{"title":"Nutrition Research","description":"\u003cp\u003e\u003cstrong\u003eNutrition Research\u003c\/strong\u003e — menghimpun fitokimia, vitamin, dan senyawa acuan untuk riset pangan fungsional, termasuk asam lemak, polifenol, dan metabolit tanaman yang menjadi objek studi nutrisi. Kategori ini menjembatani kimia bahan alam dengan penelitian gizi dan pangan.\u003c\/p\u003e\u003cp\u003eNutrition Research dipakai peneliti pangan dan gizi untuk menganalisis kandungan fitokimia dan profil asam lemak menggunakan standar GC, mengevaluasi aktivitas fitokimia seperti bakuchiol pada bahan uji in vitro, serta menyusun kurva kalibrasi vitamin dalam pengembangan produk pangan fungsional. Bahan-bahan ini juga menjadi acuan pembanding dalam studi komposisi bahan alam.\u003c\/p\u003e\u003cp\u003eContoh produk dalam koleksi ini: \u003ca href=\"\/en\/products\/tci2510s032550160\"\u003eTCI S0325 112-63-0 Methyl Linoleate [Standard Material for GC]\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b570012413\"\u003eTCI B5700 10309-37-2 Bakuchiol\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510o018044529\"\u003eTCI O0180 112-80-1 Oleic Acid\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b573912468\"\u003eTCI B5739 1022-46-4 Bentranil\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510l005036931\"\u003eTCI L0050 463-40-1 Linolenic Acid\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b595212731\"\u003eTCI B5952 69327-76-0 Buprofezin\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510m012137673\"\u003eTCI M0121 90-05-1 Guaiacol\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b603412836\"\u003eTCI B6034 55179-31-2 Bitertanol\u003c\/a\u003e.\u003c\/p\u003e\u003cp\u003ePertimbangkan kemurnian standar analitik, bentuk isomer (misalnya cis\/trans pada asam lemak), dan apakah produk disediakan sebagai bahan acuan bersertifikat untuk keperluan kuantifikasi GC. 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 Biologi Sel, sering dipakai bersamaan dalam satu alur kerja laboratorium:\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-cell-signaling-and-neuroscience\"\u003eCell Signaling and Neuroscience\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-cancer-research\"\u003eCancer Research\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-immune-system-inflammation-allergy-research\"\u003eImmune System, Inflammation, Allergy Research\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-bioactive-small-molecules\"\u003eBioactive Small Molecules\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-metabolomics\"\u003eMetabolomics\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-stem-cell-biology\"\u003eStem Cell Biology\u003c\/a\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eKoleksi ini masih terbagi menjadi 3 kelompok yang lebih spesifik:\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-phytochemicals\"\u003ePhytochemicals\u003c\/a\u003e\u003c\/li\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\/biologi-sel\"\u003eBiologi Sel\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":"tci2510b573912468","title":"TCI B5739 1022-46-4 Bentranil","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBentranil (CAS 1022-46-4) is a high-purity benzoxazinone compound supplied by TCI, commonly utilized as a reference standard and research reagent in cell biology and nutrition science. It serves as a reliable analytical standard for chromatographic method development and instrument validation in life science laboratories. The compound is also employed as a model molecule in studies investigating cellular metabolic pathways and bioactivity screening, supporting both fundamental and applied nutrition research.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"250mg","offer_id":48085900230874,"sku":"TCI2510B573912468","price":3079000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48085900263642,"sku":"TCI2510B573912469","price":9213000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5739.jpg?v=1768204440"},{"product_id":"tci2510b595212731","title":"TCI B5952 69327-76-0 Buprofezin","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B5952 Buprofezin (CAS 69327-76-0) is a high-purity chitin synthesis inhibitor widely utilized in cell biology and nutrition research laboratories for studying insect growth regulation and molting mechanisms. This compound serves as an essential reference standard for analytical testing, enzyme activity assays, and insect cell culture studies investigating the interaction between nutrition and developmental pathways. Available in 5g and 25g packaging from TCI, it is a reliable reagent for toxicology research and chitin biosynthesis pathway analysis in invertebrate model organisms.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48085911371994,"sku":"TCI2510B595212731","price":2576000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085911404762,"sku":"TCI2510B595212732","price":8935000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5952.jpg?v=1768204462"},{"product_id":"tci2510b603412836","title":"TCI B6034 55179-31-2 Bitertanol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBitertanol, with CAS number 55179-31-2, is an organic compound widely utilized in life science research, particularly in cell biology and nutrition studies. It serves as a versatile solvent and a valuable reagent in organic synthesis, supporting a range of chemical reactions in the laboratory. Its unique chemical structure enables it to participate in various biochemical processes, making it a key component in experimental setups. Bitertanol is particularly favored for its stability and controlled reactivity, which allows researchers to conduct experiments with predictable outcomes. Its non-polar nature also makes it suitable for dissolving a variety of organic compounds, enhancing its utility in different experimental contexts.\u003c\/p\u003e\n\u003cp\u003eThe chemical properties of bitertanol make it a preferred choice for laboratory use. It exhibits good solubility in organic solvents such as ethyl acetate and acetone, ensuring consistent performance in different applications. Its chemical stability ensures that it remains inert under normal laboratory conditions, reducing the risk of unwanted side reactions. Additionally, bitertanol is non-toxic at normal dosages, which contributes to its safety profile in controlled laboratory environments. These characteristics make it a reliable and dependable reagent for researchers working in both academic and industrial settings.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, bitertanol is commonly used in research related to cell biology and nutrition. Many research institutions and universities in Indonesia rely on this compound for experiments involving molecular interactions, metabolic studies, and organic synthesis. Its availability and reliable performance make it a staple in laboratories focused on advancing scientific knowledge in these fields.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eCell culture experiments benefit from bitertanol’s role as a solvent and its ability to support stable chemical environments.\u003c\/li\u003e\n\u003cli\u003eNutritional research utilizes bitertanol for studying the solubility and bioavailability of organic compounds in biological systems.\u003c\/li\u003e\n\u003cli\u003eOrganic synthesis processes rely on bitertanol’s solubility properties to dissolve reactants and facilitate chemical reactions.\u003c\/li\u003e\n\u003cli\u003eMetabolic studies use bitertanol to investigate molecular interactions and biochemical pathways in living systems.\u003c\/li\u003e\n\u003cli\u003eBiochemical assays incorporate bitertanol as a medium to ensure consistent and reproducible results in experimental setups.\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: 55179-31-2\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: Liquid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eBitertanol should be stored in a cool, dry location, away from direct sunlight and sources of heat. It is recommended to use airtight containers made of glass or high-density polyethylene to prevent contamination and evaporation. Due to its non-polar nature, it is important to handle it with care to avoid spills or exposure. In laboratory settings, proper ventilation should be ensured to maintain a safe working environment. Bitertanol is non-toxic at normal dosages, but standard safety protocols should still be followed when handling any chemical. Regular monitoring of storage conditions ensures the integrity and effectiveness of the compound in research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085916057818,"sku":"TCI2510B603412836","price":1036000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085916090586,"sku":"TCI2510B603412837","price":3636000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6034.jpg?v=1769144655"},{"product_id":"tci2510b608512896","title":"TCI B6085 4481-62-3 Betulonic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBetulonic Acid (CAS 4481-62-3) is a pentacyclic triterpenoid compound supplied by TCI, primarily utilized as a reference reagent in pharmaceutical and life science research. It is widely employed in experimental studies involving anti-inflammatory activity, cytotoxicity assays against cancer cell lines, and antiviral potential evaluation. This product is intended exclusively for laboratory research purposes and serves as a reliable standard for chromatographic analysis and synthetic derivatization of betulinic acid analogs.\u003c\/p\u003e\n\u003cp\u003e---\u003c\/p\u003e","brand":"TCI","offers":[{"title":"50mg","offer_id":48085918580954,"sku":"TCI2510B608512896","price":5250000.0,"currency_code":"IDR","in_stock":true},{"title":"250mg","offer_id":48085918613722,"sku":"TCI2510B608512897","price":16733000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6085.jpg?v=1768204482"},{"product_id":"tci2510b618613014","title":"TCI B6186 7287-19-6 Prometryn","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003ePrometryn is a triazine-class herbicide compound commonly used as a reference standard in pesticide residue analysis and environmental monitoring studies. It acts as a photosystem II inhibitor, making it a valuable tool for plant physiology research and herbicide resistance studies. This high-purity TCI product is suitable for chromatographic applications and quantitative analysis across academic and testing laboratories.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48085923889370,"sku":"TCI2510B618613014","price":2095000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085923922138,"sku":"TCI2510B618613015","price":7547000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6186.jpg?v=1768204489"},{"product_id":"tci2510b629313131","title":"TCI B6293 82657-04-3 Bifenthrin","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBifenthrin TCI B6293 is a high-purity synthetic pyrethroid reference standard for analytical and life science research. It is commonly applied in cell biology and nutrition studies to investigate xenobiotic effects on metabolic pathways, oxidative stress responses, and cellular biotransformation mechanisms. This product also serves as a reliable standard for pesticide residue analysis in food safety and environmental toxicology research.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"250mg","offer_id":48085929099482,"sku":"TCI2510B629313131","price":2297000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48085929132250,"sku":"TCI2510B629313132","price":8051000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6293.jpg?v=1769180263"},{"product_id":"tci2510b630213138","title":"TCI B6302 22150-76-1 6-Biopterin","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e6-Biopterin is a naturally occurring pteridine compound that represents the oxidized form of tetrahydrobiopterin, one of the most important cofactors in human and animal metabolism. Within the cell, its reduced derivative functions as an electron carrier for a group of hydroxylase enzymes that process aromatic amino acids. As a laboratory material, 6-biopterin is supplied as a standard compound and reference substance for biochemical and nutrition research, serving both in the construction of analytical calibration curves and as a starting point for preparing the reduced form used in enzymatic experiments.\u003c\/p\u003e\n\u003cp\u003eThe properties that make this compound valuable are its highly specific role in particular metabolic pathways and the characteristic fluorescence it exhibits as a pteridine derivative, which allows it to be detected with high sensitivity using fluorescence detectors on liquid chromatography systems. This oxidized form is considerably more stable than tetrahydrobiopterin, which oxidizes very readily on exposure to air, making 6-biopterin far more practical to store and weigh under normal laboratory conditions. Because its pteridine structure absorbs and emits light at specific wavelengths, the compound also serves as a marker that is easy to trace within complex biological mixtures.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 6-biopterin is typically handled in university biochemistry departments, nutrition research groups, and institutional research centres working on amino acid metabolism and cofactor studies. It is most often used in small quantities as an analytical reference standard, prepared fresh into working solutions for chromatographic runs or enzymatic assays. Laboratories that maintain liquid chromatography systems with fluorescence detection find it a straightforward material to incorporate into existing analytical workflows.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAnalytical calibration standard for liquid chromatography, where its well-defined identity as a reference substance allows laboratories to construct reliable calibration curves for quantifying biopterin in sample matrices.\u003c\/li\u003e\n\u003cli\u003eFluorescence detection method development, since the characteristic fluorescent behaviour of the pteridine ring permits highly sensitive detection and makes it suitable for establishing detector settings and sensitivity limits.\u003c\/li\u003e\n\u003cli\u003ePrecursor material for preparing the reduced tetrahydrobiopterin form in enzymatic experiments, giving researchers a stable starting point rather than handling the air-sensitive reduced compound directly.\u003c\/li\u003e\n\u003cli\u003eCofactor research on aromatic amino acid hydroxylases, supporting studies of the enzyme group whose activity depends on the reduced biopterin derivative acting as an electron carrier.\u003c\/li\u003e\n\u003cli\u003eNutrition and metabolic research reference material, where its specific role in defined metabolic pathways makes it a meaningful marker compound for tracing metabolism in biological 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\u003eProduct code: B6302\u003c\/li\u003e\n\u003cli\u003eCAS number: 22150-76-1\u003c\/li\u003e\n\u003cli\u003eChemical name: 6-Biopterin\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Cell Biology \u0026gt; Nutrition Research\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in standard research quantities; please confirm the currently offered pack size when ordering\u003c\/li\u003e\n\u003cli\u003eStorage: store according to the manufacturer's stated conditions on the product label and safety data sheet\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore 6-Biopterin in its original tightly closed container, following the storage conditions stated by the manufacturer on the product label and accompanying safety data sheet. As a pteridine derivative that absorbs and emits light at specific wavelengths, the material is best kept protected from light in amber or opaque containers, in a dry place away from moisture. Handle the powder inside a fume hood or well-ventilated area, using gloves, safety glasses, and a laboratory coat, and avoid generating dust during weighing. Prepare working solutions fresh where possible and label all dilutions clearly with concentration and preparation date. Consult the manufacturer's safety data sheet before first use and dispose of residues in accordance with institutional chemical waste procedures.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"50mg","offer_id":48085929427162,"sku":"TCI2510B630213138","price":3484000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6302.jpg?v=1768816025"},{"product_id":"tci2510b634113198","title":"TCI B6341 149877-41-8 Bifenazate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBifenazate (CAS 149877-41-8) is a carbazate-class acaricide widely used as a research and reference material in pesticide residue analysis and crop protection studies. Laboratories rely on it as a comparison standard for LC-MS\/MS and GC-MS methods, for method validation and recovery testing, and for research into mite resistance mechanisms linked to mitochondrial electron transport. TCI product B6341 is supplied in a 1 g pack and is intended for research and analytical use rather than as a ready-to-use agricultural product. Handle it in a fume hood with appropriate personal protective equipment, prevent release into waterways, and follow the manufacturer's Safety Data Sheet.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eChee (2006). Efficient Synthesis of Bifenazate.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.200646128\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.200646128\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eWang et al. (2023). Ferric chloride assisted QuEChERS method for separate detection of bifenazate and bifenazate-diazene in citrus fruits and its field validation. \u003cem\u003eFood Chemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.foodchem.2023.136149\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.foodchem.2023.136149\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eEuropean Food Safety Authority (2012). Modification of the existing MRLs for bifenazate in currants (red, black and white), blackberries and raspberries. \u003cem\u003eEFSA Journal\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.2903\/j.efsa.2012.2577\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.2903\/j.efsa.2012.2577\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":48085931786458,"sku":"TCI2510B634113198","price":6890000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6341.jpg?v=1768204498"},{"product_id":"tci2510b644313334","title":"TCI B6443 113558-15-9 Baohuoside I","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6443 Baohuoside I (CAS 113558-15-9) is a naturally derived prenylated flavonoid glycoside supplied strictly for research and experimental use. It is widely used as a reference compound in phytochemical profiling and in HPLC or LC-MS analysis of plant extracts. The 25 mg pack size suits analytical method development and small-scale biological studies. Store the vial tightly closed under cold, dry, light-protected conditions and allow it to reach room temperature before opening to prevent condensation.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eZhang et al. (2019). Effect of 2″-O-Rhamnosyl Icariside II, Baohuoside I and Baohuoside II in Herba Epimedii on Cytotoxicity Indices in HL-7702 and HepG2 Cells. \u003cem\u003eMolecules\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.3390\/molecules24071263\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.3390\/molecules24071263\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eMa et al. (2005). Baohuoside-1 inhibits activated T cell proliferation at G1–S phase transition. \u003cem\u003eTransplant Immunology\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.trim.2005.05.002\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.trim.2005.05.002\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eLin et al. (2026). Baohuoside I Combated Cryptocaryon irritans via Dual Targeting of Parasite Apoptosis and Host Defense Enhancement. \u003cem\u003eAntioxidants\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.3390\/antiox15030396\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.3390\/antiox15030396\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mg","offer_id":48085940502746,"sku":"TCI2510B644313334","price":7345000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6443.jpg?v=1767093684"},{"product_id":"tci2510b649213395","title":"TCI B6492 94-80-4 Butyl 2-(2,4-Dichlorophenoxy)acetate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6492, Butyl 2-(2,4-Dichlorophenoxy)acetate (CAS 94-80-4), is the butyl ester of the phenoxy compound 2,4-D, a long-studied synthetic auxin analogue. Its greater lipophilicity relative to the free acid makes it valuable for plant physiology research, tissue culture studies, and investigations of environmental hydrolysis pathways. It is also widely used as a reference material in pesticide residue analysis by GC-MS and LC-MS\/MS in food, water, and soil matrices. AMI Scientific offers this TCI product in a 1 g pack for research, testing, and analytical use only, and users should follow local regulations and hazardous waste procedures.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085943189722,"sku":"TCI2510B649213395","price":2828000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6492.jpg?v=1768204510"},{"product_id":"tci2510b654813475","title":"TCI B6548 33171-05-0 Bisdemethoxycurcumin","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBisdemethoxycurcumin (CAS 33171-05-0) is one of the three principal curcuminoids found in turmeric rhizome, differing from curcumin by the absence of methoxy groups on both aromatic rings. It is commonly used as a reference compound for curcuminoid profiling by HPLC or TLC, and for in vitro bioactivity studies where a single, defined curcuminoid is preferred over a crude extract. Curcuminoids are light sensitive and degrade under alkaline conditions, so the material should be stored cool, dry, and protected from light, with working solutions prepared fresh. AMI Scientific supplies it in a 1 g pack size for research and experimental use.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMohammadi et al. (2018). Inhibition of amyloid fibrillation of lysozyme by bisdemethoxycurcumin and diacetylbisdemethoxycurcumin. \u003cem\u003eBiophysical Chemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.bpc.2018.02.005\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.bpc.2018.02.005\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eLappichetpaiboon (2025). Anticandidal effects of bisdemethoxycurcumin \u0026amp; melatonin with dual light emitting diode in photodynamic therapy. \u003cem\u003ePhotodiagnosis and Photodynamic Therapy\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.pdpdt.2025.104797\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.pdpdt.2025.104797\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eJayaprakasha et al. (2006). Antioxidant activities of curcumin, demethoxycurcumin and bisdemethoxycurcumin. \u003cem\u003eFood Chemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.foodchem.2005.06.037\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.foodchem.2005.06.037\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085946630362,"sku":"TCI2510B654813475","price":2953000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6548.jpg?v=1767093878"},{"product_id":"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":860000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085965340890,"sku":"TCI2510C000213909","price":2853000.0,"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":455000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48085965734106,"sku":"TCI2510C001013919","price":2273000.0,"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":455000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48085965832410,"sku":"TCI2510C001113921","price":1666000.0,"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":2626000.0,"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":884000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0071.jpg?v=1767094618"},{"product_id":"tci2510c007614008","title":"TCI C0076 7080-50-4 Chloramine T Trihydrate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI Chloramine T Trihydrate (catalog C0076, CAS 7080-50-4) is one of the most widely used active-chlorine reagents in the laboratory, valued for its stable solid form and easy dissolution in water. It functions both as a general oxidant in synthetic chemistry and as an electrophilic nitrogen source in carbon–nitrogen bond forming methodologies. In biochemistry and analytical work it is well known as an oxidizing reagent for protein labelling procedures and for colorimetric and titrimetric determinations. AMI Scientific supplies this TCI product in 25g and 500g pack sizes; keep it cool, dry, light-protected, and well away from acids and reducing agents.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMekky et al. (2022). Chloramine Trihydrate‐Mediated Tandem Synthesis of New Pyrrole and\/or Arene‐Linked Mono‐ and Bis(1,3,4‐Oxadiazole) Hybrids as Potential Bacterial Biofilm and MRSA Inhibitors. \u003cem\u003eChemistry \u0026amp; Biodiversity\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/cbdv.202200338\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/cbdv.202200338\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":48085969502426,"sku":"TCI2510C007614008","price":455000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48085969535194,"sku":"TCI2510C007614009","price":1137000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0076.jpg?v=1769144594"},{"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":2197000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085975793882,"sku":"TCI2510C018114160","price":7521000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0181.jpg?v=1767094840"},{"product_id":"tci2510c020614199","title":"TCI C0206 94-74-6 (4-Chloro-2-methylphenoxy)acetic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(4-Chloro-2-methylphenoxy)acetic Acid (TCI C0206, CAS 94-74-6), commonly abbreviated as MCPA, is a solid phenoxyacetic acid compound. Laboratories use it as a reference material for phenoxy herbicide residue analysis in water, soil, and agricultural samples. It is also studied in plant physiology research because of its auxin-like activity, and its phenoxyacetate scaffold can be derivatised in organic synthesis. AMI Scientific offers this TCI product in a 25 g pack for environmental, agricultural, and quality-testing laboratories in Indonesia.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48276753318106,"sku":"TCI2510C020614199","price":657000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0206.jpg?v=1767094869"},{"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":455000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48085991751898,"sku":"TCI2510C035214420","price":1491000.0,"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":481000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48085991817434,"sku":"TCI2510C035314422","price":1062000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48085991850202,"sku":"TCI2510C035314423","price":2650000.0,"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":481000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48085993816282,"sku":"TCI2510C036214437","price":1491000.0,"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":505000.0,"currency_code":"IDR","in_stock":true},{"title":"100mL","offer_id":48085994406106,"sku":"TCI2510C037014451","price":1237000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48085994438874,"sku":"TCI2510C037014452","price":3257000.0,"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":1187000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085995127002,"sku":"TCI2510C038014468","price":6764000.0,"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":1439000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48085995946202,"sku":"TCI2510C039314489","price":4216000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48085995978970,"sku":"TCI2510C039314490","price":12038000.0,"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":834000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085996044506,"sku":"TCI2510C039414492","price":2399000.0,"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":607000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085998469338,"sku":"TCI2510C043414551","price":2550000.0,"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":3231000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0542.jpg?v=1767095451"},{"product_id":"tci2510c059814804","title":"TCI C0598 2436-73-9 Methyl 4-Chloro-2-methylphenoxyacetate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0598 Methyl 4-Chloro-2-methylphenoxyacetate (CAS 2436-73-9) is the methyl ester of a chloro- and methyl-substituted phenoxyacetic acid. It is mainly used in agrochemical research, in method development for residue analysis, and as an aromatic intermediate for further synthetic modification. The ester group can also be hydrolysed back to the free acid, making it a useful substrate for stability and transformation studies. AMI Scientific supplies this TCI product in 1 g and 25 g packs for research use.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eFerguson et al. (1997). Mechanism and Stereochemistry of the Reaction of Dichloroplatinum(II) Complexes with Diazo Compounds. X-ray Structures of Four Key Products: [(2R,3R)-Bis(diphenylphosphino)butane]chloro- [(S)-chloro(methoxycarbonyl)methyl]platinum(II), (η4-1,5-Cyclooctadiene)[3-chloro-5-(dimethoxyphosphonyl)-2- methoxy-4,1,2-platinaoxaphospholane P-oxide], (R,R)-[Chloro(dimethoxyphosphonyl)methyl][chloro- (trimethylsilyl)methyl](1,5-cyclooctadiene)platinum(II), and Chloro[chloro(dimethoxyphosphonyl)methyl](η4-1,5-cyclooctadiene)platinum(II). \u003cem\u003eOrganometallics\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1021\/om9607964\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1021\/om9607964\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":48086012559578,"sku":"TCI2510C059814804","price":455000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086012592346,"sku":"TCI2510C059814805","price":3079000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0598.jpg?v=1767095552"},{"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":758000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086018654426,"sku":"TCI2510C065514882","price":1995000.0,"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":1137000.0,"currency_code":"IDR","in_stock":true},{"title":"10g","offer_id":48086022783194,"sku":"TCI2510C070514957","price":5856000.0,"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":481000.0,"currency_code":"IDR","in_stock":true},{"title":"100mL","offer_id":48086038708442,"sku":"TCI2510C093415270","price":1162000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48086038741210,"sku":"TCI2510C093415271","price":3005000.0,"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":3005000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086039855322,"sku":"TCI2510C095515298","price":9843000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0955.jpg?v=1768816379"},{"product_id":"tci2510c109415502","title":"TCI C1094 101-10-0 2-(3-Chlorophenoxy)propionic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2-(3-Chlorophenoxy)propionic Acid (TCI C1094, CAS 101-10-0) is an aryloxypropionic acid combining an aromatic ether linkage with a chiral carboxylic acid centre. It is used as an intermediate in agrochemical-related research, as a substrate for chiral resolution studies, and as a starting point for ester and amide derivatives. AMI Scientific supplies this TCI product in a 25 g pack size suitable for laboratory research. Weigh it in a well-ventilated area with gloves and eye protection, and consult the official TCI Safety Data Sheet before use.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOliveira et al. (2024). Pre-harvest application of 2-(3-chlorophenoxy) propionic acid on pineapple plants. \u003cem\u003eComunicata Scientiae\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.14295\/cs.v16.4222\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.14295\/cs.v16.4222\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eUjang et al. (2003). The kinetic resolution of 2-(4-chlorophenoxy) propionic acid using Candida rugosa lipase. \u003cem\u003eProcess Biochemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/s0032-9592(03)00039-6\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/s0032-9592(03)00039-6\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eZakaria et al. (2007). Bacterial diversity in soil enrichment cultures amended with 2 (2‐methyl‐4‐chlorophenoxy) propionic acid (mecoprop). \u003cem\u003eEnvironmental Microbiology\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1111\/j.1462-2920.2007.01375.x\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1111\/j.1462-2920.2007.01375.x\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":48086048309466,"sku":"TCI2510C109415502","price":1389000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1094.jpg?v=1767096315"},{"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":1062000.0,"currency_code":"IDR","in_stock":true},{"title":"25mL","offer_id":48086070984922,"sku":"TCI2510C145416019","price":3131000.0,"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":1289000.0,"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":683000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48086073606362,"sku":"TCI2510C149516077","price":3963000.0,"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":2576000.0,"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":2676000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1708.jpg?v=1767097359"},{"product_id":"tci2510c197116584","title":"TCI C1971 303-98-0 Coenzyme Q10","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCoenzyme Q10, also known as ubiquinol, is an essential organic compound that plays a crucial role in cellular energy metabolism. As a key component of mitochondria, it functions as an electron acceptor in the electron transport chain, facilitating the production of ATP, which is vital for various cellular activities. This compound is widely used in life science research, particularly in biochemical and physiological studies, where its role in energy production and antioxidant activity is of significant interest. Its presence in biological systems makes it a valuable tool for understanding metabolic processes and cellular function.\u003c\/p\u003e\n\u003cp\u003eCoenzyme Q10 is a stable compound that resists degradation under normal conditions, making it suitable for a wide range of laboratory experiments. Its lipid-soluble nature allows it to dissolve in organic solvents such as ethyl acetate and chloroform, which is advantageous for chemical reactions and molecular interactions. This property enhances its utility in biochemical assays and analytical techniques. Additionally, its chemical stability ensures consistent performance in research applications, contributing to reliable experimental outcomes.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Coenzyme Q10 is commonly used in both basic and applied research. It supports studies in biochemistry, pharmacology, and biotechnology, enabling researchers to explore cellular mechanisms and drug development. Its relevance in understanding metabolic pathways and antioxidant behavior makes it a key reagent in scientific investigations. The compound's versatility and reliability make it a preferred choice for researchers across various disciplines in Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eEnergy metabolism research as it facilitates ATP production in mitochondrial processes.\u003c\/li\u003e\n\u003cli\u003eAntioxidant activity studies due to its ability to neutralize free radicals in cellular systems.\u003c\/li\u003e\n\u003cli\u003eBiochemical assays for analyzing electron transport chain efficiency in cellular respiration.\u003c\/li\u003e\n\u003cli\u003ePharmacological studies to evaluate its role in drug metabolism and therapeutic applications.\u003c\/li\u003e\n\u003cli\u003eMolecular interaction experiments because of its lipid-soluble nature and chemical stability.\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: 303-98-0\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Terpenes\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified\u003c\/li\u003e\n\u003cli\u003ePhysical form: Not specified\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eCoenzyme Q10 should be stored in a cool, dry place, away from direct light to maintain its chemical stability. It is recommended to use airtight containers to prevent moisture absorption and contamination. Since it is a lipid-soluble compound, it should be handled with care to avoid exposure to incompatible substances. Laboratory personnel should wear appropriate personal protective equipment when handling this material. Proper labeling of containers is essential for safety and traceability. Regular monitoring of storage conditions ensures the integrity of the compound for research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48086093496538,"sku":"TCI2510C197116584","price":910000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48086093529306,"sku":"TCI2510C197116585","price":4342000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1971.jpg?v=1767097603"},{"product_id":"tci2510c204216676","title":"TCI C2042 58-08-2 Caffeine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCaffeine, with CAS number 58-08-2, is a well-known alkaloid widely used in scientific experiments. As a fundamental compound in the field of biochemistry, caffeine plays a crucial role in various laboratory applications. Its complex chemical structure and pharmacological properties make it a valuable tool for researchers. In the laboratory, caffeine is often used as a starting material for the synthesis of other compounds or as a control substance in biological activity assays. Its presence in natural products such as coffee, tea, and soft drinks also makes it a familiar compound for study and analysis.\u003c\/p\u003e\n\u003cp\u003eCaffeine is favored for its chemical stability and resistance to heat, which simplifies storage and handling in laboratory settings. It dissolves well in organic solvents like ethyl acetate and ethanol, making it suitable for separation and analytical procedures. These properties contribute to its popularity in both chemical and biochemical experiments. Additionally, caffeine is non-toxic and readily available, making it a practical choice for a wide range of research applications. Its versatility and reliability have established it as a staple in many scientific laboratories.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, caffeine is particularly relevant in pharmaceutical, biochemical, and environmental research. It is frequently used in studies related to drug development, metabolic processes, and environmental contamination. Its presence in both natural and synthetic forms allows for diverse experimental approaches, supporting a broad spectrum of scientific inquiry.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003e\n\u003cstrong\u003ePharmaceutical Research\u003c\/strong\u003e: Caffeine is used to study its effects on human physiology and its role in drug formulations.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eBiochemical Analysis\u003c\/strong\u003e: It serves as a standard compound for chromatographic and spectroscopic analysis.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eEnvironmental Toxicology\u003c\/strong\u003e: Caffeine is used to assess the presence and impact of contaminants in water and soil samples.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eNeuroscience Studies\u003c\/strong\u003e: It is employed to investigate its effects on central nervous system activity in experimental models.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eMetabolic Studies\u003c\/strong\u003e: Caffeine is used to study its metabolism and excretion in biological systems, aiding in understanding drug kinetics.\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: 58-08-2\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Alkaloids\u003c\/li\u003e\n\u003cli\u003ePack Sizes: Available in various quantities as per standard laboratory requirements\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 and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eCaffeine 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 solubility in organic solvents, it is important to ensure that storage containers are sealed properly. In laboratory settings, caffeine should be handled with standard safety precautions, including the use of gloves and appropriate ventilation. Its non-toxic nature allows for relatively safe handling, but care should still be taken to avoid inhalation or ingestion. Proper storage and handling ensure the longevity and reliability of caffeine in experimental applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086098051290,"sku":"TCI2510C204216676","price":455000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48086098084058,"sku":"TCI2510C204216677","price":1591000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2042.jpg?v=1768193800"},{"product_id":"tci2510c205916703","title":"TCI C2059 133-06-2 Captan","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C2059 133-06-2 Captan is a chemical compound widely used in life science research, particularly in cellular nutrition studies. As a microbial growth inhibitor, it plays a crucial role in maintaining controlled environments within laboratory settings. Its ability to suppress the growth of both fungi and bacteria makes it an essential tool for researchers aiming to ensure the accuracy and reliability of their experimental outcomes. Captan is commonly employed in experiments where contamination by unwanted microorganisms could compromise data integrity.\u003c\/p\u003e\n\u003cp\u003eOne of the key reasons for its popularity is its stability under various environmental conditions. Captan remains effective in both liquid and solid forms, and it exhibits resistance to changes in temperature and pH levels. This versatility allows it to be used across a wide range of laboratory applications without the need for extensive modifications to experimental protocols. Additionally, its chemical stability minimizes the risk of unexpected reactions, enhancing the safety and consistency of laboratory procedures.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Captan is a preferred choice for researchers working in microbiology, cellular nutrition, and pharmaceutical development. Its availability in various packaging options ensures that it can be easily integrated into routine laboratory workflows. The compound's reliability and effectiveness make it a valuable asset for maintaining high standards of research quality in both academic and industrial settings.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMicrobial Growth Inhibition: Captan is ideal for experiments requiring controlled microbial environments, as it effectively suppresses unwanted bacterial and fungal growth.\u003c\/li\u003e\n\u003cli\u003eCellular Nutrition Studies: It supports research on nutrient absorption and metabolic pathways by maintaining sterile conditions in cell culture experiments.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical Development: Captan helps in the formulation and testing of antimicrobial agents by providing a stable, contamination-free environment.\u003c\/li\u003e\n\u003cli\u003eEnvironmental Microbiology: It is used in studies assessing the impact of environmental factors on microbial communities by preventing cross-contamination.\u003c\/li\u003e\n\u003cli\u003eBiotechnology Research: Captan ensures the purity of cultures in bioprocessing, supporting the development of bio-based products and 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: 133-06-2\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Cell Biology \u0026gt; Nutrition Research\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various packaging options\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\u003eCaptan should be stored in a cool, dry place, away from direct sunlight and sources of heat to maintain its chemical stability. It is recommended to use airtight containers to prevent moisture absorption and contamination. Due to its chemical stability, it does not require refrigeration but should be kept in a secure location to avoid accidental exposure. Laboratory personnel should handle Captan with appropriate personal protective equipment, such as gloves and safety goggles, to ensure safe usage. Regular monitoring of storage conditions is advised to maintain the integrity of the compound. Proper labeling of containers is essential to prevent mix-ups and ensure safe handling in a laboratory environment.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086100377818,"sku":"TCI2510C205916703","price":1263000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086100410586,"sku":"TCI2510C205916704","price":3434000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2059.jpg?v=1769144419"},{"product_id":"tci2510c223516932","title":"TCI C2235 1492-18-8 Calcium Folinate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C2235 Calcium Folinate is the calcium salt of folinic acid, a reduced form of folic acid that is biologically ready for use by cells without first requiring an enzymatic reduction step. The compound belongs to the group of pharmaceutical research reagents intended for experimental use, and it serves as a source of an active folate derivative within experimental systems. In life science laboratories, this material is used to trace one-carbon metabolic pathways, to support cell growth in defined media, and to study the interactions between folate and the enzymes involved in nucleotide synthesis.\u003c\/p\u003e\n\u003cp\u003eThe characteristic that makes this reagent a preferred choice is its water solubility, which is considerably better than that of free folinic acid, so stock solutions are easy to prepare for both cell culture-based experiments and enzyme assays. The calcium salt form also provides better handling stability in powder form. Because the compound is already present as a reduced folate, researchers can observe its effects directly, without the additional variable introduced by the reduction process that would otherwise take place inside the cell. This directness simplifies experimental interpretation and shortens preparation work at the bench.\u003c\/p\u003e\n\u003cp\u003eThe 1 g and 5 g pack sizes are well matched to a reagent that is generally consumed in small quantities per experiment, which suits the working pattern of most research groups. In Indonesian laboratories, this material fits routine life science work in university research units, biochemistry and pharmacy teaching laboratories, and institutional research facilities, where reduced folate derivatives are needed for metabolic pathway studies, cell culture media supplementation, and enzyme characterisation work carried out on an experimental scale.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOne-carbon metabolism pathway studies: the compound supplies an already reduced folate derivative, allowing researchers to follow carbon transfer steps without confounding effects from intracellular reduction.\u003c\/li\u003e\n\u003cli\u003eCell culture media supplementation: its high water solubility makes it straightforward to prepare and filter stock solutions that support cell growth in defined culture media formulations.\u003c\/li\u003e\n\u003cli\u003eNucleotide synthesis enzyme research: the reagent is used to examine how folate derivatives interact with the enzymes responsible for building nucleotides in experimental systems.\u003c\/li\u003e\n\u003cli\u003eFolate-enzyme interaction assays: because it is a biologically ready folate form, it can be introduced directly into enzyme assay mixtures for interaction and activity measurements.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research at experimental scale: as a pharmaceutical research reagent, it supports small-volume investigative work where an active folate source is required per experiment.\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: 1492-18-8\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Pharmaceutical Research Reagents (for Experimental Use)\u003c\/li\u003e\n\u003cli\u003ePack sizes: 1 g and 5 g\u003c\/li\u003e\n\u003cli\u003ePhysical form: powder (calcium salt form)\u003c\/li\u003e\n\u003cli\u003eStorage: store the powder under conditions that preserve its handling stability, in a closed container away from moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eKeep the powder in its original tightly closed container to protect it from moisture, since the calcium salt form is supplied and handled as a dry solid. Store containers in a cool, dry place away from direct light and heat sources, and return the container to storage promptly after each weighing so that the remaining material is not exposed for longer than necessary. Prepare aqueous stock solutions only in the quantity needed for the planned experiment, and handle the reagent in a clean, dedicated weighing area using standard laboratory personal protective equipment, including gloves, a laboratory coat, and eye protection. Use clean spatulas and glassware to avoid cross-contamination between reagents, label all prepared solutions clearly, and follow your institution's general procedures for handling research chemicals intended for experimental use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086113386714,"sku":"TCI2510C223516932","price":2020000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086113419482,"sku":"TCI2510C223516933","price":5956000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2235.jpg?v=1767097969"},{"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":1137000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086118400218,"sku":"TCI2510C230217034","price":3711000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2302.jpg?v=1767098099"},{"product_id":"tci2510c236617117","title":"TCI C2366 66215-27-8 Cyromazine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCyromazine is a chemical compound widely used in life science research, particularly in cell biology and nutrition research. It functions as a synthetic insecticide, primarily used to control disease-vectoring insects such as mosquitoes and lice. In laboratory settings, Cyromazine serves as a valuable tool for experiments involving insect population control or the testing of chemical efficacy. Its role extends beyond pest management, supporting studies on environmental health and disease transmission. As a key component in various research protocols, it enables scientists to explore biological mechanisms and develop strategies for public health interventions.\u003c\/p\u003e\n\u003cp\u003eThe chemical properties of Cyromazine make it a preferred choice for laboratory use. It exhibits chemical stability and good solubility in organic solvents, ensuring ease of handling and compatibility with a wide range of experimental conditions. Its low reactivity contributes to a relatively safe profile when used appropriately, minimizing potential hazards in the lab environment. These characteristics make it suitable for both routine and specialized research applications, enhancing its utility across different scientific disciplines.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Cyromazine is commonly used in studies related to health, environmental science, and disease management. It plays a crucial role in research focused on reducing the risk of vector-borne diseases. Its presence in laboratory settings supports the development of effective strategies for disease prevention and control, making it an essential tool for researchers in Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eInsect population control studies benefit from Cyromazine’s ability to inhibit insect reproduction, making it ideal for controlled breeding experiments.\u003c\/li\u003e\n\u003cli\u003eDisease transmission research utilizes Cyromazine to study the impact of insect vectors on public health, supporting epidemiological studies.\u003c\/li\u003e\n\u003cli\u003eEnvironmental impact assessments incorporate Cyromazine to evaluate the effectiveness of chemical interventions in reducing pest populations.\u003c\/li\u003e\n\u003cli\u003eNutritional research employs Cyromazine in experiments examining the effects of chemical compounds on insect physiology and metabolism.\u003c\/li\u003e\n\u003cli\u003eLaboratory safety protocols use Cyromazine as a reference compound for testing the efficacy of new insect control agents in controlled environments.\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: 66215-27-8\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Cell Biology \u0026gt; Nutrition Research\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various sizes as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eCyromazine should be stored in a cool, dry place, away from direct sunlight and sources of heat. It is recommended to use airtight containers to prevent moisture absorption and maintain chemical stability. Due to its low reactivity, it poses minimal risk during routine handling, but standard laboratory safety protocols should still be followed. When working with Cyromazine, ensure proper ventilation and use appropriate personal protective equipment to minimize exposure. It is important to keep the substance away from incompatible materials and ensure that storage areas are secure to prevent accidental spills or contamination.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086122463450,"sku":"TCI2510C236617117","price":1313000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086122496218,"sku":"TCI2510C236617118","price":3458000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2366.jpg?v=1768197189"},{"product_id":"tci2510c241717183","title":"TCI C2417 122008-85-9 Cyhalofop Butyl","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C2417 122008-85-9 Cyhalofop Butyl is a synthetic herbicide widely used in life science research, particularly in cell biology and nutrition studies. This chemical compound plays a crucial role in laboratory settings where researchers investigate the mechanisms of herbicide action and its impact on plant physiology. Its application extends to environmental and toxicological studies, helping scientists understand how synthetic chemicals affect ecosystems and agricultural sustainability. As a key research material, it supports the development of more effective and environmentally friendly weed control strategies.\u003c\/p\u003e\n\u003cp\u003eThe compound is valued for its chemical stability and ability to penetrate plant leaf surfaces efficiently. These properties make it a preferred choice for creating realistic and accurate experimental models. Its solubility in organic solvents further enhances its usability in various laboratory conditions, allowing for easier preparation and handling. This combination of stability, penetration, and solubility ensures consistent results in research applications, making it a reliable component in scientific studies.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Cyhalofop Butyl is commonly used in agricultural and environmental research. Scientists at universities and research institutions rely on this compound to study the effects of chemical substances on ecosystems and sustainable farming practices. Its role in understanding the environmental impact of herbicides is vital for developing safer and more sustainable agricultural solutions.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eEnvironmental toxicology studies benefit from Cyhalofop Butyl as it enables the assessment of herbicide impact on ecosystems and biodiversity.\u003c\/li\u003e\n\u003cli\u003eAgricultural research utilizes this compound to investigate weed control mechanisms and their effects on crop growth and yield.\u003c\/li\u003e\n\u003cli\u003eCell biology experiments incorporate Cyhalofop Butyl to study plant cell responses to herbicidal stress and metabolic changes.\u003c\/li\u003e\n\u003cli\u003eNutritional research employs this compound to explore the interaction between synthetic herbicides and plant nutrient uptake processes.\u003c\/li\u003e\n\u003cli\u003eEcotoxicological assessments use Cyhalofop Butyl to evaluate long-term environmental effects and potential risks to non-target organisms.\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: 122008-85-9\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Cell Biology \u0026gt; Nutrition Research\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Liquid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eCyhalofop Butyl should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to use sealed containers made of materials compatible with organic solvents to prevent contamination and evaporation. Due to its chemical nature, it is essential to handle the compound with appropriate personal protective equipment, including gloves and safety goggles. Proper ventilation should be maintained in the laboratory to minimize exposure risks. Regular monitoring of storage conditions ensures the compound remains stable and suitable for research use. Adherence to standard laboratory safety protocols is crucial when working with this synthetic herbicide.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086125445338,"sku":"TCI2510C241717183","price":1692000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086125478106,"sku":"TCI2510C241717184","price":11609000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2417.jpg?v=1769180389"},{"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":1818000.0,"currency_code":"IDR","in_stock":true},{"title":"100mg","offer_id":48086129115354,"sku":"TCI2510C248817271","price":6058000.0,"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":4392000.0,"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":17994000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2520.jpg?v=1767098452"},{"product_id":"tci2510c255417349","title":"TCI C2554 1698-60-8 Chloridazon","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eChloridazon, with CAS number 1698-60-8, is a chemical compound widely utilized in scientific research, particularly in the fields of cell biology and nutrition. It functions as an enzyme inhibitor, playing a crucial role in studying metabolic processes and biochemical reactions within cells. Its ability to modulate enzymatic activity makes it an essential tool for understanding the mechanisms of enzyme function and their impact on biological systems. In laboratory settings, Chloridazon is employed to investigate the interactions between enzymes and substrates, offering insights into the dynamics of cellular processes.\u003c\/p\u003e\n\u003cp\u003eThe chemical properties of Chloridazon, including its stability and solubility in organic solvents such as ethyl acetate and acetone, make it a preferred choice for high-precision experiments. These characteristics ensure consistent performance in various experimental conditions, allowing researchers to achieve reliable results. Additionally, its unique molecular structure enables specific inhibition of targeted enzymes, enhancing the accuracy of experimental outcomes. This specificity is vital in studies that require controlled and selective biochemical interactions.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Chloridazon is commonly used in research related to nutrition and cellular metabolism. Research institutions and universities rely on this compound to explore the relationship between nutrients and cellular function. Its availability supports the development of new methodologies and enhances the scope of scientific inquiry in these fields. The compound's versatility and reliability make it a valuable resource for researchers aiming to advance their understanding of biochemical processes.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eEnzyme Inhibition Studies - Chloridazon is ideal for investigating enzyme activity and inhibition, providing insights into metabolic pathways and biochemical reactions.\u003c\/li\u003e\n\u003cli\u003eNutritional Research - It supports studies on nutrient metabolism and cellular responses, helping researchers understand the impact of dietary components on biological systems.\u003c\/li\u003e\n\u003cli\u003eBiochemical Reaction Analysis - Its stability and solubility make it suitable for experiments requiring precise control over chemical interactions within biological systems.\u003c\/li\u003e\n\u003cli\u003eCellular Metabolism Studies - Chloridazon aids in analyzing how enzymes influence metabolic processes, offering valuable data for metabolic pathway research.\u003c\/li\u003e\n\u003cli\u003ePharmacological Research - It is used to study enzyme-targeted interventions, supporting the development of drug candidates and therapeutic strategies.\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: 1698-60-8\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 (may vary depending on supplier specifications)\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\u003eChloridazon should be stored in a cool, dry environment, 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 degradation. Due to its potential reactivity, it should be handled in a well-ventilated area, and appropriate personal protective equipment, such as gloves and safety goggles, should be worn. Avoid contact with incompatible substances, and ensure that storage areas are secure to prevent accidental exposure. Regular monitoring of storage conditions is advised to ensure the compound remains in optimal condition for use in laboratory experiments.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086132326618,"sku":"TCI2510C255417349","price":1742000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086132359386,"sku":"TCI2510C255417350","price":6032000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2554.jpg?v=1769144380"}],"url":"https:\/\/amiscientific.com\/en\/collections\/tci-l3-nutrition-research.oembed?page=39","provider":"AMI Scientific","version":"1.0","type":"link"}