{"title":"Benzothiadiazoles and Analogs [Small Molecule Semiconductor Building Blocks]","description":"\u003cp\u003e\u003cstrong\u003eBenzothiadiazoles and Analogs [Small Molecule Semiconductor Building Blocks]\u003c\/strong\u003e — mencakup inti benzotiadiazola serta analog benzoksadiazola dan benzoselenadiazola tersubstitusi brom, nitril, atau boronat, yang bersifat elektron-defisien dan terkonjugasi. Kelas ini berperan sebagai unit akseptor dalam desain molekul semikonduktor organik push-pull.\u003c\/p\u003e\u003cp\u003eTurunan bromo-benzotiadiazola dan naftobis(tiadiazola) tetraboronat digunakan peneliti elektronika organik untuk menyusun material donor-akseptor pada sel surya organik dan transistor efek medan melalui reaksi kopling Suzuki atau Stille. Analog benzoksadiazola dan benzoselenadiazola dipakai sebagai unit pembanding untuk mempelajari pengaruh heteroatom terhadap sifat elektronik molekul terkonjugasi.\u003c\/p\u003e\u003cp\u003eContoh produk dalam koleksi ini: \u003ca href=\"\/en\/products\/tci2510b547412125\"\u003eTCI B5474 1335150-10-1 2-[(7-Bromo-2,1,3-benzothiadiazol-4-yl)methylene]malononitrile\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b577412513\"\u003eTCI B5774 5,10-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)naphtho[1,2-c:5,6-c']bis([1,2,5]oxadiazole)\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b547312124\"\u003eTCI B5473 1331742-86-9 7-Bromo-2,1,3-benzothiadiazole-4-carbonitrile\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b684613754\"\u003eTCI B6846 1203707-77-0 4,4'-(Benzo[c][1,2,5]thiadiazole-4,7-diyl)dianiline\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b547012121\"\u003eTCI B5470 1467776-41-5 5,10-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)naphtho[1,2-c:5,6-c']bis([1,2,5]thiadiazole)\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b701113871\"\u003eTCI B7011 22034-13-5 4-Bromobenzo[c][1,2,5]thiadiazole\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b543312069\"\u003eTCI B5433 1071224-34-4 7-Bromo-2,1,3-benzothiadiazole-4-carboxaldehyde\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510c133715841\"\u003eTCI C1337 7116-16-7 4-Chloro-2,1,3-benzoxadiazole\u003c\/a\u003e.\u003c\/p\u003e\u003cp\u003ePerhatikan posisi dan jenis gugus reaktif (bromo, boronat ester, nitril, atau aldehida) agar cocok dengan reaksi kopling silang yang direncanakan, serta kemurnian yang sesuai untuk aplikasi semikonduktor. Seluruh produk merupakan produk asli Tokyo Chemical Industry (TCI) Jepang, dengan kemurnian, kemasan, dan kondisi penyimpanan tercantum pada halaman masing-masing item.\u003c\/p\u003e\u003cp\u003eKategori lain yang sejajar di bawah Small Molecule Semiconductor Building Blocks, sering dipakai bersamaan dalam satu alur kerja laboratorium:\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-carbazoles-small-molecule-semiconductor-building-blocks\"\u003eCarbazoles [Small Molecule Semiconductor Building Blocks]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-fluorenes-fluorenones-small-molecule-semiconductor-building-blocks\"\u003eFluorenes, Fluorenones [Small Molecule Semiconductor Building Blocks]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-thiophenes-small-molecule-semiconductor-building-blocks\"\u003eThiophenes [Small Molecule Semiconductor Building Blocks]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-anthracenes-anthraquinones-small-molecule-semiconductor-building-blocks\"\u003eAnthracenes, Anthraquinones [Small Molecule Semiconductor Building Blocks]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-small-molecule-semiconductor-building-blocks-others\"\u003eSmall Molecule Semiconductor Building Blocks (Others)\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-secondary-arylamines-small-molecule-semiconductor-building-blocks\"\u003eSecondary Arylamines [Small Molecule Semiconductor Building Blocks]\u003c\/a\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eKembali ke \u003ca href=\"\/en\/collections\/tci-l3-small-molecule-semiconductor-building-blocks\"\u003eSmall Molecule Semiconductor Building Blocks\u003c\/a\u003e. Untuk pengadaan volume besar, kemasan khusus, atau grade tertentu, hubungi tim AMI Scientific — distributor resmi TCI Japan di Indonesia — untuk pengecekan ketersediaan dan lead time langsung ke Jepang.\u003c\/p\u003e","products":[{"product_id":"tci2510b577412513","title":"TCI B5774 5,10-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)naphtho[1,2-c:5,6-c']bis([1,2,5]oxadiazole)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B5774 is a bis(pinacolatoboron)-functionalized naphtho-bisoxadiazole compound serving as a versatile diboron reagent for Suzuki-Miyaura cross-coupling reactions. This compound acts as a dual-functional building block for constructing π-conjugated polymers and small-molecule optoelectronic materials. It is particularly valuable in research involving OLEDs, organic photovoltaics, and fluorescent sensors due to the electron-accepting character of the oxadiazole core.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48085902131418,"sku":"TCI2510B577412513","price":10877000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5774.jpg?v=1769180228"},{"product_id":"tci2510b684613754","title":"TCI B6846 1203707-77-0 4,4'-(Benzo[c][1,2,5]thiadiazole-4,7-diyl)dianiline","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6846 4,4'-(Benzo[c][1,2,5]thiadiazole-4,7-diyl)dianiline pairs an electron-accepting benzothiadiazole core with two electron-donating aniline units, giving a classic donor–acceptor–donor motif. The free aromatic amines make it a ready monomer for polyimides, imine-linked polymers, and covalent organic frameworks. Its optoelectronic character supports research into fluorescent materials, organic semiconductors, and photovoltaic active layers. AMI Scientific supplies this TCI building block in 1 g and 5 g laboratory-scale packs.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085958164698,"sku":"TCI2510B684613754","price":2812000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085958197466,"sku":"TCI2510B684613755","price":9810000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6846.jpg?v=1767094317"},{"product_id":"tci2510b701113871","title":"TCI B7011 22034-13-5 4-Bromobenzo[c][1,2,5]thiadiazole","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B7011 4-Bromobenzo[c][1,2,5]thiadiazole (CAS 22034-13-5) is a widely used heterocyclic building block based on the electron-accepting benzothiadiazole core. Its single aryl bromide handle allows selective Suzuki–Miyaura, Stille, Sonogashira, and amination chemistry to attach donor fragments. The resulting donor–acceptor architectures are central to organic photovoltaics, conjugated polymers, OLED materials, and fluorescent probes. AMI Scientific supplies this building block in 5 g and 25 g pack sizes suited to routine synthetic work.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48085963735258,"sku":"TCI2510B701113871","price":2278000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085963768026,"sku":"TCI2510B701113872","price":8180000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B7011.jpg?v=1767094474"},{"product_id":"tci2510c133715841","title":"TCI C1337 7116-16-7 4-Chloro-2,1,3-benzoxadiazole","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e4-Chloro-2,1,3-benzoxadiazole (CAS 7116-16-7), also known as 4-chlorobenzofurazan, is a nitrogen-rich heterocyclic building block from TCI available at AMI Scientific. The activated chlorine atom readily undergoes nucleophilic aromatic substitution with amines, thiols, and alkoxides, giving quick access to diverse benzoxadiazole derivatives. This scaffold is widely associated with fluorescent probes, labelling reagents, and medicinal chemistry libraries. Two pack sizes are offered so laboratories can match the quantity to exploratory screening or larger synthetic campaigns.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086064038106,"sku":"TCI2510C133715841","price":4498000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086064070874,"sku":"TCI2510C133715842","price":12339000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1337.jpg?v=1768816488"},{"product_id":"tci2510d384224228","title":"TCI D3842 15155-41-6 4,7-Dibromo-2,1,3-benzothiadiazole","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D3842 4,7-Dibromo-2,1,3-benzothiadiazole, CAS number 15155-41-6, is a heterocyclic compound built around a benzothiadiazole ring carrying two bromine atoms at the 4 and 7 positions. It is one of the most important monomers in organic electronic chemistry and conjugated polymer synthesis. Its role in the laboratory is to serve as an electron-accepting unit and, at the same time, as a two-directional connection point: the two bromine atoms provide reactive positions for cross-coupling reactions, allowing the benzothiadiazole unit to be assembled together with donor units into long conjugated chains or neatly structured small molecules.\u003c\/p\u003e\n\u003cp\u003eThe property that makes this compound the preferred choice is its strong electron-withdrawing ability, which comes from the nitrogen and sulfur atoms in the ring and produces a clear acceptor character in donor–acceptor systems. This character is the basis for tuning the energy gap, the light absorption, and the charge-carrier properties of the synthesized material. The symmetrical placement of the bromine atoms makes directed polymerization straightforward, and it also allows two different groups to be attached in sequential steps. The framework is planar and thermally stable as well, so it suits materials that are processed by heating or by solution coating.\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 and conjugated polymer synthesis. It is handled in synthetic chemistry and materials chemistry work where donor–acceptor architectures are prepared step by step, then characterized and processed into thin films. Because it is supplied as a defined single compound with a stated CAS number, it fits routine research procedures in which the acceptor unit must be reproducible from one synthesis batch to the next.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eConjugated polymer synthesis — the two bromine positions act as reliable coupling handles, so the benzothiadiazole unit can be polymerized with donor comonomers into long conjugated chains.\u003c\/li\u003e\n\u003cli\u003eDonor–acceptor small molecule construction — the symmetrical dibromo substitution permits two different donor groups to be attached in sequential steps, giving neatly structured target molecules.\u003c\/li\u003e\n\u003cli\u003eOrganic electronic material development — the strong electron-withdrawing ring supplies the clear acceptor character needed when energy gap and light absorption must be deliberately tuned.\u003c\/li\u003e\n\u003cli\u003eCross-coupling reaction work — the reactive bromine sites at the 4 and 7 positions make this compound a standard substrate for building extended conjugation through cross-coupling chemistry.\u003c\/li\u003e\n\u003cli\u003eSolution-processed and thermally processed film studies — the planar, thermally stable framework suits materials intended for processing by heating or by solution coating methods.\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: 15155-41-6\u003c\/li\u003e\n\u003cli\u003eCatalogue number: D3842\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 size options when ordering\u003c\/li\u003e\n\u003cli\u003eStorage note: keep in the closed original container, in a cool, dry, well-ventilated place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the compound in its original tightly closed container in a cool, dry, well-ventilated area, protected from light and moisture and kept away from incompatible reagents. Amber glass or the supplier's original packaging is suitable; transfer only what is needed and reseal promptly to avoid moisture uptake. Handle the solid in a fume hood using gloves, safety glasses, and a laboratory coat, and avoid generating or inhaling dust. Weigh and transfer with clean, dry spatulas to prevent contamination between batches. Label all secondary containers clearly, keep the manufacturer safety data sheet accessible before first use, and dispose of residues and contaminated consumables through the laboratory's chemical waste route rather than the general drain or bin.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48275700711642,"sku":"TCI2510D384224228","price":1153000.0,"currency_code":"IDR","in_stock":false},{"title":"5g","offer_id":48275700744410,"sku":"TCI2510D384224229","price":3458000.0,"currency_code":"IDR","in_stock":false}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D3842.jpg?v=1767106648"},{"product_id":"tci2510d394424383","title":"TCI D3944 63224-42-0 4,7-Dibromo-2,1,3-benzoselenadiazole","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e4,7-Dibromo-2,1,3-benzoselenadiazole is an organic semiconductor building block built around a benzoselenadiazole core carrying two bromine atoms at the 4 and 7 positions. In materials science laboratories, this compound serves as an electron-accepting unit that is ready to be polymerized or coupled in order to construct donor-acceptor systems. The two symmetrically placed bromo groups make it an ideal bifunctional monomer for cross-coupling reactions such as Stille, Suzuki, and direct C-H coupling, allowing researchers to assemble conjugated polymers with controlled, regularly repeating chain structures.\u003c\/p\u003e\n\u003cp\u003eThe key characteristic that leads researchers to select this material is the presence of a selenium atom in place of the sulfur found in the more common benzothiadiazole framework. The selenium atom is larger and more easily polarized, and it contributes stronger intermolecular interactions, so the resulting polymers tend to display a narrower band gap, absorption shifted toward longer wavelengths, and denser chain packing within thin films. These properties are highly sought after in organic solar cell and near-infrared detector research. The benzoselenadiazole core also retains the electron-deficient character needed for a reliable acceptor unit.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this building block is typically used in university and institutional materials chemistry groups working on organic electronics, thin-film devices, and conjugated polymer synthesis. It is generally handled at the bench scale in synthesis laboratories equipped for inert-atmosphere cross-coupling work, and is commonly requested by research teams preparing donor-acceptor copolymers for photovoltaic and photodetector studies, as well as by groups characterizing optical and electronic properties of newly designed semiconducting materials.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eDonor-acceptor copolymer synthesis: the symmetric dibromo substitution provides two reliable coupling sites, letting researchers alternate this acceptor unit with donor comonomers in a regular, repeating chain sequence.\u003c\/li\u003e\n\u003cli\u003eStille cross-coupling: the aryl bromide positions react cleanly with organostannane partners, making this a standard monomer for building extended conjugated backbones under palladium catalysis.\u003c\/li\u003e\n\u003cli\u003eSuzuki cross-coupling: the same bromo groups pair with boronic acids and esters, giving materials chemists an alternative route to conjugated polymers and defined small-molecule segments.\u003c\/li\u003e\n\u003cli\u003eDirect C-H coupling polymerization: the compound can be coupled without prior stannylation or borylation, reducing synthetic steps for laboratories developing more streamlined polymer preparation routes.\u003c\/li\u003e\n\u003cli\u003eOrganic solar cell and near-infrared detector materials research: the selenium-containing core narrows the band gap and red-shifts absorption, supporting devices that must harvest longer-wavelength light.\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: 63224-42-0\u003c\/li\u003e\n\u003cli\u003eCatalog number: D3944\u003c\/li\u003e\n\u003cli\u003eCategory: Materials Science \u0026gt; Material Building Blocks \u0026gt; Polymer\/Macromolecule Semiconductor Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in standard TCI research-scale packaging; please confirm the pack size required when ordering\u003c\/li\u003e\n\u003cli\u003eStorage note: store in a cool, dry, well-ventilated place, protected from light and kept tightly closed\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the container tightly closed in a cool, dry, and well-ventilated area, away from direct sunlight, heat sources, and incompatible chemicals. Amber glass bottles or the original manufacturer container are suitable, and transferring under an inert atmosphere is advisable when the material will be used in moisture-sensitive cross-coupling reactions. Handle the compound inside a fume hood using gloves, safety glasses, and a laboratory coat, and avoid generating or inhaling dust during weighing. Keep the container clearly labelled, and always consult the manufacturer's safety data sheet before use and disposal.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086646948058,"sku":"TCI2510D394424383","price":6578000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D3944.jpg?v=1768817979"},{"product_id":"tci2510d406424548","title":"TCI D4064 18392-81-9 5,6-Dibromo-2,1,3-benzothiadiazole","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D4064 5,6-Dibromo-2,1,3-benzothiadiazole is a heterocyclic building block consisting of a benzothiadiazole core carrying two bromine atoms at the 5 and 6 positions. The benzothiadiazole core itself is widely recognized as a strong electron-withdrawing unit in organic materials chemistry, while the two bromine atoms act as reactive connection points for a range of transition metal-catalyzed cross-coupling reactions. In the laboratory, this compound serves as a monomer and a key intermediate in the assembly of conjugated polymers, small-molecule semiconductors, and purpose-designed dyes and fluorescent probes.\u003c\/p\u003e\n\u003cp\u003eThe characteristic that makes this material a preferred choice is its ability to act as an acceptor unit within donor–acceptor architectures. When paired with electron-rich units such as thiophene, fluorene, or carbazole through Suzuki, Stille, or Sonogashira coupling, the benzothiadiazole core narrows the energy band gap and shifts both absorption and emission toward longer wavelengths. The adjacent positioning of the two bromine atoms provides a distinctive substitution pattern that is useful for constructing fused frameworks as well as branched structures. The thermal stability of this heterocyclic core is also advantageous during synthetic and processing steps.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this building block is typically used in university and institutional research groups working on organic electronics, materials chemistry, and synthetic organic chemistry. It is commonly handled in multi-step synthesis programs where a defined acceptor unit is required, and in the preparation of fluorescent compounds for sensing and imaging studies. Researchers usually order it as part of a broader set of coupling partners and catalysts for planned reaction campaigns.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eConjugated polymer synthesis: the dibrominated core functions as a ready acceptor monomer that can be polymerized with electron-rich comonomers through metal-catalyzed cross-coupling to build extended conjugated backbones.\u003c\/li\u003e\n\u003cli\u003eDonor–acceptor small molecule construction: the strong electron-withdrawing benzothiadiazole unit pairs with donor fragments to narrow the energy band gap and tune electronic behavior in a controlled way.\u003c\/li\u003e\n\u003cli\u003eSuzuki, Stille, and Sonogashira coupling chemistry: both bromine atoms serve as reliable reactive handles, allowing single or double coupling with thiophene, fluorene, or carbazole partners.\u003c\/li\u003e\n\u003cli\u003eFluorescent dye and probe development: the core shifts absorption and emission toward longer wavelengths, which supports the design of tailored luminescent probes for laboratory sensing work.\u003c\/li\u003e\n\u003cli\u003eFused and branched framework building: the neighboring 5,6-substitution pattern gives a distinctive geometry suited to assembling fused ring skeletons and branched molecular architectures.\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: 18392-81-9\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003eProduct code: D4064\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in standard TCI research pack sizes; please confirm the size required when ordering\u003c\/li\u003e\n\u003cli\u003eStorage: keep in a tightly closed 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 material in its original tightly closed container in a cool, dry, well-ventilated area, protected from light and moisture and kept away from strong oxidizing agents. Amber glass or the supplier's original packaging is suitable for keeping the contents dry and shielded from light. Handle only in a chemical fume hood using appropriate personal protective equipment, including safety glasses, gloves, and a laboratory coat. Avoid generating dust, avoid inhalation and skin contact, and close the container promptly after weighing. Consult the manufacturer's safety data sheet before use, and dispose of residues and contaminated materials through your institution's chemical waste procedures.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086653993178,"sku":"TCI2510D406424548","price":8264000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D4064.jpg?v=1769141946"},{"product_id":"tci2510d448725095","title":"TCI D4487 165190-76-1 4,7-Di(2-thienyl)-2,1,3-benzothiadiazole","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e4,7-Di(2-thienyl)-2,1,3-benzothiadiazole is an organic compound widely used in electronic material research, particularly in the development of organic field-effect transistors (OFETs). This compound plays a crucial role in laboratory settings where researchers are working on flexible and lightweight electronic devices. Its unique molecular structure enables efficient electron transport, making it a key component in the fabrication of organic semiconductor layers. As a core material in advanced electronic applications, it supports innovation in next-generation electronic systems.\u003c\/p\u003e\n\u003cp\u003eThe compound is valued for its high chemical stability, ability to form smooth and uniform layers, and compatibility with a variety of substrates. These properties make it ideal for high-precision material processing techniques. Additionally, its optical characteristics open up opportunities for use in optoelectronic applications. The compound’s versatility and performance in various experimental conditions contribute to its popularity among researchers.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 4,7-Di(2-thienyl)-2,1,3-benzothiadiazole is commonly used in material science and information technology research. It is a key material for developing new electronic devices and exploring advanced semiconductor technologies. Its application is widespread in academic and industrial research settings, supporting both fundamental and applied studies in electronic materials.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic Field-Effect Transistor (OFET) Development: This compound is ideal for fabricating organic semiconductor layers due to its high electron mobility and stability, enabling efficient transistor performance.\u003c\/li\u003e\n\u003cli\u003eFlexible Electronic Device Research: Its lightweight and flexible properties make it suitable for creating bendable and wearable electronic systems.\u003c\/li\u003e\n\u003cli\u003eOptoelectronic Material Investigation: The compound’s optical properties allow it to be used in the development of light-emitting and photodetecting devices.\u003c\/li\u003e\n\u003cli\u003eSemiconductor Layer Coating: Its ability to form smooth and uniform layers makes it a preferred choice for coating processes in thin-film transistor fabrication.\u003c\/li\u003e\n\u003cli\u003eMaterial Science Research: It is frequently used in studies focused on the synthesis and characterization of new organic electronic 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: 165190-76-1\u003c\/li\u003e\n\u003cli\u003eCategory: Materials Science \u0026gt; Electronic Materials \u0026gt; Organic Transistor (OFET) Materials\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid (as per standard product description)\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct 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 direct sunlight and sources of heat. It is recommended to use airtight containers to prevent exposure to moisture and air, which may affect its stability. Proper labeling of containers is essential for safe handling and identification. Due to its chemical nature, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to ensure laboratory safety. Avoid contact with skin and eyes, and ensure adequate ventilation when working with the material. Regular monitoring of storage conditions is advised to maintain the integrity of the compound.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48086694166746,"sku":"TCI2510D448725095","price":2812000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48086694199514,"sku":"TCI2510D448725096","price":10933000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D4487.jpg?v=1768818110"},{"product_id":"tci2510d461425254","title":"TCI D4614 54286-63-4 4,7-Dibromo-2,1,3-benzoxadiazole","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e4,7-Dibromo-2,1,3-benzoxadiazole is a chemical compound widely used in scientific research, particularly in the fields of materials science and semiconductor technology. This compound serves as a foundational building block for the synthesis of complex materials with specific conductive or optical properties. In laboratory settings, it plays a crucial role in the development of both inorganic and organic materials, contributing to the creation of advanced functional materials. Its versatility makes it an essential component in the design and modification of molecular structures, supporting innovation in material science.\u003c\/p\u003e\n\u003cp\u003eThe compound is valued for its stable chemical structure and controlled reactivity, which allow it to be manipulated effectively in various synthetic processes. These properties make it a preferred choice for researchers aiming to create new materials with tailored properties. Its ability to form bonds with a wide range of functional groups enhances its utility in molecular design and functionalization. This adaptability ensures that it remains a key reagent in the synthesis of advanced materials with specific applications in electronics and optoelectronics.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 4,7-Dibromo-2,1,3-benzoxadiazole is commonly used in semiconductor technology, optical material research, and electronic applications. Researchers from academic and industrial institutions rely on this compound to develop new materials with potential applications in advanced technologies. Its role in material innovation underscores its importance in both academic and industrial research environments in Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSemiconductor material synthesis due to its role in creating conductive and optoelectronic compounds.\u003c\/li\u003e\n\u003cli\u003eOptical material development because of its ability to form functionalized structures with specific optical properties.\u003c\/li\u003e\n\u003cli\u003eOrganic semiconductor research as a building block for molecular design and functionalization.\u003c\/li\u003e\n\u003cli\u003eAdvanced electronic material fabrication due to its stability and reactivity in synthetic processes.\u003c\/li\u003e\n\u003cli\u003eMaterial modification applications where controlled reactivity and structural versatility are required.\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: 54286-63-4\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 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 sources of 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 protected from potential contaminants. In laboratory settings, it is important to handle the compound with appropriate personal protective equipment to ensure safety. Always ensure proper ventilation when working with this material to minimize any potential risks associated with its handling.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48086699573466,"sku":"TCI2510D461425254","price":1997000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48086699606234,"sku":"TCI2510D461425255","price":6578000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D4614.jpg?v=1768818156"},{"product_id":"tci2510d473425418","title":"TCI D4734 1295502-53-2 4,7-Dibromo-5,6-difluoro-2,1,3-benzothiadiazole","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e4,7-Dibromo-5,6-difluoro-2,1,3-benzothiadiazole is a fluorinated building block widely used in organic chemistry laboratories for the synthesis of complex compounds. This compound serves as a versatile intermediate in various chemical reactions, particularly those involving bromo and fluoro substitution. Its unique heterocyclic structure makes it a valuable tool for researchers aiming to develop new materials or pharmaceutical compounds. Due to its reactivity and structural versatility, it is frequently employed in synthetic pathways requiring functional group manipulation.\u003c\/p\u003e\n\u003cp\u003eThe compound is prized for its chemical stability under controlled conditions and its predictable reactivity profile. The presence of bromine and fluorine atoms in its structure significantly enhances its reactivity, allowing for flexible molecular modifications. These properties make it an ideal candidate for a wide range of chemical transformations. Additionally, its well-defined chemical behavior simplifies synthesis and characterization processes, making it a reliable choice for laboratory use.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in organic chemistry research, particularly in academic and research institutions. Its availability and consistent performance make it a preferred choice for scientists working on advanced synthetic projects. It is especially useful in studies focused on drug development, material science, and chemical innovation. Its role in supporting cutting-edge research underscores its importance in the scientific community.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of pharmaceutical compounds due to its reactivity and structural versatility.\u003c\/li\u003e\n\u003cli\u003eDevelopment of new materials through functional group modification and substitution reactions.\u003c\/li\u003e\n\u003cli\u003eResearch in chemical innovation where predictable reactivity and stability are essential.\u003c\/li\u003e\n\u003cli\u003eSynthesis of complex heterocyclic compounds for academic and industrial applications.\u003c\/li\u003e\n\u003cli\u003eExploration of fluorinated derivatives for advanced chemical transformations and 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: 1295502-53-2\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Fluorinated Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per 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 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. Avoid exposure to heat or incompatible substances to ensure safe storage and use. In laboratory settings, it is important to follow standard chemical safety protocols to minimize risks during handling and experimentation.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48086705668314,"sku":"TCI2510D473425418","price":5509000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D4734.jpg?v=1767107900"},{"product_id":"tci2510d475025434","title":"TCI D4750 1347736-74-6 4,7-Dibromo-5-fluoro-2,1,3-benzothiadiazole","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D4750 4,7-Dibromo-5-fluoro-2,1,3-benzothiadiazole is a benzothiadiazole derivative carrying two bromine atoms at the 4- and 7-positions together with a single fluorine atom at the 5-position. In materials research laboratories, this compound serves as an electron-accepting unit that is very commonly used to construct conjugated polymers and small molecules of the donor–acceptor type. The two bromine atoms provide ready-to-react coupling points for transition-metal-catalysed cross-coupling, allowing researchers to join this unit to a wide range of donor segments and build a desired electronic framework in a planned, deliberate way.\u003c\/p\u003e\n\u003cp\u003eThe main appeal of this building block lies in the presence of the fluorine atom. Fluorination of the benzothiadiazole core is known to lower the frontier orbital energy levels of conjugated materials, strengthen interchain interactions, and assist molecular ordering in thin films. These effects frequently translate into improved stability and device performance without altering the basic molecular skeleton. The benzothiadiazole core itself is a strong yet still readily processable electron acceptor, and the 4,7-dibromo substitution pattern gives a symmetric reactivity profile that simplifies copolymer design.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this material is typically used in organic electronics and polymer chemistry research groups at universities and research institutes, where donor–acceptor conjugated systems are prepared on a laboratory scale. It is handled as a synthetic intermediate within multi-step routes, drawn upon whenever a fluorinated acceptor unit with defined coupling positions is required. Because it is supplied under the TCI brand as a catalogue building block, it fits routine research workflows in which reproducible starting materials are needed for repeated synthetic campaigns.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eDonor–acceptor conjugated polymer synthesis: the two 4,7-bromine sites act as reliable coupling handles, letting researchers alternate this acceptor with chosen donor comonomers in a controlled sequence.\u003c\/li\u003e\n\u003cli\u003eTransition-metal-catalysed cross-coupling reactions: the dibromo substitution pattern is directly compatible with standard metal-catalysed coupling chemistry used to form carbon–carbon bonds between aromatic units.\u003c\/li\u003e\n\u003cli\u003eSmall-molecule organic semiconductor preparation: the compound provides a strong yet processable electron-accepting centre around which conjugated small molecules of defined architecture can be assembled.\u003c\/li\u003e\n\u003cli\u003eFrontier orbital energy level engineering: fluorination on the benzothiadiazole core lowers frontier orbital levels, giving researchers a structural means of tuning the electronic character of target materials.\u003c\/li\u003e\n\u003cli\u003eThin-film morphology and device stability studies: the fluorine substituent strengthens interchain interactions and assists molecular ordering in films, supporting work on stability and device 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: 1347736-74-6\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Fluorinated Building Blocks\u003c\/li\u003e\n\u003cli\u003eChemical name: 4,7-Dibromo-5-fluoro-2,1,3-benzothiadiazole\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in standard TCI catalogue research quantities; please confirm the pack size required when ordering\u003c\/li\u003e\n\u003cli\u003eStorage: store in a 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\u003eKeep this building block in its original tightly closed container, stored in a cool, dry, well-ventilated area away from moisture, direct sunlight, and sources of heat or ignition. Amber or opaque glass containers with chemically resistant closures are suitable for any transfer or subdivision, and containers should be clearly labelled with the chemical name and CAS number. Handle in a fume hood using safety glasses, nitrile gloves, and a laboratory coat, and avoid generating or inhaling dust when weighing solids. Follow the manufacturer's safety data sheet for detailed exposure control, incompatibility, and disposal guidance, and dispose of residues and contaminated consumables through the institution's chemical waste stream rather than general waste.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48086706290906,"sku":"TCI2510D475025434","price":1462000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48086706323674,"sku":"TCI2510D475025435","price":4610000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D4750.jpg?v=1767107929"},{"product_id":"tci2510d498525767","title":"TCI D4985 76186-72-6 4,7-Dibromo-5,6-dinitro-2,1,3-benzothiadiazole","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e4,7-Dibromo-5,6-dinitro-2,1,3-benzothiadiazole is a chemical compound widely used as a building block in the synthesis of complex heterocyclic compounds. This compound plays a crucial role in laboratory settings, particularly in organic chemistry research, where it serves as a versatile intermediate for the development of new molecules. Its unique structure allows for the incorporation of various functional groups, making it a valuable tool in the creation of compounds with specific biological or chemical properties. Due to its stability and reactivity, it is frequently employed in synthetic pathways that require precise control over molecular architecture.\u003c\/p\u003e\n\u003cp\u003eThe compound’s high chemical stability and ability to undergo multiple functional group modifications make it a preferred choice for researchers. Its complex heterocyclic framework provides a robust platform for further chemical transformations, enabling the synthesis of a wide range of derivatives. Additionally, its resistance to degradation under various reaction conditions enhances its utility in both academic and industrial research environments. These properties contribute to its widespread use in laboratories that require reliable and adaptable chemical intermediates.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in organic chemistry research, especially in the fields of pharmacology and materials science. Local researchers often rely on it as a foundational material for the development of new compounds with potential medical or industrial applications. Its availability and chemical properties make it an essential component in the synthesis of bioactive and functional materials within the scientific community.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of bioactive compounds due to its versatile functional group compatibility and structural adaptability.\u003c\/li\u003e\n\u003cli\u003eDevelopment of pharmaceutical intermediates as it supports the creation of complex heterocyclic structures with biological activity.\u003c\/li\u003e\n\u003cli\u003eMaterial science research for the synthesis of advanced polymers and functional materials with specific chemical properties.\u003c\/li\u003e\n\u003cli\u003eChemical modification studies to explore the reactivity and stability of heterocyclic frameworks under various conditions.\u003c\/li\u003e\n\u003cli\u003eAnalytical chemistry applications for the characterization of complex organic compounds through structural elucidation techniques.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 76186-72-6\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 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, and well-ventilated area 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, and well-ventilated area, away from direct light and moisture. It is recommended to use airtight containers made of materials that are chemically inert to prevent contamination or degradation. Due to its chemical reactivity, it should be handled with appropriate personal protective equipment, including gloves, safety goggles, and a lab coat. Avoid exposure to heat or open flames, as it may pose a fire hazard. Always ensure proper ventilation when working with this compound to minimize inhalation risks. Maintain a safe distance from incompatible materials to prevent unwanted chemical reactions.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086738075866,"sku":"TCI2510D498525767","price":2025000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086738108634,"sku":"TCI2510D498525768","price":7055000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D4985.jpg?v=1767108256"},{"product_id":"tci2510d528826165","title":"TCI D5288 133546-50-6 5,10-Dibromonaphtho[1,2-c:5,6-c']bis([1,2,5]thiadiazole)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e5,10-Dibromonaphtho[1,2-c:5,6-c']bis([1,2,5]thiadiazole) is a complex chemical compound widely used in materials science research. This compound plays a crucial role in the development of advanced materials, particularly in the field of organic and optoelectronic applications. As a building block for polymers and semiconductors, it is essential for creating materials with unique electronic properties. Its presence in laboratory settings enables researchers to explore new synthetic pathways and functional materials.\u003c\/p\u003e\n\u003cp\u003eThe compound's molecular structure features two bromine atoms positioned strategically, which significantly enhances its reactivity. This reactivity makes it a preferred choice for researchers aiming to modify molecular structures through substitution or other chemical reactions. Its versatility in synthetic processes allows it to be used in a variety of experimental setups, making it a valuable resource for material scientists. The compound's chemical stability and reactivity also support its use in the synthesis of advanced electronic materials.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used by researchers in materials science and high-tech industries. It is frequently employed in the development of new materials with potential applications in electronics and optoelectronics. Institutions and research centers in Indonesia rely on this compound to advance their work in material innovation and technological development. Its availability through AMI Scientific ensures that local researchers have access to this essential chemical for their experiments.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic semiconductor synthesis due to its reactivity and structural versatility for creating advanced electronic materials.\u003c\/li\u003e\n\u003cli\u003eOptoelectronic material development as it supports the formation of compounds with unique optical and electronic properties.\u003c\/li\u003e\n\u003cli\u003ePolymer modification processes where its bromine groups enable functionalization of polymer chains for improved performance.\u003c\/li\u003e\n\u003cli\u003eResearch in molecular electronics due to its ability to participate in chemical reactions that alter molecular structure.\u003c\/li\u003e\n\u003cli\u003eHigh-tech material innovation as it is a key building block for developing next-generation electronic and optoelectronic components.\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: 133546-50-6\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: 50 g\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 environment, away from direct light and moisture to maintain its stability and reactivity. It is recommended to use airtight containers made of glass or high-density polyethylene to prevent contamination and degradation. Due to its bromine content, it is important to handle it with care, using appropriate personal protective equipment such as gloves and safety goggles. In laboratory settings, it should be kept in a well-ventilated area to minimize exposure. Proper labeling and storage conditions are essential to ensure safe handling and prevent accidental use. Always follow standard laboratory safety protocols when working with this compound.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48086753083610,"sku":"TCI2510D528826165","price":10765000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D5288.jpg?v=1768818377"},{"product_id":"tci2510d549626411","title":"TCI D5496 1437229-17-8 5,10-Dibromonaphtho[1,2-c:5,6-c']bis([1,2,5]oxadiazole)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e5,10-Dibromonaphtho[1,2-c:5,6-c']bis([1,2,5]oxadiazole) is a complex chemical compound widely used in scientific research, particularly in the development of semiconductor and polymer materials. This compound plays a crucial role in laboratories where advanced material synthesis is required. Its unique molecular structure allows for chemical modifications, enabling the creation of materials with tailored electronic properties. As a building block for complex compounds, it supports innovation in various scientific disciplines.\u003c\/p\u003e\n\u003cp\u003eThe compound is valued for its chemical stability and controlled reactivity, making it ideal for high-precision chemical reactions. Its two bromine groups at specific positions provide opportunities for further functionalization, allowing researchers to fine-tune the electronic and optical properties of the resulting materials. These characteristics make it a preferred choice for applications requiring precise molecular control. Additionally, its compatibility with various synthetic methods enhances its utility in material science research.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in material science and semiconductor technology research. Scientists rely on it to develop new materials with potential applications in electronics, optoelectronics, and energy technologies. 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