{"title":"Biokimia \u0026 Reagen Hayati","description":"\u003cp\u003e\u003cstrong\u003eBiokimia \u0026amp; Reagen Hayati\u003c\/strong\u003e — menghimpun reagen hayati lintas kelas, mulai asam amino, karbohidrat, lipid, alkaloid, hingga peptida, enzim beserta substrat dan inhibitornya, probe fluoresen, dan bahan penunjang riset model penyakit hewan. Kategori ini berfungsi sebagai bahan uji dan reagen pendukung eksperimen biokimia serta biologi molekuler.\u003c\/p\u003e\u003cp\u003eReagen ini dipakai peneliti biokimia dan biologi molekuler untuk uji aktivitas enzim, deteksi luminesen atau fluoresen, penyiapan buffer biologis, hingga pelabelan biomolekul dalam eksperimen in vitro. Bahan seperti antibiotik dan senyawa bahan baku obat mentah berperan sebagai senyawa acuan untuk riset serta model eksperimen dalam studi terkait penyakit.\u003c\/p\u003e\u003cp\u003eContoh produk dalam koleksi ini: \u003ca href=\"\/en\/products\/tci2510t096051929\"\u003eTCI T0960 1731-88-0 Methyl Tridecanoate\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b552012169\"\u003eTCI B5520 714971-09-2 BMS-599626\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510s016350046\"\u003eTCI S0163 57-11-4 Stearic Acid\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b552212172\"\u003eTCI B5522 120410-24-4 Biapenem\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510o018044529\"\u003eTCI O0180 112-80-1 Oleic Acid\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b553712196\"\u003eTCI B5537 96099-84-2 N-(tert-Butoxycarbonyl)-D-threonine Methyl Ester\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510m047638178\"\u003eTCI M0476 544-63-8 Myristic Acid\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b554612203\"\u003eTCI B5546 1309649-57-7 Biotin-PEG4-Azide\u003c\/a\u003e.\u003c\/p\u003e\u003cp\u003ePerhatikan kemurnian tingkat biokimia, kondisi penyimpanan yang sesuai untuk enzim dan peptida, serta bentuk sediaan (larutan, serbuk, atau konjugat) sebelum memilih reagen. Seluruh produk merupakan produk asli Tokyo Chemical Industry (TCI) Jepang, dengan kemurnian, kemasan, dan kondisi penyimpanan tercantum pada halaman masing-masing item.\u003c\/p\u003e\u003cp\u003eKategori lain yang sejajar di bawah Life Science, sering dipakai bersamaan dalam satu alur kerja laboratorium:\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/riset-pengembangan-obat\"\u003eRiset Pengembangan Obat\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/biologi-sel\"\u003eBiologi Sel\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l2-cell-biology\"\u003eCell Biology\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l2-glycoscience\"\u003eGlycoscience\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l2-molecular-biology\"\u003eMolecular Biology\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l2-microbiology\"\u003eMicrobiology\u003c\/a\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eKoleksi ini masih terbagi menjadi 12 kelompok yang lebih spesifik:\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-pharmaceutical-research-reagents-for-experimental-use\"\u003ePharmaceutical Research Reagents (for Experimental Use)\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-amino-acids\"\u003eAmino Acids\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-carbohydrates\"\u003eCarbohydrates\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-lipids\"\u003eLipids\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-antibiotics\"\u003eAntibiotics\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-enzymes-enzyme-inhibitors-enzyme-substrates\"\u003eEnzymes, Enzyme Inhibitors, Enzyme Substrates\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-crude-medicine-ingredients-for-research-and-experimental-use\"\u003eCrude Medicine Ingredients for Research and Experimental Use\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-nucleosides-nucleotides-oligonucleotides\"\u003eNucleosides, Nucleotides, Oligonucleotides\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-phenylpropanoids-aromatic-polyketides\"\u003ePhenylpropanoids, Aromatic Polyketides\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-terpenes\"\u003eTerpenes\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-steroids\"\u003eSteroids\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-alkaloids\"\u003eAlkaloids\u003c\/a\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eKembali ke \u003ca href=\"\/en\/collections\/tci-l1-life-science\"\u003eLife Science\u003c\/a\u003e. Untuk pengadaan volume besar, kemasan khusus, atau grade tertentu, hubungi tim AMI Scientific — distributor resmi TCI Japan di Indonesia — untuk pengecekan ketersediaan dan lead time langsung ke Jepang.\u003c\/p\u003e","products":[{"product_id":"tci2510b552012169","title":"TCI B5520 714971-09-2 BMS-599626","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBMS-599626 (CAS 714971-09-2) is a research-grade compound supplied by TCI, known as a selective kinase inhibitor used in laboratory studies of HER-related cell signaling pathways. It is commonly applied in oncology research, including in vitro and in vivo assays investigating tumor growth and drug resistance mechanisms. The product is available in 10 mg and 50 mg packaging for pharmaceutical and biomedical research purposes.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"10mg","offer_id":48085885026522,"sku":"TCI2510B552012169","price":3358000.0,"currency_code":"IDR","in_stock":true},{"title":"50mg","offer_id":48085885059290,"sku":"TCI2510B552012170","price":11661000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5520.jpg?v=1771058686"},{"product_id":"tci2510b552212172","title":"TCI B5522 120410-24-4 Biapenem","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBiapenem (CAS 120410-24-4) is a carbapenem antibiotic supplied by TCI, commonly used as a reference standard in pharmaceutical and analytical laboratories. It serves as a key material for method validation, calibration, and quality control testing in drug development. The product is also widely applied in antimicrobial susceptibility testing and resistance studies, and is available in 25 mg and 100 mg pack sizes.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mg","offer_id":48085885157594,"sku":"TCI2510B552212172","price":2247000.0,"currency_code":"IDR","in_stock":true},{"title":"100mg","offer_id":48085885190362,"sku":"TCI2510B552212173","price":6890000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5522_38593186-9c2d-4eb7-82a7-949c77e5be01.jpg?v=1767862251"},{"product_id":"tci2510b554612203","title":"TCI B5546 1309649-57-7 Biotin-PEG4-Azide","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI Biotin-PEG4-Azide (B5546, CAS 1309649-57-7) is a click chemistry reagent featuring a biotin affinity tag linked via a PEG4 spacer to an azide reactive group. It is primarily used for biotinylation of alkyne-modified biomolecules through copper-catalyzed or strain-promoted azide-alkyne cycloaddition reactions. This reagent is ideal for applications in protein labeling, affinity purification, pull-down assays, and various streptavidin-based detection systems.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48085886304474,"sku":"TCI2510B554612203","price":7521000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5546.jpg?v=1767092491"},{"product_id":"tci2510b556012218","title":"TCI B5560 663171-32-2 Biotin-PEG4-Amine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBiotin-PEG4-Amine (TCI B5560, CAS 663171-32-2) is a high-purity bioconjugation reagent featuring a biotin moiety linked via a PEG4 spacer to a reactive primary amine group, enabling efficient labeling of biomolecules such as proteins, peptides, and nucleic acids. This compound facilitates covalent attachment of biotin through standard coupling chemistries, making it suitable for avidin\/streptavidin-based detection, purification, and immobilization workflows. Widely employed in chemical biology, drug discovery, and biosensor development, it serves as a versatile building block for constructing biotinylated conjugates with enhanced solubility and reduced steric hindrance.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"10mg","offer_id":48085886894298,"sku":"TCI2510B556012218","price":1439000.0,"currency_code":"IDR","in_stock":true},{"title":"50mg","offer_id":48085886927066,"sku":"TCI2510B556012219","price":5023000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5560_fb481397-bc4c-4eba-8c65-751d9f73ad13.jpg?v=1767862393"},{"product_id":"tci2510b556512224","title":"TCI B5565 1418022-42-0 Biotin-PEG11-Amine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI Biotin-PEG11-Amine (CAS 1418022-42-0) is a bioconjugation reagent featuring a biotin moiety linked to a reactive primary amine group via an 11-unit PEG spacer, designed for efficient and flexible biotinylation of biomolecules. The amine group enables covalent coupling to carboxyl groups, activated esters, or other electrophilic functional groups on proteins, antibodies, peptides, and nucleic acids, while the PEG11 spacer enhances water solubility and reduces non-specific binding. This product is widely applied in biochemical assays, affinity purification, surface functionalization, and the development of targeted delivery systems across life science and chemical biology research.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"10mg","offer_id":48085887123674,"sku":"TCI2510B556512224","price":2474000.0,"currency_code":"IDR","in_stock":true},{"title":"50mg","offer_id":48085887156442,"sku":"TCI2510B556512225","price":7748000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5565_5b4f7184-161c-4bc2-a110-888315fe290a.jpg?v=1767862412"},{"product_id":"tci2510b557712239","title":"TCI B5577 2413847-26-2 Biotin-PEG2-Hydrazide","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBiotin-PEG2-Hydrazide is a flexible bioconjugation reagent that enables selective attachment of biotin to carbonyl-containing biomolecules such as oxidized glycoproteins, carbohydrates, or aldehyde-modified oligonucleotides via hydrazide chemistry. Its PEG2 spacer enhances aqueous solubility and reduces steric hindrance, making it ideal for affinity purification, pull-down assays, and fluorescent labeling workflows in chemical biology research. The compound's strong biotin-streptavidin interaction ensures reliable detection and capture across diverse experimental platforms.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"10mg","offer_id":48085887779034,"sku":"TCI2510B557712239","price":3711000.0,"currency_code":"IDR","in_stock":true},{"title":"50mg","offer_id":48085887811802,"sku":"TCI2510B557712240","price":12922000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5577_e18bc269-39f9-4431-b16e-c996df731892.jpg?v=1767862460"},{"product_id":"tci2510b557812241","title":"TCI B5578 756525-97-0 Biotin-PEG4-Hydrazide","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBiotin-PEG4-Hydrazide (CAS 756525-97-0) is a biotinylation reagent featuring a hydrazide reactive group and a PEG4 spacer for enhanced water solubility. This TCI product is designed for selective labeling of glycoproteins and other carbonyl-containing biomolecules via hydrazide-aldehyde\/ketone conjugation chemistry. It is widely employed in streptavidin-based detection systems, protein interaction studies, and chemical biology applications requiring high-affinity biotin tagging.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"10mg","offer_id":50506879172826,"sku":"TCI2510B557812241","price":2147000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5578_9b0c0983-7a70-4bb5-8d9a-b18ed5dda187.jpg?v=1767862466"},{"product_id":"tci2510b558712254","title":"TCI B5587 186020-66-6 tert-Butyl 12-Hydroxy-4,7,10-trioxadodecanoate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e*tert*-Butyl 12-Hydroxy-4,7,10-trioxadodecanoate is a heterobifunctional PEG linker featuring a terminal hydroxyl group and a protected *tert*-butyl ester, enabling controlled stepwise conjugation. It is widely utilized in the synthesis of PEGylated biomolecules, including drug-protein conjugates, surface-modified nanoparticles, and targeted delivery systems. The trioxa spacer enhances aqueous solubility and reduces immunogenicity, making it an essential building block in chemical biology and pharmaceutical research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085889286362,"sku":"TCI2510B558712254","price":2171000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085889319130,"sku":"TCI2510B558712255","price":7547000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5587_91fe5bcc-c5e3-48be-b2eb-9ca09f5bddb5.jpg?v=1767862503"},{"product_id":"tci2510b559212263","title":"TCI B5592 132-17-2 Benztropine Mesylate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBenztropine Mesylate is a chemical compound widely used in pharmacological and biochemical research. It serves as a key reagent in experimental studies focused on anticholinergic effects and their impact on the central nervous system. This compound is essential for researchers aiming to understand the mechanisms of neurological disorders and the efficacy of neuropharmacological treatments. Its role in laboratory settings is critical for advancing knowledge in drug development and therapeutic applications.\u003c\/p\u003e\n\u003cp\u003eThe compound is known for its chemical stability and good solubility in organic solvents, making it highly suitable for a variety of chemical reactions. These properties ensure consistent performance in experimental protocols, contributing to reliable and reproducible results. Additionally, its thermal stability allows for ease of storage and use under varying laboratory conditions, enhancing its versatility in research applications.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Benztropine Mesylate is extensively used in pharmacological research across educational institutions and research organizations. It is a preferred choice for studying the mechanisms of antiparkinson drugs and their effects on neural systems. Researchers rely on its quality and reliability to conduct accurate and meaningful experiments in the field of neuropharmacology.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eParkinson’s Disease Research – This compound is used to study the effects of antiparkinson drugs on neural pathways and motor function.\u003c\/li\u003e\n\u003cli\u003eAnticholinergic Effect Testing – It helps in evaluating the impact of anticholinergic agents on the central nervous system and peripheral tissues.\u003c\/li\u003e\n\u003cli\u003eNeuropharmacological Studies – It is essential for investigating the pharmacodynamics and pharmacokinetics of neuroactive compounds.\u003c\/li\u003e\n\u003cli\u003eDrug Development Protocols – Its use supports the screening and evaluation of potential therapeutic agents for neurological disorders.\u003c\/li\u003e\n\u003cli\u003eClinical Trial Simulations – It aids in creating controlled environments to assess drug interactions and therapeutic outcomes in preclinical settings.\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: 132-17-2\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Pharmaceutical Research Reagents\u003c\/li\u003e\n\u003cli\u003ePack Sizes: Available in various quantities as per standard reagent packaging\u003c\/li\u003e\n\u003cli\u003ePhysical Form: Solid powder\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\u003eBenztropine Mesylate should be stored in a cool, dry environment to maintain its chemical stability and prevent degradation. It is recommended to keep the compound in airtight containers to avoid moisture exposure, which could affect its solubility and potency. Laboratory personnel should handle the material with care, using appropriate personal protective equipment such as gloves and safety goggles. The compound is non-hazardous under normal conditions but should be handled in a well-ventilated area to minimize inhalation risks. Proper labeling and storage practices ensure the safety of both the material and the laboratory environment.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48085889614042,"sku":"TCI2510B559212263","price":2802000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085889646810,"sku":"TCI2510B559212264","price":9793000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5592.jpg?v=1769180200"},{"product_id":"tci2510b563012321","title":"TCI B5630 292605-14-2 SB-3CT","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eSB-3CT is a potent and selective mechanism-based inhibitor of matrix metalloproteinase-2 (MMP-2) and matrix metalloproteinase-9 (MMP-9), widely utilized in biochemical and pharmacological research. It is commonly applied in studies involving cancer metastasis, angiogenesis, inflammatory processes, and extracellular matrix remodeling. This compound also serves as a valuable reference tool in the development of next-generation MMP inhibitors and in neuroscience research related to neurodegenerative disorders.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mg","offer_id":48085893185754,"sku":"TCI2510B563012321","price":6739000.0,"currency_code":"IDR","in_stock":true},{"title":"100mg","offer_id":48085893218522,"sku":"TCI2510B563012322","price":19862000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5630.jpg?v=1769180207"},{"product_id":"tci2510b570712424","title":"TCI B5707 96187-53-0 Brequinar","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBrequinar (TCI B5707, CAS 96187-53-0) is a potent dihydroorotate dehydrogenase (DHODH) inhibitor used in pharmaceutical research to study de novo pyrimidine biosynthesis. It is widely applied in experimental models of oncology, immunology, and virology to investigate cell proliferation suppression via nucleotide metabolism blockade. This product is intended strictly for laboratory and experimental use only.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"20mg","offer_id":48085898494170,"sku":"TCI2510B570712424","price":3029000.0,"currency_code":"IDR","in_stock":true},{"title":"100mg","offer_id":48085898526938,"sku":"TCI2510B570712425","price":10600000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5707.jpg?v=1771058498"},{"product_id":"tci2510b573512462","title":"TCI B5735 20898-44-6 tele-Benzyl-Nalpha-(tert-butoxycarbonyl)-L-histidine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003etele-Benzyl-Nalpha-(tert-butoxycarbonyl)-L-histidine (Boc-His(Bzl)-OH) is a doubly protected histidine derivative widely used in solid-phase peptide synthesis (SPPS). The Boc group protects the alpha-amino functionality while the benzyl group protects the imidazole side chain, ensuring regioselective coupling and minimizing undesired side reactions during peptide chain assembly. This building block is essential for synthesizing bioactive peptides, protein interaction probes, and peptide-based drug candidates in both academic and pharmaceutical research settings.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085900001498,"sku":"TCI2510B573512462","price":1465000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085900034266,"sku":"TCI2510B573512463","price":4569000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5735.jpg?v=1768204440"},{"product_id":"tci2510b574112470","title":"TCI B5741 179324-69-7 Bortezomib","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBortezomib is a chemical compound widely used in pharmacological and biochemical research, particularly in the development of cancer treatments. As a pharmaceutical research reagent, it plays a crucial role in experimental studies aimed at understanding and combating diseases such as multiple myeloma and leukemia. This compound is essential for researchers seeking to explore the mechanisms of protein degradation and its impact on cellular processes. Its application extends to various laboratory settings where precision and reliability are paramount.\u003c\/p\u003e\n\u003cp\u003eBortezomib is preferred due to its high chemical stability under specific conditions and its excellent solubility in organic solvents like ethanol and dimethyl sulfoxide (DMSO). These properties make it highly versatile for use in a wide range of biochemical experiments. Additionally, its high purity ensures accurate and reproducible results, which are vital for scientific research. The compound’s ability to selectively inhibit proteasomes makes it a valuable tool for studying protein turnover and its implications in disease progression.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, bortezomib is commonly used by researchers and scientists to investigate the effects of pharmaceutical compounds on cells and to develop new therapeutic strategies. Its role in experimental drug testing and cellular research makes it a key component in the study of cancer biology and related fields. The compound’s reliability and effectiveness make it a preferred choice for those conducting advanced biochemical and pharmacological experiments.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePharmaceutical research for drug development and testing due to its ability to inhibit proteasomes and affect protein degradation pathways.\u003c\/li\u003e\n\u003cli\u003eCancer cell studies focusing on multiple myeloma and leukemia as it targets abnormal protein accumulation in malignant cells.\u003c\/li\u003e\n\u003cli\u003eBiochemical experiments requiring high-purity reagents with consistent performance and solubility in organic solvents.\u003c\/li\u003e\n\u003cli\u003eExperimental models for understanding cellular responses to proteasome inhibitors in disease progression.\u003c\/li\u003e\n\u003cli\u003eResearch applications in pharmacology where precise and reliable reagents are essential for accurate experimental outcomes.\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: 179324-69-7\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Pharmaceutical Research Reagents\u003c\/li\u003e\n\u003cli\u003ePack sizes: As per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid (as per standard product description)\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eBortezomib should be stored in a cool, dry environment, away from direct light and moisture to maintain its chemical stability. It is recommended to use airtight containers made of glass or high-density polyethylene to prevent contamination and degradation. Due to its potential reactivity, it should be handled with appropriate personal protective equipment such as gloves and safety goggles. In laboratory settings, it should be stored separately from incompatible substances to ensure safety. Regular monitoring of storage conditions is advised to maintain the integrity and effectiveness of the compound during experimental use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"10mg","offer_id":48085900296410,"sku":"TCI2510B574112470","price":1970000.0,"currency_code":"IDR","in_stock":true},{"title":"50mg","offer_id":48085900329178,"sku":"TCI2510B574112471","price":6890000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5741_1e978569-95ee-47db-9596-fda49489a1a6.jpg?v=1767863168"},{"product_id":"tci2510b577512514","title":"TCI B5775 848695-25-0 BIIB 021","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B5775, with the CAS number 848695-25-0, is a chemical compound widely used in pharmaceutical research within laboratory settings. It belongs to the category of pharmaceutical research reagents and plays a crucial role in experimental studies aimed at drug development and biological activity analysis. This compound is essential for researchers seeking to understand how specific substances interact with living organisms or cells. Its presence in laboratory experiments helps in evaluating the efficacy and safety of potential therapeutic agents.\u003c\/p\u003e\n\u003cp\u003eThe compound is preferred due to its high purity and consistent quality, which ensures reliable and reproducible results. Its chemical stability allows it to maintain its properties under various experimental conditions, making it suitable for long-term use in research. Additionally, its resistance to degradation ensures that it remains effective even when stored for extended periods. These characteristics make it a trusted choice for scientists conducting rigorous biochemical and pharmacological studies.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, TCI B5775 is commonly used in academic and governmental research institutions. It is favored for its compliance with international standards and its availability, which supports the continuous advancement of scientific research. Its application is particularly relevant in drug development and biological activity studies, contributing to the growth of the pharmaceutical sector in Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePharmaceutical research for evaluating drug efficacy and biological activity in experimental models.\u003c\/li\u003e\n\u003cli\u003eBiochemical experiments requiring stable reagents for accurate compound interaction studies.\u003c\/li\u003e\n\u003cli\u003eDrug development projects aiming to test the pharmacological properties of new chemical entities.\u003c\/li\u003e\n\u003cli\u003eLaboratory-based toxicity studies to assess the impact of compounds on living cells and tissues.\u003c\/li\u003e\n\u003cli\u003eResearch in pharmacokinetics to analyze how substances are absorbed, distributed, and metabolized in the body.\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: 848695-25-0\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Pharmaceutical Research Reagents\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 direct sunlight and moisture.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis chemical 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. Proper labeling of storage containers is essential to ensure safe handling and prevent accidental use. Laboratory personnel should wear appropriate personal protective equipment when handling the compound. Storage conditions should be monitored regularly to ensure compliance with safety standards. The compound should not be stored near incompatible materials to avoid potential chemical reactions.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mg","offer_id":48085902164186,"sku":"TCI2510B577512514","price":3005000.0,"currency_code":"IDR","in_stock":true},{"title":"100mg","offer_id":48085902196954,"sku":"TCI2510B577512515","price":9035000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5775_21b243ef-0cee-4d1e-b9d7-d12d0a8362f0.jpg?v=1767863304"},{"product_id":"tci2510b577612516","title":"TCI B5776 356559-20-1 SB-525334","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eSB-525334 is a chemical compound classified under the category of enzyme substrates and inhibitors. It plays a crucial role in biochemical experiments by enabling researchers to study enzyme activity and catalytic reaction mechanisms. This compound is widely used in laboratories to assess the efficiency of specific enzymes, supporting both fundamental and applied research. Its presence in various biotechnological and pharmaceutical studies makes it an essential tool for understanding enzyme behavior and function.\u003c\/p\u003e\n\u003cp\u003eSB-525334 is preferred due to its chemical stability under specific conditions, ensuring accurate and consistent results. Its molecular structure allows for specific interactions with target enzymes, making it highly effective in enzyme mechanism studies. Additionally, it maintains its chemical activity over a defined period, offering reliability in diverse research scenarios. These properties make it a valuable reagent for researchers aiming to explore enzyme-substrate interactions and inhibition patterns.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, SB-525334 is a key component in biochemical and pharmacological research. It is commonly used in experiments related to enzyme activity, drug development, and metabolic pathway analysis. Its application extends to academic institutions and research centers, where it supports both teaching and advanced scientific investigations.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eEnzyme Kinetics Studies – SB-525334 is ideal for measuring enzyme activity and substrate turnover rates, providing precise data for kinetic analysis.\u003c\/li\u003e\n\u003cli\u003eDrug Development Research – It is used to evaluate enzyme inhibition and substrate specificity, aiding in the design of targeted pharmaceutical compounds.\u003c\/li\u003e\n\u003cli\u003eBiochemical Assays – Its stability and specificity make it suitable for standard biochemical assays that require controlled enzyme-substrate interactions.\u003c\/li\u003e\n\u003cli\u003eMetabolic Pathway Analysis – SB-525334 helps in tracing enzyme activity within metabolic pathways, supporting functional genomics and proteomics studies.\u003c\/li\u003e\n\u003cli\u003eTeaching and Training – It is commonly used in educational settings to demonstrate enzyme mechanisms and biochemical processes to students and researchers.\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 – 356559-20-1\u003c\/li\u003e\n\u003cli\u003eCategory – Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Enzymes, Enzyme Inhibitors, Enzyme Substrates\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 formulation\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\u003eSB-525334 should be stored in a cool, dry environment to maintain its chemical stability and activity. It is recommended to keep the compound in airtight containers to prevent moisture exposure and contamination. Proper labeling of storage containers is essential for safe handling and traceability. Laboratory personnel should wear appropriate personal protective equipment when handling the compound. Regular monitoring of storage conditions ensures the integrity of the material. Adherence to standard laboratory safety protocols minimizes risks associated with chemical exposure.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"10mg","offer_id":48085902229722,"sku":"TCI2510B577612516","price":5527000.0,"currency_code":"IDR","in_stock":true},{"title":"50mg","offer_id":48085902262490,"sku":"TCI2510B577612517","price":19938000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5776.jpg?v=1768815892"},{"product_id":"tci2510b585712620","title":"TCI B5857 114676-69-6 N-(tert-Butoxycarbonyl)-cis-4-hydroxy-D-proline Methyl Ester","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eN-(tert-Butoxycarbonyl)-cis-4-hydroxy-D-proline Methyl Ester is a chemical compound widely used in organic and biochemical research, particularly in peptide chemistry. This compound serves as a key building block in the synthesis of complex peptides and proteins, playing a crucial role in the development of bioactive molecules. Its structural complexity makes it an essential tool for scientists working on drug discovery and biotechnology applications. In laboratory settings, it is frequently employed to create modified amino acids that are integral to the design of therapeutic agents and functional biomolecules.\u003c\/p\u003e\n\u003cp\u003eThis compound is valued for its chemical stability under controlled conditions and its reactivity with various reagents during synthesis processes. Its ability to participate in specific chemical reactions makes it a preferred choice for researchers aiming to achieve precise modifications in peptide structures. The compound's high reactivity also allows for efficient and reproducible results in synthetic pathways, which is critical in both academic and industrial research environments. Its purity and consistent quality ensure reliable outcomes in experimental procedures, making it a trusted material in advanced chemical synthesis.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in pharmaceutical research, biotechnology, and biochemical analysis. It is particularly relevant in studies related to protein structure and function, as well as in the development of new therapeutic agents. Its availability in pure form and suitable packaging makes it accessible for a wide range of experimental applications, supporting innovation in both academic and industrial research sectors.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePeptide Synthesis: This compound is ideal for synthesizing complex peptides due to its reactivity and structural versatility, enabling the creation of bioactive molecules.\u003c\/li\u003e\n\u003cli\u003eDrug Discovery: It is used in the development of therapeutic agents, as it allows for the modification of amino acid sequences to enhance drug efficacy.\u003c\/li\u003e\n\u003cli\u003eBiochemical Analysis: Its role in protein structure studies makes it valuable for understanding molecular interactions and functional properties.\u003c\/li\u003e\n\u003cli\u003eBiotechnology Research: It supports the creation of modified amino acids, which are essential in the development of novel biotechnological applications.\u003c\/li\u003e\n\u003cli\u003eOrganic Chemistry Studies: Its chemical stability and reactivity make it a key reagent in synthetic pathways for advanced organic chemistry experiments.\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: 114676-69-6\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Peptide Chemistry\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid, crystalline or powder depending on packaging\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 and prevent degradation. It is recommended to keep it in airtight containers to minimize exposure to moisture and air, which can affect its reactivity. Due to its high reactivity, it should be handled with care in a well-ventilated laboratory setting, using appropriate personal protective equipment such as gloves and safety goggles. Avoid direct contact with skin and eyes, and ensure proper disposal of any unused material in accordance with local safety regulations. Proper storage and handling are essential to ensure the compound remains effective and safe for use in laboratory applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085906948314,"sku":"TCI2510B585712620","price":683000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085906981082,"sku":"TCI2510B585712621","price":1541000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5857.jpg?v=1769180240"},{"product_id":"tci2510b588712658","title":"TCI B5887 87691-27-8 cis-N-(tert-Butoxycarbonyl)-4-hydroxy-L-proline","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B5887 is cis-N-(tert-Butoxycarbonyl)-4-hydroxy-L-proline, a derivative of the amino acid proline in which the ring nitrogen has been protected with a tert-butoxycarbonyl (Boc) group and which carries a hydroxyl group at the 4-position in the cis orientation. The compound belongs to the family of peptide chemistry raw materials that are very frequently used as chiral building blocks in stepwise peptide synthesis, both on solid phase and in solution phase. The presence of two functional groups of differing reactivity, namely a free carboxylic acid and a secondary hydroxyl, makes this material a flexible starting point for chemists who wish to construct more elaborate molecular frameworks in a controlled and deliberate manner.\u003c\/p\u003e\n\u003cp\u003eThe characteristic that makes this material a preferred choice is its stereochemical purity. The compound is the cis isomer of 4-hydroxyproline, that is, the epimer of the naturally occurring trans-configured hydroxyproline, and it therefore gives researchers access to a different folding pattern of the pyrrolidine ring. That difference in hydroxyl orientation has been shown to influence the ring puckering preference and, ultimately, the conformation of the peptide chain built from it. The Boc protecting group adds a further practical advantage, since it masks the ring nitrogen during coupling steps and can be removed under acidic conditions without disturbing the stereocentres of the molecule, allowing the synthetic sequence to be planned with confidence.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, a building block of this type is typically found in university research groups, pharmaceutical development units, and contract research facilities that work on peptide synthesis and medicinal chemistry programmes. It is generally ordered in modest quantities for exploratory and method-development work rather than for bulk production, and is handled within a standard synthetic organic chemistry setup equipped with a fume hood, an analytical balance, and facilities for chromatographic purification and structural confirmation of the products obtained.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eStepwise solid-phase peptide synthesis, where the Boc-protected ring nitrogen allows the residue to be introduced into a growing chain without side reactions at the amine, while the free carboxylic acid serves as the coupling handle.\u003c\/li\u003e\n\u003cli\u003eSolution-phase peptide assembly, in which the compound acts as a defined chiral building block that can be coupled, deprotected, and extended through a planned sequence of transformations under conventional organic synthesis conditions.\u003c\/li\u003e\n\u003cli\u003eConformational studies of peptide chains, because the cis orientation of the 4-hydroxyl group alters pyrrolidine ring puckering and therefore lets researchers probe how proline stereochemistry shapes the overall peptide fold.\u003c\/li\u003e\n\u003cli\u003eMedicinal chemistry scaffold construction, where the secondary hydroxyl offers a selective attachment point for further derivatisation while the carboxylic acid remains available for amide bond formation elsewhere in the molecule.\u003c\/li\u003e\n\u003cli\u003ePreparation of non-natural proline analogues and peptidomimetics, since this epimer of natural trans-hydroxyproline gives access to structural variants that cannot be obtained directly from the naturally occurring amino acid.\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: 87691-27-8\u003c\/li\u003e\n\u003cli\u003eChemical name: cis-N-(tert-Butoxycarbonyl)-4-hydroxy-L-proline\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Peptide Chemistry\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in the catalogue pack sizes offered by the manufacturer for this item\u003c\/li\u003e\n\u003cli\u003eStorage: keep in the closed original container under the conditions stated on the manufacturer's label\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the container tightly closed in a cool, dry, and well-ventilated place, away from heat sources, direct sunlight, and moisture, following the storage conditions indicated on the manufacturer's label. Keep the material in its original container or in a chemically compatible, clearly labelled vessel, and close it promptly after each use to limit exposure to atmospheric moisture. Handle the compound in a fume hood using standard laboratory personal protective equipment, including safety glasses, gloves, and a laboratory coat. Weigh and transfer the solid carefully to avoid generating dust, avoid contact with skin and eyes, and wash hands thoroughly after handling. Consult the manufacturer's safety data sheet before use, and dispose of residues and contaminated materials in accordance with applicable laboratory waste procedures.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085908455642,"sku":"TCI2510B588712658","price":1112000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085908488410,"sku":"TCI2510B588712659","price":3257000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5887.jpg?v=1769180241"},{"product_id":"tci2510b588812660","title":"TCI B5888 866323-14-0 Belinostat","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBelinostat (TCI B5888) is a potent hydroxamate-based histone deacetylase (HDAC) inhibitor supplied as a high-purity pharmaceutical research reagent for experimental use. It is primarily employed in preclinical oncology studies to investigate epigenetic mechanisms, gene expression modulation, and apoptosis induction in various cancer cell lines. This product serves as a valuable tool in HDAC inhibitor screening, drug resistance research, and combination therapy development.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mg","offer_id":48085908521178,"sku":"TCI2510B588812660","price":2197000.0,"currency_code":"IDR","in_stock":true},{"title":"100mg","offer_id":48085908553946,"sku":"TCI2510B588812661","price":7193000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5888_d63ea2ae-929a-4256-92e9-e030d244bc08.jpg?v=1767863756"},{"product_id":"tci2510b590212675","title":"TCI B5902 581065-94-3 tert-Butyl 1-(Tosyloxy)-3,6,9,12-tetraoxapentadecan-15-oate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B5902 tert-Butyl 1-(Tosyloxy)-3,6,9,12-tetraoxapentadecan-15-oate is a heterobifunctional PEG linker designed for PEGylation applications in chemical biology research. This compound features a tosyl leaving group at one terminus for nucleophilic substitution and a tert-butyl ester-protected carboxylic acid at the other, enabling selective conjugation to biomolecules such as proteins, peptides, or small-molecule drugs. It is commonly employed in the development of drug conjugates, drug delivery systems, and biomolecular interaction studies.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085909111002,"sku":"TCI2510B590212675","price":5276000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085909143770,"sku":"TCI2510B590212676","price":17767000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5902_279b9e4a-3917-46e4-b6f3-938443d79391.jpg?v=1767863803"},{"product_id":"tci2510b592612697","title":"TCI B5926 234081-98-2 tert-Butyl Hydrogen Dodecanedioate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e*tert*-Butyl Hydrogen Dodecanedioate (CAS 234081-98-2) is a mono-protected dodecanedioic acid derivative widely used as a non-heterocyclic building block in organic synthesis. The compound features a free carboxylic acid group and a *tert*-butyl-protected counterpart, enabling selective and sequential synthetic transformations. This versatile reagent is commonly employed in peptide synthesis, bioconjugate chemistry, and the development of functional polymeric materials.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085910061274,"sku":"TCI2510B592612697","price":2878000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085910094042,"sku":"TCI2510B592612698","price":10651000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5926_240b4309-21b5-4cde-9ad3-7272c63dbd24.jpg?v=1767863872"},{"product_id":"tci2510b592712699","title":"TCI B5927 234082-00-9 tert-Butyl Hydrogen Tetradecanedioate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003etert-Butyl Hydrogen Tetradecanedioate is a mono-protected diester building block featuring one free carboxylic acid group and one tert-butyl protected carboxyl group, enabling selective stepwise reactions in complex molecule construction. This compound is widely utilized in peptide synthesis, bioactive molecule development, and pharmaceutical research for constructing compound libraries. Its tert-butyl protecting group can be readily removed under mild acidic conditions, making it an ideal choice for orthogonal protection strategies in multi-step organic synthesis.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085910126810,"sku":"TCI2510B592712699","price":4115000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5927.jpg?v=1767092950"},{"product_id":"tci2510b592812700","title":"TCI B5928 843666-40-0 18-(tert-Butoxy)-18-oxooctadecanoic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B5928 18-(tert-Butoxy)-18-oxooctadecanoic Acid (CAS 843666-40-0) is a non-heterocyclic building block featuring a long-chain octadecanoic acid backbone with a tert-butyl ester protecting group. This compound serves as a versatile intermediate in organic synthesis for constructing lipid-based molecules, functional surfactants, and bioconjugation precursors. The acid-labile tert-butoxy protection allows selective deprotection under mild conditions, making it suitable for multi-step synthetic strategies in medicinal chemistry and materials research.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"250mg","offer_id":48085910225114,"sku":"TCI2510B592812700","price":1566000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48085910257882,"sku":"TCI2510B592812701","price":5932000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5928_e8b222ac-d93c-42c2-bae3-2c84f28ba3b9.jpg?v=1767863881"},{"product_id":"tci2510b597112753","title":"TCI B5971 120638-55-3 Bromfenac Sodium Sesquihydrate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBromfenac Sodium Sesquihydrate is a potent COX-2 inhibitor widely utilized in biochemical and pharmacological research. It serves as a selective non-steroidal anti-inflammatory agent for studying arachidonic acid metabolism and prostaglandin biosynthesis pathways. This compound is commonly applied in enzyme inhibition assays, COX-2 expression studies, and as a reference standard in ophthalmic formulation development.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085912518874,"sku":"TCI2510B597112753","price":3686000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5971.jpg?v=1771057971"},{"product_id":"tci2510b600712796","title":"TCI B6007 1190-53-0 Buformin Hydrochloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBuformin Hydrochloride is a biguanide-class pharmaceutical research reagent used in experimental studies on glucose metabolism and insulin regulation. It is commonly applied in biochemical and pharmacological research focusing on AMPK signaling pathways, hepatic gluconeogenesis inhibition, and cellular glucose uptake mechanisms. This product is intended strictly for laboratory and experimental use, supporting preclinical investigations in metabolic disorders and exploratory oncology research.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"50mg","offer_id":48085914452186,"sku":"TCI2510B600712796","price":1868000.0,"currency_code":"IDR","in_stock":true},{"title":"250mg","offer_id":48085914484954,"sku":"TCI2510B600712797","price":6437000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6007.jpg?v=1769144657"},{"product_id":"tci2510b605312855","title":"TCI B6053 58816-69-6 SB 297006","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6053 (CAS 58816-69-6) is a high-quality biochemical compound supplied by Tokyo Chemical Industry, categorized under amino acids and biochemical reagents for life science research. This product is widely used in pharmacological studies involving receptor-ligand interactions, enzyme inhibition assays, and cellular signaling pathway investigations. It serves as a reliable reference standard or research tool in both academic and industrial laboratory settings.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5mg","offer_id":48085916909786,"sku":"TCI2510B605312855","price":3534000.0,"currency_code":"IDR","in_stock":true},{"title":"25mg","offer_id":48085916942554,"sku":"TCI2510B605312856","price":12367000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6053.jpg?v=1768815963"},{"product_id":"tci2510b605712863","title":"TCI B6057 50654-94-9 (tert-Butoxycarbonyl)-D-histidine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(tert-Butoxycarbonyl)-D-histidine (Boc-D-His-OH) is a protected D-histidine derivative with a Boc group attached to its amino terminus, serving as an essential building block for peptide synthesis. This high-purity reagent from TCI is commonly used in solid-phase and solution-phase peptide synthesis to introduce D-histidine residues into peptide chains, particularly for studies on stereochemical effects on biological activity. It finds broad application in peptide chemistry research, including the development of modified peptides, cyclic peptides, and peptide-based drug candidates with enhanced enzymatic stability.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085917204698,"sku":"TCI2510B605712863","price":1213000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085917237466,"sku":"TCI2510B605712864","price":4140000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6057.jpg?v=1768204481"},{"product_id":"tci2510b607412881","title":"TCI B6074 51871-62-6 N-(tert-Butoxycarbonyl)-L-beta-homophenylalanine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6074 N-(tert-Butoxycarbonyl)-L-beta-homophenylalanine (CAS 51871-62-6) is a Boc-protected beta-homologated phenylalanine derivative widely used as a building block in peptide synthesis. Its beta-homo backbone confers enhanced proteolytic stability and distinct conformational properties to synthetic peptides, making it valuable in chemical biology research and peptide drug development. Available in 250mg and 1g packaging, this high-purity reagent is ideal for both solid-phase and solution-phase peptide chemistry applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"250mg","offer_id":48085917827290,"sku":"TCI2510B607412881","price":2524000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48085917860058,"sku":"TCI2510B607412882","price":6310000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6074.jpg?v=1771058403"},{"product_id":"tci2510b608512896","title":"TCI B6085 4481-62-3 Betulonic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBetulonic Acid (CAS 4481-62-3) is a pentacyclic triterpenoid compound supplied by TCI, primarily utilized as a reference reagent in pharmaceutical and life science research. It is widely employed in experimental studies involving anti-inflammatory activity, cytotoxicity assays against cancer cell lines, and antiviral potential evaluation. This product is intended exclusively for laboratory research purposes and serves as a reliable standard for chromatographic analysis and synthetic derivatization of betulinic acid analogs.\u003c\/p\u003e\n\u003cp\u003e---\u003c\/p\u003e","brand":"TCI","offers":[{"title":"50mg","offer_id":48085918580954,"sku":"TCI2510B608512896","price":5250000.0,"currency_code":"IDR","in_stock":true},{"title":"250mg","offer_id":48085918613722,"sku":"TCI2510B608512897","price":16733000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6085.jpg?v=1768204482"},{"product_id":"tci2510b608812900","title":"TCI B6088 155976-13-9 N-(tert-Butoxycarbonyl)-L-cyclopropylglycine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI's N-(tert-Butoxycarbonyl)-L-cyclopropylglycine (Boc-L-Cpg) is a Boc-protected unnatural amino acid widely employed as a key building block in peptide synthesis. The tert-butoxycarbonyl group provides temporary N-terminal protection during solid-phase or solution-phase peptide coupling, while the cyclopropyl side chain introduces conformational rigidity into the peptide backbone. This compound is particularly valuable in chemical biology research for designing metabolically stable, constrained peptides used in enzyme inhibitor development, structure-activity relationship studies, and protein-protein interaction modulation.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48085919269082,"sku":"TCI2510B608812900","price":1465000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48085919301850,"sku":"TCI2510B608812901","price":4392000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6088.jpg?v=1768204483"},{"product_id":"tci2510b610112917","title":"TCI B6101 15706-73-7 Butyl 2-Methylbutyrate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eButyl 2-Methylbutyrate is a non-heterocyclic ester building block suitable for organic synthesis and a variety of laboratory research applications. This compound serves as a versatile precursor in esterification and transesterification reactions, as well as in the preparation of ester-based derivatives. It is also relevant to flavor and fragrance studies, where its volatile ester profile supports research in food chemistry and sensory science.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mL","offer_id":48085920022746,"sku":"TCI2510B610112917","price":733000.0,"currency_code":"IDR","in_stock":true},{"title":"100mL","offer_id":48085920055514,"sku":"TCI2510B610112918","price":1718000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6101_24ba5377-6e84-495d-9733-485cb550a980.jpg?v=1767864545"},{"product_id":"tci2510b611212931","title":"TCI B6112 73536-69-3 Bifendate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBifendate (CAS 73536-69-3) is a synthetic organic compound widely utilized in pharmaceutical research as a reference reagent and a key building block for drug development studies. It is commonly applied in pharmacological investigations focusing on hepatoprotective, anti-inflammatory, and anti-fibrotic mechanisms, serving as a reference standard in both in vitro and in vivo experimental models. This product, supplied by TCI, is intended strictly for research and experimental use in laboratory settings.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48085920579802,"sku":"TCI2510B611212931","price":1894000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085920612570,"sku":"TCI2510B611212932","price":6537000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6112_2f52f9c5-3f23-4df1-a7df-45dba3f998f0.jpg?v=1767864581"},{"product_id":"tci2510b611612934","title":"TCI B6116 10276-85-4 Benzyl Octanoate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6116 Benzyl Octanoate (CAS 10276-85-4) is a high-purity non-heterocyclic building block ester compound intended for laboratory research and organic synthesis applications. This chemical serves as a reliable precursor for the development of derivative compounds and can be employed as an analytical reference standard in various experimental workflows. It is commonly utilized in fragrance chemistry studies, esterification reaction modeling, and molecular interaction research within both academic and industrial laboratory settings.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48085920710874,"sku":"TCI2510B611612934","price":1465000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6116.jpg?v=1767093197"},{"product_id":"tci2510b612312939","title":"TCI B6123 2156642-70-3 BIP","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6123 (CAS 2156642-70-3) is a high-purity BIP (dipyrromethene boron complex) dye specifically developed for photonic materials research. This compound belongs to the dipyrromethene dye family, which is widely recognized for its excellent photostability and high fluorescence quantum yield, making it suitable for applications such as fluorescent probes in bioimaging, active layers in organic light-emitting diodes (OLEDs), and organic laser dyes. It is also utilized in the development of optical sensors and organic-based solar energy conversion systems.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5mg","offer_id":48085920907482,"sku":"TCI2510B612312939","price":2373000.0,"currency_code":"IDR","in_stock":true},{"title":"25mg","offer_id":48085920940250,"sku":"TCI2510B612312940","price":8279000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6123.jpg?v=1768815985"},{"product_id":"tci2510b614812972","title":"TCI B6148 54613-99-9 Boc-Lys(2-Cl-Z)-OH","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBoc-Lys(2-Cl-Z)-OH is a doubly protected lysine derivative widely employed as a building block in solid-phase peptide synthesis (SPPS). The Boc group protects the α-amino terminus while the 2-Cl-Z group safeguards the ε-amino side chain, enabling selective orthogonal deprotection during peptide chain elongation. This high-purity TCI reagent is suitable for the synthesis of branched peptides, cyclic peptides, and peptide conjugates in pharmaceutical and biochemical research settings.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48085922119898,"sku":"TCI2510B614812972","price":808000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085922152666,"sku":"TCI2510B614812973","price":2550000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6148.jpg?v=1768204485"},{"product_id":"tci2510b616512996","title":"TCI B6165 155206-00-1 Bimatoprost","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBimatoprost is a synthetic prostamide analog that acts as a prostaglandin F2α (FP) receptor agonist, widely utilized in biochemical and pharmacological research involving lipid signaling pathways and intraocular pressure regulation. Common research applications include glaucoma studies, hair follicle growth investigations, and adipocyte differentiation assays. This high-purity reagent from TCI is suitable for in vitro cell-based assays and receptor binding studies in life science laboratories.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5mg","offer_id":48085923135706,"sku":"TCI2510B616512996","price":5224000.0,"currency_code":"IDR","in_stock":true},{"title":"25mg","offer_id":48085923168474,"sku":"TCI2510B616512997","price":18826000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6165.jpg?v=1771058210"},{"product_id":"tci2510b627213107","title":"TCI B6272 165599-63-3 BDP FL (1mg*3)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6272 BDP FL is a boron-dipyrromethene (BODIPY) fluorescent dye specifically designed for fluorescence labeling and optical material research applications. This dye offers bright green fluorescence, high quantum yield, and excellent photostability, making it suitable for fluorescence microscopy, flow cytometry, and biosensor development. It is also widely employed in photonic material studies, dye-sensitized solar cells (DSSC), and the fabrication of fluorescent probes for metal ion and intracellular pH detection.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1set","offer_id":48085927395546,"sku":"TCI2510B627213107","price":4366000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6272.jpg?v=1769144641"},{"product_id":"tci2510b629513133","title":"TCI B6295 32602-11-2 2,3-Bis(bromomethyl)quinoxaline-6-carboxylic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2,3-Bis(bromomethyl)quinoxaline-6-carboxylic Acid is a chemical compound widely used in laboratory settings for the synthesis of complex heterocyclic compounds. This material plays a crucial role in organic chemistry research, particularly in the formation of quinoxaline-based structures. Its unique molecular structure makes it a valuable tool for chemists seeking to develop new materials and pharmaceuticals. Due to its reactivity and structural versatility, it is frequently employed in various synthetic pathways to build more intricate molecular frameworks.\u003c\/p\u003e\n\u003cp\u003eThe compound is characterized by the presence of bromomethyl groups at the 2 and 3 positions of the quinoxaline ring, which significantly enhances its reactivity in substitution and covalent reactions. The stable quinoxaline core ensures that the compound maintains its structural integrity during chemical transformations, making it a preferred choice for precise synthetic applications. Its reactivity and stability are key factors that make it an essential component in advanced chemical research.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used by chemists, pharmacologists, and material scientists for the development of new drugs and industrial chemicals. Its availability in the local market supports ongoing research efforts, enabling scientists to conduct experiments with high precision and efficiency. The compound’s role in creating complex molecular structures is vital for advancing scientific knowledge in multiple fields.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of quinoxaline derivatives due to its reactive bromomethyl groups and stable core structure.\u003c\/li\u003e\n\u003cli\u003eDevelopment of pharmaceutical compounds as a building block for drug molecule design and modification.\u003c\/li\u003e\n\u003cli\u003eCreation of advanced materials through covalent bonding reactions that require structural stability and reactivity.\u003c\/li\u003e\n\u003cli\u003eResearch in heterocyclic chemistry for the synthesis of complex ring systems with specific functional groups.\u003c\/li\u003e\n\u003cli\u003eInvestigation of chemical reactivity in substitution reactions for the preparation of functionalized compounds.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 32602-11-2\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct sunlight 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 to maintain its chemical integrity and prevent degradation. It is recommended to use airtight containers to protect it from moisture and air exposure. Due to its reactivity, it should be handled in a well-ventilated area, preferably under a fume hood, to minimize exposure. Proper personal protective equipment, such as gloves and safety goggles, should be worn when handling the material. Avoid contact with incompatible substances, and ensure that storage conditions are consistent with standard laboratory safety protocols. Regular monitoring of storage conditions is advised to ensure the compound remains stable and suitable for use in research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"10mg","offer_id":48085929165018,"sku":"TCI2510B629513133","price":3636000.0,"currency_code":"IDR","in_stock":true},{"title":"50mg","offer_id":48085929197786,"sku":"TCI2510B629513134","price":12593000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6295_17e7f8af-4c19-4865-924d-b9b5a23409a8.jpg?v=1767865175"},{"product_id":"tci2510b636213230","title":"TCI B6362 13726-76-6 Boc-Arg-OH","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6362, Boc-Arg-OH (CAS 13726-76-6), is an Nα-Boc-protected arginine derivative intended for peptide chemistry applications. The tert-butoxycarbonyl group masks the α-amino function so that coupling reactions proceed selectively, and it can subsequently be removed under acidic conditions within a Boc-based synthetic strategy. Arginine residues contribute the guanidine side chain that underpins molecular recognition, charge-driven interactions, and the design of cell-penetrating peptides. AMI Scientific offers this TCI reagent in 1 g and 5 g pack sizes for solid-phase and solution-phase peptide synthesis in research laboratories.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eImaizumi et al. (2000). Anterograde axonal transport of Boc-Arg-Val-Arg-Arg-MCA hydrolyzing enzyme in rat sciatic nerves: cleavage occurs between basic residues. \u003cem\u003eBiochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/s0167-4838(99)00239-3\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/s0167-4838(99)00239-3\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085932933338,"sku":"TCI2510B636213230","price":860000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085932966106,"sku":"TCI2510B636213231","price":2903000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6362.jpg?v=1769180264"},{"product_id":"tci2510b636413234","title":"TCI B6364 5545-52-8 Z-Asp(OtBu)-OH","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6364, Z-Asp(OtBu)-OH (CAS 5545-52-8), is a doubly protected aspartic acid derivative bearing a benzyloxycarbonyl group on the amino function and a tert-butyl ester on the side-chain carboxyl. This orthogonal arrangement lets chemists remove each protecting group under different conditions — hydrogenolysis for the Z group and acid for the tert-butyl ester — giving precise control over each synthetic step. Keeping the side chain masked helps suppress unwanted cyclisation and branching at aspartate residues during chain elongation. AMI Scientific supplies this TCI peptide-chemistry reagent in 5 g and 25 g pack sizes for research use.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eKates et al. (1995). Rearrangement of Glu(OtBu)- and Asp(OtBu)-containing peptides upon fluoride treatment in solid-phase synthesis. \u003cem\u003eLetters in Peptide Science\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1007\/bf00127267\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1007\/bf00127267\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eHamzé dkk. (2003). Synthesis of (R) and (S) enantiomers of Fmoc-protected 1,2,4-oxadiazole-containing β3-amino acids from Fmoc-(R)-β-HAsp(OtBu)-OH. \u003cem\u003eTetrahedron Letters\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/s0040-4039(03)01471-0\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/s0040-4039(03)01471-0\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48085933097178,"sku":"TCI2510B636413234","price":1112000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085933129946,"sku":"TCI2510B636413235","price":3761000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6364.jpg?v=1768197087"},{"product_id":"tci2510b638313259","title":"TCI B6383 70359-46-5 Brimonidine Tartrate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6383 Brimonidine Tartrate (CAS 70359-46-5) is the tartrate salt of a selective α2-adrenergic receptor agonist, offered strictly as a pharmaceutical research reagent for experimental use. The salt form improves aqueous handling, which makes stock solution preparation for binding assays, functional studies, and formulation work more convenient. It is widely used as a reference compound in adrenergic signalling research and as a model substance in analytical method development. Available in 100 mg and 1 g sizes, it should be kept cool, dry, and light-protected, and must never be used for human or veterinary therapeutic purposes.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003e(2024). Brimonidine tartrate: risk of serious corneal opacity. \u003cem\u003eReactions Weekly\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1007\/s40278-024-63460-z\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1007\/s40278-024-63460-z\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eDinç (2017). Continuous Wavelet Transform Methods for the Simultaneous Quantification of Brimonidine Tartrate and Timolol Maleate in an Eye Drop Formulation. \u003cem\u003eBioequivalence \u0026amp; Bioavailability International Journal\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.23880\/beba-16000105\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.23880\/beba-16000105\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eKim (2024). Charles Bonnet Syndrome Precipitated by Brimonidine Tartrate. \u003cem\u003eJournal of Medical Optometry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.62055\/xqbniayihzdr\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.62055\/xqbniayihzdr\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48085937160410,"sku":"TCI2510B638313259","price":934000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48085937193178,"sku":"TCI2510B638313260","price":5527000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6383.jpg?v=1768197091"},{"product_id":"tci2510b641713303","title":"TCI B6417 464-43-7 (+)-Borneol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6417 (+)-Borneol (CAS 464-43-7) is a bicyclic monoterpene alcohol supplied as a crude medicine ingredient intended for research and experimental use. It is commonly employed as a reference compound in phytochemical studies and in the characterisation of plant-derived extracts. The single-enantiomer form also makes it useful for stereochemistry-oriented investigations and for the synthesis of bornyl derivatives. Store the material in a tightly closed container in a cool, dry place away from light, and always consult the manufacturer's safety data sheet before handling.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMa et al. (2023). Comparison of pharmacological activity and safety of different stereochemical configurations of borneol: L-borneol, D-borneol, and synthetic borneol. \u003cem\u003eBiomedicine \u0026amp; Pharmacotherapy\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.biopha.2023.114668\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.biopha.2023.114668\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003e(2016). Preparation of borneol loaded hollow mesoporous silica nanoparticles and effect on borneol volatility. \u003cem\u003eChina Journal of Chinese Materia Medica\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.4268\/cjcmm20161510\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.4268\/cjcmm20161510\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eMa et al. (2017). Microcalorimetric study of the effect of l-borneol, d-borneol and synthetic borneol on the growth of P. aeruginosa. \u003cem\u003eJournal of Thermal Analysis and Calorimetry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1007\/s10973-017-6627-3\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1007\/s10973-017-6627-3\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085939028186,"sku":"TCI2510B641713303","price":1062000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085939060954,"sku":"TCI2510B641713304","price":3660000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6417.jpg?v=1768193707"},{"product_id":"tci2510b643713325","title":"TCI B6437 115951-16-1 1-[(tert-Butoxycarbonyl)amino]cyclohexanecarboxylic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6437 1-[(tert-Butoxycarbonyl)amino]cyclohexanecarboxylic Acid (CAS 115951-16-1) is a Boc-protected cyclic amino acid in which the amino and carboxyl groups share a quaternary carbon. Its rigid cyclohexane framework makes it valuable for designing conformationally constrained peptides and peptide analogues. The pre-installed Boc group saves a protection step and can be removed under well-established acidic conditions. Store the solid tightly sealed in a cool, dry place away from strong acids, and refer to the manufacturer's safety data sheet before handling.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBadland et al. (2010). An improved synthesis of (1R,3S)-3-[(tert-butoxycarbonyl)amino]cyclohexanecarboxylic acid. \u003cem\u003eTetrahedron: Asymmetry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.tetasy.2010.04.049\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.tetasy.2010.04.049\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eKadyrov et al. (2021). Convenient Synthesis of (R)-3-[(tert-Butoxycarbonyl)amino]piperidine and (R)-3-[(tert-Butoxycarbonyl)amino]azepane. \u003cem\u003eSynthesis\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1055\/a-1526-7657\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1055\/a-1526-7657\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003e(2012). Discussion Addendum For: Efficient Asymmetric Synthesis of N-tert-Butoxycarbonyl a-Amino Acids using 4-tert-Butoxycarbonyl-5,6-Diphenylmorpholin-2-one:. \u003cem\u003eOrganic Syntheses\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.15227\/orgsyn.089.0394\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.15227\/orgsyn.089.0394\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085939912922,"sku":"TCI2510B643713325","price":1742000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085939945690,"sku":"TCI2510B643713326","price":6082000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6437_d1e882c4-5446-4e40-b77f-bf0c8053c12b.jpg?v=1767865775"},{"product_id":"tci2510b644313334","title":"TCI B6443 113558-15-9 Baohuoside I","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6443 Baohuoside I (CAS 113558-15-9) is a naturally derived prenylated flavonoid glycoside supplied strictly for research and experimental use. It is widely used as a reference compound in phytochemical profiling and in HPLC or LC-MS analysis of plant extracts. The 25 mg pack size suits analytical method development and small-scale biological studies. Store the vial tightly closed under cold, dry, light-protected conditions and allow it to reach room temperature before opening to prevent condensation.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eZhang et al. (2019). Effect of 2″-O-Rhamnosyl Icariside II, Baohuoside I and Baohuoside II in Herba Epimedii on Cytotoxicity Indices in HL-7702 and HepG2 Cells. \u003cem\u003eMolecules\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.3390\/molecules24071263\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.3390\/molecules24071263\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eMa et al. (2005). Baohuoside-1 inhibits activated T cell proliferation at G1–S phase transition. \u003cem\u003eTransplant Immunology\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.trim.2005.05.002\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.trim.2005.05.002\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eLin et al. (2026). Baohuoside I Combated Cryptocaryon irritans via Dual Targeting of Parasite Apoptosis and Host Defense Enhancement. \u003cem\u003eAntioxidants\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.3390\/antiox15030396\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.3390\/antiox15030396\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mg","offer_id":48085940502746,"sku":"TCI2510B644313334","price":7345000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6443.jpg?v=1767093684"},{"product_id":"tci2510b646713360","title":"TCI B6467 61-12-1 Dibucaine Hydrochloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eDibucaine Hydrochloride is the water-soluble salt form of a well-characterised quinoline carboxamide local anaesthetic compound. It is widely recognised in laboratories as the selective inhibitor used in the classical dibucaine number assay for butyrylcholinesterase variants. Researchers also employ it as a reference compound in enzyme inhibition kinetics and membrane interaction studies. Supplied by TCI in 5 g and 25 g sizes, the material is intended for research and experimental use only.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eYamadori et al. (2009). Allergic contact dermatitis from dibucaine hydrochloride, chlorpheniramine maleate, and naphazoline hydrochloride in an over‐the‐counter topical antiseptic. \u003cem\u003eContact Dermatitis\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1111\/j.1600-0536.2009.01556.x\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1111\/j.1600-0536.2009.01556.x\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eLaPlanche (1991). 13C NMR Chemical Shift Assignments in Dibucaine and Dibucaine Hydrochloride Determined by Two-Dimensional NMR Spectroscopy. \u003cem\u003eSpectroscopy Letters\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1080\/00387019108020651\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1080\/00387019108020651\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eYOKOYAMA (1997). Surface Potential of Mixed Micelles Composed of Dibucaine Hydrochloride and Heptaethylene Glycol Dodecyl Ether.. \u003cem\u003eChemical and Pharmaceutical Bulletin\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1248\/cpb.45.2104\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1248\/cpb.45.2104\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48085941518554,"sku":"TCI2510B646713360","price":1010000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085941551322,"sku":"TCI2510B646713361","price":3484000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6467.jpg?v=1768816058"},{"product_id":"tci2510b648513387","title":"TCI B6485 149-64-4 Buscopan","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6485, Buscopan or hyoscine butylbromide (CAS 149-64-4), is a quaternary ammonium derivative of a tropane alkaloid and a well-known muscarinic receptor antagonist. Its high polarity and good aqueous solubility make it convenient for preparing stock solutions in in vitro pharmacology work and for use as an analytical reference standard. Common laboratory applications include HPLC and LC-MS method development, smooth muscle contraction studies, and natural product chemistry teaching. AMI Scientific supplies this TCI product in 1 g and 5 g packs strictly for research and analytical purposes, not for human diagnostic or therapeutic use.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSissons et al. (1991). The ocular effects of hyoscine-n-butylbromide (“Buscopan”) in radiological practice. \u003cem\u003eThe British Journal of Radiology\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1259\/0007-1285-64-763-584\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1259\/0007-1285-64-763-584\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eZitvast (2023). Buscopan tegen Reutelen. \u003cem\u003eNursing\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1007\/s41193-023-0736-0\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1007\/s41193-023-0736-0\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003e(1992). A comparison of intravenous and intramuscular buscopan for barium meal examinations. \u003cem\u003eClinical Radiology\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/s0009-9260(05)80810-4\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/s0009-9260(05)80810-4\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085942894810,"sku":"TCI2510B648513387","price":1742000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085942927578,"sku":"TCI2510B648513388","price":5906000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6485.jpg?v=1768204505"},{"product_id":"tci2510b648613389","title":"TCI B6486 4530-18-1 Boc-DL-Phe-OH","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6486, Boc-DL-Phe-OH (CAS 4530-18-1), is racemic phenylalanine protected at the amino group with a tert-butoxycarbonyl group. The Boc group is stable to basic and nucleophilic conditions yet readily removed under acidic treatment, making this a dependable building block for solution- and solid-phase peptide synthesis. Its racemic nature makes it particularly cost-effective for coupling method development, chiral analysis reference work, and advanced teaching laboratories. AMI Scientific offers this TCI product in 25 g and 100 g pack sizes, to be stored cool, dry, and tightly closed.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eRodriguez et al. (1990). A general route to “carba” peptide bond replacements: Unequivocal synthesis of Boc--Phe-ψ(CH2-CH2)--Ala-OH and Boc--Phe-ψ(CH2-CH2)--Ala-OH.. \u003cem\u003eTetrahedron Letters\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/s0040-4039(00)97829-8\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/s0040-4039(00)97829-8\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eHayashi et al. (2014). Development of potent antagonists for formyl peptide receptor 1 based on Boc-Phe-d-Leu-Phe-d-Leu-Phe-OH. \u003cem\u003eBioorganic \u0026amp; Medicinal Chemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.bmc.2014.06.048\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.bmc.2014.06.048\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eKarle et al. (2002). Infinite pleated β-sheet formed by the β-hairpin Boc-β-Phe-β-Phe- d -Pro-Gly-β-Phe-β-Phe-OMe. \u003cem\u003eProceedings of the National Academy of Sciences\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1073\/pnas.022616499\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1073\/pnas.022616499\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48085942960346,"sku":"TCI2510B648613389","price":1566000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48085942993114,"sku":"TCI2510B648613390","price":4544000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6486.jpg?v=1769144627"},{"product_id":"tci2510b649413397","title":"TCI B6494 3601-66-9 Boc-DL-Phg-OH","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6494, Boc-DL-Phg-OH (CAS 3601-66-9), is racemic phenylglycine protected with a tert-butoxycarbonyl group at the amino position. With the aryl ring attached directly to the alpha carbon, phenylglycine offers greater conformational rigidity than phenylalanine and a well-documented tendency toward racemisation during coupling. This makes the DL form especially useful as a reference standard for chiral chromatography method development, coupling condition evaluation, and kinetic resolution studies, in addition to routine peptide synthesis. AMI Scientific supplies this TCI product in a 25 g pack, to be kept cool, dry, tightly closed, and away from strong acid vapours.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48085943255258,"sku":"TCI2510B649413397","price":1566000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6494.jpg?v=1768204508"},{"product_id":"tci2510b654413470","title":"TCI B6544 61-75-6 Bretylium Tosylate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBretylium tosylate (CAS 61-75-6) is a quaternary ammonium compound long recognised in the literature as an adrenergic neuron blocker that interferes with norepinephrine release from sympathetic nerve terminals. It is widely used as a reference pharmacological tool in cardiovascular and autonomic nervous system research, including studies of antiarrhythmic mechanisms and cardiac repolarisation. The material is supplied strictly for research and experimental use and is not intended for human diagnostic or therapeutic application. AMI Scientific offers a 25 mg pack size suitable for isolated tissue experiments and cell-based assays.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eFallen (2000). Bretylium Tosylate (UDATE—2000). \u003cem\u003eCardiac Electrophysiology Review\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1023\/a:1026583112967\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1023\/a:1026583112967\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eMuhammad et al. (1999). The effect of bretylium tosylate on ECG-guided pericardiocentesis. \u003cem\u003eAnnals of Emergency Medicine\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/s0196-0644(99)80198-x\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/s0196-0644(99)80198-x\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eDeBehnke (1991). Effects of bretylium tosylate during experimental cardiac arrest. \u003cem\u003eThe American Journal of Emergency Medicine\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/0735-6757(91)90064-q\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/0735-6757(91)90064-q\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mg","offer_id":48085946302682,"sku":"TCI2510B654413470","price":5527000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6544.jpg?v=1768204511"},{"product_id":"tci2510b654813475","title":"TCI B6548 33171-05-0 Bisdemethoxycurcumin","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBisdemethoxycurcumin (CAS 33171-05-0) is one of the three principal curcuminoids found in turmeric rhizome, differing from curcumin by the absence of methoxy groups on both aromatic rings. It is commonly used as a reference compound for curcuminoid profiling by HPLC or TLC, and for in vitro bioactivity studies where a single, defined curcuminoid is preferred over a crude extract. Curcuminoids are light sensitive and degrade under alkaline conditions, so the material should be stored cool, dry, and protected from light, with working solutions prepared fresh. AMI Scientific supplies it in a 1 g pack size for research and experimental use.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMohammadi et al. (2018). Inhibition of amyloid fibrillation of lysozyme by bisdemethoxycurcumin and diacetylbisdemethoxycurcumin. \u003cem\u003eBiophysical Chemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.bpc.2018.02.005\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.bpc.2018.02.005\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eLappichetpaiboon (2025). Anticandidal effects of bisdemethoxycurcumin \u0026amp; melatonin with dual light emitting diode in photodynamic therapy. \u003cem\u003ePhotodiagnosis and Photodynamic Therapy\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.pdpdt.2025.104797\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.pdpdt.2025.104797\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eJayaprakasha et al. (2006). Antioxidant activities of curcumin, demethoxycurcumin and bisdemethoxycurcumin. \u003cem\u003eFood Chemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.foodchem.2005.06.037\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.foodchem.2005.06.037\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085946630362,"sku":"TCI2510B654813475","price":2953000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6548.jpg?v=1767093878"},{"product_id":"tci2510b655013477","title":"TCI B6550 26166-92-7 5-Bromo-2-(2,6-dioxopiperidin-3-yl)isoindoline-1,3-dione","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e5-Bromo-2-(2,6-dioxopiperidin-3-yl)isoindoline-1,3-dione (CAS 26166-92-7) is a brominated phthalimide–glutarimide derivative used as a cereblon-binding ligand in targeted protein degradation research. Its aryl bromide handle is well suited to palladium-catalysed cross-couplings such as Suzuki and Buchwald–Hartwig reactions, allowing convenient linker attachment during PROTAC assembly. Because of the pharmacological sensitivity of the glutarimide class, the compound should be weighed with full personal protective equipment in a fume hood and stored cool, dry, and protected from light. AMI Scientific supplies it in 1 g and 5 g pack sizes strictly for laboratory research use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085946695898,"sku":"TCI2510B655013477","price":1742000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085946728666,"sku":"TCI2510B655013478","price":6840000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6550.jpg?v=1767093886"}],"url":"https:\/\/amiscientific.com\/en\/collections\/biokimia-dan-reagen-hayati.oembed?page=108","provider":"AMI Scientific","version":"1.0","type":"link"}