{"title":"Metabolic Libraries","description":"\u003cp\u003e\u003cstrong\u003eMetabolic Libraries\u003c\/strong\u003e — menghimpun metabolit endogen dan turunannya—asam lemak seperti asam linoleat dan arakidonat, asam amino, hingga senyawa antara jalur energi seperti asetil-L-karnitin—yang mewakili titik-titik kunci jaringan metabolisme seluler. Kumpulan ini berfungsi sebagai standar rujukan untuk membangun dan memvalidasi pustaka spektral pada studi metabolomik.\u003c\/p\u003e\u003cp\u003eMetabolic Libraries dipakai peneliti metabolomik dan biokimia untuk menyusun pustaka spektral MS\/NMR, mengonfirmasi identitas puncak hasil LC-MS atau GC-MS, serta menjadi kontrol internal saat menganalisis ekstrak biologis dari sel, plasma, atau jaringan. Senyawa seperti kolin klorida atau asam amino turunan lipid juga membantu menelusuri jalur biosintesis dan perubahan profil metabolit pada berbagai kondisi eksperimen.\u003c\/p\u003e\u003cp\u003eContoh produk dalam koleksi ini: \u003ca href=\"\/en\/products\/tci2510l012437022\"\u003eTCI L0124 60-33-3 Linoleic Acid\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510c032914395\"\u003eTCI C0329 67-48-1 Choline Chloride\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510a0297431\"\u003eTCI A0297 141-43-5 2-Aminoethanol\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510c042714544\"\u003eTCI C0427 79-63-0 Lanosterol\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510a0084131\"\u003eTCI A0084 60-31-1 Acetylcholine Chloride\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510d058720091\"\u003eTCI D0587 674-26-0 DL-Mevalonolactone\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510a14782023\"\u003eTCI A1478 3483-11-2 Lithium Acetoacetate\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510e147629515\"\u003eTCI E1476 54048-10-1 Etonogestrel\u003c\/a\u003e.\u003c\/p\u003e\u003cp\u003ePerhatikan tingkat kemurnian yang tercantum, bentuk fisik (padatan, larutan, atau garam tertentu seperti hidroklorida atau asetat), serta kesesuaian struktur dan stereokimia dengan metabolit target sebelum digunakan sebagai standar analitik. Seluruh produk merupakan produk asli Tokyo Chemical Industry (TCI) Jepang, dengan kemurnian, kemasan, dan kondisi penyimpanan tercantum pada halaman masing-masing item.\u003c\/p\u003e\u003cp\u003eKategori lain yang sejajar di bawah Metabolomics, sering dipakai bersamaan dalam satu alur kerja laboratorium:\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-metabolic-pathways\"\u003eMetabolic Pathways\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-nutrition-research\"\u003eNutrition Research\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-cell-signaling-and-neuroscience\"\u003eCell Signaling and Neuroscience\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-cancer-research\"\u003eCancer Research\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-immune-system-inflammation-allergy-research\"\u003eImmune System, Inflammation, Allergy Research\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-bioactive-small-molecules\"\u003eBioactive Small Molecules\u003c\/a\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eKembali ke \u003ca href=\"\/en\/collections\/tci-l3-metabolomics\"\u003eMetabolomics\u003c\/a\u003e. Untuk pengadaan volume besar, kemasan khusus, atau grade tertentu, hubungi tim AMI Scientific — distributor resmi TCI Japan di Indonesia — untuk pengecekan ketersediaan dan lead time langsung ke Jepang.\u003c\/p\u003e","products":[{"product_id":"tci2510c032914395","title":"TCI C0329 67-48-1 Choline Chloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0329 Choline Chloride (CAS 67-48-1) is a highly water-soluble quaternary ammonium salt widely used as a phase transfer catalyst in two-phase organic reactions. It is best known as a key component of deep eutectic solvents, typically combined with hydrogen bond donors such as urea, and is central to many green chemistry and electrodeposition studies. The compound also serves as a choline source in nutrition and biochemistry research. Supplied by Tokyo Chemical Industry in 25 g and 500 g packs, it is strongly hygroscopic and must be stored tightly closed in a cool, dry, moisture-free environment.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eLin et al. (2014). Henry’s constant of carbon dioxide-aqueous deep eutectic solvent (choline chloride\/ethylene glycol, choline chloride\/glycerol, choline chloride\/malonic acid) systems. \u003cem\u003eThe Journal of Chemical Thermodynamics\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.jct.2013.08.029\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.jct.2013.08.029\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eZHANG et al. (2014). Properties and applications of choline chloride\/urea and choline chloride\/glycerol. \u003cem\u003eSCIENTIA SINICA Chimica\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1360\/n032014-00001\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1360\/n032014-00001\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eAbbas et al. (2011). Anodic Dissolution of Refractory Metals in Choline Chloride Based Binary Mixtures. \u003cem\u003eECS Transactions\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1149\/1.3566089\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1149\/1.3566089\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":48085990703322,"sku":"TCI2510C032914395","price":564000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48085990736090,"sku":"TCI2510C032914396","price":1771000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0329.jpg?v=1767095043"},{"product_id":"tci2510c042714544","title":"TCI C0427 79-63-0 Lanosterol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0427 Lanosterol (CAS 79-63-0) is a triterpenoid sterol that occupies a central position in the eukaryotic sterol biosynthesis pathway. It serves as a substrate and reference compound in studies of sterol 14α-demethylase, the enzyme targeted by azole antifungal agents. Researchers also use it to examine membrane properties, mevalonate pathway intermediates, and lens protein aggregation. The powder should be kept tightly closed in a cool, dark, and dry place, and weighed with gloves and eye protection in a well-ventilated area.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eRisley (2002). Cholesterol Biosynthesis: Lanosterol to Cholesterol. \u003cem\u003eJournal of Chemical Education\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1021\/ed079p377\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1021\/ed079p377\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eShanmugam et al. (2015). Effect of lanosterol on human cataract nucleus. \u003cem\u003eIndian Journal of Ophthalmology\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.4103\/0301-4738.176040\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.4103\/0301-4738.176040\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eTuck et al. (1991). Lanosterol 14 alpha-demethylase (P45014DM): effects of P45014DM inhibitors on sterol biosynthesis downstream of lanosterol.. \u003cem\u003eJournal of Lipid Research\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/s0022-2275(20)41987-x\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/s0022-2275(20)41987-x\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48085998207194,"sku":"TCI2510C042714544","price":4273000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0427.jpg?v=1768816243"},{"product_id":"tci2510e147629515","title":"TCI E1476 54048-10-1 Etonogestrel","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI E1476 Etonogestrel is a synthetic steroid of the progestin class, supplied by TCI within the Life Science portfolio under the biochemicals and reagents category for steroids. The compound is the active metabolite of desogestrel and is widely recognised as the active ingredient in long-acting contraceptive preparations. In the laboratory, however, its role is principally that of a reference material and research substance: it is used to establish identity and assay content in quality-control testing, to develop analytical methods in biological matrices, and to serve as a reference ligand in progesterone receptor studies and molecular endocrinology investigations.\u003c\/p\u003e\n\u003cp\u003eThe properties that make this material a preferred choice begin with its molecular architecture. Etonogestrel possesses a rigid gonane steroid skeleton bearing an ethynyl group at position 17 and an exocyclic methylene group at position 11, a combination that confers high affinity for the progesterone receptor. The sharply defined steroid structure gives the compound consistent chromatographic behaviour and a characteristic mass spectrum, two attributes that are indispensable for quantitative analysis at low concentrations. The unsaturated ketone system on the A ring additionally provides adequate ultraviolet absorption for routine detection, allowing straightforward integration into established instrumental workflows.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Etonogestrel is typically encountered in pharmaceutical quality-control units, contract analytical laboratories, and academic or institutional research groups working on hormonal preparations. It supports identity confirmation and content determination during batch release testing, underpins method development and validation work for bioanalytical assays, and provides a dependable reference point for receptor-binding and endocrinology research. Because the compound is hormonally active at very low concentrations, it is handled as a potent substance under controlled laboratory conditions.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eIdentity confirmation in pharmaceutical quality control, where the compound's characteristic retention behaviour and distinctive mass spectrum allow analysts to verify that a test sample genuinely contains Etonogestrel.\u003c\/li\u003e\n\u003cli\u003eContent and assay determination during batch release testing, since the well-defined steroid structure and adequate ultraviolet absorption support reliable quantitation against a reference standard.\u003c\/li\u003e\n\u003cli\u003eAnalytical method development for biological matrices, because the compound's consistent chromatographic behaviour makes it a stable anchor when optimising extraction, separation, and detection parameters.\u003c\/li\u003e\n\u003cli\u003eProgesterone receptor binding studies, where its high receptor affinity arising from the ethynyl and exocyclic methylene substituents makes it a suitable reference ligand for comparative binding work.\u003c\/li\u003e\n\u003cli\u003eMolecular endocrinology research, in which the compound serves as a defined progestin reference for investigating hormonal signalling pathways and the behaviour of synthetic progestins in experimental systems.\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: 54048-10-1\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Steroids\u003c\/li\u003e\n\u003cli\u003eProduct code: E1476\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in the standard TCI catalogue pack sizes; please confirm the currently listed options when ordering.\u003c\/li\u003e\n\u003cli\u003eStorage: store according to the conditions stated on the manufacturer's label and product documentation.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore Etonogestrel in its original tightly closed container, protected from light, moisture, and elevated temperature, and follow the storage conditions specified on the manufacturer's label and accompanying documentation. Amber glass vials or the supplied original packaging are appropriate containers; transfer only the quantity required for immediate work and reseal promptly. Because the compound is hormonally active at very low concentrations, handle it as a potent substance: weigh and manipulate the powder inside a fume hood or suitable containment enclosure, wear gloves, a laboratory coat, and eye protection, avoid generating dust, and prevent skin contact or inhalation. Clean balances and work surfaces after use, and dispose of residues and contaminated consumables through established chemical waste procedures. Personnel who are pregnant or may become pregnant should observe particular caution in line with institutional safety policy.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"250mg","offer_id":48086963486938,"sku":"TCI2510E147629515","price":5623000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510E1476.jpg?v=1768818838"},{"product_id":"tci2510g011031710","title":"TCI G0110 79-14-1 Glycolic Acid (ca 70% in Water, ca 12mol\/L)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eGlycolic Acid supplied as an aqueous solution of approximately 70 percent, offered by TCI under catalogue number G0110, is the simplest alpha hydroxy acid, carrying both a carboxyl group and a hydroxyl group on adjacent carbon atoms. This combination of two functional groups gives the material a dual role in the laboratory: it acts as an organic acid strong enough to adjust acidity and dissolve mineral deposits, and at the same time serves as a bifunctional building block that can undergo esterification, etherification, and condensation polymerisation into polyglycolide, a material widely studied in the field of biodegradable materials.\u003c\/p\u003e\n\u003cp\u003eThe properties that make this reagent a preferred choice begin with its very small molecular size, its complete solubility in water, and its higher acidity compared with acetic acid, a consequence of the electron-withdrawing effect of the hydroxyl group at the alpha position. Supply in aqueous solution form makes pouring and volumetric measurement straightforward, spares the user the difficulty of handling a strongly hygroscopic solid, and speeds up the preparation of working solutions because the material is already completely dissolved. Its mild chelating character is a further advantage.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories this reagent fits naturally into routine bench work where an acid of known behaviour is needed without the handling burden of a hygroscopic solid. The solution form supports direct volumetric dispensing during the preparation of working solutions, while the mild chelating character is put to use in cleaning metal surfaces and dissolving inorganic scale on equipment. Its role as a bifunctional building block also supports synthetic and materials-oriented investigations.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAcidity adjustment in aqueous systems, where the material functions as an organic acid strong enough to set and control the acidity of a solution reliably.\u003c\/li\u003e\n\u003cli\u003eDissolution of mineral deposits, where the acid strength of the reagent allows precipitated mineral matter to be brought back into solution during sample handling.\u003c\/li\u003e\n\u003cli\u003eEsterification and etherification chemistry, where the adjacent carboxyl and hydroxyl groups give two reactive handles on a single very small molecular framework.\u003c\/li\u003e\n\u003cli\u003eCondensation polymerisation into polyglycolide, supporting work on biodegradable materials, a field in which this polymer has been extensively studied by researchers.\u003c\/li\u003e\n\u003cli\u003eCleaning of metal surfaces and dissolution of inorganic scale on equipment, where the mild chelating character of the molecule assists the removal process.\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: 79-14-1\u003c\/li\u003e\n\u003cli\u003eCatalogue number: G0110\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePhysical form: aqueous solution, approximately 70 percent in water (approximately 12 mol\/L)\u003c\/li\u003e\n\u003cli\u003eStorage: keep in a closed container under the conditions stated on the supplier label\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the solution in its original tightly closed container, kept upright in a designated area for acidic reagents and away from incompatible materials. Containers should be of a material resistant to organic acids, and bottles should be closed immediately after dispensing so that the solution strength is not altered. Handle the material in a well ventilated area or fume hood, wearing safety glasses, gloves, and a laboratory coat, since this is an acidic solution capable of causing irritation on contact with skin or eyes. Wipe up spills promptly and rinse the affected surface with water. Label all working solutions clearly with contents and preparation date, and consult the supplier safety data sheet before first use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48087091216602,"sku":"TCI2510G011031710","price":507000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48087091249370,"sku":"TCI2510G011031711","price":732000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510G0110.jpg?v=1767114623"},{"product_id":"tci2510g019631803","title":"TCI G0196 79-14-1 Glycolic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eGlycolic Acid TCI G0196, with CAS number 79-14-1, is a fundamental chemical compound widely used in laboratory experiments. As a key building block in organic chemistry, it plays a crucial role in the synthesis of various compounds, including esters, carboxylic acids, and complex organic structures. Its versatility makes it an essential reagent for chemists working on diverse synthetic pathways. This compound is particularly valued for its ability to participate in high-reactivity chemical reactions and form bonds with multiple functional groups.\u003c\/p\u003e\n\u003cp\u003eThe chemical properties of Glycolic Acid make it a preferred choice in laboratory settings. It exhibits both stability and reactivity, which are essential for controlled chemical transformations. Its relatively low melting and boiling points allow for easy handling during heating and cooling processes, making it suitable for a wide range of experimental conditions. Additionally, Glycolic Acid can react with a variety of substances, including acids, bases, and organic compounds, offering flexibility in experimental design and application.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Glycolic Acid is commonly used in chemical research, educational institutions, and industrial development projects. Its relevance spans across academic and industrial applications where basic chemical compounds are required for experimentation and product development. Its availability and reliability make it a go-to reagent for both teaching and advanced research activities.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis applications benefit from Glycolic Acid's ability to form esters and carboxylic acids, supporting the creation of complex molecular structures.\u003c\/li\u003e\n\u003cli\u003eEducational laboratories use Glycolic Acid to teach fundamental chemical reactions and synthesis techniques to students at all levels.\u003c\/li\u003e\n\u003cli\u003eIndustrial research facilities rely on Glycolic Acid for the development of new chemical products and materials through controlled chemical processes.\u003c\/li\u003e\n\u003cli\u003eAnalytical chemistry experiments utilize Glycolic Acid as a reagent for testing the reactivity of various functional groups in different compounds.\u003c\/li\u003e\n\u003cli\u003eEnvironmental studies incorporate Glycolic Acid to investigate its behavior in chemical interactions and its impact on different reaction systems.\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: 79-14-1\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 standard laboratory supply options\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid, typically in crystalline or powder form\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eGlycolic 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 minimize exposure to moisture and air, which can affect its reactivity. Suitable storage conditions include a controlled temperature range, typically between 15°C and 25°C, to ensure long-term preservation. In laboratory settings, it is important to handle Glycolic Acid with care, using appropriate personal protective equipment such as gloves and safety goggles. Proper labeling and storage away from incompatible materials are essential to maintain safety and prevent accidental reactions.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48275639828698,"sku":"TCI2510G019631803","price":760000.0,"currency_code":"IDR","in_stock":false}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510G0196.jpg?v=1767114794"},{"product_id":"tci2510g031631952","title":"TCI G0316 56-81-5 Glycerol [for Electrophoresis]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI G0316 Glycerol, with CAS number 56-81-5, is a versatile chemical compound widely used in laboratory settings, particularly in electrophoresis procedures. As a key reagent, it serves as a critical component in the preparation of running gels and buffer solutions, facilitating the separation of biomolecules such as DNA and proteins. Its role in maintaining a stable and consistent environment is essential for accurate and reproducible results in molecular biology experiments.\u003c\/p\u003e\n\u003cp\u003eOne of the main reasons glycerol is preferred in laboratory applications is its unique physical and chemical properties. It is a non-volatile, highly viscous liquid with strong solvating capabilities, making it ideal for creating stable solutions. Its ability to absorb moisture and resist evaporation ensures that experimental conditions remain consistent over time. These characteristics are especially valuable in long-duration or temperature-sensitive experiments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, glycerol is commonly used in research and educational institutions. It is a staple in biochemistry and molecular biology labs, where it supports various analytical techniques. Its non-toxic and non-irritating nature also makes it suitable for use in environments where safety and comfort are priorities. Its widespread application reflects its reliability and effectiveness in maintaining the integrity of experimental procedures.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eElectrophoresis is a common application where glycerol is used to prepare running gels, providing a stable medium for the migration of DNA and protein molecules.\u003c\/li\u003e\n\u003cli\u003eBuffer solution preparation benefits from glycerol’s solvating properties, helping to maintain the pH and stability of the solution.\u003c\/li\u003e\n\u003cli\u003eSample concentration procedures often use glycerol to aid in the precipitation and isolation of biomolecules from complex mixtures.\u003c\/li\u003e\n\u003cli\u003eProtein solubilization is enhanced by glycerol’s ability to stabilize proteins in solution, preventing denaturation during storage or processing.\u003c\/li\u003e\n\u003cli\u003eCryopreservation of biological samples relies on glycerol’s ability to prevent ice crystal formation, ensuring the integrity of cells and tissues during freezing.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 56-81-5\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Stabilization of Biomolecules\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified in the provided data\u003c\/li\u003e\n\u003cli\u003ePhysical form: Liquid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eGlycerol should be stored in a cool, dry place, away from direct sunlight and sources of heat. It is recommended to use sealed, airtight containers to prevent moisture absorption and contamination. Due to its high viscosity, it is important to ensure that containers are properly labeled and stored in a designated chemical storage area. While glycerol is non-toxic and non-corrosive, it should still be handled with care to avoid spills or exposure. 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