{"title":"Linear Alkyl Sources [Material Building Blocks]","description":"\u003cp\u003e\u003cstrong\u003eLinear Alkyl Sources [Material Building Blocks]\u003c\/strong\u003e — berisi asam lemak rantai lurus, alkil halida, dan alkilamina dengan rantai karbon panjang yang berfungsi sebagai blok bangun untuk menyisipkan gugus alkil hidrofobik ke dalam suatu molekul. Senyawa ini menjadi sumber rantai alkil pada modifikasi kelarutan dan sifat permukaan material.\u003c\/p\u003e\u003cp\u003eLinear Alkyl Sources dipakai peneliti material dan kimia organik untuk sintesis surfaktan, alkilasi senyawa aromatik atau heteroatom, serta pembentukan lapisan monolayer rakitan mandiri (self-assembled monolayer). Asam lemak seperti asam stearat dan palmitat juga digunakan sebagai model rantai lipid pada riset material lunak dan formulasi berbasis alkil rantai panjang.\u003c\/p\u003e\u003cp\u003eContoh produk dalam koleksi ini: \u003ca href=\"\/en\/products\/tci2510s016350046\"\u003eTCI S0163 57-11-4 Stearic Acid\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510c014214104\"\u003eTCI C0142 109-69-3 1-Chlorobutane\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510m047638178\"\u003eTCI M0476 544-63-8 Myristic Acid\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510c016314132\"\u003eTCI C0163 112-52-7 1-Chlorododecane\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510p114546751\"\u003eTCI P1145 57-10-3 Palmitic Acid\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510c018214161\"\u003eTCI C0182 629-06-1 1-Chloroheptane\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510a0445643\"\u003eTCI A0445 110-58-7 Amylamine\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510c018314163\"\u003eTCI C0183 4860-03-1 1-Chlorohexadecane\u003c\/a\u003e.\u003c\/p\u003e\u003cp\u003ePerhatikan panjang rantai karbon, kemurnian, serta bentuk fisik senyawa (padat atau cair) karena keduanya menentukan kemudahan penanganan dan kesesuaian dengan reaksi alkilasi yang direncanakan. 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 Solubility Enhancing Reagents [Material Building Blocks], sering dipakai bersamaan dalam satu alur kerja laboratorium:\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-branched-alkyl-sources-material-building-blocks\"\u003eBranched Alkyl Sources [Material Building Blocks]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-fluorinated-alkyl-sources-material-building-blocks\"\u003eFluorinated Alkyl Sources [Material Building Blocks]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-dialkyldichlorosilanes-material-building-blocks\"\u003eDialkyldichlorosilanes [Material Building Blocks]\u003c\/a\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eKembali ke \u003ca href=\"\/en\/collections\/tci-l3-solubility-enhancing-reagents-material-building-blocks\"\u003eSolubility Enhancing Reagents [Material Building Blocks]\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":"tci2510c014214104","title":"TCI C0142 109-69-3 1-Chlorobutane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0142, 1-Chlorobutane (CAS 109-69-3), is a clear, volatile primary alkyl chloride supplied as a liquid. It is widely used as a butylating agent, as the starting material for butylmagnesium chloride Grignard reagent, and as a low-polarity solvent for extraction and chromatography. The compound is flammable and must be handled in a fume hood away from ignition sources and stored in a dedicated flammables cabinet. AMI Scientific supplies it in 25 mL and 500 mL packs in original manufacturer packaging for research, analytical, and teaching laboratories in Indonesia.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eGuerrero et al. (2015). Excess properties from pρT data for n-heptane+isomeric chlorobutane mixtures. \u003cem\u003eThermochimica Acta\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.tca.2015.06.017\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.tca.2015.06.017\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eKar et al. (2023). Cl atoms-initiated degradation of 1-Chlorobutane and 2-Chlorobutane: Kinetics, product analysis and atmospheric implications. \u003cem\u003eChemosphere\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.chemosphere.2023.139664\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.chemosphere.2023.139664\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eWisniak (1995). Isobaric vapor-liquid equilibria in the binary systems propyl bromide-i-butanol, propyl bromide-1-chlorobutane and 1-chlorobutane-methyl ethyl ketone. \u003cem\u003eThermochimica Acta\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/0040-6031(94)02209-7\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/0040-6031(94)02209-7\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mL","offer_id":48085973532890,"sku":"TCI2510C014214104","price":479000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48085973565658,"sku":"TCI2510C014214105","price":704000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0142.jpg?v=1767094761"},{"product_id":"tci2510c016314132","title":"TCI C0163 112-52-7 1-Chlorododecane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI 1-Chlorododecane (CAS 112-52-7), also known as lauryl chloride, is a long-chain alkyl halide widely used to introduce a C12 hydrophobic chain into target molecules. Its terminal chlorine is readily displaced by amines, alcohols, thiols and phenolates, making it a staple reagent for surfactant and quaternary ammonium salt synthesis. The product is available in 25 mL and 500 mL packages for both small-scale research and routine preparative work. Handle it in a fume hood with chemical-resistant gloves and eye protection, keep it away from ignition sources, and store the tightly closed container in a cool, dry, well-ventilated place.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eTurro et al. (1995). Mechanism of Dichlorination of n-Dodecane and Chlorination of 1-Chlorododecane Adsorbed on ZSM-5 Zeolite Molecular Sieves. A Supramolecular Structural Interpretation. \u003cem\u003eJournal of the American Chemical Society\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1021\/ja00122a020\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1021\/ja00122a020\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mL","offer_id":48085974581466,"sku":"TCI2510C016314132","price":507000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48085974614234,"sku":"TCI2510C016314133","price":1322000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0163.jpg?v=1769144586"},{"product_id":"tci2510c018214161","title":"TCI C0182 629-06-1 1-Chloroheptane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0182 1-Chloroheptane, CAS 629-06-1, is a straight-chain primary alkyl chloride used as a practical building block in organic synthesis. It serves as an alkylating agent for introducing an n-heptyl chain and as a precursor for organometallic reagents such as Grignard reagents. AMI Scientific offers 25 mL and 500 mL packs to suit both method development and routine synthetic work. Handle it in a fume hood with protective equipment, keep it away from ignition sources and strong oxidizers, and store it tightly closed in a cool, dry, well-ventilated area.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMelent'ev et al. (2020). Density and speed of sound of 3‑chloroheptane in the range of temperatures 233.15−393.15 K and pressures up to 196.2 MPa. \u003cem\u003eChemical Data Collections\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.cdc.2020.100451\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.cdc.2020.100451\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eSlabbinck et al. (2000). Proton acceptor site selectivity in the proton transfer from heptane radical cations to decane molecules in γ-irradiated heptane\/decane\/1-chloroheptane crystals at 77 K. \u003cem\u003eJournal of the Chemical Society, Perkin Transactions 2\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1039\/b004829l\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1039\/b004829l\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mL","offer_id":48085975826650,"sku":"TCI2510C018214161","price":564000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48085975859418,"sku":"TCI2510C018214162","price":5623000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0182.jpg?v=1768816155"},{"product_id":"tci2510c018314163","title":"TCI C0183 4860-03-1 1-Chlorohexadecane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0183 1-Chlorohexadecane, CAS 4860-03-1, is a long-chain primary alkyl chloride, also known as cetyl chloride, valued for its strongly hydrophobic C16 chain. It is widely used to prepare cationic surfactants, quaternary ammonium salts, organoclays, and other amphiphilic or soft-matter materials. AMI Scientific supplies 25 mL and 500 mL packs for both exploratory and routine synthetic work. Handle it with standard protective equipment in a well-ventilated area, keep the container tightly closed, and store it in a cool, dry place away from strong oxidizers.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eGonçalves da Silva et al. (1996). Mixed Monolayers of Heptadecanoic Acid with Chlorohexadecane and Bromohexadecane. Effects of Temperature and of Metal Ions in the Subphase. \u003cem\u003eLangmuir\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1021\/la960258w\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1021\/la960258w\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eAkimoto et al. (2000). Dechlorination of 1‐chlorohexadecane and 2‐chloronaphthalene in water under sub‐ and supercritical conditions. \u003cem\u003eThe Canadian Journal of Chemical Engineering\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/cjce.5450780617\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/cjce.5450780617\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eSapunov et al. (2024). Formation of esters by the Baeyer–Villiger reaction during oxidation of 1-chlorohexadecane with air oxygen in the presence of cobalt hydroxystearate– N-hydroxyphthalimide catalytic system. \u003cem\u003eŽurnal obŝej himii\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.31857\/s0044460x24050134\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.31857\/s0044460x24050134\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mL","offer_id":48085975924954,"sku":"TCI2510C018314163","price":816000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48085975957722,"sku":"TCI2510C018314164","price":2615000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0183.jpg?v=1768816156"},{"product_id":"tci2510c018414165","title":"TCI C0184 544-10-5 1-Chlorohexane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0184 1-Chlorohexane, CAS 544-10-5, is a simple primary alkyl chloride widely used as a building block in organic synthesis. It supports nucleophilic substitution reactions for introducing an n-hexyl group and serves as a precursor to hexylmagnesium chloride in Grignard chemistry. AMI Scientific offers 25 mL and 500 mL packs to match occasional and routine laboratory use. The liquid is flammable, so handle it in a fume hood away from ignition sources and store it tightly closed in a cool, dry, well-ventilated area.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBolotnikov et al. (2003). Speed of Sound of Hexane + 1-Chlorohexane, Hexane + 1-Iodohexane, and 1-Chlorohexane + 1-Iodohexane at Saturation Condition. \u003cem\u003eJournal of Chemical \u0026amp; Engineering Data\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1021\/je0256129\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1021\/je0256129\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eQuiñonez et al. (2017). Thermochemistry and Kinetics of the Thermal Decomposition of 1‐Chlorohexane. \u003cem\u003eInternational Journal of Chemical Kinetics\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/kin.21111\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/kin.21111\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eBolotnikov et al. (2004). Relative Permittivity for 1-Chlorohexane, 1-Iodohexane, 1-Iodoheptane, and 1-Chlorononane from (293.15 to 373.15) K and Hexane + 1-Chlorohexane from (293.15 to 333.15) K. \u003cem\u003eJournal of Chemical \u0026amp; Engineering Data\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1021\/je034205+\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1021\/je034205+\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mL","offer_id":48085975990490,"sku":"TCI2510C018414165","price":620000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48085976023258,"sku":"TCI2510C018414166","price":3626000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0184.jpg?v=1768816158"},{"product_id":"tci2510c023314242","title":"TCI C0233 2473-01-0 1-Chlorononane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0233 1-Chlorononane (CAS 2473-01-0) is a linear primary alkyl chloride bearing a terminal chlorine on a nine-carbon chain. Its primary halide character makes it a dependable SN2 alkylating agent toward amines, thiolates, cyanide, and carboxylate nucleophiles. It can also be converted to the corresponding Grignard reagent for carbon–carbon bond formation, or reacted with tertiary amines to give cationic surfactants. TCI supplies it in 25 mL and 500 mL pack sizes for synthetic, surfactant, and materials research.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBolotnikov et al. (2007). Temperature Dependence of the Speed of Sound of Nonane + 1-Chlorononane in the Range of (293.15 to 423.15) K. \u003cem\u003eJournal of Chemical \u0026amp; Engineering Data\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1021\/je700021f\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1021\/je700021f\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eBolotnikov et al. (2006). Kinematic Viscosity of 1-Iodohexane, 1-Iodoheptane, and 1-Chlorononane at Temperatures from (293.15 to 423.15) K. \u003cem\u003eJournal of Chemical \u0026amp; Engineering Data\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1021\/je060158k\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1021\/je060158k\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eBolotnikov et al. (2004). Temperature Dependence of the Thermophysical Properties of 1-Chlorohexane, 1-Iodohexane, 1-Iodoheptane, and 1-Chlorononane at Saturation Condition. \u003cem\u003eJournal of Chemical \u0026amp; Engineering Data\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1021\/je034013e\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1021\/je034013e\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mL","offer_id":48085981364442,"sku":"TCI2510C023314242","price":2503000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48085981397210,"sku":"TCI2510C023314243","price":19253000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0233.jpg?v=1769144576"},{"product_id":"tci2510c023514244","title":"TCI C0235 3386-33-2 1-Chlorooctadecane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0235 1-Chlorooctadecane (CAS 3386-33-2) is a long-chain primary alkyl chloride carrying an eighteen-carbon hydrophobic tail. The terminal chloride is readily displaced by nucleophiles to give long-chain amines, ethers, esters, and thioethers. It is widely used to prepare cationic surfactants, hydrophobic surface modifiers, and amphiphilic materials whose chain length mimics natural fatty acids. TCI provides it in 25 mL and 500 mL pack sizes; the material may solidify in cool conditions and should be warmed gently before use.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAikawa et al. (2001). Catalytic dechlorination of 1-chlorooctadecane in supercritical carbon dioxide. \u003cem\u003eApplied Catalysis B: Environmental\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/s0926-3373(01)00151-5\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/s0926-3373(01)00151-5\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eAubert et al. (2004). Incorporation of 1‐chlorooctadecane into FA and β‐hydroxy acids of Marinobacter hydrocarbonoclasticus. \u003cem\u003eLipids\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1007\/s11745-004-1204-8\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1007\/s11745-004-1204-8\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003ePeters et al. (1993). The Production of Stable Monolayers from Nonamphiphilic 1-Chlorooctadecane. \u003cem\u003eJournal of Colloid and Interface Science\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1006\/jcis.1993.1216\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1006\/jcis.1993.1216\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mL","offer_id":48085981429978,"sku":"TCI2510C023514244","price":788000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48085981462746,"sku":"TCI2510C023514245","price":2503000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0235.jpg?v=1769180298"},{"product_id":"tci2510c023614246","title":"TCI C0236 111-85-3 1-Chlorooctane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0236 1-Chlorooctane (CAS 111-85-3) is a straight-chain primary alkyl chloride used as a versatile non-heterocyclic building block. It serves as a convenient precursor to octylmagnesium chloride and as an alkylating agent for introducing an eight-carbon chain onto nucleophilic substrates. The reagent is also valued in surfactant and quaternary ammonium salt preparation, where its hydrophobic tail is essential. AMI Scientific offers this TCI product in 25 mL and 500 mL bottles to suit both exploratory and routine synthetic work.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSingh et al. (2010). Vibrational analysis of 1-chlorooctane. \u003cem\u003eIndian Journal of Physics\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1007\/s12648-010-0116-x\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1007\/s12648-010-0116-x\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eHara et al. (2024). Temperature-dependent chlorosomal self-aggregation of bacteriochlorophyll-d analogs with a branched alkyl chain in a single 1-chlorooctane solvent. \u003cem\u003eBulletin of the Chemical Society of Japan\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1093\/bulcsj\/uoae032\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1093\/bulcsj\/uoae032\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eRolińska et al. (2004). Solubilities of Some Long-Chain n-Alkanes in Dipropyl Ether, Dibutyl Ether, 1-Chlorobutane, and 1-Chlorooctane as Functions of Temperature. \u003cem\u003eJournal of Chemical \u0026amp; Engineering Data\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1021\/je030206q\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1021\/je030206q\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mL","offer_id":48085981561050,"sku":"TCI2510C023614246","price":507000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48085981593818,"sku":"TCI2510C023614247","price":1827000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0236.jpg?v=1769144574"},{"product_id":"tci2510c023714248","title":"TCI C0237 543-59-9 1-Chloropentane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0237 1-Chloropentane (CAS 543-59-9) is a primary five-carbon alkyl chloride used as a general-purpose building block in organic synthesis. It reacts cleanly in nucleophilic substitution and serves as a starting material for pentylmagnesium chloride in Grignard chemistry. Its moderate chain length makes derived products convenient to purify by distillation, which is useful in both research and teaching laboratories. AMI Scientific supplies this TCI reagent in 25 mL and 500 mL packs, with handling under a fume hood strongly recommended.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eGiner et al. (2007). Isothermal vapour–liquid equilibrium for cyclic ethers with 1-chloropentane. \u003cem\u003eFluid Phase Equilibria\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.fluid.2006.10.024\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.fluid.2006.10.024\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eMilinkevich et al. (2008). ChemInform Abstract: Synthesis of 5‐(Thiazol‐5‐yl)‐4,5‐dihydroisoxazoles from 3‐Chloropentane‐2,4‐dione.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.200848128\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.200848128\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eLorenzana et al. (1993). Excess molar volumes of (1-chloropentane or 1-chlorohexane + heptane + decane) at the temperature 298.15 K. \u003cem\u003eThe Journal of Chemical Thermodynamics\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1006\/jcht.1993.1100\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1006\/jcht.1993.1100\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mL","offer_id":48085981659354,"sku":"TCI2510C023714248","price":704000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48085981692122,"sku":"TCI2510C023714249","price":4273000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0237.jpg?v=1769144574"},{"product_id":"tci2510c059914806","title":"TCI C0599 2473-03-2 1-Chloroundecane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0599 1-Chloroundecane (CAS 2473-03-2) is a long-chain primary alkyl chloride carrying eleven carbon atoms. It is commonly used as an alkylating agent to attach a hydrophobic undecyl chain to oxygen, nitrogen, or sulfur nucleophiles, and can also be converted into organometallic reagents such as Grignard reagents. These properties make it valuable in surfactant synthesis, quaternary ammonium chemistry, and surface or materials research. AMI Scientific supplies this TCI building block in a 25 g research pack.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086012625114,"sku":"TCI2510C059914806","price":1715000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0599.jpg?v=1768816280"},{"product_id":"tci2510c060014807","title":"TCI C0600 1002-69-3 1-Chlorodecane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0600 1-Chlorodecane (CAS 1002-69-3) is a primary alkyl chloride with a ten-carbon chain. It is widely used for alkylation reactions, for preparing organometallic reagents, and for building the hydrophobic portion of surfactants and amphiphilic molecules. Its predictable behaviour also makes it a convenient working comparison substance in gas chromatography method development and in nucleophilic substitution studies. AMI Scientific offers this TCI building block in 25 mL and 500 mL packs.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eZhang et al. (2019). Photochemical degradation kinetics and mechanism of short-chain chlorinated paraffins in aqueous solution: A case of 1-chlorodecane. \u003cem\u003eEnvironmental Pollution\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.envpol.2019.01.065\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.envpol.2019.01.065\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eWang et al. (2021). Increased adverse effects during metabolic transformation of short-chain chlorinated paraffins by cytochrome P450: A theoretical insight into 1-chlorodecane. \u003cem\u003eJournal of Hazardous Materials\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.jhazmat.2020.124391\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.jhazmat.2020.124391\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eHolgado et al. (1993). Excess molar volumes and viscosities for the n-decane + 1-chlorodecane system at different temperatures. \u003cem\u003eCanadian Journal of Chemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1139\/v93-104\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1139\/v93-104\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mL","offer_id":48086012657882,"sku":"TCI2510C060014807","price":985000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48086012690650,"sku":"TCI2510C060014808","price":6437000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0600.jpg?v=1768816283"},{"product_id":"tci2510c062214829","title":"TCI C0622 2425-54-9 1-Chlorotetradecane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0622 1-Chlorotetradecane is a long-chain primary alkyl chloride used to introduce a fourteen-carbon hydrophobic tail into target molecules. It is commonly reacted with amines to prepare quaternary ammonium surfactants and phase-transfer catalysts, and can also serve as a Grignard reagent precursor. Its strongly hydrophobic chain makes it relevant to surface chemistry and self-assembly research. Supplied as a liquid in 25 mL and 500 mL packs, it should be handled in a fume hood and stored away from heat and ignition sources.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eRoshan Deen et al. (2009). Phase Behavior and Kinetics of Phase Separation of a Nonionic Microemulsion of C12E5\/Water\/1-Chlorotetradecane upon a Temperature Quench. \u003cem\u003eThe Journal of Physical Chemistry B\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1021\/jp808268m\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1021\/jp808268m\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mL","offer_id":48086015017178,"sku":"TCI2510C062214829","price":536000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48086015049946,"sku":"TCI2510C062214830","price":2784000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0622.jpg?v=1768816291"},{"product_id":"tci2510c082915116","title":"TCI C0829 506-46-7 Cerotic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0829 Cerotic Acid (CAS 506-46-7), also known as hexacosanoic acid, is a very-long-chain saturated fatty acid supplied in 1 g and 10 g packs. Its waxy character and long carbon chain make it a useful reference material in lipidomics, peroxisomal metabolism research, and studies of natural waxes. Laboratories commonly derivatise it to the corresponding methyl ester before gas chromatographic analysis, or use it directly in material and cosmetic formulation research. Weigh it with gloves and eye protection, avoid dust generation, and keep the container tightly closed in a cool, dry place.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eThirunakaran et al. (2016). Cerotic acid assisted sol-gel synthesis and electrochemical performance of double doped spinels (LiCrxMgyMn2-x-yO4) as cathode materials for lithium rechargeable batteries. \u003cem\u003ePowder Technology\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.powtec.2016.05.064\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.powtec.2016.05.064\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eMika et al. (2017). Hyper-Elongation in Colorectal Cancer Tissue – Cerotic Acid is a Potential Novel Serum Metabolic Marker of Colorectal Malignancies. \u003cem\u003eCellular Physiology and Biochemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1159\/000458431\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1159\/000458431\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eKong et al. (2021). Improving stability and efficiency of perovskite solar cells via a cerotic acid interfacial layer. \u003cem\u003eSurfaces and Interfaces\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.surfin.2021.101163\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.surfin.2021.101163\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086032089306,"sku":"TCI2510C082915116","price":5369000.0,"currency_code":"IDR","in_stock":true},{"title":"10g","offer_id":48086032122074,"sku":"TCI2510C082915117","price":24228000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0829.jpg?v=1767095852"},{"product_id":"tci2510c221316898","title":"TCI C2213 822-13-9 1-Chlorotridecane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1-Chlorotridecane (TCI C2213) is a straight-chain alkyl chloride carrying thirteen carbon atoms with a chlorine atom placed at the terminal position of the chain. The compound belongs to the family of primary haloalkanes that form the backbone of many alkylation reactions in the laboratory. Its role is to deliver a long hydrocarbon chain directly onto a target molecule, allowing researchers to adjust the lipophilicity, the length of a hydrophobic tail, or the interfacial behaviour of a compound. For that reason it is widely used in surfactant research, colloid chemistry, and the synthesis of long-chain materials.\u003c\/p\u003e\n\u003cp\u003eThe property that makes this reagent a preferred choice is the characteristic reactivity of a primary halide. Because the chlorine sits at the end of the chain, the molecule undergoes bimolecular nucleophilic substitution with minimal steric hindrance, so reactions with amines, thiols, alkoxides, phenoxides, or carbanions proceed cleanly with a limited range of side products. The long C13 chain confers strong lipophilic character and a high boiling point, which makes the compound straightforward to separate from lighter solvents during purification. As a material that is liquid at room temperature, it is also convenient to measure with a pipette whenever gradual addition is required.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent is used in university research groups, government research institutes, and industrial development laboratories that work on synthetic organic chemistry. It commonly appears in projects on surfactant development, colloid and interface studies, and the preparation of long-chain intermediates for further functionalisation. Because it is supplied as a liquid, it fits routine bench-scale work where reagents are dispensed by pipette and reactions are run in standard glassware under normal laboratory conditions.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSurfactant research: the terminal chlorine allows a thirteen-carbon hydrophobic tail to be attached to a polar head group, producing amphiphilic molecules for detergency and micelle studies.\u003c\/li\u003e\n\u003cli\u003eN-alkylation of amines: as a primary halide with minimal steric hindrance, it reacts cleanly with primary and secondary amines to build long-chain alkylammonium and amine derivatives.\u003c\/li\u003e\n\u003cli\u003eThioether synthesis: thiols and thiolate anions displace the terminal chloride efficiently, giving long-chain sulfides used in colloid chemistry and surface-modification research.\u003c\/li\u003e\n\u003cli\u003eEther preparation via Williamson synthesis: alkoxides and phenoxides substitute the chloride readily, delivering long-chain alkyl ethers with a limited number of competing side products.\u003c\/li\u003e\n\u003cli\u003eCarbon-chain extension: carbanion nucleophiles attack the terminal carbon to introduce a C13 unit, letting chemists tune lipophilicity and interfacial behaviour of a target molecule.\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: 822-13-9\u003c\/li\u003e\n\u003cli\u003eProduct code: C2213\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePhysical form: liquid at room temperature\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in standard TCI catalogue pack sizes; please confirm the pack size when ordering\u003c\/li\u003e\n\u003cli\u003eStorage: keep tightly closed in a cool, dry, 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, dry, and well-ventilated area, away from heat sources, open flames, and direct sunlight. Keep it separated from strong oxidising agents and strong bases. Original manufacturer bottles or chemically compatible glass containers with tight-sealing caps are suitable; label every transfer container clearly. Handle the liquid inside a fume hood and wear safety glasses, chemical-resistant gloves, and a laboratory coat. Use clean, dry pipettes for dispensing, close the bottle immediately after use, and consult the manufacturer's safety data sheet before starting work.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086111650010,"sku":"TCI2510C221316898","price":2924000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2213.jpg?v=1768816803"},{"product_id":"tci2510d001719297","title":"TCI D0017 334-48-5 Decanoic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eDecanoic Acid (TCI D0017, CAS 334-48-5) is an organic compound that exists as a solid with a linear carbon chain and a carboxyl group at one end. It serves as a fundamental building block in organic chemistry, widely used in laboratory settings for the synthesis of complex molecules. Its versatility makes it a key component in various chemical reactions, supporting the development of esters, amides, and heterocyclic compounds. As a core reagent, it plays a crucial role in both academic and industrial research environments.\u003c\/p\u003e\n\u003cp\u003eDecanoic Acid is prized for its chemical stability and resistance to common reagents, which simplifies handling and storage. Its high melting point ensures thermal stability, making it suitable for use in environments requiring controlled temperature conditions. Additionally, its non-toxic nature and ease of manipulation contribute to its safety profile, making it a preferred choice for both educational and research applications. These properties collectively enhance its reliability and effectiveness in laboratory workflows.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Decanoic Acid is extensively utilized in educational institutions and research facilities. It is commonly found in chemistry, pharmacy, and chemical engineering programs, where it is used to teach and conduct synthesis experiments. Its role in molecular characterization through techniques like IR and NMR spectroscopy further underscores its importance in analytical and synthetic chemistry. Its widespread use highlights its significance in advancing scientific knowledge and practical skills.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis is a primary application where Decanoic Acid serves as a versatile building block for creating complex molecules, especially in the development of esters and amides.\u003c\/li\u003e\n\u003cli\u003eMolecular characterization techniques, such as IR and NMR spectroscopy, benefit from Decanoic Acid due to its stable structure and predictable chemical behavior.\u003c\/li\u003e\n\u003cli\u003eEducational laboratories use Decanoic Acid to teach fundamental organic chemistry concepts, including functional group transformations and reaction mechanisms.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research incorporates Decanoic Acid in the synthesis of drug-related compounds, leveraging its chemical stability and reactivity.\u003c\/li\u003e\n\u003cli\u003eAnalytical chemistry applications rely on Decanoic Acid for standardization and as a reference material in various analytical procedures.\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: 334-48-5\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory supply\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct sunlight and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eDecanoic Acid should be stored in a cool, dry environment to maintain its chemical stability and prevent degradation. It is recommended to use airtight containers to protect it from moisture and contaminants. Due to its solid form, it is typically stored in sealed glass or plastic containers that are resistant to chemical reactions. Laboratory personnel should handle it with care, using appropriate personal protective equipment such as gloves and safety goggles. While it is non-toxic, proper handling ensures safety and maintains the integrity of the material during experiments. Its stable nature allows for long-term storage without significant changes in properties, making it a reliable reagent for consistent laboratory use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086331588826,"sku":"TCI2510D001719297","price":507000.0,"currency_code":"IDR","in_stock":true},{"title":"400g","offer_id":48086331621594,"sku":"TCI2510D001719298","price":760000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D0017.jpg?v=1767100652"},{"product_id":"tci2510d003119319","title":"TCI D0031 112-30-1 1-Decanol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1-Decanol is an organic compound widely utilized in various chemical experiments conducted in laboratories. As a key component in chemical synthesis, it serves as a foundational building block for the creation of more complex molecules. This versatile compound is commonly used as a precursor in the synthesis of esters, ethers, and other functional group-containing compounds. Its role in laboratory settings is critical for researchers and chemists who require reliable and stable reagents for their experiments.\u003c\/p\u003e\n\u003cp\u003eThe chemical properties of 1-Decanol make it a preferred choice for many laboratory applications. It exhibits neutral and non-reactive characteristics under normal conditions, which enhances its compatibility with a wide range of experimental setups. Additionally, its relatively high boiling point allows it to be used in reactions that require elevated temperatures. These properties contribute to its reliability and safety, making it a standard material in chemical laboratories.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 1-Decanol is frequently used in chemical research, educational institutions, and the pharmaceutical industry. Its availability and cost-effectiveness make it a practical choice for both academic and industrial applications. It is also integrated into ongoing research programs at various institutions, supporting advancements in chemical science and related fields.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eChemical synthesis: 1-Decanol is commonly used in the synthesis of esters and ethers due to its stability and reactivity in controlled environments.\u003c\/li\u003e\n\u003cli\u003eOrganic chemistry experiments: It serves as a starting material for creating more complex organic compounds, supporting educational and research activities.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research: The compound is used in the development of new drugs and chemical intermediates due to its versatile chemical properties.\u003c\/li\u003e\n\u003cli\u003eAnalytical testing: It is used as a solvent or standard in analytical procedures to ensure accurate and reproducible results.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical production: It is a key component in the manufacturing of various chemical products, including surfactants and 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: 112-30-1\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory supply sizes\u003c\/li\u003e\n\u003cli\u003ePhysical form: Liquid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct sunlight and incompatible materials\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003e1-Decanol should be stored in a cool, dry place, away from direct sunlight and sources of heat. It is recommended to keep the container tightly sealed to prevent evaporation and contamination. The compound should be stored in a well-ventilated area to ensure safe handling. It is important to avoid contact with incompatible substances such as strong oxidizers or acids. Proper labeling of containers is essential for safety and identification. Always use appropriate personal protective equipment when handling this material to minimize exposure risks.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mL","offer_id":48086333391066,"sku":"TCI2510D003119319","price":536000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48086333423834,"sku":"TCI2510D003119320","price":873000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D0031.jpg?v=1769144219"},{"product_id":"tci2510d096320635","title":"TCI D0963 112-85-6 Behenic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBehenic Acid (TCI D0963, CAS 112-85-6) is a chemical compound widely used in laboratory settings for various chemical experiments, particularly in organic synthesis. As a saturated fatty acid, it plays a crucial role in the development of esters, surfactants, and polymers due to its long molecular structure. Its chemical stability and non-reactive nature make it a reliable component in chemical research, enabling scientists to manipulate and store it over extended periods without degradation.\u003c\/p\u003e\n\u003cp\u003eOne of the key reasons behenic acid is preferred in laboratories is its chemical stability and non-polar characteristics. These properties allow it to dissolve non-polar compounds effectively, making it valuable in extraction and separation processes. Its inertness also ensures compatibility with a wide range of reagents, reducing the risk of unwanted side reactions. Additionally, its solid form facilitates easy handling and measurement, enhancing its usability in both academic and industrial research environments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, behenic acid is commonly used in chemical research and development. It is a staple in academic institutions and research centers where organic chemistry experiments are conducted. Its versatility and reliability make it a popular choice for both teaching and advanced research applications. Its availability in solid form and ease of use further contribute to its widespread adoption in the Indonesian scientific community.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis where long-chain fatty acids are needed for esterification and polymer formation.\u003c\/li\u003e\n\u003cli\u003eSurfactant and emulsifier production due to its ability to interact with both polar and non-polar substances.\u003c\/li\u003e\n\u003cli\u003ePolymer research for creating materials with specific physical and chemical properties.\u003c\/li\u003e\n\u003cli\u003eSpectroscopic and chromatographic analysis as a reference standard for compound identification.\u003c\/li\u003e\n\u003cli\u003eExtraction and purification processes for isolating non-polar compounds from complex mixtures.\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: 112-85-6\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory supply\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct sunlight and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eBehenic acid should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to use airtight containers to prevent moisture absorption and contamination. Due to its non-polar nature, it should be kept away from reactive substances to avoid unintended chemical interactions. Proper labeling of storage containers is essential for safety and traceability. In laboratory settings, it is important to handle it with appropriate personal protective equipment to ensure safe usage. Regular inspection of storage conditions helps in maintaining the integrity of the compound over time.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086415278298,"sku":"TCI2510D096320635","price":507000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48086415311066,"sku":"TCI2510D096320636","price":1181000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D0963.jpg?v=1767102327"},{"product_id":"tci2510d097820659","title":"TCI D0978 112-53-8 1-Dodecanol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1-Dodecanol is a chemical compound widely used as a foundational material in various chemical reactions and the synthesis of complex molecules. As a long-chain alcohol, it possesses a stable molecular structure that makes it a valuable precursor in the creation of other organic compounds. In the laboratory, 1-Dodecanol plays a crucial role in organic chemistry research, particularly in the synthesis of compounds with complex hydrocarbon chains. Its versatility and chemical stability make it an essential component in many synthetic processes.\u003c\/p\u003e\n\u003cp\u003eThe properties of 1-Dodecanol that make it a preferred choice include its solubility in organic solvents such as ethyl acetate and chloroform, as well as its non-polar nature. These characteristics allow it to be effectively used in solvent systems and specific chemical reactions where polarity is a key factor. Additionally, its relatively high boiling point ensures good thermal stability, making it suitable for use in high-temperature laboratory conditions. This stability contributes to its reliability in a wide range of experimental setups.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 1-Dodecanol is a vital material for both fundamental and applied chemical research. It is commonly used in experiments related to organic synthesis, chemical material development, and performance testing of materials in various industries. Its availability and consistent performance make it a go-to compound for researchers and students alike.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of hydrocarbon-based compounds due to its stable molecular structure and long carbon chain.\u003c\/li\u003e\n\u003cli\u003ePreparation of solvent systems where non-polar solvents are required for dissolving specific organic compounds.\u003c\/li\u003e\n\u003cli\u003eDevelopment of chemical materials in industrial applications requiring high thermal stability and solubility.\u003c\/li\u003e\n\u003cli\u003eResearch in polymer chemistry for creating long-chain polymers and modifying existing polymer structures.\u003c\/li\u003e\n\u003cli\u003eTesting of material performance in the chemical industry for assessing compatibility and reactivity under different conditions.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 112-53-8\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: Liquid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003e1-Dodecanol should be stored in a cool, dry location, away from direct sunlight and sources of heat. It is recommended to use airtight containers made of glass or high-density polyethylene to prevent contamination and evaporation. Due to its non-polar nature, it is important to ensure proper ventilation when handling the compound to avoid inhalation of vapors. In laboratory settings, it should be kept in a well-ventilated area, and appropriate personal protective equipment such as gloves and safety goggles should be worn during handling. Avoid contact with skin and eyes, and ensure spill containment measures are in place to prevent environmental contamination.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086416195802,"sku":"TCI2510D097820659","price":536000.0,"currency_code":"IDR","in_stock":true},{"title":"400g","offer_id":48086416228570,"sku":"TCI2510D097820660","price":957000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D0978.jpg?v=1768817362"},{"product_id":"tci2510e000427632","title":"TCI E0004 629-96-9 1-Eicosanol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1-Eicosanol is a chemical compound widely used as a foundational building block in various chemical reactions and the synthesis of complex molecules. It plays a crucial role in organic chemistry by serving as a key component in the construction of molecular structures, especially in the synthesis of compounds with long carbon chains. This material is essential for researchers aiming to develop new chemical entities or modify existing ones through functional group transformations. Its versatility makes it a valuable tool in both academic and industrial laboratory settings.\u003c\/p\u003e\n\u003cp\u003eThe chemical properties of 1-Eicosanol, including its stability and ability to interact with a range of functional groups, make it a preferred choice for laboratory applications. It is suitable for substitution reactions and coupling reactions, where its chemical inertness and reactivity are advantageous. Additionally, its relatively high melting and boiling points facilitate controlled heating and cooling processes, which are essential in many synthetic procedures. These characteristics ensure that it remains a reliable and efficient reagent in chemical synthesis.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 1-Eicosanol is extensively used in chemical research, particularly in the fields of organic synthesis, complex compound analysis, and the development of new chemical products. Its availability and compatibility with a wide range of chemical reactions make it a primary choice for researchers working on molecular structure modifications and functional group manipulations. Its application is especially prominent in academic and industrial research settings where precision and reliability are paramount.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of complex molecules requires 1-Eicosanol for its structural versatility and reactivity in building long carbon chains.\u003c\/li\u003e\n\u003cli\u003eAnalysis of complex compounds benefits from 1-Eicosanol’s stability and compatibility with various analytical techniques.\u003c\/li\u003e\n\u003cli\u003eDevelopment of new chemical products relies on 1-Eicosanol’s ability to participate in substitution and coupling reactions.\u003c\/li\u003e\n\u003cli\u003eMolecular structure modification is enhanced by 1-Eicosanol’s capacity to interact with functional groups during synthetic processes.\u003c\/li\u003e\n\u003cli\u003eResearch in chemical engineering utilizes 1-Eicosanol for its role in creating compounds with specific physical and chemical 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: 629-96-9\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 or liquid, depending on the specific product variant\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct sunlight and incompatible materials\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003e1-Eicosanol should be stored in a cool, dry environment to maintain its chemical integrity and prevent degradation. It is recommended to use sealed containers to minimize exposure to air and moisture, which could affect its stability. Proper labeling of storage containers is essential for safety and identification purposes. In laboratory settings, it should be kept away from incompatible substances such as strong oxidizers or acids to avoid potential chemical reactions. Regular monitoring of storage conditions ensures that the material remains suitable for use in chemical synthesis and research applications. Always follow standard laboratory safety protocols when handling and storing this compound.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086812786906,"sku":"TCI2510E000427632","price":1885000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48086812819674,"sku":"TCI2510E000427633","price":11328000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510E0004.jpg?v=1768818613"},{"product_id":"tci2510e000627635","title":"TCI E0006 506-30-9 Arachidic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eArachidic Acid (TCI E0006, CAS 506-30-9) is a long-chain saturated fatty acid commonly used in chemical laboratories for its structural stability and versatility in synthetic applications. As a fundamental building block in organic chemistry, it plays a crucial role in the synthesis of complex molecules, including heterocyclic and non-heterocyclic compounds. Its molecular structure, characterized by a long carbon chain, makes it an essential reagent for research involving molecular modeling and functional group manipulation. This compound is widely utilized in both academic and industrial settings due to its predictable chemical behavior and compatibility with various reaction conditions.\u003c\/p\u003e\n\u003cp\u003eThe chemical properties of Arachidic Acid make it a preferred choice for laboratory use. It exhibits high thermal stability and resistance to chemical degradation, ensuring consistent performance in prolonged experiments. Its limited solubility in organic solvents and high melting point contribute to its utility in reactions requiring controlled environmental conditions. These characteristics make it suitable for applications where stability and predictability are essential. Additionally, its inert nature allows it to be used as a reference material in analytical procedures.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Arachidic Acid is frequently employed in pure chemical research, organic synthesis, and studies on the physical and chemical properties of complex compounds. It is particularly valuable in educational institutions and research centers where the development of new chemical compounds and materials is a priority. Its availability and reliability make it a standard component in many laboratory workflows across Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePure Chemical Research: Arachidic Acid is ideal for studying the structural and functional properties of organic compounds due to its stable molecular framework.\u003c\/li\u003e\n\u003cli\u003eOrganic Synthesis: Its long carbon chain makes it a valuable reagent in the synthesis of complex molecules, including heterocyclic structures.\u003c\/li\u003e\n\u003cli\u003ePhysical Chemistry Studies: The compound’s high melting point and limited solubility are useful in experiments examining molecular behavior under extreme conditions.\u003c\/li\u003e\n\u003cli\u003eAnalytical Chemistry: Arachidic Acid serves as a reference standard in chromatographic and spectroscopic analyses due to its well-defined chemical properties.\u003c\/li\u003e\n\u003cli\u003eIndustrial Material Development: It is used in the formulation of specialty chemicals and coatings, supporting innovation in material science applications.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS Number: 506-30-9\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack Sizes: Available in standard laboratory quantities\u003c\/li\u003e\n\u003cli\u003ePhysical Form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage Note: Store in a cool, dry place away from direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eArachidic Acid should be stored in a cool, dry environment to maintain its chemical stability and prevent degradation. It is recommended to keep the compound in a tightly sealed container to minimize exposure to moisture and air. Due to its solid form, it is best stored in glass or plastic containers that are resistant to chemical corrosion. Laboratory personnel should handle the material with care, using appropriate personal protective equipment when necessary. While it is not highly reactive, it is advisable to avoid contact with strong oxidizing agents. Proper storage ensures the compound remains effective for use in chemical experiments and research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086813475034,"sku":"TCI2510E000627635","price":985000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086813507802,"sku":"TCI2510E000627636","price":7590000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510E0006.jpg?v=1767110468"},{"product_id":"tci2510h001032327","title":"TCI H0010 2363-71-5 Heneicosanoic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eHeneicosanoic Acid (HC21:0) is a saturated fatty acid with a carbon chain of 21 atoms. It serves as a key reagent in materials science, particularly in the field of colloidal quantum dot (QD) research. In the laboratory, this compound plays a vital role in the synthesis of nanoparticles with tailored optical and electronic properties. Its unique molecular structure enables precise control over the characteristics of quantum dots, making it essential for advanced optoelectronic and sensor applications.\u003c\/p\u003e\n\u003cp\u003eThe chemical stability and controlled reactivity of Heneicosanoic Acid make it a preferred choice in complex molecular synthesis. Its hydrophobic nature allows it to dissolve easily in organic solvents such as hexane and toluene, facilitating high-precision nanoparticle fabrication. Additionally, its high melting point ensures it remains chemically stable under normal storage conditions, reducing the risk of degradation during experiments. These properties contribute to its reliability in demanding research environments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Heneicosanoic Acid is commonly used in material science research, especially in the development of organic and inorganic semiconductors. Its role in colloidal quantum dot synthesis supports various applications, including optoelectronics and sensing technologies. Researchers rely on its consistent performance and chemical stability to achieve reproducible results in their experiments.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eColloidal Quantum Dot Synthesis: Heneicosanoic Acid is used to create nanoparticles with precise optical and electronic properties, essential for optoelectronic devices and sensors.\u003c\/li\u003e\n\u003cli\u003eOrganic Semiconductor Development: Its hydrophobic nature and chemical stability make it ideal for synthesizing organic semiconductors with controlled molecular structures.\u003c\/li\u003e\n\u003cli\u003eNanoparticle Surface Functionalization: The compound aids in modifying nanoparticle surfaces, enhancing their compatibility with various solvents and functional groups.\u003c\/li\u003e\n\u003cli\u003eMaterial Stability Testing: Its high melting point and chemical resistance make it suitable for experiments requiring long-term stability under varied conditions.\u003c\/li\u003e\n\u003cli\u003eSensor Fabrication: Heneicosanoic Acid contributes to the development of sensitive and durable sensors by providing a stable base for nanoparticle integration.\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: 2363-71-5\u003c\/li\u003e\n\u003cli\u003eCategory: Materials Science \u0026gt; Electronic Materials \u0026gt; Colloidal Quantum Dot (QD) Research Reagents\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid at room temperature\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\u003eHeneicosanoic Acid should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to use airtight containers to prevent moisture absorption and maintain chemical integrity. Due to its hydrophobic nature, it should be handled with care to avoid contamination from moisture or other substances. Laboratory personnel should wear appropriate personal protective equipment, including gloves and safety goggles, when handling the compound. It is important to ensure proper ventilation in the workspace to minimize exposure to vapors. The compound is non-toxic in its solid form but should still be treated with standard laboratory safety protocols to ensure a safe working environment.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087140794586,"sku":"TCI2510H001032327","price":4021000.0,"currency_code":"IDR","in_stock":true},{"title":"10g","offer_id":48087140827354,"sku":"TCI2510H001032328","price":23749000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510H0010.jpg?v=1769056251"},{"product_id":"tci2510h001932338","title":"TCI H0019 506-12-7 Heptadecanoic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eHeptadecanoic Acid (CAS 506-12-7), also known as TCI H0019, is an organic compound widely used in scientific research, particularly in the field of materials science. This material plays a crucial role in the synthesis of colloidal quantum dots (QDs), which are essential components in electronic and optical material research. In laboratory settings, Heptadecanoic Acid functions as a solvent or capping agent during the synthesis of QDs, aiding in the formation of stable crystalline structures and acting as a protective layer. Its presence ensures the quality and performance of the final quantum dot products.\u003c\/p\u003e\n\u003cp\u003eThe chemical properties of Heptadecanoic Acid make it a preferred choice for researchers. It exhibits chemical stability and good solubility in organic solvents, which are key factors in maintaining the consistency and reliability of chemical reactions. These characteristics allow it to be used in various synthetic processes where stability and reproducibility are critical. Additionally, its high melting point ensures that it remains stable under laboratory conditions, making it suitable for use in environments that require controlled temperature settings.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Heptadecanoic Acid is commonly used in technological and material research, particularly in universities and research institutions. Its application in the development of advanced materials and electronic components highlights its importance in the scientific community. Researchers rely on its consistent performance and reliability to achieve accurate and reproducible results in their experiments.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eColloidal Quantum Dot Synthesis: Heptadecanoic Acid is used as a capping agent to stabilize the colloidal quantum dots, ensuring their optical and electronic properties remain consistent during synthesis.\u003c\/li\u003e\n\u003cli\u003eOrganic Solvent in Material Processing: Its solubility in organic solvents makes it ideal for dissolving and processing various organic compounds in material science experiments.\u003c\/li\u003e\n\u003cli\u003eSurface Functionalization of Nanoparticles: The acid helps in modifying the surface of nanoparticles, enhancing their compatibility with other materials and improving their performance in electronic applications.\u003c\/li\u003e\n\u003cli\u003eCoating and Passivation of Semiconductor Nanoparticles: It acts as a protective layer, preventing unwanted reactions and improving the stability of semiconductor nanoparticles in solution.\u003c\/li\u003e\n\u003cli\u003eResearch in Electronic and Optical Materials: Its role in the synthesis of quantum dots makes it a key component in studies related to optoelectronic devices and advanced material development.\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: 506-12-7\u003c\/li\u003e\n\u003cli\u003eCategory: Materials Science \u0026gt; Electronic Materials \u0026gt; Colloidal Quantum Dot (QD) Research Reagents\u003c\/li\u003e\n\u003cli\u003ePack Sizes: Available in various sizes 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 moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eHeptadecanoic Acid should be stored in a cool, dry place, away from moisture and direct sunlight to maintain its chemical stability. It is recommended to use airtight containers to prevent exposure to air and humidity. Due to its organic nature, it should be handled in a well-ventilated area to avoid inhalation of vapors. While it is not highly reactive, it is advisable to use appropriate personal protective equipment, such as gloves and safety goggles, when handling it. The material should be kept in a secure location to prevent accidental spills or contamination. 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As a non-heterocyclic building block, it plays a crucial role in the synthesis of more complex molecules, particularly in organic and analytical chemistry. Its simple molecular structure makes it a versatile reagent for chemical reactions such as esterification and hydrolysis. This compound is commonly used as a foundational material in the development of esters, fatty acids, and other derivatives, making it a staple in many research settings.\u003c\/p\u003e\n\u003cp\u003eHeptanoic Acid is valued for its chemical stability under controlled conditions, which allows it to be used in a range of experimental setups. Its mild corrosive properties and sharp odor require careful handling, but its predictable chemical behavior makes it a preferred choice for many researchers. The compound’s compatibility with moderate to elevated temperatures enhances its utility in various synthetic processes. Its availability in multiple packaging options ensures that it can be easily adapted to different experimental scales, from small-scale research to larger industrial applications.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Heptanoic Acid is frequently utilized in chemical synthesis and analytical studies. It is a common component in organic chemistry research, where it serves as a starting material for the creation of more complex compounds. Its reliability and availability make it a go-to reagent for both academic and industrial researchers. Due to its well-documented properties and consistent performance, it remains a key element in the chemical toolkit of Indonesian laboratories.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis experiments benefit from Heptanoic Acid as a reliable building block for ester and fatty acid derivations.\u003c\/li\u003e\n\u003cli\u003eAnalytical chemistry uses Heptanoic Acid for standardization and calibration of chromatographic and spectroscopic techniques.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical processes incorporate Heptanoic Acid for the production of specialty chemicals and pharmaceutical intermediates.\u003c\/li\u003e\n\u003cli\u003eEducational laboratories rely on Heptanoic Acid for teaching fundamental chemical reactions and reaction mechanisms.\u003c\/li\u003e\n\u003cli\u003eEnvironmental studies employ Heptanoic Acid as a reference compound in the analysis of organic pollutants and degradation 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: 111-14-8\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 sizes to suit different experimental needs\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid or liquid, depending on the packaging and storage conditions\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eHeptanoic Acid should be stored in a cool, dry, and well-ventilated area away from direct sunlight. It is recommended to use sealed containers made of glass or high-density polyethylene to prevent exposure to air and moisture. Due to its mild corrosive nature, it should be handled with appropriate personal protective equipment, including gloves and safety goggles. In laboratory settings, it is important to ensure proper ventilation to mitigate the effects of its sharp odor. Storage should be in a location that is inaccessible to children and unauthorized personnel. 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Its role in the laboratory is crucial for researchers aiming to develop new materials, pharmaceuticals, or specialty chemicals. Due to its predictable behavior and compatibility with various reaction conditions, it is a reliable choice for both academic and industrial applications.\u003c\/p\u003e\n\u003cp\u003eThe physical and chemical properties of 1-Hexadecanol make it a preferred choice in laboratory work. It is non-polar, which means it dissolves more readily in organic solvents than in water. This characteristic is essential for reactions that require solubility in non-aqueous environments. Additionally, its high melting and boiling points allow it to remain stable under elevated temperature conditions, making it suitable for a wide range of experimental setups. The controlled reactivity of this compound ensures predictable outcomes in chemical reactions, enhancing the reliability of laboratory results.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 1-Hexadecanol is commonly used in chemical research, particularly in organic synthesis and formulation processes. It is also employed in educational settings to teach students about the properties and applications of long-chain alcohols. Its consistent performance and availability make it a trusted material for both research and teaching purposes, supporting the development of new chemical products and scientific knowledge.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis is a key application where 1-Hexadecanol is used as a building block for creating complex molecules due to its stable structure and predictable reactivity.\u003c\/li\u003e\n\u003cli\u003eFormulation of specialty chemicals benefits from 1-Hexadecanol’s solubility in organic solvents, allowing it to be incorporated into various chemical mixtures for industrial use.\u003c\/li\u003e\n\u003cli\u003eResearch in polymer science often utilizes 1-Hexadecanol as a component in the development of new materials due to its long carbon chain and chemical versatility.\u003c\/li\u003e\n\u003cli\u003eEducational laboratories use 1-Hexadecanol to demonstrate the properties of long-chain alcohols and their behavior in different reaction conditions.\u003c\/li\u003e\n\u003cli\u003eDevelopment of new pharmaceutical compounds frequently incorporates 1-Hexadecanol as a starting material due to its compatibility with a wide range of chemical 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: 36653-82-4\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory supply\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid at room temperature\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003e1-Hexadecanol should be stored in a cool, dry environment to maintain its chemical stability and prevent degradation. It is recommended to use airtight containers made of glass or high-density polyethylene to minimize exposure to moisture and air. Due to its non-polar nature, it should be kept separate from reactive or incompatible substances. In laboratory settings, proper ventilation is essential when handling this compound to ensure safe working conditions. Always wear appropriate personal protective equipment, such as gloves and safety goggles, when working with 1-Hexadecanol to prevent skin contact or inhalation. 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The compound serves as an important reference material in organic chemistry and food analysis laboratories, functioning both as a reagent for the formation of esters, amides, and acyl chlorides, and as a standard compound in the identification of fatty acid profiles. Its placement in the Non-Heterocyclic Building Blocks category underlines its role as a foundational material used to construct more complex derivative molecules.\u003c\/p\u003e\n\u003cp\u003eThe property that makes hexanoic acid such a widely chosen material is its amphiphilic character: a polar carboxyl group combined with a nonpolar alkyl chain. This combination allows it to dissolve readily in organic solvents while still being able to interact with aqueous phases, making it flexible for use across a range of reaction and extraction systems. Its physical form is an oily liquid with a characteristically sharp odour, so handling is customarily carried out inside a fume hood. The acidity of the carboxyl group permits neutralisation reactions, Fischer esterification, and activation into more reactive acyl derivatives.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, hexanoic acid is typically kept as a general-purpose building block on the organic synthesis bench and in analytical sections dealing with fatty acid work. Because the material is an oily liquid with a penetrating odour, routine dispensing is normally scheduled inside a working fume hood, and the container is returned to its designated chemical storage position after each use rather than being left open on the bench.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eEster synthesis — the carboxyl group undergoes Fischer esterification directly with alcohols, making this a convenient starting acid for preparing hexanoate esters in teaching and research settings.\u003c\/li\u003e\n\u003cli\u003eAmide preparation — the acid can be coupled with amines through standard activation routes, so it serves as a straightforward six-carbon acyl source for building amide-containing target molecules.\u003c\/li\u003e\n\u003cli\u003eAcyl chloride generation — conversion of the carboxyl group into a more reactive acyl derivative gives chemists an activated intermediate for onward acylation steps in multistep organic sequences.\u003c\/li\u003e\n\u003cli\u003eFatty acid profile identification — as a defined medium-chain saturated fatty acid, it works as a reference compound when analysts assign and confirm peaks in food analysis work.\u003c\/li\u003e\n\u003cli\u003eExtraction and reaction system studies — its amphiphilic nature, with both polar and nonpolar regions, lets it partition usefully between organic solvents and aqueous phases during method development.\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: 142-62-1\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in the standard TCI catalogue pack sizes for this item\u003c\/li\u003e\n\u003cli\u003ePhysical form: oily liquid with a characteristically sharp odour\u003c\/li\u003e\n\u003cli\u003eStorage: keep in a tightly closed container in a designated chemical storage area\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore hexanoic acid in a tightly closed container within a designated chemical storage area, away from incompatible materials and out of direct sunlight. Tightly sealed glass bottles with chemically resistant closures are the usual choice, since the material is an oily liquid whose sharp odour escapes readily from a loosely capped vessel. Dispensing and weighing should be performed inside a working fume hood with adequate ventilation. Laboratory staff should wear safety goggles, chemical-resistant gloves, and a laboratory coat, because the carboxyl group makes the material acidic and capable of irritating skin and eyes. 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