{"title":"Halogenated Hydrocarbons (Fluorides expected) [Non-Heterocyclic Building Blocks]","description":"\u003cp\u003e\u003cstrong\u003eHalogenated Hydrocarbons (Fluorides expected) [Non-Heterocyclic Building Blocks]\u003c\/strong\u003e — includes non-heterocyclic hydrocarbons containing one or more halogen atoms (chlorine, bromine, iodine), with emphasis on fluorinated compounds, which serve as building blocks for introducing halogen atoms into the framework of target molecules during synthesis.\u003c\/p\u003e\u003cp\u003eThese Halogenated Hydrocarbons are used as electrophiles in nucleophilic substitution reactions, Grignard reagents, and starting materials for cross-coupling reactions to build the carbon skeleton of a molecule. Fluorinated derivatives in particular are widely sought by medicinal chemistry and materials chemistry researchers because they can alter the electronic properties, lipophilicity, and metabolism of derived compounds, and are therefore often used as marker groups in fluorine-19 spectroscopy studies.\u003c\/p\u003e\u003cp\u003eExample products in this collection: \u003ca href=\"\/en\/products\/tci2510i075236002\"\u003eTCI I0752 608-28-6 2-Iodo-m-xylene\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b571412433\"\u003eTCI B5714 557-68-6 Bromoiodomethane (stabilized with Copper chip)\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510i078536046\"\u003eTCI I0785 1591-31-7 4-Iodobiphenyl\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b572112443\"\u003eTCI B5721 85531-02-8 5-(Bromomethyl)undecane\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510i079336057\"\u003eTCI I0793 2523-42-4 2-Iodofluorene\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b574212472\"\u003eTCI B5742 535934-25-9 1-Bromo-2-chloro-4-iodobenzene\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510t391655629\"\u003eTCI T3916 171408-77-8 2,2',7-Tribromo-9,9'-spirobi[fluorene]\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b574312474\"\u003eTCI B5743 21521-54-0 4-Bromo-1,2-diiodobenzene\u003c\/a\u003e.\u003c\/p\u003e\u003cp\u003ePay attention to the position and type of halogen atom, purity, and the stability of the compound toward light and heat, as some halogen derivatives are reactive and easily decompose during storage. All products are original products of Tokyo Chemical Industry (TCI) Japan, with purity, packaging, and storage conditions listed on each item's page.\u003c\/p\u003e\u003cp\u003eOther parallel categories under Non-Heterocyclic Building Blocks, often used together in one laboratory workflow:\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-carbonyl-compounds-non-heterocyclic-building-blocks\"\u003eCarbonyl Compounds [Non-Heterocyclic Building Blocks]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-nitrogen-compounds-non-heterocyclic-building-blocks\"\u003eNitrogen Compounds [Non-Heterocyclic Building Blocks]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-oxygen-compounds-non-heterocyclic-building-blocks\"\u003eOxygen Compounds [Non-Heterocyclic Building Blocks]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-sulfur-compounds-non-heterocyclic-building-blocks\"\u003eSulfur Compounds [Non-Heterocyclic Building Blocks]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-arenes-non-heterocyclic-building-blocks\"\u003eArenes [Non-Heterocyclic Building Blocks]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-alkenes-non-heterocyclic-building-blocks\"\u003eAlkenes [Non-Heterocyclic Building Blocks]\u003c\/a\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eBack to \u003ca href=\"\/en\/collections\/tci-l3-non-heterocyclic-building-blocks\"\u003eNon-Heterocyclic Building Blocks\u003c\/a\u003e. For large-volume procurement, special packaging, or specific grades, contact the AMI Scientific team — official distributor of TCI Japan in Indonesia — for availability checks and lead times directly from Japan.\u003c\/p\u003e","products":[{"product_id":"tci2510b572112443","title":"TCI B5721 85531-02-8 5-(Bromomethyl)undecane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e5-(Bromomethyl)undecane is a branched alkyl bromide that serves as a versatile non-heterocyclic building block in organic synthesis, featuring a reactive bromomethyl group ideal for nucleophilic substitution reactions to construct carbon-carbon and carbon-heteroatom bonds. It is commonly employed in the preparation of surfactants, pharmaceutical intermediates, and specialty organic compounds that benefit from its long-chain lipophilic character. This high-quality TCI product is available in 5g and 25g packaging, suitable for both small-scale exploratory research and larger preparative synthetic workflows.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48085899215066,"sku":"TCI2510B572112443","price":3307000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085899247834,"sku":"TCI2510B572112444","price":11533000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5721.jpg?v=1768815872"},{"product_id":"tci2510b580812555","title":"TCI B5808 1379440-97-7 (R)-3-(Bromomethyl)heptane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(R)-3-(Bromomethyl)heptane is a chiral alkyl bromide building block widely utilized in organic synthesis laboratories for constructing complex molecular architectures. Its reactive bromomethyl group enables efficient nucleophilic substitution reactions, allowing researchers to introduce the (R)-3-methylheptyl framework into target compounds. This compound is particularly valuable in medicinal chemistry research, asymmetric synthesis, and the development of functional materials requiring enantiomerically pure intermediates.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"250mg","offer_id":48085904523482,"sku":"TCI2510B580812555","price":6285000.0,"currency_code":"IDR","in_stock":true},{"title":"500mg","offer_id":48085904556250,"sku":"TCI2510B580812556","price":11282000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5808.jpg?v=1769180233"},{"product_id":"tci2510b594812724","title":"TCI B5948 1647-23-0 1-Bromo-3,3-dimethylbutane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1-Bromo-3,3-dimethylbutane (CAS 1647-23-0) is a non-heterocyclic organic building block supplied by TCI, widely used as a key precursor in nucleophilic substitution, Grignard, and carbon-carbon coupling reactions. Its sterically hindered tert-butyl moiety makes it particularly valuable for selectivity studies and mechanistic investigations in organic synthesis. This compound serves as an essential intermediate in pharmaceutical research, functional material development, and academic studies requiring branched aliphatic building blocks with a single reactive center.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48085911109850,"sku":"TCI2510B594812724","price":1187000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085911142618,"sku":"TCI2510B594812725","price":5250000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5948.jpg?v=1769180245"},{"product_id":"tci2510b620613033","title":"TCI B6206 2791-57-3 1-Bromo-3,7,11,15-tetramethylhexadecane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6206 (1-Bromo-3,7,11,15-tetramethylhexadecane, CAS 2791-57-3) is a long-chain alkyl bromide serving as a non-heterocyclic building block in organic synthesis. Its reactive bromo group enables key transformations such as nucleophilic substitution, Grignard reagent formation, and coupling reactions for constructing complex molecular frameworks. This compound is particularly valuable in the synthesis of bioactive molecules, functional lipids, and isoprenoid-based specialty surfactants for advanced laboratory research.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085924544730,"sku":"TCI2510B620613033","price":3508000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085924577498,"sku":"TCI2510B620613034","price":12493000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6206.jpg?v=1768816004"},{"product_id":"tci2510b644013331","title":"TCI B6440 630-17-1 1-Bromo-2,2-dimethylpropane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6440 1-Bromo-2,2-dimethylpropane (neopentyl bromide, CAS 630-17-1) is a sterically hindered alkyl bromide used as a non-heterocyclic building block. It is commonly applied to install a neopentyl group onto nucleophiles and to prepare the corresponding organometallic reagents. Its hindered structure also makes it a classic substrate for studying steric effects in nucleophilic substitution. The product is flammable, so handle it in a fume hood away from ignition sources and store it tightly closed in a cool, well-ventilated area.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48085940371674,"sku":"TCI2510B644013331","price":1894000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085940404442,"sku":"TCI2510B644013332","price":6537000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6440.jpg?v=1769144632"},{"product_id":"tci2510b645613346","title":"TCI B6456 16400-32-1 1-Bromo-2-pentyne","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6456 1-Bromo-2-pentyne (CAS 16400-32-1) is a reactive propargylic bromide supplied as a non-heterocyclic building block. It readily alkylates carbon, nitrogen, oxygen, and sulfur nucleophiles, installing a pentynyl fragment that can be elaborated further through click chemistry or metal-catalyzed coupling. The reagent is flammable and lachrymatory, so all transfers should be performed inside a fume hood with suitable protective equipment. Store it tightly closed in a cool, dark, well-ventilated area away from ignition sources and oxidizing agents.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48085940928730,"sku":"TCI2510B645613346","price":3434000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085940961498,"sku":"TCI2510B645613347","price":11962000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6456.jpg?v=1792631555"},{"product_id":"tci2510b676413681","title":"TCI B6764 2270-59-9 5-Bromo-2-methylpent-2-ene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6764 5-Bromo-2-methylpent-2-ene is an unsaturated alkyl bromide featuring a trisubstituted alkene and a terminal bromide, giving it two complementary reactive sites. The bromide readily undergoes nucleophilic substitution or conversion to organometallic reagents such as Grignard species, while the alkene remains available for epoxidation, hydration, or cyclisation chemistry. Its branched skeleton resembles an isoprenoid fragment, making it a practical building block for terpenoid-oriented synthesis and chain extension. AMI Scientific offers this TCI reagent in small research packages; handle it in a fume hood and store it cool, dark, and tightly sealed.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085955117274,"sku":"TCI2510B676413681","price":1162000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085955150042,"sku":"TCI2510B676413682","price":4013000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6764_3406ed98-c1e8-478b-ad58-c4b40219f2b7.jpg?v=1792631841"},{"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":431000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48085973565658,"sku":"TCI2510C014214105","price":633000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0142_2c0827bd-c490-46a7-9deb-a5a591f0e890.jpg?v=1792632155"},{"product_id":"tci2510c014314106","title":"TCI C0143 78-86-4 2-Chlorobutane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0143 2-Chlorobutane is a secondary alkyl halide widely used as a general-purpose building block in organic synthesis. Its chlorine atom on a secondary carbon makes it a convenient sec-butyl source for alkylation chemistry and organometallic preparation. The compound is also a classroom favourite for illustrating the balance between nucleophilic substitution and elimination pathways. AMI Scientific supplies this TCI product in 25 mL and 500 mL packs suitable for routine laboratory work.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\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\u003cli\u003eWisniak (1995). Vapor-Liquid Equilibria in the Ternary System 2-Chlorobutane + 1-Chlorobutane + Cyclohexane and Its Binaries. \u003cem\u003ePhysics and Chemistry of Liquids\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1080\/00319109508031642\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1080\/00319109508031642\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":48085973598426,"sku":"TCI2510C014314106","price":986000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48085973631194,"sku":"TCI2510C014314107","price":2853000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0143.jpg?v=1768816145"},{"product_id":"tci2510c014514110","title":"TCI C0145 591-97-9 Crotyl Chloride (cis- and trans- mixture)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0145 Crotyl Chloride is an allylic chloride supplied as a mixture of cis and trans isomers. The chlorine atom adjacent to the double bond gives it the characteristic reactivity of allylic systems, making it an efficient crotylating agent. The residual alkene provides a convenient handle for further transformations such as oxidation, hydrogenation, or olefin metathesis. AMI Scientific supplies this TCI product in 25 mL, 100 mL, and 500 mL packs for flexible laboratory use.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eHethcox et al. (2016). Iridium‐Catalyzed Stereoselective Allylic Alkylation Reactions with Crotyl Chloride. \u003cem\u003eAngewandte Chemie\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/ange.201609960\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/ange.201609960\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eHethcox et al. (2016). Iridium‐Catalyzed Stereoselective Allylic Alkylation Reactions with Crotyl Chloride. \u003cem\u003eAngewandte Chemie International Edition\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/anie.201609960\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/anie.201609960\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":48085973762266,"sku":"TCI2510C014514110","price":1616000.0,"currency_code":"IDR","in_stock":true},{"title":"100mL","offer_id":48085973795034,"sku":"TCI2510C014514111","price":4594000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48085973827802,"sku":"TCI2510C014514112","price":14915000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0145_c79ce982-3f7f-478f-8861-7fba7329c02a.jpg?v=1792632158"},{"product_id":"tci2510c016314132","title":"TCI C0163 112-52-7 1-Chlorododecane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1-Chlorododecane is an organic compound classified as a straight-chain alkyl chloride. It has twelve carbon atoms, with a chlorine atom bonded at the end of the chain. In the laboratory it is used as a non-heterocyclic building block, a starting material for attaching a dodecyl group (a long hydrocarbon chain) to a target molecule. It is used in organic synthesis, surfactant research and the development of materials based on alkyl chains. TCI supplies it under product code C0163 for research and development.\u003c\/p\u003e\n\u003cp\u003eThe defining feature of 1-Chlorododecane is the primary chloride group at the end of its long alkyl chain. The chlorine atom acts as a leaving group in nucleophilic substitution reactions. This makes the compound suitable for forming carbon–heteroatom bonds with nucleophiles such as amines, thiols, phenolates and carboxylates. The dodecyl chain is hydrophobic, so it makes the final product more lipophilic. The compound can also be used to prepare organometallic reagents. It is generally supplied as a liquid. For its physical properties, refer to the manufacturer's official data sheet.\u003c\/p\u003e\n\u003cp\u003eIn Indonesia, chemistry laboratories at universities, research institutions and industrial R\u0026amp;D facilities use materials like this regularly. Researchers working on organic synthesis, surface-active compounds or functional materials use 1-Chlorododecane to add long alkyl chains to their target molecules. Because it comes from an established brand such as TCI, research teams can expect consistent quality from batch to batch. This consistency matters for repeatable experiments, academic work and early-stage product development in local laboratories.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAlkylation in organic synthesis: the primary chloride is a good leaving group, so the compound can attach a dodecyl chain to amines, thiols, phenolates or carboxylates through nucleophilic substitution.\u003c\/li\u003e\n\u003cli\u003eSurfactant research: the long hydrophobic dodecyl chain can serve as the lipophilic tail of surface-active molecules, which is useful when studying amphiphilic compounds and how they behave.\u003c\/li\u003e\n\u003cli\u003ePreparation of organometallic reagents: the terminal alkyl chloride can be converted into organometallic intermediates, which are then used to form new carbon–carbon bonds in later synthesis steps.\u003c\/li\u003e\n\u003cli\u003eDevelopment of alkyl-chain-based materials: adding a twelve-carbon chain makes a material more lipophilic, which helps researchers who are studying how chain length affects a material's properties.\u003c\/li\u003e\n\u003cli\u003eBuilding block for target molecule design: as a non-heterocyclic building block, it is a simple and predictable way to add a straight dodecyl group to a more complex research molecule.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI (product code C0163)\u003c\/li\u003e\n\u003cli\u003eCAS number: 112-52-7\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: see the available options on the product listing\u003c\/li\u003e\n\u003cli\u003ePhysical form: generally a liquid (confirm with the manufacturer's data sheet)\u003c\/li\u003e\n\u003cli\u003eStorage: follow the storage conditions on the manufacturer's label and Safety Data Sheet\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore 1-Chlorododecane in its original tightly closed container, in a cool, dry and well-ventilated area away from heat, direct sunlight and incompatible substances such as strong oxidizing agents. Glass or chemically compatible containers are recommended. Always label containers clearly after opening. Handle the material in a fume hood or a well-ventilated workspace while wearing suitable personal protective equipment, including chemical-resistant gloves, safety glasses and a laboratory coat. Avoid contact with skin and eyes, and do not inhale vapors. Before use, read the manufacturer's Safety Data Sheet for complete hazard, first-aid and disposal information. Dispose of waste according to local regulations.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mL","offer_id":48085974581466,"sku":"TCI2510C016314132","price":455000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48085974614234,"sku":"TCI2510C016314133","price":1187000.0,"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":505000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48085975859418,"sku":"TCI2510C018214162","price":5048000.0,"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":733000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48085975957722,"sku":"TCI2510C018314164","price":2349000.0,"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":557000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48085976023258,"sku":"TCI2510C018414166","price":3257000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0184.jpg?v=1768816158"},{"product_id":"tci2510c019914184","title":"TCI C0199 107-84-6 1-Chloro-3-methylbutane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1-Chloro-3-methylbutane (TCI C0199, CAS 107-84-6), commonly known as isoamyl chloride, is a branched primary alkyl halide supplied as a liquid. It is widely used to introduce the isoamyl group into nucleophiles and to prepare Grignard reagents for further synthesis. Its primary halide structure also makes it a clear teaching example for SN2 substitution chemistry. AMI Scientific provides this TCI reagent in 25 mL and 500 mL packs for research and teaching laboratories throughout Indonesia.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mL","offer_id":48085977956570,"sku":"TCI2510C019914184","price":1415000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48085977989338,"sku":"TCI2510C019914185","price":11609000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0199.jpg?v=1769144583"},{"product_id":"tci2510c020014186","title":"TCI C0200 594-36-5 2-Chloro-2-methylbutane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2-Chloro-2-methylbutane (TCI C0200, CAS 594-36-5) is a tertiary alkyl chloride supplied as a liquid reagent. Its readiness to ionise into a tertiary carbocation makes it a standard substrate for SN1 solvolysis kinetics and elimination experiments. In synthesis it can also serve as an alkyl source in Friedel-Crafts reactions on aromatic substrates. AMI Scientific supplies this TCI product in 25 mL, 100 mL, and 500 mL packs for research and teaching laboratories in Indonesia.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mL","offer_id":48085978022106,"sku":"TCI2510C020014186","price":1465000.0,"currency_code":"IDR","in_stock":true},{"title":"100mL","offer_id":48085978054874,"sku":"TCI2510C020014187","price":3761000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48085978087642,"sku":"TCI2510C020014188","price":10675000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0200.jpg?v=1769180293"},{"product_id":"tci2510c020714201","title":"TCI C0207 513-36-0 1-Chloro-2-methylpropane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1-Chloro-2-methylpropane (TCI C0207, CAS 513-36-0), known as isobutyl chloride, is a branched primary alkyl halide supplied as a liquid. It is used to introduce the isobutyl group into nucleophiles and to prepare Grignard reagents for chain-extension chemistry. Its beta-branching also makes it a useful example when comparing steric effects on nucleophilic substitution rates. AMI Scientific supplies this TCI reagent in 25 mL and 500 mL packs for synthesis and teaching laboratories in Indonesia.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mL","offer_id":48085978710234,"sku":"TCI2510C020714201","price":834000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48085978743002,"sku":"TCI2510C020714202","price":6285000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0207.jpg?v=1768816166"},{"product_id":"tci2510c020814203","title":"TCI C0208 507-20-0 2-Chloro-2-methylpropane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2-Chloro-2-methylpropane (TCI C0208, CAS 507-20-0), widely known as tert-butyl chloride, is a tertiary alkyl halide supplied as a liquid. Its rapid ionisation to a stable tert-butyl carbocation makes it the classic substrate for SN1 solvolysis kinetics and solvent-effect studies. In synthesis it acts as a tert-butyl source for Friedel-Crafts alkylation and related derivatisation reactions. AMI Scientific offers this TCI reagent in 25 mL and 500 mL packs for research and teaching laboratories across Indonesia.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mL","offer_id":48085978808538,"sku":"TCI2510C020814203","price":455000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48085978841306,"sku":"TCI2510C020814204","price":1792000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0208.jpg?v=1768816166"},{"product_id":"tci2510c020914205","title":"TCI C0209 563-47-3 3-Chloro-2-methyl-1-propene (stabilized with Stearyl 3-(3,5-Di-tert-butyl-4-hydroxyphenyl)propionate)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e3-Chloro-2-methyl-1-propene (TCI C0209, CAS 563-47-3), known as methallyl chloride, is a reactive allylic halide stabilised with Stearyl 3-(3,5-Di-tert-butyl-4-hydroxyphenyl)propionate. Its activated allylic position allows efficient introduction of the methallyl group onto alcohols, phenols, amines, and thiols. The remaining terminal double bond can then be used in polymerisation, addition, or further functionalisation steps. AMI Scientific supplies this TCI reagent in 25 mL and 500 mL packs for organic synthesis, polymer, and materials laboratories in Indonesia.\u003c\/p\u003e\n\u003cp\u003e---\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mL","offer_id":48085978874074,"sku":"TCI2510C020914205","price":481000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48085978906842,"sku":"TCI2510C020914206","price":1137000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0209_6a56d110-68ce-4726-aa18-b7d90ca7b637.jpg?v=1792632246"},{"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":2247000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48085981397210,"sku":"TCI2510C023314243","price":17288000.0,"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":708000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48085981462746,"sku":"TCI2510C023514245","price":2247000.0,"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":455000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48085981593818,"sku":"TCI2510C023614247","price":1642000.0,"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":633000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48085981692122,"sku":"TCI2510C023714249","price":3837000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0237.jpg?v=1769144574"},{"product_id":"tci2510c026614288","title":"TCI C0266 540-54-5 1-Chloropropane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0266 1-Chloropropane (CAS 540-54-5) is a primary alkyl halide widely used as a propylating agent in nucleophilic substitution chemistry. It also serves as a precursor to n-propyl Grignard reagents and as a teaching example for SN1 and SN2 mechanism studies. The compound is a highly flammable, volatile liquid and must be handled in a fume hood away from ignition sources. It is available in 25 mL and 500 mL packs for both small-scale trials and routine synthesis.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSaheb (2013). Theoretic studies on the kinetics and mechanism of multi-channel gas-phase unimolecular reactions of 1-chloropropane and 2-chloropropane. \u003cem\u003eStructural Chemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1007\/s11224-013-0240-2\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1007\/s11224-013-0240-2\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eErmacora et al. (2014). Influence of oil composition on the formation of fatty acid esters of 2-chloropropane-1,3-diol (2-MCPD) and 3-chloropropane-1,2-diol (3-MCPD) under conditions simulating oil refining. \u003cem\u003eFood Chemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.foodchem.2014.03.130\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.foodchem.2014.03.130\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eGronert (1993). Theoretical studies of elimination reactions. 3. Gas-phase reactions of fluoride ion with 2-chloropropane and 1-chloropropane. The effect of methyl substituents. \u003cem\u003eJournal of the American Chemical Society\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1021\/ja00055a039\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1021\/ja00055a039\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":48085983658202,"sku":"TCI2510C026614288","price":581000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48085983690970,"sku":"TCI2510C026614289","price":2853000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0266.jpg?v=1769144571"},{"product_id":"tci2510c026714290","title":"TCI C0267 75-29-6 2-Chloropropane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0267 2-Chloropropane (CAS 75-29-6) is the secondary isomer of chloropropane and a convenient source of the isopropyl group in synthesis. It is used in isopropylation reactions, Friedel–Crafts alkylation, and the preparation of isopropyl organometallic reagents. Its secondary structure also makes it a valuable teaching example when comparing substitution and elimination pathways. Supplied in 25 mL and 500 mL packs, this highly flammable liquid must be handled in a fume hood away from all ignition sources.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSaheb (2013). Theoretic studies on the kinetics and mechanism of multi-channel gas-phase unimolecular reactions of 1-chloropropane and 2-chloropropane. \u003cem\u003eStructural Chemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1007\/s11224-013-0240-2\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1007\/s11224-013-0240-2\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eErmacora et al. (2014). Influence of oil composition on the formation of fatty acid esters of 2-chloropropane-1,3-diol (2-MCPD) and 3-chloropropane-1,2-diol (3-MCPD) under conditions simulating oil refining. \u003cem\u003eFood Chemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.foodchem.2014.03.130\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.foodchem.2014.03.130\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eGronert (1993). Theoretical studies of elimination reactions. 3. Gas-phase reactions of fluoride ion with 2-chloropropane and 1-chloropropane. The effect of methyl substituents. \u003cem\u003eJournal of the American Chemical Society\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1021\/ja00055a039\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1021\/ja00055a039\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":48085983756506,"sku":"TCI2510C026714290","price":481000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48085983789274,"sku":"TCI2510C026714291","price":986000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0267.jpg?v=1768816192"},{"product_id":"tci2510c027214299","title":"TCI C0272 590-21-6 1-Chloro-1-propene (cis- and trans- mixture)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0272 1-Chloro-1-propene (CAS 590-21-6) is supplied as a mixture of cis- and trans- isomers, as stated by the manufacturer. As a vinylic chloride, it behaves differently from ordinary alkyl halides and is mainly used in organometallic chemistry and transition-metal cross-coupling research. The isomer mixture also makes it useful for comparative stereochemical studies. Presented in a 10 mL pack, this highly volatile and flammable liquid must be handled in a fume hood away from ignition sources.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"10mL","offer_id":48085984280794,"sku":"TCI2510C027214299","price":4518000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0272_41cfbd81-43ff-4956-aab7-2e3715b15dc8.jpg?v=1792632304"},{"product_id":"tci2510c027414300","title":"TCI C0274 107-05-1 Allyl Chloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0274 Allyl Chloride (CAS 107-05-1) is a highly reactive allylic halide and one of the most widely used allylating agents in organic synthesis. It introduces the allyl group onto oxygen, nitrogen, sulfur, and carbon nucleophiles, and serves as a precursor to epichlorohydrin and allyl organometallic reagents. The resulting allyl group can be further elaborated through metathesis, epoxidation, hydroboration, or used as a removable protecting group. Supplied in 25 mL and 500 mL packs, it is a flammable, toxic, and strongly irritating liquid that must be handled in a fume hood.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eZulfiqar et al. (1999). Effect of allyl chloride comonomer on the thermal degradation of poly(methyl methacrylate-co-allyl chloride). \u003cem\u003ePolymer Degradation and Stability\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/s0141-3910(99)00087-7\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/s0141-3910(99)00087-7\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eYadav et al. (2004). Acetyl Chloride—Ethanol Brings About a Remarkably Efficient Conversion of Allyl Acetates into Allyl Chlorides.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.200410041\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.200410041\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eYadav et al. (2003). Acetyl chloride–ethanol brings about a remarkably efficient conversion of allyl acetates into allyl chlorides. \u003cem\u003eTetrahedron\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.tet.2003.09.063\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.tet.2003.09.063\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":48085984313562,"sku":"TCI2510C027414300","price":455000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48085984346330,"sku":"TCI2510C027414301","price":633000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0274_bd8084cd-4db9-41a4-9bf7-986260b844ed.jpg?v=1792632308"},{"product_id":"tci2510c058114775","title":"TCI C0581 563-52-0 3-Chloro-1-butene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e3-Chloro-1-butene (TCI C0581, CAS 563-52-0) is a short-chain allylic chloride with a terminal double bond, making it highly reactive toward nucleophilic substitution. It is used to introduce butenyl groups into target molecules and to study competition between direct substitution and allylic rearrangement pathways. Its terminal alkene remains available for further functionalisation in multistep synthesis. AMI Scientific offers this TCI product in 25 g and 100 g packs, handled and stored as a volatile, flammable liquid.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086011379930,"sku":"TCI2510C058114775","price":3508000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48086011412698,"sku":"TCI2510C058114776","price":12467000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0581_e1768a52-ebf3-43cd-b85d-362ce6d3e1fd.jpg?v=1792632765"},{"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":1541000.0,"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":884000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48086012690650,"sku":"TCI2510C060014808","price":5781000.0,"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":481000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48086015049946,"sku":"TCI2510C062214830","price":2500000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0622.jpg?v=1768816291"},{"product_id":"tci2510c077515028","title":"TCI C0775 42217-03-8 1-Chlorodocosane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0775 1-Chlorodocosane (CAS 42217-03-8) is a long-chain terminal alkyl chloride with a C22 hydrocarbon backbone. Its terminal chlorine provides a reactive site for nucleophilic substitution, making it an effective alkylating agent for introducing a long lipophilic tail. Typical uses include the preparation of surfactants, amphiphiles, synthetic lipid analogues, and surface-modifying agents. AMI Scientific supplies this TCI item in 5 g and 25 g pack sizes for materials, surface, and lipid research.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086027501786,"sku":"TCI2510C077515028","price":1339000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086027534554,"sku":"TCI2510C077515029","price":5048000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0775.jpg?v=1768816333"},{"product_id":"tci2510c082715115","title":"TCI C0827 2211-69-0 (Z)-2-Chloro-2-butene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0827 (Z)-2-Chloro-2-butene (CAS 2211-69-0) is a stereodefined vinylic chloride supplied in a compact 5 mL pack. As an sp2 carbon–chlorine building block, it serves as an electrophilic partner in transition-metal-catalysed cross-coupling and in the construction of substituted alkene motifs. Its defined Z geometry makes it useful for stereochemical studies and for methodology development. The compound is volatile and flammable, so chill the bottle before opening and handle it in a fume hood away from ignition sources.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5mL","offer_id":48086032023770,"sku":"TCI2510C082715115","price":4065000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0827_b28eedd5-3fc8-4029-b445-10e1a60cae3c.jpg?v=1792633104"},{"product_id":"tci2510c083415123","title":"TCI C0834 753-89-9 1-Chloro-2,2-dimethylpropane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0834 1-Chloro-2,2-dimethylpropane (CAS 753-89-9), commonly known as neopentyl chloride, is a highly branched alkyl chloride widely used as a non-heterocyclic building block. Its severely hindered structure makes it a classic model substrate for teaching and investigating nucleophilic substitution and carbocation rearrangement behaviour. AMI Scientific supplies this TCI-branded reagent in 5 mL and 25 mL packs so laboratories can match their purchase to actual experimental scale. Store the product in a cool, dry, well-ventilated area in a tightly closed container away from ignition sources, and consult the official TCI Safety Data Sheet before handling.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5mL","offer_id":48086032351450,"sku":"TCI2510C083415123","price":1768000.0,"currency_code":"IDR","in_stock":true},{"title":"25mL","offer_id":48086032384218,"sku":"TCI2510C083415124","price":4973000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0834.jpg?v=1768816348"},{"product_id":"tci2510c085215144","title":"TCI C0852 1001-89-4 2-Chloroheptane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0852 2-Chloroheptane (CAS 1001-89-4) is a secondary alkyl chloride bearing a stereogenic centre at the second carbon of a seven-carbon chain. Its secondary nature makes it an excellent model substrate for studying the competition between nucleophilic substitution and elimination pathways, as well as stereochemical outcomes. Synthetically, it serves to introduce a lipophilic heptyl chain onto nucleophiles or to prepare organometallic reagents. AMI Scientific supplies this TCI reagent in 5 mL and 25 mL packs; store it cool, dry, and tightly closed away from ignition sources.\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":"5mL","offer_id":48086033170650,"sku":"TCI2510C085215144","price":2297000.0,"currency_code":"IDR","in_stock":true},{"title":"25mL","offer_id":48086033203418,"sku":"TCI2510C085215145","price":6866000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0852.jpg?v=1768816352"},{"product_id":"tci2510c089015200","title":"TCI C0890 638-28-8 2-Chlorohexane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0890 2-Chlorohexane (CAS 638-28-8) is a secondary alkyl chloride that serves as a straightforward non-heterocyclic building block for laboratory synthesis. Its secondary carbon–chlorine bond makes it a useful substrate for alkylation chemistry, organometallic reagent preparation, and mechanistic studies of substitution versus elimination. The six-carbon chain also allows researchers to tune the lipophilic character of target molecules. Offered by AMI Scientific in 5 g and 25 g sizes, it should be kept tightly closed in a cool, dry, well-ventilated place away from heat and ignition sources.\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\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\u003cli\u003eMato et al. (2001). Study on Excess Molar Enthalpies and Excess Molar Volumes of the Binary Systems 1,2-Dichlorobenzene + (Benzene, Hexane, 1-Chlorohexane) and 1,3-Dichlorobenzene + (Benzene, Hexane, 1-Chlorohexane) at 298.15 K. \u003cem\u003eJournal of Chemical \u0026amp; Engineering Data\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1021\/je010040y\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1021\/je010040y\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086035857626,"sku":"TCI2510C089015200","price":2550000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086035890394,"sku":"TCI2510C089015201","price":8127000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0890.jpg?v=1769144539"},{"product_id":"tci2510c090115221","title":"TCI C0901 2346-81-8 3-Chlorohexane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0901 3-Chlorohexane (CAS 2346-81-8) is a secondary alkyl chloride belonging to the non-heterocyclic building block family. Its chlorine atom on a secondary carbon makes it a practical substrate for nucleophilic substitution chemistry and for introducing a hexyl fragment into target molecules. The compound is also commonly used as a precursor to organometallic reagents under anhydrous conditions and as a teaching example when comparing substitution and elimination pathways. AMI Scientific supplies this TCI product in a compact bottle format suited to laboratory-scale synthesis.\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\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\u003cli\u003eMato et al. (2001). Study on Excess Molar Enthalpies and Excess Molar Volumes of the Binary Systems 1,2-Dichlorobenzene + (Benzene, Hexane, 1-Chlorohexane) and 1,3-Dichlorobenzene + (Benzene, Hexane, 1-Chlorohexane) at 298.15 K. \u003cem\u003eJournal of Chemical \u0026amp; Engineering Data\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1021\/je010040y\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1021\/je010040y\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":"10mL","offer_id":48086036807898,"sku":"TCI2510C090115221","price":7295000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0901.jpg?v=1768816364"},{"product_id":"tci2510c119515654","title":"TCI C1195 21020-24-6 3-Chloro-1-butyne","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1195 3-Chloro-1-butyne, CAS 21020-24-6, is a compact propargylic halide that combines a terminal alkyne with a reactive carbon–chlorine bond. It is widely used for propargylation reactions, where nucleophiles displace the chloride to install a butynyl unit that remains available for further functionalisation. The retained terminal alkyne makes it a convenient precursor for copper-catalysed azide–alkyne cycloaddition, Sonogashira coupling, and alkyne-based cyclisations. AMI Scientific offers 1 g and 5 g packs for research laboratories, and this volatile, reactive reagent must be handled in a fume hood in accordance with the manufacturer's Safety Data Sheet.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086055878874,"sku":"TCI2510C119515654","price":6890000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086055911642,"sku":"TCI2510C119515655","price":15698000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1195_0e0f3af0-57c2-4383-8bc3-d6e648628908.jpg?v=1792633519"},{"product_id":"tci2510c129015777","title":"TCI C1290 503-60-6 1-Chloro-3-methyl-2-butene (stabilized with K2CO3)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1290 1-Chloro-3-methyl-2-butene (prenyl chloride, CAS 503-60-6) is a reactive allylic halide supplied stabilized with K2CO3. It is the reagent of choice for introducing the prenyl group onto oxygen, nitrogen, sulfur, and carbon nucleophiles under comparatively mild conditions. The prenyl unit is central to terpenoid and natural product synthesis as well as medicinal chemistry modification studies. AMI Scientific offers 25 mL and 250 mL pack sizes; the material is flammable, lachrymatory, and should be stored cold, dark, and tightly closed.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mL","offer_id":48086061121754,"sku":"TCI2510C129015777","price":3257000.0,"currency_code":"IDR","in_stock":true},{"title":"250mL","offer_id":48086061154522,"sku":"TCI2510C129015778","price":14335000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1290_0cf5e48c-9864-4693-a85e-5179b30a06d7.jpg?v=1792633593"},{"product_id":"tci2510c145916026","title":"TCI C1459 616-13-7 1-Chloro-2-methylbutane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1459 1-Chloro-2-methylbutane (CAS 616-13-7) is a short branched primary alkyl chloride used as a simple synthetic building block. Its primary chloride readily undergoes nucleophilic substitution, making it convenient for introducing the 2-methylbutyl group onto oxygen, nitrogen, or sulfur nucleophiles. It can also be converted into organometallic reagents for carbon-carbon bond formation and serves as a model substrate in mechanistic studies. AMI Scientific offers this TCI product in a 5 g pack; store it tightly closed in a cool, well-ventilated area away from ignition sources.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086071214298,"sku":"TCI2510C145916026","price":607000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1459.jpg?v=1769144472"},{"product_id":"tci2510c147616049","title":"TCI C1476 14753-05-0 1-Chloro-2-methylpentane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1476 1-Chloro-2-methylpentane (CAS 14753-05-0) is a branched primary alkyl chloride supplied as a non-heterocyclic building block. It serves research chemists as an alkylating agent and as a precursor for organomagnesium reagents in carbon–carbon bond formation. Available in 5 g and 25 g packs, it suits the millimole-scale workflows typical of academic and industrial R\u0026amp;D laboratories. Please refer to the manufacturer's label, Certificate of Analysis, and Safety Data Sheet for lot-specific technical and safety information.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086072328410,"sku":"TCI2510C147616049","price":1213000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086072361178,"sku":"TCI2510C147616050","price":3787000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1476.jpg?v=1768816541"},{"product_id":"tci2510c148016054","title":"TCI C1480 51575-83-8 1-Chloro-2-octyne","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1480 1-Chloro-2-octyne (CAS 51575-83-8) is a propargylic chloride bearing an internal alkyne, offering two reactive handles in a single molecule. The activated chloride readily undergoes nucleophilic substitution while the triple bond remains available for cycloaddition, coupling, or reduction chemistry. It is therefore a practical building block for constructing unsaturated carbon frameworks and heterocycles. Supplied as a 25 mL liquid pack; handle in a fume hood and consult the Safety Data Sheet before use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mL","offer_id":48086072525018,"sku":"TCI2510C148016054","price":2752000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1480_f942e54e-3106-44a7-a489-34c06b232acd.jpg?v=1792633758"},{"product_id":"tci2510c149316074","title":"TCI C1493 10297-06-0 6-Chloro-1-hexyne","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1493 6-Chloro-1-hexyne (CAS 10297-06-0) is a bifunctional building block carrying a terminal alkyne and a primary alkyl chloride separated by a six-carbon chain. The alkyne enables copper-catalysed azide–alkyne cycloaddition, Sonogashira coupling, and acetylide chemistry, while the chloride undergoes straightforward nucleophilic substitution. This orthogonal reactivity makes it a convenient linker for bioconjugation, probe synthesis, and surface functionalisation. Supplied in 5 mL and 25 mL packs; it is a volatile flammable liquid, so handle in a fume hood per the Safety Data Sheet.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5mL","offer_id":67556161945818,"sku":"TCI2510C149316074","price":1237000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1493_8d11700d-cd77-4f8f-9db7-81e8e6634c09.jpg?v=1792633767"},{"product_id":"tci2510c152216126","title":"TCI C1522 14267-92-6 5-Chloro-1-pentyne","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI 5-Chloro-1-pentyne (CAS 14267-92-6) is a bifunctional C5 building block bearing a terminal alkyne at one end and a primary alkyl chloride at the other. This complementary reactivity allows chemists to couple one terminus while reserving the other for a later transformation, making it a convenient flexible linker. It is widely used in click chemistry, Sonogashira couplings, and nucleophilic alkylation to introduce a pentynyl chain. AMI Scientific supplies it in 5 mL and 25 mL laboratory packs; please refer to the manufacturer's Safety Data Sheet for full handling and storage guidance.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5mL","offer_id":48086075605210,"sku":"TCI2510C152216126","price":1213000.0,"currency_code":"IDR","in_stock":true},{"title":"25mL","offer_id":48086075637978,"sku":"TCI2510C152216127","price":3937000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1522_e4e6643b-631c-4911-8ae4-04e035a14064.jpg?v=1792633798"},{"product_id":"tci2510c153416144","title":"TCI C1534 123-04-6 3-(Chloromethyl)heptane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1534, 3-(Chloromethyl)heptane (CAS 123-04-6), is a branched primary alkyl chloride widely used as a source of the 2-ethylhexyl group in organic synthesis. Its reactive carbon–chlorine bond makes it suitable for the alkylation of oxygen, nitrogen, and sulfur nucleophiles, as well as for the preparation of organometallic derivatives. The branched chain is often introduced to improve solubility and to reduce crystallinity in target molecules and materials. Supplied by AMI Scientific in a 5 g pack, it should be handled in a fume hood and stored in a tightly closed container in a cool, dry, well-ventilated area.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086076326106,"sku":"TCI2510C153416144","price":2095000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1534.jpg?v=1768816558"},{"product_id":"tci2510c156516194","title":"TCI C1565 1871-57-4 3-Chloro-2-chloromethyl-1-propene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1565 3-Chloro-2-chloromethyl-1-propene is a bifunctional building block bearing two reactive allylic chloromethyl groups flanking an exocyclic double bond. Its symmetry makes it a convenient reagent for double alkylation of stabilised nucleophiles, a route commonly used to assemble carbocyclic and spirocyclic frameworks. The remaining alkene offers a handle for downstream hydrogenation, oxidation, or metathesis chemistry. AMI Scientific supplies this TCI reagent in 5 g and 25 g pack sizes for both exploratory and multi-step synthetic work.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003e(2017). Selective N-Methylation of Pyrimidone with Chloro(chloromethyl)dimethylsilane–KF. \u003cem\u003eSynfacts\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1055\/s-0036-1591613\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1055\/s-0036-1591613\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086078259418,"sku":"TCI2510C156516194","price":2071000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086078292186,"sku":"TCI2510C156516195","price":6563000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1565_fd65f97e-7555-41ae-8588-cdab7bcdc71c.jpg?v=1792633868"},{"product_id":"tci2510c165316309","title":"TCI C1653 62614-70-4 cis-6-Chloro-2-hexene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1653 62614-70-4 cis-6-Chloro-2-hexene is a versatile organic compound used as a building block in the synthesis of complex molecules. This compound is widely applied in laboratory research for its reactivity and structural flexibility. It is commonly used in the development of pharmaceuticals and chemical materials. Its simple structure allows for various chemical reactions, making it a valuable tool in organic chemistry. The compound is available in different volumes, suitable for both small-scale experiments and larger research projects. Its stability and purity make it a reliable choice for Indonesian laboratories engaged in chemical research.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5mL","offer_id":48086083010778,"sku":"TCI2510C165316309","price":3029000.0,"currency_code":"IDR","in_stock":true},{"title":"25mL","offer_id":48086083043546,"sku":"TCI2510C165316310","price":10045000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1653_650f4a81-83cf-422e-8fd8-0f8a172d433f.jpg?v=1792633953"},{"product_id":"tci2510c168616353","title":"TCI C1686 591-97-9 Crotyl Chloride (cis- and trans- mixture, contains 38% 3-Chloro-1-butene at maximum)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCrotyl Chloride (cis- and trans- mixture), with CAS number 591-97-9, is a chemical building block widely used in organic synthesis. This compound is a mixture containing up to 38% 3-Chloro-1-butene and is known for its reactivity in various chemical reactions such as addition, substitution, and isomerization. It is commonly utilized in laboratory settings for the synthesis of complex organic compounds. Due to its sensitivity to moisture and air, it requires careful handling and storage. In Indonesia, this compound is essential for research in organic chemistry, pharmaceutical development, and material science, offering versatility in experimental applications.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eDong et al. (2012). Cuprous Chloride Catalyzed Isomerization of 3-Chloro-1-butene to Crotyl Chloride. \u003cem\u003eChinese Journal of Organic Chemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.6023\/cjoc1109212\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.6023\/cjoc1109212\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":48086084681946,"sku":"TCI2510C168616353","price":657000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48086084714714,"sku":"TCI2510C168616354","price":3307000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1686_6b41bc71-3209-4610-b2e3-27f45d89854f.jpg?v=1792633976"},{"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":2626000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2213.jpg?v=1768816803"},{"product_id":"tci2510c288217764","title":"TCI C2882 75-00-3 Chloroethane (ca. 17% in Ethyl Ether, ca. 2.0mol\/L)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eChloroethane is a chemical compound widely used in laboratory experiments across various fields of chemistry. As a volatile liquid, it is commonly employed as a solvent or reagent in chemical reactions that require specific conditions. Its unique chemical properties make it a versatile tool in synthetic and analytical chemistry, where it can act as a reagent or a reaction medium. This product is particularly useful in reactions involving substitution or elimination mechanisms, where its reactivity and solubility characteristics are advantageous.\u003c\/p\u003e\n\u003cp\u003eThe composition of this product includes approximately 17% chloroethane in ethyl ether, with a concentration of about 2.0 mol\/L. This formulation ensures stability while maintaining reactivity, allowing it to participate in chemical reactions without significant structural changes to the molecules involved. Its volatility and solubility in organic solvents make it a preferred choice for applications requiring controlled and efficient chemical interactions. The balanced concentration also enhances safety and ease of use in laboratory settings.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, chloroethane is frequently utilized in organic and analytical chemistry research. It plays a crucial role in both teaching and research environments, supporting experiments that require precise chemical interactions. Its availability and reliability make it a standard component in many laboratory protocols, especially in institutions focused on chemical synthesis and analysis. The product’s formulation ensures it is suitable for use in a variety of experimental setups, contributing to the efficiency and accuracy of laboratory work.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis reactions benefit from chloroethane's solubility and reactivity, enabling efficient substitution and elimination processes.\u003c\/li\u003e\n\u003cli\u003eAnalytical chemistry uses chloroethane as a solvent for sample preparation, ensuring accurate and reproducible results.\u003c\/li\u003e\n\u003cli\u003eTeaching laboratories rely on chloroethane for demonstrating basic chemical reactions and properties, enhancing student understanding.\u003c\/li\u003e\n\u003cli\u003eExtraction processes in chemical analysis utilize chloroethane for isolating compounds due to its low boiling point and solubility.\u003c\/li\u003e\n\u003cli\u003eIndustrial research applications leverage chloroethane for its versatility in creating custom chemical formulations and reaction 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: 75-00-3\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified\u003c\/li\u003e\n\u003cli\u003ePhysical form: Liquid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, well-ventilated area away from heat and direct sunlight.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eChloroethane should be stored in a cool, well-ventilated area, away from heat and direct sunlight to maintain its stability and prevent degradation. It is recommended to use sealed containers made of materials compatible with organic solvents, such as glass or high-density polyethylene. Due to its volatility, it is essential to handle the product in a fume hood to minimize exposure and ensure a safe working environment. Avoid contact with open flames or sparks, as chloroethane is highly flammable. Regularly check the container for leaks or damage to prevent accidental release. In laboratory settings, proper personal protective equipment, including gloves and safety goggles, should always be worn when handling this chemical.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mL","offer_id":48086201139418,"sku":"TCI2510C288217764","price":1718000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48086201172186,"sku":"TCI2510C288217765","price":5250000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2882_6ae7c876-1019-440d-a53d-a763d515a2c8.jpg?v=1792634941"}],"url":"https:\/\/amiscientific.com\/en\/collections\/tci-l4-halogenated-hydrocarbons-fluorides-expected-non-heterocyclic-building-blocks.oembed?page=15","provider":"AMI Scientific","version":"1.0","type":"link"}