{"title":"Benzonitriles [Liquid Crystal (LC) Building Blocks]","description":"\u003cp\u003e\u003cstrong\u003eBenzonitriles [Liquid Crystal (LC) Building Blocks]\u003c\/strong\u003e — berisi turunan benzonitril tersubstitusi dengan gugus alkoksi, benzil-oksi, halogen, trifluorometoksi, atau siklik jenuh, yang menyediakan gugus nitril polar sebagai unit ujung pada perancangan molekul kristal cair.\u003c\/p\u003e\u003cp\u003eBenzonitriles [Liquid Crystal (LC) Building Blocks] digunakan peneliti material elektro-optik untuk menyusun mesogen dengan gugus nitril terminal yang memberi momen dipol tinggi, melalui reaksi kopling karbon-karbon atau substitusi aromatik, guna mengatur sifat dielektrik dan perilaku fase pada material display kristal cair.\u003c\/p\u003e\u003cp\u003eContoh produk dalam koleksi ini: \u003ca href=\"\/en\/products\/tci2510a0493701\"\u003eTCI A0493 874-90-8 Anisonitrile\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510c013514091\"\u003eTCI C0135 623-03-0 4-Chlorobenzonitrile\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510v013556557\"\u003eTCI V0135 96184-42-8 4-(trans-4-Vinylcyclohexyl)benzonitrile\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510c044314565\"\u003eTCI C0443 105-07-7 4-Formylbenzonitrile\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510t229253574\"\u003eTCI T2292 332-25-2 4-(Trifluoromethoxy)benzonitrile\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510c044514569\"\u003eTCI C0445 619-65-8 4-Cyanobenzoic Acid\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b14266700\"\u003eTCI B1426 623-00-7 4-Bromobenzonitrile\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510c084215133\"\u003eTCI C0842 767-00-0 4-Hydroxybenzonitrile\u003c\/a\u003e.\u003c\/p\u003e\u003cp\u003ePerhatikan jenis dan posisi substituen (alkoksi, benzil-oksi, siklik jenuh, trifluorometoksi) pada cincin aromatik karena menentukan momen dipol dan sifat dielektrik molekul 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 Liquid Crystal (LC) Building Blocks, sering dipakai bersamaan dalam satu alur kerja laboratorium:\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-biphenyls-liquid-crystal-lc-building-blocks\"\u003eBiphenyls [Liquid Crystal (LC) Building Blocks]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-benzoic-acids-liquid-crystal-lc-building-blocks\"\u003eBenzoic Acids [Liquid Crystal (LC) Building Blocks]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-phenols-liquid-crystal-lc-building-blocks\"\u003ePhenols [Liquid Crystal (LC) Building Blocks]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-bromobenzenes-liquid-crystal-lc-building-blocks\"\u003eBromobenzenes [Liquid Crystal (LC) Building Blocks]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-benzaldehydes-liquid-crystal-lc-building-blocks\"\u003eBenzaldehydes [Liquid Crystal (LC) Building Blocks]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-benzeneboronic-acids-liquid-crystal-lc-building-blocks\"\u003eBenzeneboronic Acids [Liquid Crystal (LC) Building Blocks]\u003c\/a\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eKembali ke \u003ca href=\"\/en\/collections\/tci-l3-liquid-crystal-lc-building-blocks\"\u003eLiquid Crystal (LC) 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":"tci2510c013514091","title":"TCI C0135 623-03-0 4-Chlorobenzonitrile","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0135, 4-Chlorobenzonitrile (CAS 623-03-0), is a solid aromatic nitrile bearing a chlorine substituent in the para position. The nitrile group is readily converted into amines, amides, carboxylic acids, or nitrogen-rich heterocycles such as tetrazoles. Together with the aryl chloride handle for cross-coupling, this makes the compound a flexible non-heterocyclic building block for medicinal and materials chemistry. AMI Scientific supplies it in 25 g and 500 g packs in original manufacturer packaging.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAim (1994). A modified ebulliometric method for high-boiling substances: vapour pressures of 2-chlorobenzonitrile and 4-chlorobenzonitrile at temperatures from 380 K to 490 K. \u003cem\u003eThe Journal of Chemical Thermodynamics\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1006\/jcht.1994.1115\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1006\/jcht.1994.1115\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eMahajan et al. (2006). Synthesis of 2‐Amino‐5‐chlorobenzonitrile.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.200639102\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.200639102\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003e(2013). A New Synthetic Route Toward o-Chlorobenzonitrile. \u003cem\u003eChinese Journal of Applied Chemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.3724\/sp.j.1095.2013.20530\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.3724\/sp.j.1095.2013.20530\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":"25g","offer_id":48085972943066,"sku":"TCI2510C013514091","price":1799000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48085972975834,"sku":"TCI2510C013514092","price":15375000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0135.jpg?v=1768816144"},{"product_id":"tci2510c044314565","title":"TCI C0443 105-07-7 4-Formylbenzonitrile","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e4-Formylbenzonitrile (CAS 105-07-7) from TCI is a bifunctional aromatic building block bearing an aldehyde and a nitrile group in the para position. The two electron-withdrawing groups create an electron-poor ring, enhancing carbonyl reactivity toward nucleophiles in Schiff base formation, Knoevenagel condensation, and Wittig-type olefination. Its nitrile group offers orthogonal transformations into carboxylic acids, primary amines, amidines, or tetrazole rings, making stepwise synthetic design straightforward. AMI Scientific offers this reagent in 5 g and 25 g packs for exploratory and routine laboratory synthesis.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eJ. Intelli (2024). Synthesis of 4-(2,2-Difluorovinyl)benzonitrile through a Wittig-type Olefination of 4-Formylbenzonitrile. \u003cem\u003eOrganic Syntheses\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.15227\/orgsyn.101.0542\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.15227\/orgsyn.101.0542\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eLiu et al. (2017). Direct Access to Isoindolin‐1‐one Scaffolds by Copper‐Catalyzed Divergent Cyclizations of 2‐Formylbenzonitrile and Diaryliodonium Salts. \u003cem\u003eAdvanced Synthesis \u0026amp; Catalysis\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/adsc.201601403\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/adsc.201601403\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eBritton et al. (2006). 2-Formylbenzonitrile. \u003cem\u003eActa Crystallographica Section C Crystal Structure Communications\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1107\/s0108270106013138\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1107\/s0108270106013138\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":"5g","offer_id":48085999059162,"sku":"TCI2510C044314565","price":1097000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085999091930,"sku":"TCI2510C044314566","price":3092000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0443.jpg?v=1769180303"},{"product_id":"tci2510c044514569","title":"TCI C0445 619-65-8 4-Cyanobenzoic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e4-Cyanobenzoic Acid (CAS 619-65-8) from TCI is a rigid, linear aromatic building block carrying both carboxylic acid and nitrile functionalities in the para position. The carboxyl group is readily activated for amide coupling and esterification, while the nitrile can be converted into tetrazoles, amidines, or aminomethyl groups. Its linear geometry and polar nitrile make it a frequent choice for metal-organic framework linkers and liquid crystal research. AMI Scientific provides this reagent in 5 g and 25 g packs for laboratory-scale synthesis.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eWang et al. (2009). Solubility of 3,5-Dimethoxybenzoic Acid, 4-Cyanobenzoic Acid, 4-Acetoxybenzoic Acid, 3,5-Diaminobenzoic Acid, and 2,4-Dichlorobenzoic Acid in Ethanol. \u003cem\u003eJournal of Chemical \u0026amp; Engineering Data\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1021\/je900190n\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1021\/je900190n\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eHan et al. (1999). Infrared and Raman spectra of 4-cyanobenzoic acid on powdered silver. \u003cem\u003eVibrational Spectroscopy\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/s0924-2031(99)00066-1\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/s0924-2031(99)00066-1\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eHan et al. (1998). Diffuse Reflectance Infrared Spectra of 4-Nitrobenzoic Acid and 4-Cyanobenzoic Acid Self-Assembled on Fine Silver Particles. \u003cem\u003eApplied Spectroscopy\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1366\/0003702981944931\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1366\/0003702981944931\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":"5g","offer_id":48085999190234,"sku":"TCI2510C044514569","price":1322000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085999223002,"sku":"TCI2510C044514570","price":3345000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0445.jpg?v=1767095251"},{"product_id":"tci2510c084215133","title":"TCI C0842 767-00-0 4-Hydroxybenzonitrile","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0842 4-Hydroxybenzonitrile (CAS 767-00-0) is a para-substituted aromatic bearing both a phenolic hydroxyl and a nitrile group. The phenol is easily alkylated or acylated, while the nitrile can be transformed into amides, amines, tetrazoles, and other nitrogen heterocycles, making it a versatile two-way building block. It is widely applied in pharmaceutical and agrochemical intermediates as well as in liquid crystal and conjugated materials research. AMI Scientific offers this TCI reagent in 25 g and 500 g packs; store it cool, dry, protected from light, and tightly closed.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eCupples et al. (2005). Dehalogenation of the Herbicides Bromoxynil (3,5-Dibromo-4-Hydroxybenzonitrile) and Ioxynil (3,5-Diiodino-4-Hydroxybenzonitrile) by Desulfitobacterium chlororespirans. \u003cem\u003eApplied and Environmental Microbiology\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1128\/aem.71.7.3741-3746.2005\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1128\/aem.71.7.3741-3746.2005\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eVIDYASAGAR et al. (1993). ChemInform Abstract: A Novel Two‐Step Synthesis of 3,5‐Dibromo‐4‐hydroxybenzonitrile. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.199347158\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.199347158\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eMachado et al. (1995). Photolysis of bromoxynil (3,5‐dibromo‐4‐hydroxybenzonitrile) in aqueous solution. \u003cem\u003ePesticide Science\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/ps.2780450203\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/ps.2780450203\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":"25g","offer_id":48086032744666,"sku":"TCI2510C084215133","price":1069000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48086032777434,"sku":"TCI2510C084215134","price":9922000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0842.jpg?v=1768816349"},{"product_id":"tci2510c114115569","title":"TCI C1141 1443-80-7 4'-Cyanoacetophenone","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e4'-Cyanoacetophenone (CAS 1443-80-7) from TCI is a bifunctional aromatic ketone carrying a para-positioned nitrile group. The acetyl moiety supports aldol condensations, chalcone formation, and heterocycle construction, while the nitrile can be hydrolysed, reduced, or converted into tetrazole rings. This dual reactivity makes it a practical starting point for medicinal chemistry and functional materials research. AMI Scientific offers the reagent in 10 g and 25 g pack sizes for laboratory use.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eReidlinger et al. (1999). ChemInform Abstract: Cyanoacetophenone as a Synthon for 1,4,5‐Substituted Pyrazoles.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.199909139\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.199909139\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eReidlinger et al. (1998). Cyanoacetophenone as a Synthon for 1,4,5-Substituted Pyrazoles. \u003cem\u003eMonatshefte für Chemie \/ Chemical Monthly\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1007\/pl00010132\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1007\/pl00010132\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003ePark et al. (2017). A Novel Probe with a Chlorinated α-Cyanoacetophenone Acceptor Moiety Shows Near-Infrared Fluorescence Specific for Tau Fibrils. \u003cem\u003eCHEMICAL \u0026amp; PHARMACEUTICAL BULLETIN\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1248\/cpb.c17-00559\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1248\/cpb.c17-00559\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":"10g","offer_id":48086051487962,"sku":"TCI2510C114115569","price":2025000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086051520730,"sku":"TCI2510C114115570","price":3626000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1141.jpg?v=1769180328"},{"product_id":"tci2510c118215636","title":"TCI C1182 6068-72-0 4-Cyanobenzoyl Chloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1182 4-Cyanobenzoyl Chloride (CAS 6068-72-0) is an activated benzoyl chloride carrying a para-cyano group, giving a highly reactive acylating agent with a second functional handle. It reacts readily with amines, alcohols, and thiols to form amides, esters, and thioesters under mild conditions. The remaining nitrile can subsequently be reduced, hydrolysed, or converted into tetrazoles and other nitrogen heterocycles. Because it is moisture sensitive and releases corrosive hydrogen chloride on contact with water, it must be handled in a fume hood and stored tightly closed in a cool, dry place.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086055026906,"sku":"TCI2510C118215636","price":2222000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086055059674,"sku":"TCI2510C118215637","price":7422000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1182.jpg?v=1767096484"},{"product_id":"tci2510c198516603","title":"TCI C1985 874-86-2 4-Cyanobenzyl Chloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e4-Cyanobenzyl Chloride (TCI C1985), with CAS number 874-86-2, is a versatile chemical compound widely used in laboratory settings for the synthesis of complex molecules. As a key building block in organic chemistry, it serves as a foundational reagent for the development of both heterocyclic and non-heterocyclic compounds. Its presence in chemical laboratories is essential for researchers working in organic synthesis and molecular design. This compound is particularly valuable for its ability to participate in a variety of chemical reactions, making it a crucial component in the creation of new chemical entities.\u003c\/p\u003e\n\u003cp\u003eThe compound's chemical structure is stable, and its high reactivity makes it an ideal choice for substitution and nucleophilic reactions. These properties allow it to be a preferred reagent in synthetic pathways where chlorinated aromatic rings are required. Its reactivity and stability ensure that it can be reliably used in various experimental conditions, contributing to the reproducibility and success of chemical syntheses. Its role in the development of pharmaceuticals and industrial chemicals further underscores its importance in modern chemical research.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 4-Cyanobenzyl Chloride is commonly used in scientific research across multiple disciplines. It is a preferred material for academic and industrial research due to its availability and consistent quality. Its applications span from the development of new drugs to the production of industrial chemical compounds. Its use in both educational and research institutions highlights its significance in advancing chemical knowledge and innovation in Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSynthesis of heterocyclic compounds for the development of new pharmaceuticals due to its reactivity and ability to form stable intermediates.\u003c\/li\u003e\n\u003cli\u003eChlorine substitution reactions on aromatic rings in organic synthesis, making it ideal for creating complex molecular structures.\u003c\/li\u003e\n\u003cli\u003eProduction of industrial chemical compounds requiring chlorinated aromatic derivatives, supporting various manufacturing processes.\u003c\/li\u003e\n\u003cli\u003eResearch in material science for the creation of functional polymers and advanced chemical materials.\u003c\/li\u003e\n\u003cli\u003eEducational use in chemistry laboratories for teaching organic synthesis techniques and reaction mechanisms.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 874-86-2\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard chemical supply practices\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\u003e4-Cyanobenzyl Chloride 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 exposure to moisture and air. The compound should be stored in a well-ventilated area to minimize the risk of inhalation of vapors. It is important to avoid contact with incompatible materials such as strong bases or reducing agents. Proper personal protective equipment, including gloves and safety goggles, should be worn when handling this substance to ensure safety in the laboratory environment.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086094414042,"sku":"TCI2510C198516603","price":929000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086094446810,"sku":"TCI2510C198516604","price":2503000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1985.jpg?v=1769144426"},{"product_id":"tci2510c200716629","title":"TCI C2007 74448-92-3 4-(4-Chlorophenoxy)benzonitrile","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e4-(4-Chlorophenoxy)benzonitrile is a chemical compound widely used as a building block in the synthesis of complex organic compounds. This material plays a crucial role in laboratory settings where researchers aim to develop new molecules with specific biological or chemical properties. Its versatility makes it an essential component in various synthetic pathways, enabling the creation of compounds with tailored functionalities. As a key intermediate, it supports the exploration of new chemical reactions and the design of advanced molecular structures.\u003c\/p\u003e\n\u003cp\u003eThe compound is prized for its excellent solubility in organic solvents and high chemical stability. These properties ensure that it remains effective under a wide range of experimental conditions, making it a reliable choice for both academic and industrial research. Its controlled reactivity and predictable behavior in different reaction environments further enhance its utility. Additionally, its clear chemical structure allows for precise manipulation in synthetic processes, contributing to the reproducibility and success of laboratory experiments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 4-(4-Chlorophenoxy)benzonitrile is commonly used in both fundamental and applied chemical research. It is a popular choice for institutions and research centers aiming to develop new compounds with potential applications in pharmaceuticals, materials science, and environmental chemistry. Its availability and reliability make it a standard component in many research programs across the country.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis applications benefit from this compound's role as a versatile building block, enabling the creation of complex molecules with specific functional groups.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research utilizes it to develop new drug candidates, as its structure can be modified to target various biological pathways.\u003c\/li\u003e\n\u003cli\u003eMaterials science experiments leverage its chemical stability and reactivity to design advanced polymers and functional materials.\u003c\/li\u003e\n\u003cli\u003eEnvironmental chemistry studies use it to investigate the behavior of organic pollutants in different environmental matrices.\u003c\/li\u003e\n\u003cli\u003eAnalytical chemistry applications take advantage of its distinct chemical structure for use in spectroscopic and chromatographic analyses.\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: 74448-92-3\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory supply\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid, crystalline\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 chemical nature, it should be handled with appropriate personal protective equipment, including gloves and safety goggles, to ensure laboratory safety. While it is not classified as hazardous under normal conditions, it should be kept out of reach of children and stored separately from incompatible substances. Proper labeling and storage practices are essential to maintain the integrity of the compound and ensure safe handling in laboratory settings.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086095691994,"sku":"TCI2510C200716629","price":3682000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2007.jpg?v=1768816735"},{"product_id":"tci2510e087228677","title":"TCI E0872 3032-92-6 4-Ethynylbenzonitrile","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e4-Ethynylbenzonitrile is a bifunctional aromatic building block that carries a terminal ethynyl group on one side of the benzene ring and a nitrile group at the opposite para position. Bringing together two functional groups of very different character within a single linear molecule makes this compound highly useful across organic synthesis, materials chemistry, and coordination chemistry. The terminal alkyne serves as a reaction partner in a wide range of modern cross-coupling transformations, while the nitrile acts both as an electron-withdrawing group and as a precursor to amines, amides, carboxylic acids, or tetrazole rings.\u003c\/p\u003e\n\u003cp\u003eThe properties that make this compound a preferred choice are its rigid linear geometry together with the highly dependable reactivity of the terminal alkyne. The carbon–carbon triple bond bearing a terminal hydrogen atom is ready to undergo Sonogashira coupling with aryl halides, as well as copper-catalysed azide–alkyne cycloaddition, widely known as the click reaction. This click chemistry proceeds in high yield, tolerates a broad range of functional groups, and runs under mild conditions, which makes it well suited to attaching labels onto biomolecules. The strongly electron-withdrawing nitrile group increases the polarisation of the molecule, adding a further handle for tuning electronic behaviour.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories this building block is typically used in university and institutional research groups working on organic synthesis, in materials chemistry programmes constructing conjugated or coordination frameworks, and in bioconjugation work where click chemistry is used to attach reporter groups. It is normally purchased in small research quantities for method development and multi-step synthesis rather than for routine analytical testing, and it is handled in laboratories equipped with a fume hood and standard inert-atmosphere technique.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSonogashira cross-coupling: the terminal alkyne couples reliably with aryl and heteroaryl halides under palladium–copper catalysis, giving rapid access to extended conjugated aryl-alkyne scaffolds.\u003c\/li\u003e\n\u003cli\u003eCopper-catalysed azide–alkyne click chemistry: the terminal ethynyl group reacts in high yield under mild conditions, making it a dependable partner for triazole formation in modular synthesis.\u003c\/li\u003e\n\u003cli\u003eBioconjugation and molecular labelling: broad functional-group tolerance of the click reaction allows reporter groups and tags to be attached to biomolecules without disturbing sensitive functionality.\u003c\/li\u003e\n\u003cli\u003eMaterials and coordination chemistry: the rigid linear para-substituted geometry, combined with the nitrile donor site, suits the construction of conjugated materials and coordination frameworks.\u003c\/li\u003e\n\u003cli\u003eNitrile-based functional group interconversion: the cyano group serves as a versatile precursor that can be converted into amines, amides, carboxylic acids, or tetrazole rings in multi-step routes.\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\u003eCatalogue reference: E0872\u003c\/li\u003e\n\u003cli\u003eCAS number: 3032-92-6\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in research-scale packs; please confirm the currently offered sizes when ordering.\u003c\/li\u003e\n\u003cli\u003eStorage: keep in a cool, dry, well-ventilated place in a tightly closed original container, away from light and heat.\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 direct sunlight, heat, and ignition sources, and keep it away from strong oxidising agents and other incompatible chemicals. Amber glass or the manufacturer's supplied container is appropriate; for moisture- or air-sensitive handling, transfer under an inert atmosphere. Handle the compound inside a fume hood, wearing safety goggles, chemically resistant gloves, and a laboratory coat, and avoid inhalation of dust or vapour and contact with skin and eyes. Weigh and transfer carefully to prevent spillage, keep containers clearly labelled and sealed after each use, and consult the manufacturer's safety data sheet for the full hazard, first-aid, and disposal guidance before beginning work.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086903292122,"sku":"TCI2510E087228677","price":1631000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086903324890,"sku":"TCI2510E087228678","price":5623000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510E0872.jpg?v=1767111896"},{"product_id":"tci2510e098128833","title":"TCI E0981 25117-74-2 4-Ethoxybenzonitrile","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e4-Ethoxybenzonitrile is a chemical compound widely used as a foundational building block in the synthesis of complex organic molecules. Its molecular structure consists of a nitrile group and an ethoxy group, which contribute to its reactivity and versatility in chemical reactions. This compound plays a crucial role in organic chemistry laboratories, where it is employed to construct a variety of organic compounds through different synthetic pathways. Due to its ability to participate in multiple reaction types, it is a valuable resource for researchers aiming to develop new chemical entities.\u003c\/p\u003e\n\u003cp\u003eThe reactivity of 4-Ethoxybenzonitrile stems from its functional groups, making it an ideal candidate for nucleophilic substitution, condensation, and other organic transformations. Its chemical stability under controlled conditions ensures reliable performance in laboratory settings, while its reactivity allows for efficient synthesis of target molecules. The compound’s ability to interact with a wide range of reagents and solvents enhances its utility in diverse synthetic strategies. These properties make it a preferred choice for chemists working on complex molecular designs.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 4-Ethoxybenzonitrile is commonly used in organic synthesis research, particularly in the development of new pharmaceuticals and materials. Its availability in solid form and ease of handling make it a practical choice for both academic and industrial research. The compound’s role in creating complex structures underscores its importance in advancing chemical research in Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis for the development of new pharmaceutical compounds due to its versatile reactivity and structural adaptability.\u003c\/li\u003e\n\u003cli\u003eNucleophilic substitution reactions where the nitrile group acts as an electrophilic site for substitution.\u003c\/li\u003e\n\u003cli\u003eCondensation reactions to form more complex organic molecules through intermolecular bonding.\u003c\/li\u003e\n\u003cli\u003eResearch in material science for the creation of polymers and functional materials with tailored properties.\u003c\/li\u003e\n\u003cli\u003eTeaching and training in undergraduate and graduate chemistry programs to demonstrate key synthetic 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: 25117-74-2\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various 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 moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003e4-Ethoxybenzonitrile should be stored in a cool, dry environment to maintain its chemical stability and prevent degradation. It is recommended to use airtight containers made of glass or high-density polyethylene to minimize exposure to moisture and air. Due to its reactivity, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. Avoid contact with incompatible substances like strong acids or bases. Ensure proper ventilation in the laboratory when working with this compound to reduce the risk of inhalation. Regular monitoring of storage conditions is essential to maintain the integrity and safety of the material.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086914695386,"sku":"TCI2510E098128833","price":1125000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086914728154,"sku":"TCI2510E098128834","price":3964000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510E0981.jpg?v=1768818764"},{"product_id":"tci2510f022129960","title":"TCI F0221 1194-02-1 4-Fluorobenzonitrile","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e4-Fluorobenzonitrile is a chemical compound widely used as a foundational building block in the synthesis of complex organic molecules. It is a versatile reagent that plays a crucial role in laboratory settings, particularly in organic chemistry research. Its molecular structure consists of a benzene ring substituted with a fluorine atom and a nitrile group, making it an essential component in the development of compounds with specific functional properties. This compound is frequently utilized in synthetic pathways to introduce fluorine and nitrile functionalities into target molecules, enabling the creation of compounds with tailored biological or electronic characteristics.\u003c\/p\u003e\n\u003cp\u003eThe unique electronic properties of 4-Fluorobenzonitrile, derived from its fluorine substitution, make it a preferred choice in chemical synthesis. The fluorine atom influences the reactivity and stability of the molecule, allowing it to participate effectively in various reaction mechanisms such as nucleophilic, electrophilic, and substitution reactions. Its chemical stability under general laboratory conditions further enhances its reliability as a reagent. The presence of the nitrile group adds to its versatility, enabling it to react with a wide range of functional groups, making it a valuable tool for researchers aiming to modify molecular structures with precision.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 4-Fluorobenzonitrile is commonly used by chemists and researchers in the development of new compounds. It is an essential material for those working on drug discovery, material science, and advanced organic synthesis projects. Its availability through reliable suppliers like AMI Scientific ensures that Indonesian researchers have access to high-quality reagents necessary for their work. This compound supports the advancement of scientific research by providing a stable and reactive building block for complex molecule synthesis.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of pharmaceuticals and agrochemicals due to its reactivity and functional group versatility.\u003c\/li\u003e\n\u003cli\u003eModification of molecular structures in drug discovery projects to enhance biological activity and selectivity.\u003c\/li\u003e\n\u003cli\u003eDevelopment of electronic materials through its nitrile group, which can influence molecular conductivity and stability.\u003c\/li\u003e\n\u003cli\u003eResearch in fluorinated compounds for applications in polymer science and specialty chemical manufacturing.\u003c\/li\u003e\n\u003cli\u003eSynthesis of complex organic molecules requiring precise functional group introduction and structural modification.\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: 1194-02-1\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Fluorinated Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Liquid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and incompatible materials\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003e4-Fluorobenzonitrile should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to keep the compound in a tightly sealed container to prevent exposure to moisture and air. Due to its chemical reactivity, it should be stored separately from strong oxidizers and reducing agents to avoid potential hazardous reactions. Laboratory personnel should handle the compound with appropriate personal protective equipment, including gloves and safety goggles, to ensure safe handling. Proper ventilation is also essential when working with this compound to minimize inhalation risks. Regular monitoring of storage conditions is advised to maintain the integrity and safety of the material.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086987571418,"sku":"TCI2510F022129960","price":1041000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48086987604186,"sku":"TCI2510F022129961","price":3036000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48086987636954,"sku":"TCI2510F022129962","price":10484000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510F0221.jpg?v=1769142334"},{"product_id":"tci2510h077833451","title":"TCI H0778 60484-67-5 4-Heptylbenzonitrile","description":"\u003cp\u003e\u003cstrong\u003e4-Heptylbenzonitrile\u003c\/strong\u003e (CAS 60484-67-5) is a high-quality chemical from TCI, supplied as \u003cstrong\u003eGC Grade \/ for 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Indonesia.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48087403921626,"sku":"TCI2510I066135879","price":1827000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48087403954394,"sku":"TCI2510I066135880","price":6297000.0,"currency_code":"IDR","in_stock":true}]},{"product_id":"tci2510t030751115","title":"TCI T0307 104-85-8 p-Tolunitrile","description":"\u003cp\u003e\u003cstrong\u003ep-Tolunitrile\u003c\/strong\u003e (CAS 104-85-8) is a high-quality chemical from TCI, supplied as \u003cstrong\u003eGC Grade \/ for Synthesis\u003c\/strong\u003e.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eApplication:\u003c\/strong\u003e Synthesis reagent for a wide range of organic chemistry transformations in laboratory and industrial settings.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eSpecifications:\u003c\/strong\u003e\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003eMolecular formula: C8H7N\u003c\/li\u003e\n\u003cli\u003eCAS number: 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Indonesia.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48088305795290,"sku":"TCI2510T030751115","price":732000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48088305828058,"sku":"TCI2510T030751116","price":1997000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48088305860826,"sku":"TCI2510T030751117","price":5595000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510T0307.jpg?v=1768363109"},{"product_id":"tci2510a0695919","title":"TCI A0695 873-74-5 4-Aminobenzonitrile","description":"\u003cp\u003e\u003cstrong\u003e4-Aminobenzonitrile\u003c\/strong\u003e (CAS 873-74-5) is a high-quality chemical from TCI, supplied as \u003cstrong\u003eGC Grade \/ for Synthesis\u003c\/strong\u003e.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eApplication:\u003c\/strong\u003e Synthesis reagent for a wide range of organic chemistry transformations in laboratory and 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