{"title":"C-X(Non-Halogen) Bond Formation [Synthetic Reagents]","description":"\u003cp\u003e\u003cstrong\u003eC-X(Non-Halogen) Bond Formation [Synthetic Reagents]\u003c\/strong\u003e adalah kelompok produk di bawah Synthetic Reagents (Chemistry), dengan \u003cstrong\u003e375 produk\u003c\/strong\u003e tersedia.\u003c\/p\u003e\u003cp\u003eContoh produk pada kategori ini: \u003cem\u003e8-Aminoquinoline\u003c\/em\u003e, \u003cem\u003e1,1'-(Azodicarbonyl)dipiperidine\u003c\/em\u003e, \u003cem\u003e4-Amino-1,2,4-triazole\u003c\/em\u003e, \u003cem\u003eDiisopropyl Azodicarboxylate (40% in Toluene, ca. 1.9mol\/L)\u003c\/em\u003e. Seluruh produk merupakan produk asli Tokyo Chemical Industry (TCI) Jepang dengan spesifikasi kemurnian yang tercantum pada masing-masing item.\u003c\/p\u003e\u003cp\u003eKategori lain yang sejajar di bawah Synthetic Reagents, sering dipakai bersamaan dalam satu alur kerja laboratorium:\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-acids-bases-synthetic-reagents\"\u003eAcids, Bases [Synthetic Reagents]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-aryne-precursors-heteroaryne-precursors\"\u003eAryne Precursors, Heteroaryne Precursors\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-c-c-bond-formation-synthetic-reagents\"\u003eC-C Bond Formation [Synthetic Reagents]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-c-x-halogen-bond-formation-synthetic-reagents\"\u003eC-X(Halogen) Bond Formation [Synthetic Reagents]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-chelation-complexation-compounds\"\u003eChelation\/Complexation Compounds\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-coupling-synthetic-reagents\"\u003eCoupling [Synthetic Reagents]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-dehydrating-reagents-synthetic-reagents\"\u003eDehydrating Reagents [Synthetic Reagents]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-fluorination-reagents-synthetic-reagents\"\u003eFluorination Reagents [Synthetic Reagents]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-hypervalent-iodine-compounds-synthetic-reagents\"\u003eHypervalent Iodine Compounds [Synthetic Reagents]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-inorganic-salts-synthetic-reagents\"\u003eInorganic Salts [Synthetic Reagents]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-oxidation-synthetic-reagents\"\u003eOxidation [Synthetic Reagents]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-phase-transfer-catalysts\"\u003ePhase Transfer Catalysts\u003c\/a\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eProduk pada kategori ini dipakai dalam riset sintesis, pengembangan material, maupun analisis laboratorium, tergantung karakter senyawanya. Perhatikan kemurnian, kemasan, dan kondisi penyimpanan yang tercantum pada tiap produk karena keduanya memengaruhi hasil percobaan. Untuk kebutuhan volume besar atau spesifikasi khusus, tim kami dapat membantu mengecek ketersediaan langsung ke TCI Jepang.\u003c\/p\u003e\u003cp\u003eKembali ke \u003ca href=\"\/en\/collections\/reagen-sintesis-organik\"\u003eSynthetic Reagents\u003c\/a\u003e.\u003c\/p\u003e\u003cp\u003eAMI Scientific adalah distributor resmi TCI Japan di Indonesia. Hubungi kami untuk harga, ketersediaan, dan lead time pengiriman.\u003c\/p\u003e","products":[{"product_id":"tci2510b643513320","title":"TCI B6435 2488525-05-7 [[[1,1'-Biphenyl]-4-yloxy]imino]-lambda4-sulfanone","description":"\u003ch3\u003eDeskripsi\u003c\/h3\u003e\n\u003cp\u003eTCI B6435 [[[1,1'-Biphenyl]-4-yloxy]imino]-lambda4-sulfanone dengan nomor CAS 2488525-05-7 adalah reagen sintesis modern dengan gugus fungsi N-sulfinilamin yang khas. Bagian bifenil-4-iloksi pada molekul berperan sebagai gugus yang menstabilkan sekaligus mengarahkan reaktivitas reagen. Senyawa seperti ini termasuk kelompok reagen khusus yang relatif baru dikembangkan.\u003c\/p\u003e\n\u003cp\u003eTCI menempatkan produk ini pada kategori Synthetic Reagents untuk pembentukan ikatan C–X non-halogen. Reagen dalam kelompok ini dirancang untuk memperkenalkan heteroatom seperti nitrogen dan belerang ke dalam kerangka organik, khususnya melalui reaksi dengan nukleofil atau reagen organologam. Pendekatan tersebut menawarkan rute yang lebih langsung dibandingkan jalur multitahap konvensional.\u003c\/p\u003e\n\u003cp\u003eProduk tersedia dalam kemasan kecil yang sesuai dengan pola pemakaian reagen khusus di laboratorium riset. AMI Scientific menyediakannya bagi peneliti yang mengeksplorasi metodologi sintesis mutakhir, terutama di bidang kimia medisinal dan pengembangan reaksi baru. Untuk kondisi reaksi yang optimal, peneliti disarankan merujuk literatur dan dokumen teknis resmi dari produsen.\u003c\/p\u003e\n\u003ch3\u003eAplikasi Laboratorium\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePembentukan ikatan C–X non-halogen — sesuai peruntukan kategori reagen sintetik ini.\u003c\/li\u003e\n\u003cli\u003eReaksi dengan reagen organologam — memperkenalkan fragmen berbasis belerang–nitrogen pada substrat.\u003c\/li\u003e\n\u003cli\u003eSintesis turunan sulfur–nitrogen — mendukung penyusunan gugus fungsi yang sulit diakses jalur biasa.\u003c\/li\u003e\n\u003cli\u003ePengembangan metodologi organik — menjadi reagen uji dalam penelitian reaksi baru.\u003c\/li\u003e\n\u003cli\u003eRiset kimia medisinal — membantu eksplorasi gugus fungsi alternatif dalam desain molekul.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpesifikasi\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMerek: TCI\u003c\/li\u003e\n\u003cli\u003eNomor CAS: 2488525-05-7\u003c\/li\u003e\n\u003cli\u003eKategori: Chemistry \u0026gt; Synthetic Reagents \u0026gt; C-X(Non-Halogen) Bond Formation [Synthetic Reagents]\u003c\/li\u003e\n\u003cli\u003eVarian\/kemasan: 1 g dan 5 g\u003c\/li\u003e\n\u003cli\u003eBentuk fisik: rujuk dokumen teknis resmi produsen untuk penampakan produk\u003c\/li\u003e\n\u003cli\u003eCatatan penyimpanan: simpan tertutup rapat di tempat sejuk, kering, dan terlindung dari cahaya\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003ePenanganan dan Penyimpanan\u003c\/h3\u003e\n\u003cp\u003eReagen sintesis khusus seperti ini sebaiknya ditangani di lemari asam dengan sarung tangan dan kacamata pelindung, serta dijauhkan dari kelembapan. Gunakan teknik penanganan yang menjaga bahan tetap kering, misalnya dengan wadah tertutup rapat dan pengambilan yang cepat dan terencana. Karena termasuk reagen reaktif, selalu baca lembar data keselamatan (SDS) serta dokumen teknis resmi produsen sebelum digunakan.\u003c\/p\u003e\n\u003ch3\u003eEnglish\u003c\/h3\u003e\n\u003cp\u003eTCI B6435 [[[1,1'-Biphenyl]-4-yloxy]imino]-lambda4-sulfanone (CAS 2488525-05-7) is a specialty synthetic reagent classified for non-halogen C–X bond formation. Reagents of this N-sulfinylamine type are used to introduce sulfur- and nitrogen-containing fragments into organic frameworks, typically through reactions with nucleophiles or organometallic partners. It is aimed at researchers exploring modern synthetic methodology and medicinal chemistry applications. Handle the reagent in a fume hood, protect it from moisture, and consult the manufacturer's technical documentation and safety data sheet before use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085939749082,"sku":"TCI2510B643513320","price":4358000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085939781850,"sku":"TCI2510B643513321","price":19927000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6435.jpg?v=1768204502"},{"product_id":"tci2510b655213480","title":"TCI B6552 2763205-15-6 2',7'-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)spiro[cyclopenta[2,1-b:3,4-b']dipyridine-5,9'-fluorene]","description":"\u003ch3\u003eDeskripsi\u003c\/h3\u003e\n\u003cp\u003eTCI B6552 adalah 2',7'-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)spiro[cyclopenta[2,1-b:3,4-b']dipyridine-5,9'-fluorene], sebuah senyawa spiro terkonjugasi yang membawa dua gugus ester boronat pinakol pada posisi 2' dan 7'. Rangka spiro yang menyatukan unit fluorena dengan unit cyclopenta-dipiridina memberikan struktur tiga dimensi yang kaku dan tegak lurus, arsitektur yang banyak dicari dalam desain material fungsional. Kehadiran atom nitrogen piridinik pada salah satu sisi rangka menjadikan molekul ini tidak sekadar kerangka hidrokarbon, melainkan juga kandidat ligan pendonor nitrogen. Kombinasi tersebut menempatkannya pada kategori Nitrogen-Donor Ligands dalam katalog TCI.\u003c\/p\u003e\n\u003cp\u003eDua gugus pinacol boronate pada molekul ini berfungsi sebagai titik sambung yang sangat andal untuk reaksi kopling silang terkatalisis paladium, terutama kopling Suzuki–Miyaura. Sifat difungsional tersebut memungkinkan senyawa dipakai sebagai monomer inti dalam pembentukan oligomer maupun polimer terkonjugasi, atau sebagai pusat percabangan untuk molekul besar berbentuk bintang. Dibandingkan asam boronat bebas, bentuk ester pinakol umumnya lebih mudah ditangani dan dimurnikan melalui kromatografi. Hal ini memberi keleluasaan bagi peneliti yang membangun pustaka material secara bertahap.\u003c\/p\u003e\n\u003cp\u003eDi laboratorium riset material organik, senyawa dengan pola spiro seperti ini menarik karena mampu menekan agregasi antarmolekul dan menjaga sifat pembentukan lapisan tipis yang baik. Unit dipiridina yang miskin elektron dapat dipadukan dengan segmen kaya elektron untuk menyusun sistem donor–akseptor. AMI Scientific menyediakan produk ini dalam kemasan kecil yang sesuai untuk tahap penapisan sintesis dan optimasi kondisi reaksi. Setiap detail struktur dan data analitik sebaiknya dirujuk pada dokumen resmi TCI yang menyertai produk.\u003c\/p\u003e\n\u003ch3\u003eAplikasi Laboratorium\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eKopling Suzuki–Miyaura — dua gugus boronat pinakol menjadikannya monomer difungsional yang siap disambungkan dengan aril halida.\u003c\/li\u003e\n\u003cli\u003eSintesis polimer terkonjugasi — rangka spiro kaku membantu menghasilkan rantai dengan kelarutan dan morfologi lapisan yang terkendali.\u003c\/li\u003e\n\u003cli\u003eRiset material OLED dan optoelektronik organik — arsitektur spirobifluorena banyak dipelajari sebagai kerangka host maupun pemancar.\u003c\/li\u003e\n\u003cli\u003eDesain ligan pendonor nitrogen — atom nitrogen piridinik dapat berkoordinasi dengan pusat logam transisi untuk kajian katalisis.\u003c\/li\u003e\n\u003cli\u003eKonstruksi molekul donor–akseptor — segmen dipiridina yang miskin elektron cocok dipasangkan dengan blok kaya elektron.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpesifikasi\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMerek: TCI\u003c\/li\u003e\n\u003cli\u003eNomor CAS: 2763205-15-6\u003c\/li\u003e\n\u003cli\u003eKategori: Chemistry \u0026gt; Catalysis and Inorganic Chemistry \u0026gt; Nitrogen-Donor Ligands [Catalysis]\u003c\/li\u003e\n\u003cli\u003eVarian\/kemasan: 100 mg dan 500 mg\u003c\/li\u003e\n\u003cli\u003eBentuk fisik: padatan organik; rujuk label dan lembar data resmi TCI untuk deskripsi rinci\u003c\/li\u003e\n\u003cli\u003ePenyimpanan: tempat sejuk, kering, dan terlindung cahaya, sesuai anjuran pada kemasan\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003ePenanganan dan Penyimpanan\u003c\/h3\u003e\n\u003cp\u003eTangani senyawa ini di dalam lemari asam menggunakan sarung tangan, kacamata pelindung, dan jas laboratorium. Ester boronat sebaiknya dijauhkan dari kelembapan berlebih dan wadah ditutup rapat setiap selesai digunakan, karena paparan uap air dapat memengaruhi kualitas bahan. Ikuti seluruh anjuran penyimpanan dan pembuangan limbah yang tercantum pada lembar data keselamatan resmi produk.\u003c\/p\u003e\n\u003ch3\u003eEnglish\u003c\/h3\u003e\n\u003cp\u003eTCI B6552 is a spiro-linked building block bearing two pinacol boronate groups at the 2' and 7' positions of a spiro[cyclopenta-dipyridine-fluorene] framework. Its difunctional boronate handles make it a convenient monomer for palladium-catalysed Suzuki–Miyaura cross-coupling and for the assembly of conjugated oligomers and polymers. The rigid, orthogonal spiro geometry combined with electron-poor pyridine nitrogens is of particular interest in organic optoelectronic material research and in nitrogen-donor ligand design. AMI Scientific supplies this TCI product in 100 mg and 500 mg pack sizes; always consult the official TCI documentation and safety data sheet before use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48085946859738,"sku":"TCI2510B655213480","price":2194000.0,"currency_code":"IDR","in_stock":true},{"title":"500mg","offer_id":48085946892506,"sku":"TCI2510B655213481","price":7618000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6552.jpg?v=1767093890"},{"product_id":"tci2510b708213900","title":"TCI B7082 3075704-21-8 [1,2-Bis(ethoxycarbonyl)hydrazineyl]triphenylphosphonium Trifluoromethanesulfonate","description":"\u003ch3\u003eDeskripsi\u003c\/h3\u003e\n\u003cp\u003eTCI B7082 [1,2-Bis(ethoxycarbonyl)hydrazineyl]triphenylphosphonium Trifluoromethanesulfonate adalah reagen garam fosfonium yang dikembangkan untuk mempermudah reaksi tipe Mitsunobu. Secara struktur, reagen ini merupakan adduk terbentuk antara trifenilfosfina dan azodikarboksilat dietil yang telah distabilkan sebagai garam triflat. Dengan demikian, peneliti tidak perlu lagi mencampurkan fosfina dan reagen azo secara terpisah pada saat reaksi.\u003c\/p\u003e\n\u003cp\u003eKeunggulan utama pendekatan ini terletak pada kepraktisan dan keamanan penanganan. Reagen azodikarboksilat cair dikenal peka terhadap panas dan guncangan, sedangkan bentuk garam padat jauh lebih mudah ditimbang dan disimpan. Selain itu, stoikiometri reaksi menjadi lebih pasti karena kedua komponen sudah tergabung dalam satu molekul dengan perbandingan tetap.\u003c\/p\u003e\n\u003cp\u003eReaksi Mitsunobu sendiri sangat bernilai karena memungkinkan penggantian gugus hidroksil dengan nukleofil disertai inversi konfigurasi pada karbon stereogenik. Kemampuan ini menjadikannya alat penting dalam sintesis produk alami, nukleosida, dan senyawa aktif farmasi. AMI Scientific menyediakan kemasan 1 g, 5 g, dan 25 g agar dapat menyesuaikan skala uji coba hingga sintesis multi-gram.\u003c\/p\u003e\n\u003ch3\u003eAplikasi Laboratorium\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eReaksi Mitsunobu — mengubah alkohol menjadi ester, eter, atau amina terlindungi dengan inversi stereokimia.\u003c\/li\u003e\n\u003cli\u003ePembentukan ikatan C–O dan C–N — memfasilitasi kopling dehidratif antara alkohol dan nukleofil berproton asam.\u003c\/li\u003e\n\u003cli\u003eSintesis nukleosida dan analognya — berguna untuk memasang basa nitrogen pada kerangka gula.\u003c\/li\u003e\n\u003cli\u003eKimia medisinal — mempermudah modifikasi gugus hidroksil pada tahap akhir sintesis kandidat senyawa.\u003c\/li\u003e\n\u003cli\u003eAlternatif praktis reagen azo cair — mengurangi risiko penanganan dan memperbaiki reprodusibilitas stoikiometri.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpesifikasi\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMerek: TCI\u003c\/li\u003e\n\u003cli\u003eNomor CAS: 3075704-21-8\u003c\/li\u003e\n\u003cli\u003eKategori: Chemistry \u0026gt; Synthetic Reagents \u0026gt; C-X(Non-Halogen) Bond Formation\u003c\/li\u003e\n\u003cli\u003eKode produk: B7082\u003c\/li\u003e\n\u003cli\u003eVarian\/kemasan: 1 g, 5 g, dan 25 g\u003c\/li\u003e\n\u003cli\u003ePenyimpanan: simpan di tempat sejuk dan kering, hindari panas berlebih; ikuti petunjuk pada label resmi TCI.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003ePenanganan dan Penyimpanan\u003c\/h3\u003e\n\u003cp\u003eMeskipun bentuk garamnya lebih stabil daripada azodikarboksilat cair, reagen ini tetap harus dijauhkan dari sumber panas, api, dan reduktor kuat. Timbang di lingkungan kering karena garam triflat cenderung higroskopis, lalu segera tutup rapat wadahnya. Gunakan sarung tangan dan kacamata pengaman, serta lakukan penanganan di lemari asam sesuai prosedur laboratorium yang berlaku.\u003c\/p\u003e\n\u003ch3\u003eEnglish\u003c\/h3\u003e\n\u003cp\u003eTCI B7082 is a preformed phosphonium salt derived from triphenylphosphine and a dialkyl azodicarboxylate, stabilized as its trifluoromethanesulfonate. It streamlines Mitsunobu-type dehydrative couplings by combining both reagent components in a single, easily weighed solid. This avoids handling heat- and shock-sensitive liquid azodicarboxylates while fixing the reagent stoichiometry. Offered in 1 g, 5 g, and 25 g sizes, it should be kept dry, cool, and away from heat sources and strong reducing agents.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085964980442,"sku":"TCI2510B708213900","price":816000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085965013210,"sku":"TCI2510B708213901","price":2053000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085965045978,"sku":"TCI2510B708213902","price":6409000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B7082.jpg?v=1768204524"},{"product_id":"tci2510c038414469","title":"TCI C0384 13395-16-9 Bis(2,4-pentanedionato)copper(II)","description":"\u003ch3\u003eDeskripsi\u003c\/h3\u003e\n\u003cp\u003eTCI C0384 Bis(2,4-pentanedionato)copper(II), yang lebih dikenal sebagai tembaga(II) asetilasetonat, adalah kompleks koordinasi tembaga dengan dua ligan β-diketonat. Struktur kelat yang stabil membuat senyawa ini mudah ditangani, larut dalam banyak pelarut organik, dan dapat menguap tanpa terurai pada kondisi tertentu. Karakter tersebut menjadikannya salah satu sumber tembaga yang populer dalam kimia sintesis maupun ilmu material.\u003c\/p\u003e\n\u003cp\u003eDalam katalisis, kompleks ini kerap dipakai sebagai prekursor katalis tembaga untuk reaksi pembentukan ikatan karbon–karbon dan karbon–heteroatom, termasuk kajian aktivasi ikatan C–H. Ligan asetilasetonat berperan menstabilkan pusat logam sekaligus mudah tergantikan ketika sistem katalitik terbentuk di dalam campuran reaksi. Karena itu, senyawa ini banyak digunakan pada pengembangan metodologi sintesis organik modern.\u003c\/p\u003e\n\u003cp\u003eDi luar katalisis homogen, senyawa ini juga dimanfaatkan sebagai prekursor pada penumbuhan lapisan tipis berbasis tembaga dan pembuatan nanopartikel oksida tembaga. Fleksibilitas penggunaan tersebut membuatnya relevan bagi laboratorium kimia organik, anorganik, maupun material di perguruan tinggi dan industri. AMI Scientific menyediakan kemasan riset serta kemasan besar untuk kebutuhan skala berulang.\u003c\/p\u003e\n\u003ch3\u003eAplikasi Laboratorium\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePrekursor katalis tembaga — menyediakan pusat Cu(II) yang stabil untuk berbagai transformasi organik.\u003c\/li\u003e\n\u003cli\u003eRiset aktivasi ikatan C–H — dipakai dalam pengembangan metodologi fungsionalisasi langsung ikatan C–H.\u003c\/li\u003e\n\u003cli\u003eReaksi kopling dan sikloadisi terkatalisis tembaga — berperan sebagai sumber logam pada sistem katalitik homogen.\u003c\/li\u003e\n\u003cli\u003eSintesis material tembaga dan oksida tembaga — berfungsi sebagai prekursor untuk lapisan tipis dan nanopartikel.\u003c\/li\u003e\n\u003cli\u003eStudi kimia koordinasi β-diketonat — menjadi kompleks model untuk kajian struktur dan reaktivitas kelat logam.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpesifikasi\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMerek: TCI (Tokyo Chemical Industry), kode produk C0384\u003c\/li\u003e\n\u003cli\u003eNomor CAS: 13395-16-9\u003c\/li\u003e\n\u003cli\u003eKategori: Chemistry \u0026gt; Catalysis and Inorganic Chemistry \u0026gt; C-H Activation [Catalysis]\u003c\/li\u003e\n\u003cli\u003eVarian\/kemasan: 25 g dan 250 g\u003c\/li\u003e\n\u003cli\u003eBentuk fisik: padatan kristalin berwarna (kompleks tembaga(II) asetilasetonat)\u003c\/li\u003e\n\u003cli\u003eCatatan penyimpanan: simpan dalam wadah tertutup rapat di tempat sejuk dan kering, jauh dari kelembapan\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003ePenanganan dan Penyimpanan\u003c\/h3\u003e\n\u003cp\u003eGunakan sarung tangan, pelindung mata, dan lakukan penimbangan pada area berventilasi baik untuk menghindari terhirupnya debu halus. Tutup wadah segera setelah digunakan agar produk terhindar dari kelembapan yang dapat memengaruhi kinerjanya sebagai prekursor katalis. Jauhkan dari bahan pengoksidasi kuat dan buang residu maupun larutan bekas melalui jalur limbah kimia sesuai prosedur institusi serta Safety Data Sheet TCI.\u003c\/p\u003e\n\u003ch3\u003eEnglish\u003c\/h3\u003e\n\u003cp\u003eTCI C0384 Bis(2,4-pentanedionato)copper(II), CAS 13395-16-9, is the well-known copper(II) acetylacetonate chelate used as a versatile copper source in synthesis and materials science. Its stable β-diketonate framework makes the complex convenient to weigh and dissolve, while the ligands are readily displaced once the active catalytic species forms. It is commonly applied as a catalyst precursor in copper-mediated coupling and C–H functionalisation studies, and as a precursor for copper-based thin films and nanoparticles. AMI Scientific supplies it in 25 g and 250 g packs; store in a tightly closed container in a cool, dry place.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48085995159770,"sku":"TCI2510C038414469","price":676000.0,"currency_code":"IDR","in_stock":true},{"title":"250g","offer_id":48085995192538,"sku":"TCI2510C038414470","price":2784000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0384.jpg?v=1767095147"},{"product_id":"tci2510c044114561","title":"TCI C0441 105-56-6 Ethyl Cyanoacetate","description":"\u003ch3\u003eDeskripsi\u003c\/h3\u003e\n\u003cp\u003eTCI C0441 Ethyl Cyanoacetate adalah salah satu reagen metilen aktif paling banyak dipakai dalam kimia organik sintetik. Gugus nitril dan ester yang mengapit satu unit metilen membuat proton di posisi tersebut mudah dilepas oleh basa lemah sekalipun. Karena itu senyawa ini menjadi nukleofil karbon yang andal pada berbagai jenis reaksi pembentukan ikatan karbon-karbon.\u003c\/p\u003e\n\u003cp\u003ePenerapannya sangat luas, mulai dari kondensasi Knoevenagel, alkilasi, adisi Michael, hingga reaksi Gewald untuk membentuk cincin aminotiofena. Senyawa ini juga menjadi bahan awal klasik dalam pembuatan pirazolon, piridin tersubstitusi, dan berbagai heterosiklik bernitrogen lainnya. Ketersediaannya yang stabil dan reaktivitasnya yang dapat diprediksi membuatnya menjadi reagen rutin di banyak laboratorium.\u003c\/p\u003e\n\u003cp\u003eProduk dipasok oleh TCI dalam dua ukuran kemasan sehingga cocok untuk penelitian harian maupun sintesis berskala lebih besar. Dokumen mutu pabrikan menjadi acuan spesifikasi setiap lot yang diterima. AMI Scientific menyediakannya bagi laboratorium kimia organik, farmasi, dan industri riset di Indonesia.\u003c\/p\u003e\n\u003ch3\u003eAplikasi Laboratorium\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eKondensasi Knoevenagel — membentuk turunan sianoakrilat terkonjugasi yang menjadi dasar banyak sintesis lanjutan.\u003c\/li\u003e\n\u003cli\u003eReaksi Gewald — menghasilkan turunan 2-aminotiofena yang banyak dipakai dalam kimia medisinal.\u003c\/li\u003e\n\u003cli\u003eSintesis pirazolon dan piridin tersubstitusi — berperan sebagai sumber unit metilen aktif pada siklisasi.\u003c\/li\u003e\n\u003cli\u003eAdisi Michael dan alkilasi — memperluas kerangka karbon melalui reaksi dengan akseptor dan halida alkil.\u003c\/li\u003e\n\u003cli\u003eIntermediet zat warna dan bahan aktif — menyediakan gugus penarik elektron pada sistem terkonjugasi fungsional.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpesifikasi\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMerek: TCI (Tokyo Chemical Industry), kode katalog C0441\u003c\/li\u003e\n\u003cli\u003eNomor CAS: 105-56-6\u003c\/li\u003e\n\u003cli\u003eKategori: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003eVarian\/kemasan: 25 g dan 500 g\u003c\/li\u003e\n\u003cli\u003eBentuk fisik: cairan jernih tidak berwarna hingga sedikit kekuningan\u003c\/li\u003e\n\u003cli\u003eCatatan penyimpanan: simpan di tempat sejuk, kering, dan berventilasi baik sesuai anjuran label dan SDS pabrikan\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003ePenanganan dan Penyimpanan\u003c\/h3\u003e\n\u003cp\u003eLakukan penakaran di lemari asam menggunakan sarung tangan, kacamata pelindung, dan jas laboratorium karena uapnya dapat mengiritasi mata serta saluran napas. Tutup wadah rapat setelah digunakan untuk mencegah penyerapan uap air yang dapat memengaruhi hasil reaksi. Simpan terpisah dari basa kuat, amina, dan bahan pengoksidasi, serta buang limbah sesuai prosedur pengelolaan limbah kimia institusi.\u003c\/p\u003e\n\u003ch3\u003eEnglish\u003c\/h3\u003e\n\u003cp\u003eTCI C0441 Ethyl Cyanoacetate (CAS 105-56-6) is one of the most widely used active methylene reagents in synthetic organic chemistry. Its acidic methylene position readily forms carbon nucleophiles for Knoevenagel condensations, alkylations, and Michael additions. It is also the standard starting material for the Gewald reaction and for the synthesis of pyrazolones, substituted pyridines, and other nitrogen heterocycles. The liquid should be dispensed in a fume hood with gloves and eye protection and stored tightly closed in a cool, dry, well-ventilated place.\u003c\/p\u003e\n\u003ch3\u003eReferensi Ilmiah\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eHoelz (2011). Ethyl cyanoacetate (CAS No. 105-56-6). \u003cem\u003eRevista Virtual de Química\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.5935\/1984-6835.20110025\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.5935\/1984-6835.20110025\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eSemmes dkk. (2015). Arylation of diethyl malonate and ethyl cyanoacetate catalyzed by palladium\/di-tert-butylneopentylphosphine. \u003cem\u003eTetrahedron Letters\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.tetlet.2015.01.072\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.tetlet.2015.01.072\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eBaku State University dkk. (2023). SYNTHESIS BASED ON ETHYL CYANOACETATE. \u003cem\u003eChemical Problems\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.32737\/2221-8688-2023-4-323-330\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.32737\/2221-8688-2023-4-323-330\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferensi dihimpun otomatis dari Crossref dan setiap DOI diverifikasi keberadaannya. AMI Scientific tidak berafiliasi dengan penulis maupun penerbit.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48085998829786,"sku":"TCI2510C044114561","price":507000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48085998862554,"sku":"TCI2510C044114562","price":1097000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0441.jpg?v=1767095243"},{"product_id":"tci2510c097615333","title":"TCI C0976 15074-54-1 2-Chlorophenyl Phosphorodichloridate [Phosphorylating Agent]","description":"\u003ch3\u003eDeskripsi\u003c\/h3\u003e\n\u003cp\u003eTCI C0976 2-Chlorophenyl Phosphorodichloridate adalah reagen fosforilasi yang tersedia dalam kemasan 5 g. Senyawa ini membawa gugus fosfor(V) dengan dua atom klorin reaktif serta satu gugus 2-klorofenoksi, sebuah kombinasi yang dirancang untuk memasukkan unit fosfat secara bertahap dan terkendali. Gugus 2-klorofenil berfungsi sebagai pelindung fosfat yang dapat dilepas pada tahap akhir sintesis.\u003c\/p\u003e\n\u003cp\u003eReagen jenis ini secara historis memegang peran penting dalam sintesis oligonukleotida melalui pendekatan fosfotriester, di mana ikatan internukleotida dibangun satu per satu dengan kontrol tinggi. Kedua ikatan P–Cl bereaksi cepat dengan alkohol maupun gugus hidroksil nukleosida, sehingga pembentukan ikatan fosfat dapat berlangsung dalam kondisi yang relatif ringan. Di luar kimia nukleotida, reagen ini juga dipakai untuk menyiapkan berbagai ester fosfat pada penelitian sintesis organik dan biokimia.\u003c\/p\u003e\n\u003cp\u003eKarena reaktivitas tinggi terhadap air, produk dikemas dalam ukuran kecil 5 g agar bahan tidak terlalu lama terbuka dan tetap terjaga mutunya. Penggunaan reagen ini menuntut teknik kerja anhidrat serta perencanaan reaksi yang cermat. AMI Scientific menyediakannya untuk laboratorium yang telah terbiasa menangani reagen sensitif kelembapan.\u003c\/p\u003e\n\u003ch3\u003eAplikasi Laboratorium\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSintesis oligonukleotida — membentuk ikatan internukleotida pada pendekatan fosfotriester dengan gugus pelindung yang dapat dilepas.\u003c\/li\u003e\n\u003cli\u003ePembuatan ester fosfat — dua ikatan P–Cl reaktif memungkinkan fosforilasi alkohol dan fenol secara langsung.\u003c\/li\u003e\n\u003cli\u003eFosforilasi nukleosida — digunakan untuk memasang unit fosfat pada gugus hidroksil gula.\u003c\/li\u003e\n\u003cli\u003eSintesis fosfat terlindung — gugus 2-klorofenil bertindak sebagai pelindung sementara pada fosfat.\u003c\/li\u003e\n\u003cli\u003eRiset biokimia dan kimia bahan alam — mendukung penyiapan analog fosfat untuk studi mekanisme enzim.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpesifikasi\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMerek: TCI (kode produk C0976)\u003c\/li\u003e\n\u003cli\u003eNomor CAS: 15074-54-1\u003c\/li\u003e\n\u003cli\u003eKategori: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003eVarian\/kemasan: 5 g\u003c\/li\u003e\n\u003cli\u003eBentuk fisik: cairan pada suhu ruang\u003c\/li\u003e\n\u003cli\u003eCatatan penyimpanan: sangat sensitif terhadap kelembapan; simpan di tempat sejuk dan kering, wadah tertutup rapat, sebaiknya di bawah atmosfer gas inert\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003ePenanganan dan Penyimpanan\u003c\/h3\u003e\n\u003cp\u003eReagen ini bereaksi dengan air dan dapat melepaskan hidrogen klorida, sehingga penanganan wajib dilakukan di lemari asam dengan teknik anhidrat, misalnya menggunakan jarum suntik kering dan aliran nitrogen atau argon. Kenakan sarung tangan tahan bahan kimia, kacamata pelindung, dan jas laboratorium, serta hindari segala kontak dengan uap air. Tutup wadah rapat segera setelah pengambilan dan buang limbah melalui prosedur penanganan bahan korosif yang berlaku.\u003c\/p\u003e\n\u003ch3\u003eEnglish\u003c\/h3\u003e\n\u003cp\u003eTCI C0976 2-Chlorophenyl Phosphorodichloridate (CAS 15074-54-1) is a moisture-sensitive phosphorylating agent supplied in a 5 g pack. Its two reactive P–Cl bonds react readily with alcohols and nucleoside hydroxyl groups, while the 2-chlorophenyl group acts as a removable phosphate protecting group. It is classically associated with phosphotriester approaches to oligonucleotide synthesis and with the preparation of protected phosphate esters. Use strict anhydrous technique in a fume hood, wear chemical-resistant gloves and eye protection, and keep the container tightly sealed, preferably under inert gas.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086041231578,"sku":"TCI2510C097615333","price":704000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0976.jpg?v=1767096129"},{"product_id":"tci2510c097815336","title":"TCI C0978 207121-42-4 Barium 2-Cyanoethylphosphate Hydrate [Phosphorylating Agent]","description":"\u003ch3\u003eDeskripsi\u003c\/h3\u003e\n\u003cp\u003eTCI C0978 Barium 2-Cyanoethylphosphate Hydrate adalah reagen fosforilasi berbentuk garam barium yang tersedia dalam kemasan 5 g dan 25 g. Senyawa ini menyediakan unit fosfat yang telah dilengkapi gugus pelindung 2-sianoetil, sebuah gugus yang secara luas dikenal dapat dilepas dengan mudah pada kondisi basa ringan. Bentuk garam padat membuatnya lebih mudah ditimbang dan disimpan dibandingkan reagen fosforilasi berbentuk cairan reaktif.\u003c\/p\u003e\n\u003cp\u003eDalam praktiknya, reagen ini dipakai untuk memperkenalkan gugus monofosfat pada alkohol, nukleosida, gula, dan berbagai substrat hidroksil lain dengan bantuan agen pengaktif seperti karbodiimida. Setelah pembentukan ikatan fosfat, gugus 2-sianoetil dapat dihilangkan melalui eliminasi berbasis basa untuk mengungkap fosfat bebas. Kation barium umumnya ditukar terlebih dahulu menggunakan resin penukar ion atau diendapkan sebagai sulfat, bergantung pada protokol yang digunakan.\u003c\/p\u003e\n\u003cp\u003eDua pilihan kemasan memberi keleluasaan antara pekerjaan penapisan skala kecil dan sintesis rutin yang lebih besar. Reagen ini banyak digunakan pada laboratorium kimia nukleotida, biokimia, dan kimia karbohidrat. AMI Scientific menyediakan produk TCI ini untuk mendukung riset di bidang tersebut.\u003c\/p\u003e\n\u003ch3\u003eAplikasi Laboratorium\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eFosforilasi nukleosida — memasang gugus monofosfat terlindung pada gugus hidroksil nukleosida.\u003c\/li\u003e\n\u003cli\u003eSintesis fosfat gula — digunakan dalam kimia karbohidrat untuk menyiapkan ester fosfat sakarida.\u003c\/li\u003e\n\u003cli\u003ePenyiapan monoester fosfat — reagen padat yang praktis untuk fosforilasi alkohol sederhana.\u003c\/li\u003e\n\u003cli\u003eKimia gugus pelindung fosfat — gugus 2-sianoetil dapat dilepas pada kondisi basa ringan tanpa merusak substrat sensitif.\u003c\/li\u003e\n\u003cli\u003eRiset biokimia — mendukung pembuatan analog fosfat untuk studi substrat dan inhibitor enzim.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpesifikasi\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMerek: TCI (kode produk C0978)\u003c\/li\u003e\n\u003cli\u003eNomor CAS: 207121-42-4\u003c\/li\u003e\n\u003cli\u003eKategori: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003eVarian\/kemasan: 5 g, 25 g\u003c\/li\u003e\n\u003cli\u003eBentuk fisik: padatan (garam barium terhidrat)\u003c\/li\u003e\n\u003cli\u003eCatatan penyimpanan: simpan di tempat sejuk dan kering dalam wadah tertutup rapat, terlindung dari kelembapan berlebih\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003ePenanganan dan Penyimpanan\u003c\/h3\u003e\n\u003cp\u003eGaram barium bersifat toksik apabila tertelan atau terhirup, sehingga penimbangan sebaiknya dilakukan di lemari asam atau timbangan berpelindung dengan sarung tangan, kacamata, dan masker debu. Hindari terbentuknya debu halus dan cuci tangan setelah selesai bekerja. Simpan terpisah dari asam kuat, dan tangani limbah yang mengandung barium melalui jalur limbah logam berat sesuai ketentuan laboratorium.\u003c\/p\u003e\n\u003ch3\u003eEnglish\u003c\/h3\u003e\n\u003cp\u003eTCI C0978 Barium 2-Cyanoethylphosphate Hydrate (CAS 207121-42-4) is a solid phosphorylating reagent available in 5 g and 25 g packs. It delivers a phosphate unit already carrying a 2-cyanoethyl protecting group, which can later be removed under mild basic conditions. The reagent is commonly applied to nucleosides, sugars, and simple alcohols, typically with a coupling activator, and the barium counterion is exchanged or precipitated as required. Because barium salts are toxic, weigh the material with gloves and dust protection, keep it dry and tightly closed, and dispose of residues through heavy-metal waste channels.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086041362650,"sku":"TCI2510C097815336","price":1743000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086041395418,"sku":"TCI2510C097815337","price":5876000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0978.jpg?v=1767096137"},{"product_id":"tci2510c121015673","title":"TCI C1210 5381-99-7 2-Chloro-4H-1,3,2-benzodioxaphosphorin-4-one","description":"\u003ch3\u003eDeskripsi\u003c\/h3\u003e\n\u003cp\u003eTCI C1210 2-Chloro-4H-1,3,2-benzodioxaphosphorin-4-one adalah reagen fosfor(III) bersiklus yang dikenal luas di kalangan kimiawan nukleotida sebagai pereaksi fosfitilasi. Struktur cincin benzodioksafosforin dengan atom klor terikat pada fosfor menjadikannya sangat reaktif terhadap gugus hidroksil. Produk ini dipasok oleh TCI untuk keperluan riset sintesis kimia tingkat lanjut.\u003c\/p\u003e\n\u003cp\u003eReagen ini umumnya digunakan untuk memasukkan atom fosfor ke dalam molekul yang memiliki gugus hidroksil bebas, misalnya pada nukleosida, gula, atau alkohol lain. Setelah fosfitilasi, intermediet yang terbentuk dapat dioksidasi, disulfurisasi, atau direaksikan lebih lanjut untuk menghasilkan berbagai turunan fosfat, tiofosfat, dan fosfat siklik. Efisiensi jalur inilah yang membuat reagen tersebut menjadi pilihan pada penelitian nukleotida dan analog nukleotida.\u003c\/p\u003e\n\u003cp\u003eAMI Scientific menyediakan produk ini bagi laboratorium kimia nukleotida, kimia medisinal, dan sintesis organik lanjut. Kemasan 5 g dan 25 g memberikan pilihan sesuai intensitas pemakaian di laboratorium masing-masing. Mengingat sifatnya yang sangat peka terhadap kelembapan, reagen ini sebaiknya ditangani oleh personel yang terbiasa dengan teknik kerja bebas air.\u003c\/p\u003e\n\u003ch3\u003eAplikasi Laboratorium\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eReagen fosfitilasi — mereaksikan gugus hidroksil bebas menjadi intermediet fosfor(III) secara efisien.\u003c\/li\u003e\n\u003cli\u003eSintesis nukleotida dan analognya — mendukung pembuatan turunan fosfat dan tiofosfat pada riset asam nukleat.\u003c\/li\u003e\n\u003cli\u003ePembentukan fosfat siklik — berguna dalam penyiapan struktur fosfat berbentuk cincin.\u003c\/li\u003e\n\u003cli\u003eSintesis prodrug berbasis fosfor — dipakai pada penelitian kimia medisinal yang melibatkan gugus fosfat termodifikasi.\u003c\/li\u003e\n\u003cli\u003eKimia organofosfor umum — menjadi sumber gugus fosfor reaktif untuk berbagai transformasi lanjutan.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpesifikasi\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMerek: TCI (kode produk C1210)\u003c\/li\u003e\n\u003cli\u003eNomor CAS: 5381-99-7\u003c\/li\u003e\n\u003cli\u003eKategori: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003eVarian\/kemasan: 5 g dan 25 g\u003c\/li\u003e\n\u003cli\u003eBentuk fisik: padatan kristalin yang sangat peka terhadap kelembapan\u003c\/li\u003e\n\u003cli\u003eCatatan penyimpanan: simpan dalam wadah tertutup rapat di bawah gas inert dan pada kondisi kering sesuai petunjuk penyimpanan produsen.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003ePenanganan dan Penyimpanan\u003c\/h3\u003e\n\u003cp\u003eReagen ini bereaksi cepat dengan air, sehingga penimbangan dan pemindahan sebaiknya dilakukan di dalam glovebox atau menggunakan teknik Schlenk dengan aliran gas inert. Gunakan pelarut kering, alat gelas yang telah dikeringkan, serta alat pelindung diri lengkap termasuk sarung tangan dan kacamata pelindung. Jauhkan dari kelembapan udara, alkohol, dan basa, dan selalu ikuti Safety Data Sheet resmi TCI untuk penanganan serta pembuangan limbah organofosfor.\u003c\/p\u003e\n\u003ch3\u003eEnglish\u003c\/h3\u003e\n\u003cp\u003eTCI C1210 2-Chloro-4H-1,3,2-benzodioxaphosphorin-4-one, CAS 5381-99-7, is a cyclic phosphorus(III) chloride reagent widely used for phosphitylation of free hydroxyl groups. It reacts readily with nucleosides, sugars, and other alcohols to give phosphorus(III) intermediates that can subsequently be oxidised, sulfurised, or cyclised. Because of this, it is a standard tool in nucleotide chemistry, cyclic phosphate synthesis, and phosphorus-containing prodrug research. AMI Scientific supplies 5 g and 25 g packs; the reagent is highly moisture sensitive and must be handled under dry, inert conditions in line with the manufacturer's Safety Data Sheet.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086056534234,"sku":"TCI2510C121015673","price":1857000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086056567002,"sku":"TCI2510C121015674","price":5567000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1210.jpg?v=1767096538"},{"product_id":"tci2510c124215716","title":"TCI C1242 2942-58-7 Diethyl Cyanophosphonate","description":"\u003ch3\u003eDeskripsi\u003c\/h3\u003e\n\u003cp\u003eTCI C1242 Diethyl Cyanophosphonate adalah reagen kopling yang dikenal luas dalam sintesis organik, sering disingkat sebagai DEPC. Reagen ini banyak digunakan untuk mengaktifkan asam karboksilat sehingga dapat bereaksi dengan amina membentuk ikatan amida. Karena efektivitasnya, DEPC menjadi salah satu pilihan dalam pembentukan ikatan peptida.\u003c\/p\u003e\n\u003cp\u003eSelain untuk sintesis amida dan peptida, DEPC juga dimanfaatkan dalam pembentukan ester serta beberapa transformasi organik lain yang memerlukan aktivasi gugus karboksil. Reagen ini kerap dipilih ketika peneliti membutuhkan kondisi reaksi yang relatif ringan dan tingkat rasemisasi yang terkendali. Penggunaannya umumnya dikombinasikan dengan basa amina tersier dalam pelarut organik yang sesuai.\u003c\/p\u003e\n\u003cp\u003eAMI Scientific menyediakan produk TCI ini bagi laboratorium sintesis organik, kimia medisinal, dan penelitian peptida di Indonesia. Kemasan 5 g dan 25 g memberi keleluasaan sesuai frekuensi penggunaan di laboratorium. Seluruh data teknis dan prosedur penggunaan sebaiknya dirujuk pada dokumen resmi dari produsen.\u003c\/p\u003e\n\u003ch3\u003eAplikasi Laboratorium\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePembentukan ikatan amida — mengaktifkan asam karboksilat untuk bereaksi dengan amina.\u003c\/li\u003e\n\u003cli\u003eSintesis peptida — digunakan sebagai reagen kopling dengan kecenderungan rasemisasi yang terkendali.\u003c\/li\u003e\n\u003cli\u003eSintesis ester — membantu aktivasi gugus karboksil dalam pembentukan ikatan ester.\u003c\/li\u003e\n\u003cli\u003eRiset kimia medisinal — mendukung penyusunan cepat analog senyawa berbasis amida.\u003c\/li\u003e\n\u003cli\u003eTransformasi organik lanjutan — dipakai dalam berbagai reaksi yang memerlukan aktivasi asam karboksilat.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpesifikasi\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMerek: TCI (kode produk C1242)\u003c\/li\u003e\n\u003cli\u003eNomor CAS: 2942-58-7\u003c\/li\u003e\n\u003cli\u003eKategori: Chemistry \u0026gt; Synthetic Reagents \u0026gt; Coupling [Synthetic Reagents]\u003c\/li\u003e\n\u003cli\u003eVarian\/kemasan: 5 g dan 25 g\u003c\/li\u003e\n\u003cli\u003eBentuk fisik: umumnya berupa cairan; konfirmasikan pada lembar data resmi TCI\u003c\/li\u003e\n\u003cli\u003eCatatan penyimpanan: simpan di tempat sejuk dan kering, terlindung dari kelembapan, dalam wadah tertutup rapat\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003ePenanganan dan Penyimpanan\u003c\/h3\u003e\n\u003cp\u003eReagen ini tergolong sangat berbahaya dan hanya boleh ditangani oleh personel terlatih di dalam lemari asam dengan alat pelindung diri lengkap. Hindari kontak dengan air atau kelembapan karena senyawa sianofosfonat dapat terurai dan melepaskan gas yang sangat beracun. Gunakan teknik bebas udara bila diperlukan, jangan sekali-kali membuang sisa reagen ke saluran air, dan patuhi sepenuhnya Safety Data Sheet resmi TCI.\u003c\/p\u003e\n\u003ch3\u003eEnglish\u003c\/h3\u003e\n\u003cp\u003eTCI C1242 Diethyl Cyanophosphonate (DEPC) is a well-established coupling reagent for activating carboxylic acids toward amide and ester bond formation. It is frequently applied in peptide synthesis, where it offers effective coupling under comparatively mild conditions. The reagent is highly toxic and moisture-sensitive, and hydrolysis can release extremely hazardous gas, so it must be handled only by trained personnel in a fume hood. Available in 5 g and 25 g packs, it must be stored, used, and disposed of strictly in accordance with the official TCI safety data sheet.\u003c\/p\u003e\n\u003ch3\u003eReferensi Ilmiah\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eGUZMAN dkk. (1997). ChemInform Abstract: A Convenient Method for the Phosphorylation of Phenols with Diethyl Cyanophosphonate.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.199747196\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.199747196\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eGuzmán dkk. (1997). A Convenient Method for the Phosphorylation of Phenols with Diethyl Cyanophosphonate. \u003cem\u003eSynthetic Communications\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1080\/00397919708005008\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1080\/00397919708005008\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eDemir dkk. (2009). Cyanide Ion Promoted Addition of Acylphosphonates to Diethyl Cyanophosphonate: Synthesis of Phosphonocyanohydrin O-Phosphates. \u003cem\u003eSynthesis\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1055\/s-0029-1216634\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1055\/s-0029-1216634\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferensi dihimpun otomatis dari Crossref dan setiap DOI diverifikasi keberadaannya. AMI Scientific tidak berafiliasi dengan penulis maupun penerbit.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086058598618,"sku":"TCI2510C124215716","price":1799000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086058631386,"sku":"TCI2510C124215717","price":5904000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1242.jpg?v=1768204586"},{"product_id":"tci2510c154516159","title":"TCI C1545 3724-43-4 (Chloromethylene)dimethyliminium Chloride","description":"\u003ch3\u003eDeskripsi\u003c\/h3\u003e\n\u003cp\u003eTCI C1545 (Chloromethylene)dimethyliminium Chloride adalah bentuk terisolasi dari reagen Vilsmeier, salah satu reagen aktivasi paling dikenal dalam kimia organik. Tersedianya reagen ini sebagai padatan siap pakai menghilangkan kebutuhan untuk membuatnya secara in situ dari dimetilformamida dan klorida asam. Hal tersebut memberikan kendali stoikiometri yang lebih baik serta hasil yang lebih konsisten antar-percobaan.\u003c\/p\u003e\n\u003cp\u003eReagen ini bekerja sebagai elektrofil kuat yang mampu memformilasi cincin aromatik dan heteroaromatik kaya elektron pada reaksi Vilsmeier–Haack. Selain itu, ia juga banyak dipakai untuk mengaktifkan gugus hidroksil dan karboksilat, mendehidrasi amida menjadi nitril, serta mengubah alkohol menjadi klorida. Dalam ranah glikosains, sifat dehidratifnya dimanfaatkan pada aktivasi donor gula dan transformasi terkait.\u003c\/p\u003e\n\u003cp\u003eAMI Scientific menyediakan produk ini dalam dua pilihan kemasan agar sesuai dengan kebutuhan riset maupun sintesis yang lebih rutin. Karena reagen ini sangat peka terhadap kelembapan, penanganan yang tepat menjadi kunci untuk menjaga kinerjanya. Kode katalog dan nomor CAS yang jelas memudahkan penelusuran dokumen resmi produsen.\u003c\/p\u003e\n\u003ch3\u003eAplikasi Laboratorium\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eReaksi Vilsmeier–Haack — memformilasi senyawa aromatik dan heteroaromatik kaya elektron menjadi aldehida.\u003c\/li\u003e\n\u003cli\u003eAktivasi asam karboksilat — membentuk spesies teraktivasi untuk pembentukan amida dan ester.\u003c\/li\u003e\n\u003cli\u003eDehidrasi amida menjadi nitril — memberikan jalur konversi yang efisien pada kondisi ringan.\u003c\/li\u003e\n\u003cli\u003eKonversi alkohol menjadi klorida — memanfaatkan sifat elektrofilik dan dehidratif reagen.\u003c\/li\u003e\n\u003cli\u003eAplikasi glikosains — dipakai dalam aktivasi dan transformasi turunan karbohidrat.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpesifikasi\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMerek: TCI (kode katalog C1545)\u003c\/li\u003e\n\u003cli\u003eNomor CAS: 3724-43-4\u003c\/li\u003e\n\u003cli\u003eKategori: Chemistry \u0026gt; Chemical Biology \u0026gt; Glycoscience\u003c\/li\u003e\n\u003cli\u003eVarian\/kemasan: 25 g dan 250 g\u003c\/li\u003e\n\u003cli\u003eBentuk fisik: padatan yang sangat peka terhadap kelembapan\u003c\/li\u003e\n\u003cli\u003eCatatan penyimpanan: simpan dalam wadah tertutup rapat pada kondisi kering, sesuai anjuran resmi produsen.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003ePenanganan dan Penyimpanan\u003c\/h3\u003e\n\u003cp\u003eReagen ini bereaksi dengan air, karena itu penimbangan sebaiknya dilakukan di dalam glove box atau di bawah aliran gas inert dengan peralatan yang benar-benar kering. Gunakan lemari asam, sarung tangan, dan pelindung mata, serta hindari kontak dengan alkohol, basa, dan bahan pengoksidasi. Tutup wadah segera setelah pengambilan dan simpan sesuai ketentuan pada lembar data keselamatan resmi TCI.\u003c\/p\u003e\n\u003ch3\u003eEnglish\u003c\/h3\u003e\n\u003cp\u003eTCI C1545, (Chloromethylene)dimethyliminium Chloride (CAS 3724-43-4), is the isolated form of the Vilsmeier reagent, supplied as a ready-to-use solid rather than generated in situ. It acts as a powerful electrophilic and dehydrating agent, enabling Vilsmeier–Haack formylation of electron-rich aromatics, activation of carboxylic acids, dehydration of amides to nitriles, and conversion of alcohols to chlorides. Within glycoscience, its dehydrative activation chemistry is applied to carbohydrate donors and related transformations. Offered by AMI Scientific in 25 g and 250 g packs, this highly moisture-sensitive solid must be weighed under dry inert conditions and stored tightly closed.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086076883162,"sku":"TCI2510C154516159","price":3092000.0,"currency_code":"IDR","in_stock":true},{"title":"250g","offer_id":48086076915930,"sku":"TCI2510C154516160","price":17173000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1545.jpg?v=1767097106"},{"product_id":"tci2510c175716420","title":"TCI C1757 245365-64-4 N-Benzyloxycarbonyl-2-nitrobenzenesulfonamide","description":"\u003ch3\u003eDeskripsi\u003c\/h3\u003e\n\u003cp\u003eN-Benzyloxycarbonyl-2-nitrobenzenesulfonamide adalah senyawa kimia yang digunakan dalam berbagai reaksi sintetik di laboratorium. Bahan ini termasuk dalam kategori reaktif sintetik yang memiliki fungsi penting dalam pembentukan ikatan C-X (non-halogen) dalam proses sintesis senyawa organik. Senyawa ini sering ditemukan dalam reaksi substitusi, reaksi pembentukan ikatan, serta reaksi penggabungan molekul kompleks. Dalam laboratorium, senyawa ini menjadi alat penting untuk mempercepat proses sintesis dan memperoleh senyawa target dengan presisi tinggi.\u003c\/p\u003e\n\u003cp\u003eKarakteristik utama dari N-Benzyloxycarbonyl-2-nitrobenzenesulfonamide adalah kemampuannya untuk berpartisipasi dalam reaksi kimia yang melibatkan pembentukan ikatan karbon-oksigen atau karbon-sulfur. Senyawa ini memiliki struktur kimia yang stabil dan dapat bereaksi dengan berbagai reaktif lain seperti amina, asam, atau basa. Karena sifatnya yang reaktif dan spesifik, senyawa ini dipilih untuk aplikasi yang memerlukan reaksi presisi dan kontrol tinggi.\u003c\/p\u003e\n\u003cp\u003eDalam konteks laboratorium Indonesia, senyawa ini digunakan secara luas dalam penelitian kimia organik, baik di universitas, institusi penelitian, maupun perusahaan farmasi. Bahan ini sangat relevan untuk penelitian yang berkaitan dengan sintesis senyawa aktif biologis, pengembangan obat, dan modifikasi senyawa kimia. Dengan sifat reaktifnya, senyawa ini menjadi pilihan utama dalam berbagai eksperimen sintetik yang memerlukan keakuratan dan keandalan hasil.\u003c\/p\u003e\n\u003ch3\u003eAplikasi Laboratorium\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSintesis senyawa organik kompleks yang memerlukan reaksi substitusi presisi\u003c\/li\u003e\n\u003cli\u003eReaksi pembentukan ikatan karbon-oksigen dalam proses kimia organik\u003c\/li\u003e\n\u003cli\u003ePenelitian tentang modifikasi senyawa aktif biologis untuk pengembangan obat\u003c\/li\u003e\n\u003cli\u003eEksperimen kimia yang melibatkan reaksi dengan amina atau asam\u003c\/li\u003e\n\u003cli\u003ePengembangan senyawa kimia baru dalam bidang farmasi dan material\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpesifikasi\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMerek: TCI\u003c\/li\u003e\n\u003cli\u003eNomor CAS: 245365-64-4\u003c\/li\u003e\n\u003cli\u003eKategori: Chemistry \u0026gt; Synthetic Reagents \u0026gt; C-X(Non-Halogen) Bond Formation [Synthetic Reagents]\u003c\/li\u003e\n\u003cli\u003eVarian\/kemasan: 5g, 25g\u003c\/li\u003e\n\u003cli\u003eBentuk fisik: Padatan kristalin\u003c\/li\u003e\n\u003cli\u003eCatatan penyimpanan: Simpan dalam wadah tertutup rapat di tempat sejuk dan kering\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003ePenanganan dan Penyimpanan\u003c\/h3\u003e\n\u003cp\u003eSenyawa ini harus disimpan dalam wadah tertutup rapat di tempat sejuk dan kering, menjauh dari paparan sinar matahari langsung dan sumber panas. Karena sifat reaktifnya, bahan ini harus ditangani dengan hati-hati, menggunakan alat pelindung seperti sarung tangan dan masker. Pastikan wadah penyimpanan tidak terbuka dan tidak terkontaminasi oleh bahan kimia lain. Penyimpanan yang tepat akan memperpanjang masa pakai dan menjaga kualitas senyawa secara optimal.\u003c\/p\u003e\n\u003ch3\u003eEnglish\u003c\/h3\u003e\n\u003cp\u003eN-Benzyloxycarbonyl-2-nitrobenzenesulfonamide is a synthetic reagent widely used in organic chemistry for the formation of C-X (non-halogen) bonds. This compound is known for its ability to participate in substitution reactions and molecular coupling processes, making it essential in the synthesis of complex organic compounds. Its stable structure allows it to react selectively with various reagents such as amines, acids, and bases. In laboratory applications, it is commonly used in research related to the development of bioactive compounds and pharmaceuticals. Due to its reactivity and specificity, this compound is a preferred choice for experiments requiring precision and controlled chemical reactions. Its versatility makes it a valuable tool for both academic and industrial research in Indonesia.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086087106778,"sku":"TCI2510C175716420","price":2840000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086087139546,"sku":"TCI2510C175716421","price":8826000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1757.jpg?v=1769144442"},{"product_id":"tci2510c216016823","title":"TCI C2160 534-17-8 Cesium Carbonate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI Cesium Carbonate, catalog code C2160, is an inorganic salt of the alkali metal cesium that has become one of the most popular bases in modern organic synthesis. In the laboratory this compound is used primarily as a proton-scavenging base in alkylation reactions, transition-metal-catalyzed cross-coupling reactions, and nucleophilic aromatic substitution reactions. Its presence on the reagent shelf of a synthesis laboratory means that many transformations that previously proceeded only with difficulty under conventional bases can now be carried out under considerably milder conditions.\u003c\/p\u003e\n\u003cp\u003eThe property that most often leads chemists to select cesium carbonate is its relatively good solubility in polar aprotic organic solvents such as DMF, DMSO, and acetonitrile, far exceeding that of the corresponding potassium or sodium carbonate salts. The cesium cation is large and has low polarizing power, so its ion pairing is loose; this leaves the accompanying nucleophilic anion more reactive, an effect widely known as the cesium effect. Its basicity is moderate, strong enough to deprotonate phenols, thiols, amides, or dicarbonyl compounds, yet mild enough to leave sensitive functional groups intact. The compound is also hygroscopic, which must be taken into account during handling.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent is typically found in university organic synthesis and medicinal chemistry groups, in research institute laboratories, and in pharmaceutical and fine chemical development units where coupling and alkylation reactions are run routinely. Because the local climate is humid throughout the year, laboratories here pay particular attention to keeping the container tightly closed and limiting exposure to open air, so that the reagent retains its performance from one experiment to the next.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAlkylation of phenols and thiols — the moderate basicity deprotonates these substrates cleanly while the loose cesium ion pair keeps the resulting anion highly nucleophilic toward the alkylating agent.\u003c\/li\u003e\n\u003cli\u003eTransition-metal-catalyzed cross-coupling reactions — serves as the proton-scavenging base that keeps the catalytic cycle turning over without attacking sensitive functional groups elsewhere in the substrate.\u003c\/li\u003e\n\u003cli\u003eNucleophilic aromatic substitution — good solubility in DMF, DMSO, and acetonitrile allows the base to work in the homogeneous polar aprotic media these substitutions normally require.\u003c\/li\u003e\n\u003cli\u003eN-alkylation of amides and related nitrogen nucleophiles — basicity sufficient to deprotonate the amide nitrogen while remaining mild enough to preserve other functionality in the molecule.\u003c\/li\u003e\n\u003cli\u003eDeprotonation and functionalization of dicarbonyl compounds — generates the stabilized enolate under milder conditions than conventional carbonate bases permit, which is useful for multi-step synthetic sequences.\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: 534-17-8\u003c\/li\u003e\n\u003cli\u003eCatalog code: C2160\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Catalysis and Inorganic Chemistry \u0026gt; Main-group Elements [Catalysis and Inorganic Chemistry]\u003c\/li\u003e\n\u003cli\u003eChemical class: inorganic alkali metal salt (cesium carbonate)\u003c\/li\u003e\n\u003cli\u003eStorage note: hygroscopic material; keep the container tightly closed and protected from moisture. Pack sizes available on request.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore cesium carbonate in its original tightly closed container, in a dry place away from direct exposure to humid air, since the material is hygroscopic and readily takes up atmospheric moisture. Chemically resistant containers with well-sealed caps are appropriate, and transferring the reagent inside a glove box or under a dry inert atmosphere is advisable when reaction results are sensitive to water content. Weigh out only the quantity needed and close the container immediately afterwards. Handle the material in a fume hood using safety glasses, gloves, and a laboratory coat, avoid contact with skin and eyes and inhalation of the dust, and consult the manufacturer's safety data sheet before use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086107914458,"sku":"TCI2510C216016823","price":1406000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48086107947226,"sku":"TCI2510C216016824","price":3682000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2160.jpg?v=1767097850"},{"product_id":"tci2510c223116927","title":"TCI C2231 3570-58-9 2-Chloroethyl Methanesulfonate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C2231 2-Chloroethyl Methanesulfonate is a non-heterocyclic building block belonging to the mesylate ester family, widely applied as a two-ended alkylating reagent in organic synthesis. Its molecular structure carries a mesylate group serving as an excellent leaving group at one end and a chlorine atom at the other, giving researchers two reactive sites with clearly differentiated levels of reactivity. This configuration is particularly useful for introducing a two-carbon bridge into a target molecule in stepwise fashion, then closing it through a cyclization reaction. The compact size of the molecule makes it an economical choice from an atom-economy standpoint in synthetic design.\u003c\/p\u003e\n\u003cp\u003eThe principal advantage of a mesylate over aromatic sulfonates lies in its lower molecular weight, so the mass of reagent required per mole is smaller and the methanesulfonate by-product is more easily separated during the purification stage. The mesylate group is also far more readily displaced than chloride or bromide, which means nucleophilic substitution can proceed at low temperature with a weak base, making it suitable for substrates that are sensitive to harsh conditions. The reactivity difference between the mesylate end and the chloride end allows reactions to be directed selectively to one site before the second site is engaged.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this building block is typically found in university organic chemistry research groups, pharmaceutical and medicinal chemistry programmes, and industrial R\u0026amp;D units engaged in intermediate preparation. It is handled in fume hoods on a research and pilot scale, where the ability to run substitution steps under mild conditions is valued in facilities that do not always have access to specialised low-temperature or inert-atmosphere equipment. Its role as a compact bifunctional linker makes it a practical stock item for multi-step synthesis work.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eStepwise alkylation of nucleophiles, where the highly labile mesylate end reacts first under mild conditions while the chloride end remains available for a later, separate transformation.\u003c\/li\u003e\n\u003cli\u003eIntroduction of two-carbon bridges into target molecules, allowing researchers to extend a scaffold by a short ethylene linker before closing the structure through a subsequent cyclization step.\u003c\/li\u003e\n\u003cli\u003eRing-closing and cyclization chemistry, in which the two differentiated reactive ends are engaged in sequence so that intramolecular bond formation completes the desired ring system.\u003c\/li\u003e\n\u003cli\u003ePreparation of synthetic intermediates in medicinal and pharmaceutical chemistry research, where mild substitution conditions protect sensitive functional groups elsewhere in the substrate molecule.\u003c\/li\u003e\n\u003cli\u003eBifunctional linker chemistry for joining two distinct nucleophilic partners, exploiting the clear reactivity gap between the mesylate and chloride termini to control the order of coupling.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI (Tokyo Chemical Industry)\u003c\/li\u003e\n\u003cli\u003eCAS number: 3570-58-9\u003c\/li\u003e\n\u003cli\u003eChemical name: 2-Chloroethyl Methanesulfonate\u003c\/li\u003e\n\u003cli\u003eCatalogue code: C2231\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in standard TCI research-scale packaging; please confirm the size options when ordering\u003c\/li\u003e\n\u003cli\u003eStorage: keep in the original tightly closed container under the conditions stated on the manufacturer's label and safety data sheet\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the container tightly closed in a cool, dry, well-ventilated area away from heat, ignition sources, moisture, and incompatible materials such as strong bases and strong oxidising agents, following the conditions specified on the manufacturer's label and safety data sheet. Keep the material in its original supplier container, or in a chemically compatible, clearly labelled vessel if transfer is necessary. Handle only inside a functioning fume hood, wearing safety glasses, chemical-resistant gloves, and a laboratory coat. As an alkylating agent, this compound should be treated with particular care: avoid skin contact, eye contact, and inhalation of vapours, minimise the quantity handled on the open bench, and consult the safety data sheet before use, spill clean-up, or waste disposal.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086113190106,"sku":"TCI2510C223116927","price":4189000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2231.jpg?v=1767097961"},{"product_id":"tci2510c230417037","title":"TCI C2304 578743-87-0 Chloro[1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene]copper(I)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eChloro[1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene]copper(I) is a copper-based chemical compound widely used in catalytic reactions, particularly in carbon-hydrogen (C-H) activation processes. This compound plays a crucial role in modern laboratory settings by enabling the efficient transformation of complex organic molecules. Its unique structure, containing a copper(I) ion and an imidazol-2-ylidene ligand, allows it to act as a highly effective catalyst in various synthetic pathways. Due to its stability and reactivity, it is an essential tool for researchers working in catalysis and inorganic chemistry.\u003c\/p\u003e\n\u003cp\u003eThe compound is favored for its exceptional catalytic activity and chemical stability. It maintains its structural integrity under a range of reaction conditions, making it suitable for both academic and industrial applications. Its ability to selectively activate C-H bonds makes it particularly valuable in the development of new synthetic methods. Additionally, its compatibility with a wide range of organic substrates enhances its versatility in laboratory settings. These properties make it a preferred choice for chemists seeking reliable and efficient catalytic solutions.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is frequently used in research focused on organic chemistry, catalysis, and inorganic chemistry. It supports the development of new chemical processes and the synthesis of complex molecules. Its application is especially relevant in academic and research institutions where advanced catalytic techniques are required. The compound’s reliability and performance make it a key component in the chemical research toolkit of Indonesian scientists.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eC-H Activation Reactions: This compound is ideal for C-H activation due to its ability to selectively activate carbon-hydrogen bonds, enabling the synthesis of complex organic molecules with high efficiency.\u003c\/li\u003e\n\u003cli\u003eOrganic Synthesis: It is widely used in organic synthesis to facilitate various reactions such as substitution and oxidation, providing a stable and reactive catalytic environment.\u003c\/li\u003e\n\u003cli\u003eCatalytic Oxidation Processes: The compound's unique structure allows it to act as a catalyst in oxidation reactions, enhancing reaction rates and selectivity in laboratory settings.\u003c\/li\u003e\n\u003cli\u003eInorganic Chemistry Research: Its role in inorganic chemistry is significant, particularly in the study of metal-ligand interactions and catalytic mechanisms.\u003c\/li\u003e\n\u003cli\u003eAdvanced Catalytic Studies: Researchers use it to explore new catalytic pathways and improve existing synthetic methods, contributing to the advancement of chemical research.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 578743-87-0\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Catalysis and Inorganic Chemistry \u0026gt; C-H Activation [Catalysis]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified\u003c\/li\u003e\n\u003cli\u003ePhysical form: Not specified\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry place away from moisture and direct sunlight to maintain its stability and effectiveness. It is recommended to use airtight containers made of materials such as glass or 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. In laboratory settings, it is important to ensure proper ventilation to minimize exposure to any potential vapors. Always follow standard safety protocols when working with catalytic materials to ensure a safe and controlled environment.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48086118629594,"sku":"TCI2510C230417037","price":1294000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48086118662362,"sku":"TCI2510C230417038","price":3852000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2304.jpg?v=1767098104"},{"product_id":"tci2510c240517170","title":"TCI C2405 852445-83-1 Chloro[1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene]gold(I)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eChloro[1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene]gold(I) is a chemical compound used in catalytic reactions, particularly in C-H activation processes. This compound is a metal complex with a unique structure and highly effective catalytic properties. In the laboratory, it plays a crucial role in accelerating chemical reactions that require C-H bond activation, such as the synthesis of complex organic compounds. Its stability and reactivity make it a valuable tool for researchers working in catalysis and organic chemistry.\u003c\/p\u003e\n\u003cp\u003eThe compound’s high catalytic efficiency and stability under specific conditions make it a preferred choice for various scientific applications. Its structure, featuring a gold(I) ion bonded to an imidazole ligand, allows it to interact effectively with relevant substrates. This unique molecular configuration enhances its ability to facilitate complex chemical transformations. The compound’s reactivity and stability ensure consistent performance in laboratory settings, making it a reliable option for advanced research.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in research related to organic chemistry, catalysis, and the synthesis of complex compounds. It supports studies that require precise and efficient C-H activation, contributing to advancements in chemical research. Its versatility and effectiveness make it a key component in various scientific investigations conducted in Indonesian academic and research institutions.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eC-H Activation Reactions: This compound is ideal for activating carbon-hydrogen bonds, enabling the synthesis of complex organic molecules with high efficiency.\u003c\/li\u003e\n\u003cli\u003eOrganic Synthesis: It is widely used in the development of new organic compounds, particularly in reactions requiring selective and efficient catalytic activity.\u003c\/li\u003e\n\u003cli\u003eCatalytic Research: Its unique structure and catalytic properties make it a valuable tool for studying catalytic mechanisms and improving reaction conditions.\u003c\/li\u003e\n\u003cli\u003eIndustrial Chemistry Applications: It supports the development of new chemical processes in industrial settings, particularly those involving complex catalytic systems.\u003c\/li\u003e\n\u003cli\u003eAcademic Research: It is frequently used in academic laboratories for teaching and research purposes, helping students and researchers explore advanced catalytic 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: 852445-83-1\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Catalysis and Inorganic Chemistry \u0026gt; C-H Activation [Catalysis]\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\u003eThis compound should be stored in a cool, dry environment to maintain its stability and effectiveness. It is recommended to keep it in a tightly sealed container to prevent exposure to moisture and air. Due to its chemical nature, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles. Avoid direct contact with skin and inhalation of vapors. Ensure proper ventilation in the laboratory when working with this material. Regular inspection of storage conditions is advised to ensure long-term integrity and safety.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48086124953818,"sku":"TCI2510C240517170","price":2924000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2405.jpg?v=1767098290"},{"product_id":"tci2510c266217500","title":"TCI C2662 12148-71-9 (1,5-Cyclooctadiene)(methoxy)iridium(I) Dimer","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(1,5-Cyclooctadiene)(methoxy)iridium(I) Dimer is a chemical compound widely used in catalytic reactions, particularly in C-H activation processes. As a metal complex, it plays a crucial role in facilitating complex chemical transformations within laboratory settings. Its chiral structure allows it to act as an efficient catalyst in various organic and inorganic reactions. This compound is especially valuable in research involving substitution, oxidation, and C-H bond activation due to its unique reactivity and stability under controlled conditions. Its ability to mediate these reactions makes it a key component in modern catalytic studies.\u003c\/p\u003e\n\u003cp\u003eThe compound is preferred for its strong catalytic properties and its ability to interact with a wide range of organic substrates. Its stability in specific conditions, combined with its sensitivity to moisture and oxygen, makes it a versatile yet carefully handled material. The solid form of the compound allows for easy handling and storage, while its reactivity ensures it remains effective in catalytic applications. These properties make it a reliable choice for researchers seeking high-efficiency catalytic solutions.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in catalytic research for both academic and industrial applications. It is a popular choice among research institutions aiming to develop environmentally friendly and efficient catalytic technologies. Its role in advancing chemical processes has made it a sought-after material in the field of catalysis within Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eC-H Activation Reactions: This compound is ideal for C-H activation due to its ability to mediate complex organic transformations efficiently.\u003c\/li\u003e\n\u003cli\u003eOrganic Substitution Reactions: Its chiral structure and catalytic properties make it suitable for promoting substitution reactions in organic chemistry.\u003c\/li\u003e\n\u003cli\u003eOxidation Processes: The compound facilitates oxidation reactions by acting as a catalyst, enhancing reaction efficiency and selectivity.\u003c\/li\u003e\n\u003cli\u003eIndustrial Catalytic Processes: Its stability and reactivity make it a preferred choice for industrial applications requiring high-performance catalysts.\u003c\/li\u003e\n\u003cli\u003eEnvironmental Catalytic Research: It is used in developing green and sustainable catalytic technologies, supporting eco-friendly chemical processes.\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: 12148-71-9\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Catalysis and Inorganic Chemistry \u0026gt; C-H Activation [Catalysis]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified in the provided data\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Should be stored in a dry, inert atmosphere to prevent degradation\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a dry, cool environment away from moisture and oxygen to maintain its stability and catalytic activity. It is recommended to use airtight containers made of inert materials such as glass or stainless steel to prevent exposure to air and humidity. Due to its sensitivity, it should be handled in a controlled laboratory setting with appropriate safety measures in place. Researchers should ensure that the compound is kept in a secure location to avoid accidental exposure or contamination. Proper labeling and storage conditions are essential to preserve its effectiveness and ensure safe usage in laboratory environments.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48086179971290,"sku":"TCI2510C266217500","price":2138000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48086180004058,"sku":"TCI2510C266217501","price":7252000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2662.jpg?v=1767098614"},{"product_id":"tci2510c270917560","title":"TCI C2709 152120-62-2 N-(Carbobenzoxy)-1H-pyrazole-1-carboxamidine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eN-(Carbobenzoxy)-1H-pyrazole-1-carboxamidine is a chemical compound widely used in organic synthesis reactions, particularly in the formation of heterocyclic compounds. This material plays a crucial role in laboratory settings where researchers aim to develop complex molecular structures. Its unique chemical structure enables it to participate in various substitution and reaction mechanisms under controlled conditions. As a versatile building block, it supports the creation of compounds with potential applications in pharmaceutical and medicinal chemistry.\u003c\/p\u003e\n\u003cp\u003eThe compound’s chemical stability under specific conditions, combined with its reactivity towards acids, bases, and organic solvents, makes it a preferred choice for synthetic chemists. Its ability to undergo substitution reactions and its compatibility with a range of reagents contribute to its utility in advanced synthetic pathways. The structural complexity of N-(Carbobenzoxy)-1H-pyrazole-1-carboxamidine also allows for the design of molecules with tailored biological activities, making it a key component in drug discovery and development.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is frequently used by chemists and pharmacologists to synthesize new compounds with potential medical or industrial applications. Its availability in solid form and its reactivity in substitution reactions make it a valuable resource for researchers working on complex molecular synthesis projects. The compound is essential for advancing chemical research and innovation in both academic and industrial settings.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis for creating heterocyclic compounds due to its reactive functional groups and structural versatility.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research for developing compounds with biological activity, as it can be modified to target specific molecular interactions.\u003c\/li\u003e\n\u003cli\u003eMedicinal chemistry applications where the compound serves as a building block for drug molecule design and optimization.\u003c\/li\u003e\n\u003cli\u003eAcademic research in chemistry departments focusing on synthetic methodologies and reaction mechanisms.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical development for producing specialized compounds used in various sectors such as agriculture and materials science.\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: 152120-62-2\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\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to use airtight containers to prevent exposure to moisture and contaminants. Due to its reactivity with acids and bases, it should be handled with appropriate personal protective equipment. Storage conditions should avoid direct sunlight and high humidity to prevent degradation. Laboratory personnel should ensure proper ventilation when working with this compound to minimize any potential hazards. Regular monitoring of storage conditions is advised to maintain the integrity of the material during long-term use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086192783578,"sku":"TCI2510C270917560","price":873000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086192816346,"sku":"TCI2510C270917561","price":2559000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2709.jpg?v=1767098672"},{"product_id":"tci2510c332618356","title":"TCI C3326 1620086-77-2 5-Chlorosaligenyl-N,N-diisopropylphosphoramidite","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e5-Chlorosaligenyl-N,N-diisopropylphosphoramidite is a chemical compound widely used in chemical biology, particularly in nucleic acid chemistry. It serves as a key precursor in the synthesis of phosphoramidite nucleotides, which are essential components in the production of oligonucleotides. This compound plays a crucial role in molecular biology laboratories where the construction of DNA or RNA strands is required for various experimental applications. Its chemical structure enables specific reactions under controlled conditions, making it a versatile tool in modern biochemical research.\u003c\/p\u003e\n\u003cp\u003eThe compound is valued for its reactivity and stability under specific conditions. Its ability to selectively bind to nucleotide bases ensures accuracy and precision in nucleic acid synthesis. This makes it particularly suitable for applications requiring high fidelity, such as DNA sequencing or probe design. The compound’s stability also allows for reliable performance in laboratory settings, contributing to the reproducibility of experimental results. These properties make it a preferred choice for researchers working in nucleic acid chemistry.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 5-Chlorosaligenyl-N,N-diisopropylphosphoramidite is commonly used by researchers in universities, research centers, and biotechnology labs. It supports studies in genetics, biomedicine, and chemical biology, which are rapidly growing fields in Indonesia. Its application is essential for advancing research in molecular biology and related disciplines, providing a foundation for innovative scientific discoveries.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eDNA sequencing relies on this compound to synthesize oligonucleotide probes with high specificity and accuracy.\u003c\/li\u003e\n\u003cli\u003eOligonucleotide synthesis benefits from its reactivity, enabling the precise construction of DNA and RNA strands.\u003c\/li\u003e\n\u003cli\u003ePCR experiments use this compound to create primers that ensure accurate amplification of target DNA sequences.\u003c\/li\u003e\n\u003cli\u003eProbe design in molecular biology requires its selective binding properties to generate reliable hybridization results.\u003c\/li\u003e\n\u003cli\u003eGenetic research utilizes this compound to develop custom nucleic acid sequences for functional and structural studies.\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: 1620086-77-2\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Nucleic Acid Chemistry\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified\u003c\/li\u003e\n\u003cli\u003ePhysical form: Not specified\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light\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 to maintain its stability and reactivity. It is recommended to use airtight containers to prevent exposure to moisture and air, which could affect its chemical integrity. Due to its chemical nature, it should be handled in a well-ventilated area, and appropriate personal protective equipment such as gloves and safety goggles should be worn. Avoid contact with skin and eyes, and ensure that spill containment measures are in place. Proper disposal should follow local regulations to ensure safety and environmental compliance.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48086233317594,"sku":"TCI2510C332618356","price":2531000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48086233350362,"sku":"TCI2510C332618357","price":8910000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3326.jpg?v=1771057910"},{"product_id":"tci2510d068620257","title":"TCI D0686 137-18-8 p-Xyloquinone","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003ep-Xyloquinone is a chemical compound widely used in laboratory settings for the synthesis of complex molecules. As a building block in organic chemistry, it plays a crucial role in the development of heterocyclic compounds and other specialized chemical structures. Its unique reactivity and stability make it a valuable tool for chemists working on a variety of synthetic pathways. This compound is commonly found in pharmaceutical and chemical industries, where it serves as a key intermediate in the production of drugs and industrial chemicals.\u003c\/p\u003e\n\u003cp\u003eThe chemical and physical properties of p-Xyloquinone contribute to its popularity among researchers. It possesses a stable aromatic structure and exhibits high reactivity, making it suitable for substitution and oxidation reactions. These characteristics allow it to be used in a wide range of experimental applications, from basic research to advanced chemical synthesis. Its consistent performance and high purity ensure reliable results in laboratory experiments, making it a preferred choice for scientists seeking precision and reproducibility.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, p-Xyloquinone is frequently used in organic chemistry research, particularly in academic institutions and research organizations. It is an essential component in the synthesis of various compounds with specific structural requirements. Due to its availability and reliability, it is commonly selected for experiments that require high accuracy and consistency. Its role in chemical synthesis supports the development of new compounds with potential applications in medicine and industry.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis applications benefit from p-Xyloquinone due to its reactivity and ability to form complex molecular structures.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research utilizes this compound as a building block for the synthesis of drug molecules and active pharmaceutical ingredients.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical production relies on p-Xyloquinone for the creation of specialized compounds used in various commercial applications.\u003c\/li\u003e\n\u003cli\u003eAcademic research in chemistry uses p-Xyloquinone to explore new synthetic pathways and molecular structures.\u003c\/li\u003e\n\u003cli\u003eAnalytical chemistry experiments incorporate p-Xyloquinone to test reaction mechanisms and chemical behavior under different conditions.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 137-18-8\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various sizes as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003ep-Xyloquinone should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep the compound in a sealed container to prevent exposure to moisture and air. Suitable storage containers include glass or high-density polyethylene vessels that are resistant to chemical reactions. Due to its reactivity, it is important to handle p-Xyloquinone with care, using appropriate personal protective equipment such as gloves and safety goggles. Avoid direct contact with skin and eyes, and ensure proper ventilation in the laboratory when working with this compound. Regular monitoring of storage conditions will help ensure the compound remains in optimal condition for use in experiments.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086400172250,"sku":"TCI2510D068620257","price":816000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086400205018,"sku":"TCI2510D068620258","price":2503000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086400237786,"sku":"TCI2510D068620259","price":9501000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D0686.jpg?v=1767101773"},{"product_id":"tci2510d072020315","title":"TCI D0720 110-70-3 N,N'-Dimethylethylenediamine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eN,N’-Dimethylethylenediamine (DMEDA), with the CAS number 110-70-3, is a versatile chemical compound widely used in laboratory settings for its reactivity and functional properties. As a building block in organic synthesis, DMEDA plays a crucial role in the development of complex molecules, including pharmaceuticals, industrial chemicals, and food additives. Its unique structure, featuring two amine groups connected by an ethylene chain, allows it to participate in various chemical reactions, making it a valuable tool for chemists. Due to its ability to act as a strong base and electron donor, DMEDA is frequently employed in reactions requiring pH control or bond cleavage.\u003c\/p\u003e\n\u003cp\u003eDMEDA is particularly favored for its strong basicity and reactivity towards electrophilic and reactive species. These characteristics make it an ideal choice for applications such as condensation, reduction, and the formation of new chemical bonds. Its high boiling point also allows for its use in reactions that require elevated temperatures without significant evaporation. The compound’s stability and reactivity ensure that it remains a preferred reagent in many synthetic pathways, especially in the production of pharmaceutical intermediates and specialty chemicals.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, DMEDA is commonly used in the synthesis of organic compounds, particularly in the pharmaceutical and chemical industries. It is a key component in the development of new drugs and industrial materials. Its availability through suppliers like AMI Scientific ensures that researchers have access to this essential building block for their experiments and production processes. The compound’s reliability and effectiveness make it a staple in both academic and industrial research settings in Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis is a primary application where DMEDA is used to build complex molecules due to its reactivity and ability to act as a nucleophile.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research benefits from DMEDA’s role in the synthesis of drug intermediates, where its basicity and reactivity aid in forming key molecular structures.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical production relies on DMEDA for the creation of specialty chemicals, as its stability and reactivity support efficient synthetic pathways.\u003c\/li\u003e\n\u003cli\u003eFood additive development uses DMEDA in the formulation of flavor compounds and preservatives, leveraging its chemical versatility and safety profile.\u003c\/li\u003e\n\u003cli\u003eAnalytical chemistry applications benefit from DMEDA’s use in pH control and as a reagent in various spectroscopic and chromatographic 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: 110-70-3\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 supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Liquid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct sunlight and incompatible materials\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eDMEDA should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to use airtight containers made of materials compatible with its chemical properties, such as glass or high-density polyethylene. Due to its strong basicity and reactivity, it should be kept separate from acids, oxidizing agents, and other reactive substances. Proper ventilation is essential during handling to minimize exposure to vapors. Always wear appropriate personal protective equipment, including gloves, goggles, and a lab coat, when working with DMEDA to ensure safety in the laboratory environment.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5mL","offer_id":48086402334938,"sku":"TCI2510D072020315","price":1322000.0,"currency_code":"IDR","in_stock":true},{"title":"25mL","offer_id":48086402367706,"sku":"TCI2510D072020316","price":3993000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D0720.jpg?v=1767101862"},{"product_id":"tci2510d105920766","title":"TCI D1059 2524-64-3 Diphenyl Chlorophosphate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eDiphenyl Chlorophosphate is a chemical compound widely used as a building block in organic synthesis. It serves as a versatile reagent that enables substitution reactions and other chemical transformations under various laboratory conditions. This compound is particularly valuable for its ability to participate in the formation of ester and phosphate bonds, making it essential in the development of complex molecular structures. Its role in organic chemistry is critical, especially in research settings where precise control over chemical reactions is required.\u003c\/p\u003e\n\u003cp\u003eThe chemical properties of Diphenyl Chlorophosphate make it a preferred choice for laboratory applications. It exhibits stability under certain conditions but is highly reactive towards water and other polar substances. This reactivity necessitates careful handling and storage to maintain its integrity. Its ability to engage in multiple types of chemical reactions also makes it a valuable tool for chemists seeking to explore diverse synthetic pathways. The compound’s reactivity and versatility contribute to its widespread use in both academic and industrial research.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Diphenyl Chlorophosphate is commonly used in organic chemistry research, particularly in universities and research institutions focused on the synthesis of new compounds. Its application is prevalent in projects involving esterification, phosphate ester formation, and other synthetic processes. The compound’s utility in creating complex molecules has made it an essential component of many chemical research programs in Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic Synthesis: Diphenyl Chlorophosphate is widely used in the synthesis of esters and phosphate esters due to its reactivity and versatility in forming complex molecular structures.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical Research: It is a key reagent in the development of new pharmaceutical compounds, particularly in the formation of phosphate ester linkages.\u003c\/li\u003e\n\u003cli\u003eAcademic Research: Universities and research institutions use it extensively in teaching and research to demonstrate chemical reactivity and synthetic techniques.\u003c\/li\u003e\n\u003cli\u003eIndustrial Chemistry: It is employed in industrial settings for the production of various chemical intermediates and specialty compounds.\u003c\/li\u003e\n\u003cli\u003eAnalytical Chemistry: It serves as a standard reagent for testing and characterizing other chemical compounds in analytical laboratories.\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: 2524-64-3\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 supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid or liquid, depending on the specific product variant\u003c\/li\u003e\n\u003cli\u003eStorage note: Requires storage in a cool, dry place away from moisture and incompatible substances\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eDiphenyl Chlorophosphate should be stored in a cool, dry environment to prevent degradation. It is essential to keep the compound away from moisture and polar solvents to maintain its chemical integrity. Suitable containers should be sealed and made of materials that do not react with the compound, such as glass or inert polymer. Due to its reactivity, it is recommended to handle the material with appropriate personal protective equipment, including gloves and safety goggles. Proper ventilation should be maintained in the laboratory to minimize exposure. Regular monitoring of storage conditions is necessary to ensure the compound remains stable and safe for use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086420521178,"sku":"TCI2510D105920766","price":732000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48086420553946,"sku":"TCI2510D105920767","price":1913000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48086420586714,"sku":"TCI2510D105920768","price":5144000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D1059.jpg?v=1767102466"},{"product_id":"tci2510d129421008","title":"TCI D1294 1188-33-6 N,N-Dimethylformamide Diethyl Acetal [for Esterification]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D1294 N,N-Dimethylformamide Diethyl Acetal [for Esterification] is an organic synthesis reagent from the formamide acetal family, formulated specifically for esterification work. The reagent supplies an ethyl group, allowing carboxylic acids to be converted into their corresponding ethyl esters without a strong acid catalyst and without prolonged reflux in an excess of alcohol. As a non-heterocyclic building block, it holds an important position in both synthesis and analytical laboratories, because it shortens the working sequence and reduces the risk of damaging other sensitive functional groups present on the target molecule.\u003c\/p\u003e\n\u003cp\u003eThe principal advantage of this reagent lies in its mild, essentially neutral reaction conditions. Substrates carrying acid-labile groups, additional ester linkages, or stereogenic centres can therefore be processed with a lower risk of racemisation and decomposition than would be expected under classical acid-catalysed esterification. Beyond esterification, the formamide acetal framework is also able to react with active methylene compounds to form enaminone derivatives, although the product's primary intended use is genuinely directed towards esterification reactions. It is supplied as a moisture-sensitive liquid, so the best results are obtained only when the reagent is handled and stored correctly.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent is typically used in university and institutional research groups working on organic synthesis, in medicinal and natural-product chemistry projects where sensitive intermediates must be esterified, and in analytical laboratories that prepare ester derivatives prior to instrumental measurement. Because it removes the need for strongly acidic conditions and extended reflux, it fits well into routine bench workflows where sample quantities are limited and functional-group integrity has to be preserved.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eEthyl ester preparation from carboxylic acids: supplies the ethyl group directly, so conversion proceeds without a strong acid catalyst or a large excess of ethanol under prolonged reflux.\u003c\/li\u003e\n\u003cli\u003eEsterification of acid-sensitive substrates: the mild, nearly neutral conditions allow molecules bearing acid-labile protecting groups or additional ester linkages to be converted with reduced decomposition.\u003c\/li\u003e\n\u003cli\u003eDerivatisation of stereogenic compounds: because harsh acidic media are avoided, substrates containing stereogenic centres can be esterified with a lower risk of racemisation during the reaction.\u003c\/li\u003e\n\u003cli\u003eEnaminone synthesis from active methylene compounds: the formamide acetal framework reacts with active methylene substrates to build enaminone derivatives useful as intermediates in further synthetic sequences.\u003c\/li\u003e\n\u003cli\u003eSample derivatisation in analytical laboratories: forming ester derivatives shortens the preparation sequence and helps preserve other sensitive functional groups on the analyte before instrumental analysis.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 1188-33-6\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003eProduct designation: D1294, N,N-Dimethylformamide Diethyl Acetal [for Esterification]\u003c\/li\u003e\n\u003cli\u003ePhysical form: liquid, moisture sensitive\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in the pack sizes offered for this catalogue item\u003c\/li\u003e\n\u003cli\u003eStorage: keep tightly closed and protected from moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eBecause this reagent is a moisture-sensitive liquid, it should be stored in a tightly closed original container and protected from atmospheric humidity; best results are obtained only when the reagent is kept dry. Store in a cool, well-ventilated area away from heat, ignition sources, and incompatible materials, and keep the container closed when not in use. Dispense in a fume hood using dry glassware and dry syringes or cannulas, and minimise the time the container remains open. Wear safety glasses, chemical-resistant gloves, and a laboratory coat while handling. Return the container to storage promptly after use and follow the manufacturer's safety data sheet together with local laboratory waste-disposal procedures.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5mL","offer_id":48086433038554,"sku":"TCI2510D129421008","price":1125000.0,"currency_code":"IDR","in_stock":true},{"title":"25mL","offer_id":48086433071322,"sku":"TCI2510D129421009","price":3149000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D1294.jpg?v=1767102837"},{"product_id":"tci2510d130121014","title":"TCI D1301 6006-65-1 N,N-Dimethylformamide Dipropyl Acetal [for Esterification]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D1301 N,N-Dimethylformamide Dipropyl Acetal [for Esterification] is a member of the formamide acetal family carrying two propoxy groups, prepared specifically for esterification reactions in both synthesis and analytical laboratories. The reagent allows carboxylic acids to be converted directly into their propyl esters without a strong acid catalyst and without the need to add excess alcohol under prolonged reflux conditions. As a non-heterocyclic building block, it complements the dimethyl and diethyl variants within the same family of reagents, giving researchers a choice of ester alkyl group according to the demands of a particular analysis or synthetic target.\u003c\/p\u003e\n\u003cp\u003eThe distinguishing feature of this reagent lies in its propyl chain, which is longer than either the methyl or ethyl equivalent, producing ester derivatives with different polarity and different retention behaviour in chromatographic analysis. This difference is especially valuable when the peak of a methyl or ethyl derivative overlaps with components of the sample matrix, since the analyst can select propyl derivatisation instead to obtain better separation. The reaction conditions are mild and close to neutral, which preserves the integrity of other functional groups present in the molecule and reduces the risk of unwanted side reactions during derivatisation.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, reagents of this type are used in university synthesis groups, government research institutes, and analytical service laboratories that prepare samples for chromatographic determination. Because it works under gentle, near-neutral conditions and avoids the handling of strong acid catalysts, it fits well into routine sample-preparation workflows where a straightforward and reproducible derivatisation step is required before instrumental measurement, and where the choice of alkyl group must be adapted to the sample matrix at hand.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eDirect esterification of carboxylic acids: converts the acid group into the corresponding propyl ester in a single step, without a strong acid catalyst or a large excess of alcohol under long reflux.\u003c\/li\u003e\n\u003cli\u003eDerivatisation for chromatographic analysis: forms propyl ester derivatives with polarity and retention characteristics that differ from methyl and ethyl analogues, giving analysts an alternative when peaks overlap.\u003c\/li\u003e\n\u003cli\u003eResolution of matrix interference problems: when methyl or ethyl derivative peaks coincide with sample matrix components, switching to propyl derivatisation shifts retention and delivers better chromatographic separation.\u003c\/li\u003e\n\u003cli\u003eSynthesis of propyl esters on substrates with sensitive functionality: the mild, near-neutral reaction conditions preserve other functional groups on the molecule that acidic esterification methods could damage.\u003c\/li\u003e\n\u003cli\u003eBuilding block work in non-heterocyclic organic synthesis: serves alongside the dimethyl and diethyl acetal variants so researchers can select the ester alkyl group that matches their synthetic target.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 6006-65-1\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003eProduct code: D1301\u003c\/li\u003e\n\u003cli\u003eApplication grade: supplied as a reagent designated for esterification\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in the packaging options offered by the manufacturer for this catalogue item\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the reagent in its original tightly closed container, protected from moisture, in a cool and well-ventilated area away from direct sunlight and sources of ignition. Acetal reagents of this type are moisture-sensitive, so containers should be resealed promptly after use and, where practical, handled under a dry inert atmosphere. Dispense and transfer the material inside a fume hood using clean, dry glassware and dry syringes or cannulas. Laboratory personnel should wear safety goggles, chemical-resistant gloves, and a laboratory coat, and should avoid inhaling vapours or allowing contact with skin and eyes. Keep the reagent separate from strong acids and strong oxidising agents, and consult the manufacturer's safety data sheet before use and before disposal of residues.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5mL","offer_id":48086433267930,"sku":"TCI2510D130121014","price":1097000.0,"currency_code":"IDR","in_stock":true},{"title":"25mL","offer_id":48086433300698,"sku":"TCI2510D130121015","price":3149000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D1301.jpg?v=1767102850"},{"product_id":"tci2510d130221016","title":"TCI D1302 18503-90-7 N,N-Dimethylformamide Dibutyl Acetal [for Esterification]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eN,N-Dimethylformamide Dibutyl Acetal (DMFDBA), with CAS number 18503-90-7, is a chemical compound widely utilized in laboratory settings for esterification reactions. As a key building block in organic synthesis, it plays a vital role in the formation of esters from carboxylic acids. Its stability and reactivity make it a versatile reagent for creating complex molecular structures. This compound is particularly favored for its ability to participate in both esterification and other organic transformations, making it an essential component in synthetic chemistry workflows.\u003c\/p\u003e\n\u003cp\u003eDMFDBA is known for its excellent solubility in organic solvents, which facilitates mixing and reaction processes in laboratory experiments. Its chemical properties allow it to react efficiently with a variety of acids and alcohols, enhancing its utility in esterification reactions. The compound’s stability under various reaction conditions ensures consistent results, making it a reliable choice for researchers. Additionally, its dual role as both a reagent and a solvent increases its flexibility in different experimental setups, contributing to its widespread use in chemical laboratories.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, DMFDBA is commonly used in organic chemistry research, compound development, and industrial chemical production. It supports academic institutions and research centers in advancing chemical knowledge and innovation. Its availability and effectiveness make it a standard material in both educational and industrial chemical applications within the country.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis for esterification reactions due to its reactivity with carboxylic acids and alcohols.\u003c\/li\u003e\n\u003cli\u003eDevelopment of new chemical compounds in research laboratories requiring reliable reagents for complex molecular structures.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical production where DMFDBA is used as a building block for ester formation processes.\u003c\/li\u003e\n\u003cli\u003eEducational institutions for teaching and conducting experiments in organic chemistry courses.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research for the synthesis of ester-based compounds used in drug development.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 18503-90-7\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory supply formats\u003c\/li\u003e\n\u003cli\u003ePhysical form: Liquid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct sunlight and incompatible materials\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eDMFDBA should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to keep it in a tightly sealed container to prevent evaporation and contamination. Due to its chemical nature, it should be stored separately from strong oxidizing agents and acids to avoid potential reactions. Proper ventilation is essential when handling this compound to minimize inhalation risks. Laboratory personnel should wear appropriate personal protective equipment, such as gloves and safety goggles, when working with DMFDBA to ensure safe handling and reduce exposure risks. Regular monitoring of storage conditions is advised to maintain the compound's integrity and ensure compliance with safety standards.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5mL","offer_id":48086433333466,"sku":"TCI2510D130221016","price":1462000.0,"currency_code":"IDR","in_stock":true},{"title":"25mL","offer_id":48086433366234,"sku":"TCI2510D130221017","price":4582000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D1302.jpg?v=1767102854"},{"product_id":"tci2510d130321018","title":"TCI D1303 36805-97-7 N,N-Dimethylformamide Di-tert-butyl Acetal [for Esterification]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eN,N-Dimethylformamide Di-tert-butyl Acetal is a chemical compound widely used in laboratory settings for its role in esterification reactions. As a key building block in organic synthesis, it enables the formation of esters through efficient and controlled chemical processes. This compound is particularly valued for its ability to react with various carboxylic acids, making it a versatile reagent in synthetic chemistry. Its stability and reactivity make it a reliable choice for researchers working on complex molecular structures.\u003c\/p\u003e\n\u003cp\u003eThe compound's chemical properties, including its stability and reactivity, make it a preferred choice for laboratory applications. It is known for its ability to undergo esterification efficiently, which is crucial in the synthesis of ester compounds with diverse industrial and pharmaceutical applications. Its non-heterocyclic nature allows it to be used in a wide range of chemical reactions without interfering with other functional groups. This makes it a go-to material for chemists seeking reliable and consistent results.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, N,N-Dimethylformamide Di-tert-butyl Acetal is commonly used in organic chemistry research. It is a staple in both academic and industrial settings, where its reliability and efficiency are highly appreciated. Its availability in liquid form and ease of use further contribute to its popularity among researchers. Its non-volatile nature also ensures safety during handling and storage, making it a trusted reagent in controlled laboratory environments.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis for esterification reactions due to its efficient and stable chemical properties.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research for the development of ester-based compounds with therapeutic applications.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemistry applications where ester compounds are required for product formulation.\u003c\/li\u003e\n\u003cli\u003eAcademic research in chemical laboratories for teaching and experimental purposes.\u003c\/li\u003e\n\u003cli\u003ePolymer science for the synthesis of ester-functionalized polymers with specific properties.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 36805-97-7\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities\u003c\/li\u003e\n\u003cli\u003ePhysical form: Liquid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry place away from direct sunlight to maintain its stability and reactivity. It is recommended to use airtight containers to prevent exposure to moisture and air, which could affect its performance. Due to its chemical nature, it should be handled in a well-ventilated area, and appropriate personal protective equipment should be worn. While it is relatively stable under normal storage conditions, it should not be exposed to extreme temperatures or incompatible substances. Proper labeling and safe storage practices are essential to ensure the safety of laboratory personnel and the integrity of the compound.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5mL","offer_id":48086433431770,"sku":"TCI2510D130321018","price":4077000.0,"currency_code":"IDR","in_stock":true},{"title":"25mL","offer_id":48086433464538,"sku":"TCI2510D130321019","price":14194000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D1303.jpg?v=1767102858"},{"product_id":"tci2510d133221062","title":"TCI D1332 4637-24-5 N,N-Dimethylformamide Dimethyl Acetal [for Esterification] (0.5mL*10)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D1332 N,N-Dimethylformamide Dimethyl Acetal [for Esterification] is a methylating reagent supplied in a specially prepared format of ten glass ampoules, each containing 0.5 mL. Widely known by the abbreviation DMF-DMA, this reagent converts carboxylic acids into their corresponding methyl esters quickly and cleanly, without requiring a strong acid catalyst or an excess of solvent. In the laboratory it plays an essential role during sample preparation prior to gas chromatographic analysis, because free carboxylic acids tend to produce broadened, asymmetric peaks on the column.\u003c\/p\u003e\n\u003cp\u003eThe qualities that make analysts choose this reagent lie in its single-dose ampoule packaging and the purity maintained specifically for esterification work. Each ampoule holds a pre-measured quantity, so the analyst does not need to open a large bulk container repeatedly, and the risk of quality deterioration through contact with atmospheric moisture is kept to a minimum. The methylation reaction proceeds at moderate temperature within a short time and generates volatile by-products, which therefore do not interfere with chromatographic injection.\u003c\/p\u003e\n\u003cp\u003eBeyond esterification, DMF-DMA is also widely used as an enaminone-forming reagent and as a one-carbon unit source in synthetic chemistry. In Indonesian laboratories this combination of roles suits analytical services, university research groups, and quality control units that prepare acidic samples for gas chromatography while also running small-scale building block synthesis. The ten-ampoule set allows a single delivery to cover several separate work sessions.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMethyl ester preparation from carboxylic acids: the reagent performs the conversion rapidly and cleanly without a strong acid catalyst or excess solvent, simplifying the workflow.\u003c\/li\u003e\n\u003cli\u003eSample derivatisation before gas chromatography: free carboxylic acids give broad, asymmetric peaks, so converting them to methyl esters improves peak shape on the column.\u003c\/li\u003e\n\u003cli\u003eRoutine analytical sample preparation: each pre-measured ampoule removes the need to repeatedly open a bulk container, which keeps handling consistent between analytical batches.\u003c\/li\u003e\n\u003cli\u003eEnaminone formation in synthetic chemistry: DMF-DMA is widely employed as an enaminone-forming reagent, making this pack useful for building block work beyond esterification.\u003c\/li\u003e\n\u003cli\u003eOne-carbon unit introduction: the reagent serves as a source of a single carbon unit, supporting synthetic routes that require this fragment in non-heterocyclic building block chemistry.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 4637-24-5\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack size: 0.5 mL × 10 ampoules per set\u003c\/li\u003e\n\u003cli\u003eGrade note: supplied as a reagent for esterification\u003c\/li\u003e\n\u003cli\u003eStorage: keep ampoules sealed and protected from moisture until use\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the ampoules in their original packaging in a cool, dry place away from direct sunlight and sources of heat, keeping each unit sealed until the moment of use so that contact with atmospheric moisture is avoided. Because the material is sensitive to water vapour, the single-dose ampoule format should be used as intended: open one ampoule per working session rather than transferring the contents into a larger shared container. Handle the reagent in a fume hood with appropriate gloves, safety glasses, and a laboratory coat, and open glass ampoules carefully to avoid cuts. Prepare and transfer the reagent using clean, dry glassware, and dispose of residues and empty ampoules through the laboratory's chemical waste procedure.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1set","offer_id":48086435168474,"sku":"TCI2510D133221062","price":2194000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D1332.jpg?v=1767102920"},{"product_id":"tci2510d159521401","title":"TCI D1595 4909-78-8 N,N-Dimethylformamide Dineopentyl Acetal [for Esterification]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eN,N-Dimethylformamide Dineopentyl Acetal (DMF-DIPA) is a chemical compound widely used in laboratory settings for its role in esterification reactions. As a key reagent, it serves as a versatile source of ester groups that can react with various substrates to form new organic compounds. This compound is particularly valuable in synthetic chemistry due to its ability to act both as a solvent and a reactive component, streamlining the synthesis process without the need for additional reagents. Its application spans multiple areas of organic chemistry, making it an essential material for researchers and chemists working in both academic and industrial environments.\u003c\/p\u003e\n\u003cp\u003eDMF-DIPA is preferred for its chemical stability under controlled conditions and its reactivity in a wide range of chemical environments. It possesses a high boiling point, which allows it to be used in reactions requiring elevated temperatures. Its ability to participate in esterification reactions makes it a reliable choice for producing ester derivatives. Additionally, its dual functionality as a solvent and reagent enhances its utility in complex synthesis pathways. These properties make DMF-DIPA a go-to compound in Indonesian laboratories where efficiency and reliability are paramount.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, DMF-DIPA is commonly used in organic chemistry research, especially in the pharmaceutical and chemical industries. It plays a crucial role in the synthesis of complex organic molecules, contributing to the development of new drugs and materials. Its availability and effectiveness make it a staple in many research facilities across Indonesia, supporting both academic and industrial chemical innovation.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eEsterification Reactions: DMF-DIPA is ideal for esterification due to its ability to provide ester groups, facilitating the formation of ester derivatives in organic synthesis.\u003c\/li\u003e\n\u003cli\u003eOrganic Synthesis: It is widely used in the synthesis of complex organic compounds, acting as both a solvent and reactive component to enhance reaction efficiency.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical Research: Its role in producing ester derivatives makes it valuable in drug development and compound modification processes.\u003c\/li\u003e\n\u003cli\u003eIndustrial Chemistry: DMF-DIPA supports the production of various chemical products by enabling efficient and reliable esterification pathways.\u003c\/li\u003e\n\u003cli\u003eAnalytical Chemistry: It is used as a solvent in analytical procedures to dissolve and process organic compounds for further analysis.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 4909-78-8\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory supply\u003c\/li\u003e\n\u003cli\u003ePhysical form: Liquid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from heat and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eDMF-DIPA should be stored in a cool, dry environment, away from heat and direct sunlight to maintain its chemical stability. It is recommended to use sealed containers made of materials compatible with organic solvents, such as glass or high-density polyethylene. Due to its reactivity, it should be handled in a well-ventilated area, and appropriate personal protective equipment should be worn. Avoid exposure to oxygen and heat to prevent degradation. Proper storage ensures the compound remains effective for its intended applications in laboratory settings.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5mL","offer_id":48086449520858,"sku":"TCI2510D159521401","price":1210000.0,"currency_code":"IDR","in_stock":true},{"title":"25mL","offer_id":48086449553626,"sku":"TCI2510D159521402","price":3542000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D1595.jpg?v=1767103306"},{"product_id":"tci2510d207122115","title":"TCI D2071 4637-24-5 N,N-Dimethylformamide Dimethyl Acetal [for Esterification]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D2071 N,N-Dimethylformamide Dimethyl Acetal, commonly abbreviated as DMF-DMA, is a versatile liquid reagent prepared specifically for esterification work. In the laboratory it acts as a mild methylating agent that rapidly converts carboxylic acids into their methyl esters without requiring strong mineral acids or hazardous diazomethane. This role is particularly important during sample preparation prior to gas chromatographic analysis, because many organic acids are insufficiently volatile and are difficult to separate cleanly until they have been converted into their more readily analysed ester derivatives.\u003c\/p\u003e\n\u003cp\u003eThe properties that make this reagent a preferred choice are its selective reactivity and its comparatively gentle reaction conditions. The aminal acetal group in its structure readily releases methanol and forms a reactive intermediate species, so esterification can proceed under moderate heating with by-products that are easily evaporated away. DMF-DMA is also well known as an enaminone-forming reagent and as a one-carbon source for heterocyclic synthesis, including pyrazoles, pyrimidines, and isoxazoles, so a single bottle can support several different kinds of work at once.\u003c\/p\u003e\n\u003cp\u003eBecause it is supplied in liquid form, the reagent is straightforward to measure and to add directly to a reaction mixture or to a derivatisation vial. In Indonesian laboratories this suits routine analytical service work, teaching and research laboratories in organic synthesis, and quality control settings where organic acid content is determined by gas chromatography. Its dual usefulness in both derivatisation and synthetic chemistry makes it a practical item to keep on hand where a single reagent inventory has to serve mixed workloads.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMethyl ester derivatisation for gas chromatography — converts poorly volatile organic acids into methyl esters that elute and separate far more cleanly, improving peak shape and quantitation in routine GC analysis.\u003c\/li\u003e\n\u003cli\u003eMild esterification of carboxylic acids — provides a route to methyl esters without strong mineral acid catalysts or hazardous diazomethane, which simplifies both the procedure and the safety controls required.\u003c\/li\u003e\n\u003cli\u003eEnaminone formation in organic synthesis — reacts with activated methyl and methylene compounds to give enaminone intermediates that serve as flexible platforms for further ring-forming chemistry.\u003c\/li\u003e\n\u003cli\u003eHeterocyclic building block chemistry — acts as a one-carbon source in the construction of pyrazoles, pyrimidines, and isoxazoles, supporting medicinal and materials-oriented synthetic programmes.\u003c\/li\u003e\n\u003cli\u003eTeaching and research laboratory synthesis exercises — its moderate reaction conditions and easily evaporated by-products make reaction workup and product isolation more manageable for students and researchers alike.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 4637-24-5\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003eProduct code: D2071\u003c\/li\u003e\n\u003cli\u003ePhysical form: liquid reagent, specified for esterification use\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in the standard TCI catalogue pack sizes for this item; please confirm the required size when ordering\u003c\/li\u003e\n\u003cli\u003eStorage: keep tightly closed in a cool, dry, well-ventilated area away from moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the reagent in its original tightly closed container in a cool, dry, and well-ventilated chemical store, away from heat sources, ignition sources, and direct sunlight. Because the acetal group releases methanol on reaction, keep the container sealed against atmospheric moisture and reclose it promptly after each withdrawal; amber glass or the supplier's original glass packaging is appropriate. Handle and dispense in a fume hood, wearing safety glasses, chemically resistant gloves, and a laboratory coat. Use clean, dry glassware and dry syringes or pipettes when transferring, avoid contact with strong acids and oxidising agents, and consult the manufacturer's safety data sheet before first use and before disposal of residues.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mL","offer_id":48086491660506,"sku":"TCI2510D207122115","price":1969000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D2071.jpg?v=1767104141"},{"product_id":"tci2510d223422345","title":"TCI D2234 527-61-7 2,6-Dimethyl-1,4-benzoquinone","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2,6-Dimethyl-1,4-benzoquinone is a chemical compound widely used in laboratory settings for its versatility in organic synthesis. As a building block in chemical reactions, it plays a crucial role in the development of complex organic molecules. Its aromatic structure, featuring two methyl groups at positions 2 and 6, along with two keto groups at positions 1 and 4, makes it a valuable intermediate in various synthetic pathways. This compound is particularly useful in oxidation and reduction reactions due to its stable yet reactive nature. It is commonly found in both academic and industrial research environments, where its chemical properties support a wide range of experimental applications.\u003c\/p\u003e\n\u003cp\u003eThe compound’s chemical properties make it a preferred choice for laboratory use. It is non-colored, solid in form, and soluble in organic solvents, which simplifies its handling and integration into chemical processes. Its relatively high melting and boiling points allow for efficient thermal processing in laboratory settings. These physical characteristics contribute to its reliability in synthetic procedures, enabling consistent results. The compound’s stability under controlled conditions ensures that it remains effective for multiple applications without degrading prematurely.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 2,6-Dimethyl-1,4-benzoquinone is frequently used in organic chemistry research and pharmaceutical development. Its role in synthesizing compounds with pharmaceutical and industrial applications makes it an essential material for researchers. Many institutions and laboratories in Indonesia rely on this compound for its predictable performance and compatibility with various chemical processes.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis is a key application where 2,6-Dimethyl-1,4-benzoquinone is used for its ability to participate in oxidation and reduction reactions, making it ideal for creating complex organic molecules.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research benefits from this compound due to its role in the synthesis of various drug compounds, supporting the development of new therapeutic agents.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical processes often incorporate this material because of its stability and reactivity, allowing it to be used in the production of specialty chemicals and intermediates.\u003c\/li\u003e\n\u003cli\u003eAnalytical chemistry laboratories use it as a reference standard for identifying and quantifying compounds in various samples through spectroscopic and chromatographic methods.\u003c\/li\u003e\n\u003cli\u003ePolymer science research employs this compound in the development of new materials, leveraging its chemical structure to create polymers with specific functional properties.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 527-61-7\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory requirements\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct sunlight and incompatible materials\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its chemical integrity. It is recommended to use airtight containers to prevent exposure to moisture and air, which could affect its stability. Due to its chemical nature, it should be kept away from strong oxidizing or reducing agents to avoid unwanted reactions. Proper labeling of storage containers is essential for safety and identification. In laboratory settings, personal protective equipment such as gloves and goggles should be worn when handling this material to ensure safe usage. 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