{"title":"Phytochemicals","description":"\u003cp\u003e\u003cstrong\u003ePhytochemicals\u003c\/strong\u003e — compiles plant-derived secondary metabolites, such as flavonoids, polyphenols, alkaloids, terpenoids, and carotenoids, which serve as reference compounds in various studies of food chemistry, nutrition, and natural product composition analysis.\u003c\/p\u003e\u003cp\u003eThese phytochemicals are used as analytical standards in chromatography (HPLC, LC-MS) to identify and quantify bioactive components in plant extracts, foods, or supplements. Nutrition and food chemistry researchers also use them as reference compounds in in vitro antioxidant activity assays, studies of plant metabolite biosynthetic pathways, and the development of analytical methods for functional food composition.\u003c\/p\u003e\u003cp\u003eExample products in this collection: \u003ca href=\"\/en\/products\/tci2510m012137673\"\u003eTCI M0121 90-05-1 Guaiacol\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b570012413\"\u003eTCI B5700 10309-37-2 Bakuchiol\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510g001131577\"\u003eTCI G0011 149-91-7 Gallic Acid\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b608512896\"\u003eTCI B6085 4481-62-3 Betulonic Acid\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510c230217033\"\u003eTCI C2302 458-37-7 Curcumin (Synthetic)\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b644313334\"\u003eTCI B6443 113558-15-9 Baohuoside I\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510a0443641\"\u003eTCI A0443 29883-15-6 Amygdalin\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b654813475\"\u003eTCI B6548 33171-05-0 Bisdemethoxycurcumin\u003c\/a\u003e.\u003c\/p\u003e\u003cp\u003ePay attention to analytical purity, source of isolation, and the crystal form or standard solution suitable for calibration needs of chromatographic methods in analyzing the phytochemical content of a sample. All products are genuine Tokyo Chemical Industry (TCI) Japan products, with purity, packaging, and storage conditions listed on each item's page.\u003c\/p\u003e\u003cp\u003eOther parallel categories under Nutrition Research, often used together in one laboratory workflow:\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-vitamins-nutrition-research\"\u003eVitamins [Nutrition Research]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-functional-food-research\"\u003eFunctional Food Research\u003c\/a\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eBack to \u003ca href=\"\/en\/collections\/tci-l3-nutrition-research\"\u003eNutrition Research\u003c\/a\u003e. For large-volume procurement, special packaging, or specific grades, contact the AMI Scientific team — official TCI Japan distributor in Indonesia — for availability checks and lead time directly from Japan.\u003c\/p\u003e","products":[{"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":5300000.0,"currency_code":"IDR","in_stock":true},{"title":"250mg","offer_id":48085918613722,"sku":"TCI2510B608512897","price":16783000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6085_23b229c2-4408-40c7-853c-af4d0bbbd87a.jpg?v=1792631170"},{"product_id":"tci2510b644313334","title":"TCI B6443 113558-15-9 Baohuoside I","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6443 is Baohuoside I, CAS number 113558-15-9, a natural compound in the flavonoid glycoside class known to come from plants of the genus Epimedium. It belongs to the Crude Medicine Ingredients for Research and Experimental Use category within Life Science, Biochemicals and Reagents. In the laboratory, Baohuoside I serves as a reference standard or test material for phytochemical and biological research into the active components of medicinal plants. It is intended for research and experimental use only.\u003c\/p\u003e\n\u003cp\u003eAs a flavonoid glycoside, Baohuoside I has a flavonoid skeleton bonded to a sugar group. This structure affects its solubility and how it behaves in chromatographic analysis, which matters when separation methods are being developed and checked. Researchers prefer reference materials with a clearly stated CAS number because they can then identify a compound in a plant extract by comparing retention times or spectral data against a known substance. Baohuoside I is also used as a test compound in in vitro studies of the biological activity of natural products. Purity and lot-specific characteristics should be checked on the manufacturer's label and certificate of analysis.\u003c\/p\u003e\n\u003cp\u003eIndonesia has a strong tradition of research into medicinal plants and jamu, so this material is relevant to pharmacy, chemistry and biology laboratories at universities, research institutes and natural product development teams. Researchers who study plant-derived compounds can use Baohuoside I as a comparison standard when they characterize extracts. It also gives a consistent reference point for experimental work on flavonoid glycosides, which supports reproducible results across studies and between laboratories working on similar plant material.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePhytochemical reference standard: a clearly identified compound with a defined CAS number lets researchers confirm Baohuoside I in plant extracts by comparing results against a known material.\u003c\/li\u003e\n\u003cli\u003eChromatographic identification: comparing retention times with this reference material helps analysts identify peaks for Baohuoside I in complex extracts from Epimedium species and related botanical samples.\u003c\/li\u003e\n\u003cli\u003eSpectral comparison: spectral data recorded from the reference compound give a benchmark for checking structural identity when characterizing isolated or partially purified flavonoid glycoside fractions.\u003c\/li\u003e\n\u003cli\u003eIn vitro biological activity studies: Baohuoside I is used as a test compound in experiments on the biological activity of natural products, so researchers can study a defined substance instead of a crude mixture.\u003c\/li\u003e\n\u003cli\u003eMedicinal plant and jamu research: laboratories studying the active components of traditional medicinal plants can use this compound as a consistent reference for flavonoid glycoside content in their work.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI (product code B6443)\u003c\/li\u003e\n\u003cli\u003eCAS number: 113558-15-9\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Crude Medicine Ingredients for Research and Experimental Use\u003c\/li\u003e\n\u003cli\u003eCompound class: flavonoid glycoside\u003c\/li\u003e\n\u003cli\u003ePack sizes and physical form: please confirm with the product listing and the manufacturer's label\u003c\/li\u003e\n\u003cli\u003eStorage: follow the conditions on the manufacturer's label and certificate of analysis\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore Baohuoside I under the conditions stated on the manufacturer's label and certificate of analysis. Keep it in its original, tightly sealed container, protected from moisture, heat and direct light, and reseal the container promptly after each use to protect the material. Handle the compound in a clean, well-ventilated area and wear standard personal protective equipment, including gloves, a laboratory coat and safety glasses. Avoid inhaling dust and avoid contact with skin and eyes. Read the safety data sheet before use, label all prepared solutions clearly, and dispose of waste according to institutional and local regulations. This product is for research and experimental use only.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mg","offer_id":48085940502746,"sku":"TCI2510B644313334","price":7395000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6443_26e2fe86-7e89-47f7-b5f9-a2e06fed657d.jpg?v=1792631550"},{"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":3003000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6548_c8b6fc48-ed03-405e-9513-8fcde39c1676.jpg?v=1792631663"},{"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":910000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085965340890,"sku":"TCI2510C000213909","price":2903000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0002_e9ad7a26-14f2-438e-a98c-5fdb7d262044.jpg?v=1792631965"},{"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":505000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48085965734106,"sku":"TCI2510C001013919","price":2323000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0010_d12ca12a-d097-4435-bf40-f058e12413b3.jpg?v=1792631972"},{"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":505000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48085965832410,"sku":"TCI2510C001113921","price":1716000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0011_cb3e79c9-b135-46ce-976d-0c5910405e50.jpg?v=1792631975"},{"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_4ab9f6a5-4e7d-4d66-b54a-4e52e3bcc188.jpg?v=1792632032"},{"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":2247000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085975793882,"sku":"TCI2510C018114160","price":7571000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0181_2c61e9a8-246a-4840-b408-1354ed47d7ef.jpg?v=1792632216"},{"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_e316f869-3e84-44eb-8904-7702acc79f11.jpg?v=1792632419"},{"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":531000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48085991817434,"sku":"TCI2510C035314422","price":1112000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48085991850202,"sku":"TCI2510C035314423","price":2700000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0353_29c7ea3f-3ec7-47c1-9d35-51fa12453cb9.jpg?v=1792632423"},{"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":"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":1489000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48085995946202,"sku":"TCI2510C039314489","price":4266000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48085995978970,"sku":"TCI2510C039314490","price":12088000.0,"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":884000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085996044506,"sku":"TCI2510C039414492","price":2449000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0394_c18c1ea2-5c9c-4304-b28f-f183982d17c0.jpg?v=1792632497"},{"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":808000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086018654426,"sku":"TCI2510C065514882","price":2045000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0655_c6da8aba-348a-4bfd-87a2-e5f687b97206.jpg?v=1792632881"},{"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":"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":2726000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1708_e66af60d-2b28-4cb5-85ae-a28e9fbb935d.jpg?v=1792633993"},{"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":505000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48086098084058,"sku":"TCI2510C204216677","price":1641000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2042_d5a4e8d3-a5d9-4ac8-bbff-4d50be64a87a.jpg?v=1792634185"},{"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":1187000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086118400218,"sku":"TCI2510C230217034","price":3761000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2302_823cf16f-3f38-4327-8317-f81e9309d14e.jpg?v=1792634423"},{"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":1868000.0,"currency_code":"IDR","in_stock":true},{"title":"100mg","offer_id":48086129115354,"sku":"TCI2510C248817271","price":6108000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2488_9fc86d53-dadf-4f2c-b253-9032db9c3daf.jpg?v=1792634605"},{"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":4442000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2505_da37926e-294f-4b9e-9f57-aca23056b93a.jpg?v=1792634616"},{"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":18044000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2520_9a702fb0-25cc-4026-8a4a-46fbd5c0c2eb.jpg?v=1792634634"},{"product_id":"tci2510c273717595","title":"TCI C2737 34157-83-0 Celastrol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCelastrol is a chemical compound widely used in scientific research, particularly in the fields of biochemistry and pharmacology. It serves as a key reagent in laboratory experiments aimed at exploring its biological activities, including anti-inflammatory, antitumor, and antiviral effects. This compound is essential for researchers seeking to understand the mechanisms of drug action and the body's response to various medical conditions. Its versatility makes it a valuable tool in both academic and industrial research settings.\u003c\/p\u003e\n\u003cp\u003eCelastrol is favored for its stable chemical properties and solubility in organic solvents such as ethyl acetate and ethanol. These characteristics allow it to be easily incorporated into a wide range of chemical and biochemical analyses. Additionally, its complex molecular structure enables it to interact with multiple molecular targets within the body, making it a preferred choice for pharmacological studies. The compound’s unique properties support its use in experiments requiring specific biological activities.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Celastrol is commonly used in research focused on drug development, particularly in the study of cancer therapies and autoimmune diseases. It is also utilized in academic institutions for teaching and experimental purposes. Researchers in Indonesia rely on Celastrol to conduct experiments that require a compound with well-defined biological activity and chemical stability. Its presence in laboratory workflows underscores its importance in advancing scientific knowledge in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAnti-inflammatory Research: Celastrol is used to study its effects on inflammation, making it ideal for experiments involving inflammatory disease models.\u003c\/li\u003e\n\u003cli\u003eAntitumor Studies: Its potential as an antitumor agent supports its use in cancer research, particularly in drug discovery and mechanism studies.\u003c\/li\u003e\n\u003cli\u003eAntiviral Investigations: Celastrol’s antiviral properties make it a valuable reagent for studying viral infections and potential therapeutic applications.\u003c\/li\u003e\n\u003cli\u003ePharmacological Screening: Its complex structure and biological activity make it suitable for screening compounds with specific molecular targets.\u003c\/li\u003e\n\u003cli\u003eDrug Development Protocols: Celastrol is integrated into protocols for developing new drugs, especially in the context of autoimmune and oncological research.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 34157-83-0\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Crude Medicine Ingredients for Research and Experimental Use\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eCelastrol should be stored in a cool, dry place, away from direct sunlight and moisture. It is recommended to use airtight containers to prevent contamination and maintain its chemical stability. Due to its solubility in organic solvents, it should be handled in a well-ventilated area to minimize exposure. Laboratory personnel should wear appropriate personal protective equipment, such as gloves and safety goggles, when handling the compound. Proper disposal procedures should be followed to ensure compliance with safety and environmental regulations. Regular monitoring of storage conditions is essential to preserve the integrity of the compound for research use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mg","offer_id":48086194520282,"sku":"TCI2510C273717595","price":9338000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2737_f6988ac8-098d-4fa0-8ae1-dc60801bc576.jpg?v=1792634812"},{"product_id":"tci2510c285417731","title":"TCI C2854 77-53-2 Cedrol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCedrol (77-53-2) is an organic compound classified as a phenolic compound, widely utilized in life science research. It plays a crucial role in biochemical and pharmaceutical studies, serving as a key reagent in experimental setups. Its unique chemical structure and biological activity make it an essential component for researchers working on drug development, organic synthesis, and bioactive compound analysis. Cedrol is particularly valued for its versatility in supporting a wide range of scientific inquiries, from basic research to advanced experimental applications.\u003c\/p\u003e\n\u003cp\u003eCedrol is preferred due to its moderate polarity and solubility in organic solvents such as ethyl acetate and ethanol. These properties enable it to be effectively used in various chemical reactions and synthesis processes. Its high biological activity, including antioxidant and antimicrobial properties, further enhances its applicability in health-related research. The compound’s stability under specific conditions also contributes to its reliability in laboratory settings, ensuring consistent results over time.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Cedrol is commonly used in pharmaceutical, biotechnology, and chemical research. It is a staple in academic and industrial research institutions, supporting the development of new drugs and bioactive compounds. Its availability and well-documented properties make it a trusted choice for researchers aiming to advance scientific knowledge and innovation.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePharmaceutical research utilizes Cedrol for the development of new drugs due to its bioactive properties and chemical versatility.\u003c\/li\u003e\n\u003cli\u003eOrganic synthesis experiments benefit from Cedrol’s solubility in organic solvents and its role in complex molecule creation.\u003c\/li\u003e\n\u003cli\u003eAntimicrobial studies often incorporate Cedrol because of its known antimicrobial activity, aiding in the evaluation of natural compounds.\u003c\/li\u003e\n\u003cli\u003eBiochemical assays use Cedrol as a reagent to test the effects of phenolic compounds on cellular processes and enzyme activity.\u003c\/li\u003e\n\u003cli\u003eHealth-related research employs Cedrol to explore its antioxidant properties and potential applications in therapeutic formulations.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 77-53-2\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Crude Medicine Ingredients for Research and Experimental Use\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory supply\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid or liquid, depending on the specific product variant\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct sunlight and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eCedrol should be stored in a cool, dry environment to maintain its chemical stability and prevent degradation. It is recommended to keep it in airtight containers to minimize exposure to moisture and air, which can affect its quality over time. When handling Cedrol, researchers should use appropriate personal protective equipment, such as gloves and safety goggles, to ensure safety. It is important to avoid contact with skin and eyes, and to work in a well-ventilated area to reduce inhalation risks. Proper labeling of storage containers is essential for safe handling and to prevent accidental misuse. Regular monitoring of storage conditions ensures the compound remains suitable for use in laboratory applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086199795930,"sku":"TCI2510C285417731","price":1641000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086199828698,"sku":"TCI2510C285417732","price":5577000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2854_fa797f1c-0445-46c8-99aa-6ec185927c8c.jpg?v=1792634914"},{"product_id":"tci2510c344218482","title":"TCI C3442 6199-67-3 Cucurbitacin B","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCucurbitacin B is a chemical compound classified under alkaloids and widely used in pharmacological and biochemical research. As a key component of plants in the Cucurbitaceae family, it plays a significant role in the development of pharmaceuticals and bioactive compounds. In laboratory settings, it serves as a fundamental reagent for the synthesis of new compounds and the investigation of biological activities such as antioxidant, antitumor, and anti-inflammatory effects. Its presence in experimental research contributes to the understanding of natural products and their therapeutic potential.\u003c\/p\u003e\n\u003cp\u003eCucurbitacin B is valued for its complex molecular structure, which provides unique reactivity in chemical reactions. It is insoluble in water but more soluble in organic solvents such as ethyl acetate and ethanol, making it versatile for various extraction and synthesis processes. Its stability under certain conditions allows for safe handling and storage, enhancing its usability in laboratory environments. These properties make it a preferred choice for researchers seeking reliable and consistent results in their experiments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Cucurbitacin B is commonly used in applied research such as the development of modern traditional medicines, pharmacological effect studies of plants, and research on antioxidant effects in various disease conditions. Its application supports both academic and industrial research, contributing to advancements in pharmaceutical science and natural product chemistry.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePharmacological research for studying the biological effects of natural compounds in drug development.\u003c\/li\u003e\n\u003cli\u003eBiochemical studies to analyze the molecular mechanisms of antioxidant and anti-inflammatory activities.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical synthesis as a starting material for the creation of new therapeutic agents.\u003c\/li\u003e\n\u003cli\u003ePlant-based drug discovery to evaluate the potential of Cucurbitaceae species in traditional medicine.\u003c\/li\u003e\n\u003cli\u003eToxicological testing to assess the safety and efficacy of compounds derived from natural sources.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 6199-67-3\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Pharmaceutical Research Reagents\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eCucurbitacin B should be stored in a cool, dry environment to maintain its stability and prevent degradation. It is recommended to keep it in a tightly sealed container to minimize exposure to moisture and air. Due to its insolubility in water, it is advisable to use glass or plastic containers that are resistant to chemical reactions. Laboratory personnel should handle the compound with care, using appropriate personal protective equipment to ensure safety. Proper labeling and storage conditions are essential to maintain the integrity of the compound during experimental use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5mg","offer_id":48086247211226,"sku":"TCI2510C344218482","price":3307000.0,"currency_code":"IDR","in_stock":true},{"title":"25mg","offer_id":48086247243994,"sku":"TCI2510C344218483","price":11533000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3442_1fe3e03e-09f1-4d27-bd75-d5ec1ea61f39.jpg?v=1792635288"},{"product_id":"tci2510c345018493","title":"TCI C3450 70831-56-0 Chicoric Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eChicoric Acid is a chemical compound widely used in scientific research, particularly in the fields of cell biology and nutrition. As a bioactive compound, it is commonly found in extracts of certain plants and has the potential to influence physiological and metabolic processes in organisms. In laboratory settings, Chicoric Acid serves as a key reagent for the synthesis of other compounds or as a test material in nutritional and pharmacological studies. Its chemical structure is complex, and its chemical properties are stable, making it suitable for a variety of research conditions.\u003c\/p\u003e\n\u003cp\u003eOne of the main reasons Chicoric Acid is preferred in laboratories is its antioxidant and anti-inflammatory properties. These characteristics make it a valuable tool in studies related to health and disease. Its ability to modulate biological activities also enhances its relevance in research that requires compounds with clear biological effects. Additionally, its stability under various experimental conditions ensures consistent results, which is crucial for reliable scientific outcomes.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Chicoric Acid is commonly used in public health, nutritional, and pharmacological research. Researchers often employ this compound to explore the effects of natural substances on human and animal physiology. Its versatility and biological activity make it a preferred choice for studies aiming to understand the impact of plant-derived compounds on health and disease mechanisms. The compound's broad applications support its continued use in diverse scientific investigations.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eNutritional Research: Chicoric Acid is used to study the bioavailability and metabolic effects of plant-derived compounds in dietary contexts.\u003c\/li\u003e\n\u003cli\u003ePharmacological Studies: It serves as a model compound to investigate the pharmacological properties of natural substances and their therapeutic potential.\u003c\/li\u003e\n\u003cli\u003eCell Biology Experiments: Its role in modulating cellular processes makes it valuable for studying cellular responses to bioactive compounds.\u003c\/li\u003e\n\u003cli\u003eHealth and Disease Research: The compound's antioxidant and anti-inflammatory properties are explored in studies related to chronic diseases and immune responses.\u003c\/li\u003e\n\u003cli\u003ePublic Health Investigations: It is utilized to assess the impact of natural compounds on public health outcomes and nutritional status.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 70831-56-0\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Cell Biology \u0026gt; Nutrition Research\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory supply\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid, crystalline powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eChicoric Acid should be stored in a cool, dry environment, away from direct light and moisture to maintain its chemical stability. It is recommended to use airtight containers to prevent exposure to air and humidity, which could affect its integrity. As a solid, crystalline powder, it should be handled with care to avoid contamination. In laboratory settings, it is important to ensure proper ventilation when working with the compound to minimize inhalation risks. Always use appropriate personal protective equipment, such as gloves and safety goggles, when handling or transferring Chicoric Acid. Proper storage and handling practices are essential to preserve its quality and ensure safe usage in research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"10mg","offer_id":48086248554714,"sku":"TCI2510C345018493","price":2247000.0,"currency_code":"IDR","in_stock":true},{"title":"50mg","offer_id":48086248587482,"sku":"TCI2510C345018494","price":7622000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3450.jpg?v=1768817095"},{"product_id":"tci2510c347718527","title":"TCI C3477 3650-09-7 Carnosic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCarnosic Acid is a naturally occurring phenolic compound widely found in plants such as rosemary and sage. This compound plays a vital role in biochemical and pharmacological research due to its potent antioxidant properties. In the laboratory, it serves as a key reagent for studying antioxidant effects, free radical scavenging, and the mechanisms of biological activity. Its natural origin and well-documented properties make it a reliable choice for researchers seeking to explore the therapeutic potential of plant-derived compounds.\u003c\/p\u003e\n\u003cp\u003eCarnosic Acid is valued for its complex chemical structure, which provides both reactivity and stability under specific conditions. Its strong antioxidant activity makes it an ideal candidate for experiments aimed at inhibiting oxidative damage. Additionally, its good solubility in organic solvents enhances its usability in various chemical reactions and experimental formulations. These characteristics make it a preferred choice for researchers in both academic and industrial settings.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Carnosic Acid is commonly used in research related to health, environmental science, and pharmaceutical development. Its relevance in natural product research has made it a staple in studies focused on the biological effects of phenolic compounds. Researchers in Indonesia rely on its consistent quality and well-defined properties to support their experimental work across multiple scientific disciplines.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAntioxidant Activity Studies: Carnosic Acid is used to investigate its ability to neutralize free radicals and prevent oxidative damage in cellular and tissue systems.\u003c\/li\u003e\n\u003cli\u003eFree Radical Scavenging Research: It is employed to evaluate its effectiveness in scavenging reactive oxygen species, contributing to understanding its protective mechanisms.\u003c\/li\u003e\n\u003cli\u003eNatural Product Development: Carnosic Acid supports the formulation of pharmaceutical and cosmetic products derived from natural sources due to its bioactive properties.\u003c\/li\u003e\n\u003cli\u003eBiological Mechanism Exploration: It is utilized to study the molecular pathways involved in the biological activity of phenolic compounds.\u003c\/li\u003e\n\u003cli\u003eEnvironmental Toxicology Studies: Carnosic Acid is used to assess its impact on environmental systems and its potential role in bioremediation processes.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS Number: 3650-09-7\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Crude Medicine Ingredients for Research and Experimental Use\u003c\/li\u003e\n\u003cli\u003ePack Sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical Form: Solid (as per standard product description)\u003c\/li\u003e\n\u003cli\u003eStorage Note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eCarnosic Acid should be stored in a cool, dry place, away from direct light and moisture to maintain its chemical integrity. It is recommended to use airtight containers to prevent exposure to air and humidity, which may affect its stability. Due to its chemical reactivity, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. It is important to ensure that storage conditions are consistent and free from contaminants to preserve its potency. In laboratory settings, proper labeling and secure storage are essential to prevent accidental exposure and ensure safe handling.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"20mg","offer_id":48086251962586,"sku":"TCI2510C347718527","price":1842000.0,"currency_code":"IDR","in_stock":true},{"title":"100mg","offer_id":48086251995354,"sku":"TCI2510C347718528","price":7672000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3477_18c5433a-15e2-4c89-b3e1-12c15d136e66.jpg?v=1792635332"},{"product_id":"tci2510c350118561","title":"TCI C3501 61281-38-7 Schisandrin A","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eSchisandrin A is a bioactive compound belonging to the class of phytochemicals, primarily found in the *Schisandra chinensis* plant. This compound plays a vital role in biochemical and pharmacological research, serving as a key reagent for studying the biological effects of natural substances. In laboratory settings, it is used to investigate the mechanisms of action of natural compounds on biological systems, making it an essential tool for researchers in life sciences. Its unique molecular structure and significant biological activity contribute to its importance in experimental studies aimed at understanding the therapeutic potential of plant-derived compounds.\u003c\/p\u003e\n\u003cp\u003eThe compound's complex structure and notable biological activity make it a preferred choice for researchers. Schisandrin A exhibits significant antioxidant properties, enabling it to reduce oxidative stress and enhance cellular function. These properties are crucial in studies related to drug development, antioxidant research, and alternative therapy exploration. Its chemical stability under certain conditions further enhances its usability in laboratory experiments, ensuring consistent results across multiple trials. This stability and potency make it a reliable reagent for both academic and industrial research applications.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Schisandrin A is widely utilized in pharmaceutical and biomedical research. It is commonly found in research institutions and universities where scientists investigate the pharmacological effects of natural compounds. Its role in developing new therapeutic approaches and understanding the mechanisms of plant-based treatments makes it a valuable resource for researchers in Indonesia. Its availability and reliability ensure that it remains a key component in various experimental studies conducted within the country.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBiochemical Research: Schisandrin A is ideal for studying the biological effects of natural compounds due to its bioactive properties and molecular complexity.\u003c\/li\u003e\n\u003cli\u003ePharmacological Studies: It is used to explore the therapeutic potential of plant-derived substances, particularly in drug development and alternative medicine research.\u003c\/li\u003e\n\u003cli\u003eAntioxidant Activity Analysis: Its ability to reduce oxidative stress makes it suitable for experiments investigating antioxidant mechanisms in biological systems.\u003c\/li\u003e\n\u003cli\u003eCellular Function Studies: The compound's impact on cellular function supports research into how natural compounds influence cellular processes and health.\u003c\/li\u003e\n\u003cli\u003eAlternative Therapy Exploration: Schisandrin A is utilized to examine the efficacy of natural remedies in treating various conditions and diseases.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 61281-38-7\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Crude Medicine Ingredients for Research and Experimental Use\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified\u003c\/li\u003e\n\u003cli\u003ePhysical form: Not specified\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eSchisandrin A should be stored in a cool, dry place away from direct sunlight to maintain its chemical stability. It is recommended to use airtight containers to prevent moisture absorption and contamination. Proper labeling of storage containers is essential for safe handling and identification. Laboratory personnel should wear appropriate personal protective equipment when handling the compound to ensure safety. Avoid exposure to high temperatures and ensure good ventilation in the workspace. Regular monitoring of storage conditions helps maintain the integrity of the compound for reliable experimental results.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mg","offer_id":48086256353498,"sku":"TCI2510C350118561","price":3458000.0,"currency_code":"IDR","in_stock":true},{"title":"100mg","offer_id":48086256386266,"sku":"TCI2510C350118562","price":10171000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3501_bff9dced-25bb-4fb7-a12b-7d07b82c3922.jpg?v=1792635355"},{"product_id":"tci2510c361918719","title":"TCI C3619 7540-51-4 (-)-beta-Citronellol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(-)-beta-Citronellol is a chiral compound widely used in organic synthesis, particularly in asymmetric chemistry. It serves as a key building block for the synthesis of various chiral molecules with specific biological activities. This compound is essential in laboratories where precise control over stereochemistry is required. Its unique molecular structure makes it valuable for creating complex organic molecules with defined stereo configurations. In the field of pharmaceutical research, (-)-beta-Citronellol plays a critical role in the development of new drugs with enhanced efficacy and selectivity.\u003c\/p\u003e\n\u003cp\u003eThe compound is known for its chemical stability and clear chiral structure, which facilitates isomer separation and asymmetric reactions. Its stability under various laboratory conditions ensures consistent performance in synthetic processes. Additionally, (-)-beta-Citronellol has a distinct aroma, making it suitable for applications in fragrance and flavor industries. These properties make it a preferred choice for researchers seeking reliable and versatile chiral building blocks.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, (-)-beta-Citronellol is commonly used in organic chemistry and pharmaceutical research. Its relevance extends to academic and industrial settings where the synthesis of chiral compounds is essential. The compound supports both fundamental research and applied projects, contributing to advancements in drug development and cosmetic formulations. Its availability and reliability make it a valuable resource for scientists in Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis applications benefit from (-)-beta-Citronellol's chiral structure, enabling the creation of complex molecules with precise stereochemistry.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research utilizes this compound for the synthesis of chiral drugs, ensuring optimal biological activity and reduced side effects.\u003c\/li\u003e\n\u003cli\u003eCosmetic formulation processes incorporate (-)-beta-Citronellol due to its aromatic properties, enhancing the sensory qualities of products.\u003c\/li\u003e\n\u003cli\u003eAsymmetric catalysis relies on this compound to produce enantiomerically pure compounds, improving reaction efficiency and selectivity.\u003c\/li\u003e\n\u003cli\u003eIndustrial fragrance development uses (-)-beta-Citronellol for its distinctive scent, contributing to the creation of high-quality perfumes and flavorings.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 7540-51-4\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: As per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Liquid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003e(-)-beta-Citronellol should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to keep the compound in a tightly sealed container to prevent moisture absorption and contamination. Due to its chemical stability, it does not require refrigeration but should be protected from prolonged exposure to air. In laboratory settings, proper ventilation is essential when handling this compound to ensure safe working conditions. Always use appropriate personal protective equipment, such as gloves and safety goggles, to minimize exposure risks. The compound is non-hazardous under normal storage conditions but should be handled with care to maintain its integrity and effectiveness.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5mL","offer_id":48275733905626,"sku":"TCI2510C361918719","price":808000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3619.jpg?v=1769144262"},{"product_id":"tci2510c366018755","title":"TCI C3660 77-54-3 Cedryl Acetate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCedryl Acetate (TCI C3660), with the CAS number 77-54-3, is a chemical compound widely used in laboratory settings for its versatility in organic chemistry and biochemical research. It belongs to the terpene family, a group of naturally occurring compounds known for their diverse chemical and biological properties. This compound is commonly utilized as a reagent in the synthesis of complex organic molecules, making it a valuable tool for researchers in life sciences. Its role extends to studies involving fragrance and the physical properties of organic materials, where it serves as a key component in understanding molecular behavior.\u003c\/p\u003e\n\u003cp\u003eCedryl Acetate is favored for its chemical stability and solubility in organic solvents such as ethyl acetate and chloroform. These characteristics make it an ideal choice for chemical reactions requiring organic solvents. Additionally, its distinct aroma contributes to its relevance in aroma research and the development of fragrance-related compounds. The compound is non-toxic and relatively safe under normal usage conditions, which enhances its appeal in laboratory environments. Its stability and solubility ensure consistent performance across various experimental setups.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Cedryl Acetate is frequently used in chemical and pharmaceutical research, particularly in organic synthesis and fragrance studies. Its application spans across academic and industrial research settings, supporting the development of new compounds and the analysis of molecular properties. Its availability and reliability make it a preferred choice for researchers working on projects related to organic chemistry and biochemistry.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic Synthesis: Cedryl Acetate is ideal for organic synthesis due to its solubility in organic solvents and chemical stability, allowing for efficient reaction conditions.\u003c\/li\u003e\n\u003cli\u003eAroma Research: Its distinct aroma makes it a key component in studies related to fragrance and the sensory properties of organic compounds.\u003c\/li\u003e\n\u003cli\u003ePhysical Property Testing: It is used to assess the volatility and stability of organic compounds, providing valuable data for material characterization.\u003c\/li\u003e\n\u003cli\u003eBiochemical Studies: Cedryl Acetate supports research into the chemical behavior of terpenoids, contributing to understanding their biological and chemical properties.\u003c\/li\u003e\n\u003cli\u003eIndustrial Research: Its versatility and reliability make it a preferred choice for pharmaceutical and chemical industries conducting compound development and analysis.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS Number: 77-54-3\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Terpenes\u003c\/li\u003e\n\u003cli\u003ePack Sizes: Available in various sizes as per standard laboratory requirements\u003c\/li\u003e\n\u003cli\u003ePhysical Form: Liquid\u003c\/li\u003e\n\u003cli\u003eStorage Note: Store in a cool, dark place away from direct sunlight and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eCedryl Acetate should be stored in a cool, dark place, away from direct sunlight and moisture to maintain its chemical stability. It is recommended to use airtight containers made of glass or high-density polyethylene to prevent contamination and evaporation. Due to its solubility in organic solvents, it should be kept separate from incompatible materials to avoid unintended reactions. In laboratory settings, proper ventilation is essential to ensure safe handling. Always use appropriate personal protective equipment, such as gloves and safety goggles, when working with this compound. Its non-toxic nature makes it relatively safe, but standard laboratory safety protocols should still be followed to ensure optimal handling and storage conditions.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086275227866,"sku":"TCI2510C366018755","price":1642000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48086275260634,"sku":"TCI2510C366018756","price":4947000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3660.jpg?v=1768817134"},{"product_id":"tci2510c392119039","title":"TCI C3921 4547-24-4 Corosolic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCorosolic Acid is a chemical compound widely used in life science research and biochemical experiments. As a key component in natural products such as the leaves of the breadfruit tree, it has gained significant attention for its potential pharmacological properties. In laboratory settings, this compound serves as an essential reagent for studying biological activities, including antioxidant, anti-inflammatory, and antidiabetic effects. Its role in experimental research makes it a valuable tool for scientists exploring natural remedies and therapeutic applications.\u003c\/p\u003e\n\u003cp\u003eThe unique molecular structure of Corosolic Acid allows it to interact with various biological pathways, making it a preferred choice for researchers. It is chemically stable under certain conditions and is commonly available in crystalline form, which facilitates its use in laboratory experiments. Its non-toxic nature and measurable biological activity further enhance its appeal in scientific studies. These properties contribute to its widespread use in both academic and industrial research environments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Corosolic Acid is frequently utilized in applied research projects, including the development of herbal medicines, pharmacological effect studies, and biochemical experiments. Its relevance extends to researchers interested in natural compounds and their applications in healthcare. The compound's versatility and reliability make it a go-to material for various scientific investigations in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePharmacological research for studying anti-inflammatory and antioxidant properties due to its bioactive nature.\u003c\/li\u003e\n\u003cli\u003eDevelopment of herbal medicines as a key ingredient in natural product formulations for therapeutic applications.\u003c\/li\u003e\n\u003cli\u003eBiochemical experiments to analyze molecular interactions and biological pathway mechanisms.\u003c\/li\u003e\n\u003cli\u003eAntidiabetic studies to evaluate the compound's potential in managing blood sugar levels.\u003c\/li\u003e\n\u003cli\u003eNatural product screening to identify new compounds with therapeutic potential in traditional medicine.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 4547-24-4\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Crude Medicine Ingredients for Research and Experimental Use\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities\u003c\/li\u003e\n\u003cli\u003ePhysical form: Crystalline\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eCorosolic Acid should be stored in a cool, dry environment to maintain its stability and prevent degradation. It is recommended to keep the compound in a sealed container to avoid exposure to moisture and air. Since it is non-toxic, general laboratory safety protocols should still be followed when handling. The compound is stable under normal laboratory conditions but should be protected from extreme temperatures. Proper labeling and storage in a designated chemical cabinet are essential for safe handling and easy access. Always ensure that the workspace is clean and free from contaminants to preserve the integrity of the compound during experiments.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48086303834330,"sku":"TCI2510C392119039","price":8353000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3921_a25b0888-f4ad-4e2b-8135-8a552745d4ae.jpg?v=1792635644"},{"product_id":"tci2510d024219593","title":"TCI D0242 72-48-0 Alizarin","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eAlizarin TCI D0242, with CAS number 72-48-0, is a chemical compound widely used as a pigment in laboratory experiments. It is a key component in various analytical and experimental processes, particularly in the fields of chemistry, biology, and pharmacy. This compound is commonly employed for its ability to absorb and reflect specific wavelengths of light, making it an essential tool in staining and visualization techniques. Its presence in laboratory settings allows researchers to identify and analyze organic compounds effectively. Alizarin is also valuable in qualitative testing, where its reactivity with certain substances helps in determining the presence of specific ions or compounds.\u003c\/p\u003e\n\u003cp\u003eOne of the main reasons alizarin is preferred in laboratory applications is its stability under controlled conditions and its solubility in organic solvents. These properties make it suitable for a wide range of experimental setups, from basic research to advanced analytical procedures. Its ability to bind with other compounds enhances its utility in both qualitative and quantitative analysis. Additionally, alizarin’s consistent performance and reliability contribute to its popularity among scientists and researchers. Its physical form and chemical behavior make it a versatile reagent that can be adapted to various experimental needs.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, alizarin is frequently used in chemical, biological, and pharmaceutical research. It plays a crucial role in educational institutions and research facilities where staining and visualization techniques are required. Its availability in a 25-gram package makes it convenient for both small-scale experiments and larger research projects. Alizarin’s application in these settings highlights its importance as a fundamental reagent in the scientific community.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAlizarin is used in chemical analysis for identifying organic compounds due to its distinct absorption and reflection properties.\u003c\/li\u003e\n\u003cli\u003eIt is commonly applied in biological research for staining and visualizing cellular structures, aiding in microscopic examination.\u003c\/li\u003e\n\u003cli\u003eAlizarin supports pharmaceutical studies by helping in the detection and analysis of specific compounds in drug formulations.\u003c\/li\u003e\n\u003cli\u003eIt is utilized in qualitative testing to detect the presence of certain ions or functional groups in a sample.\u003c\/li\u003e\n\u003cli\u003eAlizarin is employed in educational settings to demonstrate staining techniques and light interaction in chemistry and biology classes.\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: 72-48-0\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Stains and Dyes (for Research and Experimental Use) \u0026gt; Pigments (for Research and Experimental Use)\u003c\/li\u003e\n\u003cli\u003ePack sizes: 25 grams\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eAlizarin should be stored in a cool, dry place away from direct sunlight and moisture. It is recommended to keep it in a sealed container to prevent exposure to air and contaminants. Due to its chemical nature, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. Alizarin is not flammable but may react with strong oxidizing agents. It is important to ensure proper ventilation when working with this compound to avoid inhalation of any vapors. Storage in a well-ventilated area helps maintain its stability and effectiveness for laboratory use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086360883418,"sku":"TCI2510D024219593","price":1112000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D0242_569a7be6-2214-447a-a1e8-086e20b5fbb2.jpg?v=1792636025"},{"product_id":"tci2510d054020024","title":"TCI D0540 11024-24-1 Digitonin","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eDigitonin from TCI (product code D0540) is a steroidal saponin obtained from the plant Digitalis purpurea. Each molecule combines a steroidal aglycone with a sugar chain. This structure makes it amphiphilic and places it among the glycoscience compounds. In cell biology and biochemistry laboratories, Digitonin is known as a mild detergent that can form pores in cholesterol-rich membranes. Researchers use it to permeabilize cells, isolate organelles and solubilize membrane protein complexes without disrupting their native structure.\u003c\/p\u003e\n\u003cp\u003eDigitonin's main advantage is its ability to form complexes with cholesterol. The plasma membrane is rich in cholesterol, while the inner mitochondrial membrane and the endoplasmic reticulum contain much less. At the right concentration, Digitonin can selectively perforate the plasma membrane and leave the organelles inside the cell intact. As a mild nonionic detergent, it also preserves the interactions between protein subunits. For this reason, it is a preferred reagent for analyzing mitochondrial respiratory chain complexes and membrane protein supercomplexes.\u003c\/p\u003e\n\u003cp\u003eIn Indonesia, Digitonin is used in molecular biology, biochemistry and medical research laboratories at universities, research institutes and life-science facilities. Typical work includes studies of cell physiology, mitochondrial function and membrane proteins, where intact organelles or native protein assemblies are essential. Its selective action on cholesterol-rich membranes makes it a practical tool for researchers who need to reach the cell interior in a controlled way. It also lets them extract membrane complexes without losing information about how the subunits are organized.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eCell permeabilization: Digitonin selectively forms pores in the cholesterol-rich plasma membrane, giving reagents access to the cytosol while internal organelle membranes remain largely intact.\u003c\/li\u003e\n\u003cli\u003eOrganelle isolation: Because cholesterol-poor membranes such as the inner mitochondrial membrane and the endoplasmic reticulum are less affected, Digitonin helps release and separate organelles in their intact form.\u003c\/li\u003e\n\u003cli\u003eSolubilization of membrane protein complexes: As a mild nonionic detergent, Digitonin extracts membrane proteins while preserving the native interactions between subunits that harsher detergents would disrupt.\u003c\/li\u003e\n\u003cli\u003eAnalysis of mitochondrial respiratory chain complexes: Its gentle action keeps respiratory chain complexes assembled, so researchers can study their composition and organization close to their native state.\u003c\/li\u003e\n\u003cli\u003eMembrane protein supercomplex studies: Digitonin keeps higher-order assemblies of membrane proteins intact, which supports research into how these supercomplexes form and work together in biological membranes.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI (product code D0540)\u003c\/li\u003e\n\u003cli\u003eCAS number: 11024-24-1\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Glycoscience\u003c\/li\u003e\n\u003cli\u003ePack sizes: see the available options on the product listing\u003c\/li\u003e\n\u003cli\u003ePhysical form: refer to the TCI specification sheet and certificate of analysis\u003c\/li\u003e\n\u003cli\u003eStorage: follow the storage conditions stated on the TCI label and Safety Data Sheet\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore Digitonin under the conditions specified on the TCI label and Safety Data Sheet. Keep it in its original tightly closed container in a dry, well-ventilated area, away from incompatible materials and direct heat or light. Handle it in a well-ventilated space or fume hood, and wear suitable gloves, safety glasses and a lab coat. Avoid breathing in dust and avoid contact with skin or eyes. Weigh and prepare solutions carefully to keep dust generation to a minimum. Label every working solution clearly. Read the Safety Data Sheet before use, and dispose of waste according to institutional and local regulations for chemical waste.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48086390079706,"sku":"TCI2510D054020024","price":1616000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D0540_5da2c1af-e101-4dec-9bc2-3c65ce5482a2.jpg?v=1792636217"},{"product_id":"tci2510d054220026","title":"TCI D0542 71-63-6 Digitoxin","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eDigitoxin is a chemical compound belonging to the group of digitalis glycosides, widely used in biochemical and pharmacological research. It plays a crucial role in laboratories where studies on cardiac function and pharmacological mechanisms are conducted. As a key component in the development of cardiac medications, Digitoxin is essential for understanding how certain compounds affect heart muscle contractions and overall cardiovascular function. Its presence in pharmaceutical products makes it a valuable tool for researchers aiming to explore the therapeutic potential of natural compounds.\u003c\/p\u003e\n\u003cp\u003eDigitoxin is characterized by its complex molecular structure, which includes both glycoside and steroid groups. These structural features contribute to its limited solubility in water and greater solubility in organic solvents, making it ideal for chromatographic and spectroscopic analyses. Its stability under certain conditions further enhances its usability in long-term research projects. These properties make Digitoxin a preferred choice for scientists working in analytical and experimental settings.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Digitoxin is commonly used in pharmacological and biochemical studies, particularly in research focused on cardiovascular systems. It is also utilized in the development of new therapeutic agents and in understanding the mechanisms of existing cardiac treatments. Its relevance in both academic 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\u003eCardiac Pharmacology Research: Digitoxin is used to investigate the effects of cardiac glycosides on heart muscle contractions and their therapeutic potential.\u003c\/li\u003e\n\u003cli\u003eBiochemical Analysis: Its molecular structure makes it suitable for spectroscopic and chromatographic studies to determine its chemical behavior and interactions.\u003c\/li\u003e\n\u003cli\u003eDrug Development Studies: Researchers use Digitoxin to explore its pharmacological properties and potential applications in new drug formulations.\u003c\/li\u003e\n\u003cli\u003eToxicology Testing: Digitoxin is employed to assess its toxicity and biological effects on various cell types and tissues.\u003c\/li\u003e\n\u003cli\u003eCardiovascular Mechanism Studies: It aids in understanding how cardiac glycosides influence heart function and cellular signaling pathways.\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: 71-63-6\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Glycoscience\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\u003eDigitoxin should be stored in a cool, dry place away from direct light to maintain its stability and prevent degradation. It is recommended to use airtight containers to minimize exposure to moisture and contaminants. Due to its limited water solubility, it is advisable to handle it in a well-ventilated area to avoid inhalation of dust particles. Laboratory personnel should wear appropriate personal protective equipment, such as gloves and safety goggles, when handling this compound. Proper labeling of containers is essential to ensure safe handling and prevent accidental exposure. Regular monitoring of storage conditions will help maintain the integrity of the compound for research purposes.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48086390145242,"sku":"TCI2510D054220026","price":3660000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D0542_80b2f720-3f69-4873-8ed2-e8bb1c8727a2.jpg?v=1792636219"},{"product_id":"tci2510d056320055","title":"TCI D0563 117-10-2 Chrysazin","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eChrysazin is a chemical compound widely used in various chemical reactions for the synthesis of complex molecules. As a key building block in organic chemistry, it serves as a foundational material for the creation of heterocyclic compounds and other organic substances. Its role in the laboratory is critical, especially in reactions involving substitution or molecular combination. Chrysazin is valued for its stable molecular structure and high reactivity, making it a versatile reagent in diverse chemical processes.\u003c\/p\u003e\n\u003cp\u003eThe compound’s non-heterocyclic nature makes it an ideal choice for synthesizing molecules that require a simple yet flexible base structure. This characteristic allows researchers to efficiently modify molecular structures, enhancing the efficiency of chemical synthesis. Its stability and reactivity ensure consistent performance across a range of experimental conditions, making it a reliable material for both academic and industrial applications.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Chrysazin is commonly used in chemical research, including the synthesis of pharmaceutical compounds, industrial chemicals, and materials science. It plays a vital role in educational and research institutions, supporting the development of knowledge and skills in organic chemistry. Its relevance spans across various fields, contributing to innovation and scientific advancement in the chemical industry.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSynthesis of heterocyclic compounds for the development of new pharmaceuticals due to its structural versatility and reactivity.\u003c\/li\u003e\n\u003cli\u003eOrganic chemistry research where stable and reactive building blocks are required for complex molecule creation.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical production where non-heterocyclic compounds are needed for the formulation of various products.\u003c\/li\u003e\n\u003cli\u003eMaterial science experiments involving molecular modification and structural flexibility for advanced material development.\u003c\/li\u003e\n\u003cli\u003eEducational purposes in chemistry laboratories to teach fundamental concepts of organic synthesis and molecular structure.\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: 117-10-2\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities\u003c\/li\u003e\n\u003cli\u003ePhysical form: 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\u003eChrysazin should be stored in a cool, dry environment to maintain its stability and prevent degradation. It is recommended to keep the compound in airtight containers to avoid exposure to moisture and air, which can affect its reactivity. Proper labeling of storage containers is essential for safety and identification. In a laboratory setting, it is important to handle the compound with care, using appropriate personal protective equipment such as gloves and safety goggles. Storage should be in a location that is inaccessible to unauthorized personnel and away from incompatible substances. Regular monitoring of storage conditions ensures the integrity and usability of the material for research and experimentation.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086391554266,"sku":"TCI2510D056320055","price":3710000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D0563_787a78db-9cbf-4c16-8310-1b999ce63778.jpg?v=1792636239"},{"product_id":"tci2510d060020115","title":"TCI D0600 59-92-7 3-(3,4-Dihydroxyphenyl)-L-alanine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e3-(3,4-Dihydroxyphenyl)-L-alanine, commonly known as L-DOPA, is a chemical compound that plays a crucial role in chemical biology and peptide chemistry. It is widely used in laboratory settings for its ability to participate in various biochemical reactions. This compound is particularly important in the study of neurotransmitter metabolism and has been extensively researched in the context of Parkinson’s disease. Due to its reactivity and structural complexity, L-DOPA is a valuable tool for researchers seeking to explore the mechanisms of biological processes and develop new therapeutic agents.\u003c\/p\u003e\n\u003cp\u003eL-DOPA is preferred for its chemical versatility and biological activity. Its ability to interact with a wide range of reagents and catalysts makes it ideal for organic synthesis and drug development. The compound’s stability under certain conditions further enhances its usability in laboratory environments. Additionally, its role in the biosynthesis of dopamine makes it a key component in studies related to neurochemistry and pharmacology. These properties collectively make L-DOPA a highly sought-after material in both academic and industrial research.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, L-DOPA is frequently used in pharmacological, biochemical, and health sciences research. It is a staple in university research facilities and scientific institutions focused on biomedical innovation. Its relevance spans across multiple disciplines, making it an essential compound for researchers aiming to advance knowledge in chemical and biological sciences. The compound’s broad applications ensure its continued importance in the scientific community.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eNeurochemical research utilizes L-DOPA to study dopamine synthesis and its role in neurological disorders.\u003c\/li\u003e\n\u003cli\u003ePeptide chemistry applications benefit from L-DOPA's structural properties for synthesizing bioactive compounds.\u003c\/li\u003e\n\u003cli\u003ePharmacological studies rely on L-DOPA to develop and test new therapeutic agents for Parkinson’s disease.\u003c\/li\u003e\n\u003cli\u003eBiochemical experiments use L-DOPA to investigate enzyme activity and metabolic pathways.\u003c\/li\u003e\n\u003cli\u003eBiomedical research incorporates L-DOPA to explore its potential in drug development and 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: 59-92-7\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Peptide Chemistry\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities\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\u003eL-DOPA should be stored in a cool, dry environment to maintain its chemical integrity. It is recommended to keep the compound in a tightly sealed container to prevent moisture absorption and contamination. Due to its reactivity, it should be handled in a well-ventilated area, ideally with appropriate personal protective equipment. Avoid exposure to strong oxidizing agents or incompatible substances. Proper labeling and storage conditions ensure the compound remains stable and safe for use in laboratory settings. Regular monitoring of storage conditions is advised to maintain optimal performance and safety.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086393880794,"sku":"TCI2510D060020115","price":733000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086393913562,"sku":"TCI2510D060020116","price":1868000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48086393946330,"sku":"TCI2510D060020117","price":5326000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D0600_d92e0e33-cbce-43c0-9792-3cbb6d55baf1.jpg?v=1792636272"},{"product_id":"tci2510d176521659","title":"TCI D1765 530-59-6 3,5-Dimethoxy-4-hydroxycinnamic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e3,5-Dimethoxy-4-hydroxycinnamic Acid is a chemical compound widely used in laboratory settings for its versatility in synthetic chemistry. It serves as a key building block in the synthesis of complex organic molecules and molecular modifications. This compound is particularly valuable for researchers working on the development of new compounds with potential applications in pharmaceuticals, biochemistry, and materials science. Its chemical structure provides a foundation for further functionalization, making it a crucial component in many experimental protocols.\u003c\/p\u003e\n\u003cp\u003eThe compound is known for its polar nature and ability to form hydrogen bonds, which are essential for participating in substitution and oxidation reactions. These properties make it a preferred choice for chemists seeking reliable and consistent results in their experiments. Its high purity and molecular consistency ensure that it meets the rigorous standards required for scientific research. This reliability is especially important in reproducible and accurate experimental outcomes.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 3,5-Dimethoxy-4-hydroxycinnamic Acid is commonly used in scientific research across various institutions, including universities and research centers. It plays a significant role in organic and biochemical studies, contributing to the development of new compounds with potential therapeutic or industrial applications. Its relevance in these fields continues to grow as researchers explore its properties and potential uses.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis applications benefit from this compound's reactivity and structural versatility, enabling the creation of complex molecules with tailored properties.\u003c\/li\u003e\n\u003cli\u003eBiochemical research utilizes its polar nature and hydrogen bonding capabilities, which are essential for enzyme interactions and molecular recognition processes.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical development leverages its potential as a precursor for drug candidates with antioxidant and anti-inflammatory properties.\u003c\/li\u003e\n\u003cli\u003eMaterial science experiments use its chemical stability and reactivity to design new polymers and functional materials with specific properties.\u003c\/li\u003e\n\u003cli\u003eAnalytical chemistry applications take advantage of its detectability and reactivity in spectroscopic and chromatographic analyses.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 530-59-6\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment, away from direct light and moisture to maintain its chemical integrity. It is recommended to use airtight containers to prevent exposure to air and humidity, which could affect its stability. Proper labeling of storage containers is essential for safety and traceability. In laboratory settings, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to minimize exposure. Due to its polar nature, it is advisable to avoid contact with incompatible substances. Regular inspection of storage conditions ensures that the compound remains in optimal condition for use in experiments.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086473670874,"sku":"TCI2510D176521659","price":2045000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086473703642,"sku":"TCI2510D176521660","price":6840000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D1765_5c4be171-f017-4271-8cb1-78fea90b0b44.jpg?v=1792637332"},{"product_id":"tci2510d182821755","title":"TCI D1828 20830-75-5 Digoxin","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eDigoxin is a chemical compound classified under the category of digitalis glycosides, commonly used in biochemical and pharmacological research. As a key component in the study of cardiac physiology, it plays a vital role in understanding the mechanisms of action of cardiac medications. Its strong pharmacological activity makes it an essential tool for investigating the effects of drugs on the cardiovascular system. In the laboratory, Digoxin is widely utilized for its ability to modulate heart rate and contractility, making it a valuable asset in pharmacological studies and drug development.\u003c\/p\u003e\n\u003cp\u003eDigoxin is known for its chemical stability under controlled conditions, which ensures consistent results in experimental settings. However, it is highly sensitive to moisture and light, requiring careful handling and storage to maintain its integrity. These properties make it a preferred choice for researchers who require reliable and reproducible data. Its availability in solid form simplifies its use in both qualitative and quantitative analyses, enhancing its versatility in various laboratory applications.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Digoxin is frequently used in public health and pharmaceutical research. It serves as a critical reagent for studying the pharmacological effects and mechanisms of action of drugs in human physiology. Its application supports the development of more effective and safe therapeutic options for the Indonesian population. Researchers rely on Digoxin to advance their understanding of cardiovascular diseases and improve treatment strategies.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePharmacological research for studying cardiac drug mechanisms and effects on heart function.\u003c\/li\u003e\n\u003cli\u003eDevelopment of new pharmaceuticals by analyzing the pharmacological properties of Digoxin.\u003c\/li\u003e\n\u003cli\u003eToxicological studies to evaluate the safety and potential side effects of the compound.\u003c\/li\u003e\n\u003cli\u003eBiochemical experiments to investigate the interaction of Digoxin with cellular and molecular targets.\u003c\/li\u003e\n\u003cli\u003ePublic health research to understand the impact of cardiac medications on human health and disease management.\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: 20830-75-5\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Glycoscience\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory requirements\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Must be stored 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\u003eDigoxin should be stored in a cool, dry environment, away from direct light and moisture to maintain its chemical stability. It is recommended to use airtight containers made of glass or high-density polyethylene to prevent exposure to humidity. Due to its sensitivity, it is important to handle Digoxin with clean, dry gloves and avoid contact with moisture during preparation. In laboratory settings, it should be kept in a designated storage area with controlled environmental conditions to ensure its integrity. Always follow standard safety protocols when handling this compound to prevent degradation and ensure accurate experimental results.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48086477865178,"sku":"TCI2510D182821755","price":1060000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48086477897946,"sku":"TCI2510D182821756","price":4240000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D1828_f2744b41-867d-4676-888c-41e2ab8b68a0.jpg?v=1792637381"},{"product_id":"tci2510d266822983","title":"TCI D2668 486-66-8 Daidzein","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eDaidzein is a chemical compound classified as an isoflavone, naturally found in various plants, particularly legumes such as soybeans. It plays a crucial role in scientific research, especially in biochemical and pharmacological studies. This compound is widely used in laboratories to investigate the biological effects of natural substances, including their impact on metabolism and overall health. Its presence in research settings allows scientists to explore its potential applications in drug development and nutritional studies.\u003c\/p\u003e\n\u003cp\u003eDaidzein is valued for its chemical stability and controlled reactivity, making it suitable for a range of laboratory experiments. Its molecular structure enables interactions with various enzymes and receptors in the body, which is essential for studying biological mechanisms. Additionally, its non-toxic nature and ability to be used in controlled dosages make it a safe option for scientific experiments. The purity of the compound also facilitates accurate analysis and testing in laboratory environments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Daidzein is commonly used in research related to natural compounds and their biological effects. It is a key component in studies focused on antioxidant properties and hormonal activity. Its availability in pure form supports detailed scientific investigations and contributes to the advancement of biochemical and pharmacological research in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBiochemical Research: Daidzein is used to study the biochemical pathways and interactions of natural compounds in biological systems.\u003c\/li\u003e\n\u003cli\u003ePharmacological Studies: It is employed in drug development to evaluate the potential therapeutic effects of isoflavones.\u003c\/li\u003e\n\u003cli\u003eNutritional Analysis: Daidzein helps in understanding the role of plant-derived compounds in human metabolism and health.\u003c\/li\u003e\n\u003cli\u003eHormonal Activity Research: Its hormonal properties make it valuable for studying the impact of natural substances on endocrine systems.\u003c\/li\u003e\n\u003cli\u003eAntioxidant Testing: Daidzein is used to assess the antioxidant capacity of natural compounds in various experimental models.\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: 486-66-8\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\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\u003eDaidzein 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. Laboratory personnel should handle the compound with care, using appropriate personal protective equipment such as gloves and safety goggles. Since it is non-toxic, it is generally safe to handle, but standard laboratory safety protocols should still be followed. Proper labeling of storage containers is essential to ensure safe handling and prevent accidental exposure. Regular monitoring of storage conditions will help maintain the integrity of the compound for research purposes.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086571778266,"sku":"TCI2510D266822983","price":4871000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D2668_9cc851de-4f30-4707-9502-49f10e26636e.jpg?v=1792638184"},{"product_id":"tci2510d390824332","title":"TCI D3908 520-27-4 Diosmin","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D3908 Diosmin is a naturally occurring flavonoid glycoside that belongs to the fields of glycoscience and chemical biology. Structurally, the compound is a flavone bound to a sugar unit, combining the character of an aromatic aglycone with a carbohydrate portion. In the laboratory, Diosmin serves as both a comparison standard and a test material in natural product research, in studies of the biological activity of flavonoids, and in the development of analytical methods for determining active compound content in plant extracts and herbal-based products. This combination of roles makes it a routine item on the bench for groups working on plant-derived bioactive molecules.\u003c\/p\u003e\n\u003cp\u003eThe characteristic that leads researchers to select this material is its clearly defined glycosidic structure, which makes it suitable for use as an identity marker in both chromatographic and spectroscopic analysis. The sugar portion influences solubility and the behaviour of the compound in mixed-solvent systems, while the flavone framework provides a chromophore that responds well to ultraviolet detectors. As a TCI product supplied at research reagent quality, the compound helps confirm that a peak observed on an instrument genuinely originates from the intended analyte rather than from some other component of the sample matrix.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Diosmin is widely used in natural product pharmaceutical research and in laboratory work concerned with the characterisation of plant-derived flavonoids. It supports method development and verification activities where a defined reference material is required to interpret instrument output with confidence, particularly in studies of extracts and herbal-based preparations that form a substantial part of the local research landscape.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eReference standard in natural product analysis — the defined glycosidic structure allows analysts to confirm the identity of a flavonoid peak observed in a plant extract rather than relying on retention behaviour alone.\u003c\/li\u003e\n\u003cli\u003eChromatographic method development — the flavone chromophore gives a strong ultraviolet detector response, making the compound a practical marker when establishing separation conditions for flavonoid-containing samples.\u003c\/li\u003e\n\u003cli\u003eSpectroscopic identity confirmation — the well-characterised aglycone and sugar combination provides a consistent spectral signature that can be compared directly against signals recorded from unknown or partially purified samples.\u003c\/li\u003e\n\u003cli\u003eFlavonoid biological activity studies — as a test material in chemical biology work, Diosmin allows researchers to examine how a glycosylated flavone behaves in comparison with related aglycone structures.\u003c\/li\u003e\n\u003cli\u003eHerbal product quality evaluation — the material serves as a comparison substance when verifying that an active compound reported in a herbal-based preparation is genuinely present and not a matrix artefact.\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: 520-27-4\u003c\/li\u003e\n\u003cli\u003eCatalogue number: D3908\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Glycoscience\u003c\/li\u003e\n\u003cli\u003eCompound class: Natural flavonoid glycoside (flavone linked to a sugar unit)\u003c\/li\u003e\n\u003cli\u003eGrade: Research reagent quality\u003c\/li\u003e\n\u003cli\u003ePack sizes and physical form: please refer to the current TCI catalogue listing for this item\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the container in a cool, dry place, kept tightly closed and protected from light and moisture, in line with the storage instructions printed on the manufacturer's label for this item. Keep the material in its original container wherever possible; if it must be transferred, use clean, dry, chemically compatible glass or suitable plastic vessels that can be sealed and clearly labelled with the compound name, catalogue number, and CAS number. Handle the substance in a well-ventilated area or fume hood, wear a laboratory coat, safety glasses, and appropriate gloves, and avoid generating dust when weighing out portions. Use clean, dry spatulas to prevent contamination that would compromise the material's value as a reference standard, and allow the container to reach ambient temperature before opening so that condensation does not affect the contents. Consult the manufacturer's safety data sheet before first use and follow local institutional rules for chemical waste disposal.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086644719834,"sku":"TCI2510D390824332","price":1313000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086644752602,"sku":"TCI2510D390824333","price":3987000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D3908_c059087c-8eb9-4f7a-881d-5b7c06abeb24.jpg?v=1792638951"},{"product_id":"tci2510d392024350","title":"TCI D3920 552-66-9 Daidzin","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D3920 Daidzin is an isoflavone glycoside that belongs to the group of chemical biology compounds used in the field of glycoscience. Structurally, this compound is the glycosylated form of the isoflavone daidzein, combining an isoflavone core with a sugar unit. In the laboratory, Daidzin is widely used as an analytical reference material and as a test substance in natural product research, particularly in studies of the isoflavone content of soybeans and their derived products, which are common subjects of food and pharmaceutical research.\u003c\/p\u003e\n\u003cp\u003eThe characteristic that makes this compound important is its clearly defined structure as a marker for glycosylated isoflavones, which helps researchers distinguish the glycoside form from the aglycone form within a single sample. The sugar portion influences solubility and retention time in chromatographic analysis, while the isoflavone core provides a characteristic ultraviolet absorbance that is easily monitored by a detector. Because it is supplied as a TCI research reagent, this compound supports accurate peak identification and reliable quantification results in both routine analytical work and method development.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Daidzin is relevant to soybean-based functional food research, where soy and its fermented and processed derivatives are studied extensively. It supports laboratories working on natural product characterization, food composition studies, and pharmaceutical research that requires a defined isoflavone reference. Its role as a glycosylated isoflavone marker makes it suitable for both academic research groups and analytical service laboratories carrying out routine identification and quantification work.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eIsoflavone reference material in chromatographic analysis, where its defined structure and characteristic ultraviolet absorbance allow reliable peak identification against sample chromatograms.\u003c\/li\u003e\n\u003cli\u003eQuantification of isoflavones in soybean and soy-derived products, since a defined glycoside reference supports dependable calculation of content in food research samples.\u003c\/li\u003e\n\u003cli\u003eDifferentiation of glycoside and aglycone forms in a single sample, because Daidzin represents the glycosylated form while daidzein represents the corresponding aglycone.\u003c\/li\u003e\n\u003cli\u003eAnalytical method development for natural product research, as the sugar unit gives a distinct retention behaviour useful for optimising separation and detection conditions.\u003c\/li\u003e\n\u003cli\u003eGlycoscience and chemical biology studies of isoflavone glycosides, where the combination of an isoflavone core with a sugar unit serves as a well-characterised test substance.\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: 552-66-9\u003c\/li\u003e\n\u003cli\u003eProduct Code: D3920\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Glycoscience\u003c\/li\u003e\n\u003cli\u003eCompound Class: Isoflavone glycoside (glycosylated form of daidzein)\u003c\/li\u003e\n\u003cli\u003eStorage: Store according to the conditions stated on the manufacturer's product label and safety data sheet\u003c\/li\u003e\n\u003cli\u003ePack sizes: Please refer to the available pack size options for this product\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore this compound in its original tightly closed container, protected from light and moisture, and follow the storage temperature stated on the manufacturer's label and safety data sheet. Suitable containers are the original amber glass or sealed vial supplied, kept in a dedicated reagent cabinet or refrigerated storage as indicated. Handle the material in a well-ventilated area or fume hood while wearing a laboratory coat, safety glasses, and appropriate gloves. Avoid generating dust when weighing, close the container promptly after use, and keep it away from strong oxidising agents. Prepare solutions using clean glassware and label all dilutions clearly. Review the safety data sheet before first use and dispose of residues and contaminated materials in accordance with applicable laboratory waste procedures.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mg","offer_id":48086645473498,"sku":"TCI2510D392024350","price":5603000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D3920_1873400b-3602-4655-b87f-b04f501c10f7.jpg?v=1792638963"},{"product_id":"tci2510d398624435","title":"TCI D3986 478-43-3 4,5-Dihydroxyanthraquinone-2-carboxylic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D3986 4,5-Dihydroxyanthraquinone-2-carboxylic Acid (CAS 478-43-3), widely known among researchers as rhein, is a hydroxylated anthraquinone derivative that carries a carboxylic acid group on its tricyclic framework. In the laboratory this material plays a dual role: it serves as a non-heterocyclic building block for organic synthesis, and at the same time it functions as a reference compound in natural product research, particularly in studies of secondary metabolites of the anthraquinone class that are commonly found in plants of the Polygonaceae and Fabaceae families. Its presence helps researchers establish the identity of isolated compounds with greater confidence.\u003c\/p\u003e\n\u003cp\u003eThe characteristic that makes this material a frequent choice is its combination of functional groups that is rich yet still manageable: two phenolic hydroxyl groups that are weakly acidic and capable of forming intramolecular hydrogen bonds with the quinone carbonyl groups, plus a single carboxylic acid group that provides a clear derivatisation point for both esterification and amidation. The anthraquinone framework supplies a strongly conjugated chromophore system, so the compound is easily monitored with a UV-Vis detector in HPLC as well as by spectrophotometric scanning. This makes it convenient to track through reaction sequences and analytical workflows alike.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this profile fits the work routinely carried out in university natural product groups, pharmacy and pharmacognosy laboratories, and chemical synthesis laboratories. It is used as a comparison standard when confirming anthraquinone metabolites isolated from local plant material, and as a starting scaffold when researchers need to prepare derivatives around the anthraquinone core. Because it is detected readily by common UV-Vis instrumentation, it integrates well with the analytical equipment already available in most institutional laboratories.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eNatural product reference compound — used as a comparison marker so anthraquinone metabolites isolated from Polygonaceae and Fabaceae plant material can be identified with greater confidence.\u003c\/li\u003e\n\u003cli\u003eNon-heterocyclic building block for organic synthesis — the intact anthraquinone framework serves as a starting scaffold for researchers preparing structurally related target compounds.\u003c\/li\u003e\n\u003cli\u003eCarboxyl-directed derivatisation chemistry — the single carboxylic acid group provides a clear and well-defined point of attachment for esterification and amidation reactions.\u003c\/li\u003e\n\u003cli\u003eHPLC method development and analysis — the strongly conjugated anthraquinone chromophore is readily monitored with a UV-Vis detector, making the compound convenient for chromatographic work.\u003c\/li\u003e\n\u003cli\u003eUV-Vis spectrophotometric studies — the same conjugated chromophore system allows straightforward spectrophotometric scanning, supporting characterisation work and routine verification of isolated fractions.\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: 478-43-3\u003c\/li\u003e\n\u003cli\u003eChemical name: 4,5-Dihydroxyanthraquinone-2-carboxylic Acid (also known as rhein)\u003c\/li\u003e\n\u003cli\u003eProduct code: D3986\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in standard TCI research-scale packaging; please refer to the current catalogue listing for available options\u003c\/li\u003e\n\u003cli\u003eStorage: store according to the storage conditions stated on the product label and in the accompanying documentation\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the container tightly closed in a cool, dry, well-ventilated place, away from direct sunlight and sources of heat or ignition, and follow the specific storage conditions indicated on the product label and Safety Data Sheet. Keep the material in its original supplier container, or in a chemically compatible, clearly labelled amber glass container if transfer is necessary, since the conjugated chromophore makes light protection sensible. Handle in a fume hood using standard personal protective equipment — safety goggles, gloves, and a laboratory coat — and avoid the generation and inhalation of dust when weighing the solid. Wash hands thoroughly after handling, keep the container closed when not in use, and dispose of residues and contaminated materials in accordance with applicable laboratory and institutional waste procedures. Always consult the Safety Data Sheet before first use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48086649602266,"sku":"TCI2510D398624435","price":4013000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48086649635034,"sku":"TCI2510D398624436","price":12998000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D3986_0fdfc12c-3f70-42f4-a1bf-74ad181f78a7.jpg?v=1792639020"},{"product_id":"tci2510d516726024","title":"TCI D5167 19057-60-4 Dioscin","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eDioscin, with the CAS number 19057-60-4, is a chemical compound classified under the category of steroid saponins. It plays a significant role in laboratory research, particularly in the fields of chemical biology and glycoscience. As a naturally occurring compound derived from specific plant sources, Dioscin is widely used in scientific studies to explore its biological activities. Its presence in various biochemical experiments makes it an essential component for researchers aiming to understand its potential therapeutic applications.\u003c\/p\u003e\n\u003cp\u003eThe compound is valued for its stability under certain conditions and its solubility in organic solvents such as ethyl acetate and ethanol. These properties make it a preferred choice for laboratory use, as they allow for consistent and reliable results in experimental settings. Additionally, Dioscin's ability to interact with various enzymes and biological receptors enhances its utility in pharmacological and biochemical investigations. Its molecular structure also contributes to its significance in organic chemistry research.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Dioscin is commonly utilized in research related to public health and pharmaceutical development. Its potential as a natural compound for drug discovery and health supplement formulation has made it a key material for scientists working in both academic and industrial settings. The compound's versatility and chemical properties support its widespread application across multiple scientific disciplines.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePharmacological research utilizes Dioscin to study its anti-inflammatory and anti-tumor properties, aiding in drug development.\u003c\/li\u003e\n\u003cli\u003eBiochemical experiments benefit from Dioscin's solubility in organic solvents, enabling effective extraction and analysis.\u003c\/li\u003e\n\u003cli\u003eGlycoscience studies leverage Dioscin's molecular structure to explore its role in carbohydrate metabolism and enzyme interactions.\u003c\/li\u003e\n\u003cli\u003eAnti-oxidant research incorporates Dioscin to assess its potential in neutralizing free radicals and protecting cellular components.\u003c\/li\u003e\n\u003cli\u003eHealth-related research in Indonesian labs uses Dioscin to investigate its therapeutic applications in natural medicine and herbal formulations.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 19057-60-4\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Glycoscience\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eDioscin should be stored in a cool, dry environment to maintain its chemical stability and prevent degradation. It is recommended to keep the compound in a sealed container to avoid exposure to moisture and air, which can affect its integrity. Suitable storage containers include glass or high-density polyethylene vessels that are resistant to chemical reactions. In laboratory settings, it is important to handle Dioscin with appropriate personal protective equipment, such as gloves and safety goggles, to ensure safe handling. The compound is generally non-hazardous but should be treated with care to avoid contamination. Regular monitoring of storage conditions ensures the compound remains suitable for use in research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"250mg","offer_id":48086747873498,"sku":"TCI2510D516726024","price":6360000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D5167_a1f79c62-ddd0-4b1e-a407-821481889577.jpg?v=1792639785"},{"product_id":"tci2510d569626671","title":"TCI D5696 611-59-6 1,7-Dimethylxanthine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D5696 1,7-Dimethylxanthine is a xanthine-class alkaloid compound widely known as paraxanthine, the principal metabolite of caffeine in the human body. The material is supplied as a pure, reagent-grade substance, allowing it to be treated as a reference material in biochemistry, pharmacology, and analytical chemistry laboratories. Its role at the bench is highly specific: it serves as both an identity comparator and a quantitative comparator whenever researchers need to confirm that a peak appearing on a chromatogram genuinely originates from paraxanthine rather than from caffeine, theophylline, or theobromine, whose underlying structures are closely similar.\u003c\/p\u003e\n\u003cp\u003eThe characteristic that makes this compound the preferred choice is the placement of its methyl groups at positions 1 and 7 of the xanthine core, which produces a distinctive ultraviolet absorption pattern and mass spectrometric fragmentation pattern that can be distinguished from those of the other dimethylxanthine isomers. As an alkaloid solid, the material is stable enough to be weighed and dissolved into a stock solution, which makes the preparation of graded calibration series straightforward. It is precisely this clarity of identity that gives the material its value: a single correct comparator compound determines data quality far more decisively than almost any other variable in the workflow.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this material fits naturally into the daily routine of university research groups, pharmacology departments, and analytical service units that work with caffeine metabolism and related xanthine compounds. It is typically weighed out to build stock and working solutions, then carried through chromatographic and spectrometric runs as the identity and quantity reference. Because a reliable comparator underpins every subsequent number reported, it occupies a small but decisive place on the reagent shelf.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eChromatographic identity confirmation: run alongside unknown samples so that a suspected paraxanthine peak can be matched against a known comparator rather than assigned by retention time alone.\u003c\/li\u003e\n\u003cli\u003eCalibration series preparation: weighed accurately and dissolved into a stock solution, then diluted stepwise to build the graded standard curve that quantitative measurements of paraxanthine depend upon.\u003c\/li\u003e\n\u003cli\u003eCaffeine metabolism studies: used as the authentic reference for the principal human metabolite of caffeine, letting pharmacology researchers track and confirm metabolic conversion with a defined comparator.\u003c\/li\u003e\n\u003cli\u003eIsomer discrimination work: its methyl groups at positions 1 and 7 give ultraviolet and mass fragmentation patterns distinguishable from theophylline, theobromine, and caffeine in mixed samples.\u003c\/li\u003e\n\u003cli\u003eAnalytical method development and verification: serves as the known input against which a newly built or revised analytical procedure is checked for correct response, separation, and identification.\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: 611-59-6\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Alkaloids\u003c\/li\u003e\n\u003cli\u003ePack Sizes: available in the standard TCI catalogue pack sizes for this item; please confirm the specific pack when ordering.\u003c\/li\u003e\n\u003cli\u003ePhysical Form: solid (alkaloid)\u003c\/li\u003e\n\u003cli\u003eStorage: store according to the conditions stated on the manufacturer's label and accompanying documentation.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the container closed and protected from moisture and direct light, in a cool, dry place consistent with the conditions stated on the manufacturer's label. Keep the material in its original tightly sealed container, or transfer it to a clean, chemically compatible glass vial with a secure closure if aliquots are prepared. Handle the solid in a well-ventilated area or a fume hood, using gloves, safety glasses, and a laboratory coat, and avoid generating or inhaling dust during weighing. Allow a cold container to reach room temperature before opening to prevent condensation. Label all prepared stock and working solutions clearly with the compound identity and preparation date, and consult the supplier's safety data sheet before first use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mg","offer_id":48086775496922,"sku":"TCI2510D569626671","price":2979000.0,"currency_code":"IDR","in_stock":true},{"title":"100mg","offer_id":48086775529690,"sku":"TCI2510D569626672","price":7193000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D5696.jpg?v=1768818494"},{"product_id":"tci2510d611227153","title":"TCI D6112 522-66-7 (-)-Dihydroquinine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(-)-Dihydroquinine is a chiral compound widely used in asymmetric synthesis to produce molecules with specific stereochemical configurations. In the laboratory, it functions as a chiral reagent that directs chemical reactions toward the desired product by influencing the reaction pathway. This compound is particularly valuable in organic chemistry and pharmaceutical research, where precise control over molecular structure is essential. Its role as a chiral catalyst allows for the efficient synthesis of complex molecules with high enantioselectivity, making it a key component in modern synthetic strategies.\u003c\/p\u003e\n\u003cp\u003eOne of the key properties that make (-)-Dihydroquinine a preferred choice is its ability to act as an effective chiral catalyst in asymmetric reactions. Its complex molecular structure enables specific interactions with substrates, enhancing both the efficiency and selectivity of the reaction. Additionally, its stability under various reaction conditions contributes to its reliability in laboratory settings. These characteristics make it a versatile tool for researchers aiming to develop new compounds with biological activity or industrial applications.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, (-)-Dihydroquinine is commonly used in research focused on organic chemistry and asymmetric synthesis. It is particularly relevant for institutions engaged in drug discovery, pharmaceutical development, and chemical innovation. Its application supports the creation of compounds with specific stereochemistry, which is crucial for the development of new medicines and specialized chemical products.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric synthesis is a key application where (-)-Dihydroquinine is used to produce chiral compounds with high enantioselectivity, making it ideal for pharmaceutical and organic chemistry research.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research benefits from (-)-Dihydroquinine’s ability to direct reactions toward specific stereoisomers, which is essential for drug development and compound optimization.\u003c\/li\u003e\n\u003cli\u003eOrganic chemistry experiments often utilize this compound to explore new synthetic pathways and improve reaction efficiency through chiral catalysis.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical synthesis relies on (-)-Dihydroquinine to create compounds with defined stereochemistry, supporting the production of specialty chemicals and materials.\u003c\/li\u003e\n\u003cli\u003eAcademic research in Indonesia uses (-)-Dihydroquinine to advance studies in synthetic chemistry, contributing to the development of new methodologies and compounds.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 522-66-7\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Catalysts, Chiral Ligands, Chiral Reagents\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: Store in a cool, dry place away from light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003e(-)-Dihydroquinine should be stored in a cool, dry place away from direct light to maintain its chemical integrity. It is recommended to use airtight containers to prevent moisture absorption and contamination. Due to its chiral nature, it is important to handle the compound with care to avoid any unintended stereochemical changes. Proper labeling and storage conditions are essential to ensure its effectiveness in laboratory applications. Always follow standard safety protocols when handling chiral compounds, including the use of appropriate personal protective equipment. The compound is generally stable under normal laboratory conditions but should be kept in a controlled environment to preserve its properties for extended use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086792241370,"sku":"TCI2510D611227153","price":2045000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086792274138,"sku":"TCI2510D611227154","price":6990000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D6112_845e1a40-401a-4709-8d01-4ca376ae461f.jpg?v=1792640374"},{"product_id":"tci2510d616927214","title":"TCI D6169 944-73-0 1,3-Dimethyluric Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1,3-Dimethyluric Acid is a chemical compound widely used in chemical and biochemical experiments. It plays a crucial role in laboratory settings, particularly in research involving alkaloids and organic compound metabolism. This compound serves as a key reagent or building block in the synthesis of complex molecules, contributing to various scientific investigations. Its presence is essential in studies that require precise chemical reactions and controlled environments. Due to its versatility, it is a valuable asset in both academic and industrial research.\u003c\/p\u003e\n\u003cp\u003eThe compound is favored for its stable chemical properties and controlled reactivity, making it suitable for a wide range of applications. Its molecular structure allows for specific interactions with other compounds under controlled conditions, enhancing its utility in synthetic processes. Additionally, its resistance to degradation ensures long-term storage and consistent performance in experiments. These characteristics make it a reliable choice for laboratories requiring high precision and accuracy in their work.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 1,3-Dimethyluric Acid is commonly used in chemical, pharmaceutical, and biotechnology research. It is frequently found in experiments related to alkaloid synthesis and chemical reactions that require specific reagents. Its availability in the market supports ongoing scientific activities, ensuring that researchers have access to a high-quality compound for their experiments.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAlkaloid Synthesis: 1,3-Dimethyluric Acid is ideal for alkaloid synthesis due to its molecular structure that facilitates specific chemical interactions.\u003c\/li\u003e\n\u003cli\u003eOrganic Compound Metabolism Studies: It is used in research on organic compound metabolism because of its stability and controlled reactivity.\u003c\/li\u003e\n\u003cli\u003eBiochemical Reactions: The compound is suitable for biochemical reactions requiring precise reagents with predictable behavior.\u003c\/li\u003e\n\u003cli\u003eDrug Development Research: Its use in pharmaceutical research supports the development of new compounds with specific chemical properties.\u003c\/li\u003e\n\u003cli\u003eChemical Synthesis Experiments: It serves as a building block for the synthesis of complex molecules in various chemical experiments.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 944-73-0\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Alkaloids\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities\u003c\/li\u003e\n\u003cli\u003ePhysical form: 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\u003e1,3-Dimethyluric Acid should be stored in a cool, dry place, away from direct sunlight and moisture. It is recommended to keep it in a sealed container to prevent contamination and maintain its chemical integrity. Due to its stable nature, it does not require refrigeration but should be protected from environmental factors that could affect its purity. In laboratory settings, it is important to handle the compound with care, using appropriate personal protective equipment. Regular inspection of storage conditions ensures the compound remains suitable for use in experiments. Proper labeling and organization of storage areas help maintain a safe and efficient laboratory environment.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"250mg","offer_id":48086794338522,"sku":"TCI2510D616927214","price":5224000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D6169_b6d3fe25-f048-47c8-81ca-494ad6794917.jpg?v=1792640421"},{"product_id":"tci2510d633627379","title":"TCI D6336 523-87-5 Dimenhydrinate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eDimenhydrinate (523-87-5) is a chemical compound widely used in laboratory experiments, particularly in the fields of bio-pharmaceuticals and organic chemistry. As an alkaloid derived from specific plant sources, it exhibits antihistaminic properties, making it a valuable reagent for various scientific applications. Its chemical stability and solubility in organic solvents such as ethyl acetate and ethanol further enhance its utility in laboratory settings. This compound is commonly used as a starting material for the synthesis of other compounds or in biological activity assays.\u003c\/p\u003e\n\u003cp\u003eDimenhydrinate is preferred due to its stable chemical properties and ease of availability. It dissolves well in organic solvents, which simplifies its use in analytical procedures. Its molecular structure is well-defined, allowing for accurate identification through techniques like UV-Vis spectroscopy and chromatography. These characteristics make it a reliable and versatile reagent for researchers working in biochemistry and pharmacology. The compound's consistent performance and compatibility with various analytical methods contribute to its popularity in scientific research.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Dimenhydrinate is frequently used in pharmacological, pharmaceutical, and organic chemistry research. It plays a key role in drug development and clinical testing, supporting studies aimed at understanding its biological effects and therapeutic potential. Its presence in research institutions highlights its importance in advancing scientific knowledge and innovation in the field of medicinal chemistry.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePharmacological research utilizes Dimenhydrinate to study antihistaminic effects and drug interactions in biological systems.\u003c\/li\u003e\n\u003cli\u003eOrganic chemistry experiments often employ it as a starting material for the synthesis of complex molecules and derivatives.\u003c\/li\u003e\n\u003cli\u003eBiochemical assays use Dimenhydrinate to evaluate its biological activity and potential therapeutic applications.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical development incorporates it in the formulation of drugs and the testing of new compounds for efficacy.\u003c\/li\u003e\n\u003cli\u003eAnalytical chemistry relies on Dimenhydrinate for its solubility and stability, making it suitable for spectroscopic and chromatographic analysis.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 523-87-5\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: 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\u003eDimenhydrinate should be stored in a cool, dry place, away from direct sunlight and moisture. It is recommended to keep the compound in a sealed container to prevent exposure to air and humidity. Suitable storage containers include glass or plastic vessels with tight-fitting lids. Due to its chemical stability, it does not require refrigeration under normal conditions. In laboratory settings, it is important to handle Dimenhydrinate with care, using appropriate personal protective equipment when necessary. Proper labeling and storage practices ensure the compound remains safe and effective for use in research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086802792666,"sku":"TCI2510D633627379","price":1792000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086802825434,"sku":"TCI2510D633627380","price":6132000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D6336_d33a51b7-f52f-4718-b112-f6b1e1eaa7b6.jpg?v=1792640496"},{"product_id":"tci2510d647927519","title":"TCI D6479 22608-11-3 Demethoxycurcumin","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eDemethoxycurcumin is a chemical compound belonging to the curcuminoid family, naturally occurring in turmeric plants. It is widely used in scientific research to investigate the biological properties and pharmacological activities of this compound. In the laboratory, Demethoxycurcumin serves as a key reagent in experiments related to antioxidants, inflammation, and anti-cancer effects. Its presence in natural products makes it a valuable tool for studying the therapeutic potential of plant-derived compounds.\u003c\/p\u003e\n\u003cp\u003eThis compound is preferred due to its stable chemical structure and reactive nature, which allows it to participate in various chemical reactions and molecular synthesis processes. Its strong antioxidant and anti-inflammatory properties make it an ideal choice for pharmacological and biochemical research. The high purity and consistent quality of Demethoxycurcumin ensure reliable results in experimental studies, making it a trusted material for researchers.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Demethoxycurcumin is commonly used by research institutions and universities to study the biological effects of natural compounds. It is also utilized as a raw material in the development of pharmaceuticals and health supplements. Its role in scientific investigations highlights its importance in advancing knowledge in the field of natural product research.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAnti-inflammatory Research: Demethoxycurcumin is widely used to study its anti-inflammatory properties, making it ideal for experiments on inflammatory diseases and immune responses.\u003c\/li\u003e\n\u003cli\u003eAntioxidant Studies: Its strong antioxidant activity makes it a preferred compound for research on oxidative stress and free radical scavenging mechanisms.\u003c\/li\u003e\n\u003cli\u003eCancer Research: Demethoxycurcumin is frequently employed in experiments investigating its potential anti-cancer effects, including cell proliferation inhibition and apoptosis induction.\u003c\/li\u003e\n\u003cli\u003ePharmacological Development: Its natural origin and bioactive properties make it suitable for the development of new drugs and health supplements.\u003c\/li\u003e\n\u003cli\u003eBiochemical Analysis: It is used in biochemical experiments to study the interaction of natural compounds with biological systems and cellular processes.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 22608-11-3\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Crude Medicine Ingredients for Research and Experimental Use\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid 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\u003eDemethoxycurcumin should be stored in a cool, dry environment, away from direct light and moisture to maintain its chemical stability. It is recommended to use airtight containers to prevent contamination and degradation. Due to its reactive nature, it should be handled with appropriate laboratory safety measures, such as wearing gloves and safety goggles. Proper ventilation is essential when working with this compound to avoid inhalation of fine particles. It is important to keep it away from incompatible substances to ensure safe storage and usage in the laboratory. Regular inspection of storage conditions is advised to maintain the integrity and quality of the compound.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"10mg","offer_id":48086808428762,"sku":"TCI2510D647927519","price":2802000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D6479_89e6324f-a4aa-460e-b516-a6a46e7475f9.jpg?v=1792640566"},{"product_id":"tci2510e002427651","title":"TCI E0024 66778-17-4 Esculin Sesquihydrate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eEsculin Sesquihydrate is a chemical compound widely used in chemical and biochemical experiments, particularly in the study of glycosides and enzymatic activity. This compound plays a crucial role in laboratories conducting research on carbohydrate metabolism or enzymatic reactions. Its unique chemical structure allows it to interact with enzymes such as β-glukosidase, making it essential for enzyme activity assays. Esculin Sesquihydrate is a key reagent in various analytical and research applications due to its specific reactivity and utility in biochemical pathways.\u003c\/p\u003e\n\u003cp\u003eOne of the main reasons for its preference in laboratories is its chemical stability under controlled conditions, despite its sensitivity to moisture and light. It exists as white crystalline solids that dissolve easily in water, simplifying the preparation of solutions for experiments. These physical properties make it highly suitable for use in precise and consistent chemical procedures. Its solubility and crystalline form also contribute to its reliability in laboratory settings where accuracy is paramount.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Esculin Sesquihydrate is commonly used in pharmaceutical, biochemical, and medical research. It is frequently found in studies examining the effects of enzymes on specific substrates and in the development of chemical analysis methods. Its availability in the local market ensures that researchers have access to this essential compound for their experimental needs. The compound's versatility and reliability make it a valuable asset in various scientific investigations.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eEnzymatic Activity Assays – Esculin Sesquihydrate is ideal for testing β-glukosidase activity due to its specific reactivity with this enzyme.\u003c\/li\u003e\n\u003cli\u003eCarbohydrate Metabolism Studies – It is used to investigate metabolic pathways involving glycosides and their breakdown.\u003c\/li\u003e\n\u003cli\u003eBiochemical Research – Its role in glycoscience makes it a key component in studies related to sugar metabolism and enzyme function.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical Development – It supports the analysis of drug interactions and enzyme-based therapeutic approaches.\u003c\/li\u003e\n\u003cli\u003eAnalytical Chemistry Techniques – Esculin Sesquihydrate is used in developing and validating chemical analysis methods for enzyme activity.\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: 66778-17-4\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Glycoscience\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: White crystalline solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eEsculin Sesquihydrate should be stored in a cool, dry environment to prevent degradation due to moisture and light exposure. It is recommended to use airtight containers to maintain its chemical stability. The compound is sensitive to humidity, so it should be kept in a desiccated environment whenever possible. Proper labeling of containers is essential to ensure safe handling and prevent cross-contamination. Laboratory personnel should wear appropriate personal protective equipment when handling this compound. Regular monitoring of storage conditions is advised to maintain the integrity of the material for experimental use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086813999322,"sku":"TCI2510E002427651","price":1439000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086814032090,"sku":"TCI2510E002427652","price":4921000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510E0024_4e0a0c74-357b-41c0-a82c-bea9e494b66f.jpg?v=1792640649"},{"product_id":"tci2510e021027917","title":"TCI E0210 93-28-7 Eugenol Acetate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eEugenol Acetate (TCI E0210) is a chemical compound widely used in laboratory experiments, particularly in organic chemistry and biochemistry. As an ester derivative of eugenol, it is a key reagent in the study of phenylpropanoids and aromatic polyketides. This compound plays a crucial role in the synthesis of complex organic molecules and serves as a valuable tool in qualitative and quantitative analysis. Its stability and reactivity make it a versatile component in various experimental setups, supporting both research and educational activities in Indonesian laboratories.\u003c\/p\u003e\n\u003cp\u003eThe chemical properties of Eugenol Acetate make it a preferred choice for laboratory use. It exhibits a stable chemical structure, which ensures consistent performance across different experimental conditions. Its characteristic aroma aids in visual identification, while its solubility in organic solvents like ethyl acetate and ethanol enhances its utility in analytical procedures. The presence of an aromatic ring and an ester group contributes to its chemical stability, allowing it to be stored under appropriate conditions without significant degradation. These features make it a reliable and efficient reagent for a wide range of laboratory applications.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Eugenol Acetate is commonly used in research focused on secondary plant metabolites and their biochemical pathways. It is a staple in both academic and industrial research settings, supporting studies on natural products, pharmacology, and chemical synthesis. Its availability and reliability ensure that it remains a key component in the toolkit of researchers and students alike, facilitating accurate and reproducible results in various scientific investigations.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eUsed in the synthesis of complex organic compounds due to its reactivity and stability, making it ideal for chemical synthesis experiments.\u003c\/li\u003e\n\u003cli\u003eApplied in qualitative and quantitative analysis for its distinct aroma and solubility properties, aiding in accurate identification and measurement.\u003c\/li\u003e\n\u003cli\u003eUtilized in the study of phenylpropanoids and aromatic polyketides, supporting research on plant-derived secondary metabolites.\u003c\/li\u003e\n\u003cli\u003eEmployed in pharmacological research for its potential role in drug development and natural product isolation.\u003c\/li\u003e\n\u003cli\u003eFound in educational settings for teaching organic chemistry and biochemical techniques through hands-on experimentation.\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: 93-28-7\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Phenylpropanoids, Aromatic Polyketides\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities as specified by supplier\u003c\/li\u003e\n\u003cli\u003ePhysical form: Liquid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct sunlight and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eEugenol Acetate should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep it in a tightly sealed container to prevent exposure to moisture and air, which may affect its integrity. Due to its solubility in organic solvents, it should be stored in containers that are resistant to such substances. Laboratory personnel should handle the compound with care, using appropriate personal protective equipment when necessary. Proper labeling of storage containers is essential to ensure safe handling and prevent accidental exposure. Regular monitoring of storage conditions helps maintain the compound's effectiveness and safety in laboratory settings.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086825042138,"sku":"TCI2510E021027917","price":455000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510E0210.jpg?v=1768818650"}],"url":"https:\/\/amiscientific.com\/en\/collections\/tci-l4-phytochemicals.oembed?page=14","provider":"AMI Scientific","version":"1.0","type":"link"}