{"title":"Nucleic Acid Detection Substrates and Reagents","description":"\u003cp\u003e\u003cstrong\u003eNucleic Acid Detection Substrates and Reagents\u003c\/strong\u003e — berisi substrat kromogenik, reagen pewarnaan, dan senyawa turunan tetrazolium maupun indolil-glikosida yang menghasilkan sinyal warna terukur saat bereaksi dengan enzim penanda. Golongan ini berfungsi sebagai komponen deteksi dalam berbagai teknik biologi molekuler di laboratorium riset.\u003c\/p\u003e\u003cp\u003eNucleic Acid Detection Substrates and Reagents digunakan peneliti biologi molekuler pada teknik seperti Western blotting, uji enzim reporter (misalnya beta-galaktosidase), dan pewarnaan koloni untuk memvisualisasikan hasil reaksi secara kualitatif maupun semi-kuantitatif. Produk siap pakai seperti larutan TMB atau 4-kloro-1-naftol mempermudah alur kerja deteksi tanpa persiapan reagen tambahan.\u003c\/p\u003e\u003cp\u003eContoh produk dalam koleksi ini: \u003ca href=\"\/en\/products\/tci2510a0257366\"\u003eTCI A0257 22198-72-7 4-Aminoantipyrine Hydrochloride [for Biochemical Research]\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510c229117021\"\u003eTCI C2291 604-44-4 4-Chloro-1-naphthol [for Biochemical Research]\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510i078136040\"\u003eTCI I0781 146-68-9 2-(4-Iodophenyl)-3-(4-nitrophenyl)-5-phenyltetrazolium Chloride [for Biochemical Research]\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510c237117127\"\u003eTCI C2371 138182-21-5 6-Chloro-3-indolyl beta-D-Galactopyranoside [for Biochemical Research]\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510i084036121\"\u003eTCI I0840 540-38-5 4-Iodophenol [for Biochemical Research]\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510c299017903\"\u003eTCI C2990 5496-32-2 2-(4-Chlorophenyl)-4,5-diphenylimidazole\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510t385555563\"\u003eTCI T3855 TMB [for Western blotting] (Ready-to-use solution)\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510c338418427\"\u003eTCI C3384 4-Chloro-1-naphthol (Ready-to-use solution) [for Western blotting]\u003c\/a\u003e.\u003c\/p\u003e\u003cp\u003ePerhatikan bentuk sediaan (bubuk murni atau larutan siap pakai) serta kesesuaian substrat dengan sistem enzim reporter yang digunakan dalam protokol deteksi molekuler. 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 Molecular Biology, sering dipakai bersamaan dalam satu alur kerja laboratorium:\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-plant-biotechnology\"\u003ePlant Biotechnology\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-proteomics\"\u003eProteomics\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-regenerative-medicine-research-reagents\"\u003eRegenerative Medicine Research Reagents\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-antioxidants-life-science\"\u003eAntioxidants [Life Science]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-epigenetics\"\u003eEpigenetics\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-nucleic-acid-detection-and-hybridization\"\u003eNucleic Acid Detection and Hybridization\u003c\/a\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eKembali ke \u003ca href=\"\/en\/collections\/tci-l2-molecular-biology\"\u003eMolecular Biology\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":"tci2510c229117021","title":"TCI C2291 604-44-4 4-Chloro-1-naphthol [for Biochemical Research]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e4-Chloro-1-naphthol is a chemical compound widely used in biochemical research. It is a key reagent in laboratory settings where precise chemical reactions are required. This compound features an aromatic structure with a chlorine substituent at the C-4 position, which enhances its reactivity in various chemical processes. Its versatility makes it a valuable tool for researchers working on enzyme reactions and analytical methods. Due to its stability and reactivity, it is frequently used in experiments that demand accuracy and reproducibility.\u003c\/p\u003e\n\u003cp\u003eThe compound's chemical properties make it a preferred choice for laboratory applications. It exhibits solubility in organic solvents such as ethyl acetate and ethanol, allowing for easy incorporation into reaction mixtures. Its ability to participate in electrophilic substitution reactions further expands its utility in synthetic chemistry. Additionally, its resistance to degradation under standard laboratory conditions ensures long-term stability and reliability of experimental results. These characteristics make it a reliable and effective reagent for biochemical research.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 4-Chloro-1-naphthol is commonly used in biochemical research, including enzyme studies and analytical method development. Its role is crucial in experiments that require precise chemical interactions and stable reagents. Researchers in Indonesia rely on this compound for its consistent performance and compatibility with various experimental protocols. Its widespread use highlights its importance in both academic and industrial research settings.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eEnzyme Kinetics Studies: This compound is ideal for enzyme reaction experiments due to its reactivity and stability, allowing accurate measurement of enzyme activity.\u003c\/li\u003e\n\u003cli\u003eQuantitative Analysis Development: Its solubility and chemical behavior make it suitable for creating reagents used in quantitative testing methods.\u003c\/li\u003e\n\u003cli\u003eSynthetic Organic Chemistry: The compound's ability to undergo electrophilic substitution reactions makes it a valuable reagent in organic synthesis.\u003c\/li\u003e\n\u003cli\u003eBiochemical Assay Preparation: It is commonly used in preparing substrates for biochemical assays that require controlled chemical reactions.\u003c\/li\u003e\n\u003cli\u003eSpectroscopic Analysis: Its distinct chemical properties make it useful in spectroscopic studies for identifying and analyzing molecular structures.\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: 604-44-4\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Antibodies \u0026gt; Antibody Supplementary Products\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\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\u003eThis compound should be stored in a cool, dry place away from direct light to maintain its stability and effectiveness. It is recommended to use airtight containers to prevent moisture absorption, which can affect its chemical properties. Due to its reactivity, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. It is important to ensure good ventilation when working with this material to avoid inhalation of vapors. Proper storage and handling practices help preserve the compound's integrity and ensure safe laboratory operations.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086117777626,"sku":"TCI2510C229117021","price":657000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086117810394,"sku":"TCI2510C229117022","price":1792000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2291.jpg?v=1767098083"},{"product_id":"tci2510c237117127","title":"TCI C2371 138182-21-5 6-Chloro-3-indolyl beta-D-Galactopyranoside [for Biochemical Research]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e6-Chloro-3-indolyl β-D-galactopyranoside is a chemical compound widely used in biochemical research, particularly in the study of carbohydrate metabolism and enzymatic activity. This compound serves as a substrate for β-galactosidase, a key enzyme in enzymatic and genetic analysis. Its role in laboratories is critical for assessing enzyme activity, especially in genetic and biochemical research contexts. It is a fundamental reagent for researchers aiming to understand enzyme function and genetic expression mechanisms.\u003c\/p\u003e\n\u003cp\u003eThe compound is preferred due to its high purity and specificity in reacting with β-galactosidase. Its molecular structure is stable and soluble in organic solvents, making it easy to handle and incorporate into various experimental protocols. These properties ensure reliable and consistent results in laboratory settings. Its stability and solubility also contribute to its effectiveness in different experimental conditions.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 6-Chloro-3-indolyl β-D-galactopyranoside is commonly used by researchers in universities and research institutions. It plays a vital role in studies involving genes and proteins, especially in biotechnology and molecular biology. Its relevance in scientific research makes it an essential tool for advancing knowledge in these fields.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eEnzymatic Activity Assays: This compound is ideal for measuring β-galactosidase activity, providing accurate and reproducible results in enzymatic studies.\u003c\/li\u003e\n\u003cli\u003eGenetic Expression Analysis: It is used in reporter gene assays to monitor gene expression, offering a reliable method for studying genetic regulation.\u003c\/li\u003e\n\u003cli\u003eMolecular Biology Research: Its role as a substrate supports experiments in molecular biology, particularly in cloning and gene expression studies.\u003c\/li\u003e\n\u003cli\u003eBiochemical Pathway Studies: It aids in understanding carbohydrate metabolism and enzyme kinetics, contributing to broader biochemical research.\u003c\/li\u003e\n\u003cli\u003eBiotechnology Applications: It is valuable in biotechnology for developing and testing new enzymatic processes and genetic tools.\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: 138182-21-5\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 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\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 to maintain its stability and effectiveness. It is recommended to use airtight containers to prevent moisture absorption and contamination. Due to its chemical nature, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to ensure laboratory safety. Proper ventilation should be maintained when working with this compound to minimize exposure. It is important to follow standard laboratory safety protocols to ensure safe handling and storage practices.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"20mg","offer_id":48086123217114,"sku":"TCI2510C237117127","price":1137000.0,"currency_code":"IDR","in_stock":true},{"title":"100mg","offer_id":48086123249882,"sku":"TCI2510C237117128","price":2878000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2371.jpg?v=1767098219"},{"product_id":"tci2510c299017903","title":"TCI C2990 5496-32-2 2-(4-Chlorophenyl)-4,5-diphenylimidazole","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2-(4-Chlorophenyl)-4,5-diphenylimidazole is a chemical compound widely used in life science research, particularly in molecular biology. It plays a crucial role in nucleic acid detection and hybridization processes, enabling scientists to study molecular interactions and develop diagnostic techniques. This compound is essential in laboratories where precise and reliable results are required for genetic and biochemical analyses. Its unique chemical structure allows it to interact effectively with various biomolecules, making it a valuable tool in advanced research settings.\u003c\/p\u003e\n\u003cp\u003eThe compound is preferred due to its high specificity and stability under controlled laboratory conditions. Its ability to bind with molecules containing phenyl and imidazole groups makes it ideal for applications requiring high selectivity. Additionally, its chemical properties ensure consistent performance across different experimental protocols, enhancing the accuracy of research outcomes. These characteristics make it a reliable choice for researchers working on complex molecular studies.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 2-(4-Chlorophenyl)-4,5-diphenylimidazole is commonly used in genetic, biochemical, and molecular diagnostic research. Due to its limited availability in the local market, it is often imported by research institutions and universities to support specialized studies. Its application in these settings highlights its importance in advancing scientific understanding and innovation in the life sciences.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eNucleic Acid Hybridization: This compound is ideal for hybridization experiments due to its ability to bind specifically with complementary nucleic acid strands, enhancing detection accuracy.\u003c\/li\u003e\n\u003cli\u003eMolecular Interaction Studies: Its chemical structure allows it to interact with various biomolecules, making it suitable for studying molecular interactions in complex biological systems.\u003c\/li\u003e\n\u003cli\u003eDiagnostic Assay Development: The compound's high specificity supports the creation of diagnostic assays, enabling precise identification of genetic markers and mutations.\u003c\/li\u003e\n\u003cli\u003eGenetic Research: It is used in genetic studies to analyze DNA and RNA structures, contributing to the understanding of gene expression and function.\u003c\/li\u003e\n\u003cli\u003eBiochemical Analysis: Its stability and reactivity make it a valuable tool for biochemical experiments requiring precise molecular interactions and binding properties.\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: 5496-32-2\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Molecular Biology \u0026gt; Nucleic Acid Detection and Hybridization\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 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 contaminants. Due to its chemical nature, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. Storage should be in a secure location that is inaccessible to unauthorized personnel. Regular monitoring of storage conditions is advised to ensure the compound remains stable and suitable for use in laboratory applications. Proper labeling of containers is essential for safe handling and to prevent accidental exposure.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48086206349530,"sku":"TCI2510C299017903","price":1415000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2990.jpg?v=1768816981"},{"product_id":"tci2510d192821913","title":"TCI D1928 54970-72-8 Sodium 3,5-Dichloro-2-hydroxybenzenesulfonate [for Biochemical Research]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eSodium 3,5-Dichloro-2-hydroxybenzenesulfonate is a chemical compound widely used in biochemical research for its role in nucleic acid detection and hybridization processes. This reagent is essential in molecular biology applications where precise control over DNA and RNA interactions is required. It is commonly employed in laboratory settings to facilitate hybridization reactions, enabling the identification and analysis of genetic material with high accuracy. Its chemical stability and functional versatility make it a reliable component in various experimental protocols.\u003c\/p\u003e\n\u003cp\u003eThis compound is preferred due to its consistent chemical properties and ability to act as a pH buffer or a molecular binding agent. Its stability under various experimental conditions ensures reliable results, making it a trusted choice for researchers. The compound’s capacity to interact with specific molecules enhances its utility in molecular binding assays and hybridization techniques. Its predictable behavior and compatibility with other reagents contribute to its widespread use in laboratory environments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Sodium 3,5-Dichloro-2-hydroxybenzenesulfonate is commonly used in biomedical research, diagnostic testing, and academic studies. It plays a key role in DNA and RNA detection methods, supporting the development of sensitive and efficient analytical techniques. Its application is particularly relevant in molecular biology laboratories where accurate and reproducible results are critical. The compound's reliability and effectiveness make it a valuable tool for scientific research in Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eNucleic Acid Hybridization: This compound is ideal for hybridization reactions as it stabilizes DNA-RNA interactions, enhancing the accuracy of hybridization assays.\u003c\/li\u003e\n\u003cli\u003eMolecular Biology Research: It supports various molecular biology experiments by acting as a buffer and facilitating molecular binding processes.\u003c\/li\u003e\n\u003cli\u003eDiagnostic Testing: Its role in DNA and RNA detection makes it suitable for diagnostic applications requiring precise and sensitive analysis.\u003c\/li\u003e\n\u003cli\u003eBiochemical Analysis: The compound is used in biochemical research to control pH and enable specific molecular interactions during analytical procedures.\u003c\/li\u003e\n\u003cli\u003eEducational Research: It is commonly used in academic settings to teach and demonstrate molecular biology techniques and hybridization methods.\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: 54970-72-8\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Molecular Biology \u0026gt; Nucleic Acid Detection and Hybridization\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 and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eSodium 3,5-Dichloro-2-hydroxybenzenesulfonate should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep the compound in a sealed container to prevent moisture absorption and contamination. The storage area should be free from direct sunlight and excessive humidity to ensure the integrity of the material. Proper labeling of containers is essential for safe handling and easy identification. Laboratory personnel should wear appropriate personal protective equipment when handling the compound to minimize exposure risks. Regular inspection of storage conditions is advised to maintain optimal quality and safety standards in the laboratory.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086483828954,"sku":"TCI2510D192821913","price":1289000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086483861722,"sku":"TCI2510D192821914","price":3231000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D1928.jpg?v=1768817532"},{"product_id":"tci2510d375624119","title":"TCI D3756 91-95-2 3,3'-Diaminobenzidine [for Biochemical Research]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e3,3'-Diaminobenzidine, commonly abbreviated as DAB, is a tetra-amino aromatic compound prepared for biochemical research purposes. Its molecule consists of two directly linked benzene rings, each carrying two amino groups, which provides four nucleophilic centres together with a readily oxidised pi-electron system. Its principal role in the laboratory is as a chromogenic substrate in reactions catalysed by peroxidase enzymes, where DAB is oxidised and precipitates as an insoluble brown product exactly at the site of the enzyme. In addition, this tetra-amino framework is also used as a monomer and building block in heterocyclic synthesis.\u003c\/p\u003e\n\u003cp\u003eThe characteristics that make DAB such a widely chosen reagent are the stability, contrast, and strong adherence of its oxidation precipitate to tissues or membranes. The brown colour that forms is insoluble in both water and alcohol, so preparations can be dehydrated, cleared, and mounted in a permanent medium without any loss of signal. It is precisely this property that allows stained preparations to be archived and re-examined years later. As a free base, the compound is generally dissolved first in a suitable solvent before use in the working system.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this material is typically handled in biochemistry, molecular biology, histology, and pathology work, where peroxidase-based detection is a routine part of the workflow. It is also drawn on by organic and materials synthesis groups that require a non-heterocyclic building block with multiple amino centres. Supplied as a TCI catalogue item under the Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks category, it is ordered by university research units, hospital laboratories, and industrial R\u0026amp;D facilities alike.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eImmunohistochemistry (IHC) detection: DAB oxidised by horseradish peroxidase deposits an insoluble brown precipitate directly at the antigen site, giving sharp, high-contrast localisation on tissue sections.\u003c\/li\u003e\n\u003cli\u003eWestern blot membrane development: the precipitate adheres firmly to the blotting membrane and does not wash away, producing permanent visible bands that require no imaging equipment to read.\u003c\/li\u003e\n\u003cli\u003eImmunocytochemistry on cultured cells: because the coloured product is insoluble in water and alcohol, stained cell preparations survive dehydration and clearing without any loss of signal intensity.\u003c\/li\u003e\n\u003cli\u003eEnzyme histochemistry and peroxidase activity mapping: the reaction proceeds precisely where the enzyme is located, so endogenous or introduced peroxidase activity can be mapped with good spatial fidelity.\u003c\/li\u003e\n\u003cli\u003eHeterocyclic and polymer synthesis: the four amino groups on a directly linked biphenyl framework make this a versatile monomer and building block for condensation into heterocyclic ring systems.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI (Tokyo Chemical Industry), catalogue number D3756\u003c\/li\u003e\n\u003cli\u003eCAS number: 91-95-2\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003eGrade: [for Biochemical Research]\u003c\/li\u003e\n\u003cli\u003eChemical form: free base of the tetra-amino aromatic compound, dissolved in a suitable solvent before use\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in the standard TCI research pack sizes; storage conditions follow the manufacturer's label\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the container tightly closed in a cool, dry place away from direct sunlight, heat sources, and strong oxidising agents, following the storage conditions stated on the manufacturer's label. Amber glass or the original supplier container is preferred, since the compound is readily oxidised and light exposure should be minimised. Handle weighing and dissolution inside a fume hood, and wear a laboratory coat, nitrile gloves, and eye protection throughout. Avoid raising dust, and do not inhale or allow contact with skin. Prepare working solutions fresh where possible and keep them protected from light. Collect residues and used solutions as designated chemical waste for disposal in accordance with applicable institutional and local regulations.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086636200154,"sku":"TCI2510D375624119","price":708000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086636232922,"sku":"TCI2510D375624120","price":2071000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D3756.jpg?v=1767106510"},{"product_id":"tci2510d375724121","title":"TCI D3757 868272-85-9 3,3'-Diaminobenzidine Tetrahydrochloride Hydrate [for Biochemical Research]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D3757 3,3'-Diaminobenzidine Tetrahydrochloride Hydrate is the hydrated tetrahydrochloride salt form of DAB, prepared specifically for biochemical research and classified within antibody supplementary products. Like its free base counterpart, this compound functions as a chromogenic substrate for peroxidase enzymes, particularly horseradish peroxidase conjugated to secondary antibodies. When the enzyme acts in the presence of hydrogen peroxide, DAB is oxidised and precipitates as an insoluble brown reaction product, allowing the position of an antigen in tissue or a protein band on a membrane to be observed directly by eye or under an ordinary light microscope.\u003c\/p\u003e\n\u003cp\u003eThe principal advantage of the tetrahydrochloride salt form lies in its ease of handling. As a salt, this compound is considerably more soluble in water and aqueous buffers than the free base, so working solutions can be prepared quickly without the need for additional organic solvents. The salt form is also generally more stable against oxidation during storage, which reduces the risk of the material darkening before it is used. The properties of the final reaction product remain equally advantageous: the brown precipitate that forms adheres strongly and resists dehydration and subsequent processing steps.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this product is typically used wherever peroxidase-based antibody detection is routine. It serves immunohistochemistry benches in hospital and university pathology units, research groups working on tissue localisation studies, and laboratories performing membrane-based protein detection. Because the salt dissolves readily in aqueous buffer, it suits facilities that prefer straightforward reagent preparation, and the stable brown product allows slides and membranes to be archived and re-examined long after the staining run is complete.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eImmunohistochemistry on tissue sections — the insoluble brown precipitate marks antigen position directly on the slide and remains visible under an ordinary light microscope without specialised optics.\u003c\/li\u003e\n\u003cli\u003eWestern blot and membrane-based protein detection — DAB oxidation produces a permanent brown band on the membrane, giving a visual record of the target protein that needs no imaging equipment.\u003c\/li\u003e\n\u003cli\u003eHorseradish peroxidase conjugate detection systems — the compound acts as the chromogenic substrate for HRP linked to secondary antibodies, completing the enzyme-based signal generation step.\u003c\/li\u003e\n\u003cli\u003eRoutine diagnostic and teaching histology preparations — because the reaction product resists dehydration and further processing, stained slides can be mounted, archived and reviewed repeatedly.\u003c\/li\u003e\n\u003cli\u003eGeneral biochemical research on peroxidase activity — the salt dissolves quickly in aqueous buffer, so working solutions for enzyme-linked assays can be prepared without organic solvents.\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: 868272-85-9\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Antibodies \u0026gt; Antibody Supplementary Products\u003c\/li\u003e\n\u003cli\u003eProduct code: D3757\u003c\/li\u003e\n\u003cli\u003eChemical form: tetrahydrochloride salt, hydrate; grade stated for biochemical research\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in the pack sizes offered by the manufacturer for this catalogue item\u003c\/li\u003e\n\u003cli\u003eStorage: store as directed for the product; keep protected from light and air to limit oxidation\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eKeep the container tightly closed and store it in a cool, dark place, since DAB salts darken on exposure to light and air. Original manufacturer packaging or amber glass with a well-sealed cap is suitable; transfer only the quantity needed for immediate use and reseal promptly. Prepare working solutions fresh in aqueous buffer and handle them in a fume hood where practicable. Wear gloves, a laboratory coat and eye protection, avoid skin contact and inhalation of the powder, and collect DAB-containing waste separately for disposal according to institutional chemical waste procedures.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086636265690,"sku":"TCI2510D375724121","price":1213000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086636298458,"sku":"TCI2510D375724122","price":3231000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D3757.jpg?v=1767106514"},{"product_id":"tci2510d386524268","title":"TCI D3865 120-83-2 2,4-Dichlorophenol [for Biochemical Research]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D3865 2,4-Dichlorophenol [for Biochemical Research] is a chlorinated phenol derivative prepared for biochemical research purposes while also serving as a non-heterocyclic building block in synthetic chemistry. Its molecule consists of a benzene ring bearing a phenolic hydroxyl group together with two chlorine atoms located at the two and four positions. The presence of these chlorine atoms raises the acidity of the hydroxyl group compared with ordinary phenol, so the compound is readily deprotonated to form a reactive phenoxide. In the laboratory, its principal role is as a starting material for the formation of aryl ethers and as a model compound in environmental studies.\u003c\/p\u003e\n\u003cp\u003eThe properties that make this material a preferred choice are the combination of increased acidity, the stability of the aromatic ring, and a clearly defined substitution pattern. Because the two chlorine substituents occupy known positions, reaction outcomes are predictable and the compound behaves consistently as a synthetic intermediate. The phenoxide that forms upon deprotonation can be reacted with alkyl halides or with chloroacetic acid to construct aryloxy derivatives, a route that underpins the synthesis of many agrochemical compounds. The aromatic ring itself remains stable through these transformations, allowing the reactive hydroxyl position to be addressed selectively without disturbing the rest of the structure.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in biochemical and environmental work as a substrate or standard. Typical contexts include research on microbial degradation, peroxidase and laccase enzyme assays, and studies of chlorinated phenol toxicity. The designation as a grade for biochemical research confirms its suitability for these applications, making it appropriate for university research groups, environmental laboratories, and synthesis laboratories that prepare aryloxy derivatives.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAryl ether synthesis — the increased acidity of the hydroxyl group allows straightforward deprotonation to the phenoxide, which then reacts with alkyl halides to build ether linkages.\u003c\/li\u003e\n\u003cli\u003eAryloxy derivative preparation — reaction of the phenoxide with chloroacetic acid produces aryloxy compounds, the fundamental route on which the synthesis of many agrochemical substances is based.\u003c\/li\u003e\n\u003cli\u003eMicrobial degradation research — the compound serves as a defined substrate or standard, letting researchers track the breakdown of chlorinated phenols by microorganisms under controlled conditions.\u003c\/li\u003e\n\u003cli\u003ePeroxidase and laccase enzyme assays — its well-defined phenolic structure makes it a consistent substrate for measuring the oxidative activity of these enzymes in biochemical studies.\u003c\/li\u003e\n\u003cli\u003eChlorinated phenol toxicity studies — as a model compound in environmental work, it provides a representative chlorinated phenol for investigating toxicity behaviour and related environmental effects.\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: 120-83-2\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003eGrade: for Biochemical Research\u003c\/li\u003e\n\u003cli\u003eChemical class: chlorinated phenol derivative; non-heterocyclic building block\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in the pack sizes offered for this catalogue item\u003c\/li\u003e\n\u003cli\u003eStorage: store according to the manufacturer's instructions on the product label\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the container tightly closed in a cool, dry, well-ventilated area away from direct sunlight, heat sources, and incompatible materials, following the storage conditions stated by the manufacturer on the product label. Keep the material in its original supplier container or in a chemically compatible, clearly labelled vessel that is resistant to phenolic compounds. Handle the substance in a fume hood and wear appropriate personal protective equipment, including safety goggles, chemical-resistant gloves, and a laboratory coat, since chlorinated phenols can irritate skin, eyes, and the respiratory tract. Avoid the formation of dust during weighing, close the container immediately after use, and consult the manufacturer's safety data sheet before handling, storage, or waste disposal.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086642196698,"sku":"TCI2510D386524268","price":481000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086642229466,"sku":"TCI2510D386524269","price":1187000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D3865.jpg?v=1768817964"},{"product_id":"tci2510d386624270","title":"TCI D3866 121-69-7 N,N-Dimethylaniline [for Biochemical Research]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D3866 N,N-Dimethylaniline is a classic tertiary aromatic amine consisting of a benzene ring bearing a dimethylamino group, prepared in a grade intended for biochemical research. The compound is one of the best-known reagents in organic chemistry and plays a triple role as a building block, an organic base, and a catalyst. The lone pair on the nitrogen is conjugated with the aromatic ring, which makes the ring strongly electron-rich and readily susceptible to electrophilic substitution at the para position. This property is precisely what makes it an important starting material for the synthesis of dyes and analytical reagents.\u003c\/p\u003e\n\u003cp\u003eThe characteristic that makes it so widely chosen is its moderate basicity combined with the fact that it is not excessively nucleophilic, because the nitrogen is already fully substituted. The compound is therefore effective as an acid scavenger in acylation and sulfonylation reactions without itself reacting with the substrate. In polymer chemistry, tertiary aromatic amines are well known as accelerators that speed up the decomposition of organic peroxides, so that radical polymerization can proceed at room temperature. In the analytical field, the reactivity of its ring is exploited in coupling reactions that yield coloured products.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent belongs to the Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks category and is typically kept as a standing item on the organic synthesis bench. It is drawn on for routine acylation and sulfonylation work, for the preparation of dye intermediates, and for polymer and adhesive formulation studies in academic, government, and industrial research settings. The biochemical research grade makes it suitable for work where a well-characterised, consistently supplied tertiary amine reagent is required.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAcid scavenging in acylation reactions: its moderate basicity binds the liberated acid effectively while the fully substituted nitrogen prevents unwanted attack on the substrate itself.\u003c\/li\u003e\n\u003cli\u003eSulfonylation chemistry: it neutralises the acid generated during sulfonyl chloride couplings, keeping the reaction medium controlled without competing nucleophilically for the sulfonylating agent.\u003c\/li\u003e\n\u003cli\u003eDye and pigment intermediate synthesis: the strongly electron-rich ring undergoes electrophilic substitution readily at the para position, giving the coupling reactivity that dye chemistry depends upon.\u003c\/li\u003e\n\u003cli\u003eRoom-temperature radical polymerization: as a tertiary aromatic amine accelerator it promotes decomposition of organic peroxides, allowing cure and polymerization to proceed without external heating.\u003c\/li\u003e\n\u003cli\u003eColorimetric analytical reagent preparation: the reactive aromatic ring participates in coupling reactions that generate coloured products, making it useful in the formulation of analytical detection 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: 121-69-7\u003c\/li\u003e\n\u003cli\u003eCatalogue number: D3866\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003eGrade: for Biochemical Research\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in the standard TCI catalogue pack sizes; please confirm the size required when ordering\u003c\/li\u003e\n\u003cli\u003eStorage: store in a tightly closed container in a cool, dark, well-ventilated place\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, dark, and well-ventilated area, away from heat, ignition sources, and direct sunlight, and separated from strong oxidising agents and acids. Keep the material in its original supplier packaging or in a compatible, clearly labelled, chemically resistant container, and reseal it immediately after each use to limit exposure to air and moisture. As with all aromatic amines, handle the compound in a functioning fume hood and wear appropriate personal protective equipment, including chemical-resistant gloves, safety goggles, and a laboratory coat. Avoid inhalation of vapours and any contact with skin or eyes, use compatible transfer tools, and manage residues and empty packaging in accordance with your institution's chemical waste procedures. Always consult the manufacturer's safety data sheet before first use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086642295002,"sku":"TCI2510D386624270","price":481000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086642327770,"sku":"TCI2510D386624271","price":1263000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D3866.jpg?v=1769141923"},{"product_id":"tci2510d386824274","title":"TCI D3868 91-67-8 N,N-Diethyl-m-toluidine [for Biochemical Research]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D3868 N,N-Diethyl-m-toluidine is a tertiary aromatic amine that carries two ethyl groups on the nitrogen atom together with a methyl group at the meta position of the benzene ring, supplied in a grade intended for biochemical research. The compound belongs to the non-heterocyclic building block family and functions in the laboratory as an organic base, a radical reaction accelerator, and a synthetic intermediate. Researchers working in organic synthesis and polymer chemistry rely on this class of substituted aniline derivative as a versatile starting material for constructing more elaborate molecular architectures.\u003c\/p\u003e\n\u003cp\u003eThe combination of alkyl groups on both the nitrogen and the aromatic ring makes the molecule more hydrophobic and more readily miscible with organic matrices than simple aniline, a practical advantage in resin formulations and polymer systems. The principal property behind its selection is its ability to accelerate the decomposition of organic peroxides, allowing radical polymerization to be initiated without heating. This amine-peroxide redox system underpins acrylate and methacrylate resins that cure at room temperature, a chemistry widely studied for materials and biomaterials applications. The tertiary nitrogen is also basic yet sterically shielded, which makes it useful as an acid scavenger in acylation reactions, while the electron-rich aromatic ring opens pathways for electrophilic substitution and diazo coupling in dye synthesis.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent is typically found in university organic chemistry and polymer research groups, materials science laboratories, and institutional research centers investigating self-curing resin systems. It is used at bench scale in synthesis and formulation studies where a room-temperature curing accelerator or a hindered organic base is required, and it also serves as an intermediate in method development work supporting dye chemistry and fine chemical synthesis programs.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eRoom-temperature radical polymerization: the amine accelerates organic peroxide decomposition so acrylate and methacrylate systems cure without any external heating step.\u003c\/li\u003e\n\u003cli\u003eSelf-curing resin formulation studies: its hydrophobic alkyl substitution allows easy blending into organic resin matrices where simple aniline would disperse poorly.\u003c\/li\u003e\n\u003cli\u003eAcid scavenging in acylation reactions: the sterically shielded tertiary nitrogen remains basic enough to bind liberated acid without competing as a nucleophile.\u003c\/li\u003e\n\u003cli\u003eDye synthesis via diazo coupling: the electron-rich aromatic ring readily undergoes coupling reactions, making it a practical coupling component for colorant preparation.\u003c\/li\u003e\n\u003cli\u003eNon-heterocyclic building block synthesis: it serves as a versatile intermediate for electrophilic aromatic substitution routes toward more complex substituted aromatic amine targets.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eProduct code: D3868\u003c\/li\u003e\n\u003cli\u003eCAS number: 91-67-8\u003c\/li\u003e\n\u003cli\u003eChemical name: N,N-Diethyl-m-toluidine [for Biochemical Research]\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003eStorage: store according to the manufacturer's instructions stated on the product label\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the container tightly closed in a cool, dry, and well-ventilated area, away from direct sunlight, heat sources, and open flame. Keep it separated from organic peroxides and other oxidizing agents, since the accelerating reactivity that makes this amine useful can also cause unintended reactions in storage. Use the original manufacturer's container or a compatible amber glass bottle with a chemically resistant closure. Handle inside a fume hood while wearing safety goggles, chemical-resistant gloves, and a laboratory coat. Avoid inhalation of vapors and contact with skin or eyes, transfer with clean dry glassware, and always consult the manufacturer's safety data sheet before use and before disposal.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086642426074,"sku":"TCI2510D386824274","price":481000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086642458842,"sku":"TCI2510D386824275","price":1415000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D3868.jpg?v=1768817967"},{"product_id":"tci2510d393124365","title":"TCI D3931 536-46-9 N,N-Dimethyl-1,4-phenylenediamine Dihydrochloride [for Biochemical Research]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D3931 N,N-Dimethyl-1,4-phenylenediamine Dihydrochloride [for Biochemical Research] is the dihydrochloride salt of a para-phenylenediamine derivative that carries two methyl groups on one of its nitrogen atoms. The compound is a classic chromogenic reagent, and its role in the laboratory is to develop colour when it undergoes oxidation or reacts with certain analytes, so that the presence of a substance that was originally colourless can be followed visually or measured quantitatively with a spectrophotometer. This product class is categorised as a supplementary material for biochemical research and antibody-based work.\u003c\/p\u003e\n\u003cp\u003eThe property that makes this reagent a preferred choice is the ease with which it is oxidised into a strongly coloured species, combined with its good solubility in water thanks to the dihydrochloride salt form. The salt form also makes the powder more stable to handle and weigh than the free base, which darkens in air far more readily. Because the response is sensitive and relatively rapid, the reagent is suited both to qualitative bench-top tests and to colorimetric methods that require absorbance readings. The electron-donating character of the dimethylamino group is what underlies this colour formation behaviour.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent fits routine analytical and biochemical research work where a colour-forming indicator is needed to confirm or measure a reaction. It is typically used in university research laboratories, biochemistry and life science units, and analytical laboratories that run colorimetric procedures. Because it serves as a supplementary product for antibody-related work, it is generally kept on hand as part of the reagent stock supporting detection and staining workflows rather than as a bulk consumable.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eColorimetric assay development: the reagent forms a strongly coloured oxidation product, allowing colourless analytes to be quantified by absorbance measurement on a standard laboratory spectrophotometer.\u003c\/li\u003e\n\u003cli\u003eQualitative bench-top screening tests: because the colour response is sensitive and relatively rapid, results can be judged visually without instrumentation during preliminary or routine confirmation work.\u003c\/li\u003e\n\u003cli\u003eAntibody-based detection support: it is classified as an antibody supplementary product, so it serves as the colour-generating component in detection systems built around antibody reagents.\u003c\/li\u003e\n\u003cli\u003eOxidation-based indicator chemistry: the electron-donating dimethylamino group makes the molecule readily oxidised, so it acts as a reliable visual indicator of oxidising conditions in a reaction system.\u003c\/li\u003e\n\u003cli\u003eGeneral biochemical research reagent preparation: its good water solubility in the dihydrochloride form makes it convenient to dissolve into aqueous working solutions for biochemical 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: 536-46-9\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Antibodies \u0026gt; Antibody Supplementary Products\u003c\/li\u003e\n\u003cli\u003eGrade \/ designation: for Biochemical Research\u003c\/li\u003e\n\u003cli\u003ePhysical form: solid powder (dihydrochloride salt)\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in standard TCI catalogue pack sizes; please confirm the required size when ordering\u003c\/li\u003e\n\u003cli\u003eStorage: keep in a tightly closed container, protected from air and light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the reagent in a tightly closed container, protected from air and light, and keep it in a cool, dry place away from oxidising agents. Amber glass bottles or the original supplier container are suitable, and the container should be reclosed promptly after each use because phenylenediamine derivatives darken on exposure to air. Weigh the powder in a well-ventilated area or fume hood, and prepare aqueous solutions fresh where the method allows. Wear gloves, safety glasses and a laboratory coat during handling, avoid contact with skin and eyes and avoid inhaling dust, and dispose of residues and contaminated materials according to the chemical waste procedures of your laboratory.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086646161626,"sku":"TCI2510D393124365","price":481000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086646194394,"sku":"TCI2510D393124366","price":1010000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D3931.jpg?v=1769141930"},{"product_id":"tci2510d400524464","title":"TCI D4005 333338-18-4 Disodium 4-Nitrophenyl Phosphate Hexahydrate [for Biochemical Research]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eDisodium 4-Nitrophenyl Phosphate Hexahydrate, commonly abbreviated as pNPP, is a chromogenic substrate that forms the backbone of many phosphatase-based enzymatic assays in biochemical laboratories. The compound acts as a phosphate group donor that is hydrolysed by alkaline phosphatase and acid phosphatase alike, releasing 4-nitrophenol, which develops a bright yellow colour under alkaline conditions. That colour change is measured spectrophotometrically, allowing enzyme activity to be quantified in a way that is simple, rapid, and free of complicated instrumentation. In everyday practice, pNPP serves as the bridge between an enzyme reaction that cannot be seen and an optical signal that is easy to read.\u003c\/p\u003e\n\u003cp\u003eThe characteristics that make this material such a widely chosen reagent are its good solubility in water and aqueous buffers, its stability as a hydrated disodium salt, and its low background absorbance before the reaction proceeds, so that the signal-to-noise ratio is preserved. The hexahydrate form makes weighing and dissolution straightforward at small scale, while the hydrolysis product carries a strong absorption coefficient in the visible wavelength region. The grade offered here is intended for biochemical research, matching the demands of work where reaction responses must be consistent and reproducible from one run to the next.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, pNPP is routinely used across university biochemistry teaching and research labs, clinical and diagnostic development settings, and enzyme-focused work in food, agricultural, and environmental laboratories. It appears wherever phosphatase activity has to be measured with a plate reader or a conventional spectrophotometer, and it is equally common as the detection substrate in alkaline phosphatase-conjugated immunoassay workflows, where it supports antibody-based detection alongside other antibody supplementary products.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAlkaline phosphatase activity assays — pNPP is hydrolysed efficiently by the enzyme and yields a bright yellow product under alkaline conditions, so activity can be quantified directly by absorbance.\u003c\/li\u003e\n\u003cli\u003eAcid phosphatase activity assays — the same substrate serves acid phosphatase reactions, letting a single reagent cover both enzyme classes and simplifying reagent inventory in a working biochemistry laboratory.\u003c\/li\u003e\n\u003cli\u003eELISA and immunoassay detection — as a chromogenic substrate for alkaline phosphatase-conjugated antibodies, it converts specific binding events into a readable optical signal in microplate formats.\u003c\/li\u003e\n\u003cli\u003eEnzyme kinetics and inhibitor screening — its low background absorbance and strong product absorption give a clean, linear optical readout suitable for rate measurements and inhibition studies.\u003c\/li\u003e\n\u003cli\u003eBiochemistry teaching and method development — good aqueous solubility and easy small-scale weighing in the hexahydrate form make it practical for student practicals and for validating new assay protocols.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eProduct code: D4005\u003c\/li\u003e\n\u003cli\u003eCAS Number: 333338-18-4\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Antibodies \u0026gt; Antibody Supplementary Products\u003c\/li\u003e\n\u003cli\u003ePhysical form: hydrated disodium salt (hexahydrate), water-soluble\u003c\/li\u003e\n\u003cli\u003eGrade: for biochemical research\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in standard TCI catalogue pack sizes — please confirm the size required when ordering\u003c\/li\u003e\n\u003cli\u003eStorage: store as directed on the product label; keep containers tightly closed and protected from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the material in its original tightly closed container in a cool, dry place, protected from light and moisture, since the hydrated salt is hygroscopic in character and its assay performance depends on an intact, low-background reagent. Amber glass or opaque containers are preferred for prepared stock solutions, and solutions should be made fresh in the appropriate buffer where assay sensitivity matters. Handle the powder in a well-ventilated area or fume hood, wearing gloves, safety glasses, and a laboratory coat, and avoid generating dust. Use clean, dry spatulas to prevent moisture ingress into the bulk container, label all prepared solutions clearly with the preparation date, and follow the manufacturer's safety data sheet together with your institutional waste-handling procedures for disposal.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":50506821304538,"sku":"TCI2510D400524464","price":708000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D4005.jpg?v=1767106935"},{"product_id":"tci2510d417824692","title":"TCI D4178 1752-94-9 4-(4,5-Diphenyl-1H-imidazol-2-yl)phenol [for Biochemical Research]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D4178 is 4-(4,5-Diphenyl-1H-imidazol-2-yl)phenol, supplied with the designation [for Biochemical Research]. Structurally, it is a derivative of lophine (2,4,5-triphenylimidazole) in which the phenyl group at the 2-position has been replaced by a 4-hydroxyphenyl group. The compound belongs to the family of luminescent compounds and detection reagents used in life science research. In the laboratory, it serves as a luminescence-active compound and as a substrate or enhancer in detection systems based on oxidative reactions, particularly those involving hydrogen peroxide and peroxidase enzymes, making it relevant to the development of sensitive biochemical analytical methods.\u003c\/p\u003e\n\u003cp\u003eThe property that makes this material attractive is its triphenyl-substituted imidazole core, which is highly conjugated and widely recognized as a classical chemiluminescent scaffold. The lophine framework is able to emit light when it undergoes oxidation under appropriate conditions, and the addition of a phenolic hydroxyl group at the para position provides two advantages at once: it increases the ease with which the molecule is oxidized, while also supplying a functional group that can be further derivatized or can interact through hydrogen bonding. The extended aromatic system likewise renders the compound fluorescent, broadening the range of optical measurements in which it can participate.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, a reagent of this type is typically found in university research groups, biochemistry and analytical chemistry laboratories, and institutional research centres working on luminescence-based detection. It is generally handled at small scale on the laboratory bench, where researchers prepare solutions for oxidative detection experiments and optical measurements. Because it is designated for biochemical research, it is intended for research use and method development rather than routine production or clinical diagnostic work.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eChemiluminescence detection studies: the lophine-derived imidazole core emits light upon oxidation, making the compound a well-established scaffold for developing and evaluating light-emitting analytical reactions.\u003c\/li\u003e\n\u003cli\u003eHydrogen peroxide detection systems: the compound acts as a substrate or enhancer in oxidative detection schemes where hydrogen peroxide is the analyte or the driving oxidant of the reaction.\u003c\/li\u003e\n\u003cli\u003ePeroxidase-based assay development: it participates in detection systems involving peroxidase enzymes, supporting the construction of sensitive enzymatic assays for biochemical research applications.\u003c\/li\u003e\n\u003cli\u003eFluorescence measurement work: the extended aromatic conjugation of the triphenyl-substituted imidazole makes the molecule fluorescent, allowing its use in optical characterization and fluorescence-based experiments.\u003c\/li\u003e\n\u003cli\u003eSynthetic derivatization and probe design: the para-positioned phenolic hydroxyl group provides a reactive handle for further chemical modification or for hydrogen-bonding interactions in designed probe molecules.\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: 1752-94-9\u003c\/li\u003e\n\u003cli\u003eChemical name: 4-(4,5-Diphenyl-1H-imidazol-2-yl)phenol, designated [for Biochemical Research]\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Luminescent Compounds\/Detection\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in the standard research-scale pack sizes offered by the manufacturer; please confirm the required packaging when ordering\u003c\/li\u003e\n\u003cli\u003eStorage note: store in a tightly closed container, protected from light, in a cool and dry place\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the reagent in its original tightly closed container, kept in a cool, dry and well-ventilated area away from direct sunlight and from strong oxidizing agents, since the compound is designed to be readily oxidized. Amber glass or otherwise light-protected containers are appropriate, and the container should be resealed promptly after each use to limit exposure to moisture and air. Handle the material inside a fume hood using standard personal protective equipment, including a laboratory coat, chemical-resistant gloves and safety glasses. Avoid generating dust, avoid inhalation and skin or eye contact, and wash hands thoroughly after handling. Always consult the manufacturer's safety data sheet before use, and dispose of residues and contaminated materials in accordance with applicable chemical waste procedures.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48086674899162,"sku":"TCI2510D417824692","price":1718000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D4178.jpg?v=1767107168"},{"product_id":"tci2510d465525312","title":"TCI D4655 29898-72-4 4-(4,5-Diphenyl-1H-imidazol-2-yl)benzonitrile","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D4655 4-(4,5-Diphenyl-1H-imidazol-2-yl)benzonitrile is a heterocyclic intermediate that combines an imidazole core bearing two phenyl substituents with a benzonitrile ring at the 2-position. Structurally, it belongs to the family of triphenylimidazole or lophine derivatives, a group of compounds widely recognised in chemiluminescence studies and fluorescent materials research. In the laboratory, this compound serves as a molecular building block for further synthesis and, at the same time, as a chromophore whose optical properties can be studied directly in work on sensors and functional materials.\u003c\/p\u003e\n\u003cp\u003eSeveral properties make this material a preferred choice. The imidazole core provides donor nitrogen atoms and an N–H proton that can participate in hydrogen bonding as well as metal ion binding, while the two phenyl groups extend the conjugated system and therefore support light-emitting behaviour. The nitrile group on the phenyl ring acts both as an electron-withdrawing substituent and as a synthetic handle that can be converted into an amide, a carboxylic acid, an amine, a tetrazole, or other heterocycles. Donor–acceptor combinations of this kind are widely used by researchers to tune the electronic properties and optical response of a molecule.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, a compound of this type is typically handled in university and institutional research groups working on organic synthesis, photophysics, and functional materials. It is normally used at small research scale, weighed out for exploratory synthesis, derivatisation studies, or spectroscopic characterisation rather than for routine bulk work. Because it functions as both an intermediate and a chromophore, it fits naturally into projects that move from synthesis through to optical measurement within the same laboratory.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eHeterocyclic building block synthesis — the reactive nitrile group and substituted imidazole core allow controlled elaboration into amides, carboxylic acids, amines, tetrazoles, and further heterocyclic systems.\u003c\/li\u003e\n\u003cli\u003eChemiluminescence research — as a member of the triphenylimidazole or lophine family, it belongs to a compound class long established in the study of light-emitting chemical reactions.\u003c\/li\u003e\n\u003cli\u003eFluorescent materials development — the extended conjugation contributed by the two phenyl rings supports emissive behaviour, making the molecule useful for preparing and evaluating fluorescent compounds.\u003c\/li\u003e\n\u003cli\u003eChemical sensor studies — the imidazole N–H proton and donor nitrogen atoms can participate in hydrogen bonding and metal ion binding, giving a recognition site for analyte-responsive systems.\u003c\/li\u003e\n\u003cli\u003eDonor–acceptor molecular design — pairing the electron-rich imidazole with the electron-withdrawing nitrile lets researchers systematically tune electronic structure and optical response in functional molecules.\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: 29898-72-4\u003c\/li\u003e\n\u003cli\u003eChemical name: 4-(4,5-Diphenyl-1H-imidazol-2-yl)benzonitrile\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003eCatalogue code: D4655\u003c\/li\u003e\n\u003cli\u003eStorage: store in the original, tightly closed container as indicated on the manufacturer's label\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eKeep the product in its original, tightly closed container and store it in a cool, dry, well-ventilated place away from direct sunlight, moisture, and incompatible chemicals. Amber glass or the supplied container is suitable, and containers should be resealed promptly after each use to limit exposure to air and humidity. Handle the solid in a fume hood or a well-ventilated area, using safety glasses, gloves, and a laboratory coat, and avoid generating or inhaling dust during weighing and transfer. Label all working solutions clearly, keep the manufacturer's safety data sheet accessible, and follow institutional procedures for chemical waste disposal.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48086701539546,"sku":"TCI2510D465525312","price":3534000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D4655.jpg?v=1767107802"},{"product_id":"tci2510f096831001","title":"TCI F0968 2284-96-0 2-(4-Fluorophenyl)-4,5-diphenylimidazole","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2-(4-Fluorophenyl)-4,5-diphenylimidazole is a chemical compound widely used in research applications within the life sciences. This compound plays a crucial role in molecular biology, particularly in the detection and hybridization of nucleic acids. Its complex structure, composed of an imidazole ring with two phenyl groups attached, makes it a valuable tool for studying molecular interactions. This compound is commonly found in laboratory settings where precision and specificity in chemical reactions are essential. Its ability to interact with biological molecules such as DNA and RNA enhances its utility in various scientific investigations.\u003c\/p\u003e\n\u003cp\u003eThe compound's high reactivity and structural complexity make it a preferred choice for researchers seeking compounds with strong binding affinity. Its chemical properties allow it to participate in a range of biochemical reactions, making it suitable for applications that require precise molecular interactions. The presence of fluorine in its molecular structure also contributes to its unique reactivity, which is advantageous in certain analytical techniques. These characteristics make it an essential component in many laboratory workflows, especially those involving nucleic acid analysis.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is frequently used in molecular biology research, particularly in the development of nucleic acid detection methods. Researchers in health and biotechnology sectors rely on this compound to accelerate molecular analysis and testing processes. Its application is especially relevant in diagnostic and research settings where accurate and reliable results are critical. The compound's versatility and effectiveness make it a key material in advancing scientific research in Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eNucleic Acid Hybridization: This compound is ideal for hybridization studies due to its ability to bind with DNA and RNA, enabling precise detection of target sequences.\u003c\/li\u003e\n\u003cli\u003eMolecular Interaction Studies: Its complex structure allows for detailed analysis of molecular interactions, making it suitable for research into biomolecular behavior.\u003c\/li\u003e\n\u003cli\u003eDiagnostic Reagent Development: The compound's reactivity and specificity are beneficial in creating reagents for diagnostic assays and nucleic acid detection kits.\u003c\/li\u003e\n\u003cli\u003eBiochemical Assay Optimization: Its high affinity for biological molecules helps in refining and optimizing biochemical assays for improved accuracy.\u003c\/li\u003e\n\u003cli\u003eResearch in Genetic Analysis: It supports genetic research by facilitating the study of nucleic acid interactions in various biological 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: 2284-96-0\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Molecular Biology \u0026gt; Nucleic Acid Detection and Hybridization\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid, crystalline powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\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 safe handling and easy identification. In laboratory settings, it should be handled with appropriate personal protective equipment, including gloves and safety goggles, to ensure safety. Regular inspection of storage conditions is advised to ensure optimal preservation of the compound's properties. Always follow standard laboratory safety protocols when working with this material to minimize risks.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48087048650970,"sku":"TCI2510F096831001","price":2878000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510F0968.jpg?v=1769142436"},{"product_id":"tci2510h138034217","title":"TCI H1380 13599-84-3 6-Hydroxybenzothiazole","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI H1380 6-Hydroxybenzothiazole is an aromatic heterocyclic compound that combines a benzothiazole ring with a hydroxyl group at the six position. In organic synthesis laboratories, this compound serves as a building block, that is, a starting scaffold that already carries two reactive points at once: a phenolic hydroxyl group that is readily alkylated or acylated, and a thiazole ring that supplies nitrogen and sulfur atoms for coordination as well as for further substitution. Its role saves synthetic steps because researchers do not need to construct the benzothiazole ring from simpler starting materials.\u003c\/p\u003e\n\u003cp\u003eThe characteristics that make this compound a preferred choice are the combination of aromatic ring stability with the directed reactivity of the phenol group. The benzothiazole scaffold is widely recognised as a pharmacophore core in many active molecules, and at the same time as a structural component of light-emitting systems such as luciferin. The hydroxyl position at number six imparts a distinctive electronic pattern, so that the derivatives obtained possess absorption and emission properties that are attractive to researchers working on luminescent materials.\u003c\/p\u003e\n\u003cp\u003eThis compound is also available in reagent purity, making it suitable for milligram-scale reactions that demand reliable outcomes. In Indonesian laboratories, that combination fits the typical working pattern of university and institutional research groups, where heterocyclic building blocks are consumed in small quantities across exploratory synthetic routes. Researchers preparing benzothiazole derivatives for medicinal chemistry programmes or for fluorescent probe development can begin directly from this intermediate rather than assembling the ring system themselves.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eHeterocyclic derivative synthesis, because the intact benzothiazole ring removes the need to build the scaffold from simpler precursors and shortens the overall synthetic route considerably.\u003c\/li\u003e\n\u003cli\u003ePhenolic alkylation and acylation chemistry, since the hydroxyl group at position six is readily converted into ethers or esters under standard conditions.\u003c\/li\u003e\n\u003cli\u003eMedicinal chemistry exploration, as the benzothiazole scaffold is widely recognised as a pharmacophore core present in many biologically active molecules of research interest.\u003c\/li\u003e\n\u003cli\u003eLuminescent materials research, because the six-hydroxyl substitution pattern gives derivatives absorption and emission characteristics attractive to investigators working on light-emitting compounds.\u003c\/li\u003e\n\u003cli\u003eCoordination and further substitution studies, given that the thiazole ring supplies both nitrogen and sulfur atoms as available donor and reaction sites.\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: 13599-84-3\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003eGrade: reagent purity, suitable for milligram-scale synthetic work\u003c\/li\u003e\n\u003cli\u003ePack sizes: please refer to the catalogue listing for the available pack configurations\u003c\/li\u003e\n\u003cli\u003eStorage: keep in the closed original container under the conditions stated on the manufacturer label\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the container tightly closed in a cool, dry and well-ventilated area, away from direct sunlight and from incompatible reagents such as strong oxidising agents. The original manufacturer packaging is the most suitable container; where transfer is necessary, use clean amber glass with a chemically resistant closure to limit light and moisture exposure. Handle the material inside a fume hood, wearing safety glasses, a laboratory coat and appropriate chemical-resistant gloves. Avoid generating dust when weighing, close the container immediately after use, and consult the manufacturer safety data sheet before first handling and before disposal.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":50506755440858,"sku":"TCI2510H138034217","price":2676000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510H1380.jpg?v=1767117924"},{"product_id":"tci2510m215540316","title":"TCI M2155 4338-98-1 3-Methyl-2-benzothiazolinonehydrazone Hydrochloride [for Biochemical Research]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e3-Methyl-2-benzothiazolinonehydrazone Hydrochloride is a chemical compound widely used in biochemical research. This compound plays a crucial role in laboratory settings, particularly in the synthesis of heterocyclic compounds. It serves as a building block for creating complex molecular structures, which are essential for various scientific applications. Its versatility makes it a valuable resource for researchers working on diverse biochemical processes.\u003c\/p\u003e\n\u003cp\u003eThe compound is known for its chemical stability under specific conditions, which enhances its usability in long-term experiments. Its reactivity also makes it suitable for a range of chemical reactions that require a readily available substrate. This stability and reactivity contribute to its popularity among scientists who need reliable and consistent results. Additionally, its availability in various packaging options ensures that it meets the needs of different experimental scales.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in biochemical research, especially in the analysis of proteins and enzymes. It is also integral to chemical experiments that require heterocyclic compounds for the synthesis of more complex molecules. Its reliability and effectiveness make it a preferred choice for researchers aiming to achieve accurate and reproducible outcomes.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBiochemical Synthesis: This compound is ideal for synthesizing heterocyclic compounds, which are essential in drug development and molecular biology research.\u003c\/li\u003e\n\u003cli\u003eProtein Analysis: It is frequently used in enzyme and protein studies due to its ability to participate in complex chemical reactions.\u003c\/li\u003e\n\u003cli\u003eEnzyme Kinetics Studies: Its reactivity makes it suitable for experiments that require substrates that can undergo rapid and controlled chemical transformations.\u003c\/li\u003e\n\u003cli\u003eStructural Chemistry Research: It supports the creation of complex molecular structures, aiding in the study of molecular interactions and bonding.\u003c\/li\u003e\n\u003cli\u003eAnalytical Chemistry Applications: It is used in analytical procedures that require precise chemical reagents for accurate results.\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: 4338-98-1\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various packaging options to suit different experimental needs\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\u003eThis compound 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 moisture absorption. Due to its reactivity, it should be handled with care in a well-ventilated area. Avoid exposure to strong oxidizing agents or incompatible materials. Proper labeling and storage conditions are essential to ensure safety and maintain the integrity of the compound. Always follow standard laboratory safety protocols when handling and using this material.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087654203610,"sku":"TCI2510M215540316","price":657000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48087654236378,"sku":"TCI2510M215540317","price":1415000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510M2155.jpg?v=1767126165"},{"product_id":"tci2510m232540565","title":"TCI M2325 30686-73-8 4-(2-Methyl-4-thiazolyl)phenol [for Biochemical Research]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI M2325 4-(2-Methyl-4-thiazolyl)phenol [for Biochemical Research] is a compound built on a combined thiazole–phenol framework, in which a thiazole core bearing a methyl group at the 2-position is linked directly to a 4-hydroxyphenyl group. The product is supplied under the specific designation \"for Biochemical Research\", indicating that it is intended for biochemical research purposes rather than for general use. In the laboratory, this compound serves as an intermediate and as a basic scaffold in the development of luminescent compounds, detection reagents, and probe molecules that exploit the optical behaviour of the thiazole–phenol core.\u003c\/p\u003e\n\u003cp\u003eThe characteristic that makes this material attractive is the conjugated system formed between the aromatic phenol ring and the heteroatom-rich thiazole ring. That conjugation gives rise to distinctive light absorption and emission behaviour that responds to the surrounding chemical environment, an essential foundation for the design of optical probes. The phenolic hydroxyl group provides a highly useful point of attachment: it can be etherified, esterified, phosphorylated, or fitted with a sugar moiety, so that the optical properties of the compound can be \"switched off\" and then restored once a specific enzyme cleaves the capping group.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is typically used in university research groups, biochemistry and molecular biology laboratories, and institutional research units working on detection chemistry. It is normally handled in small quantities as a starting scaffold for synthesising probe molecules, or as a reference material in experiments that examine the optical response of thiazole–phenol systems. Its role suits research-scale work rather than routine or bulk production activities.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eLuminescent compound development: the conjugated thiazole–phenol framework provides the optical core that researchers modify to build new light-emitting molecules for biochemical study.\u003c\/li\u003e\n\u003cli\u003eOptical probe design: the phenolic hydroxyl group offers a defined attachment point for capping groups, allowing probe molecules whose optical signal can be switched off and later restored.\u003c\/li\u003e\n\u003cli\u003eEnzyme-responsive reagent preparation: etherified, esterified, phosphorylated, or glycosylated derivatives can be prepared so that enzymatic cleavage of the capping group regenerates the optical response.\u003c\/li\u003e\n\u003cli\u003eDetection reagent synthesis: the compound functions as a synthetic intermediate from which detection reagents relying on thiazole–phenol optical behaviour are constructed in the laboratory.\u003c\/li\u003e\n\u003cli\u003eBiochemical research reference material: supplied specifically for biochemical research, it serves as a defined scaffold for comparison studies of thiazole–phenol optical and chemical behaviour.\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: 30686-73-8\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Luminescent Compounds\/Detection\u003c\/li\u003e\n\u003cli\u003eProduct code: M2325\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in research-scale laboratory pack sizes; please confirm the sizes currently offered when ordering\u003c\/li\u003e\n\u003cli\u003eStorage: store according to the manufacturer's stated conditions on the product label and safety data sheet\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the compound in a cool, dry place away from direct sunlight, moisture, and sources of heat or ignition, following the storage conditions stated by the manufacturer on the product label and safety data sheet. Keep it in its original tightly closed container, or in a clean amber glass container if transfer is required, since compounds with conjugated aromatic systems may be light-sensitive. Handle the material in a fume hood, wearing a laboratory coat, safety goggles, and suitable chemical-resistant gloves. Avoid inhaling dust and avoid direct contact with skin and eyes. Because this material is intended for biochemical research only, it should be handled exclusively by trained laboratory personnel, and the container should be clearly labelled and kept separate from incompatible chemicals.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48087673798874,"sku":"TCI2510M232540565","price":1162000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48087673831642,"sku":"TCI2510M232540566","price":6814000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510M2325.jpg?v=1767126460"},{"product_id":"tci2510n041843148","title":"TCI N0418 369-07-3 2-Nitrophenyl beta-D-Galactopyranoside [Substrate for beta-D-Galactosidase]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2-Nitrophenyl beta-D-Galactopyranoside is a chemical compound used as a substrate for the enzyme beta-D-galactosidase. It plays a critical role in biochemical and enzymatic analysis within laboratory settings. This compound is widely utilized in research to measure the activity of beta-D-galactosidase, an essential enzyme in carbohydrate metabolism. Its ability to react with the enzyme produces a colored product, making it ideal for colorimetric assays. This makes it a fundamental tool in biochemical studies and enzyme kinetics research.\u003c\/p\u003e\n\u003cp\u003eThe compound’s molecular structure allows it to bind efficiently with beta-D-galactosidase, ensuring accurate and reliable results in enzymatic reactions. Its chemical properties and reactivity make it a preferred choice in various laboratory applications. Its stability and predictable behavior under controlled conditions contribute to its reliability in experimental setups. These characteristics ensure consistent performance, which is vital for scientific accuracy and reproducibility.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 2-Nitrophenyl beta-D-Galactopyranoside is commonly used in biochemical research, particularly in enzyme activity analysis and metabolic studies. It is a key component in experiments requiring precise measurement of enzymatic activity. Many research institutions and universities rely on this compound for its effectiveness and consistency in experimental procedures. Its use supports a wide range of scientific investigations in the field of glycoscience and chemical biology.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eEnzyme Activity Assays: This compound is ideal for measuring beta-D-galactosidase activity due to its ability to produce a detectable color change when reacted with the enzyme.\u003c\/li\u003e\n\u003cli\u003eMetabolic Pathway Studies: It is used to investigate carbohydrate metabolism by assessing the activity of beta-D-galactosidase in various biological samples.\u003c\/li\u003e\n\u003cli\u003eBiochemical Research: Its role as a substrate makes it essential for studies involving enzyme kinetics and substrate specificity in glycoscience.\u003c\/li\u003e\n\u003cli\u003eColorimetric Analysis: The colored product formed during the reaction allows for precise and quantitative measurement of enzymatic activity.\u003c\/li\u003e\n\u003cli\u003eEducational Experiments: It is commonly used in academic settings to teach students about enzyme function and biochemical reactions.\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: 369-07-3\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: 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\u003eThis compound should be stored in a cool, dry place, away from direct light to maintain its stability and effectiveness. It is recommended to use airtight containers to prevent moisture absorption, which could affect its chemical integrity. Proper labeling of storage containers is essential for safe handling and easy identification. Laboratory personnel should wear appropriate personal protective equipment, such as gloves and safety goggles, when handling this material. It should be kept out of reach of children and stored separately from incompatible substances. Regular monitoring of storage conditions ensures the compound remains suitable for use in experimental procedures.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087813718234,"sku":"TCI2510N041843148","price":808000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48087813751002,"sku":"TCI2510N041843149","price":2247000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48087813783770,"sku":"TCI2510N041843150","price":8051000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510N0418.jpg?v=1767129806"},{"product_id":"tci2510n045243192","title":"TCI N0452 81012-89-7 Monosodium 1-Naphthyl Phosphate Monohydrate [Substrate for Phosphatase]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eMonosodium 1-Naphthyl Phosphate Monohydrate is a chemical compound used as a substrate for phosphatase enzyme activity. It plays a crucial role in biochemical assays, particularly in measuring the activity of enzymes involved in phosphate degradation. In laboratory settings, this compound serves as an essential reagent for quantifying enzyme activity with high accuracy and reliability. Its application spans various research fields, including biochemistry, pharmacology, and biomedical studies.\u003c\/p\u003e\n\u003cp\u003eThis compound is valued for its high reactivity and purity, making it a preferred choice for scientific research. It exhibits a stable chemical structure and dissolves easily in organic solvents such as ethanol and acetone, which simplifies its use in diverse chemical and biochemical reactions. The consistent reactivity of Monosodium 1-Naphthyl Phosphate Monohydrate ensures minimal variation in test results, enhancing the reliability of experimental outcomes. Its stability and resistance to degradation further contribute to its popularity in laboratory applications.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Monosodium 1-Naphthyl Phosphate Monohydrate is commonly used in biomedical and biochemical research. It is a key component in enzyme activity assays, supporting studies related to enzyme kinetics and metabolic pathways. Its widespread use in academic and research institutions underscores its importance in advancing scientific knowledge in Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eEnzyme Activity Assays – This compound is ideal for measuring phosphatase activity due to its high reactivity and specificity.\u003c\/li\u003e\n\u003cli\u003eBiochemical Research – It supports studies on metabolic pathways and enzyme function, providing reliable data for scientific analysis.\u003c\/li\u003e\n\u003cli\u003ePharmacological Studies – Used in drug development to assess enzyme inhibition and metabolic interactions in biological systems.\u003c\/li\u003e\n\u003cli\u003eBiomedical Investigations – Facilitates research on cellular processes and enzyme-related diseases, contributing to medical advancements.\u003c\/li\u003e\n\u003cli\u003eAnalytical Chemistry – Its solubility and stability make it suitable for various analytical techniques requiring precise reagent performance.\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: 81012-89-7\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Antibodies \u0026gt; Antibody Supplementary Products\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities\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\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 sunlight and moisture. It is recommended to use airtight containers to prevent contamination and maintain its chemical integrity. Due to its reactivity, 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. Avoid contact with incompatible substances to prevent any adverse chemical reactions. Proper storage conditions help preserve the compound’s stability and effectiveness for extended use in laboratory applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087816372442,"sku":"TCI2510N045243192","price":834000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48087816405210,"sku":"TCI2510N045243193","price":2247000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48087816437978,"sku":"TCI2510N045243194","price":8732000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510N0452.jpg?v=1767129866"},{"product_id":"tci2510n061643406","title":"TCI N0616 3150-24-1 4-Nitrophenyl beta-D-Galactopyranoside [Substrate for beta-Galactosidase]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e4-Nitrophenyl beta-D-Galactopyranoside is a chemical compound used as a substrate for beta-galactosidase enzymes. It plays a crucial role in biochemical and molecular biology laboratories, particularly in enzyme activity assays. This compound is widely utilized to measure the activity of beta-galactosidase, an enzyme involved in the breakdown of beta-galactose. Its specificity makes it a reliable tool for enzyme kinetics and metabolic studies. Due to its high reactivity and stability, it is a preferred choice for researchers aiming for accurate and reproducible results.\u003c\/p\u003e\n\u003cp\u003eThe compound exhibits chemical stability and is easily soluble in organic solvents such as ethanol and acetone. These properties make it suitable for a variety of experimental conditions. Its high purity and controlled reactivity ensure consistent performance in laboratory settings. Additionally, its availability in multiple packaging sizes allows for flexibility in experimental scale, from small-scale research to larger studies. This versatility enhances its utility across different laboratory applications.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 4-Nitrophenyl beta-D-Galactopyranoside is commonly used in biochemical research, especially in enzyme studies and carbohydrate metabolism. It is a staple in molecular biology and cellular physiology experiments. Many research institutions and universities rely on this compound for its reliability and precision. Its application is essential for understanding enzymatic processes and their biological significance.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eEnzyme Activity Assays: This substrate is ideal for measuring beta-galactosidase activity, enabling researchers to assess enzyme kinetics and catalytic efficiency.\u003c\/li\u003e\n\u003cli\u003eCarbohydrate Metabolism Studies: It supports investigations into the breakdown of beta-galactose, providing insights into metabolic pathways and enzyme function.\u003c\/li\u003e\n\u003cli\u003eMolecular Biology Research: Its use in enzyme assays aids in studying gene expression and protein function in cellular processes.\u003c\/li\u003e\n\u003cli\u003eBiochemical Analysis: It is a key component in biochemical experiments requiring precise and reproducible enzyme activity measurements.\u003c\/li\u003e\n\u003cli\u003eCellular Physiology Investigations: It helps in understanding how enzymes interact with cellular components and influence metabolic 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: 3150-24-1\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Glycoscience\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various sizes to suit different experimental needs\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\u003eThis compound should be stored in a cool, dry environment, away from direct light to maintain its chemical stability. It is recommended to use airtight containers to prevent moisture absorption and contamination. Due to its reactivity, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. It is important to ensure that the compound is stored separately from incompatible substances to avoid any potential chemical interactions. In laboratory settings, proper labeling and storage protocols are essential to maintain safety and prevent accidental exposure. Always follow standard laboratory safety practices when handling and storing this material.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087828562138,"sku":"TCI2510N061643406","price":1868000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48087828594906,"sku":"TCI2510N061643407","price":5755000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510N0616.jpg?v=1767130131"},{"product_id":"tci2510n086443702","title":"TCI N0864 90-15-3 1-Naphthol [for Biochemical Research]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1-Naphthol [for Biochemical Research] from TCI, catalogue code N0864, is also known as α-naphthol. It is a phenolic compound derived from naphthalene, with a hydroxyl group at the 1-position of the ring system. The \"for Biochemical Research\" grade means the material is prepared for biochemical research work. TCI lists it as a supplementary product for antibody and immunochemistry work. In the laboratory, α-naphthol is a well-known reagent in several classic colour tests. It is also used in detection systems based on coupling reactions with diazonium salts.\u003c\/p\u003e\n\u003cp\u003eResearchers choose this material because its electron-rich naphthalene ring reacts readily with electrophilic reagents and forms clearly coloured products. This reactivity is the basis for its use in the Molisch test for carbohydrates, the Voges–Proskauer test in microbiology, and the Sakaguchi test for arginine. In histochemistry and immunochemistry, naphthol derivatives can form coloured precipitates after reacting with diazonium salts, which lets researchers see where enzyme activity is located. Because it is a biochemical research grade, laboratories can have more confidence that their test results will be consistent from run to run.\u003c\/p\u003e\n\u003cp\u003eIn Indonesia, 1-naphthol is widely needed by microbiology, biochemistry, and immunochemistry laboratories. University teaching laboratories use it for practical sessions that demonstrate classic qualitative tests for carbohydrates and amino acids. Clinical and food microbiology laboratories rely on it for the Voges–Proskauer test, which is part of routine bacterial identification. Research groups working on enzyme histochemistry and antibody-based detection also keep it on hand for colour development steps.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMolisch test for carbohydrates: α-naphthol reacts with furfural derivatives formed from carbohydrates under acidic conditions, producing a distinct coloured ring that indicates carbohydrates are present in the sample.\u003c\/li\u003e\n\u003cli\u003eVoges–Proskauer test in microbiology: 1-naphthol is a key reagent in this test for acetoin production, helping laboratories tell bacterial species apart during routine identification of microbial isolates.\u003c\/li\u003e\n\u003cli\u003eSakaguchi test for arginine: the electron-rich naphthol ring takes part in the colour-forming reaction that detects the guanidino group of arginine, making it useful for qualitative amino acid analysis.\u003c\/li\u003e\n\u003cli\u003eEnzyme histochemistry and visualisation: naphthol compounds couple with diazonium salts to form coloured precipitates, allowing researchers to locate enzyme activity directly in tissue sections or on membranes.\u003c\/li\u003e\n\u003cli\u003eImmunochemistry support work: TCI classifies this reagent as an antibody supplementary product, so it suits colour development and detection steps that accompany antibody-based assays in research laboratories.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI (catalogue code N0864)\u003c\/li\u003e\n\u003cli\u003eCAS number: 90-15-3\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Antibodies \u0026gt; Antibody Supplementary Products\u003c\/li\u003e\n\u003cli\u003eGrade: for Biochemical Research\u003c\/li\u003e\n\u003cli\u003ePack sizes: as listed on the product page, according to the TCI catalogue\u003c\/li\u003e\n\u003cli\u003eStorage: keep tightly closed in a cool, dry, dark place; see the supplier's Safety Data Sheet for specific conditions\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eKeep 1-Naphthol in its original, tightly sealed container, away from light, moisture, and heat. Store it in a cool, dry, well-ventilated area, separate from strong oxidising agents and incompatible chemicals. Amber glass or other light-protective containers help preserve the reagent's quality. Handle it only in a well-ventilated area or a fume hood. Wear suitable gloves, safety glasses, and a laboratory coat, and do not inhale dust or let it touch the skin or eyes. Wash hands thoroughly after handling. Before use, read the Safety Data Sheet from the manufacturer, and dispose of waste according to local regulations.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087845142746,"sku":"TCI2510N086443702","price":455000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48087845175514,"sku":"TCI2510N086443703","price":960000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510N0864.jpg?v=1767130445"},{"product_id":"tci2510n088243725","title":"TCI N0882 37-87-6 Naphthol AS-BI beta-D-Glucuronide [for Biochemical Research]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eNaphthol AS-BI beta-D-Glucuronide is a chemical compound widely utilized in biochemical research. It serves as a specialized substrate in enzymatic reactions, particularly in the assessment of beta-glucuronidase enzyme activity. This compound plays a crucial role in laboratory settings by enabling researchers to study carbohydrate metabolism and the degradation of complex molecules. Its application is fundamental in understanding enzymatic mechanisms and their impact on biological processes.\u003c\/p\u003e\n\u003cp\u003eThe compound is favored for its chemical stability under specific conditions, allowing for consistent results across repeated experiments. Its solubility in organic solvents makes it highly versatile for use in various biochemical reactions. These properties ensure that it remains a reliable and accurate choice for researchers seeking precise and reproducible outcomes. Additionally, its specificity enhances its utility in targeted enzymatic studies, making it a preferred material in both academic and industrial research environments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Naphthol AS-BI beta-D-Glucuronide is commonly used in biomedical, pharmacological, and biotechnological research. It is a key component in experiments related to enzyme activity, metabolic pathways, and drug development. Its widespread application across these fields highlights its importance as a standard reagent in both academic and applied research settings. Researchers in Indonesia rely on this compound for its reliability and effectiveness in producing high-quality experimental data.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eEnzyme Activity Assays: This substrate is ideal for measuring beta-glucuronidase activity, providing accurate and reproducible results in enzyme kinetics studies.\u003c\/li\u003e\n\u003cli\u003eMetabolic Pathway Analysis: Its role in carbohydrate metabolism makes it suitable for investigating metabolic processes in biological systems.\u003c\/li\u003e\n\u003cli\u003eDrug Development Research: It is used in studies to evaluate enzyme interactions and metabolic transformations of pharmaceutical compounds.\u003c\/li\u003e\n\u003cli\u003eBiotechnology Applications: Its specificity supports research in recombinant enzyme systems and bioconversion processes.\u003c\/li\u003e\n\u003cli\u003eBiochemical Screening: It serves as a standard substrate for screening enzyme inhibitors and activators in various experimental setups.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 37-87-6\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Enzymes, Enzyme Inhibitors, Enzyme Substrates\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities\u003c\/li\u003e\n\u003cli\u003ePhysical form: 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 stability. It is recommended to use airtight containers to prevent contamination and degradation. Due to its organic nature, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to ensure laboratory safety. Avoid exposure to heat or prolonged storage in humid conditions to preserve its integrity. Regular inspection of storage conditions is advised to ensure optimal performance in experimental applications. Proper labeling and secure storage are essential to prevent accidental use or contamination.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mg","offer_id":48087846781146,"sku":"TCI2510N088243725","price":1515000.0,"currency_code":"IDR","in_stock":true},{"title":"100mg","offer_id":48087846813914,"sku":"TCI2510N088243726","price":4518000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510N0882.jpg?v=1769181103"},{"product_id":"tci2510o023644601","title":"TCI O0236 30431-54-0 Bis[3,4,6-trichloro-2-(pentyloxycarbonyl)phenyl] Oxalate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBis[3,4,6-trichloro-2-(pentyloxycarbonyl)phenyl] Oxalate is a specialized organic compound used in various laboratory reactions, particularly in the field of organic synthesis. As a building block in chemical research, it plays a crucial role in the development of complex molecular structures. Its unique chemical structure allows it to participate in multiple functional group reactions, making it a valuable tool for chemists seeking to create new compounds with specific properties. This compound is widely utilized in both academic and industrial research settings due to its versatility and reactivity.\u003c\/p\u003e\n\u003cp\u003eThe compound's chemical properties make it a preferred choice for advanced chemical applications. Its molecular structure contains chlorine atoms and a pentyloxycarbonyl group, which contribute to its reactivity and functional versatility. These features enable it to undergo substitution reactions and other organic transformations, making it suitable for a wide range of synthetic pathways. The presence of these functional groups also allows for precise control over reaction outcomes, which is essential in laboratory settings where accuracy and reproducibility are critical.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in organic chemistry research, especially in projects involving the synthesis of pharmaceutical compounds. Its ability to participate in various chemical reactions and its structural complexity make it a key component in the development of new drugs and chemical materials. Researchers in Indonesia rely on this compound for its reliability and effectiveness in complex synthetic processes.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic Synthesis: This compound is ideal for creating complex molecules due to its reactivity and functional group versatility.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical Research: Its structural features make it suitable for drug development and compound modification.\u003c\/li\u003e\n\u003cli\u003eFunctional Group Manipulation: The presence of chlorine and carbonyl groups allows for precise chemical transformations.\u003c\/li\u003e\n\u003cli\u003eAdvanced Chemical Reactions: It supports a variety of synthetic pathways in laboratory settings requiring high precision.\u003c\/li\u003e\n\u003cli\u003eCompound Modification: Its ability to react with different functional groups makes it useful in modifying existing chemical structures.\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: 30431-54-0\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 powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Requires dry, cool storage away from moisture and air exposure\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a dry, cool environment to maintain its chemical stability. It is recommended to keep it in a sealed container to prevent exposure to moisture and air, which can degrade its properties. Due to its sensitivity, it should be handled in a controlled laboratory setting with appropriate safety measures. Avoid direct contact with skin and inhalation of vapors. Proper ventilation is essential when working with this material. 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This material plays a crucial role in the analysis of phosphatase activity, which is essential for studying dephosphorylation processes within cells. In laboratory settings, it is widely utilized to assess the rate of enzymatic reactions and to evaluate the efficiency of phosphatase activity. Its stability and reactivity make it a valuable reagent for both research and diagnostic applications.\u003c\/p\u003e\n\u003cp\u003eThe compound is preferred due to its excellent stability under specific conditions, which simplifies handling and storage. It is also water-soluble, making it easy to dissolve for use in chemical reactions. Its specific chemical properties ensure compatibility with targeted phosphatase enzymes, enhancing its effectiveness in experimental setups. These characteristics collectively make it a reliable and versatile choice for laboratory use.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is extensively used in biochemical research and diagnostic testing. It supports a wide range of studies, including enzyme activity assays and molecular biology experiments. 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It is recommended to use airtight containers to prevent exposure to humidity, which could affect its performance. Due to its water solubility, it should be handled 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 the compound. Proper labeling of containers is essential to ensure safe handling and prevent accidental exposure. Regular monitoring of storage conditions is advised to ensure the compound remains in optimal condition for use in experiments.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087952490714,"sku":"TCI2510P026345559","price":1289000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48087952523482,"sku":"TCI2510P026345560","price":3937000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510P0263.jpg?v=1767132877"},{"product_id":"tci2510p114446750","title":"TCI P1144 615-28-1 1,2-Phenylenediamine Dihydrochloride [for Biochemical Research]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1,2-Phenylenediamine Dihydrochloride is a chemical compound widely used in biochemical research and organic synthesis. It serves as a key building block in the development of complex molecules, particularly in studies involving aromatic amines. This compound is essential for researchers aiming to explore molecular reactivity and structural properties. Its role in laboratory settings is critical, especially in experiments requiring controlled chemical reactions with high reactivity and stability. Due to its versatility, it is frequently utilized in both academic and industrial research environments.\u003c\/p\u003e\n\u003cp\u003eThe compound’s aromatic structure enables it to participate in substitution and condensation reactions, making it a preferred choice for synthetic chemists. Its solubility in organic solvents further enhances its utility in various synthesis processes. These properties allow for greater control over reaction conditions, ensuring consistent results. Additionally, its chemical stability and reactivity make it a reliable material for experiments that demand precise manipulation of chemical processes.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 1,2-Phenylenediamine Dihydrochloride is commonly used in pharmacological, organic chemistry, and biochemical research. It supports studies on molecular interactions and the development of new compounds. Researchers in educational institutions and research organizations rely on this compound for experiments requiring aromatic amines with specific reactivity and structural characteristics.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis experiments benefit from its aromatic structure and reactivity, enabling the creation of complex molecules.\u003c\/li\u003e\n\u003cli\u003eBiochemical research utilizes its properties for studying molecular reactivity and structural behavior in chemical reactions.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical development uses it as a building block for synthesizing compounds with specific functional groups.\u003c\/li\u003e\n\u003cli\u003eAnalytical chemistry applications rely on its solubility and stability for accurate chemical analysis and reaction control.\u003c\/li\u003e\n\u003cli\u003eResearch in molecular biology employs it to investigate interactions between aromatic compounds and biological 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: 615-28-1\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 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 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 stability. It is recommended to use airtight containers to prevent exposure to air and humidity. Due to its potential reactivity, it should be handled with appropriate safety measures, such as wearing gloves and safety goggles. It is important to ensure proper ventilation when working with this material to minimize inhalation risks. Storage conditions should be consistent to avoid degradation and maintain the integrity of the compound for laboratory use. Always follow standard laboratory safety protocols when handling and storing this chemical.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48088030904538,"sku":"TCI2510P114446750","price":581000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510P1144.jpg?v=1767134361"},{"product_id":"tci2510p180547490","title":"TCI P1805 95-54-5 1,2-Phenylenediamine [for Biochemical Research]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1,2-Phenylenediamine is a chemical compound widely used in biochemical and biomedical research. It serves as a key substrate in various chemical reactions, particularly in the development of detection and analysis methods for proteins. In the laboratory, this compound is commonly used as a component in enzymatic reactions and in protein precipitation processes. Its reactivity makes it an essential material for the creation of specialized reagents used in biochemical analysis. Due to its chemical structure, it exhibits stability under certain conditions but is highly sensitive to oxidation and light exposure.\u003c\/p\u003e\n\u003cp\u003eThis compound is preferred for its versatility and reactivity in laboratory settings. Its solubility in organic solvents allows it to be easily incorporated into a wide range of experimental procedures. The ability to participate in multiple chemical reactions makes it a valuable tool for researchers working on enzyme activity studies and molecular interaction analyses. Its chemical properties also support its use in the development of analytical methods, enhancing the accuracy and reliability of experimental results.\u003c\/p\u003e\n\u003cp\u003eIn the context of research in Indonesia, 1,2-Phenylenediamine is a crucial material in biochemical and pharmaceutical laboratories. It is frequently used by research institutions and universities for enzyme activity studies, analytical method development, and molecular interaction research. Its availability and chemical properties make it a reliable choice for scientists conducting advanced biochemical experiments in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eEnzymatic Reaction Studies – This compound is ideal for studying enzyme activity due to its reactivity and ability to participate in enzymatic processes.\u003c\/li\u003e\n\u003cli\u003eProtein Precipitation – It is commonly used in protein precipitation techniques to isolate and analyze specific proteins in solution.\u003c\/li\u003e\n\u003cli\u003eBiochemical Reagent Development – Its chemical properties make it suitable for creating specialized reagents used in analytical methods.\u003c\/li\u003e\n\u003cli\u003eMolecular Interaction Research – The compound's ability to form complexes with other molecules supports studies on molecular interactions.\u003c\/li\u003e\n\u003cli\u003eDetection and Analysis Methods – It serves as a substrate in the development of detection methods for proteins and other biomolecules.\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: 95-54-5\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Antibodies \u0026gt; Antibody Supplementary Products\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: Must be stored in a cool, dark place to prevent oxidation and degradation.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003e1,2-Phenylenediamine should be stored in a cool, dark environment to prevent oxidation and maintain its chemical integrity. It is recommended to use airtight containers to minimize exposure to air and light, which can lead to degradation. Due to its reactivity, it should be handled with care and stored away from strong oxidizing agents. Proper labeling of containers is essential for safety and traceability. Laboratory personnel should wear appropriate personal protective equipment, such as gloves and safety goggles, when handling this compound. Regular monitoring of storage conditions ensures the compound remains stable and suitable for use in research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48088074748122,"sku":"TCI2510P180547490","price":708000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48088074780890,"sku":"TCI2510P180547491","price":1792000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510P1805.jpg?v=1767135262"},{"product_id":"tci2510s081750447","title":"TCI S0817 82611-85-6 Sodium 3-(N-Ethylanilino)propanesulfonate [for Biochemical Research]","description":"\u003cp\u003e\u003cstrong\u003eSodium 3-(N-Ethylanilino)propanesulfonate [for Biochemical Research]\u003c\/strong\u003e (CAS 82611-85-6) is a high-quality chemical from TCI, supplied as \u003cstrong\u003eHPLC Grade\u003c\/strong\u003e.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eApplication:\u003c\/strong\u003e Synthesis reagent for a wide range of organic chemistry transformations in laboratory and industrial settings.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eSpecifications:\u003c\/strong\u003e\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003eMolecular formula: C11H16NNaO3S\u003c\/li\u003e\n\u003cli\u003eCAS number: 82611-85-6\u003c\/li\u003e\n\u003cli\u003ePurity: \u0026gt;98.0%(HPLC)\u003c\/li\u003e\n\u003cli\u003eTCI product code: S0817\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003e\u003cstrong\u003eSynonyms:\u003c\/strong\u003e 3-(N-Ethylanilino)propanesulfonic Acid Sodium Salt; 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