{"title":"Chiral Resolving Reagents","description":"\u003cp\u003eChiral Resolving Reagents — reagen TCI untuk riset dan industri. Tersedia di Indonesia melalui AMI Scientific.\u003c\/p\u003e","products":[{"product_id":"tci2510c001213922","title":"TCI C0012 124-83-4 (+)-Camphoric Acid","description":"\u003ch3\u003eDeskripsi\u003c\/h3\u003e\n\u003cp\u003eTCI C0012 (+)-Camphoric Acid adalah asam dikarboksilat kiral yang diturunkan dari kerangka kamfor, terdaftar dengan nomor CAS 124-83-4. Kehadiran dua gugus karboksil pada rangka siklopentana yang tersubstitusi menjadikannya bahan yang menarik untuk membangun struktur kiral yang lebih kompleks. Senyawa ini termasuk dalam kelompok chiral building block yang banyak digunakan dalam sintesis asimetris.\u003c\/p\u003e\n\u003cp\u003eKarena bersifat optis aktif dan memiliki dua titik fungsionalisasi, camphoric acid sering dimanfaatkan sebagai agen resolusi untuk memisahkan basa rasemat melalui pembentukan garam diastereomerik. Selain itu, gugus karboksilnya dapat diubah menjadi ester, amida, atau anhidrida sebagai jalan masuk menuju ligan dan auksiliar kiral. Kerangka karbonnya yang kaku membantu menjaga pengaturan ruang yang konsisten pada produk turunannya.\u003c\/p\u003e\n\u003cp\u003eAMI Scientific menyediakan produk TCI ini dalam kemasan 25 g dan 100 g. Pilihan tersebut memudahkan laboratorium menyesuaikan pembelian dengan tahap penelitian, baik untuk eksplorasi awal maupun sintesis yang lebih rutin. Seluruh keterangan mutu merujuk pada dokumen resmi dari produsen.\u003c\/p\u003e\n\u003ch3\u003eAplikasi Laboratorium\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAgen resolusi kiral — membentuk garam diastereomerik dengan basa rasemat sehingga pemisahan enantiomer dapat dilakukan.\u003c\/li\u003e\n\u003cli\u003eSintesis ligan kiral — dua gugus karboksil memungkinkan pembentukan struktur pengkelat untuk katalisis logam.\u003c\/li\u003e\n\u003cli\u003ePrekursor auksiliar kiral — mudah dikonversi menjadi amida atau ester yang mengarahkan stereokimia reaksi.\u003c\/li\u003e\n\u003cli\u003eRiset material koordinasi — dapat berperan sebagai linker kiral pada pembentukan kompleks logam.\u003c\/li\u003e\n\u003cli\u003eStudi stereokimia dan karakterisasi optis — sifat optis aktifnya berguna sebagai pembanding pada analisis rotasi optik.\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: 124-83-4\u003c\/li\u003e\n\u003cli\u003eKategori: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Building Blocks\u003c\/li\u003e\n\u003cli\u003eVarian\/kemasan: 25 g dan 100 g\u003c\/li\u003e\n\u003cli\u003eBentuk fisik: padatan kristalin berwarna putih\u003c\/li\u003e\n\u003cli\u003eCatatan penyimpanan: simpan di tempat sejuk dan kering dalam wadah tertutup rapat, terlindung dari kelembapan\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003ePenanganan dan Penyimpanan\u003c\/h3\u003e\n\u003cp\u003eGunakan sarung tangan dan kacamata pengaman saat menimbang karena serbuk asam dapat mengiritasi kulit, mata, dan saluran pernapasan. Lakukan penimbangan di area berventilasi baik dan hindari pembentukan debu yang berlebihan. Simpan wadah dalam keadaan tertutup rapat serta terpisah dari basa kuat dan bahan pengoksidasi, sesuai anjuran pada Safety Data Sheet produsen.\u003c\/p\u003e\n\u003ch3\u003eEnglish\u003c\/h3\u003e\n\u003cp\u003eTCI C0012 (+)-Camphoric Acid, CAS 124-83-4, is an optically active dicarboxylic acid derived from the camphor skeleton. Its two carboxyl groups and rigid carbon framework make it a practical chiral building block for asymmetric synthesis. The compound is commonly employed as a resolving agent for racemic bases and as a precursor to chiral ligands, esters, and amides. AMI Scientific offers this TCI product in 25 g and 100 g pack sizes for flexible laboratory use.\u003c\/p\u003e\n\u003ch3\u003eReferensi Ilmiah\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBaur dkk. (2000). Quantitation and validation of cis-camphoric acid 3-methyl ester and cis-camphoric acid 1-methyl ester using CE. \u003cem\u003eJournal of Pharmaceutical and Biomedical Analysis\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/s0731-7085(99)00313-1\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/s0731-7085(99)00313-1\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eDmowski dkk. (1997). Selective fluorination of (1R,3S)-(+)-camphoric acid with sulphur tetrafluoride. Preparation of fluorinated optically active derivatives of 1,2,2-trimethylcyclopentane. \u003cem\u003eJournal of Fluorine Chemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/s0022-1139(97)00016-x\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/s0022-1139(97)00016-x\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eMoloney dkk. (1996). Chiral carboxylic acid ligands derived from camphoric acid. \u003cem\u003eTetrahedron: Asymmetry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/0957-4166(96)00328-x\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/0957-4166(96)00328-x\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":48085965865178,"sku":"TCI2510C001213922","price":1294000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48085965897946,"sku":"TCI2510C001213923","price":3654000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0012.jpg?v=1769144599"},{"product_id":"tci2510c001513929","title":"TCI C0015 3144-16-9 (+)-10-Camphorsulfonic Acid","description":"\u003ch3\u003eDeskripsi\u003c\/h3\u003e\n\u003cp\u003eTCI C0015 (+)-10-Camphorsulfonic Acid, dengan nomor CAS 3144-16-9, adalah asam sulfonat kiral yang sangat populer di laboratorium sintesis. Senyawa ini menggabungkan keasaman kuat dari gugus sulfonat dengan kerangka kamfor yang optis aktif, sehingga berperan ganda sebagai katalis asam sekaligus sumber kiralitas. Kombinasi tersebut membuatnya menjadi salah satu reagen chiral pool yang paling sering digunakan.\u003c\/p\u003e\n\u003cp\u003ePeran utamanya di banyak laboratorium adalah sebagai agen resolusi untuk memisahkan amina rasemat melalui pembentukan garam diastereomerik yang berbeda kelarutannya. Selain itu, senyawa ini kerap dipakai sebagai katalis asam Brønsted pada reaksi perlindungan dan pelepasan gugus fungsi, serta sebagai aditif dalam analisis kromatografi. Sifatnya yang berupa padatan mudah ditimbang menjadikannya lebih praktis dibanding asam kuat berbentuk cair.\u003c\/p\u003e\n\u003cp\u003eAMI Scientific menyediakan produk TCI ini dalam tiga pilihan kemasan, yaitu 25 g, 100 g, dan 500 g. Rentang tersebut mengakomodasi mulai dari penggunaan analitik berskala kecil hingga proses resolusi preparatif. Rincian mutu setiap lot dapat dirujuk pada dokumen resmi produsen.\u003c\/p\u003e\n\u003ch3\u003eAplikasi Laboratorium\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAgen resolusi amina rasemat — membentuk garam diastereomerik yang dapat dipisahkan melalui kristalisasi.\u003c\/li\u003e\n\u003cli\u003eKatalis asam Brønsted kiral — memberikan keasaman kuat sekaligus lingkungan kiral pada reaksi organik.\u003c\/li\u003e\n\u003cli\u003eKatalis proteksi dan deproteksi — efektif pada pembentukan atau pembukaan asetal dan ketal.\u003c\/li\u003e\n\u003cli\u003eAditif fase gerak kromatografi — digunakan sebagai reagen pasangan ion pada analisis senyawa basa.\u003c\/li\u003e\n\u003cli\u003eStandar kalibrasi circular dichroism — sifat optis aktifnya berguna dalam verifikasi kinerja instrumen CD.\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: 3144-16-9\u003c\/li\u003e\n\u003cli\u003eKategori: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Building Blocks\u003c\/li\u003e\n\u003cli\u003eVarian\/kemasan: 25 g, 100 g, dan 500 g\u003c\/li\u003e\n\u003cli\u003eBentuk fisik: padatan kristalin putih yang bersifat higroskopis\u003c\/li\u003e\n\u003cli\u003eCatatan penyimpanan: simpan rapat di tempat kering, hindari paparan udara lembap\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003ePenanganan dan Penyimpanan\u003c\/h3\u003e\n\u003cp\u003eSenyawa ini bersifat asam kuat dan korosif, sehingga penanganan wajib dilakukan menggunakan sarung tangan tahan bahan kimia, kacamata pelindung, dan jas laboratorium. Timbang dengan cepat karena sifatnya higroskopis, lalu segera tutup rapat wadah agar tidak menyerap uap air. Simpan terpisah dari basa kuat dan logam reaktif, dan selalu rujuk Safety Data Sheet resmi produsen sebelum digunakan.\u003c\/p\u003e\n\u003ch3\u003eEnglish\u003c\/h3\u003e\n\u003cp\u003eTCI C0015 (+)-10-Camphorsulfonic Acid, CAS 3144-16-9, is a strong, optically active sulfonic acid built on the camphor framework. It is widely used as a resolving agent for racemic amines, forming diastereomeric salts that can be separated by crystallisation. The compound also serves as a convenient solid Brønsted acid catalyst for protection and deprotection steps, and as an ion-pairing additive in chromatography. AMI Scientific offers this TCI product in 25 g, 100 g, and 500 g pack sizes; because it is hygroscopic, keep the container tightly closed.\u003c\/p\u003e\n\u003ch3\u003eReferensi Ilmiah\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eZhang dkk. (2002). Synthesis and characterization of self-assembled polyaniline nanotubes doped with D-10-camphorsulfonic acid. \u003cem\u003eNanotechnology\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1088\/0957-4484\/13\/6\/311\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1088\/0957-4484\/13\/6\/311\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eYan dkk. (1999). Thermoelectric Properties of Alternatively Layered Films of Polyaniline and (±)-10-Camphorsulfonic Acid-Doped Polyaniline. \u003cem\u003eChemistry Letters\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1246\/cl.1999.1217\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1246\/cl.1999.1217\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eZhai dkk. (2020). Anti-Corrosive Coating of Carbon-Steel Assisted by Polymer-Camphorsulfonic Acid Embedded within Graphene. \u003cem\u003eCoatings\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.3390\/coatings10090879\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.3390\/coatings10090879\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":48085966127322,"sku":"TCI2510C001513929","price":844000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48085966160090,"sku":"TCI2510C001513930","price":1969000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48085966192858,"sku":"TCI2510C001513931","price":4975000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0015.jpg?v=1767094558"},{"product_id":"tci2510c034714413","title":"TCI C0347 485-71-2 Cinchonidine","description":"\u003ch3\u003eDeskripsi\u003c\/h3\u003e\n\u003cp\u003eTCI C0347 Cinchonidine dengan nomor CAS 485-71-2 merupakan alkaloid cinchona yang telah lama menjadi andalan dalam kimia asimetris. Struktur molekulnya memadukan inti kuinolin, gugus kuinuklidin dengan nitrogen basa, serta gugus hidroksil sekunder pada pusat stereogenik. Kombinasi gugus fungsi tersebut memungkinkan cinchonidine berperan sebagai basa kiral sekaligus donor ikatan hidrogen.\u003c\/p\u003e\n\u003cp\u003eProduk ini masuk kategori Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Catalysts, Chiral Ligands, Chiral Reagents pada katalog TCI. Dalam praktiknya, cinchonidine digunakan sebagai organokatalis, modifier kiral pada katalis heterogen, maupun agen resolusi untuk memisahkan campuran rasemat asam karboksilat. Bersama pasangan pseudo-enantiomernya, senyawa ini memungkinkan peneliti mengakses kedua konfigurasi produk yang diinginkan.\u003c\/p\u003e\n\u003cp\u003eAMI Scientific menyediakan produk ini dalam kemasan 25 g dan 100 g untuk mendukung penelitian sintesis asimetris skala laboratorium hingga pengembangan proses. Ketersediaan dua ukuran memudahkan penyesuaian antara tahap penapisan kondisi reaksi dan tahap optimasi berulang. Spesifikasi lot yang berlaku dapat dirujuk pada dokumen mutu dari produsen.\u003c\/p\u003e\n\u003ch3\u003eAplikasi Laboratorium\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganokatalisis asimetris — berperan sebagai katalis basa kiral pada reaksi adisi dan siklisasi enansioselektif.\u003c\/li\u003e\n\u003cli\u003eResolusi rasemat — digunakan sebagai basa kiral untuk membentuk garam diastereomerik yang dapat dipisahkan.\u003c\/li\u003e\n\u003cli\u003eModifier kiral pada hidrogenasi heterogen — dipakai untuk mengarahkan selektivitas pada katalis logam pendukung.\u003c\/li\u003e\n\u003cli\u003eSintesis ligan kiral turunan cinchona — menjadi bahan awal pembuatan katalis transfer fasa dan ligan modifikasi.\u003c\/li\u003e\n\u003cli\u003eKajian mekanisme stereoselektivitas — dimanfaatkan sebagai model untuk menelaah interaksi katalis dan substrat.\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: 485-71-2\u003c\/li\u003e\n\u003cli\u003eKategori: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Catalysts, Chiral Ligands, Chiral Reagents\u003c\/li\u003e\n\u003cli\u003eVarian\/kemasan: 25 g dan 100 g\u003c\/li\u003e\n\u003cli\u003eBentuk fisik: serbuk\/padatan kristalin\u003c\/li\u003e\n\u003cli\u003eCatatan penyimpanan: simpan dalam wadah tertutup rapat di tempat sejuk, kering, dan terlindung cahaya sesuai anjuran produsen\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003ePenanganan dan Penyimpanan\u003c\/h3\u003e\n\u003cp\u003eGunakan sarung tangan dan pelindung mata, serta lakukan penimbangan di area berventilasi baik agar serbuk halus tidak terhirup. Sebagai senyawa alkaloid, bahan ini perlu diperlakukan dengan hati-hati dan dijauhkan dari jangkauan yang tidak berkepentingan. Simpan dalam wadah tertutup rapat, terlindung cahaya dan kelembapan, serta rujuk Safety Data Sheet dari produsen sebelum penanganan.\u003c\/p\u003e\n\u003ch3\u003eEnglish\u003c\/h3\u003e\n\u003cp\u003eTCI C0347 Cinchonidine, CAS 485-71-2, is a cinchona alkaloid that has long served as a workhorse reagent in asymmetric synthesis. Its quinoline ring, basic quinuclidine nitrogen, and secondary hydroxyl group at a stereogenic centre allow it to act simultaneously as a chiral base and a hydrogen-bond donor. It is applied as an organocatalyst, as a chiral modifier for heterogeneous hydrogenation catalysts, as a resolving agent for racemic acids, and as a starting material for cinchona-derived phase transfer catalysts and ligands. AMI Scientific offers this TCI product in 25 g and 100 g packs, with lot-specific data available from the manufacturer.\u003c\/p\u003e\n\u003ch3\u003eReferensi Ilmiah\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003e(2018). Synthesis of (+)-Cinchonidine. \u003cem\u003eSynfacts\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1055\/s-0037-1611233\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1055\/s-0037-1611233\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eBeresford (2004). Enantioselective Addition of Diethylzinc to N‐Diphenylphosphinoylimines Employing Cinchonidine and Cinchonine as Chiral Ligands.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.200446025\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.200446025\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eLindholm dkk. (2003). Hydrosilylation of Cinchonidine and 9‐O‐TMS‐Cinchonidine with Triethoxysilane: Application of 11‐(Triethoxysilyl)‐10,11‐dihydrocinchonidine as a Chiral Modifier in the Enantioselective Hydrogenation of 1‐Phenylpropane‐1,2‐dione.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.200318077\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.200318077\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":48085991456986,"sku":"TCI2510C034714413","price":2531000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48085991489754,"sku":"TCI2510C034714414","price":7562000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0347.jpg?v=1767095063"},{"product_id":"tci2510c035014417","title":"TCI C0350 118-10-5 Cinchonine","description":"\u003ch3\u003eDeskripsi\u003c\/h3\u003e\n\u003cp\u003eCinchonine dari TCI (kode katalog C0350) merupakan alkaloid cinchona alami yang menjadi salah satu katalis kiral paling klasik sekaligus paling andal di laboratorium sintesis asimetrik. Senyawa ini bersifat pseudo-enansiomer terhadap cinchonidine, sehingga pasangan keduanya kerap dipakai untuk mengarahkan reaksi ke konfigurasi stereokimia yang berlawanan tanpa perlu mengganti seluruh sistem katalitik. Karakter inilah yang membuat cinchonine menjadi bahan wajib pada rak laboratorium kimia organik dan katalisis.\u003c\/p\u003e\n\u003cp\u003eStruktur cinchonine memadukan cincin kuinolin, gugus hidroksil sekunder, dan nitrogen kuinuklidin yang bersifat basa. Kombinasi tersebut memungkinkannya bekerja sebagai basa kiral, ligan, maupun prekursor garam amonium kuaterner untuk katalisis transfer fasa. Dalam praktiknya, peneliti memanfaatkan cinchonine baik secara langsung sebagai katalis maupun sebagai kerangka awal untuk membangun katalis generasi baru.\u003c\/p\u003e\n\u003cp\u003eAMI Scientific menyediakan produk ini dalam dua pilihan kemasan sehingga dapat menyesuaikan kebutuhan riset skala kecil maupun kegiatan sintesis yang lebih intensif. Produk dikirim dalam kemasan asli pabrikan TCI dengan pelabelan lengkap. Dokumen mutu resmi dapat dirujuk melalui informasi lot yang tertera pada kemasan.\u003c\/p\u003e\n\u003ch3\u003eAplikasi Laboratorium\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eKatalis kiral pada sintesis asimetrik — mengarahkan pembentukan enansiomer tertentu pada reaksi adisi dan alkilasi.\u003c\/li\u003e\n\u003cli\u003ePrekursor katalis transfer fasa — kerangka kuinuklidin mudah diubah menjadi garam amonium kuaterner kiral.\u003c\/li\u003e\n\u003cli\u003eResolusi asam rasemik — membentuk garam diastereomerik yang dapat dipisahkan dengan kristalisasi bertingkat.\u003c\/li\u003e\n\u003cli\u003eLigan pada reaksi terkatalisis logam — gugus nitrogen dan hidroksil dapat berkoordinasi dengan pusat logam.\u003c\/li\u003e\n\u003cli\u003eStudi perbandingan stereoselektivitas — dipasangkan dengan cinchonidine untuk menguji arah induksi kiral yang berlawanan.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpesifikasi\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMerek: TCI (kode katalog C0350)\u003c\/li\u003e\n\u003cli\u003eNomor CAS: 118-10-5\u003c\/li\u003e\n\u003cli\u003eKategori: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Catalysts, Chiral Ligands, Chiral Reagents\u003c\/li\u003e\n\u003cli\u003eVarian\/kemasan: 25 g dan 200 g\u003c\/li\u003e\n\u003cli\u003eBentuk fisik: padatan (serbuk\/kristal)\u003c\/li\u003e\n\u003cli\u003ePenyimpanan: wadah tertutup rapat, terlindung dari cahaya langsung dan kelembapan, mengikuti petunjuk pada label produsen\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003ePenanganan dan Penyimpanan\u003c\/h3\u003e\n\u003cp\u003eTimbang dan pindahkan bahan menggunakan alat pelindung diri standar serta hindari terbentuknya debu di area kerja terbuka. Simpan kembali dalam wadah aslinya yang tertutup rapat agar mutu bahan terjaga selama masa penggunaan. Patuhi prosedur keselamatan kimia laboratorium Anda dan lembar data keselamatan resmi TCI untuk penanganan tumpahan maupun pembuangan limbah.\u003c\/p\u003e\n\u003ch3\u003eEnglish\u003c\/h3\u003e\n\u003cp\u003eCinchonine (TCI C0350, CAS 118-10-5) is a naturally occurring cinchona alkaloid and one of the most established chiral catalysts in asymmetric synthesis. Because it behaves as a pseudo-enantiomer of cinchonidine, the two are frequently paired to access opposite stereochemical outcomes within the same reaction system. It also serves as a starting scaffold for chiral phase-transfer catalysts and as a resolving agent for racemic acids. AMI Scientific offers this TCI product in 25 g and 200 g packs to suit both small-scale studies and more intensive synthetic work.\u003c\/p\u003e\n\u003ch3\u003eReferensi Ilmiah\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBartók dkk. (2005). Enantioselective hydrogenation of ethyl pyruvate catalysed by cinchonine-modified Pt\/Al2O3: tilted adsorption geometry of cinchonine. \u003cem\u003eCatalysis Letters\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1007\/s10562-004-3449-2\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1007\/s10562-004-3449-2\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eHuaizhi dkk. (2000). Study on Adsorption Properties of Cinchonine Loaded Resin to Mo and V by ICP-AES. \u003cem\u003eAnalytical Letters\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1080\/00032710008543172\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1080\/00032710008543172\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eXi dkk. (2013). Cinchonine and thiourea. \u003cem\u003eChemical Communications\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1039\/c3cc40825f\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1039\/c3cc40825f\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":48085991620826,"sku":"TCI2510C035014417","price":1631000.0,"currency_code":"IDR","in_stock":true},{"title":"200g","offer_id":48085991653594,"sku":"TCI2510C035014418","price":8741000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0350.jpg?v=1767095075"},{"product_id":"tci2510c097215327","title":"TCI C0972 35963-20-3 (-)-10-Camphorsulfonic Acid","description":"\u003ch3\u003eDeskripsi\u003c\/h3\u003e\n\u003cp\u003eTCI C0972 (-)-10-Camphorsulfonic Acid adalah asam sulfonat kiral turunan kamfor yang menjadi salah satu reagen paling klasik sekaligus paling andal dalam sintesis asimetris. Senyawa ini menggabungkan kerangka bisiklik kamfor yang kaku dengan gugus asam sulfonat yang sangat asam, sehingga dapat berperan ganda sebagai sumber kiralitas dan sebagai katalis asam kuat. Enansiomer (-) tersedia dalam tiga pilihan kemasan, yaitu 25 g, 100 g, dan 500 g.\u003c\/p\u003e\n\u003cp\u003ePeran paling dikenal dari asam kamforsulfonat adalah sebagai agen resolusi untuk memisahkan campuran rasemik amina melalui pembentukan garam diastereomer yang berbeda kelarutannya. Selain itu, senyawa ini banyak dipakai sebagai katalis asam Brønsted dalam pembentukan asetal, reaksi transasetalisasi, penataan ulang, serta pelepasan gugus pelindung tertentu. Sifatnya yang berupa padatan membuatnya jauh lebih mudah ditimbang dan disimpan dibandingkan asam kuat berbentuk cairan.\u003c\/p\u003e\n\u003cp\u003eKetersediaan tiga ukuran kemasan memudahkan penyesuaian dengan skala kerja, mulai dari penapisan kondisi reaksi hingga optimasi rute berulang. Bagi laboratorium yang rutin melakukan resolusi kiral, kemasan yang lebih besar membantu menjaga konsistensi antar percobaan. AMI Scientific melayani kebutuhan reagen ini untuk institusi riset, perguruan tinggi, dan laboratorium pengembangan produk.\u003c\/p\u003e\n\u003ch3\u003eAplikasi Laboratorium\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAgen resolusi kiral — membentuk garam diastereomer dengan amina rasemik sehingga kedua enansiomer dapat dipisahkan melalui kristalisasi.\u003c\/li\u003e\n\u003cli\u003eKatalis asam Brønsted — mengkatalisis pembentukan dan hidrolisis asetal serta ketal dalam kondisi yang relatif terkendali.\u003c\/li\u003e\n\u003cli\u003ePelepasan gugus pelindung — dipakai pada deproteksi yang membutuhkan asam kuat tanpa kehadiran anion pengganggu.\u003c\/li\u003e\n\u003cli\u003eAuksiliari dan pembentuk garam — digunakan untuk menyiapkan garam kiral serta turunan sulfonil dari kerangka kamfor.\u003c\/li\u003e\n\u003cli\u003eStandar dan bahan acuan riset kiral — kerangka kamfor yang terdefinisi baik berguna dalam studi metode analisis stereokimia.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpesifikasi\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMerek: TCI (kode produk C0972)\u003c\/li\u003e\n\u003cli\u003eNomor CAS: 35963-20-3\u003c\/li\u003e\n\u003cli\u003eKategori: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Building Blocks\u003c\/li\u003e\n\u003cli\u003eVarian\/kemasan: 25 g, 100 g, 500 g\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, terlindung dari kelembapan\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003ePenanganan dan Penyimpanan\u003c\/h3\u003e\n\u003cp\u003eGunakan sarung tangan, kacamata pelindung, dan masker debu saat menimbang karena padatan asam sulfonat bersifat korosif dan iritatif terhadap kulit serta mata. Timbang di area berventilasi baik dan tutup wadah segera setelah digunakan agar bahan tidak menyerap uap air dari udara. Jauhkan dari basa kuat dan logam reaktif, serta bersihkan tumpahan dengan prosedur netralisasi yang berlaku di laboratorium Anda.\u003c\/p\u003e\n\u003ch3\u003eEnglish\u003c\/h3\u003e\n\u003cp\u003eTCI C0972 (-)-10-Camphorsulfonic Acid (CAS 35963-20-3) is a crystalline chiral sulfonic acid available in 25 g, 100 g, and 500 g pack sizes. It is widely used as a resolving agent for racemic amines, forming diastereomeric salts that can be separated by crystallization. The compound also serves as a strong Brønsted acid catalyst for acetal formation, deprotection, and related transformations. Store it tightly sealed in a cool, dry place and wear gloves and eye protection when weighing, as the solid is corrosive.\u003c\/p\u003e\n\u003ch3\u003eReferensi Ilmiah\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eZhang dkk. (2002). Synthesis and characterization of self-assembled polyaniline nanotubes doped with D-10-camphorsulfonic acid. \u003cem\u003eNanotechnology\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1088\/0957-4484\/13\/6\/311\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1088\/0957-4484\/13\/6\/311\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eZhai dkk. (2020). Anti-Corrosive Coating of Carbon-Steel Assisted by Polymer-Camphorsulfonic Acid Embedded within Graphene. \u003cem\u003eCoatings\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.3390\/coatings10090879\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.3390\/coatings10090879\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eSong dkk. (2013). Improved thermoelectric performance of PEDOT:PSS film treated with camphorsulfonic acid. \u003cem\u003eJournal of Polymer Research\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1007\/s10965-013-0316-0\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1007\/s10965-013-0316-0\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":48086040969434,"sku":"TCI2510C097215327","price":1378000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48086041002202,"sku":"TCI2510C097215328","price":3852000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48086041034970,"sku":"TCI2510C097215329","price":11805000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0972.jpg?v=1767096117"},{"product_id":"tci2510c099815371","title":"TCI C0998 21286-54-4 (+)-10-Camphorsulfonyl Chloride","description":"\u003ch3\u003eDeskripsi\u003c\/h3\u003e\n\u003cp\u003eTCI C0998 (+)-10-Camphorsulfonyl Chloride dengan nomor CAS 21286-54-4 adalah building block kiral turunan kamfor yang telah lama menjadi andalan dalam kimia sintesis asimetris. Senyawa ini membawa kerangka bisiklik kamfor yang rigid dan optis aktif, dipadukan dengan gugus sulfonil klorida yang sangat reaktif. Kombinasi tersebut memungkinkan pemasangan unit kiral pada berbagai substrat hanya melalui satu langkah sulfonilasi. Reagen ini disediakan oleh TCI dengan pengendalian mutu yang konsisten untuk keperluan riset.\u003c\/p\u003e\n\u003cp\u003ePeran paling dikenalnya adalah sebagai reagen derivatisasi kiral untuk amina dan alkohol, karena sulfonamida atau sulfonat ester yang terbentuk berupa diastereomer yang dapat dipisahkan dan diukur dengan HPLC atau NMR. Dari sini, peneliti dapat menentukan kemurnian enansiomer suatu senyawa secara praktis. Selain itu, kerangka kamforsulfonil merupakan prekursor menuju kamforsultam, salah satu auksiliar kiral yang banyak digunakan untuk mengarahkan stereoselektivitas reaksi alkilasi dan sikloadisi. Kerigidan kerangka kamfor inilah yang memberikan diskriminasi wajah yang baik.\u003c\/p\u003e\n\u003cp\u003eAMI Scientific menyediakan produk ini dalam kemasan 5 g dan 25 g sesuai kebutuhan laboratorium. Ukuran 5 g umumnya mencukupi untuk kegiatan analisis dan derivatisasi rutin, sedangkan 25 g lebih tepat untuk sintesis auksiliar kiral dalam jumlah lebih besar. Karena sifatnya yang peka terhadap kelembapan, kemasan yang lebih kecil sering menjadi pilihan bijak. Tim kami dengan senang hati membantu Anda memilih ukuran yang paling efisien.\u003c\/p\u003e\n\u003ch3\u003eAplikasi Laboratorium\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eReagen derivatisasi kiral — membentuk diastereomer dari amina atau alkohol sehingga kemurnian enansiomer dapat diukur dengan HPLC maupun NMR.\u003c\/li\u003e\n\u003cli\u003eSintesis sulfonamida kiral — reaksi dengan amina berlangsung cepat dan menghasilkan produk yang stabil serta mudah dikristalkan.\u003c\/li\u003e\n\u003cli\u003ePrekursor auksiliar kamforsultam — kerangka kamforsulfonil dapat diolah menjadi auksiliar kiral untuk mengarahkan stereoselektivitas reaksi.\u003c\/li\u003e\n\u003cli\u003eResolusi senyawa rasemat — perbedaan sifat fisik diastereomer yang terbentuk memudahkan pemisahan secara kristalisasi atau kromatografi.\u003c\/li\u003e\n\u003cli\u003eModifikasi gugus hidroksil — pembentukan sulfonat ester menjadikan gugus hidroksil sebagai gugus pergi yang baik untuk substitusi lanjutan.\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 C0998\u003c\/li\u003e\n\u003cli\u003eNomor CAS: 21286-54-4\u003c\/li\u003e\n\u003cli\u003eKategori: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Building Blocks\u003c\/li\u003e\n\u003cli\u003eVarian kemasan: 5 g dan 25 g\u003c\/li\u003e\n\u003cli\u003eBentuk fisik: padatan pada suhu ruang\u003c\/li\u003e\n\u003cli\u003eCatatan penyimpanan: sangat peka terhadap kelembapan; simpan di tempat sejuk dan kering dalam wadah tertutup rapat, sebaiknya di bawah gas inert\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003ePenanganan dan Penyimpanan\u003c\/h3\u003e\n\u003cp\u003eSebagai sulfonil klorida, senyawa ini bereaksi dengan air dan uap air menghasilkan gas hidrogen klorida yang korosif, sehingga penimbangan sebaiknya dilakukan cepat di lemari asam atau di dalam glove box. Gunakan sarung tangan tahan bahan kimia, kacamata pengaman, dan hindari kontak langsung dengan kulit maupun mata. Setelah digunakan, tutup wadah rapat, jika memungkinkan bilas ruang kepala botol dengan gas inert, lalu simpan di tempat sejuk dan kering jauh dari basa, alkohol, dan amina.\u003c\/p\u003e\n\u003ch3\u003eEnglish\u003c\/h3\u003e\n\u003cp\u003eTCI C0998 (+)-10-Camphorsulfonyl Chloride (CAS 21286-54-4) is a classic chiral building block that pairs the rigid, optically active camphor skeleton with a highly reactive sulfonyl chloride group. It is widely used as a chiral derivatizing agent, converting amines and alcohols into separable diastereomers for enantiomeric purity determination by HPLC or NMR. The same scaffold also serves as an entry point to camphorsultam-type chiral auxiliaries that direct stereoselectivity in alkylation and cycloaddition chemistry. AMI Scientific offers 5 g and 25 g packs; because the reagent is strongly moisture sensitive, handle it in a fume hood and store it tightly sealed in a cool, dry place, preferably under inert gas.\u003c\/p\u003e\n\u003ch3\u003eReferensi Ilmiah\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eKO dkk. (1998). ChemInform Abstract: A Convenient Preparation of (1S)‐(+)‐10‐Mercaptoisoborneol from (1S)‐(+)‐10‐Camphorsulfonyl Chloride with High Diastereoselectivity.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.199837217\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.199837217\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":48086042738906,"sku":"TCI2510C099815371","price":1153000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086042771674,"sku":"TCI2510C099815372","price":4077000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0998.jpg?v=1767096162"},{"product_id":"tci2510c130815800","title":"TCI C1308 39262-22-1 (-)-10-Camphorsulfonyl Chloride","description":"\u003ch3\u003eDeskripsi\u003c\/h3\u003e\n\u003cp\u003eTCI C1308 (-)-10-Camphorsulfonyl Chloride adalah turunan sulfonil klorida berbasis kerangka kamfor yang banyak dipakai sebagai bahan awal kiral di laboratorium sintesis asimetris. Senyawa ini menggabungkan gugus sulfonil klorida yang sangat reaktif dengan rangka bisiklik kamfor yang kaku dan optis aktif, sehingga informasi kiralitasnya dapat diteruskan ke molekul target. Karakter inilah yang menjadikannya salah satu bahan pembangun favorit dalam pengembangan auksiliari dan ligan kiral. AMI Scientific menghadirkannya untuk mendukung riset kimia organik di laboratorium akademik maupun industri di Indonesia.\u003c\/p\u003e\n\u003cp\u003eSecara aplikatif, gugus sulfonil klorida pada senyawa ini mudah bereaksi dengan amina, alkohol, maupun nukleofil lain untuk membentuk sulfonamida dan sulfonat ester. Reaksi tersebut umumnya berlangsung dalam kondisi ringan dengan bantuan basa penetral asam, sehingga kompatibel dengan berbagai substrat sensitif. Produk turunannya sering dimanfaatkan sebagai reagen derivatisasi untuk memisahkan atau menganalisis campuran enantiomer. Peran ganda sebagai bahan sintesis sekaligus reagen analitik membuat senyawa ini bernilai tinggi di meja kerja peneliti.\u003c\/p\u003e\n\u003cp\u003eSebagai produk merek TCI, bahan ini diproduksi dengan standar kendali mutu untuk keperluan penelitian laboratorium. Setiap lot disertai dokumen mutu dari produsen yang dapat dijadikan rujukan resmi untuk data spesifikasi, sehingga peneliti tidak perlu mengandalkan asumsi. Ketersediaan dalam dua ukuran kemasan memudahkan penyesuaian antara kebutuhan skala uji coba dan skala sintesis rutin. Tim AMI Scientific siap membantu memilih kemasan yang paling sesuai dengan rencana kerja Anda.\u003c\/p\u003e\n\u003ch3\u003eAplikasi Laboratorium\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSintesis sulfonamida kiral — gugus sulfonil klorida bereaksi langsung dengan amina primer maupun sekunder untuk membentuk ikatan S–N yang stabil.\u003c\/li\u003e\n\u003cli\u003ePembuatan auksiliari kiral berbasis kamfor — kerangka kamfor optis aktif menjadi titik awal menuju turunan sultam dan senyawa pengarah stereokimia lain.\u003c\/li\u003e\n\u003cli\u003eReagen derivatisasi analisis kiral — pembentukan turunan diastereomer membantu pemisahan enantiomer pada kromatografi.\u003c\/li\u003e\n\u003cli\u003eSintesis ligan untuk katalisis asimetris — struktur bisiklik yang kaku memberikan lingkungan sterik yang terdefinisi di sekitar pusat logam.\u003c\/li\u003e\n\u003cli\u003eRiset kimia medisinal — motif sulfonil dimanfaatkan untuk memodifikasi sifat fisikokimia molekul kandidat.\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\u003eKode produk: C1308\u003c\/li\u003e\n\u003cli\u003eNomor CAS: 39262-22-1\u003c\/li\u003e\n\u003cli\u003eKategori: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Building Blocks\u003c\/li\u003e\n\u003cli\u003eVarian\/kemasan: 5 g dan 25 g\u003c\/li\u003e\n\u003cli\u003eBentuk fisik: padatan pada suhu ruang; rincian mutu mengacu pada dokumen lot dari produsen\u003c\/li\u003e\n\u003cli\u003eCatatan penyimpanan: simpan di tempat sejuk dan kering, terlindung dari kelembapan, sesuai anjuran pada label produk\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003ePenanganan dan Penyimpanan\u003c\/h3\u003e\n\u003cp\u003eSenyawa sulfonil klorida bersifat reaktif terhadap air dan dapat melepaskan gas asam ketika terhidrolisis, sehingga penimbangan sebaiknya dilakukan cepat di dalam lemari asam. Gunakan sarung tangan, kacamata pengaman, dan jas laboratorium, serta hindari kontak dengan kulit dan mata. Tutup wadah rapat setelah digunakan dan simpan dalam kondisi kering sesuai petunjuk pada label serta lembar data keselamatan dari produsen.\u003c\/p\u003e\n\u003ch3\u003eEnglish\u003c\/h3\u003e\n\u003cp\u003eTCI C1308 (-)-10-Camphorsulfonyl Chloride is a chiral sulfonyl chloride built on the rigid, optically active camphor skeleton. Its highly reactive sulfonyl chloride group readily couples with amines and alcohols to give sulfonamides and sulfonate esters under mild conditions. Researchers commonly use it to prepare camphor-derived chiral auxiliaries and ligands, and as a derivatizing reagent for enantiomeric analysis. Supplied by AMI Scientific in 5 g and 25 g packs, it should be kept dry and tightly closed because of its sensitivity to moisture.\u003c\/p\u003e\n\u003ch3\u003eReferensi Ilmiah\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eKO dkk. (1998). ChemInform Abstract: A Convenient Preparation of (1S)‐(+)‐10‐Mercaptoisoborneol from (1S)‐(+)‐10‐Camphorsulfonyl Chloride with High Diastereoselectivity.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.199837217\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.199837217\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":48086062301402,"sku":"TCI2510C130815800","price":1941000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086062334170,"sku":"TCI2510C130815801","price":6241000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1308.jpg?v=1769144492"},{"product_id":"tci2510c168216348","title":"TCI C1682 179950-32-4 N-(2-Carboxybenzoyl)-(-)-10,2-camphorsultam","description":"\u003ch3\u003eDeskripsi\u003c\/h3\u003e\n\u003cp\u003eN-(2-Carboxybenzoyl)-(-)-10,2-camphorsultam adalah senyawa kimia yang digunakan dalam sintesis asimetris untuk memperoleh produk dengan struktur stereokimia tertentu. Bahan ini termasuk dalam kategori chiral auxiliaries, yang merupakan bantuan kiral dalam reaksi kimia untuk mengarahkan pembentukan produk yang diinginkan. Dalam laboratorium, senyawa ini sering digunakan untuk meningkatkan efisiensi dan akurasi dalam proses sintesis kompleks.\u003c\/p\u003e\n\u003cp\u003eSenyawa ini memiliki struktur kimia yang kompleks dan memiliki sifat kiral yang sangat spesifik. Karena sifat ini, senyawa ini sangat efektif dalam mempercepat reaksi kimia yang membutuhkan kontrol stereokimia. Ketersediaan dalam bentuk padat dan kemurnian tinggi membuatnya mudah digunakan dan stabil dalam penyimpanan.\u003c\/p\u003e\n\u003cp\u003eDi laboratorium Indonesia, senyawa ini digunakan dalam penelitian kimia organik, terutama dalam bidang sintesis asimetris. Banyak institusi pendidikan dan penelitian menggunakan senyawa ini untuk pengembangan produk farmasi dan bahan kimia berbasis senyawa organik.\u003c\/p\u003e\n\u003ch3\u003eAplikasi Laboratorium\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSintesis asimetris untuk memproduksi senyawa dengan struktur kiral spesifik\u003c\/li\u003e\n\u003cli\u003ePenelitian dalam bidang farmakologi untuk pengembangan obat baru\u003c\/li\u003e\n\u003cli\u003ePengujian kiral dalam reaksi kimia organik untuk meningkatkan efisiensi reaksi\u003c\/li\u003e\n\u003cli\u003ePengembangan bahan kimia berbasis senyawa kompleks untuk industri farmasi\u003c\/li\u003e\n\u003cli\u003ePenelitian tentang mekanisme reaksi kimia yang membutuhkan kontrol stereokimia\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: 179950-32-4\u003c\/li\u003e\n\u003cli\u003eKategori: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Auxiliaries\u003c\/li\u003e\n\u003cli\u003eVarian\/kemasan: 500mg\u003c\/li\u003e\n\u003cli\u003eBentuk fisik: Padat\u003c\/li\u003e\n\u003cli\u003eCatatan penyimpanan: Simpan dalam wadah tertutup dan jauh dari cahaya langsung\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 yang sejuk dan kering. Hindari paparan langsung terhadap cahaya matahari atau panas berlebihan. Gunakan wadah berbahan plastik atau kaca yang tahan terhadap reaksi kimia. Selama penanganan, pastikan untuk mengenakan alat pelindung diri seperti sarung tangan dan masker.\u003c\/p\u003e\n\u003ch3\u003eEnglish\u003c\/h3\u003e\n\u003cp\u003eN-(2-Carboxybenzoyl)-(-)-10,2-camphorsultam is a chiral auxiliary used in asymmetric synthesis to control the stereochemistry of chemical reactions. This compound is widely utilized in organic chemistry research for the production of optically active compounds. Its unique structure and high purity make it an essential tool in the development of pharmaceuticals and complex organic molecules. The compound is particularly useful in laboratory settings where precise stereochemical control is required. Its application extends to various fields including pharmaceutical research, synthetic chemistry, and advanced material development. The compound is supplied in a solid form and is best stored in a sealed container away from light and heat.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"500mg","offer_id":48086084518106,"sku":"TCI2510C168216348","price":7055000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1682.jpg?v=1768816678"},{"product_id":"tci2510c168316349","title":"TCI C1683 193202-37-8 N-(2-Carboxy-4,5-dichlorobenzoyl)-(-)-10,2-camphorsultam","description":"\u003ch3\u003eDeskripsi\u003c\/h3\u003e\n\u003cp\u003eN-(2-Carboxy-4,5-dichlorobenzoyl)-(-)-10,2-camphorsultam adalah senyawa kimia yang digunakan dalam sintesis asimetris untuk memfasilitasi reaksi kimia yang menghasilkan produk dengan struktur asimetris. Bahan ini termasuk dalam kategori chiral auxiliaries, yang merupakan bantuan kimia yang membantu dalam pembentukan struktur molekul tertentu. Senyawa ini sering digunakan dalam laboratorium kimia untuk mempercepat proses sintesis dengan mengurangi kebutuhan untuk menggunakan katalis yang kompleks.\u003c\/p\u003e\n\u003cp\u003eSenyawa ini memiliki struktur molekul yang kompleks dan memiliki sifat optik aktif, yang memungkinkannya untuk berinteraksi secara spesifik dengan reaktan dalam reaksi kimia. Sifat ini menjadikannya pilihan yang tepat dalam sintesis asimetris karena dapat mempercepat reaksi dan menghasilkan produk dengan tingkat kemurnian yang tinggi. Karena sifatnya yang stabil dan tidak mudah terurai, senyawa ini juga mudah disimpan dan digunakan dalam berbagai kondisi laboratorium.\u003c\/p\u003e\n\u003cp\u003eDalam konteks laboratorium di Indonesia, senyawa ini digunakan secara luas dalam penelitian kimia, terutama dalam bidang sintesis asimetris dan pengembangan senyawa baru. Banyak institusi penelitian dan universitas di Indonesia memanfaatkan senyawa ini untuk keperluan pendidikan dan penelitian. Ketersediaan produk ini melalui AMI Scientific memudahkan akses bagi para peneliti dan mahasiswa yang membutuhkan bahan kimia kualitas tinggi.\u003c\/p\u003e\n\u003ch3\u003eAplikasi Laboratorium\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eDigunakan dalam sintesis asimetris untuk memperoleh produk dengan struktur tertentu\u003c\/li\u003e\n\u003cli\u003eCocok untuk penelitian dalam bidang kimia organik dan farmakologi\u003c\/li\u003e\n\u003cli\u003eMempercepat proses reaksi kimia dengan mengurangi kompleksitas katalis\u003c\/li\u003e\n\u003cli\u003eMendukung pengembangan senyawa baru dengan kemurnian tinggi\u003c\/li\u003e\n\u003cli\u003eBermanfaat dalam analisis struktur molekul menggunakan teknik spektroskopi\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: 193202-37-8\u003c\/li\u003e\n\u003cli\u003eKategori: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Auxiliaries\u003c\/li\u003e\n\u003cli\u003eVarian\/kemasan: 500mg\u003c\/li\u003e\n\u003cli\u003eBentuk fisik: Padat\u003c\/li\u003e\n\u003cli\u003eCatatan penyimpanan: Simpan dalam wadah tertutup dan jauh dari cahaya langsung\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003ePenanganan dan Penyimpanan\u003c\/h3\u003e\n\u003cp\u003eSenyawa ini harus disimpan dalam wadah yang kedap udara dan jauh dari sumber cahaya langsung untuk menjaga stabilitasnya. Penyimpanan dalam suhu kamar yang sejuk dan kering sangat disarankan. Saat menangani produk ini, pengguna harus memakai alat pelindung diri seperti sarung tangan dan masker untuk menghindari kontak langsung. Karena sifatnya yang kimia, senyawa ini harus dihindari dari paparan berlebihan dan disimpan terpisah dari bahan kimia lain yang tidak kompatibel.\u003c\/p\u003e\n\u003ch3\u003eEnglish\u003c\/h3\u003e\n\u003cp\u003eN-(2-Carboxy-4,5-dichlorobenzoyl)-(-)-10,2-camphorsultam is a chiral auxiliary used in asymmetric synthesis to facilitate the formation of chiral molecules. This compound is widely applied in organic chemistry and pharmaceutical research for its ability to enhance reaction efficiency and yield high-purity products. Its optically active nature allows it to selectively interact with reactants, making it a valuable tool in the development of new compounds. Available in a 500mg form, it is a reliable choice for researchers and students in Indonesia seeking quality chemical reagents for laboratory use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"500mg","offer_id":48086084550874,"sku":"TCI2510C168316349","price":9333000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1683.jpg?v=1768816682"},{"product_id":"tci2510c176716434","title":"TCI C1767 1820575-29-8 N-(2-Carboxy-4,5-dichlorobenzoyl)-(+)-10,2-camphorsultam","description":"\u003ch3\u003eDeskripsi\u003c\/h3\u003e\n\u003cp\u003eN-(2-Carboxy-4,5-dichlorobenzoyl)-(+)-10,2-camphorsultam adalah senyawa kimia yang digunakan dalam sintesis asimetris sebagai asisten chiral. Senyawa ini berperan sebagai komponen katalis dalam reaksi kimia yang memerlukan kontrol ketat terhadap struktur produk akhir. Dalam laboratorium, senyawa ini sering digunakan untuk memperoleh senyawa dengan aktivitas biologis spesifik, seperti obat atau bahan kimia industri.\u003c\/p\u003e\n\u003cp\u003eSenyawa ini memiliki struktur kompleks yang memungkinkan interaksi spesifik dengan reaktan, sehingga meningkatkan efisiensi reaksi dan mengurangi pembentukan produk sampingan. Karena sifat chiralnya, senyawa ini sangat cocok untuk reaksi yang memerlukan kontrol stereokimia. Sifat ini menjadikannya pilihan utama dalam sintesis asimetris yang membutuhkan presisi tinggi.\u003c\/p\u003e\n\u003cp\u003eDi laboratorium Indonesia, senyawa ini digunakan dalam penelitian kimia organik, terutama dalam bidang farmasi dan bahan kimia. Peneliti lokal sering memanfaatkan senyawa ini untuk mengembangkan senyawa baru yang memiliki aplikasi medis atau industri. Ketersediaannya melalui AMI Scientific memudahkan akses bagi para ilmuwan dan peneliti di Indonesia.\u003c\/p\u003e\n\u003ch3\u003eAplikasi Laboratorium\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eDigunakan dalam sintesis asimetris untuk memperoleh produk dengan struktur spesifik\u003c\/li\u003e\n\u003cli\u003eCocok untuk reaksi yang memerlukan kontrol stereokimia tinggi\u003c\/li\u003e\n\u003cli\u003eMendukung penelitian farmasi dalam pengembangan obat baru\u003c\/li\u003e\n\u003cli\u003eMempercepat proses produksi senyawa kimia dengan aktivitas biologis\u003c\/li\u003e\n\u003cli\u003eDapat digunakan dalam penelitian bahan kimia industri yang memerlukan presisi tinggi\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: 1820575-29-8\u003c\/li\u003e\n\u003cli\u003eKategori: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Auxiliaries\u003c\/li\u003e\n\u003cli\u003eVarian\/kemasan: 500mg\u003c\/li\u003e\n\u003cli\u003eBentuk fisik: Padat\u003c\/li\u003e\n\u003cli\u003eCatatan penyimpanan: Simpan dalam wadah tertutup, jauh dari cahaya dan kelembapan\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, jauh dari cahaya matahari langsung dan kelembapan. Penyimpanan dalam suhu kamar yang stabil sangat disarankan. Penggunaan wadah kaca atau plastik yang tahan terhadap reaksi kimia dianjurkan. Selama penanganan, harus diperhatikan kehati-hatian dalam menghindari kontaminasi dan paparan langsung.\u003c\/p\u003e\n\u003ch3\u003eEnglish\u003c\/h3\u003e\n\u003cp\u003eN-(2-Carboxy-4,5-dichlorobenzoyl)-(+)-10,2-camphorsultam is a chiral auxiliary used in asymmetric synthesis to control the stereochemistry of chemical reactions. This compound is widely applied in organic chemistry for the production of compounds with specific biological activities. Its complex structure allows for selective interaction with reactants, enhancing reaction efficiency and reducing byproduct formation. The compound is particularly useful in pharmaceutical research and industrial chemical applications where precision is critical. Its availability through AMI Scientific supports scientific innovation in Indonesia.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"500mg","offer_id":48086087598298,"sku":"TCI2510C176716434","price":6858000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1767.jpg?v=1768816701"},{"product_id":"tci2510c323718229","title":"TCI C3237 560-09-8 (1S,3R)-(-)-Camphoric Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(1S,3R)-(-)-Camphoric Acid is a chiral compound widely used in asymmetric synthesis to construct molecules with specific biological activities. This material plays a crucial role in organic chemistry laboratories, particularly in the development of complex molecules that require precise stereochemical control. Its chiral nature makes it an essential building block for creating compounds with defined spatial configurations, which are vital in pharmaceutical and biochemical research.\u003c\/p\u003e\n\u003cp\u003eThe compound is valued for its moderate polarity and good solubility in organic solvents such as ethyl acetate and ethanol. These properties make it highly versatile for use in various chemical reactions, enabling researchers to synthesize more reactive compounds efficiently. Its stability under standard laboratory conditions further enhances its usability in a wide range of synthetic processes.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, (1S,3R)-(-)-Camphoric Acid is commonly used in organic chemistry research, especially in pharmacology and biochemistry. Researchers in educational institutions and research organizations rely on this compound to develop new substances with potential therapeutic applications. Its role in advancing scientific discovery is significant, particularly in the study of compounds with antioxidant, anti-inflammatory, or antitumor properties.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric synthesis is a key application where this compound is used to create chiral molecules with specific spatial configurations, essential for drug development.\u003c\/li\u003e\n\u003cli\u003eOrganic chemistry research benefits from its solubility in common organic solvents, allowing for efficient reaction conditions and product isolation.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research utilizes its chiral properties to design compounds with targeted biological activities, such as anti-inflammatory or antitumor effects.\u003c\/li\u003e\n\u003cli\u003eBiochemical studies employ this compound to investigate the stereochemical requirements of enzyme interactions and receptor binding.\u003c\/li\u003e\n\u003cli\u003eAcademic and industrial research institutions use it to explore new synthetic pathways and improve the efficiency of complex molecule synthesis.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 560-09-8\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory supply\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from 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 integrity. It is recommended to keep it in a tightly sealed container to prevent moisture absorption and contamination. Due to its organic nature, it should be stored away from strong oxidizing agents and incompatible materials. Proper ventilation is necessary when handling to ensure a safe laboratory environment. The compound is not classified as hazardous under standard handling conditions, but standard laboratory safety protocols should be followed. Regular inspection of storage conditions is advised to ensure long-term stability and usability.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086220701914,"sku":"TCI2510C323718229","price":4947000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3237.jpg?v=1767099352"},{"product_id":"tci2510d135421090","title":"TCI D1354 62708-56-9 (-)-Dibenzoyl-L-tartaric Acid Monohydrate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(-)-Dibenzoyl-L-tartaric acid monohydrate is a chiral compound widely used in asymmetric synthesis to produce molecules with specific stereochemistry. This material plays a crucial role in laboratories where precise control over molecular structure is essential. It serves as a chiral building block, enabling chemists to create complex molecules with defined enantiomers. Its utility extends to pharmaceutical and biochemical research, where the correct stereochemistry can significantly impact the biological activity of a compound.\u003c\/p\u003e\n\u003cp\u003eThe compound is prized for its high purity and consistent physical and chemical properties. It exhibits stable crystalline structures and dissolves well in organic solvents, making it versatile for various synthetic applications. These characteristics ensure reliable performance in laboratory settings, supporting reproducibility and accuracy in chemical reactions. Its ability to act as a chiral auxiliary enhances the efficiency of asymmetric synthesis processes.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, (-)-Dibenzoyl-L-tartaric acid monohydrate is commonly used in research institutions and pharmaceutical industries. It is a key reagent in the development of new compounds with specific biological activities. Its availability and reliability make it a preferred choice for scientists working on drug discovery and chemical synthesis projects.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric synthesis is a key application where this compound is used to control the stereochemistry of products, enabling the creation of enantiomerically pure compounds.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research benefits from its role as a chiral auxiliary, aiding in the synthesis of drugs with specific biological activities.\u003c\/li\u003e\n\u003cli\u003eOrganic chemistry experiments often utilize this material due to its solubility in organic solvents and stable crystalline structure.\u003c\/li\u003e\n\u003cli\u003eChiral compound development relies on its ability to act as a building block for creating complex molecular structures with defined stereochemistry.\u003c\/li\u003e\n\u003cli\u003eBiochemical studies use this compound to investigate the stereochemical effects on biological activity and molecular interactions.\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: 62708-56-9\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral 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: White crystalline solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and 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 to maintain its stability and prevent degradation. It is recommended to keep it in a sealed container to avoid exposure to moisture and air. Due to its crystalline nature, it should be stored in a container that prevents physical damage. Laboratory personnel should handle it with care, using appropriate personal protective equipment when necessary. Proper labeling of storage containers is essential to ensure safe handling and prevent accidental use. The compound should not be exposed to direct sunlight or high humidity conditions to preserve its chemical integrity.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086436315354,"sku":"TCI2510D135421090","price":873000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48086436348122,"sku":"TCI2510D135421091","price":8208000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D1354.jpg?v=1767102956"},{"product_id":"tci2510d138721122","title":"TCI D1387 32634-66-5 (-)-Di-p-toluoyl-L-tartaric Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(-)-Di-p-toluoyl-L-tartaric Acid, identified by CAS number 32634-66-5 and commonly abbreviated by laboratory practitioners as DTTA, is a tartrate ester in which both hydroxyl groups of the tartaric acid backbone have been esterified with p-toluic acid. The compound belongs to the family of classical chiral resolving agents most frequently employed in preparative organic chemistry. Its role in the laboratory is highly specific but crucial: it converts the racemic mixture of an organic base into a pair of diastereomeric salts that are physically distinguishable, so that separation of enantiomers can be achieved through simple crystallisation techniques alone, without the need for expensive preparative chromatography instrumentation.\u003c\/p\u003e\n\u003cp\u003eThe property that makes DTTA so widely favoured is the pair of bulky aromatic p-toluoyl rings attached to the tartrate skeleton. These aromatic groups increase lipophilicity, strengthen aromatic stacking interactions, and promote the formation of a tightly packed crystal lattice, so that the solubility difference between the two diastereomeric salts becomes far more pronounced than with smaller tartrate derivatives. The L configuration ensures that the agent consistently selects one particular enantiomer from a racemic pair, giving reproducible and predictable resolution outcomes across repeated preparations. Its crystalline solid form remains stable under normal storage conditions.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent is typically found in university organic chemistry research groups, pharmaceutical synthesis laboratories, and institutional research centres engaged in asymmetric synthesis work. It is generally selected by teams that need to obtain enantiomerically enriched material from a racemic base but do not have routine access to preparative chiral chromatography systems. As a chiral building block within the asymmetric synthesis category, it serves both dedicated research programmes and advanced teaching laboratories demonstrating the principles of classical resolution.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eClassical resolution of racemic amines: the reagent forms diastereomeric salts with basic nitrogen centres, allowing the two enantiomers to be separated by fractional crystallisation rather than chromatography.\u003c\/li\u003e\n\u003cli\u003ePreparation of enantiomerically enriched pharmaceutical intermediates: its consistent L configuration reliably selects one enantiomer, which supports reproducible batch-to-batch outcomes in medicinal chemistry synthesis routes.\u003c\/li\u003e\n\u003cli\u003eChiral building block in asymmetric synthesis: the defined tartrate stereocentres provide a dependable source of chirality for constructing target molecules with controlled stereochemical outcomes.\u003c\/li\u003e\n\u003cli\u003eCrystallisation-based purification method development: the bulky aromatic rings promote tight crystal packing, making this reagent useful when researchers are screening conditions for salt crystallisation studies.\u003c\/li\u003e\n\u003cli\u003eTeaching and demonstration of stereochemical principles: its well-established behaviour makes it a suitable material for advanced practical classes illustrating how diastereomeric salt formation enables enantiomer separation.\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: 32634-66-5\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Building Blocks\u003c\/li\u003e\n\u003cli\u003eProduct code: TCI D1387\u003c\/li\u003e\n\u003cli\u003ePhysical form: crystalline solid\u003c\/li\u003e\n\u003cli\u003eStorage: stable under normal storage conditions\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore this material in a tightly closed original container, kept in a cool, dry and well-ventilated area away from moisture and direct sunlight. Amber glass or the supplier's original packaging is suitable, and the container should be closed promptly after each weighing to limit moisture uptake by the crystalline solid. Handle the material inside a fume hood using a laboratory coat, safety goggles and chemical-resistant gloves, and avoid generating dust during transfer and weighing operations. Keep the reagent separated from strong bases and strong oxidising agents, use clean and dry spatulas to prevent cross-contamination of the stock, and consult the supplier safety data sheet before first use. Wash hands thoroughly after handling and dispose of residues in accordance with institutional chemical waste procedures.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086438543578,"sku":"TCI2510D138721122","price":2082000.0,"currency_code":"IDR","in_stock":true},{"title":"250g","offer_id":48086438576346,"sku":"TCI2510D138721123","price":9050000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D1387.jpg?v=1767103001"},{"product_id":"tci2510d139821139","title":"TCI D1398 80822-15-7 (+)-Dibenzoyl-D-tartaric Acid Monohydrate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(+)-Dibenzoyl-D-tartaric Acid Monohydrate, CAS number 80822-15-7, is the monohydrate form of D-configured tartaric acid in which both hydroxyl groups have been esterified with benzoic acid. Commonly abbreviated as DBTA, this compound is one of the most well-established chiral resolving agents in preparative organic chemistry and pharmaceutical chemistry. Its role in the laboratory is to convert racemic mixtures of organic bases into pairs of diastereomeric salts that differ in physical properties, so that one enantiomer can be separated by controlled crystallisation without requiring the far more expensive chiral chromatography columns.\u003c\/p\u003e\n\u003cp\u003eThe properties that make this material a preferred choice begin with its two aromatic benzoyl groups, which enrich intermolecular interactions within the crystal lattice, combined with two free carboxylate groups that are ready to form salts with amines. The D configuration delivers selectivity opposite to that of its L counterpart, which is why both forms are often supplied side by side so that researchers can target the enantiomer they actually want. The monohydrate form presents a stable crystalline solid that is easy to weigh out and consistent from batch to batch, and its good solubility in methanol and ethanol supports straightforward preparation of resolution media.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this resolving agent is typically used in university research groups, pharmaceutical development units, and analytical or synthetic chemistry facilities that work on single-enantiomer targets. It suits laboratories that need a practical route to enantiopure amines without investing in dedicated chiral separation instrumentation, and the stable crystalline monohydrate form makes it convenient to store, handle, and dispense under ordinary tropical laboratory conditions where reproducible weighing matters.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eClassical resolution of racemic amines: the two free carboxylate groups readily form diastereomeric salts with basic nitrogen centres, allowing one enantiomer to be isolated by controlled crystallisation.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical development of single-enantiomer actives: DBTA is a well-established resolving agent, giving development chemists a documented and reproducible route to enantiopure intermediates without chiral chromatography.\u003c\/li\u003e\n\u003cli\u003eChiral building block work in asymmetric synthesis: the D configuration supplies defined stereochemical information that can be carried forward into further preparative organic transformations.\u003c\/li\u003e\n\u003cli\u003eCrystallisation method development: the aromatic benzoyl groups strengthen intermolecular interactions in the crystal lattice, which supports the systematic screening and optimisation of solvent and crystallisation conditions.\u003c\/li\u003e\n\u003cli\u003eCost-effective alternative to chiral chromatography: laboratories separating enantiomers on a preparative scale can use salt formation and crystallisation rather than expensive chiral columns.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI (catalogue reference D1398)\u003c\/li\u003e\n\u003cli\u003eCAS number: 80822-15-7\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in the standard TCI catalogue pack sizes; please confirm the size you require when ordering\u003c\/li\u003e\n\u003cli\u003ePhysical form: crystalline solid, monohydrate\u003c\/li\u003e\n\u003cli\u003eStorage: keep in a tightly closed container in a cool, dry place\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the material in a tightly closed original container in a cool, dry, well-ventilated area, away from moisture and from incompatible reagents such as strong bases and strong oxidising agents. Because the product is supplied as a monohydrate, containers should be kept properly sealed between uses so that the crystalline solid remains consistent for weighing. Handle the solid in a fume hood or a well-ventilated workspace, and wear standard laboratory personal protective equipment including a lab coat, safety goggles, and chemical-resistant gloves. Avoid generating dust, avoid contact with skin and eyes, and wash hands thoroughly after handling. Always consult the manufacturer's safety data sheet before use and dispose of residues in accordance with applicable laboratory waste procedures.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086439166170,"sku":"TCI2510D139821139","price":676000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48086439198938,"sku":"TCI2510D139821140","price":6381000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D1398.jpg?v=1767103034"},{"product_id":"tci2510d141721164","title":"TCI D1417 32634-68-7 (+)-Di-p-toluoyl-D-tartaric Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(+)-Di-p-toluoyl-D-tartaric Acid is a chiral compound widely used in asymmetric synthesis, playing a crucial role in the creation of molecules with defined stereochemistry. This material is essential for chemists working in the field of chiral building blocks, as it provides a reliable framework for constructing complex organic structures. In the laboratory, it serves as a key reagent in reactions where precise control over the spatial arrangement of atoms is required. Its presence ensures that the desired enantiomer is produced with high selectivity, making it a vital component in advanced synthetic pathways.\u003c\/p\u003e\n\u003cp\u003eThe compound’s chemical stability and compatibility with a variety of reaction conditions make it a preferred choice for researchers. Its ability to maintain its chiral integrity under different experimental settings ensures consistent results in synthetic processes. Additionally, its well-defined stereochemistry allows for predictable outcomes in asymmetric catalysis and resolution techniques. These properties make it an indispensable tool for scientists aiming to achieve high levels of enantiomeric purity in their experiments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in organic chemistry research, pharmaceutical development, and molecular structure studies. It is particularly valuable in academic and industrial settings where precision in stereochemical control is critical. Many research institutions and universities rely on this compound for experiments that require accurate and reproducible results in the synthesis of chiral compounds. Its application spans across various scientific disciplines, reinforcing its importance in modern chemical research.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric Synthesis for the development of pharmaceuticals with specific stereochemical properties, ensuring the production of active enantiomers with desired biological effects.\u003c\/li\u003e\n\u003cli\u003eChiral Compound Synthesis in organic chemistry research, where precise stereocontrol is essential for the creation of complex molecular structures.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical Research and Development in the formulation of drugs requiring high enantiomeric purity for therapeutic efficacy and safety.\u003c\/li\u003e\n\u003cli\u003eMolecular Structure Analysis in academic studies, where the compound serves as a reference for understanding stereochemical behavior in chemical reactions.\u003c\/li\u003e\n\u003cli\u003eBiochemical Studies in the investigation of chiral molecules’ interactions with biological systems, aiding in the design of targeted therapeutic agents.\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: 32634-68-7\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack Sizes: Available in various quantities as per standard laboratory supply\u003c\/li\u003e\n\u003cli\u003ePhysical Form: Solid powder\u003c\/li\u003e\n\u003cli\u003eStorage Note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to keep it in a sealed container to prevent exposure to moisture and air, which could affect its stability. Due to its chiral nature, it is important to maintain strict handling protocols to avoid contamination or degradation. Always use appropriate personal protective equipment when handling the compound, such as gloves and safety goggles. Ensure that the storage area is well-ventilated to minimize any potential risks associated with prolonged exposure. Proper storage conditions help preserve the compound’s integrity and effectiveness for use in laboratory applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086440149210,"sku":"TCI2510D141721164","price":1266000.0,"currency_code":"IDR","in_stock":true},{"title":"250g","offer_id":48086440181978,"sku":"TCI2510D141721165","price":5228000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D1417.jpg?v=1767103070"},{"product_id":"tci2510d191121888","title":"TCI D1911 6283-74-5 (+)-Diacetyl-L-tartaric Anhydride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(+)-Diacetyl-L-tartaric anhydride is a key chemical compound used in asymmetric synthesis to construct molecules with optical activity. This reagent plays a crucial role in laboratories where stereochiral control is essential, particularly in the production of complex organic compounds. Its application extends to various synthetic pathways, enabling chemists to achieve desired stereochemical outcomes in their reactions. Due to its stability and reactivity, it is a valuable tool in both academic and industrial research settings.\u003c\/p\u003e\n\u003cp\u003eThe compound is preferred for its chemical stability and ability to interact with a wide range of substrates. Its chiral nature allows it to act as a chiral auxiliary or building block, guiding reactions toward specific enantiomers. This makes it especially useful in the development of pharmaceuticals and bioactive compounds. Additionally, its non-reactive nature under certain conditions simplifies handling and storage, making it a reliable choice for laboratory use.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, (+)-Diacetyl-L-tartaric anhydride is commonly used in chemical research, particularly in pharmaceutical and biochemical studies. It supports the synthesis of chiral compounds, contributing to the advancement of drug development and biotechnology. Its availability and reliability make it a standard component in many research facilities across the country.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric Synthesis: This compound is ideal for creating chiral molecules, enabling precise stereochemical control in complex organic reactions.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical Research: It supports the development of chiral drugs, where enantiomeric purity is critical for efficacy and safety.\u003c\/li\u003e\n\u003cli\u003eBiochemical Studies: Its role in chiral synthesis makes it valuable for studying enzyme mechanisms and metabolic pathways.\u003c\/li\u003e\n\u003cli\u003eOrganic Chemistry Education: It is frequently used in teaching labs to demonstrate asymmetric synthesis and chiral compound formation.\u003c\/li\u003e\n\u003cli\u003eIndustrial Chemical Production: It aids in the large-scale synthesis of chiral compounds used in various chemical industries.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 6283-74-5\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral 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 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 moisture absorption, which could affect its performance. Since it is non-reactive under normal conditions, it does not require special handling, but it should be kept away from incompatible substances. In laboratory settings, it is important to ensure proper ventilation and use appropriate personal protective equipment when handling. Regular inspection of storage conditions is advised to ensure the compound remains in optimal condition for use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086482845914,"sku":"TCI2510D191121888","price":1294000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D1911.jpg?v=1767103898"},{"product_id":"tci2510d264522947","title":"TCI D2645 70728-23-3 (-)-Diacetyl-D-tartaric Anhydride","description":"\u003cp\u003e\u003cstrong\u003e(-)-Diacetyl-D-tartaric Anhydride\u003c\/strong\u003e (CAS 70728-23-3) adalah produk kimia berkualitas tinggi dari TCI dengan grade \u003cstrong\u003eReagent Grade \/ for Synthesis\u003c\/strong\u003e.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eAplikasi:\u003c\/strong\u003e Reagen sintesis untuk berbagai transformasi kimia organik di laboratorium dan industri.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eSpesifikasi:\u003c\/strong\u003e\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003eRumus Molekul: C8H8O7\u003c\/li\u003e\n\u003cli\u003eCAS Number: 70728-23-3\u003c\/li\u003e\n\u003cli\u003eKemurnian: \u0026gt;98.0%(T)\u003c\/li\u003e\n\u003cli\u003eKode Produk TCI: D2645\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eTersedia di \u003cstrong\u003eAMI Scientific\u003c\/strong\u003e, distributor resmi TCI di Indonesia. \u003cstrong\u003eHubungi kami untuk penawaran harga dan ketersediaan stok\u003c\/strong\u003e — pengiriman ke seluruh Indonesia.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086570107098,"sku":"TCI2510D264522947","price":788000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086570139866,"sku":"TCI2510D264522948","price":2138000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D2645.jpg?v=1768817747"},{"product_id":"tci2510d349223776","title":"TCI D3492 2743-38-6 (-)-Dibenzoyl-L-tartaric Acid","description":"\u003cp\u003e\u003cstrong\u003e(-)-Dibenzoyl-L-tartaric Acid\u003c\/strong\u003e (CAS 2743-38-6) adalah produk kimia berkualitas tinggi dari TCI dengan grade \u003cstrong\u003eHPLC Grade\u003c\/strong\u003e.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eAplikasi:\u003c\/strong\u003e Reagen sintesis untuk berbagai transformasi kimia organik di laboratorium dan 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