{"title":"Phytochemicals","description":"\u003cp\u003e\u003cstrong\u003ePhytochemicals\u003c\/strong\u003e — menghimpun senyawa metabolit sekunder yang berasal dari tumbuhan, seperti flavonoid, polifenol, alkaloid, terpenoid, dan karotenoid, yang berperan sebagai senyawa acuan pada berbagai studi kimia pangan, nutrisi, dan analisis komposisi bahan alam.\u003c\/p\u003e\u003cp\u003ePhytochemicals ini dipakai sebagai standar analitik pada kromatografi (HPLC, LC-MS) untuk mengidentifikasi dan mengukur kadar komponen bioaktif dalam ekstrak tumbuhan, makanan, atau suplemen. Peneliti nutrisi dan kimia pangan juga memanfaatkannya sebagai senyawa acuan pada uji aktivitas antioksidan in vitro, studi jalur biosintesis metabolit tumbuhan, serta pengembangan metode analisis komposisi bahan pangan fungsional.\u003c\/p\u003e\u003cp\u003eContoh produk dalam koleksi ini: \u003ca href=\"\/en\/products\/tci2510m012137673\"\u003eTCI M0121 90-05-1 Guaiacol\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b570012413\"\u003eTCI B5700 10309-37-2 Bakuchiol\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510g001131577\"\u003eTCI G0011 149-91-7 Gallic Acid\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b608512896\"\u003eTCI B6085 4481-62-3 Betulonic Acid\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510c230217033\"\u003eTCI C2302 458-37-7 Curcumin (Synthetic)\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b644313334\"\u003eTCI B6443 113558-15-9 Baohuoside I\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510a0443641\"\u003eTCI A0443 29883-15-6 Amygdalin\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b654813475\"\u003eTCI B6548 33171-05-0 Bisdemethoxycurcumin\u003c\/a\u003e.\u003c\/p\u003e\u003cp\u003ePerhatikan kemurnian analitik, sumber asal isolasi, serta bentuk kristal atau larutan standar yang sesuai untuk kebutuhan kalibrasi metode kromatografi pada analisis kandungan fitokimia dalam suatu sampel. 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 Nutrition Research, sering dipakai bersamaan dalam satu alur kerja laboratorium:\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-vitamins-nutrition-research\"\u003eVitamins [Nutrition Research]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-functional-food-research\"\u003eFunctional Food Research\u003c\/a\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eKembali ke \u003ca href=\"\/en\/collections\/tci-l3-nutrition-research\"\u003eNutrition Research\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":"tci2510b570012413","title":"TCI B5700 10309-37-2 Bakuchiol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBakuchiol is a naturally occurring meroterpene phenol isolated from *Psoralea corylifolia* seeds, widely employed as a reference standard in biochemical and pharmacological research. It is commonly applied in studies investigating retinol-like gene expression modulation, collagen and elastin synthesis, as well as antioxidant and anti-inflammatory activities. This compound also serves as a key material in natural cosmeceutical formulation development and antimicrobial screening assays.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"250mg","offer_id":48085897871578,"sku":"TCI2510B570012413","price":6269000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5700.jpg?v=1768815865"},{"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":5847000.0,"currency_code":"IDR","in_stock":true},{"title":"250mg","offer_id":48085918613722,"sku":"TCI2510B608512897","price":18635000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6085.jpg?v=1768204482"},{"product_id":"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":8180000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6443.jpg?v=1767093684"},{"product_id":"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":3289000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6548.jpg?v=1767093878"},{"product_id":"tci2510b683813743","title":"TCI B6838 218600-53-4 Bardoxolone Methyl","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6838 Bardoxolone Methyl (CDDO-Me, CAS 218600-53-4) is a synthetic oleanane triterpenoid widely used as a reference tool in oxidative stress and inflammation research. It is best known as a potent activator of the Keap1–Nrf2 pathway and a modulator of NF-κB-driven inflammatory signalling in cell models. Typical experiments involve preparing a DMSO stock, treating cultured cells, and measuring antioxidant response gene expression, phase II enzyme levels, or cytokine output. Supplied in a 250 mg pack, this biologically active solid should be weighed in a fume hood, stored cold and protected from light, and aliquoted to avoid repeated freeze–thaw cycles.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eYoshioka et al. (2025). Multi-Omics Reveal Antioxidant Effects of Bardoxolone Methyl in the Phase 2 Study of Bardoxolone Methyl in Patients with CKD and Type 2 Diabetes Study. \u003cem\u003eKidney360\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.34067\/kid.0000000853\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.34067\/kid.0000000853\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eKernel Networks Inc. (2019). A Clinical Pharmacology Study of Bardoxolone Methyl in Healthy Adults. \u003cem\u003eCase Medical Research\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.31525\/ct1-nct04023903\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.31525\/ct1-nct04023903\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eFu et al. (2013). Efficient and Scalable Synthesis of Bardoxolone Methyl (CDDO-methyl Ester). \u003cem\u003eOrganic Letters\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1021\/ol400399x\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1021\/ol400399x\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":"250mg","offer_id":48085957640410,"sku":"TCI2510B683813743","price":8826000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6838.jpg?v=1769144609"},{"product_id":"tci2510c000213908","title":"TCI C0002 331-39-5 Caffeic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0002 Caffeic Acid is a naturally occurring hydroxycinnamic acid found widely in coffee, fruits, vegetables, and medicinal plants. Its catechol moiety confers strong radical-scavenging and metal-chelating behavior, making it a common reference compound in antioxidant assays. It also serves as an HPLC standard for polyphenol quantification and as a useful non-heterocyclic building block for synthesis. Available in 5 g and 25 g packs, it should be stored cool, dry, and shielded from light to limit oxidative darkening.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eTosovic (2017). Spectroscopic features of caffeic acid: Theoretical study. \u003cem\u003eKragujevac Journal of Science\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.5937\/kgjsci1739099t\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.5937\/kgjsci1739099t\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eQin et al. (2021). Interaction between caffeic acid\/caffeic acid phenethyl ester and micellar casein. \u003cem\u003eFood Chemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.foodchem.2021.129154\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.foodchem.2021.129154\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eKhim Phin et al. (2009). In Vitro Synergy Effect of Syringic Acid, Caffeic Acid and 4-hydroxybenzoic Acid against Ganoderma boninense. \u003cem\u003eInternational Journal of Engineering and Technology\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.7763\/ijet.2009.v1.53\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.7763\/ijet.2009.v1.53\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":48085965308122,"sku":"TCI2510C000213908","price":957000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085965340890,"sku":"TCI2510C000213909","price":3177000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0002.jpg?v=1767094529"},{"product_id":"tci2510c001013918","title":"TCI C0010 464-49-3 (+)-Camphor","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0010 (+)-Camphor, CAS 464-49-3, is an enantiomerically defined bicyclic ketone widely used as a chiral pool starting material. Its rigid bornane framework provides a reliable steric environment for asymmetric induction, making it valuable for preparing chiral auxiliaries, ligands, and resolving agents. The reactive C-2 ketone allows straightforward conversion into oximes, imines, alcohols, and other functionalised derivatives. AMI Scientific supplies this TCI product in 25 g and 500 g pack sizes for both method development and routine synthetic work.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003e(2016). Camphor. \u003cem\u003eReactions Weekly\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1007\/s40278-016-16081-z\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1007\/s40278-016-16081-z\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eSahana et al. (2012). Camphor poisoning. \u003cem\u003eIndian Pediatrics\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1007\/s13312-012-0174-6\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1007\/s13312-012-0174-6\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eMONEY (1996). ChemInform Abstract: Remote Functionalization of Camphor: Application to Natural Product Synthesis. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.199649291\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.199649291\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":48085965701338,"sku":"TCI2510C001013918","price":507000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48085965734106,"sku":"TCI2510C001013919","price":2531000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0010.jpg?v=1767094541"},{"product_id":"tci2510c001113920","title":"TCI C0011 76-22-2 (+\/-)-Camphor","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0011 (+\/-)-Camphor, CAS 76-22-2, is the racemic form of the well-known bicyclic terpenoid ketone. It is intended for applications where optical purity is not required, serving as an economical non-heterocyclic building block for general synthetic work. The reactive carbonyl group readily undergoes reduction, oximation, and condensation reactions, while its ready sublimation makes it a classic teaching material. AMI Scientific provides this TCI product in 25 g and 500 g pack sizes for research and teaching laboratories alike.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eChan et al. (2009). Status epilepticus after topical application of a solution containing camphor. \u003cem\u003eEmergency Medicine Journal\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1136\/emj.2008.063198\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1136\/emj.2008.063198\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eYE et al. (1991). ChemInform Abstract: Selective Anodic Oxidation of Camphor.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.199142265\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.199142265\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eSTINSON (1998). Chiral camphor carries acetate in asymmetric condensation. \u003cem\u003eChemical \u0026amp; Engineering News Archive\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1021\/cen-v076n005.p029\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1021\/cen-v076n005.p029\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":48085965799642,"sku":"TCI2510C001113920","price":507000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48085965832410,"sku":"TCI2510C001113921","price":1857000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0011.jpg?v=1767094545"},{"product_id":"tci2510c001913937","title":"TCI C0019 56-25-7 Cantharidin","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCantharidin, with the CAS number 56-25-7, is a chemical compound widely utilized in biochemical and pharmacological experiments. It is a potent toxin and is commonly used as a testing agent in research focused on enzyme and receptor mechanisms. As an alkaloid, its complex structure makes it a valuable subject for structure-function studies. In the laboratory, it plays a critical role in assessing cellular responses to specific stimuli, particularly in toxicity and pharmacological effect investigations. Its unique ability to elicit specific biological responses makes it an essential tool for scientific research.\u003c\/p\u003e\n\u003cp\u003eCantharidin is preferred due to its chemical stability under controlled conditions and its ability to interact with various proteins and enzymes. These properties make it an effective tool for molecular interaction studies. Despite its stability, it is highly sensitive to environmental changes, which requires careful handling and storage to maintain its integrity. Its versatility in triggering specific biological responses further enhances its value in experimental settings. Researchers rely on its predictable behavior in controlled environments to obtain reliable and reproducible results.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Cantharidin is commonly used in biochemistry and pharmacology research. It is essential for studies involving cellular toxicity, enzyme inhibition, and receptor activation. Its application is particularly relevant in academic and research institutions where biochemical experiments are conducted. The compound's role in understanding molecular interactions and biological responses makes it a key component in many scientific investigations. Its use is well-established in both teaching and research laboratories across Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBiochemical Research: Cantharidin is used to study enzyme inhibition and receptor activation, providing insights into molecular interactions.\u003c\/li\u003e\n\u003cli\u003eToxicology Studies: Its potent toxicity makes it ideal for assessing cellular responses to toxic agents and evaluating drug effects.\u003c\/li\u003e\n\u003cli\u003ePharmacological Testing: The compound is employed to investigate the mechanisms of drug action and biological responses in controlled environments.\u003c\/li\u003e\n\u003cli\u003eStructural-Functional Analysis: Its complex alkaloid structure supports research on how molecular architecture influences biological activity.\u003c\/li\u003e\n\u003cli\u003eCellular Response Evaluation: Cantharidin helps researchers analyze how cells react to specific stimuli, particularly in toxicity and pharmacological studies.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 56-25-7\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 standard laboratory quantities\u003c\/li\u003e\n\u003cli\u003ePhysical form: Crystalline solid\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eCantharidin should be stored in a cool, dry place away from direct sunlight and moisture. It is recommended to use airtight containers to prevent exposure to air and humidity. Due to its sensitivity to environmental changes, it is important to maintain stable storage conditions to preserve its chemical integrity. Proper labeling and secure storage are essential to prevent accidental exposure. Laboratory personnel should wear appropriate personal protective equipment when handling this compound. Regular monitoring of storage conditions ensures that the material remains effective for research purposes.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48085966389466,"sku":"TCI2510C001913937","price":2924000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0019.jpg?v=1769144597"},{"product_id":"tci2510c007113999","title":"TCI C0071 94-41-7 Chalcone","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0071 Chalcone (CAS 94-41-7) is an α,β-unsaturated aromatic ketone that serves as a versatile building block in organic and medicinal chemistry. It is widely used as a Michael acceptor, a precursor to pyrazolines and flavanones, and a model substrate in asymmetric catalysis and photochemical studies. TCI offers the compound in a 25 g pack size suitable for routine synthetic work. Store it in a tightly closed container away from light and moisture, and handle with appropriate protective equipment.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePatil et al. (2010). ChemInform Abstract: Chalcone — A Versatile Molecule. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.201025251\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.201025251\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eLi et al. (2006). Highly Stereoselective Nitration of Chalcone Derivatives with Nitric Oxide.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.200641082\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.200641082\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eAbe et al. (2010). ChemInform Abstract: Structure and Function of the Chalcone Synthase Superfamily of Plant Type III Polyketide Synthases. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.201037269\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.201037269\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":48276755841242,"sku":"TCI2510C007113999","price":985000.0,"currency_code":"IDR","in_stock":false}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0071.jpg?v=1767094618"},{"product_id":"tci2510c018114159","title":"TCI C0181 327-97-9 Chlorogenic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0181 Chlorogenic Acid, CAS 327-97-9, is a naturally occurring polyphenol widely studied in phytochemical and natural product research. It is frequently used as a reference compound for polyphenol quantification, antioxidant assays, and extraction method validation. AMI Scientific supplies it in 1 g and 5 g packs, suitable for pharmaceutical, food science, and biotechnology laboratories. The material is intended for research and experimental use only; store it tightly closed, protected from light and moisture, and handle it with standard laboratory protective equipment.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eWei et al. (2011). Isolation of Chlorogenic Acid from Flaveria bidentis (L.) Kuntze by CCC and Synthesis of Chlorogenic Acid-Intercalated Layered Double Hydroxide. \u003cem\u003eChromatographia\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1007\/s10337-010-1877-2\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1007\/s10337-010-1877-2\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eWeidel et al. (2014). A Rapid Method for Quantifying Chlorogenic Acid Levels in Potato Samples. \u003cem\u003eJournal of AOAC International\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.5740\/jaoacint.13-099\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.5740\/jaoacint.13-099\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eHolowinski et al. (2022). Chlorogenic acid-water complexes in chlorogenic acid containing food products. \u003cem\u003eJournal of Food Composition and Analysis\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.jfca.2022.104509\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.jfca.2022.104509\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":48085975761114,"sku":"TCI2510C018114159","price":2447000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085975793882,"sku":"TCI2510C018114160","price":8376000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0181.jpg?v=1767094840"},{"product_id":"tci2510c035214419","title":"TCI C0352 14371-10-9 trans-Cinnamaldehyde","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003etrans-Cinnamaldehyde (TCI C0352, CAS 14371-10-9) is a conjugated aromatic aldehyde best known as the principal aroma compound of cinnamon. In the laboratory it functions as a versatile non-heterocyclic building block, offering both a reactive carbonyl group and a conjugated double bond in a single molecule. It is commonly used as a model substrate in iminium organocatalysis, Michael additions, and heterocycle construction. AMI Scientific supplies it in 25 mL and 500 mL packs, and handling in a fume hood with appropriate personal protective equipment is strongly recommended.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eGholivand et al. (2008). Simultaneous Determination of Trans-Cinnamaldehyde and Benzaldehyde in Different Real Samples by Differential Pulse Polarography and Study of Heat Stability of Trans-Cinnamaldehyde. \u003cem\u003eAnalytical Letters\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1080\/00032710802507893\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1080\/00032710802507893\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eAli et al. (2021). Trans-Cinnamaldehyde Attenuates Enterococcus faecalis Virulence and Inhibits Biofilm Formation. \u003cem\u003eAntibiotics\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.3390\/antibiotics10060702\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.3390\/antibiotics10060702\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eSwales et al. (1996). Studies on trans-cinnamaldehyde II: Mechanisms of cytotoxicity in rat isolated hepatocytes. \u003cem\u003eToxicology in Vitro\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/0887-2333(95)00105-0\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/0887-2333(95)00105-0\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":"25mL","offer_id":48085991719130,"sku":"TCI2510C035214419","price":507000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48085991751898,"sku":"TCI2510C035214420","price":1659000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0352.jpg?v=1767095079"},{"product_id":"tci2510c035314421","title":"TCI C0353 140-10-3 trans-Cinnamic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003etrans-Cinnamic Acid (TCI C0353, CAS 140-10-3) is a fundamental unsaturated aromatic carboxylic acid and a widely used non-heterocyclic building block. Its conjugated alkene and carboxyl group allow straightforward conversion into esters, amides, and reduced derivatives. The compound is also a classic substrate for solid-state [2+2] photodimerisation studies and for evaluating selective hydrogenation catalysts. AMI Scientific offers 25 g, 100 g, and 500 g packs to support teaching laboratories, routine research, and larger synthetic campaigns.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSALUM et al. (2013). High Purity cis-Cinnamic Acid Preparation for Studying Physiological Role of trans-Cinnamic and cis-Cinnamic Acids in Higher Plants. \u003cem\u003eEnvironment Control in Biology\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.2525\/ecb.51.1\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.2525\/ecb.51.1\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eKokkinou et al. (2000). The crystal structure of the 1:1 complex of β-cyclodextrin with trans-cinnamic acid. \u003cem\u003eCarbohydrate Research\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/s0008-6215(00)00091-4\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/s0008-6215(00)00091-4\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eKhoj et al. (2017). Structural Diversity of Solid Solutions Formed between 3-Chloro-trans-cinnamic acid and 3-Bromo-trans-cinnamic Acid. \u003cem\u003eCrystal Growth \u0026amp; Design\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1021\/acs.cgd.6b01675\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1021\/acs.cgd.6b01675\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":48085991784666,"sku":"TCI2510C035314421","price":536000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48085991817434,"sku":"TCI2510C035314422","price":1181000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48085991850202,"sku":"TCI2510C035314423","price":2952000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0353.jpg?v=1767095083"},{"product_id":"tci2510c036214436","title":"TCI C0362 4407-36-7 (E)-Cinnamyl Alcohol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(E)-Cinnamyl Alcohol (TCI C0362, CAS 4407-36-7) is an E-configured aromatic allylic alcohol used both as a fragrance component and as a versatile synthetic building block. It is a classic substrate for Sharpless asymmetric epoxidation, palladium-catalysed allylic substitution, and selective oxidation to cinnamaldehyde. The hydroxyl group is readily esterified, etherified, or converted into a leaving group for further transformations. AMI Scientific offers 25 g and 500 g packs in original TCI packaging, with handling under standard laboratory personal protective equipment recommended.\u003c\/p\u003e\n\u003cp\u003e---\u003c\/p\u003e\n\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMee et al. (2004). Characterization of Cinnamyl Alcohol Dehydrogenase. \u003cem\u003eEndoscopy\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1055\/s-2004-834497\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1055\/s-2004-834497\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eNAKAGAWA-IZUMI et al. (2003). Analysis of cinnamyl alcohol- and cinnamyl aldehyde end groups in lignin by trimethylsilylation\/pyrolysis-gas chromatography. \u003cem\u003eBUNSEKI KAGAKU\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.2116\/bunsekikagaku.52.1159\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.2116\/bunsekikagaku.52.1159\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eZhao et al. (2005). Carbon Dioxide‐Expanded Liquid Substrate Phase: An Effective Medium for Selective Hydrogenation of Cinnamaldehyde to Cinnamyl Alcohol.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.200512081\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.200512081\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":48085993783514,"sku":"TCI2510C036214436","price":536000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48085993816282,"sku":"TCI2510C036214437","price":1659000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0362.jpg?v=1769144563"},{"product_id":"tci2510c037014450","title":"TCI C0370 106-22-9 beta-Citronellol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0370 beta-Citronellol (CAS 106-22-9) is a monoterpenoid alcohol found in the essential oils of roses, citronella, and related aromatic plants. Its primary hydroxyl group and trisubstituted double bond make it a classic terpene building block for oxidation, esterification, epoxidation, and cyclisation chemistry. Laboratories also rely on it as a reference compound in GC-MS profiling of essential oils and in studies of biological and repellent activity. AMI Scientific stocks this TCI product in 25 mL, 100 mL, and 500 mL bottles so that volatile material can be matched to actual usage rates.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eNaresh Yadav et al. (2018). Highly Efficient Stereoselective Glycosylation of \u0026amp;beta;-Citronellol. \u003cem\u003eAsian Journal of Organic \u0026amp; Medicinal Chemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.14233\/ajomc.2018.ajomc-p109\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.14233\/ajomc.2018.ajomc-p109\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eMaulina et al. (2025). In silico study of beta citronellol compound in lime plant (Citrus aurantifolia) as a drug candidate for enterovirus disease. \u003cem\u003eGreen and Tropical Laboratory for Sustainability\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.22219\/gtlabs.v2i1.41033\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.22219\/gtlabs.v2i1.41033\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":"25mL","offer_id":48085994373338,"sku":"TCI2510C037014450","price":564000.0,"currency_code":"IDR","in_stock":true},{"title":"100mL","offer_id":48085994406106,"sku":"TCI2510C037014451","price":1378000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48085994438874,"sku":"TCI2510C037014452","price":3626000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0370.jpg?v=1768816223"},{"product_id":"tci2510c038014467","title":"TCI C0380 64-86-8 Colchicine (contains 5% Ethyl Acetate at maximum)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0380 Colchicine, CAS 64-86-8, is a plant-derived alkaloid widely used as a tubulin-binding inhibitor of microtubule polymerisation. By arresting dividing cells in metaphase, it is a standard tool for chromosome preparation, cell cycle studies, and antimitotic research, and is also applied in plant polyploidy induction work. This TCI grade is specified to contain a maximum of 5% ethyl acetate as residual solvent, which should be considered when preparing solutions. The material is highly toxic, intended strictly for trained laboratory research use, and is offered by AMI Scientific in 500 mg and 5 g packs.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"500mg","offer_id":48085995094234,"sku":"TCI2510C038014467","price":1322000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085995127002,"sku":"TCI2510C038014468","price":7534000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0380.jpg?v=1767095143"},{"product_id":"tci2510c039314488","title":"TCI C0393 501-98-4 trans-p-Coumaric Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0393 trans-p-Coumaric Acid, CAS 501-98-4, is a hydroxycinnamic acid that occupies a central position in the plant phenylpropanoid pathway. It serves as a precursor to lignin, flavonoids, and related phenolic metabolites, and is routinely used as a reference standard for phenolic quantification in natural product and food analysis. Its antioxidant character and characteristic UV absorption also make it useful in radical-scavenging assays and as a matrix material in certain mass spectrometry techniques. Available from AMI Scientific in 25 g, 100 g, and 500 g packs, it should be stored cool, dry, and protected from light to preserve the trans configuration.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48085995913434,"sku":"TCI2510C039314488","price":1603000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48085995946202,"sku":"TCI2510C039314489","price":4695000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48085995978970,"sku":"TCI2510C039314490","price":13407000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0393.jpg?v=1768816230"},{"product_id":"tci2510c039414491","title":"TCI C0394 614-60-8 trans-o-Coumaric Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI trans-o-Coumaric Acid (catalogue number C0394) is a hydroxycinnamic acid derivative widely used as a starting material in organic synthesis. Its combination of a carboxylic acid group and an ortho-positioned phenolic hydroxyl provides two selective reaction sites for building coumarin scaffolds and related phenolic structures. Researchers in natural product chemistry also employ it as a reference compound when profiling plant-derived phenolics. Available in 5 g and 25 g packs, it suits both exploratory studies and larger synthetic campaigns.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48085996011738,"sku":"TCI2510C039414491","price":929000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085996044506,"sku":"TCI2510C039414492","price":2671000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0394.jpg?v=1767095163"},{"product_id":"tci2510c043414550","title":"TCI C0434 458-37-7 Curcumin (Natural)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCurcumin (Natural) TCI C0434, with CAS number 458-37-7, is a chemical compound widely used in scientific experiments, particularly in the fields of chemistry and biology. As a natural pigment derived from the root of the turmeric plant, it serves as a valuable dye in laboratory settings. This compound is commonly used to create colorimetric solutions for various analytical processes, including color tests, compound identification, and the study of chemical and biological properties. Its presence in pure form allows researchers to precisely control concentration levels and chemical reactions, making it an essential tool in experimental research.\u003c\/p\u003e\n\u003cp\u003eCurcumin is valued for its chemical stability under certain conditions, although it is highly sensitive to light and oxidation. These properties make it a preferred choice for applications where accurate and consistent results are crucial. Its natural origin also adds to its appeal, especially in studies focused on bioactive compounds. The compound’s antioxidant properties further enhance its utility in pharmacological and nutritional research, offering researchers a versatile material for a wide range of investigations.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, curcumin is frequently used in research related to the bioactivity of natural compounds. It plays a key role in studies examining anti-inflammatory and antioxidant effects, contributing to advancements in both scientific and applied research. Its availability and reliability make it a staple in many research environments, supporting the pursuit of knowledge in various scientific disciplines.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eColorimetric analysis is a common application where curcumin is used to detect and quantify specific compounds through color changes, making it ideal for qualitative and quantitative testing.\u003c\/li\u003e\n\u003cli\u003eBioactivity studies benefit from curcumin’s natural origin and antioxidant properties, enabling researchers to investigate its effects on cellular processes and biological systems.\u003c\/li\u003e\n\u003cli\u003eChemical identification processes rely on curcumin’s distinct color properties, allowing for the visualization and analysis of compounds in solution.\u003c\/li\u003e\n\u003cli\u003ePharmacological research utilizes curcumin to explore its potential therapeutic applications, particularly in inflammation and oxidative stress-related conditions.\u003c\/li\u003e\n\u003cli\u003eNutritional studies incorporate curcumin to assess its role in dietary supplements and its impact on human health, supporting research in food science and health sciences.\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: 458-37-7\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Stains and Dyes (for Research and Experimental Use) \u0026gt; Basic Dyes (for Research and Experimental Use)\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified in the provided data\u003c\/li\u003e\n\u003cli\u003ePhysical form: Not specified in the provided data\u003c\/li\u003e\n\u003cli\u003eStorage note: Must be stored in a cool, dark place to prevent degradation due to light and oxidation\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eCurcumin should be stored in a cool, dark environment to maintain its chemical integrity and prevent degradation caused by light exposure and oxidation. It is recommended to keep it in airtight containers to minimize contact with air and moisture. Due to its sensitivity, it is important to avoid prolonged exposure to heat and direct sunlight. In laboratory settings, curcumin should be handled with care to prevent contamination and ensure accurate experimental results. Proper labeling and storage conditions are essential for maintaining the quality and effectiveness of this compound in research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085998436570,"sku":"TCI2510C043414550","price":676000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085998469338,"sku":"TCI2510C043414551","price":2840000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0434.jpg?v=1767095223"},{"product_id":"tci2510c054214729","title":"TCI C0542 470-82-6 1,8-Cineole","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0542 1,8-Cineole (CAS 470-82-6), also known as eucalyptol, is a cyclic monoterpene ether found in eucalyptus and cajuput essential oils. It is widely used as a reference standard in gas chromatography and in natural product research on terpene composition. The product is supplied as a liquid in a 25 mL bottle, convenient for preparing calibration solutions. Keep the bottle tightly closed in a cool, well-ventilated area away from heat and ignition sources.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eCarman et al. (1996). 7,9-Dihydroxy-1,8-cineole and 2α,7-Dihydroxy-1,8-cineole: Two New Possum Urinary Metabolites. \u003cem\u003eAustralian Journal of Chemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1071\/ch9960741\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1071\/ch9960741\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eAK (2023). 1,8-Cineole an Underappreciated Anti Inflammatory Therapeutic. \u003cem\u003eInternational Journal of Pharmacognosy \u0026amp; Chinese Medicine\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.23880\/ipcm-16000238\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.23880\/ipcm-16000238\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eMIYAZAWA et al. (1992). ChemInform Abstract: Biotransformation of 1,4‐Cineole to 3‐endo‐Hydroxy‐1,4‐cineole by Aspergillus niger.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.199220263\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.199220263\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":"25mL","offer_id":48086007808218,"sku":"TCI2510C054214729","price":3598000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0542.jpg?v=1767095451"},{"product_id":"tci2510c065514881","title":"TCI C0655 14755-02-3 trans-m-Coumaric Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0655 trans-m-Coumaric Acid (CAS 14755-02-3), also known as trans-3-hydroxycinnamic acid, is a phenolic acid belonging to the hydroxycinnamic acid family. Its combination of a phenolic hydroxyl group and an unsaturated carboxylic acid side chain makes it a useful reference compound in plant metabolite, food chemistry, and antioxidant research. The same functional groups provide convenient handles for derivatisation into esters, amides, or ethers in organic synthesis. AMI Scientific offers this TCI product in 5 g and 25 g packs for research use; store it tightly closed in a cool, dry, light-protected place and review the manufacturer's Safety Data Sheet before handling.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086018621658,"sku":"TCI2510C065514881","price":844000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086018654426,"sku":"TCI2510C065514882","price":2222000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0655.jpg?v=1767095625"},{"product_id":"tci2510c070514956","title":"TCI C0705 225937-10-0 (+)-Catechin Hydrate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0705 (+)-Catechin Hydrate, CAS 225937-10-0, is a flavan-3-ol polyphenol supplied as a hydrated solid for research and experimental use. It is widely used as a reference standard in total flavonoid assays, HPLC quantification, and antioxidant screening methods such as DPPH and ABTS. AMI Scientific supplies this TCI reagent in 1 g and 10 g packs for pharmaceutical, food science, and natural product laboratories. Because catechin is sensitive to light, air, and moisture, store it refrigerated in a tightly closed, light-protected container and use clean, dry tools when weighing.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eIvanova et al. (2020). Investigation of Anti-Proliferative Effects of Natural Products Quercetin Hydrate and Catechin Hydrate on Leukemia Lymphocytes. \u003cem\u003eRevista de Chimie\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.37358\/rc.20.11.8377\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.37358\/rc.20.11.8377\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eSamanta et al. (2016). Formulation of Catechin Hydrate Nanocapsule and Study of its Bioavailability. \u003cem\u003eMedicinal chemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.4172\/2161-0444.1000376\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.4172\/2161-0444.1000376\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eKhattab et al. (2021). Modulatory effects of catechin hydrate on benzo[a]pyrene-induced nephrotoxicity in adult male albino rats. \u003cem\u003eToxicology Research\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1093\/toxres\/tfab029\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1093\/toxres\/tfab029\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":48086022750426,"sku":"TCI2510C070514956","price":1266000.0,"currency_code":"IDR","in_stock":true},{"title":"10g","offer_id":48086022783194,"sku":"TCI2510C070514957","price":6521000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0705.jpg?v=1767095668"},{"product_id":"tci2510c093415269","title":"TCI C0934 470-82-6 1,8-Cineole","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1,8-Cineole, also known as eucalyptol, is a bicyclic monoterpenoid ether and the principal aromatic constituent of eucalyptus essential oil. Its bridged ether structure gives it good chemical stability, and it is frequently used as an analytical reference standard for the identification and quantification of eucalyptol in essential oils by GC and GC-MS. Beyond analysis, it serves as a starting material for terpenoid derivatisation and as a model compound in phytochemical and bioactivity studies. TCI supplies this flammable liquid in 25 mL, 100 mL, and 500 mL packs; keep containers tightly closed, protected from light, and away from ignition sources.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eCarman et al. (1996). 7,9-Dihydroxy-1,8-cineole and 2α,7-Dihydroxy-1,8-cineole: Two New Possum Urinary Metabolites. \u003cem\u003eAustralian Journal of Chemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1071\/ch9960741\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1071\/ch9960741\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eAK (2023). 1,8-Cineole an Underappreciated Anti Inflammatory Therapeutic. \u003cem\u003eInternational Journal of Pharmacognosy \u0026amp; Chinese Medicine\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.23880\/ipcm-16000238\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.23880\/ipcm-16000238\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eMIYAZAWA et al. (1992). ChemInform Abstract: Biotransformation of 1,4‐Cineole to 3‐endo‐Hydroxy‐1,4‐cineole by Aspergillus niger.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.199220263\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.199220263\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":"25mL","offer_id":48086038675674,"sku":"TCI2510C093415269","price":536000.0,"currency_code":"IDR","in_stock":true},{"title":"100mL","offer_id":48086038708442,"sku":"TCI2510C093415270","price":1294000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48086038741210,"sku":"TCI2510C093415271","price":3345000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0934.jpg?v=1768816372"},{"product_id":"tci2510c095515297","title":"TCI C0955 6003-94-7 Chelidonic Acid Monohydrate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0955 Chelidonic Acid Monohydrate (CAS 6003-94-7) is a pyranone-based dicarboxylic acid supplied as the monohydrate. Its symmetric dicarboxylate arrangement and ring carbonyl make it useful as a bifunctional monomer and as a linker in coordination and metal-organic framework research. It also serves as a starting scaffold for further heterocyclic transformations and as a reference compound in natural product studies. Supplied in 5 g and 25 g packs, it should be stored tightly closed in a cool, dry place, and the hydrate form should be accounted for in stoichiometric calculations.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSchmidt (1999). Chelidonic Acid as Precursor for 2,5-Desoxy-C-glycosides. \u003cem\u003eHETEROCYCLES\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.3987\/com-98-8348\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.3987\/com-98-8348\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eDZULKAFLI (2019). IDENTIFICATION OF CHELIDONIC ACID AND ASPARAGINE IN Ganoderma boninense– INOCULATED OIL PALM SEEDLINGS. \u003cem\u003eJournal of Oil Palm Research\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.21894\/jopr.2019.0008\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.21894\/jopr.2019.0008\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eJadreško et al. (2016). Electrochemical Characteristics of 4‐oxo‐4H‐pyran‐dicarboxylic Acid (Chelidonic Acid) and some of its Metal Complexes. \u003cem\u003eElectroanalysis\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/elan.201600355\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/elan.201600355\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":48086039822554,"sku":"TCI2510C095515297","price":3345000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086039855322,"sku":"TCI2510C095515298","price":10961000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0955.jpg?v=1768816379"},{"product_id":"tci2510c145416018","title":"TCI C1454 5949-05-3 (-)-Citronellal","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1454 (-)-Citronellal (CAS 5949-05-3) is a chiral terpenoid aldehyde and a classic chiral pool starting material. Its aldehyde group, isolated alkene, and stereogenic centre make it ideal for stereocontrolled cyclisation chemistry, most notably the carbonyl-ene route to isopulegol. It is also widely used in terpenoid derivatisation, Lewis acid catalyst benchmarking, and flavour and fragrance research. AMI Scientific offers this TCI product in 5 mL and 25 mL packs; store it tightly closed and protected from light and air as directed by the manufacturer.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eJacob et al. (2009). ChemInform Abstract: Atom‐Economic Synthesis of Functionalized Octahydroacridines from Citronellal or 3‐(Phenylthio)‐citronellal.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.200951168\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.200951168\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eLu et al. (2014). Antioxidant Activity Determination of Citronellal and Crude Extracts of \u0026amp;lt;i\u0026amp;gt;Cymbopogon citratus\u0026amp;lt;\/i\u0026amp;gt; by 3 Different Methods. \u003cem\u003ePharmacology \u0026amp;amp; Pharmacy\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.4236\/pp.2014.54047\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.4236\/pp.2014.54047\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eJacob et al. (2009). Atom-Economic Synthesis of Functionalized Octahydroacridines from Citronellal or 3-(Phenylthio)-citronellal. \u003cem\u003eSynthetic Communications\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1080\/00397910802663469\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1080\/00397910802663469\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":"5mL","offer_id":48086070952154,"sku":"TCI2510C145416018","price":1181000.0,"currency_code":"IDR","in_stock":true},{"title":"25mL","offer_id":48086070984922,"sku":"TCI2510C145416019","price":3486000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1454.jpg?v=1768816527"},{"product_id":"tci2510c146616036","title":"TCI C1466 7540-51-4 (-)-beta-Citronellol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1466 (-)-beta-Citronellol is a chiral monoterpene alcohol with a characteristic rose-like floral aroma. It is widely used as a naturally derived chiral building block in asymmetric synthesis, where its primary hydroxyl group and alkene provide two convenient handles for further derivatisation. The compound also serves as a reference material in essential oil analysis and in fragrance and flavour research. AMI Scientific supplies it as a liquid in original TCI packaging, and containers should be kept tightly sealed away from heat and light to preserve quality.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eNaresh Yadav et al. (2018). Highly Efficient Stereoselective Glycosylation of \u0026amp;beta;-Citronellol. \u003cem\u003eAsian Journal of Organic \u0026amp; Medicinal Chemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.14233\/ajomc.2018.ajomc-p109\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.14233\/ajomc.2018.ajomc-p109\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eMaulina et al. (2025). In silico study of beta citronellol compound in lime plant (Citrus aurantifolia) as a drug candidate for enterovirus disease. \u003cem\u003eGreen and Tropical Laboratory for Sustainability\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.22219\/gtlabs.v2i1.41033\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.22219\/gtlabs.v2i1.41033\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":"25mL","offer_id":48086071705818,"sku":"TCI2510C146616036","price":1434000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1466.jpg?v=1768816533"},{"product_id":"tci2510c149516076","title":"TCI C1495 7689-03-4 (S)-(+)-Camptothecin","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1495 (S)-(+)-Camptothecin (CAS 7689-03-4) is a pentacyclic quinoline alkaloid and a well-characterised topoisomerase I inhibitor. It is catalogued as a research reagent for pharmaceutical development, particularly for antibody-drug conjugate preparation, where its scaffold underpins an important class of payloads. Laboratories also use it as a positive control in cytotoxicity assays and as a starting material for analog synthesis. Supplied in 100 mg and 1 g packs; treat as a cytotoxic compound and follow the Safety Data Sheet and institutional handling procedures.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eA et al. (2016). ANNUAL VARIATION IN CAMPTOTHECIN AND 9-METHOXY CAMPTOTHECIN ACCUMULATION AND ITS DETERMINATION IN DIFFERENT PARTS OF NOTHAPODYTES NIMMONIANA BY HPLC ANALYSIS. \u003cem\u003eBulletin of Pharmaceutical Research\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.21276\/bpr.2016.6.1.3\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.21276\/bpr.2016.6.1.3\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003e(2002). Crystal Form of A Camptothecin Derivative. \u003cem\u003eJournal of Korean Pharmaceutical Sciences\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.4333\/kps.2002.32.2.081\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.4333\/kps.2002.32.2.081\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003e(2018). Characterization of Camptothecin-induced Genomic Changes in the Camptothecin-resistant T-ALL-derived Cell Line CPT-K5. \u003cem\u003eCancer Genomics \u0026amp; Proteomics\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.21873\/cgp.20068\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.21873\/cgp.20068\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":48086073573594,"sku":"TCI2510C149516076","price":760000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48086073606362,"sku":"TCI2510C149516077","price":4414000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1495.jpg?v=1767097022"},{"product_id":"tci2510c165216308","title":"TCI C1652 480-40-0 Chrysin","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eChrysin is a chemical compound belonging to the phenylpropanoid and aromatic polyketide family. It is widely used in biochemical and pharmacological research due to its antioxidant properties and potential pharmacological effects. Found naturally in plants such as *Tanacetum corymbosum* and *Curcuma longa*, Chrysin is also synthesized in laboratories. In research settings, it serves as a building block for the synthesis of other compounds and as a testing agent in studies on biological activities. Chrysin has a stable molecular structure and is soluble in organic solvents like ethyl acetate and ethanol, making it suitable for various chemical reactions and extraction processes. Its strong antioxidant properties make it a preferred choice in studies related to free radical effects on cells and tissues. In Indonesian laboratories, Chrysin is commonly used in research on health, environment, and biotechnology, particularly in studies on antioxidant effects on human cells and the development of herbal medicines. Its versatility makes it a popular choice among researchers in various educational and research institutions across Indonesia.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOliyapour et al. (2023). Chrysin and chrysin-loaded nanocarriers induced immunogenic cell death on B16 melanoma cells. \u003cem\u003eMedical Oncology\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1007\/s12032-023-02145-z\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1007\/s12032-023-02145-z\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eMohos et al. (2018). Interaction of Chrysin and Its Main Conjugated Metabolites Chrysin-7-Sulfate and Chrysin-7-Glucuronide with Serum Albumin. \u003cem\u003eInternational Journal of Molecular Sciences\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.3390\/ijms19124073\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.3390\/ijms19124073\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003e(2017). Modulatory effect of chrysin against acrylamide-induced neurotoxicity in rats. \u003cem\u003eEgyptian Journal of Pure and Applied Science\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.21608\/ejaps.2017.183753\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.21608\/ejaps.2017.183753\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":48086082978010,"sku":"TCI2510C165216308","price":2868000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1652.jpg?v=1768816592"},{"product_id":"tci2510c170816373","title":"TCI C1708 502-47-6 Citronellic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCitronellic Acid (TCI C1708) is a versatile organic compound widely used in chemical laboratories for its role as a building block in synthetic reactions. With a stable molecular structure, it is commonly employed in the synthesis of esters, fatty acids, and other complex organic compounds. Its unique chemical properties make it suitable for various applications in pharmaceutical research, cosmetic development, and environmental analysis. This compound is particularly relevant in Indonesian laboratories, where it supports both academic and industrial research in chemistry and related fields. Its ability to react with various reagents makes it an essential tool for chemists working on new compound development and molecular structure studies.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOhashi et al. (2021). Biosyntheses of geranic acid and citronellic acid from monoterpene alcohols by Saccharomyces cerevisiae. \u003cem\u003eBioscience, Biotechnology, and Biochemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1093\/bbb\/zbab039\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1093\/bbb\/zbab039\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eKim (2024). Citronellic Acid Improves Skin Barrier Function by Activation of PPAR-α. \u003cem\u003eNatural Product Sciences\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.20307\/nps.2024.30.4.268\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.20307\/nps.2024.30.4.268\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eRychlicka et al. (2018). Lipase-Catalyzed Acidolysis of Egg-Yolk Phosphatidylcholine with Citronellic Acid. New Insight into Synthesis of Isoprenoid-Phospholipids. \u003cem\u003eMolecules\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.3390\/molecules23020314\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.3390\/molecules23020314\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":"25mL","offer_id":48086085402842,"sku":"TCI2510C170816373","price":2980000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1708.jpg?v=1767097359"},{"product_id":"tci2510c230217033","title":"TCI C2302 458-37-7 Curcumin (Synthetic)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCurcumin (Synthetic) TCI C2302 is a chemical compound widely utilized in scientific research, particularly in the fields of biochemistry and pharmaceutical sciences. As a synthetic derivative of curcumin found naturally in turmeric, it serves as a key reagent in experimental studies aimed at understanding biological mechanisms and therapeutic potential. Its versatility makes it an essential component in laboratories conducting research on antioxidant, anti-inflammatory, and pharmacological properties of natural compounds. This compound is frequently employed in both qualitative and quantitative analyses, supporting a broad range of scientific investigations.\u003c\/p\u003e\n\u003cp\u003eCurcumin is prized for its chemical stability and solubility in organic solvents such as ethyl acetate and ethanol, which facilitates its use in various chemical reactions and analytical procedures. Its ability to react effectively with different substrates enhances its applicability in biological assays, making it a preferred choice for researchers seeking reliable and consistent results. Additionally, its high purity ensures accuracy in experiments that require precise measurements and reproducible outcomes. These properties contribute to its widespread use in both academic and industrial research settings.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, curcumin is commonly used in studies related to health, pharmacology, and nutrition. It is a favored material for investigating the bioavailability and efficacy of natural compounds, supporting research into potential therapeutic applications. Its availability and reliability make it a go-to option for scientists working on projects that require a stable and high-quality reagent. This compound plays a crucial role in advancing scientific knowledge and innovation in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBiochemical Research: Curcumin is used to study antioxidant and anti-inflammatory properties due to its chemical stability and reactivity.\u003c\/li\u003e\n\u003cli\u003ePharmacological Studies: It supports research into drug development by analyzing its pharmacological effects and biological interactions.\u003c\/li\u003e\n\u003cli\u003eNutritional Analysis: Curcumin is employed in studies assessing the bioavailability and health benefits of natural compounds in food.\u003c\/li\u003e\n\u003cli\u003eSynthetic Chemistry: Its solubility in organic solvents makes it ideal for chemical synthesis and compound modification.\u003c\/li\u003e\n\u003cli\u003eAnalytical Chemistry: It is used as a reagent in chromatographic and spectroscopic analyses due to its consistent chemical behavior.\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: 458-37-7\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Crude Medicine Ingredients for Research and Experimental Use\u003c\/li\u003e\n\u003cli\u003ePack Sizes: As per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical Form: Powder\u003c\/li\u003e\n\u003cli\u003eStorage Note: Store in a cool, dry place away from light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eCurcumin should be stored in a cool, dry environment, away from direct sunlight and moisture to maintain its chemical stability. It is recommended to keep it in a tightly sealed container to prevent contamination and degradation. Due to its organic nature, it is best stored in glass or high-density polyethylene containers to ensure safety and purity. Avoid exposure to strong oxidizing agents or reactive substances to prevent unwanted chemical reactions. Proper labeling and storage conditions are essential to ensure its integrity and usability in laboratory settings. Always handle with care, using appropriate personal protective equipment when necessary.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086118367450,"sku":"TCI2510C230217033","price":1266000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086118400218,"sku":"TCI2510C230217034","price":4133000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2302.jpg?v=1767098099"},{"product_id":"tci2510c248817270","title":"TCI C2488 3650-09-7 Carnosic Acid (Synthetic)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCarnosic Acid (TCI C2488) is a synthetic compound widely used in scientific research, particularly in biochemical and pharmacological studies. Derived from sage leaves, this compound plays a crucial role in laboratories where researchers investigate antioxidant, anti-inflammatory, and pharmacological properties. Its molecular structure is complex, making it a valuable reagent for various experimental applications. Carnosic Acid is commonly used as a building block in the synthesis of other compounds or as a test material in studies related to health and environmental science. Its chemical stability and solubility in organic solvents make it a versatile choice for a wide range of experimental procedures.\u003c\/p\u003e\n\u003cp\u003eThis compound is preferred due to its chemical stability, solubility in organic solvents, and consistent purity. Its ability to interact with free radicals makes it ideal for assessing antioxidant activity in chemical reactions and biological systems. The availability of Carnosic Acid in pure form and precise concentrations ensures accuracy and reliability in research settings. These properties make it a reliable and essential component in many laboratory protocols, especially those involving oxidative stress studies and pharmacological testing.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Carnosic Acid is frequently used in research related to health, environmental science, and pharmacology. It is a common material in studies focused on natural products, drug development, and bioactive compound analysis. Its role in assessing antioxidant and anti-inflammatory effects supports its use in both academic and industrial research environments. The compound’s versatility and reliability make it a preferred choice for researchers seeking precise and reproducible results.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAntioxidant Activity Testing: Carnosic Acid is used to evaluate the scavenging ability of free radicals in biological and chemical systems.\u003c\/li\u003e\n\u003cli\u003ePharmacological Research: It serves as a key reagent in studies investigating the therapeutic potential of natural compounds.\u003c\/li\u003e\n\u003cli\u003eEnvironmental Toxicology Studies: Carnosic Acid helps assess the impact of pollutants on biological systems and oxidative stress.\u003c\/li\u003e\n\u003cli\u003eDrug Development and Synthesis: It is used as a building block in the synthesis of novel compounds with potential therapeutic applications.\u003c\/li\u003e\n\u003cli\u003eBioactive Compound Analysis: It is employed in the identification and quantification of bioactive components in plant extracts and natural products.\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: 3650-09-7\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Crude Medicine Ingredients for Research and Experimental Use\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory requirements\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eCarnosic Acid should be stored in a cool, dry place, away from direct light and moisture to maintain its chemical stability. It is recommended to use airtight containers made of glass or polyethylene to prevent contamination and degradation. Due to its organic nature, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. It is important to ensure that the storage area is well-ventilated to minimize exposure to airborne particles. Regular monitoring of storage conditions is advised to maintain the integrity of the compound for experimental use. Proper labeling and safe handling procedures are essential to prevent accidental spills or contamination in the laboratory environment.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"20mg","offer_id":48086129082586,"sku":"TCI2510C248817270","price":2025000.0,"currency_code":"IDR","in_stock":true},{"title":"100mg","offer_id":48086129115354,"sku":"TCI2510C248817271","price":6746000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2488.jpg?v=1767098410"},{"product_id":"tci2510c250517279","title":"TCI C2505 481-74-3 Chrysophanic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eChrysophanic Acid is a chemical compound widely used in various chemical experiments and scientific research. As a non-heterocyclic building block, it possesses a simple molecular structure yet holds significant potential for the synthesis of complex compounds. This compound is commonly utilized as a foundational material in the development of bioactive substances, including pharmaceuticals and antioxidants. In laboratory settings, it plays a crucial role in qualitative and quantitative analysis, aiding in the identification of specific compounds within samples. Its chemical stability under certain conditions makes it a reliable and versatile material for a wide range of chemical reactions.\u003c\/p\u003e\n\u003cp\u003eChrysophanic Acid is preferred due to its chemical stability, high reactivity, and consistent quality. Its ability to remain intact without easily degrading ensures predictable results in experimental processes. The compound’s high purity and consistent quality make it a trusted choice for researchers requiring precise and reliable materials. Its reactivity allows it to participate effectively in various synthetic pathways, making it suitable for diverse chemical applications. These properties contribute to its popularity among scientists and researchers working in both academic and industrial laboratories.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Chrysophanic Acid is commonly used in scientific research, particularly in the fields of organic chemistry and pharmacy. It supports studies related to drug development, compound synthesis, and analytical chemistry. Its availability and reliability make it a key component in many research projects, ensuring accurate and reproducible results. The compound’s role in both basic and applied research underscores its importance in the scientific community in Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis applications benefit from Chrysophanic Acid’s reactivity and structural versatility, enabling the creation of complex molecules.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research utilizes this compound as a building block for developing bioactive compounds and drug candidates.\u003c\/li\u003e\n\u003cli\u003eAnalytical chemistry relies on Chrysophanic Acid for identifying and quantifying specific compounds in samples due to its chemical stability.\u003c\/li\u003e\n\u003cli\u003eBioactive compound development leverages its properties to synthesize antioxidants and other therapeutic agents.\u003c\/li\u003e\n\u003cli\u003eEnvironmental studies may use Chrysophanic Acid to analyze organic pollutants and their interactions in natural samples.\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: 481-74-3\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\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\u003eChrysophanic Acid 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 avoid exposure to moisture and air, which could affect its purity. Laboratory personnel should handle the compound with care, using appropriate personal protective equipment such as gloves and safety goggles. Due to its reactivity, it should be stored separately from incompatible substances to prevent unwanted chemical reactions. Proper labeling of storage containers is essential to ensure safe handling and easy identification. Regular monitoring of storage conditions helps maintain the compound’s integrity and ensures its suitability for scientific use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48086129410266,"sku":"TCI2510C250517279","price":4891000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2505.jpg?v=1767098422"},{"product_id":"tci2510c252017305","title":"TCI C2520 117048-59-6 Combretastatin A4","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCombretastatin A4 is a chemical compound widely utilized in life science research, particularly in biochemical and reagent applications. As a key component of the *Combretaceae* plant family, it serves as a crucial research material for experimental studies. This compound is commonly used in laboratories to investigate its biological activities, including its effects on cancer cells and antioxidant properties. Its role in scientific research is significant due to its potential therapeutic applications and its relevance in pharmacological studies.\u003c\/p\u003e\n\u003cp\u003eThe unique chemical structure of Combretastatin A4 contributes to its effectiveness in various biological assays. It exhibits potent anti-cancer properties by inhibiting the growth of malignant cells and enhancing immune responses. These characteristics make it a preferred choice for researchers aiming to explore new therapeutic targets. Additionally, its stability under different laboratory conditions ensures reliable results, making it a valuable tool in both academic and industrial research settings.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Combretastatin A4 is frequently used by researchers in academic institutions and research centers. It is integral to studies focused on cancer and metabolic diseases, supporting the development of new drugs and treatment strategies. Its availability and consistent quality make it a reliable material for experimental work, contributing to the advancement of scientific knowledge in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eCancer Research: Combretastatin A4 is used to study its anti-cancer effects on various cell lines, aiding in the development of novel therapeutic strategies.\u003c\/li\u003e\n\u003cli\u003eAntioxidant Studies: Its antioxidant properties make it suitable for experiments investigating free radical scavenging and oxidative stress reduction.\u003c\/li\u003e\n\u003cli\u003ePharmacological Investigations: The compound is employed to evaluate its potential in drug development and its interaction with biological systems.\u003c\/li\u003e\n\u003cli\u003eImmunological Research: It is used to assess its impact on immune cell function and response to pathogens.\u003c\/li\u003e\n\u003cli\u003eMetabolic Disease Studies: Combretastatin A4 is utilized to explore its role in metabolic disorders and potential therapeutic applications.\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: 117048-59-6\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Crude Medicine Ingredients for Research and Experimental Use\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified\u003c\/li\u003e\n\u003cli\u003ePhysical form: Not specified\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eCombretastatin A4 should be stored in a cool, dry, and well-ventilated area away from direct sunlight. It is recommended to keep the compound in a sealed container to prevent moisture absorption and contamination. Due to its chemical stability, it can be stored at room temperature for extended periods. Researchers should handle the compound with appropriate personal protective equipment, including gloves and safety goggles, to ensure safety during preparation and use. Proper labeling of containers is essential to avoid misidentification. In laboratory settings, it should be stored in a designated chemical storage area that complies with standard safety protocols.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"250mg","offer_id":48086130327770,"sku":"TCI2510C252017305","price":20039000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2520.jpg?v=1767098452"},{"product_id":"tci2510c260917430","title":"TCI C2609 485-35-8 (-)-Cytisine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(-)-Cytisine is a naturally occurring alkaloid widely used in scientific research, particularly in the fields of biochemistry and pharmacology. As a key reagent in laboratory settings, it plays a crucial role in both qualitative and quantitative analysis. Its chemical structure allows it to interact with various biological systems, making it an essential tool for studying the effects of alkaloids on neural pathways and metabolic processes. This compound is commonly utilized in experiments aimed at understanding the pharmacological properties of natural substances and their potential therapeutic applications.\u003c\/p\u003e\n\u003cp\u003eThe chemical stability of (-)-Cytisine under controlled conditions makes it a preferred choice for researchers seeking reliable and consistent results. Its ability to serve as a building block in the synthesis of other bioactive compounds further enhances its value in laboratory work. Additionally, its molecular complexity supports advanced research applications, such as drug development and the analysis of natural compounds. These properties ensure that (-)-Cytisine remains a versatile and essential component in many scientific investigations.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, (-)-Cytisine is frequently used by researchers in pharmacology, biochemistry, and health sciences. Its role in studying the pharmacological effects of natural compounds supports the development of new therapeutic agents. The compound's reliability and versatility make it a valuable resource for both academic and industrial research, contributing to the advancement of scientific knowledge in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eUsed in pharmacological research to study the effects of alkaloids on neural and metabolic systems.\u003c\/li\u003e\n\u003cli\u003eApplied in biochemical experiments to analyze the interaction of alkaloids with biological molecules.\u003c\/li\u003e\n\u003cli\u003eEmployed in the synthesis of bioactive compounds for drug development and therapeutic applications.\u003c\/li\u003e\n\u003cli\u003eUtilized in analytical chemistry for qualitative and quantitative analysis of alkaloid compounds.\u003c\/li\u003e\n\u003cli\u003eIncorporated in health sciences research to explore the potential of natural compounds in treating diseases.\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: 485-35-8\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Alkaloids\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities\u003c\/li\u003e\n\u003cli\u003ePhysical form: Crystalline solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003e(-)-Cytisine should be stored in a cool, dry place, away from direct light and sources of heat. It is recommended to use airtight containers to prevent moisture absorption and contamination. Due to its toxic and potentially irritating properties, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles. In laboratory settings, it is important to follow standard safety protocols to minimize exposure. Proper ventilation should be maintained when working with this compound to ensure a safe working environment. Always label containers clearly to avoid confusion and ensure safe handling.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48086135341274,"sku":"TCI2510C260917430","price":2531000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48086135374042,"sku":"TCI2510C260917431","price":10933000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2609.jpg?v=1768816894"},{"product_id":"tci2510c273717595","title":"TCI C2737 34157-83-0 Celastrol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCelastrol is a chemical compound widely used in scientific research, particularly in the fields of biochemistry and pharmacology. It serves as a key reagent in laboratory experiments aimed at exploring its biological activities, including anti-inflammatory, antitumor, and antiviral effects. This compound is essential for researchers seeking to understand the mechanisms of drug action and the body's response to various medical conditions. Its versatility makes it a valuable tool in both academic and industrial research settings.\u003c\/p\u003e\n\u003cp\u003eCelastrol is favored for its stable chemical properties and solubility in organic solvents such as ethyl acetate and ethanol. These characteristics allow it to be easily incorporated into a wide range of chemical and biochemical analyses. Additionally, its complex molecular structure enables it to interact with multiple molecular targets within the body, making it a preferred choice for pharmacological studies. The compound’s unique properties support its use in experiments requiring specific biological activities.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Celastrol is commonly used in research focused on drug development, particularly in the study of cancer therapies and autoimmune diseases. It is also utilized in academic institutions for teaching and experimental purposes. Researchers in Indonesia rely on Celastrol to conduct experiments that require a compound with well-defined biological activity and chemical stability. Its presence in laboratory workflows underscores its importance in advancing scientific knowledge in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAnti-inflammatory Research: Celastrol is used to study its effects on inflammation, making it ideal for experiments involving inflammatory disease models.\u003c\/li\u003e\n\u003cli\u003eAntitumor Studies: Its potential as an antitumor agent supports its use in cancer research, particularly in drug discovery and mechanism studies.\u003c\/li\u003e\n\u003cli\u003eAntiviral Investigations: Celastrol’s antiviral properties make it a valuable reagent for studying viral infections and potential therapeutic applications.\u003c\/li\u003e\n\u003cli\u003ePharmacological Screening: Its complex structure and biological activity make it suitable for screening compounds with specific molecular targets.\u003c\/li\u003e\n\u003cli\u003eDrug Development Protocols: Celastrol is integrated into protocols for developing new drugs, especially in the context of autoimmune and oncological research.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 34157-83-0\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Crude Medicine Ingredients for Research and Experimental Use\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eCelastrol should be stored in a cool, dry place, away from direct sunlight and moisture. It is recommended to use airtight containers to prevent contamination and maintain its chemical stability. Due to its solubility in organic solvents, it should be handled in a well-ventilated area to minimize exposure. Laboratory personnel should wear appropriate personal protective equipment, such as gloves and safety goggles, when handling the compound. Proper disposal procedures should be followed to ensure compliance with safety and environmental regulations. Regular monitoring of storage conditions is essential to preserve the integrity of the compound for research use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mg","offer_id":48086194520282,"sku":"TCI2510C273717595","price":10344000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2737.jpg?v=1767098713"},{"product_id":"tci2510c285417731","title":"TCI C2854 77-53-2 Cedrol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCedrol (77-53-2) is an organic compound classified as a phenolic compound, widely utilized in life science research. It plays a crucial role in biochemical and pharmaceutical studies, serving as a key reagent in experimental setups. Its unique chemical structure and biological activity make it an essential component for researchers working on drug development, organic synthesis, and bioactive compound analysis. Cedrol is particularly valued for its versatility in supporting a wide range of scientific inquiries, from basic research to advanced experimental applications.\u003c\/p\u003e\n\u003cp\u003eCedrol is preferred due to its moderate polarity and solubility in organic solvents such as ethyl acetate and ethanol. These properties enable it to be effectively used in various chemical reactions and synthesis processes. Its high biological activity, including antioxidant and antimicrobial properties, further enhances its applicability in health-related research. The compound’s stability under specific conditions also contributes to its reliability in laboratory settings, ensuring consistent results over time.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Cedrol is commonly used in pharmaceutical, biotechnology, and chemical research. It is a staple in academic and industrial research institutions, supporting the development of new drugs and bioactive compounds. Its availability and well-documented properties make it a trusted choice for researchers aiming to advance scientific knowledge and innovation.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePharmaceutical research utilizes Cedrol for the development of new drugs due to its bioactive properties and chemical versatility.\u003c\/li\u003e\n\u003cli\u003eOrganic synthesis experiments benefit from Cedrol’s solubility in organic solvents and its role in complex molecule creation.\u003c\/li\u003e\n\u003cli\u003eAntimicrobial studies often incorporate Cedrol because of its known antimicrobial activity, aiding in the evaluation of natural compounds.\u003c\/li\u003e\n\u003cli\u003eBiochemical assays use Cedrol as a reagent to test the effects of phenolic compounds on cellular processes and enzyme activity.\u003c\/li\u003e\n\u003cli\u003eHealth-related research employs Cedrol to explore its antioxidant properties and potential applications in therapeutic formulations.\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: 77-53-2\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Crude Medicine Ingredients for Research and Experimental Use\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory supply\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid or liquid, depending on the specific product variant\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\u003eCedrol 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 quality over time. When handling Cedrol, researchers should use appropriate personal protective equipment, such as gloves and safety goggles, to ensure safety. It is important to avoid contact with skin and eyes, and to work in a well-ventilated area to reduce inhalation risks. Proper labeling of storage containers is essential for safe handling and to prevent accidental misuse. Regular monitoring of storage conditions ensures the compound remains suitable for use in laboratory applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086199795930,"sku":"TCI2510C285417731","price":1771000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086199828698,"sku":"TCI2510C285417732","price":6156000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2854.jpg?v=1767098891"},{"product_id":"tci2510c336318400","title":"TCI C3363 35825-57-1 Cryptotanshinone","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCryptotanshinone is a naturally occurring compound derived from the *Salvia miltiorrhiza* plant, commonly known as *Danshen* in traditional Chinese medicine. This compound plays a significant role in life science laboratories, where it is utilized for studying its biological activities, including antioxidant, anti-inflammatory, and potential therapeutic effects on chronic diseases. Its presence in research settings allows scientists to explore its pharmacological properties and mechanisms of action. Due to its stability and availability, Cryptotanshinone is a valuable resource for experimental studies in both academic and industrial research environments.\u003c\/p\u003e\n\u003cp\u003eThe compound's unique molecular structure enables it to interact with various biological targets such as enzymes and cell receptors, making it a versatile tool in biochemical research. Its chemical properties also allow for testing its stability under different experimental conditions, which is crucial for reproducibility and accuracy in scientific studies. Additionally, its high purity and consistent quality ensure reliable results, making it a preferred choice for researchers seeking precision in their experiments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Cryptotanshinone is widely used in health and pharmacology-related research. Local research institutions frequently incorporate this compound into their studies to investigate its potential applications in drug development and disease treatment. Its relevance in both traditional and modern scientific contexts underscores its importance in the Indonesian scientific community.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePharmacological research for studying the compound's therapeutic potential in chronic disease treatment\u003c\/li\u003e\n\u003cli\u003eBiochemical experiments to analyze its antioxidant and anti-inflammatory properties\u003c\/li\u003e\n\u003cli\u003eDrug development studies to evaluate its interaction with biological targets such as enzymes and receptors\u003c\/li\u003e\n\u003cli\u003eStability testing under various experimental conditions to ensure reproducibility of results\u003c\/li\u003e\n\u003cli\u003eResearch on traditional Chinese medicine to explore its modern scientific applications\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: 35825-57-1\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Crude Medicine Ingredients for Research and Experimental Use\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard research quantities\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eCryptotanshinone should be stored in a cool, dry environment to maintain its stability and prevent degradation. It is recommended to use airtight containers to protect it from moisture and contaminants. Due to its chemical nature, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to ensure laboratory safety. The compound is generally non-hazardous but should be stored away from incompatible substances. Regular monitoring of storage conditions is essential to maintain its quality and effectiveness for research purposes. Proper labeling and documentation of storage locations are also important for safe laboratory management.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mg","offer_id":48086237708506,"sku":"TCI2510C336318400","price":2306000.0,"currency_code":"IDR","in_stock":true},{"title":"100mg","offer_id":48086237741274,"sku":"TCI2510C336318401","price":6493000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3363.jpg?v=1767099508"},{"product_id":"tci2510c343918478","title":"TCI C3439 4871-97-0 Curcumol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCurcumol is a naturally occurring compound found in curcuma extracts, particularly from the rhizomes of the turmeric plant. It plays a significant role in life science research, especially in the study of bioactive compounds with potential pharmacological applications. As a key component of the curcuminoid family, Curcumol is widely used in laboratories for its unique chemical properties and biological activities. Its presence in natural extracts makes it a valuable resource for researchers exploring the therapeutic potential of plant-derived compounds.\u003c\/p\u003e\n\u003cp\u003eCurcumol is prized for its stable chemical and physical properties, as well as its ability to dissolve in organic solvents, making it versatile for various laboratory procedures. Its significant antioxidant and anti-inflammatory activities further enhance its utility in experimental settings. These characteristics make Curcumol a preferred choice for researchers seeking reliable and effective compounds for drug development and disease mechanism studies. Additionally, its relatively low toxicity and safety profile contribute to its widespread use in experimental research.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Curcumol is extensively utilized in pharmacology, biochemical, and pharmaceutical research. It is commonly applied in antioxidant activity tests, inflammatory response studies, and drug formulation experiments. Its role in understanding the biological mechanisms of diseases and the development of new therapeutic agents underscores its importance in the scientific community. The compound’s availability and consistent quality make it a staple in many research settings across Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAntioxidant Activity Testing – Curcumol is used to evaluate the antioxidant potential of natural extracts and synthetic compounds due to its inherent antioxidant properties.\u003c\/li\u003e\n\u003cli\u003eInflammatory Response Studies – Its anti-inflammatory activity makes it ideal for investigating the mechanisms of inflammation and the efficacy of anti-inflammatory agents.\u003c\/li\u003e\n\u003cli\u003eDrug Development Research – Curcumol serves as a starting material for the synthesis of new compounds and is used in the development of pharmaceutical formulations.\u003c\/li\u003e\n\u003cli\u003eBioavailability Studies – Its solubility in organic solvents facilitates its use in experiments assessing the absorption and distribution of bioactive compounds.\u003c\/li\u003e\n\u003cli\u003eToxicity Assessment – Curcumol’s low toxicity profile makes it suitable for safety testing and evaluation of potential therapeutic agents.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand – TCI\u003c\/li\u003e\n\u003cli\u003eCAS Number – 4871-97-0\u003c\/li\u003e\n\u003cli\u003eCategory – Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Crude Medicine Ingredients for Research and Experimental Use\u003c\/li\u003e\n\u003cli\u003ePack Sizes – Available in various quantities as per standard laboratory supply options\u003c\/li\u003e\n\u003cli\u003ePhysical Form – Solid, typically in powder form\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\u003eCurcumol 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 minimize exposure to moisture and air, which can affect its integrity. Due to its solubility in organic solvents, it is important to handle it with care to avoid contamination. Standard laboratory safety practices should be followed, including the use of appropriate personal protective equipment when handling. Proper storage conditions ensure that Curcumol remains effective and safe for use in research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"10mg","offer_id":48086247014618,"sku":"TCI2510C343918478","price":4779000.0,"currency_code":"IDR","in_stock":true},{"title":"50mg","offer_id":48086247047386,"sku":"TCI2510C343918479","price":14334000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3439.jpg?v=1767099585"},{"product_id":"tci2510c344218482","title":"TCI C3442 6199-67-3 Cucurbitacin B","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCucurbitacin B is a chemical compound classified under alkaloids and widely used in pharmacological and biochemical research. As a key component of plants in the Cucurbitaceae family, it plays a significant role in the development of pharmaceuticals and bioactive compounds. In laboratory settings, it serves as a fundamental reagent for the synthesis of new compounds and the investigation of biological activities such as antioxidant, antitumor, and anti-inflammatory effects. Its presence in experimental research contributes to the understanding of natural products and their therapeutic potential.\u003c\/p\u003e\n\u003cp\u003eCucurbitacin B is valued for its complex molecular structure, which provides unique reactivity in chemical reactions. It is insoluble in water but more soluble in organic solvents such as ethyl acetate and ethanol, making it versatile for various extraction and synthesis processes. Its stability under certain conditions allows for safe handling and storage, enhancing its usability in laboratory environments. These properties make it a preferred choice for researchers seeking reliable and consistent results in their experiments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Cucurbitacin B is commonly used in applied research such as the development of modern traditional medicines, pharmacological effect studies of plants, and research on antioxidant effects in various disease conditions. Its application supports both academic and industrial research, contributing to advancements in pharmaceutical science and natural product chemistry.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePharmacological research for studying the biological effects of natural compounds in drug development.\u003c\/li\u003e\n\u003cli\u003eBiochemical studies to analyze the molecular mechanisms of antioxidant and anti-inflammatory activities.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical synthesis as a starting material for the creation of new therapeutic agents.\u003c\/li\u003e\n\u003cli\u003ePlant-based drug discovery to evaluate the potential of Cucurbitaceae species in traditional medicine.\u003c\/li\u003e\n\u003cli\u003eToxicological testing to assess the safety and efficacy of compounds derived from natural sources.\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: 6199-67-3\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 standard laboratory quantities\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eCucurbitacin B should be stored in a cool, dry environment to maintain its stability and prevent degradation. It is recommended to keep it in a tightly sealed container to minimize exposure to moisture and air. Due to its insolubility in water, it is advisable to use glass or plastic containers that are resistant to chemical reactions. Laboratory personnel should handle the compound with care, using appropriate personal protective equipment to ensure safety. Proper labeling and storage conditions are essential to maintain the integrity of the compound during experimental use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5mg","offer_id":48086247211226,"sku":"TCI2510C344218482","price":3682000.0,"currency_code":"IDR","in_stock":true},{"title":"25mg","offer_id":48086247243994,"sku":"TCI2510C344218483","price":12844000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3442.jpg?v=1768204774"},{"product_id":"tci2510c345018493","title":"TCI C3450 70831-56-0 Chicoric Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eChicoric Acid is a chemical compound widely used in scientific research, particularly in the fields of cell biology and nutrition. As a bioactive compound, it is commonly found in extracts of certain plants and has the potential to influence physiological and metabolic processes in organisms. In laboratory settings, Chicoric Acid serves as a key reagent for the synthesis of other compounds or as a test material in nutritional and pharmacological studies. Its chemical structure is complex, and its chemical properties are stable, making it suitable for a variety of research conditions.\u003c\/p\u003e\n\u003cp\u003eOne of the main reasons Chicoric Acid is preferred in laboratories is its antioxidant and anti-inflammatory properties. These characteristics make it a valuable tool in studies related to health and disease. Its ability to modulate biological activities also enhances its relevance in research that requires compounds with clear biological effects. Additionally, its stability under various experimental conditions ensures consistent results, which is crucial for reliable scientific outcomes.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Chicoric Acid is commonly used in public health, nutritional, and pharmacological research. Researchers often employ this compound to explore the effects of natural substances on human and animal physiology. Its versatility and biological activity make it a preferred choice for studies aiming to understand the impact of plant-derived compounds on health and disease mechanisms. The compound's broad applications support its continued use in diverse scientific investigations.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eNutritional Research: Chicoric Acid is used to study the bioavailability and metabolic effects of plant-derived compounds in dietary contexts.\u003c\/li\u003e\n\u003cli\u003ePharmacological Studies: It serves as a model compound to investigate the pharmacological properties of natural substances and their therapeutic potential.\u003c\/li\u003e\n\u003cli\u003eCell Biology Experiments: Its role in modulating cellular processes makes it valuable for studying cellular responses to bioactive compounds.\u003c\/li\u003e\n\u003cli\u003eHealth and Disease Research: The compound's antioxidant and anti-inflammatory properties are explored in studies related to chronic diseases and immune responses.\u003c\/li\u003e\n\u003cli\u003ePublic Health Investigations: It is utilized to assess the impact of natural compounds on public health outcomes and nutritional status.\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: 70831-56-0\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Cell Biology \u0026gt; Nutrition Research\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory supply\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid, crystalline powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eChicoric Acid 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 to prevent exposure to air and humidity, which could affect its integrity. As a solid, crystalline powder, it should be handled with care to avoid contamination. In laboratory settings, it is important to ensure proper ventilation when working with the compound to minimize inhalation risks. Always use appropriate personal protective equipment, such as gloves and safety goggles, when handling or transferring Chicoric Acid. Proper storage and handling practices are essential to preserve its quality and ensure safe usage in research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"10mg","offer_id":48086248554714,"sku":"TCI2510C345018493","price":2447000.0,"currency_code":"IDR","in_stock":true},{"title":"50mg","offer_id":48086248587482,"sku":"TCI2510C345018494","price":8432000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3450.jpg?v=1768817095"},{"product_id":"tci2510c347718527","title":"TCI C3477 3650-09-7 Carnosic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCarnosic Acid is a naturally occurring phenolic compound widely found in plants such as rosemary and sage. This compound plays a vital role in biochemical and pharmacological research due to its potent antioxidant properties. In the laboratory, it serves as a key reagent for studying antioxidant effects, free radical scavenging, and the mechanisms of biological activity. Its natural origin and well-documented properties make it a reliable choice for researchers seeking to explore the therapeutic potential of plant-derived compounds.\u003c\/p\u003e\n\u003cp\u003eCarnosic Acid is valued for its complex chemical structure, which provides both reactivity and stability under specific conditions. Its strong antioxidant activity makes it an ideal candidate for experiments aimed at inhibiting oxidative damage. Additionally, its good solubility in organic solvents enhances its usability in various chemical reactions and experimental formulations. These characteristics make it a preferred choice for researchers in both academic and industrial settings.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Carnosic Acid is commonly used in research related to health, environmental science, and pharmaceutical development. Its relevance in natural product research has made it a staple in studies focused on the biological effects of phenolic compounds. Researchers in Indonesia rely on its consistent quality and well-defined properties to support their experimental work across multiple scientific disciplines.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAntioxidant Activity Studies: Carnosic Acid is used to investigate its ability to neutralize free radicals and prevent oxidative damage in cellular and tissue systems.\u003c\/li\u003e\n\u003cli\u003eFree Radical Scavenging Research: It is employed to evaluate its effectiveness in scavenging reactive oxygen species, contributing to understanding its protective mechanisms.\u003c\/li\u003e\n\u003cli\u003eNatural Product Development: Carnosic Acid supports the formulation of pharmaceutical and cosmetic products derived from natural sources due to its bioactive properties.\u003c\/li\u003e\n\u003cli\u003eBiological Mechanism Exploration: It is utilized to study the molecular pathways involved in the biological activity of phenolic compounds.\u003c\/li\u003e\n\u003cli\u003eEnvironmental Toxicology Studies: Carnosic Acid is used to assess its impact on environmental systems and its potential role in bioremediation processes.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS Number: 3650-09-7\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Crude Medicine Ingredients for Research and Experimental Use\u003c\/li\u003e\n\u003cli\u003ePack Sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical Form: Solid (as per standard product description)\u003c\/li\u003e\n\u003cli\u003eStorage Note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eCarnosic Acid should be stored in a cool, dry place, away from direct light and moisture to maintain its chemical integrity. It is recommended to use airtight containers to prevent exposure to air and humidity, which may affect its stability. Due to its chemical reactivity, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. It is important to ensure that storage conditions are consistent and free from contaminants to preserve its potency. In laboratory settings, proper labeling and secure storage are essential to prevent accidental exposure and ensure safe handling.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"20mg","offer_id":48086251962586,"sku":"TCI2510C347718527","price":1997000.0,"currency_code":"IDR","in_stock":true},{"title":"100mg","offer_id":48086251995354,"sku":"TCI2510C347718528","price":8489000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3477.jpg?v=1767099647"},{"product_id":"tci2510c349418553","title":"TCI C3494 2415-24-9 Catalpol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCatalpol is a chemical compound classified under glycosides, widely utilized in chemical and biological research. It plays a significant role in laboratory settings where the study of bioactive compounds, pharmacological effects, and antioxidant activities is required. As a key component in various scientific investigations, Catalpol is essential for experiments involving molecular structure analysis, biological activity testing, and molecular interaction studies in biological environments. Its presence in research areas such as pharmacology and phytochemistry highlights its importance in understanding natural compounds and their potential therapeutic applications.\u003c\/p\u003e\n\u003cp\u003eCatalpol is valued for its chemical stability and solubility in specific organic solvents like ethyl acetate and acetone. These properties make it highly compatible with analytical techniques such as chromatography and spectroscopy, enabling accurate and reliable experimental results. Additionally, its antitumor and anti-inflammatory properties have made it a sought-after material in both pharmacological and biochemical studies. The compound’s versatility and effectiveness in various experimental setups contribute to its popularity among researchers.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Catalpol is commonly used in pharmaceutical, molecular biology, and organic chemistry research. It is a preferred choice for experiments requiring high biological activity, especially in studies involving natural compounds. Its consistent performance and reliability make it a trusted material for researchers aiming to explore the potential of bioactive substances in both academic and applied settings.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eUsed in pharmacological research for studying the antitumor and anti-inflammatory effects of natural compounds.\u003c\/li\u003e\n\u003cli\u003eApplied in biochemical studies to analyze the antioxidant properties of bioactive substances.\u003c\/li\u003e\n\u003cli\u003eEmployed in molecular biology experiments for investigating molecular interactions and structural analysis.\u003c\/li\u003e\n\u003cli\u003eUtilized in organic chemistry for the synthesis and characterization of glycoside derivatives.\u003c\/li\u003e\n\u003cli\u003eIntegrated into analytical techniques such as HPLC and UV-Vis spectroscopy for compound identification and quantification.\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: 2415-24-9\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Glycoscience\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory requirements\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eCatalpol 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 solubility in organic solvents, it should be handled in a well-ventilated area to avoid inhalation of vapors. Laboratory personnel should wear appropriate personal protective equipment, including gloves and safety goggles, when handling the compound. Catalpol is non-hazardous under normal conditions but should be kept out of reach of children and not exposed to incompatible materials. Proper labeling and storage practices ensure the safety and effectiveness of the compound in research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"250mg","offer_id":48086255141082,"sku":"TCI2510C349418553","price":7027000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3494.jpg?v=1767099684"},{"product_id":"tci2510c350118561","title":"TCI C3501 61281-38-7 Schisandrin A","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eSchisandrin A is a bioactive compound belonging to the class of phytochemicals, primarily found in the *Schisandra chinensis* plant. This compound plays a vital role in biochemical and pharmacological research, serving as a key reagent for studying the biological effects of natural substances. In laboratory settings, it is used to investigate the mechanisms of action of natural compounds on biological systems, making it an essential tool for researchers in life sciences. Its unique molecular structure and significant biological activity contribute to its importance in experimental studies aimed at understanding the therapeutic potential of plant-derived compounds.\u003c\/p\u003e\n\u003cp\u003eThe compound's complex structure and notable biological activity make it a preferred choice for researchers. Schisandrin A exhibits significant antioxidant properties, enabling it to reduce oxidative stress and enhance cellular function. These properties are crucial in studies related to drug development, antioxidant research, and alternative therapy exploration. Its chemical stability under certain conditions further enhances its usability in laboratory experiments, ensuring consistent results across multiple trials. This stability and potency make it a reliable reagent for both academic and industrial research applications.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Schisandrin A is widely utilized in pharmaceutical and biomedical research. It is commonly found in research institutions and universities where scientists investigate the pharmacological effects of natural compounds. Its role in developing new therapeutic approaches and understanding the mechanisms of plant-based treatments makes it a valuable resource for researchers in Indonesia. Its availability and reliability ensure that it remains a key component in various experimental studies conducted within the country.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBiochemical Research: Schisandrin A is ideal for studying the biological effects of natural compounds due to its bioactive properties and molecular complexity.\u003c\/li\u003e\n\u003cli\u003ePharmacological Studies: It is used to explore the therapeutic potential of plant-derived substances, particularly in drug development and alternative medicine research.\u003c\/li\u003e\n\u003cli\u003eAntioxidant Activity Analysis: Its ability to reduce oxidative stress makes it suitable for experiments investigating antioxidant mechanisms in biological systems.\u003c\/li\u003e\n\u003cli\u003eCellular Function Studies: The compound's impact on cellular function supports research into how natural compounds influence cellular processes and health.\u003c\/li\u003e\n\u003cli\u003eAlternative Therapy Exploration: Schisandrin A is utilized to examine the efficacy of natural remedies in treating various conditions and diseases.\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: 61281-38-7\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Crude Medicine Ingredients for Research and Experimental Use\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified\u003c\/li\u003e\n\u003cli\u003ePhysical form: Not specified\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eSchisandrin A should be stored in a cool, dry place away from direct sunlight to maintain its chemical stability. It is recommended to use airtight containers to prevent moisture absorption and contamination. Proper labeling of storage containers is essential for safe handling and identification. Laboratory personnel should wear appropriate personal protective equipment when handling the compound to ensure safety. Avoid exposure to high temperatures and ensure good ventilation in the workspace. Regular monitoring of storage conditions helps maintain the integrity of the compound for reliable experimental results.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mg","offer_id":48086256353498,"sku":"TCI2510C350118561","price":3852000.0,"currency_code":"IDR","in_stock":true},{"title":"100mg","offer_id":48086256386266,"sku":"TCI2510C350118562","price":11328000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3501.jpg?v=1767099688"},{"product_id":"tci2510c350718570","title":"TCI C3507 529-53-3 Scutellarein","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eScutellarein is a phenylpropanoid compound with a complex chemical structure, widely used in life science research. It is commonly found in plant extracts, particularly from the Apiaceae family, such as carrot and parsley leaves. In the laboratory, Scutellarein serves as a key reagent for the synthesis of other compounds or as a control in biological activity assays. Its role spans multiple disciplines, including biochemistry and pharmacology, where it is employed to study molecular interactions and metabolic pathways.\u003c\/p\u003e\n\u003cp\u003eScutellarein is preferred due to its high purity and chemical stability, making it reliable for precise experimental applications. Its unique chemical properties allow it to bind to specific proteins and influence cellular metabolic pathways. Additionally, Scutellarein exhibits strong antioxidant activity, which makes it valuable in health and pharmacological research. These characteristics ensure its consistency and effectiveness in various experimental settings.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Scutellarein is frequently used in molecular biology, pharmacology, and ecological studies. Researchers rely on its consistent quality and well-documented properties to conduct experiments that require accuracy and reproducibility. Its presence in research programs focused on drug development and natural product analysis underscores its importance in the scientific community.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMolecular biology research utilizes Scutellarein to study protein-ligand interactions and signaling pathways in cellular systems.\u003c\/li\u003e\n\u003cli\u003ePharmacological studies employ Scutellarein to assess its antioxidant properties and potential therapeutic applications in drug development.\u003c\/li\u003e\n\u003cli\u003eBiochemical experiments benefit from Scutellarein’s stability and purity, making it ideal for synthetic reactions and standardization processes.\u003c\/li\u003e\n\u003cli\u003eEcological research incorporates Scutellarein to analyze plant-derived compounds and their environmental impacts.\u003c\/li\u003e\n\u003cli\u003eAnalytical chemistry applications use Scutellarein as a reference standard for chromatographic and spectroscopic analyses.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 529-53-3\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Phenylpropanoids, Aromatic Polyketides\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid, crystalline powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eScutellarein 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 to prevent contamination and degradation. Due to its high purity, it is important to handle Scutellarein with care to avoid exposure to air and moisture, which could affect its integrity. In laboratory settings, proper personal protective equipment should be worn when handling this compound. Regular monitoring of storage conditions ensures the material remains suitable for use in research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"10mg","offer_id":48086256746714,"sku":"TCI2510C350718570","price":3626000.0,"currency_code":"IDR","in_stock":true},{"title":"50mg","offer_id":48086256779482,"sku":"TCI2510C350718571","price":11637000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3507.jpg?v=1771057934"},{"product_id":"tci2510c358418676","title":"TCI C3584 3895-92-9 Chelerythrine Chloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eChelerythrine Chloride is a chemical compound widely utilized in scientific research, particularly in the fields of biochemistry and pharmacology. This compound is derived from the plant *Chelidonium majus* and is recognized for its significant pharmacological activity. In laboratory settings, it serves as a key reagent for various experiments, including the study of biological mechanisms, drug development, and the investigation of natural compounds. Its role is essential in advancing research that explores the potential therapeutic applications of plant-derived substances.\u003c\/p\u003e\n\u003cp\u003eChelerythrine Chloride is valued for its complex chemical structure and polar nature, which allows it to dissolve in organic solvents such as ethyl acetate and methanol. These properties make it highly versatile for use in chemical reactions and extraction processes. Additionally, its stability under certain conditions ensures that it remains effective for extended periods, facilitating long-term research projects. This combination of solubility and stability makes it a preferred choice for researchers working with natural compounds.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Chelerythrine Chloride is commonly used in research focused on the biological effects of natural substances. It plays a vital role in the development of pharmaceutical products and biomedical research aimed at treating chronic diseases. Its presence in research studies helps scientists better understand the pharmacological properties of plant-derived compounds, contributing to the advancement of medical science in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eDrug development research utilizes Chelerythrine Chloride to study the pharmacological properties of natural compounds and their potential therapeutic applications.\u003c\/li\u003e\n\u003cli\u003eAnti-inflammatory and antioxidant activity testing benefits from its ability to interact with biological systems, making it ideal for evaluating natural compound efficacy.\u003c\/li\u003e\n\u003cli\u003eBiochemical experiments leverage its solubility in organic solvents to facilitate extraction and reaction processes in laboratory settings.\u003c\/li\u003e\n\u003cli\u003eNatural product isolation and purification studies rely on its chemical structure and stability to ensure consistent results in research.\u003c\/li\u003e\n\u003cli\u003eChronic disease research incorporates Chelerythrine Chloride to explore its potential role in developing treatments for long-term health conditions.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 3895-92-9\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Crude Medicine Ingredients for Research and Experimental Use\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard research 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 light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eChelerythrine Chloride should be stored in a cool, dry environment, away from direct sunlight and moisture to maintain its chemical integrity. It is recommended to use airtight containers made of glass or high-density polyethylene to prevent contamination and degradation. Due to its polar nature, it is important to handle the compound with care during preparation and use to avoid any unintended chemical interactions. In laboratory settings, proper personal protective equipment such as gloves and safety goggles should be worn when handling this compound to ensure safety. Regular monitoring of storage conditions is also advised to ensure the compound remains stable and effective for research purposes.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mg","offer_id":48086267527386,"sku":"TCI2510C358418676","price":8124000.0,"currency_code":"IDR","in_stock":true},{"title":"100mg","offer_id":48086267560154,"sku":"TCI2510C358418677","price":22457000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3584.jpg?v=1767099809"},{"product_id":"tci2510c361918719","title":"TCI C3619 7540-51-4 (-)-beta-Citronellol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(-)-beta-Citronellol is a chiral compound widely used in organic synthesis, particularly in asymmetric chemistry. It serves as a key building block for the synthesis of various chiral molecules with specific biological activities. This compound is essential in laboratories where precise control over stereochemistry is required. Its unique molecular structure makes it valuable for creating complex organic molecules with defined stereo configurations. In the field of pharmaceutical research, (-)-beta-Citronellol plays a critical role in the development of new drugs with enhanced efficacy and selectivity.\u003c\/p\u003e\n\u003cp\u003eThe compound is known for its chemical stability and clear chiral structure, which facilitates isomer separation and asymmetric reactions. Its stability under various laboratory conditions ensures consistent performance in synthetic processes. Additionally, (-)-beta-Citronellol has a distinct aroma, making it suitable for applications in fragrance and flavor industries. These properties make it a preferred choice for researchers seeking reliable and versatile chiral building blocks.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, (-)-beta-Citronellol is commonly used in organic chemistry and pharmaceutical research. Its relevance extends to academic and industrial settings where the synthesis of chiral compounds is essential. The compound supports both fundamental research and applied projects, contributing to advancements in drug development and cosmetic formulations. Its availability and reliability make it a valuable resource for scientists in Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis applications benefit from (-)-beta-Citronellol's chiral structure, enabling the creation of complex molecules with precise stereochemistry.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research utilizes this compound for the synthesis of chiral drugs, ensuring optimal biological activity and reduced side effects.\u003c\/li\u003e\n\u003cli\u003eCosmetic formulation processes incorporate (-)-beta-Citronellol due to its aromatic properties, enhancing the sensory qualities of products.\u003c\/li\u003e\n\u003cli\u003eAsymmetric catalysis relies on this compound to produce enantiomerically pure compounds, improving reaction efficiency and selectivity.\u003c\/li\u003e\n\u003cli\u003eIndustrial fragrance development uses (-)-beta-Citronellol for its distinctive scent, contributing to the creation of high-quality perfumes and flavorings.\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: 7540-51-4\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: As per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Liquid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003e(-)-beta-Citronellol should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to keep the compound in a tightly sealed container to prevent moisture absorption and contamination. Due to its chemical stability, it does not require refrigeration but should be protected from prolonged exposure to air. In laboratory settings, proper ventilation is essential when handling this compound to ensure safe working conditions. Always use appropriate personal protective equipment, such as gloves and safety goggles, to minimize exposure risks. The compound is non-hazardous under normal storage conditions but should be handled with care to maintain its integrity and effectiveness.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5mL","offer_id":48275733905626,"sku":"TCI2510C361918719","price":901000.0,"currency_code":"IDR","in_stock":false}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3619.jpg?v=1769144262"},{"product_id":"tci2510c364818739","title":"TCI C3648 106-23-0 (+\/-)-Citronellal","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(+\/-)-Citronellal is a versatile organic compound widely used in laboratory settings, particularly in biochemical and chemical research. As a member of the terpene family, it plays a crucial role in various experimental applications, including the study of natural compounds and synthetic chemistry. Its unique chemical structure and reactivity make it an essential reagent for researchers working in life sciences and related fields. This compound is commonly found in both academic and industrial laboratories, where it serves as a building block for more complex molecules and aids in the development of new chemical compounds.\u003c\/p\u003e\n\u003cp\u003e(+\/-)-Citronellal is valued for its stability, reactivity, and distinct aroma, which closely resembles that of citronella oil. These properties make it a preferred choice for experiments involving oxidation and reduction reactions, as well as for the synthesis of various organic compounds. Its volatility and solubility in organic solvents further enhance its utility in laboratory procedures. The compound's ability to participate in multiple chemical reactions without significant degradation ensures its reliability in a wide range of experimental conditions. Additionally, its availability in different packaging formats makes it convenient for both small-scale and large-scale laboratory use.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, (+\/-)-Citronellal is frequently used in research related to natural compounds, especially in the field of pharmacology. It is also employed in the study of fragrance chemistry and as a component in the development of natural products. Due to its chemical properties and widespread availability, it remains a key reagent in both academic and applied research settings in Indonesia. Its role in supporting scientific inquiry and innovation is well recognized among researchers and laboratory professionals.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eUsed in biochemical research for studying natural compounds and their interactions with biological systems.\u003c\/li\u003e\n\u003cli\u003eApplied in fragrance chemistry to analyze and synthesize aromatic compounds with natural characteristics.\u003c\/li\u003e\n\u003cli\u003eUtilized in synthetic chemistry for oxidation and reduction reactions to create complex organic molecules.\u003c\/li\u003e\n\u003cli\u003eEmployed in pharmacological studies to evaluate the properties of natural products and their potential therapeutic applications.\u003c\/li\u003e\n\u003cli\u003eIntegrated into analytical procedures for the identification and quantification of terpene derivatives in various samples.\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: 106-23-0\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Terpenes\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various sizes as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Liquid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dark place away from direct sunlight and heat sources\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003e(+\/-)-Citronellal should be stored in a cool, dark location, away from direct sunlight and heat sources to maintain its chemical stability. It is recommended to use sealed glass containers to prevent evaporation due to its volatile nature. Proper ventilation is essential when handling this compound to minimize exposure. Laboratory personnel should wear appropriate personal protective equipment, including gloves and safety goggles, to avoid direct contact with the skin or eyes. Due to its reactivity, it should be kept away from incompatible materials such as strong oxidizing agents. Regular monitoring of storage conditions ensures the compound remains safe and effective for use in research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mL","offer_id":48086273720538,"sku":"TCI2510C364818739","price":1799000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3648.jpg?v=1768817134"},{"product_id":"tci2510c366018755","title":"TCI C3660 77-54-3 Cedryl Acetate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCedryl Acetate (TCI C3660), with the CAS number 77-54-3, is a chemical compound widely used in laboratory settings for its versatility in organic chemistry and biochemical research. It belongs to the terpene family, a group of naturally occurring compounds known for their diverse chemical and biological properties. This compound is commonly utilized as a reagent in the synthesis of complex organic molecules, making it a valuable tool for researchers in life sciences. Its role extends to studies involving fragrance and the physical properties of organic materials, where it serves as a key component in understanding molecular behavior.\u003c\/p\u003e\n\u003cp\u003eCedryl Acetate is favored for its chemical stability and solubility in organic solvents such as ethyl acetate and chloroform. These characteristics make it an ideal choice for chemical reactions requiring organic solvents. Additionally, its distinct aroma contributes to its relevance in aroma research and the development of fragrance-related compounds. The compound is non-toxic and relatively safe under normal usage conditions, which enhances its appeal in laboratory environments. Its stability and solubility ensure consistent performance across various experimental setups.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Cedryl Acetate is frequently used in chemical and pharmaceutical research, particularly in organic synthesis and fragrance studies. Its application spans across academic and industrial research settings, supporting the development of new compounds and the analysis of molecular properties. Its availability and reliability make it a preferred choice for researchers working on projects related to organic chemistry and biochemistry.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic Synthesis: Cedryl Acetate is ideal for organic synthesis due to its solubility in organic solvents and chemical stability, allowing for efficient reaction conditions.\u003c\/li\u003e\n\u003cli\u003eAroma Research: Its distinct aroma makes it a key component in studies related to fragrance and the sensory properties of organic compounds.\u003c\/li\u003e\n\u003cli\u003ePhysical Property Testing: It is used to assess the volatility and stability of organic compounds, providing valuable data for material characterization.\u003c\/li\u003e\n\u003cli\u003eBiochemical Studies: Cedryl Acetate supports research into the chemical behavior of terpenoids, contributing to understanding their biological and chemical properties.\u003c\/li\u003e\n\u003cli\u003eIndustrial Research: Its versatility and reliability make it a preferred choice for pharmaceutical and chemical industries conducting compound development and analysis.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS Number: 77-54-3\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Terpenes\u003c\/li\u003e\n\u003cli\u003ePack Sizes: Available in various sizes as per standard laboratory requirements\u003c\/li\u003e\n\u003cli\u003ePhysical Form: Liquid\u003c\/li\u003e\n\u003cli\u003eStorage Note: Store in a cool, dark place away from direct sunlight and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eCedryl Acetate should be stored in a cool, dark place, away from direct sunlight 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 evaporation. Due to its solubility in organic solvents, it should be kept separate from incompatible materials to avoid unintended reactions. In laboratory settings, proper ventilation is essential to ensure safe handling. Always use appropriate personal protective equipment, such as gloves and safety goggles, when working with this compound. Its non-toxic nature makes it relatively safe, but standard laboratory safety protocols should still be followed to ensure optimal handling and storage conditions.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086275227866,"sku":"TCI2510C366018755","price":1827000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48086275260634,"sku":"TCI2510C366018756","price":5509000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3660.jpg?v=1768817134"},{"product_id":"tci2510c387418988","title":"TCI C3874 603-56-5 Chrysosptertin B","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eChrysosptertin B is a naturally occurring compound widely used in life sciences research, particularly in biochemistry and pharmaceutical studies. As a key component in certain plant extracts, it serves as a valuable research material for investigating the biological activity of natural compounds. Its presence in various botanical sources makes it a critical reagent for scientists exploring the potential of plant-derived substances in drug development and therapeutic applications. This compound plays a pivotal role in understanding the molecular mechanisms underlying biological processes in both human and animal systems.\u003c\/p\u003e\n\u003cp\u003eChrysosptertin B is prized for its chemical stability and ease of identification, which are essential for high-precision laboratory experiments. Its complex molecular structure offers a unique platform for studying biochemical interactions and pharmacological effects. Additionally, the compound exhibits promising antitumor and antioxidant properties, making it a subject of interest in medical research. These characteristics ensure its reliability and relevance in scientific investigations, supporting the development of new therapeutic strategies and bioactive compounds.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Chrysosptertin B is commonly used in pharmacological and biochemical research. It supports studies related to drug development, bioactive compound analysis, and the exploration of natural products for medicinal applications. Its availability facilitates scientific innovation and contributes to the advancement of health sciences and life sciences research in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBiochemical Research: Chrysosptertin B is used to study the biochemical properties of natural compounds and their interactions with biological systems.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical Development: The compound aids in the discovery and development of new drugs by analyzing its pharmacological effects and potential therapeutic applications.\u003c\/li\u003e\n\u003cli\u003eAntioxidant Studies: Its antioxidant properties make it suitable for experiments investigating free radical scavenging and oxidative stress mechanisms.\u003c\/li\u003e\n\u003cli\u003eTumor Research: Chrysosptertin B is utilized in cancer-related studies to explore its antitumor activity and potential as a therapeutic agent.\u003c\/li\u003e\n\u003cli\u003eNatural Product Analysis: It serves as a key reagent in the identification and characterization of bioactive compounds derived from plant sources.\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: 603-56-5\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Crude Medicine Ingredients for Research and Experimental Use\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory supply\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid or powder, depending on the specific product 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\u003eChrysosptertin B should be stored in a cool, dry environment to maintain its chemical stability and prevent degradation. It is recommended to keep the compound in a tightly sealed container to minimize exposure to moisture and air. Laboratory personnel should handle the material with care, using appropriate personal protective equipment such as gloves and safety goggles. Due to its potential reactivity, it should be stored away from incompatible substances. Regular monitoring of storage conditions ensures the integrity of the compound, supporting reliable and reproducible research outcomes. Proper handling and storage practices are essential to maintain the quality and effectiveness of Chrysosptertin B in scientific applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mg","offer_id":48086298427610,"sku":"TCI2510C387418988","price":10989000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3874.jpg?v=1767100218"},{"product_id":"tci2510c392119039","title":"TCI C3921 4547-24-4 Corosolic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCorosolic Acid is a chemical compound widely used in life science research and biochemical experiments. As a key component in natural products such as the leaves of the breadfruit tree, it has gained significant attention for its potential pharmacological properties. In laboratory settings, this compound serves as an essential reagent for studying biological activities, including antioxidant, anti-inflammatory, and antidiabetic effects. Its role in experimental research makes it a valuable tool for scientists exploring natural remedies and therapeutic applications.\u003c\/p\u003e\n\u003cp\u003eThe unique molecular structure of Corosolic Acid allows it to interact with various biological pathways, making it a preferred choice for researchers. It is chemically stable under certain conditions and is commonly available in crystalline form, which facilitates its use in laboratory experiments. Its non-toxic nature and measurable biological activity further enhance its appeal in scientific studies. These properties contribute to its widespread use in both academic and industrial research environments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Corosolic Acid is frequently utilized in applied research projects, including the development of herbal medicines, pharmacological effect studies, and biochemical experiments. Its relevance extends to researchers interested in natural compounds and their applications in healthcare. The compound's versatility and reliability make it a go-to material for various scientific investigations in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePharmacological research for studying anti-inflammatory and antioxidant properties due to its bioactive nature.\u003c\/li\u003e\n\u003cli\u003eDevelopment of herbal medicines as a key ingredient in natural product formulations for therapeutic applications.\u003c\/li\u003e\n\u003cli\u003eBiochemical experiments to analyze molecular interactions and biological pathway mechanisms.\u003c\/li\u003e\n\u003cli\u003eAntidiabetic studies to evaluate the compound's potential in managing blood sugar levels.\u003c\/li\u003e\n\u003cli\u003eNatural product screening to identify new compounds with therapeutic potential in traditional medicine.\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: 4547-24-4\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Crude Medicine Ingredients for Research and Experimental Use\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities\u003c\/li\u003e\n\u003cli\u003ePhysical form: Crystalline\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\u003eCorosolic Acid should be stored in a cool, dry environment to maintain its stability and prevent degradation. It is recommended to keep the compound in a sealed container to avoid exposure to moisture and air. Since it is non-toxic, general laboratory safety protocols should still be followed when handling. The compound is stable under normal laboratory conditions but should be protected from extreme temperatures. Proper labeling and storage in a designated chemical cabinet are essential for safe handling and easy access. Always ensure that the workspace is clean and free from contaminants to preserve the integrity of the compound during experiments.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48086303834330,"sku":"TCI2510C392119039","price":9248000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3921.jpg?v=1767100310"}],"url":"https:\/\/amiscientific.com\/en\/collections\/tci-l4-phytochemicals.oembed?page=18","provider":"AMI Scientific","version":"1.0","type":"link"}