronic devices.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085886697690,"sku":"TCI2510B555312212","price":3401000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5553.jpg?v=1768815816"},{"product_id":"tci2510b569012399","title":"TCI B5690 178931-63-0 5,5''-Bis(trimethylstannyl)-2,2':5',2''-terthiophene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B5690 (CAS 178931-63-0) is a high-purity 5,5''-Bis(trimethylstannyl)-2,2':5',2''-terthiophene reagent primarily used as a key precursor in Stille cross-coupling reactions for constructing terthiophene-based molecular architectures. This organotin compound serves as an essential building block in the synthesis of conjugated polymers and oligomers for organic electronic applications, including organic semiconductors, organic photovoltaics (OPV), and organic field-effect transistors (OFET). Supplied in a 200 mg packaging from TCI, this reagent meets the rigorous demands of advanced materials research and synthetic organic chemistry laboratories.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48276771209434,"sku":"TCI2510B569012399","price":2503000.0,"currency_code":"IDR","in_stock":false}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5690.jpg?v=1769180213"},{"product_id":"tci2510b639513276","title":"TCI B6395 86134-26-1 2,5-Bis(trimethylstannyl)thiophene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6395, 2,5-bis(trimethylstannyl)thiophene (CAS 86134-26-1), is a bifunctional organotin reagent designed for Stille cross-coupling and Stille polycondensation. Its two trimethylstannyl groups make it a standard donor comonomer for building conjugated donor-acceptor polymers used in organic photovoltaics, OFETs, and electrochromic materials. It is equally useful for assembling well-defined thiophene oligomers by double coupling with aryl halides. Available in 1 g and 5 g sizes, this toxic, moisture- and light-sensitive reagent must be handled in a fume hood under inert gas, with all tin-containing waste collected separately.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSsebuwufu (1990). Synthesis of 1,2-bis(diphenylphosphino)ethane-bis-(trimethylstannyl)palladium(II) and its infrared spectrum; the infrared and raman spectra of 1,2-bis(diphenylphosphino)ethane-bis-(trimethylstannyl)platinum(II). \u003cem\u003eInorganica Chimica Acta\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/s0020-1693(00)80205-4\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/s0020-1693(00)80205-4\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eSchulz et al. (1993). Umsetzung von Bis(trimethylgermyl)acetylen und Bis(trimethylstannyl)acetylen mit Diboran(4)-Derivaten \/ Reaction of Bis(trimethylgermyl)acetylene and Bis(trimethylstannyl)acetylene with Diborane(4)-Derivatives. \u003cem\u003eZeitschrift für Naturforschung B\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1515\/znb-1993-0604\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1515\/znb-1993-0604\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eVasisht et al. (1997). Synthesis and characterization of sodium bis(trimethylstannyl) amide and bis(trimethylsilyl) bis(trimethylstannyl) -phospha-tetrazene. \u003cem\u003eJournal of Organometallic Chemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/s0022-328x(97)00093-4\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/s0022-328x(97)00093-4\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085937881306,"sku":"TCI2510B639513276","price":1799000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085937914074,"sku":"TCI2510B639513277","price":6269000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6395.jpg?v=1768197095"},{"product_id":"tci2510c271517570","title":"TCI C2715 25796-77-4 4H-Cyclopenta[1,2-b:5,4-b']dithiophen-4-one","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C2715, also known as 4H-Cyclopenta[1,2-b:5,4-b']dithiophen-4-one with CAS number 25796-77-4, is a specialized chemical compound used in materials science research. It serves as a fundamental building block in the development of organic semiconductor materials. This compound is widely utilized in the synthesis of complex molecules, particularly in the field of optoelectronic devices. Its unique molecular structure makes it a valuable tool for researchers aiming to innovate in advanced material technologies.\u003c\/p\u003e\n\u003cp\u003eThe compound is favored for its complex molecular structure and its ability to form stable bonds with various other molecules. Its dithiophene ring system contributes to high chemical stability and good electrical conductivity, making it ideal for use in semiconductor applications. These properties enable it to be a preferred choice for scientists working on organic electronics and photovoltaic materials. The optical properties of this compound also make it relevant for applications involving light and energy.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used by researchers in material technology and renewable energy fields. It plays a key role in the development of more efficient and environmentally friendly semiconductor materials. Local researchers appreciate its availability and effectiveness in their studies, making it a reliable component in their experimental workflows.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic Semiconductor Development: This compound is essential for creating advanced organic semiconductor materials used in optoelectronic devices.\u003c\/li\u003e\n\u003cli\u003eOrganic Solar Cell Research: Its high conductivity and stability make it suitable for use in organic photovoltaic cell synthesis.\u003c\/li\u003e\n\u003cli\u003eLED Material Synthesis: The compound's optical properties are ideal for developing materials used in light-emitting diodes.\u003c\/li\u003e\n\u003cli\u003eMaterial Stability Testing: Its chemical stability allows it to be used in experiments that require long-term material performance evaluation.\u003c\/li\u003e\n\u003cli\u003eRenewable Energy Innovation: It supports research into sustainable energy solutions by enabling the development of efficient semiconductor 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: 25796-77-4\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 direct 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. It is recommended to use airtight containers to prevent exposure to air and humidity. Due to its chemical stability, it does not require refrigeration but should be kept in a secure location to avoid contamination. Laboratory personnel should handle it with appropriate personal protective equipment, such as gloves and safety goggles, to ensure safe handling. It is important to maintain proper ventilation in the workspace to minimize any potential exposure. Regular inspection of storage conditions ensures the compound remains in optimal condition for research use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48086193504474,"sku":"TCI2510C271517570","price":4919000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2715.jpg?v=1769180413"},{"product_id":"tci2510c302117948","title":"TCI C3021 389-58-2 4H-Cyclopenta[2,1-b:3,4-b']dithiophene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e4H-Cyclopenta[2,1-b:3,4-b']dithiophene, commonly abbreviated as CPDT, is a small molecule semiconductor building block composed of two thiophene rings bridged by a single cyclopentane ring. This bridged architecture is what makes it one of the most important donor units in organic electronics research. Because both thiophene rings are locked into the same plane, the molecule is rigid and coplanar, so pi electron delocalization proceeds efficiently and the band gap of materials constructed from it can be pushed to a narrower value.\u003c\/p\u003e\n\u003cp\u003eThe characteristic that makes CPDT such a widely chosen unit is the sp³ carbon bridge at the C4 position, which is readily deprotonated and alkylated. Researchers routinely install long alkyl chains at that position to improve the solubility of the resulting polymers in organic solvents without disturbing the conjugated system, an advantage that is difficult to achieve with other donor units. In addition, the alpha positions on both thiophene rings are highly responsive to halogenation, stannylation, and borylation, so the compound is ready to be carried into Stille and Suzuki polymerizations. The electron rich nature of the dithiophene core also makes it a suitable partner for electron accepting units.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this building block is typically found in university and institutional research groups working on organic electronics and functional polymer materials. It is used at the synthesis bench where conjugated monomers are prepared, functionalized, and then advanced into polymerization steps, with the resulting materials characterized by the spectroscopic and electrochemical instrumentation available in the same facility. Because it serves as a starting intermediate rather than a finished device material, it is generally ordered in small research quantities.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eDonor–acceptor conjugated polymer synthesis: the electron rich dithiophene core pairs with electron accepting comonomers to produce low band gap polymers for organic electronic studies.\u003c\/li\u003e\n\u003cli\u003eStille and Suzuki cross-coupling polymerization: the alpha positions of both thiophene rings accept stannylation or borylation cleanly, giving monomers ready for step-growth coupling chemistry.\u003c\/li\u003e\n\u003cli\u003eAlkylation chemistry at the C4 bridge: the sp³ bridging carbon is easily deprotonated and alkylated, letting researchers tune polymer solubility without perturbing the conjugated backbone.\u003c\/li\u003e\n\u003cli\u003eOrganic photovoltaic material development: the rigid coplanar structure promotes efficient pi electron delocalization, a property sought when designing light absorbing donor materials for organic solar cell research.\u003c\/li\u003e\n\u003cli\u003eSmall molecule semiconductor building block studies: the compound serves as a core scaffold for structure–property investigations comparing bridged donor units across different conjugated material systems.\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: 389-58-2\u003c\/li\u003e\n\u003cli\u003eCategory: Materials Science \u0026gt; Material Building Blocks \u0026gt; Small Molecule Semiconductor Building Blocks\u003c\/li\u003e\n\u003cli\u003eProduct code: TCI C3021\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in research scale quantities; please confirm the currently offered pack size when ordering.\u003c\/li\u003e\n\u003cli\u003eStorage note: store in a cool, dark place in a tightly sealed container.\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, dark, and well ventilated place, away from heat, direct sunlight, and sources of ignition. Amber glass or the supplier's original packaging is preferred to limit light exposure, and containers should be kept sealed to avoid moisture uptake and contamination between uses. Handle in a fume hood while wearing safety glasses, gloves, and a laboratory coat, and avoid inhalation of dust or contact with skin and eyes. Weigh and transfer with clean, dry spatulas, close the container promptly after use, and consult the manufacturer's safety data sheet before handling or disposal.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48086209626330,"sku":"TCI2510C302117948","price":3626000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48086209659098,"sku":"TCI2510C302117949","price":12732000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3021.jpg?v=1768816991"},{"product_id":"tci2510c330118321","title":"TCI C3301 635305-24-7 5-Chloro-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e5-Chloro-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene is a specialized chemical compound widely used in organic chemistry laboratories. It plays a crucial role in various synthetic processes, particularly in the development of heterocyclic compounds. This reagent is essential for facilitating coupling reactions, such as S-N coupling and the Suzuki-Miyaura reaction, which are fundamental in the synthesis of complex organic molecules. Its unique structure, incorporating both boron and chlorine functionalities, makes it a versatile tool in modern chemical research.\u003c\/p\u003e\n\u003cp\u003eThe compound's chemical properties, including its reactivity and stability under controlled conditions, make it a preferred choice for researchers. Its ability to participate in multiple reaction pathways enhances its utility in synthetic chemistry. The presence of the boronic acid group allows it to act as a key intermediate in cross-coupling reactions, which are vital for the creation of new compounds with specific biological or material properties. This reagent is especially valuable in applications requiring high selectivity and efficiency.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in pharmaceutical and materials science research. It is an essential component in the development of new drugs and advanced materials. Due to its complex molecular structure, it is often employed in studies aimed at understanding and improving the reactivity of organic compounds. Its application is widespread in academic and industrial settings, contributing to the advancement of scientific knowledge and innovation.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eUsed in pharmaceutical research for the synthesis of bioactive compounds due to its reactivity in coupling reactions.\u003c\/li\u003e\n\u003cli\u003eApplied in materials science for the development of new polymers and functional materials through cross-coupling processes.\u003c\/li\u003e\n\u003cli\u003eEmployed in synthetic organic chemistry for the preparation of heterocyclic compounds with specific structural features.\u003c\/li\u003e\n\u003cli\u003eUtilized in academic research for exploring new reaction mechanisms and synthetic pathways in organic chemistry.\u003c\/li\u003e\n\u003cli\u003eIntegrated into drug discovery programs to facilitate the construction of complex molecular frameworks with therapeutic potential.\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: 635305-24-7\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 supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid or liquid, depending on the specific formulation\u003c\/li\u003e\n\u003cli\u003eStorage note: Requires dry and cool storage to prevent moisture and oxidation\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a dry, cool environment away from moisture and oxidizing agents to maintain its chemical stability. It is recommended to use airtight containers made of inert materials such as glass or polyethylene to prevent exposure to humidity. Due to its sensitivity to moisture, handling should be done in a controlled atmosphere with appropriate safety measures. The compound should be kept in a well-ventilated area to minimize the risk of inhalation. Proper labeling and storage conditions are essential to ensure the integrity and safety of the material during laboratory use. Always follow standard laboratory safety protocols when working with this reagent.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086230630618,"sku":"TCI2510C330118321","price":1097000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086230663386,"sku":"TCI2510C330118322","price":3824000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3301.jpg?v=1768204758"},{"product_id":"tci2510c340018448","title":"TCI C3400 120659-34-9 3-Cyclohexylthiophene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e3-Cyclohexylthiophene is an organic compound widely utilized in scientific research, particularly in the field of semiconductor materials. This compound plays a crucial role in the development of advanced materials with tailored electronic properties. Its unique chemical structure enables it to serve as a building block in the synthesis of complex molecules, offering researchers the ability to manipulate electronic behavior and chemical reactivity. In laboratory settings, it is a key component in the creation of functional materials that require precise chemical interactions.\u003c\/p\u003e\n\u003cp\u003eThe compound is valued for its high reactivity and compatibility with various functional groups, making it an ideal candidate for synthetic processes that demand precision. Its ability to form specific chemical bonds under controlled conditions allows for the production of materials with desired properties. Additionally, its chemical stability under certain conditions ensures consistent performance and reliability in laboratory experiments. These characteristics make it a preferred choice for researchers aiming to develop innovative semiconductor materials.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 3-Cyclohexylthiophene is commonly used in research related to the synthesis of advanced electronic materials. Its application extends to studies involving organic semiconductors and nanomaterials, where its chemical properties are essential for achieving desired outcomes. The compound's versatility and reliability make it a valuable resource for scientists working on cutting-edge material development projects.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSemiconductor material synthesis due to its ability to form complex molecular structures with tailored electronic properties.\u003c\/li\u003e\n\u003cli\u003eOrganic electronics research as it enables the creation of functional materials with specific conductivity characteristics.\u003c\/li\u003e\n\u003cli\u003eNanomaterial development because of its compatibility with various functional groups and reactivity in controlled environments.\u003c\/li\u003e\n\u003cli\u003eChemical synthesis of advanced compounds requiring precise reactivity and bonding capabilities.\u003c\/li\u003e\n\u003cli\u003eMaterial characterization studies due to its stable chemical properties under specific experimental 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: 120659-34-9\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 or liquid, depending on supplier packaging\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct sunlight and incompatible substances\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003e3-Cyclohexylthiophene 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 air. Due to its reactivity, it should be kept away from strong oxidizing agents and incompatible materials. Proper ventilation is essential when handling the compound to minimize inhalation risks. Laboratory personnel should wear appropriate personal protective equipment, including gloves and safety goggles, to ensure safe handling. The compound should be stored in a secure location to prevent accidental spills or contamination.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086243475674,"sku":"TCI2510C340018448","price":2053000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086243508442,"sku":"TCI2510C340018449","price":7983000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3400.jpg?v=1768817089"},{"product_id":"tci2510d418124695","title":"TCI D4181 51285-60-0 4,4'-Dibromo-2,2'-bithiophene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D4181 is 4,4'-Dibromo-2,2'-bithiophene, a bithiophene derivative carrying bromine atoms at the 4 and 4' positions of the two thiophene rings. As a heterocyclic building block, this compound occupies an important place in the synthesis of conjugated materials because it supplies a ready-made bithiophene framework together with two reactive sites available for further elaboration. In the laboratory it serves as a monomer and as a synthetic intermediate for constructing oligothiophenes, substituted polythiophenes, and a wide range of small conjugated molecules studied in organic electronics and photochemistry.\u003c\/p\u003e\n\u003cp\u003eThe principal advantage of this compound lies in its beta-bromination pattern, at the 4 and 4' positions rather than the more common alpha positions. This arrangement leaves the 5 and 5' positions free, so that polymerization or chain extension can be directed toward the ring termini, while the beta bromine atoms act as handles for installing side groups through palladium-catalysed cross-coupling or through halogen–metal exchange. The carbon–bromine bonds on the thiophene rings are sufficiently reactive for Suzuki, Stille, Negishi, and Kumada reactions, which makes the compound a flexible platform for designing conjugated architectures with controlled substitution.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, materials of this type are typically used by university and institutional research groups working on organic semiconductors, conjugated polymers, and photoactive small molecules. It is normally handled in synthetic chemistry laboratories equipped for cross-coupling work, where it is weighed out in small quantities for multi-step preparations, purified intermediates, and structure–property studies. Because it functions as a starting material rather than a finished formulation, it is generally ordered in research-scale quantities to support ongoing method development and materials synthesis projects.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eConjugated polymer synthesis: the bithiophene core provides an extended conjugated unit while the free 5 and 5' positions allow chain growth to proceed along the polymer backbone.\u003c\/li\u003e\n\u003cli\u003ePalladium-catalysed cross-coupling chemistry: the reactive carbon–bromine bonds participate readily in Suzuki, Stille, Negishi, and Kumada couplings for attaching aryl or alkyl partners.\u003c\/li\u003e\n\u003cli\u003eOligothiophene preparation: researchers use this building block to assemble defined thiophene sequences whose chain length and substitution pattern can be controlled step by step.\u003c\/li\u003e\n\u003cli\u003eOrganic electronics materials research: the compound serves as a precursor for semiconducting small molecules and polymers investigated for their charge-transport and optical behaviour.\u003c\/li\u003e\n\u003cli\u003eSide-chain functionalisation via halogen–metal exchange: the beta bromine atoms can be converted into organometallic intermediates, giving access to substituents that tune solubility and 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: 51285-60-0\u003c\/li\u003e\n\u003cli\u003eChemical name: 4,4'-Dibromo-2,2'-bithiophene\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 research-scale packaging; please confirm the sizes currently listed for this catalogue number\u003c\/li\u003e\n\u003cli\u003eStorage note: keep in the tightly closed original container, protected from light and moisture\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 place, away from direct sunlight, heat sources, and incompatible chemicals. The original manufacturer packaging is the most suitable container; if the material is transferred, use a clean, dry, chemically resistant vessel with a secure closure and a clear label. Handle the compound in a fume hood, wearing safety goggles, a laboratory coat, and suitable chemical-resistant gloves. Avoid inhalation of dust and contact with skin or eyes, keep the container closed when not in use, and consult the manufacturer's safety data sheet before use and disposal.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086677029082,"sku":"TCI2510D418124695","price":5004000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086677061850,"sku":"TCI2510D418124696","price":17370000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D4181.jpg?v=1768818041"},{"product_id":"tci2510d429024844","title":"TCI D4290 960524-18-9 3-Dodecyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D4290 is 3-Dodecyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene, a thiophene derivative carrying a pinacol boronate ester group at the 2-position and a long dodecyl alkyl chain at the 3-position. The compound belongs to the family of material building blocks for small molecule semiconductors and acts as the boron partner in cross-coupling reactions. In materials and organic electronics laboratories, reagents of this type serve as the primary building blocks used to construct the conjugated chains that become the active layer of optoelectronic devices.\u003c\/p\u003e\n\u003cp\u003eThe main advantage of this material lies in its pinacol boronate group, which is considerably more stable and easier to handle than a free boronic acid, so weighing and storage become far more practical without excessive concern over dehydration or the formation of boroxine anhydrides. This group reacts cleanly under Suzuki–Miyaura conditions with palladium catalysts, delivering carbon–carbon bonds directed to a specific position on the thiophene ring. The long dodecyl chain provides high solubility in common organic solvents, an essential requirement if the resulting polymers or oligomers are to be processed by solution techniques such as spin coating.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, a building block of this kind is typically used by university and institutional research groups working on organic electronics, conjugated polymers, and semiconducting thin films. It fits synthetic workflows where a defined thiophene fragment must be coupled reproducibly into a larger conjugated backbone, and where the resulting material has to remain soluble enough for solution processing and subsequent device fabrication and characterisation.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSuzuki–Miyaura cross-coupling synthesis: the pinacol boronate group reacts cleanly with palladium catalysts, giving directed carbon–carbon bond formation at a defined thiophene position.\u003c\/li\u003e\n\u003cli\u003eConjugated polymer preparation: serves as a boron-bearing monomer for building extended conjugated chains used as the active layer in optoelectronic devices.\u003c\/li\u003e\n\u003cli\u003eSmall molecule semiconductor construction: functions as a defined thiophene building block that can be assembled into larger semiconducting molecular architectures for organic electronics research.\u003c\/li\u003e\n\u003cli\u003eSolution-processable material development: the long dodecyl chain confers high solubility in common organic solvents, supporting spin coating and other solution deposition techniques.\u003c\/li\u003e\n\u003cli\u003eRegiodefined thiophene functionalisation: substitution at the 2- and 3-positions allows researchers to control where coupling occurs along the thiophene unit during synthesis.\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: 960524-18-9\u003c\/li\u003e\n\u003cli\u003eChemical name: 3-Dodecyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene\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 research pack sizes; please confirm the currently offered packaging when ordering.\u003c\/li\u003e\n\u003cli\u003eStorage: keep in a tightly closed original 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 material in its original tightly closed container, protected from moisture and direct sunlight, and follow the storage conditions specified on the manufacturer's label and safety data sheet. Boronate esters are best kept dry and, where recommended, under an inert atmosphere to preserve reagent quality. Handle the compound in a fume hood using appropriate personal protective equipment, including safety glasses, gloves, and a laboratory coat. Weigh and transfer with clean, dry glassware or spatulas to avoid contamination, keep containers away from ignition sources and incompatible chemicals, and dispose of residues and contaminated materials according to institutional chemical waste procedures.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086683025626,"sku":"TCI2510D429024844","price":3654000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086683058394,"sku":"TCI2510D429024845","price":11749000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D4290.jpg?v=1769141976"},{"product_id":"tci2510d429124846","title":"TCI D4291 1173788-58-3 4-Dodecyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D4291 is 4-Dodecyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene, a thiophene isomer that carries a pinacol boronate ester group at the 2-position and a dodecyl chain at the 4-position. The compound belongs to the family of material building blocks for small molecule semiconductors and is used as the boron component in palladium-catalysed cross-coupling reactions. Because the alkyl chain sits in a different position than in the 3-dodecyl isomer, it represents a distinct choice for researchers who want to control the substitution pattern and the side-chain arrangement of the conjugated materials they design.\u003c\/p\u003e\n\u003cp\u003eThe properties that make this building block attractive are the stability of the pinacol boronate group towards routine laboratory handling combined with its good reactivity under Suzuki–Miyaura conditions. Because the dodecyl chain is located at the 4-position, the distance between the alkyl group and the boron reaction centre is larger, so the steric environment around the newly formed bond differs from that of the other isomers. This in turn influences the torsion angle between units, the arrangement of chains in the solid state, and the effective conjugation length of the final material. The long alkyl chain still provides adequate solubility for solution processing.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent is typically used in academic and institutional research groups working on organic electronics and conjugated polymer chemistry, where thiophene-based monomers are coupled step by step to build defined molecular architectures. It suits work carried out at the synthesis scale, where a boronate partner with a known substitution pattern is required to compare isomers, and it fits laboratories that already run palladium-catalysed coupling chemistry and need a well-defined side-chain-bearing thiophene boronate for their material design programmes.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSuzuki–Miyaura cross-coupling: the pinacol boronate group at the 2-position transfers the thiophene unit efficiently under palladium catalysis while remaining stable enough for routine weighing and transfer in the laboratory.\u003c\/li\u003e\n\u003cli\u003eConjugated polymer synthesis: the reagent serves as the boron-bearing monomer that couples with halogenated partners, allowing researchers to extend conjugation length in a controlled, stepwise manner.\u003c\/li\u003e\n\u003cli\u003eSmall molecule semiconductor construction: as a material building block, it introduces an alkylated thiophene unit into defined molecular architectures intended for organic electronic applications and structure–property studies.\u003c\/li\u003e\n\u003cli\u003eIsomer comparison studies: the 4-dodecyl substitution pattern lets researchers evaluate how alkyl chain placement, rather than chain length, affects torsion angles and solid-state chain packing relative to the 3-dodecyl isomer.\u003c\/li\u003e\n\u003cli\u003eSolution-processable material preparation: the long dodecyl chain imparts adequate solubility to the resulting materials, supporting synthetic routes that end in solution-based processing and film formation work.\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: 1173788-58-3\u003c\/li\u003e\n\u003cli\u003eChemical name: 4-Dodecyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene\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: please refer to the packaging options listed for this catalogue item\u003c\/li\u003e\n\u003cli\u003eStorage: store as indicated on the manufacturer's label and in the accompanying documentation\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the container in a cool, dry place, tightly closed and protected from moisture, following the storage conditions stated on the manufacturer's label. Keep the material in its original supplier container, or in a clean, well-sealed and clearly labelled vessel of compatible material, and return it promptly after each use to limit exposure to air and humidity. Handle the compound in a well-ventilated area or fume hood, wear gloves, safety glasses and a laboratory coat, and avoid contact with skin, eyes and clothing. Weigh and transfer with clean, dry tools to preserve the integrity of the boronate group, and consult the safety data sheet before use and for waste disposal.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086683091162,"sku":"TCI2510D429124846","price":2110000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086683123930,"sku":"TCI2510D429124847","price":7983000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D4291.jpg?v=1769141976"},{"product_id":"tci2510d437624954","title":"TCI D4376 89088-95-9 2,5-Dibromothiophene 1,1-Dioxide","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2,5-Dibromothiophene 1,1-Dioxide is a chemical compound widely used in scientific research, particularly in the fields of organic chemistry and materials science. As a key building block in the development of advanced materials, this compound plays a crucial role in the synthesis of complex molecules. Its unique structure enables it to participate in various chemical reactions, making it an essential component for researchers aiming to create materials with specific electronic or optical properties. This compound is particularly valuable for those working on semiconductor and polymer-based materials due to its reactivity and structural versatility.\u003c\/p\u003e\n\u003cp\u003eThe compound's high reactivity is attributed to the presence of bromine and oxygen atoms in its molecular structure. These functional groups enhance its ability to undergo chemical transformations, making it a preferred choice for synthetic applications. Its heterocyclic nature further contributes to its chemical versatility, allowing it to be used as a precursor in the synthesis of a wide range of compounds. The combination of reactivity and structural complexity makes it a favored material in laboratories focused on organic synthesis and material development.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 2,5-Dibromothiophene 1,1-Dioxide is commonly used in research related to semiconductors and polymers. Its ability to participate in complex chemical reactions and its role as a building block for advanced materials make it a highly sought-after compound among researchers and students. The compound's significance in modern material science ensures its continued use in both academic and industrial research settings.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSemiconductor material synthesis due to its reactivity and structural versatility, enabling the creation of advanced electronic materials.\u003c\/li\u003e\n\u003cli\u003ePolymer development as a building block for creating materials with specific optical and electronic properties.\u003c\/li\u003e\n\u003cli\u003eOrganic chemistry research for synthesizing complex molecules with tailored chemical functionalities.\u003c\/li\u003e\n\u003cli\u003eMaterial characterization studies to understand the behavior of heterocyclic compounds in different environments.\u003c\/li\u003e\n\u003cli\u003eAdvanced functional material research for applications in optoelectronics and nanotechnology.\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: 89088-95-9\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: As available from supplier\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Keep 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 integrity. It is recommended to use airtight containers to prevent exposure to air and humidity, which can affect its stability. Due to its reactivity, 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 compound to minimize inhalation risks. It is important to store it separately from incompatible materials to avoid any potential chemical interactions. Following these guidelines ensures safe and effective use in laboratory environments.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086689317082,"sku":"TCI2510D437624954","price":4498000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D4376.jpg?v=1768818081"},{"product_id":"tci2510d487425615","title":"TCI D4874 4861-61-4 2-Dodecylthiophene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2-Dodecylthiophene (TCI D4874), with CAS number 4861-61-4, is a chemical compound widely used in laboratory settings as a building block for the synthesis of heterocyclic compounds. This versatile reagent plays a crucial role in organic chemistry by enabling the creation of complex molecular structures through controlled chemical modifications. Its unique structure, consisting of a thiophene ring substituted with a dodecyl chain, makes it a valuable tool for researchers aiming to develop new pharmaceuticals, advanced materials, and specialized chemical products.\u003c\/p\u003e\n\u003cp\u003eThe chemical stability and controlled reactivity of 2-Dodecylthiophene make it a preferred choice in synthetic chemistry. It dissolves well in organic solvents such as ethyl acetate and chloroform, facilitating its use in various reaction types, including substitution, oxidation, and covalent bonding. These properties ensure that it remains a reliable and efficient reagent in the hands of chemists. Its ability to participate in multiple chemical reactions without significant degradation further enhances its utility in laboratory applications.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 2-Dodecylthiophene is commonly used in organic chemistry and pharmaceutical research. It is an essential component in the development of new compounds and is frequently employed in academic and industrial research settings. Its availability and ease of use make it a practical choice for both educational institutions and research organizations in Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of heterocyclic compounds due to its thiophene ring and alkyl chain structure, enabling precise molecular modifications.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research for the development of new drugs, as it can be used as a building block in complex molecule synthesis.\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\u003eEducational use in chemistry laboratories for teaching synthetic methods and reaction mechanisms.\u003c\/li\u003e\n\u003cli\u003eIndustrial research and development for the production of specialty chemicals and chemical intermediates.\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: 4861-61-4\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 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 light and incompatible materials\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003e2-Dodecylthiophene should be stored in a cool, dry place, away from direct sunlight and sources of heat. It is recommended to keep the container tightly sealed to prevent evaporation and contamination. Suitable storage containers include glass or high-density polyethylene (HDPE) bottles, which are resistant to chemical reactions and provide a secure seal. General laboratory precautions include handling the compound in a well-ventilated area or fume hood to minimize exposure. It is important to avoid contact with skin and eyes, and to use appropriate personal protective equipment such as gloves and safety goggles when handling the substance. Proper labeling of containers is essential to ensure safe storage and handling practices.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1mL","offer_id":48086730899674,"sku":"TCI2510D487425615","price":1490000.0,"currency_code":"IDR","in_stock":true},{"title":"5mL","offer_id":48086730932442,"sku":"TCI2510D487425616","price":5537000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D4874.jpg?v=1767108111"},{"product_id":"tci2510d502125826","title":"TCI D5021 1231160-83-0 2,5-Dibromo-N-(2-ethylhexyl)-3,4-thiophenedicarboximide","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2,5-Dibromo-N-(2-ethylhexyl)-3,4-thiophenedicarboximide is a chemical compound widely used in scientific research, particularly in the fields of materials science and organic chemistry. This compound plays a crucial role in the development of semiconductor materials and polymers due to its unique molecular structure. Its presence in laboratory settings enables researchers to explore advanced chemical reactions and material synthesis. The compound is valued for its versatility and potential applications in creating materials with specific optical and electronic properties.\u003c\/p\u003e\n\u003cp\u003eThe compound’s chemical stability and controlled reactivity make it a preferred choice for high-precision chemical processes. Its thiophene ring structure contributes to its electronic properties, which are essential for applications in optoelectronic devices and advanced material formulations. The ability to modify its molecular structure further enhances its utility in research focused on molecular engineering and functional material development. These characteristics allow it to be a key component in the synthesis of materials with tailored properties.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in research related to semiconductor materials, polymer development, and optoelectronic applications. Its role in molecular modification and material innovation makes it a valuable resource for researchers aiming to advance technological applications. The compound’s stability and reactivity are particularly important in creating new materials with specific electronic and optical properties. Its use is widespread in academic and industrial research settings in Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSemiconductor Material Development: This compound is ideal for synthesizing semiconductor materials due to its electronic properties and structural versatility, enabling the creation of advanced electronic components.\u003c\/li\u003e\n\u003cli\u003ePolymer Synthesis: Its thiophene ring structure makes it suitable for polymer synthesis, allowing the development of materials with tailored optical and electrical characteristics.\u003c\/li\u003e\n\u003cli\u003eOptoelectronic Research: The compound’s electronic properties are well-suited for research in optoelectronic devices, such as organic light-emitting diodes and photovoltaic materials.\u003c\/li\u003e\n\u003cli\u003eMolecular Modification Studies: Its reactivity and structural flexibility make it a preferred choice for studies involving molecular engineering and functional material design.\u003c\/li\u003e\n\u003cli\u003eAdvanced Material Innovation: The compound supports the development of new materials with specific properties, making it essential in cutting-edge material research.\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: 1231160-83-0\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: As per manufacturer specifications\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 light 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. In laboratory settings, it is important to handle the compound with appropriate personal protective equipment, including gloves and safety goggles, to ensure safety during synthesis and experimentation. Proper ventilation should be maintained when working with the compound to minimize exposure. Regular monitoring of storage conditions is advised to ensure the compound remains in optimal condition for research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48086740500698,"sku":"TCI2510D502125826","price":2082000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48086740533466,"sku":"TCI2510D502125827","price":7195000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D5021.jpg?v=1768818285"},{"product_id":"tci2510d524026102","title":"TCI D5240 24769-39-9 2-Decylthiophene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2-Decylthiophene (TCI D5240), with CAS number 24769-39-9, is a versatile organic compound widely used in laboratory settings for synthetic chemistry applications. As a heterocyclic building block, it plays a crucial role in the development of complex molecular structures. This compound is particularly valuable for its ability to participate in various chemical reactions, including substitution, addition, and functional group modifications. Its stability and reactivity make it a reliable choice for researchers aiming to synthesize thiophenes and their derivatives.\u003c\/p\u003e\n\u003cp\u003eThe compound’s reactivity and stability are key factors that make it a preferred choice in synthetic chemistry. It exhibits good solubility in organic solvents such as ethyl acetate and acetone, which facilitates its use in both solution-based and solid-phase reactions. Its predictable behavior under different reaction conditions allows for precise control over the synthesis process, making it an essential tool in organic laboratories. The compound’s molecular structure also supports a wide range of chemical transformations, enhancing its utility in diverse research applications.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 2-Decylthiophene is commonly used in organic chemistry research, especially in the synthesis of heterocyclic compounds. It is a key reagent in the development of new chemical materials and pharmaceutical intermediates. Due to its reactivity and solubility, it is frequently employed in both academic and industrial research settings, contributing to the advancement of chemical synthesis techniques in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of heterocyclic compounds due to its reactivity and structural versatility.\u003c\/li\u003e\n\u003cli\u003eDevelopment of pharmaceutical intermediates through functional group modifications.\u003c\/li\u003e\n\u003cli\u003ePreparation of thiophenes and their derivatives in synthetic chemistry experiments.\u003c\/li\u003e\n\u003cli\u003eUse in reaction optimization studies requiring stable and predictable chemical behavior.\u003c\/li\u003e\n\u003cli\u003eSupport for research in new material development through controlled chemical transformations.\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: 24769-39-9\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; 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 light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003e2-Decylthiophene should be stored in a cool, dry environment, away from direct light and moisture to maintain its chemical stability. It is recommended to use airtight containers made of materials such as glass or high-density polyethylene to prevent contamination and evaporation. Due to its reactivity, it should be handled in a well-ventilated area, ideally with appropriate personal protective equipment. Avoid exposure to strong oxidizing agents or incompatible substances. Always follow standard laboratory safety protocols to ensure safe handling and storage. Regular monitoring of storage conditions is advised to maintain the integrity of the compound.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1mL","offer_id":48086750789850,"sku":"TCI2510D524026102","price":1631000.0,"currency_code":"IDR","in_stock":true},{"title":"5mL","offer_id":48086750822618,"sku":"TCI2510D524026103","price":5256000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D5240.jpg?v=1767108541"},{"product_id":"tci2510d524126104","title":"TCI D5241 160096-74-2 2,5-Dibromo-3-tetradecylthiophene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2,5-Dibromo-3-tetradecylthiophene is a chemical compound widely utilized in scientific research, particularly in the development of organic semiconductor materials. This compound serves as a fundamental building block in the synthesis of conductive polymers and semiconductors with unique electronic properties. Its molecular structure combines a thiophene ring with a long hydrocarbon chain, enabling it to participate in complex chemical reactions that lead to the formation of advanced materials. In the laboratory, it is a key component in the creation of innovative materials that are essential for modern electronic and optoelectronic applications.\u003c\/p\u003e\n\u003cp\u003eThe compound is valued for its chemical stability under controlled conditions, which allows for consistent results in experimental processes. Its sensitivity to moisture and light, however, necessitates careful handling and storage to maintain its integrity. The ability to form well-defined crystalline structures makes it ideal for applications requiring precise control over material synthesis. These characteristics make it a preferred choice for researchers working on advanced material development and electronic device fabrication.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 2,5-Dibromo-3-tetradecylthiophene is commonly used in material science and semiconductor technology research. It is a critical reagent for institutions and universities engaged in the development of organic photovoltaic cells and flexible electronic devices. Its role in these studies underscores its importance in advancing technological innovation within the scientific community.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic semiconductor synthesis: This compound is ideal for creating organic semiconductors due to its molecular structure that facilitates charge transport properties.\u003c\/li\u003e\n\u003cli\u003eConductive polymer development: Its long hydrocarbon chain contributes to the formation of conductive polymers with enhanced electrical conductivity.\u003c\/li\u003e\n\u003cli\u003eFlexible electronics research: The compound supports the development of flexible electronic devices by enabling the synthesis of materials with mechanical flexibility.\u003c\/li\u003e\n\u003cli\u003eOrganic photovoltaic cell fabrication: It is used in the production of organic solar cells due to its ability to form stable and efficient semiconductor layers.\u003c\/li\u003e\n\u003cli\u003eMaterial characterization studies: Its crystalline structure allows for detailed analysis in material science experiments, aiding in the understanding of material 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: 160096-74-2\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 various quantities as per standard laboratory supply\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 light and moisture to maintain its chemical stability. It is recommended to use sealed containers made of materials that are chemically inert, such as glass or high-density polyethylene, to prevent contamination and degradation. Due to its sensitivity to environmental factors, it is important to handle it with care during preparation and use. Always ensure proper ventilation in the laboratory when working with this compound. Regular monitoring of storage conditions is advised to ensure the material remains suitable for research applications. Laboratory personnel should wear appropriate personal protective equipment, including gloves and safety goggles, to minimize exposure risks.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086750888154,"sku":"TCI2510D524126104","price":1490000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086750920922,"sku":"TCI2510D524126105","price":5116000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D5241.jpg?v=1768818336"},{"product_id":"tci2510d524226106","title":"TCI D5242 178452-13-6 2,5-Dibromo-3-hexadecylthiophene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2,5-Dibromo-3-hexadecylthiophene is a chemical compound widely used in material science research, particularly in the development of organic semiconductor materials. This compound plays a crucial role in the synthesis of complex molecular structures, serving as a foundational building block for advanced polymer and macromolecule applications. Its unique chemical structure, featuring a thiophene ring with a long alkyl chain and bromo groups, makes it highly versatile for various synthetic pathways. In the laboratory, it is essential for creating materials with tailored electronic properties, supporting innovation in semiconductor technology and electronic device fabrication.\u003c\/p\u003e\n\u003cp\u003eThe compound’s chemical properties make it a preferred choice for researchers seeking materials with specific electronic behaviors. Its stability under controlled conditions allows for reliable synthesis processes, while its sensitivity to UV light and oxidation necessitates careful handling. The presence of a long alkyl chain influences its solubility characteristics, making it more soluble in non-polar solvents like hexane and toluene. These properties enable precise control over material morphology and performance, which is critical for applications in advanced electronics and optoelectronics.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 2,5-Dibromo-3-hexadecylthiophene is commonly used in semiconductor material research, especially in the development of organic solar cells and electronic components. Its role in creating materials with tunable electronic properties supports the growth of local research in renewable energy and advanced electronics. The compound’s utility in these contexts underscores its importance in the scientific community.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic Semiconductor Development: This compound is ideal for synthesizing organic semiconductors due to its tunable electronic properties and structural versatility.\u003c\/li\u003e\n\u003cli\u003ePolymer Synthesis: It serves as a key building block for creating macromolecules with specific electrical and optical characteristics.\u003c\/li\u003e\n\u003cli\u003eElectronic Device Fabrication: Its use in material synthesis supports the development of advanced electronic components and optoelectronic devices.\u003c\/li\u003e\n\u003cli\u003eSolar Cell Research: The compound is utilized in the creation of organic photovoltaic materials, contributing to renewable energy innovation.\u003c\/li\u003e\n\u003cli\u003eMaterial Characterization Studies: Its unique chemical structure makes it suitable for studies aimed at understanding molecular behavior and electronic 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: 178452-13-6\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 various quantities as per standard laboratory supply\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid or crystalline, depending on storage conditions\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dark place away from UV light and oxidizing agents\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, dark environment to prevent degradation due to UV exposure and oxidation. A suitable container would be a sealed, airtight glass or plastic vessel, preferably with a desiccant to maintain dryness. It is important to handle the material with appropriate personal protective equipment, such as gloves and safety goggles, to avoid direct contact. Due to its low solubility in polar solvents, it is recommended to use non-polar solvents for dissolution. Always ensure proper ventilation when working with this compound to minimize inhalation risks. Regular monitoring of storage conditions is essential to maintain its chemical integrity and ensure safe laboratory practices.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086750986458,"sku":"TCI2510D524226106","price":1799000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086751019226,"sku":"TCI2510D524226107","price":6184000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D5242.jpg?v=1768818338"},{"product_id":"tci2510d524326108","title":"TCI D5243 205235-01-4 2,5-Dibromo-3-octadecylthiophene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2,5-Dibromo-3-octadecylthiophene is a chemical compound widely utilized in materials science research, particularly in the development of organic semiconductor materials. This compound plays a crucial role in laboratory settings where the synthesis of advanced electronic materials is required. Its unique molecular structure makes it a valuable building block for creating materials with tailored electronic properties. Researchers in Indonesia and globally rely on this compound to explore new avenues in semiconductor technology and functional material design.\u003c\/p\u003e\n\u003cp\u003eThe compound’s molecular structure, consisting of a long carbon chain and a thiophene ring, contributes to its electronic properties, making it a preferred choice for organic semiconductor applications. Its stability under certain conditions and the ability to undergo chemical reactions under controlled environments enhance its utility in synthetic processes. The compound’s high melting and boiling points also make it suitable for use in high-temperature laboratory procedures. These characteristics collectively make it a versatile and reliable material for advanced research.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 2,5-Dibromo-3-octadecylthiophene is commonly used in semiconductor material research and development. Its application is particularly relevant in the study of organic conductive materials and optoelectronic devices. Due to its chemical stability and reactivity, it is a key component in the synthesis of various functional materials. Researchers in Indonesia frequently use this compound to advance their work in material science and semiconductor technology.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic Semiconductor Synthesis: This compound is ideal for synthesizing organic semiconductors due to its unique molecular structure and electronic properties.\u003c\/li\u003e\n\u003cli\u003eConductive Polymer Development: Its long carbon chain and thiophene ring make it suitable for creating conductive polymers with enhanced performance.\u003c\/li\u003e\n\u003cli\u003eOptoelectronic Material Research: The compound's optical response properties are valuable in studying materials for optoelectronic applications.\u003c\/li\u003e\n\u003cli\u003eMaterial Characterization Studies: Its chemical stability allows it to be used in various characterization techniques to analyze material behavior.\u003c\/li\u003e\n\u003cli\u003eAdvanced Electronic Device Prototyping: It serves as a building block for creating prototypes of next-generation electronic devices.\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: 205235-01-4\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 various 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 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 integrity. It is recommended to use airtight containers to prevent exposure to air and moisture, which could affect its stability. Laboratory personnel should handle the compound with care, using appropriate personal protective equipment such as gloves and safety goggles. Due to its chemical nature, it should be stored separately from incompatible substances to avoid any potential reactions. Proper labeling of storage containers is essential for safety and identification purposes. Always ensure that storage conditions comply with standard laboratory safety protocols to minimize risks associated with chemical handling.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086751051994,"sku":"TCI2510D524326108","price":1857000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D5243.jpg?v=1768818341"},{"product_id":"tci2510d524726112","title":"TCI D5247 302912-44-3 2,5-Dibromo-3-cyclohexylthiophene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2,5-Dibromo-3-cyclohexylthiophene is a chemical compound widely used in scientific research, particularly in the field of materials science and technology. This compound plays a crucial role in the development of advanced materials, serving as a building block for the synthesis of organic compounds with unique electronic properties. Its molecular structure enables it to participate in various chemical reactions, making it a versatile component in laboratory settings. Due to its stability and controlled reactivity, it is often selected for experiments that require precise chemical interactions and controlled synthesis processes.\u003c\/p\u003e\n\u003cp\u003eThe compound's key properties include its ability to interact effectively with a range of reagents, supporting substitution and covalent reactions. Its solubility in organic solvents further enhances its utility, as it simplifies processing and synthesis procedures in the lab. These characteristics make it an ideal choice for researchers aiming to develop new materials with tailored electronic and structural properties. The stability of the compound also ensures that it remains safe for use in controlled laboratory environments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 2,5-Dibromo-3-cyclohexylthiophene is commonly used in the development of novel materials for electronic and semiconductor applications. Its role in creating advanced polymers and semiconductors aligns with the growing demand for innovative materials in both academic and industrial research. Researchers in Indonesia rely on this compound to explore new chemical pathways and improve the performance of materials used in modern technology.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eUsed in semiconductor material synthesis due to its ability to form stable organic compounds with unique electronic properties.\u003c\/li\u003e\n\u003cli\u003eApplied in polymer research for creating advanced macromolecules with tailored structural and functional characteristics.\u003c\/li\u003e\n\u003cli\u003eUtilized in organic electronics development for its role in synthesizing materials with high conductivity and stability.\u003c\/li\u003e\n\u003cli\u003eEmployed in material characterization studies to test the reactivity and compatibility of new chemical compounds.\u003c\/li\u003e\n\u003cli\u003eIntegrated into research projects focused on developing environmentally sustainable materials with enhanced performance.\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: 302912-44-3\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: Not specified\u003c\/li\u003e\n\u003cli\u003ePhysical form: Not specified\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and incompatible substances.\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 and sources of heat. It is recommended to use airtight containers to prevent exposure to moisture and air. Due to its chemical nature, it should be kept separate from incompatible substances such as strong oxidizers or acids. Proper ventilation is essential when handling the material to minimize inhalation risks. Laboratory personnel should wear appropriate personal protective equipment, including gloves and safety goggles, to ensure safe handling. Regular monitoring of storage conditions is advised to maintain the integrity and stability of the compound.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086751215834,"sku":"TCI2510D524726112","price":7083000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D5247.jpg?v=1768818340"},{"product_id":"tci2510d537426264","title":"TCI D5374 5556-13-8 4,4'-Dibromo-3,3'-bithiophene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e4,4'-Dibromo-3,3'-bithiophene is a chemical compound that plays a crucial role in organic chemistry and material science research. As a heterocyclic building block, it serves as a versatile intermediate for the synthesis of complex molecules. Its unique structure makes it an essential tool for researchers aiming to modify heterocyclic frameworks to achieve desired electronic or optical properties. This compound is widely used in laboratory settings to facilitate chemical reactions that involve substitution or coupling of heterocyclic chains.\u003c\/p\u003e\n\u003cp\u003eThe compound's high reactivity is primarily due to the presence of two bromine atoms at the 4 and 4' positions of the bithiophene core. These bromine groups enhance the molecule's ability to participate in various chemical transformations, such as substitution, coupling, or arylation reactions. The reactivity of 4,4'-Dibromo-3,3'-bithiophene makes it a preferred choice for applications requiring precise structural modifications. Its chemical stability and predictable reactivity ensure reliable results in synthetic processes.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 4,4'-Dibromo-3,3'-bithiophene is commonly used in organic material research, particularly in the development of compounds for organic electronics and photovoltaic applications. Researchers rely on this compound to create functional materials with specific electronic properties. Its availability and chemical properties make it a standard reagent in academic and industrial research settings across Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic electronics research benefits from this compound as it enables the synthesis of conjugated polymers used in flexible displays and sensors.\u003c\/li\u003e\n\u003cli\u003ePhotovoltaic material development utilizes the compound to create organic semiconductors that enhance solar cell efficiency.\u003c\/li\u003e\n\u003cli\u003eHeterocyclic synthesis projects rely on its reactivity for constructing complex molecular frameworks with tailored electronic properties.\u003c\/li\u003e\n\u003cli\u003eMaterial science experiments use it to design new compounds with specific optical and electrical behaviors for advanced applications.\u003c\/li\u003e\n\u003cli\u003eChemical modification studies employ it as a starting material for creating derivatives with enhanced functional properties in various industries.\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: 5556-13-8\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\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 sources of moisture. It is recommended to use airtight containers to prevent exposure to air and humidity, which could affect its chemical stability. Due to its bromine content, it is important to handle the compound with care, using appropriate personal protective equipment such as gloves and safety goggles. It should be kept in a well-ventilated area to minimize inhalation risks. Avoid contact with incompatible materials, and ensure proper disposal according to local regulations. Regular monitoring of storage conditions ensures the compound remains suitable for use in laboratory applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086756720858,"sku":"TCI2510D537426264","price":6184000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D5374.jpg?v=1767108666"},{"product_id":"tci2510d549226405","title":"TCI D5492 132814-91-6 3,3'''-Dihexyl-2,2':5',2'':5'',2'''-quaterthiophene (contains 3% Dichloromethane at maximum)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e3,3'''-Dihexyl-2,2':5',2'':5'',2'''-quaterthiophene is an organic compound widely used in semiconductor material research. This compound plays a crucial role in the synthesis and characterization of organic conductive materials, particularly in the development of optoelectronic devices such as solar cells and light-emitting diodes. In the laboratory, it serves as a foundational building block for creating materials with high electrical conductivity and chemical stability. Its unique molecular structure enables it to be a key component in the design of advanced electronic materials.\u003c\/p\u003e\n\u003cp\u003eThe compound's molecular structure consists of four thiophene units connected by hexyl chains, which contribute to its high electronic conductivity and chemical stability. These properties make it a preferred choice for researchers working on organic semiconductors. The inclusion of up to 3% dichloromethane ensures the compound remains stable and free from unwanted contaminants, maintaining its integrity during experimental processes. This purity level is essential for accurate and reproducible results in material science studies.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is frequently used by researchers in the fields of materials science and semiconductor technology. It is a vital component in the development of new materials with unique electronic properties, especially in the energy sector. Its application supports innovation in sustainable and efficient electronic devices, making it an essential tool for scientific advancement in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic Semiconductor Synthesis: This compound is ideal for creating organic semiconductors due to its high electronic conductivity and stable molecular structure.\u003c\/li\u003e\n\u003cli\u003eOptoelectronic Device Development: It is used in the fabrication of solar cells and LEDs, where its conductive properties are essential for efficient energy conversion and light emission.\u003c\/li\u003e\n\u003cli\u003eMaterial Characterization Studies: Researchers use it to analyze the electrical and chemical properties of new semiconductor materials under various conditions.\u003c\/li\u003e\n\u003cli\u003eEnergy Research Applications: It supports the development of advanced materials for renewable energy technologies, contributing to sustainable energy solutions.\u003c\/li\u003e\n\u003cli\u003ePolymer Science Investigations: Its molecular structure makes it a valuable component in the study of polymer-based electronic materials and their performance characteristics.\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: 132814-91-6\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: Not specified\u003c\/li\u003e\n\u003cli\u003ePhysical form: Not specified\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 light and moisture to maintain its stability and prevent degradation. It is recommended to use airtight containers to minimize exposure to air and contaminants. Due to its chemical nature, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to ensure laboratory safety. While it contains up to 3% dichloromethane, it is not classified as a hazardous material under standard laboratory conditions. Proper ventilation should be maintained when working with the compound to ensure a safe working environment. Regular monitoring of storage conditions is advised to maintain the integrity of the material for research purposes.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48086762356954,"sku":"TCI2510D549226405","price":2615000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D5492.jpg?v=1768818444"},{"product_id":"tci2510d552526448","title":"TCI D5525 250726-93-3 2-(2,3-Dihydrothieno[3,4-b][1,4]dioxin-5-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eThe TCI D5525 is a complex organic compound with a unique molecular structure that combines a thieno[3,4-b][1,4]dioxin ring and a dioxaborolane ring. This compound plays a crucial role in laboratory research, particularly in the field of materials science and technology. It serves as a building block for the development of small molecule semiconductors, enabling the synthesis of advanced materials with tailored properties. Its presence in research labs is essential for exploring new applications in electronic and optoelectronic devices.\u003c\/p\u003e\n\u003cp\u003eThe compound is valued for its chemical stability and controlled reactivity, making it a preferred choice for researchers seeking high-quality starting materials. Its specific chemical properties, including the presence of boron and oxygen groups, allow for precise chemical reactions such as substitution and coupling. These characteristics are vital for the synthesis of complex molecules, which are often required in cutting-edge material research. The molecule's ability to participate in the formation of intricate molecular structures further enhances its utility in the development of novel materials.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in advanced material research. It is integral to projects focused on semiconductor development and electrochemical applications. Its reliability and performance make it a trusted component in the synthesis of complex compounds, supporting scientific innovation in both academic and industrial research settings.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSmall Molecule Semiconductor Synthesis: This compound is ideal for creating advanced semiconductor materials due to its unique molecular structure and reactivity.\u003c\/li\u003e\n\u003cli\u003eElectrochemical Research: Its chemical stability allows it to be used in electrochemical studies, contributing to the development of new energy storage solutions.\u003c\/li\u003e\n\u003cli\u003eOptoelectronic Device Development: The compound's properties make it suitable for the synthesis of materials used in optoelectronic applications, such as sensors and displays.\u003c\/li\u003e\n\u003cli\u003eCoupling Reaction Applications: The presence of boron and oxygen groups enables it to participate in coupling reactions, which are essential for constructing complex molecular frameworks.\u003c\/li\u003e\n\u003cli\u003eMaterial Innovation Projects: It supports the creation of novel materials by providing a reliable and versatile building block for chemical synthesis.\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: 250726-93-3\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: Not specified\u003c\/li\u003e\n\u003cli\u003ePhysical form: Not specified\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\u003eThis compound should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep it in a sealed container to prevent exposure to moisture and air. Due to its chemical nature, it should be handled with care in a well-ventilated laboratory setting. Avoid direct contact with skin and eyes, and use appropriate personal protective equipment when handling. Ensure that storage conditions are suitable for maintaining the integrity of the compound during long-term use. Proper storage ensures that the material remains effective for its intended applications in scientific research.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086763962586,"sku":"TCI2510D552526448","price":3121000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D5525.jpg?v=1768818457"},{"product_id":"tci2510d554426472","title":"TCI D5544 211181-63-4 (4-Dodecyl-2-thienyl)trimethylstannane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(4-Dodecyl-2-thienyl)trimethylstannane is an organotin compound widely used in material science research, particularly in the development of semiconductor materials. This compound serves as a key building block in the synthesis of complex molecules with applications in optoelectronic technologies and semiconductor devices. In the laboratory, it plays a crucial role in the creation of materials with tailored electronic properties, enabling the design of advanced functional materials for modern technological applications. Its unique molecular structure supports a wide range of chemical reactivity, making it an essential component in various synthetic processes.\u003c\/p\u003e\n\u003cp\u003eThe compound's high reactivity and structural versatility make it a preferred choice for researchers working on semiconductor and optoelectronic material synthesis. Its molecular framework combines a long hydrocarbon chain with a thienyl group, enhancing its compatibility with a variety of chemical reactions. This allows it to act as a versatile intermediate in the development of new materials with specific optical and electronic characteristics. The compound's stability and reactivity balance make it ideal for use in controlled laboratory environments where precise chemical reactions are required.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, (4-Dodecyl-2-thienyl)trimethylstannane is commonly used in material science and semiconductor technology research. Researchers from academic institutions and research centers utilize this compound for experiments involving the synthesis of novel materials. Its role in creating materials with specific electronic and optical properties makes it a valuable tool in the advancement of semiconductor and optoelectronic technologies in Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSemiconductor material synthesis: This compound is ideal for creating advanced semiconductor materials due to its reactivity and structural versatility, enabling the development of materials with tailored electronic properties.\u003c\/li\u003e\n\u003cli\u003eOptoelectronic device fabrication: Its unique molecular structure allows it to be used in the production of optoelectronic components, enhancing the performance of light-sensitive and conductive materials.\u003c\/li\u003e\n\u003cli\u003eOrganic semiconductor research: The compound's ability to form stable chemical bonds makes it suitable for studying organic semiconductors, supporting research into new material applications.\u003c\/li\u003e\n\u003cli\u003eMolecular building block experimentation: It serves as a fundamental component in the synthesis of complex molecules, allowing researchers to explore new chemical pathways and material properties.\u003c\/li\u003e\n\u003cli\u003eMaterial characterization studies: Its well-defined structure enables precise analysis in material characterization, aiding in the understanding of electronic and optical behavior in new 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: 211181-63-4\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 various quantities as per standard laboratory supply\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid or liquid, depending on specific formulation\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\u003eThis compound should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to use airtight containers to prevent exposure to moisture and air, which could affect its reactivity. Due to its organotin nature, it should be handled with care to avoid direct contact with skin or inhalation. Laboratory personnel should wear appropriate personal protective equipment, including gloves and safety goggles, when working with this material. It is also advisable to keep it away from incompatible substances to ensure safe storage and usage in the laboratory.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086764781786,"sku":"TCI2510D554426472","price":3570000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D5544.jpg?v=1769142117"},{"product_id":"tci2510d558726535","title":"TCI D5587 67061-73-8 Dithieno[3,2-b:2',3'-d]thiophene-2,6-dicarboxaldehyde","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eDithieno[3,2-b:2',3'-d]thiophene-2,6-dicarboxaldehyde is a complex organic compound widely used in laboratory settings for its unique molecular structure and reactivity. As a heterocyclic building block, it plays a crucial role in the synthesis of various organic compounds, particularly those with specific biological or optical properties. This compound is commonly employed in advanced chemical research to create new materials and pharmaceuticals. Its versatility makes it an essential tool for chemists working on innovative projects.\u003c\/p\u003e\n\u003cp\u003eThe compound's chemical stability under controlled conditions, combined with its sensitivity to moisture and air, makes it a preferred choice for specialized applications. Its ability to participate in targeted chemical reactions ensures precision in synthetic processes. These properties are highly valued in research environments where accuracy and reproducibility are critical. The compound’s reactivity and structural complexity enable scientists to design and synthesize compounds with tailored functionalities.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is frequently used in organic chemistry research, especially in the synthesis of heterocyclic compounds. It is a key component in studies related to pharmaceutical development, material science, and optical technologies. Many research institutions and universities rely on this compound to advance their scientific work and develop new applications in various fields.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of heterocyclic compounds due to its reactive functional groups and structural versatility.\u003c\/li\u003e\n\u003cli\u003eDevelopment of pharmaceuticals with specific biological activities through controlled chemical modifications.\u003c\/li\u003e\n\u003cli\u003eCreation of optically active materials for use in advanced technological applications.\u003c\/li\u003e\n\u003cli\u003eResearch in material science for the design of new polymers and functional materials.\u003c\/li\u003e\n\u003cli\u003eInvestigation of chemical reactivity patterns in synthetic pathways for complex molecule construction.\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: 67061-73-8\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 laboratory supply standards.\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid, typically in crystalline or powder form.\u003c\/li\u003e\n\u003cli\u003eStorage note: Requires storage in a dry, cool, and airtight environment to prevent degradation.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a dry, cool, and airtight container to prevent exposure to moisture and air, which can lead to degradation. It is recommended to use glass or sealed plastic containers that are resistant to chemical reactions. Laboratory personnel should handle the compound with care, using appropriate personal protective equipment such as gloves and safety goggles. Due to its sensitivity, it should be used in a controlled environment to ensure stability and safety. Regular monitoring of storage conditions is essential to maintain the compound's integrity and effectiveness in research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48086767042778,"sku":"TCI2510D558726535","price":6578000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D5587.jpg?v=1767108928"},{"product_id":"tci2510d572926703","title":"TCI D5729 32431-85-9 2,5-Dibromo-3-fluorothiophene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2,5-Dibromo-3-fluorothiophene is a fluorinated building block based on a thiophene ring, carrying two bromine atoms at the 2- and 5-positions and a single fluorine atom at the 3-position. This substitution pattern makes it a highly useful starting material in the synthesis of conjugated compounds, because the two bromo groups act as reactive connection points for transition-metal-catalysed cross-coupling reactions. In laboratory practice, the compound is frequently used to construct thiophene oligomers and polymers, to assemble acceptor–donor units, and to prepare fluorinated heterocyclic derivatives that are difficult to obtain through direct synthetic routes.\u003c\/p\u003e\n\u003cp\u003eThe advantage that leads researchers to select this material lies in the role of the fluorine atom. Fluorine is strongly electronegative yet small in size, so it can lower the energy levels of the molecular orbitals without introducing significant steric disturbance to chain packing density. In materials research practice, this is often associated with improved stability towards oxidation and more ordered chain arrangement. At the same time, the two bromine atoms at the terminal positions of the ring provide good and well-directed reactivity in Suzuki, Stille, and Kumada couplings, allowing chain extension to be carried out in a controlled manner.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this building block is typically used in university and institutional research groups working on organic electronic materials, conjugated polymers, and fluorinated heterocyclic chemistry. It is normally handled at small synthetic scale on the bench or in a fume hood, as part of multi-step routes where the dibrominated core is elaborated stepwise. Supplied under the TCI brand, it fits research settings that require a defined, reproducible fluorinated intermediate rather than one prepared in-house.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eCross-coupling synthesis: the two terminal bromine atoms serve as reactive handles for transition-metal-catalysed Suzuki, Stille, and Kumada reactions, giving directed and controllable bond formation.\u003c\/li\u003e\n\u003cli\u003eThiophene oligomer construction: the difunctional 2,5-substitution pattern allows stepwise chain extension, so researchers can build defined oligomeric sequences from a single reliable core unit.\u003c\/li\u003e\n\u003cli\u003eConjugated polymer preparation: symmetrical dibromination at both ring termini supports polymerisation routes in which the fluorinated thiophene is incorporated repeatedly along the backbone.\u003c\/li\u003e\n\u003cli\u003eAcceptor–donor unit assembly: the electron-withdrawing fluorine substituent lowers molecular orbital energy levels, making this unit useful when assembling acceptor–donor architectures for organic electronic materials.\u003c\/li\u003e\n\u003cli\u003eFluorinated heterocycle derivatisation: the compound gives access to fluorinated heterocyclic derivatives that are difficult to obtain by direct synthetic routes starting from unsubstituted thiophenes.\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: D5729\u003c\/li\u003e\n\u003cli\u003eCAS number: 32431-85-9\u003c\/li\u003e\n\u003cli\u003eChemical name: 2,5-Dibromo-3-fluorothiophene\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Fluorinated Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in standard research quantities as offered by TCI; please confirm the required pack size when ordering\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 place, away from direct sunlight, heat sources, and incompatible materials, and follow the storage conditions stated 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, and reseal it promptly after each use to limit exposure to moisture and air. All handling should take place in a fume hood by trained personnel wearing appropriate personal protective equipment, including safety glasses, gloves, and a laboratory coat. Consult the safety data sheet before use, and dispose of residues and contaminated materials in accordance with applicable laboratory waste procedures.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086776545498,"sku":"TCI2510D572926703","price":4133000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086776578266,"sku":"TCI2510D572926704","price":14334000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D5729.jpg?v=1767109136"},{"product_id":"tci2510e115029059","title":"TCI E1150 204905-77-1 3,4-Ethylenedioxythiophene-2-carboxaldehyde","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e3,4-Ethylenedioxythiophene-2-carboxaldehyde is a chemical compound widely used in semiconductor material research. This compound serves as a foundational building block for creating conductive films and electrode components with high conductivity. In laboratory settings, it plays a crucial role in the synthesis of organic materials that find applications in electrochemistry and optoelectronics. Its versatility makes it an essential tool for researchers aiming to develop advanced materials with superior performance.\u003c\/p\u003e\n\u003cp\u003eThe compound’s chemical stability and controlled reactivity make it a preferred choice for material synthesis. Its molecular structure, consisting of a thiophene ring connected by an ethylenedioxy group, provides excellent chemical stability and allows for specific chemical reactions under controlled conditions. These characteristics enable precise control over the synthesis process, making it ideal for applications requiring high accuracy and reproducibility.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in research focused on organic semiconductors and conductive materials. Its solubility in organic solvents facilitates its use in various experimental setups. Researchers in Indonesia rely on this compound for developing innovative materials with tailored properties for advanced technological applications.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eConductive Film Synthesis: This compound is ideal for creating conductive films due to its ability to form stable and conductive structures when processed appropriately.\u003c\/li\u003e\n\u003cli\u003eElectrode Material Development: It is used in the fabrication of electrode components because of its high conductivity and chemical stability, enhancing the performance of electrochemical devices.\u003c\/li\u003e\n\u003cli\u003eOrganic Semiconductor Research: Its molecular structure makes it suitable for synthesizing organic semiconductors, which are essential in optoelectronic applications.\u003c\/li\u003e\n\u003cli\u003eElectrochemical Sensor Fabrication: The compound’s reactivity and solubility allow for the creation of sensitive and reliable electrochemical sensors.\u003c\/li\u003e\n\u003cli\u003eMaterial Characterization Studies: It is frequently used in studies that require precise control over chemical reactions and material properties for advanced 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: 204905-77-1\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 various 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 stability. It is recommended to use airtight containers made of glass or high-density polyethylene to prevent contamination and degradation. Due to its reactivity, it should be handled with appropriate personal protective equipment, including gloves and safety goggles. In laboratory settings, it is important to ensure proper ventilation when working with this compound to minimize exposure. Always follow standard safety protocols when handling chemical substances to ensure a safe working environment.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086929244378,"sku":"TCI2510E115029059","price":1041000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086929277146,"sku":"TCI2510E115029060","price":3373000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510E1150.jpg?v=1768818791"},{"product_id":"tci2510e129429258","title":"TCI E1294 4891-44-5 2-(2-Ethylhexyl)thiophene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2-(2-Ethylhexyl)thiophene is a chemical compound widely used as a building block in the synthesis of heterocyclic compounds. Its core structure is based on a thiophene ring, which contains a single sulfur atom and is known for its aromatic properties. This compound plays a crucial role in organic chemistry laboratories, where it is employed to construct complex molecular structures through various chemical reactions. Due to its versatility and chemical stability, it is a fundamental component in the development of new materials and pharmaceutical compounds.\u003c\/p\u003e\n\u003cp\u003eThe compound's stability and controlled reactivity make it a preferred choice for researchers aiming to modify heterocyclic rings. Its solubility in organic solvents simplifies handling and reaction processes, allowing for efficient synthesis under laboratory conditions. Additionally, its predictable chemical behavior enables precise control over reaction outcomes, making it a reliable reagent in synthetic pathways. These properties contribute to its widespread use in both academic and industrial research settings.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 2-(2-Ethylhexyl)thiophene is commonly utilized in organic chemistry research, particularly in institutions focused on heterocyclic synthesis. It is also employed in the development of new materials and pharmacological studies. Its role in advancing scientific research makes it an essential compound for chemists working in both educational and applied research environments.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eHeterocyclic Compound Synthesis: This compound is ideal for constructing complex molecular structures due to its thiophene ring and functional groups, enabling the development of new pharmaceuticals and materials.\u003c\/li\u003e\n\u003cli\u003eOrganic Chemistry Research: Its stability and reactivity make it a key reagent in synthetic pathways, supporting the creation of novel compounds with specific properties.\u003c\/li\u003e\n\u003cli\u003eMaterial Development: The compound is used in the synthesis of conductive materials and polymers, offering potential applications in electronics and nanotechnology.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical Research: Its ability to participate in various chemical reactions makes it valuable in the design of bioactive molecules and drug candidates.\u003c\/li\u003e\n\u003cli\u003eEducational Purposes: It is frequently used in teaching laboratories to demonstrate synthetic techniques and the behavior of heterocyclic 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: 4891-44-5\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 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 substances\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 tightly sealed containers to prevent exposure to air and moisture. Due to its chemical nature, it should be kept separate from strong oxidizing agents and incompatible materials to avoid potential reactions. In laboratory settings, proper personal protective equipment such as gloves and safety goggles should always be worn when handling the compound. Regular monitoring of storage conditions is essential to maintain its stability and ensure safe usage in research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1mL","offer_id":48086945890522,"sku":"TCI2510E129429258","price":1827000.0,"currency_code":"IDR","in_stock":true},{"title":"5mL","offer_id":48086945923290,"sku":"TCI2510E129429259","price":6269000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510E1294.jpg?v=1767112649"},{"product_id":"tci2510e129529260","title":"TCI E1295 1390584-88-9 2-[5-(2-Ethylhexyl)-2-thienyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eThis chemical compound, TCI E1295 1390584-88-9, is an organoboron reagent with a complex molecular structure featuring a thienyl group and a tetramethylcycloborane moiety. It plays a crucial role in organic chemistry, particularly in the synthesis of heterocyclic compounds and coupling reactions. Its unique structure enables it to participate in a wide range of chemical transformations, making it a valuable tool in modern synthetic chemistry. In laboratory settings, it is widely used for its reactivity and specificity in various synthetic pathways.\u003c\/p\u003e\n\u003cp\u003eThe compound is known for its chemical stability under controlled conditions, although it is sensitive to oxidation and moisture. Its high reactivity and ability to form stable complexes with transition metals make it a preferred choice for advanced synthetic applications. The presence of the thienyl group enhances its versatility, allowing it to be used in multiple reaction types. These properties contribute to its popularity among chemists working on complex molecule synthesis.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent is commonly used by researchers and scientists in the field of organic synthesis. Its reliability and effectiveness in producing high-quality chemical compounds make it a key component in both academic and industrial research settings. The compound's application in various synthetic processes underscores its importance in the chemical research landscape of Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003e\n\u003cstrong\u003eSuzuki-Miyaura Coupling Reactions\u003c\/strong\u003e: This reagent is ideal for coupling reactions due to its ability to form stable boronic acid derivatives, enhancing the efficiency of cross-coupling processes.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eHeterocyclic Compound Synthesis\u003c\/strong\u003e: Its complex structure allows it to participate in the formation of various heterocyclic rings, making it essential for the synthesis of bioactive molecules.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eOrganic Synthesis of Aromatic Compounds\u003c\/strong\u003e: The compound's reactivity supports the creation of aromatic structures, which are fundamental in pharmaceutical and material science research.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eTransition Metal Complex Formation\u003c\/strong\u003e: Its capacity to bind with transition metals expands its utility in catalytic systems and advanced synthetic methodologies.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eHigh-Specificity Reaction Pathways\u003c\/strong\u003e: The compound's unique properties enable it to be used in reactions requiring precise control and selectivity, enhancing the success rate of complex syntheses.\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: 1390584-88-9\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 supply\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid or liquid, depending on the specific formulation\u003c\/li\u003e\n\u003cli\u003eStorage note: Should be stored in a dry, cool, and well-ventilated area away from moisture and oxidizing agents\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a dry, cool, and well-ventilated environment to prevent moisture exposure and oxidation. It is recommended to use airtight containers made of glass or inert plastic to maintain its stability. Due to its sensitivity to moisture, it should be handled with care, and all operations should be conducted in a controlled atmosphere. Proper personal protective equipment, such as gloves and safety goggles, should be worn during handling. Regular monitoring of storage conditions is essential to ensure the compound remains effective for laboratory use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086946021594,"sku":"TCI2510E129529260","price":5876000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510E1295.jpg?v=1768205282"},{"product_id":"tci2510e135529337","title":"TCI E1355 1224430-50-5 4-(2-Ethylhexyl)-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e4-(2-Ethylhexyl)-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene is a specialized organoboron compound widely used in chemical laboratories for its reactivity and structural versatility. This reagent plays a crucial role in synthetic chemistry, particularly in the development of complex organic molecules. Its unique molecular structure makes it an essential component in various coupling reactions, such as the Suzuki-Miyaura reaction, which is fundamental in the synthesis of pharmaceuticals and advanced materials. Due to its functional group diversity, it is a key tool for chemists aiming to create new compounds with tailored properties.\u003c\/p\u003e\n\u003cp\u003eThe compound's stability under controlled conditions, combined with its reactivity in specific environments, makes it a preferred choice for researchers. It is particularly sensitive to moisture and oxidation, which necessitates careful handling and storage. Its ability to participate in a wide range of chemical transformations, including cross-coupling and functional group modifications, enhances its utility in synthetic pathways. This reagent is also valued for its compatibility with inert atmospheres and low-temperature conditions, which are common in advanced organic synthesis protocols.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is frequently used in organic chemistry research, especially in institutions focused on the synthesis of complex molecules. Its availability and effectiveness in producing high-quality results make it a go-to reagent for scientists working on drug development, material science, and other specialized fields. Its role in enabling precise and efficient chemical reactions underscores its importance in modern laboratory practices.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis in pharmaceutical research due to its role in coupling reactions that produce complex molecular structures.\u003c\/li\u003e\n\u003cli\u003eDevelopment of advanced materials where precise functional group modifications are required for enhanced properties.\u003c\/li\u003e\n\u003cli\u003eDrug discovery projects that rely on the synthesis of bioactive compounds with specific molecular frameworks.\u003c\/li\u003e\n\u003cli\u003eAcademic research in chemical engineering focusing on the design of novel synthetic methodologies.\u003c\/li\u003e\n\u003cli\u003eIndustrial applications in chemical manufacturing where stable and reactive reagents are essential for process optimization.\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: 1224430-50-5\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 supply practices.\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid or liquid depending on the specific formulation and supplier packaging.\u003c\/li\u003e\n\u003cli\u003eStorage note: Requires dry, cool, and inert atmosphere storage to prevent degradation.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a dry, cool environment away from moisture and oxidizing agents to maintain its chemical integrity. It is recommended to use sealed containers made of inert materials such as glass or polyethylene to prevent exposure to air and humidity. Laboratory personnel should handle the material with care, using appropriate personal protective equipment to avoid direct contact. Due to its sensitivity, it should be kept in a controlled atmosphere, such as under nitrogen, to minimize the risk of oxidation. Proper labeling and storage conditions are essential to ensure safety and effectiveness in research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086951100634,"sku":"TCI2510E135529337","price":3570000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086951133402,"sku":"TCI2510E135529338","price":12367000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510E1355.jpg?v=1768205295"},{"product_id":"tci2510e139729405","title":"TCI E1397 1231160-82-9 5-(2-Ethylhexyl)-4H-thieno[3,4-c]pyrrole-4,6(5H)-dione","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e5-(2-Ethylhexyl)-4H-thieno[3,4-c]pyrrole-4,6(5H)-dione is a specialized chemical compound used in material science research, particularly in the development of organic semiconductor materials. This compound plays a critical role in the synthesis of intermediate compounds that are essential for creating advanced electronic materials. Its molecular structure provides the foundation for materials with unique electronic properties, making it a key component in the fabrication of organic light-emitting diodes (OLEDs) and other organic electronic devices.\u003c\/p\u003e\n\u003cp\u003eThe compound's chemical stability under controlled conditions makes it ideal for laboratory synthesis and characterization processes. Its thieno[3,4-c]pyrrole-4,6(5H)-dione structure offers thermal stability and the ability to form bonds with various functional groups, enhancing its versatility in material design. These properties make it a preferred choice for researchers aiming to develop materials with controlled reactivity and stability.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is widely used in material and semiconductor technology research. It is a common reagent in academic and industrial settings where the development of advanced electronic materials is a priority. Its application supports innovation in fields such as optoelectronics and nanotechnology, contributing to the growth of Indonesia’s scientific research capabilities.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic Semiconductor Development: This compound is essential for creating organic semiconductors used in OLEDs and flexible electronics due to its stable molecular structure and functional group compatibility.\u003c\/li\u003e\n\u003cli\u003eIntermediate Synthesis for Electronic Materials: It is frequently used in the synthesis of intermediate compounds that are crucial for the production of high-performance electronic materials.\u003c\/li\u003e\n\u003cli\u003eMaterial Characterization Studies: Its chemical stability allows for accurate and reproducible results in material characterization techniques such as spectroscopy and chromatography.\u003c\/li\u003e\n\u003cli\u003eResearch in Optoelectronic Devices: The compound supports the development of optoelectronic devices by providing a reliable base for material synthesis and functionalization.\u003c\/li\u003e\n\u003cli\u003eAcademic and Industrial R\u0026amp;D: It is a key reagent in both academic and industrial research settings, enabling the exploration of new material properties and 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: 1231160-82-9\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 various quantities as per standard laboratory supply practices\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid (as per standard chemical specifications)\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct 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 chemical stability. It is recommended to use airtight containers made of 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 labeling of storage containers is essential to prevent accidental exposure and ensure safe usage. The compound should be kept in a well-ventilated area to minimize any potential risks associated with its chemical properties.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086957064410,"sku":"TCI2510E139729405","price":8096000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510E1397.jpg?v=1768818830"},{"product_id":"tci2510f054830434","title":"TCI F0548 1369328-62-0 5'-Formyl-2,2'-bithiophene-5-boronic Acid (contains varying amounts of Anhydride)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e5'-Formyl-2,2'-bithiophene-5-boronic Acid is a chemical compound widely used in organic reactions, particularly in the synthesis of heterocyclic compounds and complex molecules. This reagent contains both a boronic acid group and a formyl group, which contribute to its reactivity and specificity in various chemical transformations. Its unique molecular structure makes it a valuable tool in synthetic chemistry, especially in the development of advanced materials and electronic components. Due to its complex structure and the presence of anhydride, this compound exhibits high reactivity and can participate in a wide range of chemical interactions.\u003c\/p\u003e\n\u003cp\u003eThe compound's reactivity is enhanced by its ability to form stable intermediates during coupling and substitution reactions. Its chemical versatility allows it to be used in multiple synthetic pathways, making it a preferred choice for researchers working on complex molecule synthesis. The presence of the boronic acid group also facilitates its use in cross-coupling reactions, which are essential in the creation of functionalized organic compounds. These properties make it a key reagent in both academic and industrial research settings.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in organic chemistry research, especially in the development of materials with applications in electronics and advanced chemical synthesis. It is also integral to studies involving the synthesis of heterocyclic compounds and complex molecular structures. Its role in scientific innovation is significant, supporting the development of new materials and chemical processes in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of heterocyclic compounds due to its reactivity and functional groups.\u003c\/li\u003e\n\u003cli\u003eDevelopment of complex molecular structures in material science research.\u003c\/li\u003e\n\u003cli\u003eCross-coupling reactions for functionalization of organic molecules.\u003c\/li\u003e\n\u003cli\u003eSynthesis of electronic materials for advanced applications in semiconductor technology.\u003c\/li\u003e\n\u003cli\u003eResearch in chemical engineering for the creation of new polymers and nanomaterials.\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: 1369328-62-0\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 supplier specifications\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 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, away from moisture and direct sunlight to maintain its stability and reactivity. It is recommended to use airtight containers to prevent exposure to air and moisture, which could affect its chemical properties. Due to its reactive nature, it should be handled in a well-ventilated laboratory setting, with appropriate personal protective equipment such as gloves and safety goggles. It is important to avoid contact with incompatible substances and to follow standard chemical safety protocols to ensure safe handling and storage. Proper labeling and storage conditions are essential to maintain the integrity of the compound and ensure safe usage in laboratory settings.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087012966618,"sku":"TCI2510F054830434","price":11103000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510F0548.jpg?v=1768205359"},{"product_id":"tci2510f080130772","title":"TCI F0801 17303-83-2 3-Formyl-2-thiopheneboronic Acid (contains varying amounts of Anhydride)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI F0801 3-Formyl-2-thiopheneboronic Acid is a dual-functional organoboron reagent designed for the demands of modern organic synthesis, particularly the construction of carbon–carbon bonds. The compound is built around a thiophene core, a five-membered heterocycle encountered very frequently in the molecular frameworks of pharmaceuticals and organic electronic materials. The second position carries a boronic acid group that acts as the nucleophilic partner in cross-coupling reactions, while the third position bears a formyl (aldehyde) group that supplies a second reactive site. This combination makes it a highly valued starting material for synthetic chemistry laboratories, medicinal chemistry programmes, and research into thiophene-based functional materials.\u003c\/p\u003e\n\u003cp\u003eThe most distinctive characteristic of this reagent is its bifunctional nature. Researchers can engage the boronic acid group first through a Suzuki–Miyaura reaction with an aryl halide, then elaborate the still-intact aldehyde group through condensation, reduction, reductive amination, or the construction of further heterocyclic rings. A stepwise approach of this kind shortens synthetic routes and reduces the need for protecting-group manipulations. The material is supplied as containing varying amounts of the corresponding anhydride, which is normal for boronic acids of this class and is accounted for in routine stoichiometric calculations.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent is typically used in university and institutional research groups working on synthetic organic chemistry, medicinal chemistry, and organic electronic materials. It suits methodology development, the preparation of thiophene-containing intermediates, and small-scale exploratory syntheses where a compact bifunctional building block saves both time and reagents. Because it is supplied in laboratory-scale packaging from TCI, it fits well into the workflow of research groups that order defined quantities for specific project stages rather than bulk production.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSuzuki–Miyaura cross-coupling: the boronic acid group at position two transfers the thiophene unit to aryl or heteroaryl halides under palladium catalysis, giving biaryl products with the aldehyde preserved for later use.\u003c\/li\u003e\n\u003cli\u003eMedicinal chemistry building block: the thiophene core is a recurring motif in drug scaffolds, and two orthogonal reactive handles allow rapid assembly of analogue libraries from a single common intermediate.\u003c\/li\u003e\n\u003cli\u003eOrganic electronic materials research: thiophene-based frameworks underpin many conjugated systems, and this reagent introduces a thiophene unit already carrying an aldehyde for further conjugation or condensation chemistry.\u003c\/li\u003e\n\u003cli\u003eHeterocycle construction: the free formyl group serves as the entry point for cyclisation and condensation sequences that build additional fused or pendant heterocyclic rings onto the coupled product.\u003c\/li\u003e\n\u003cli\u003eAldehyde derivatisation chemistry: after coupling, the intact aldehyde can be carried into reductive amination, reduction to the alcohol, or condensation with amines and active methylene compounds without extra protecting steps.\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: 17303-83-2\u003c\/li\u003e\n\u003cli\u003eProduct Code: F0801\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 anhydride\u003c\/li\u003e\n\u003cli\u003ePackaging: supplied in laboratory-scale research pack sizes as listed by the manufacturer\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 place, protected from moisture and away from direct sunlight, following the storage conditions stated on the manufacturer's label and Safety Data Sheet. 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It serves as a key reagent in the synthesis of heterocyclic compounds and complex molecular structures, making it essential for advanced chemical research. This compound is particularly valuable in the field of organoboron chemistry, where it contributes to the development of new materials and pharmaceutical compounds. Its unique chemical properties allow it to participate in multiple reaction pathways, enhancing its utility across different experimental applications.\u003c\/p\u003e\n\u003cp\u003eThe compound is known for its high reactivity and ability to form stable bonds with organic ligands and metals. These properties make it a preferred choice for reactions such as the Suzuki-Miyaura and Heck coupling reactions, which are fundamental in organic synthesis. Its stability under certain conditions ensures reliable results, making it a trusted reagent in both academic and industrial laboratories. The combination of reactivity and stability allows researchers to achieve precise and consistent outcomes in their experiments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, (5-Formylthiophen-3-yl)boronic Acid is commonly used in organic chemistry research, especially in the synthesis of complex compounds and drug development. Its availability and reliability make it a staple in chemical laboratories, supporting a wide range of experimental needs. The compound's role in creating new molecular structures underscores its importance in advancing scientific research in Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of heterocyclic compounds due to its reactivity and ability to form stable bonds with various ligands.\u003c\/li\u003e\n\u003cli\u003eUse in Suzuki-Miyaura coupling reactions for efficient cross-coupling of aryl halides with boronic acids.\u003c\/li\u003e\n\u003cli\u003eApplication in Heck reactions for the formation of carbon-carbon bonds in complex molecule synthesis.\u003c\/li\u003e\n\u003cli\u003eSupport in the development of pharmaceutical compounds through its role in creating boron-containing structures.\u003c\/li\u003e\n\u003cli\u003eUtilization in material science research for the synthesis of advanced 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: 175592-59-3\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron [Organometallic Reagents]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Varies as per supplier\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\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\u003eThis compound should be stored in a cool, dry environment to maintain its stability and prevent degradation. It is recommended to keep it in a sealed container to avoid exposure to moisture, which can affect its reactivity. Due to its chemical nature, it should be handled in a well-ventilated area to minimize inhalation risks. Laboratory personnel should wear appropriate personal protective equipment, such as gloves and safety goggles, when handling the material. Proper disposal methods should be followed to ensure compliance with environmental and safety regulations. The compound is not classified as hazardous under standard laboratory conditions, but standard chemical safety protocols should still be observed.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087055499482,"sku":"TCI2510F106531137","price":6493000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48087055532250,"sku":"TCI2510F106531138","price":23861000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510F1065.jpg?v=1769142450"},{"product_id":"tci2510f113331233","title":"TCI F1133 21512-16-3 5-Formylthiophene-2-carbonitrile","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e5-Formylthiophene-2-carbonitrile is a chemical compound widely used in laboratory settings as a building block for the synthesis of complex heterocyclic compounds. Its unique molecular structure combines a thiophene ring with both a formyl and a nitrile group, making it highly versatile in organic chemistry applications. This compound plays a crucial role in the development of new molecules with specific biological activities, such as pharmaceuticals and specialty chemicals. Due to its reactivity and structural complexity, it is a valuable tool for researchers aiming to modify heterocyclic rings in various synthetic pathways.\u003c\/p\u003e\n\u003cp\u003eThe compound's polar nature allows it to participate in both nucleophilic and electrophilic reactions, enhancing its utility in synthetic processes. Its ability to form new compounds through chemical reactions makes it a preferred choice among organic chemists and medicinal researchers. The high reactivity and functional group diversity of 5-Formylthiophene-2-carbonitrile enable it to be a key component in the design of molecules with targeted biological properties. This makes it an essential reagent in advanced chemical synthesis.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 5-Formylthiophene-2-carbonitrile is commonly used by chemists and pharmacologists in the development of new compounds with potential medical or industrial applications. Its availability in the local market supports research efforts without the need for expensive imports. This accessibility ensures that researchers can conduct experiments efficiently and effectively, contributing to scientific advancements in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of heterocyclic compounds due to its functional groups and reactivity.\u003c\/li\u003e\n\u003cli\u003eDevelopment of pharmaceuticals and specialty chemicals through ring modification reactions.\u003c\/li\u003e\n\u003cli\u003eResearch in medicinal chemistry for the creation of bioactive molecules with therapeutic potential.\u003c\/li\u003e\n\u003cli\u003eUse in academic and industrial laboratories for the synthesis of complex organic structures.\u003c\/li\u003e\n\u003cli\u003eSupport for drug discovery projects requiring versatile building blocks for molecular design.\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: 21512-16-3\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: As available from supplier\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid (may vary depending on supplier)\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\u003e5-Formylthiophene-2-carbonitrile should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep it in airtight containers to prevent exposure to moisture and air, which can affect its reactivity. Due to its polar nature, it may absorb moisture from the atmosphere, so desiccant packaging is advisable. The compound should be handled in a well-ventilated area to minimize inhalation risks. Avoid direct contact with skin and eyes, and use appropriate personal protective equipment when handling. It is important to store the compound away from incompatible materials to ensure safety in the laboratory setting.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087061987546,"sku":"TCI2510F113331233","price":2727000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48087062020314,"sku":"TCI2510F113331234","price":10652000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510F1133.jpg?v=1767114179"},{"product_id":"tci2510h129434092","title":"TCI H1294 883742-29-8 4-Hexyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene","description":"\u003cp\u003e\u003cstrong\u003e4-Hexyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene\u003c\/strong\u003e (CAS 883742-29-8) 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 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: C16H27BO2S\u003c\/li\u003e\n\u003cli\u003eCAS number: 883742-29-8\u003c\/li\u003e\n\u003cli\u003ePurity: \u0026gt;98.0%(GC)\u003c\/li\u003e\n\u003cli\u003eTCI product code: H1294\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003e\u003cstrong\u003eSynonyms:\u003c\/strong\u003e 2-(4-Hexyl-2-thienyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane; 4-Hexyl-2-thiopheneboronic Acid Pinacol Ester\u003c\/p\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 Indonesia.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087269507290,"sku":"TCI2510H129434092","price":4217000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48087269540058,"sku":"TCI2510H129434093","price":14390000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510H1294.jpg?v=1768205558"},{"product_id":"tci2510h129834096","title":"TCI H1298 850881-09-3 3-Hexyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene","description":"\u003cp\u003e\u003cstrong\u003e3-Hexyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene\u003c\/strong\u003e (CAS 850881-09-3) 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 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