{"title":"Benzaldehydes [Liquid Crystal (LC) Building Blocks]","description":"\u003cp\u003e\u003cstrong\u003eBenzaldehydes [Liquid Crystal (LC) Building Blocks]\u003c\/strong\u003e — menghimpun turunan benzaldehida tersubstitusi gugus alkoksi, boronat, trifluorometoksi, atau bromofenoksi yang gugus karbonilnya menjadi titik sambung reaksi kondensasi maupun kopling silang. Senyawa ini berperan sebagai unit inti aromatik untuk pembentukan mesogen dalam material kristal cair.\u003c\/p\u003e\u003cp\u003eBenzaldehida tersubstitusi seperti 3,4,5-tris(dodesiloksi)benzaldehida dan turunan boronat ester digunakan peneliti material display untuk menyusun molekul kristal cair kalamitik melalui reaksi Suzuki atau kondensasi Knoevenagel. p-Anisaldehida dan 4-hidroksibenzaldehida juga umum dipakai sebagai bahan awal sintesis mesogen aromatik pada riset kimia material.\u003c\/p\u003e\u003cp\u003eContoh produk dalam koleksi ini: \u003ca href=\"\/en\/products\/tci2510h019832626\"\u003eTCI H0198 123-08-0 4-Hydroxybenzaldehyde\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510d112420847\"\u003eTCI D1124 24083-16-7 4-Decyloxybenzaldehyde\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510t025951034\"\u003eTCI T0259 104-87-0 p-Tolualdehyde\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510d568226652\"\u003eTCI D5682 307498-21-1 3-Dodecylbenzaldehyde\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510a0480678\"\u003eTCI A0480 123-11-5 p-Anisaldehyde\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510e004227678\"\u003eTCI E0042 10031-82-0 4-Ethoxybenzaldehyde\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510t362455281\"\u003eTCI T3624 117241-32-4 3,4,5-Tris(dodecyloxy)benzaldehyde\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510e032528046\"\u003eTCI E0325 4748-78-1 4-Ethylbenzaldehyde\u003c\/a\u003e.\u003c\/p\u003e\u003cp\u003eSesuaikan panjang rantai alkoksi dan jenis gugus reaktif (aldehida bebas, boronat ester, atau halida) dengan tahap sintesis mesogen yang dituju, serta perhatikan kemurnian untuk menghindari pengotor yang memengaruhi sifat fase cair-kristal. Seluruh produk merupakan produk asli Tokyo Chemical Industry (TCI) Jepang, dengan kemurnian, kemasan, dan kondisi penyimpanan tercantum pada halaman masing-masing item.\u003c\/p\u003e\u003cp\u003eKategori lain yang sejajar di bawah Liquid Crystal (LC) Building Blocks, sering dipakai bersamaan dalam satu alur kerja laboratorium:\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-biphenyls-liquid-crystal-lc-building-blocks\"\u003eBiphenyls [Liquid Crystal (LC) Building Blocks]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-benzoic-acids-liquid-crystal-lc-building-blocks\"\u003eBenzoic Acids [Liquid Crystal (LC) Building Blocks]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-phenols-liquid-crystal-lc-building-blocks\"\u003ePhenols [Liquid Crystal (LC) Building Blocks]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-bromobenzenes-liquid-crystal-lc-building-blocks\"\u003eBromobenzenes [Liquid Crystal (LC) Building Blocks]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-benzeneboronic-acids-liquid-crystal-lc-building-blocks\"\u003eBenzeneboronic Acids [Liquid Crystal (LC) Building Blocks]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-chiral-compounds-liquid-crystal-lc-building-blocks\"\u003eChiral Compounds [Liquid Crystal (LC) Building Blocks]\u003c\/a\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eKembali ke \u003ca href=\"\/en\/collections\/tci-l3-liquid-crystal-lc-building-blocks\"\u003eLiquid Crystal (LC) Building Blocks\u003c\/a\u003e. Untuk pengadaan volume besar, kemasan khusus, atau grade tertentu, hubungi tim AMI Scientific — distributor resmi TCI Japan di Indonesia — untuk pengecekan ketersediaan dan lead time langsung ke Jepang.\u003c\/p\u003e","products":[{"product_id":"tci2510d112420847","title":"TCI D1124 24083-16-7 4-Decyloxybenzaldehyde","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e4-Decyloxybenzaldehyde is a chemical compound widely used as a building block in the synthesis of complex organic compounds. It serves as a versatile intermediate in various chemical reactions, enabling the modification of carbon chains through its aldehyde functional group and long hydrocarbon chain. This compound plays a crucial role in organic chemistry by offering a stable and reactive platform for further chemical transformations. Its structural simplicity and functional versatility make it an essential tool for researchers aiming to design and synthesize new molecules with specific properties.\u003c\/p\u003e\n\u003cp\u003eThe compound's stability and controlled reactivity make it a preferred choice in laboratory settings. Its ability to participate in nucleophilic reactions, substitution reactions, and condensation reactions enhances its utility in synthetic pathways. Additionally, its capacity to form bonds with various functional groups allows for the creation of more complex molecular structures. These properties ensure that 4-Decyloxybenzaldehyde remains a valuable reagent in both academic and industrial research environments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 4-Decyloxybenzaldehyde is commonly used in research and development projects, particularly in pharmaceutical and materials science applications. It is a key component in experiments requiring specific molecular structures and controlled reactivity. Its use supports the development of new compounds with potential applications in drug discovery and advanced material synthesis, contributing to scientific innovation in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis projects benefit from 4-Decyloxybenzaldehyde due to its reactivity and structural versatility, allowing for the creation of complex molecules with tailored properties.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research utilizes this compound as a building block for the synthesis of drug candidates, offering a stable and modifiable platform for functional group manipulation.\u003c\/li\u003e\n\u003cli\u003eMaterials science applications leverage its hydrocarbon chain and aldehyde group to develop new polymers and functional materials with unique chemical properties.\u003c\/li\u003e\n\u003cli\u003eAcademic research in chemistry often incorporates this compound to explore reaction mechanisms and synthetic pathways in undergraduate and graduate studies.\u003c\/li\u003e\n\u003cli\u003eIndustrial R\u0026amp;D uses it as a key intermediate in the production of specialty chemicals, supporting innovation in chemical manufacturing processes.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 24083-16-7\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Liquid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and incompatible substances\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003e4-Decyloxybenzaldehyde should be stored in a cool, dry environment, away from direct light and sources of heat. It is recommended to keep the compound in a sealed container to prevent evaporation and contamination. Due to its chemical nature, it should be stored separately from strong oxidizing agents and reactive materials to ensure safety. In laboratory settings, proper ventilation is essential when handling this compound to minimize exposure. Always use appropriate personal protective equipment, such as gloves and safety goggles, to protect against potential skin or eye contact. Regular inspection of storage conditions is advised to maintain the integrity and safety of the compound.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086425927898,"sku":"TCI2510D112420847","price":2559000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086425960666,"sku":"TCI2510D112420848","price":6690000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D1124.jpg?v=1768817388"},{"product_id":"tci2510d568226652","title":"TCI D5682 307498-21-1 3-Dodecylbenzaldehyde","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D5682 3-Dodecylbenzaldehyde is an aromatic aldehyde that carries a twelve-carbon dodecyl chain at the meta position relative to the aldehyde group. The material is classified as a non-heterocyclic building block, and its role in the laboratory is to supply a highly reactive aldehyde group together with a long hydrocarbon tail that imparts lipophilic character. That combination makes the compound a practical starting point for constructing molecules that must dissolve well in organic solvents or must be able to self-assemble at interfaces, something that is difficult to achieve when researchers work with plain benzaldehyde bearing no substituent.\u003c\/p\u003e\n\u003cp\u003eThe property that makes this compound a preferred choice lies in the versatility of the aldehyde carbonyl group, which is ready to enter condensation reactions with amines to form imines or Schiff bases, reduction reactions to the corresponding alcohol, oxidation to the carboxylic acid, and chain-extension reactions such as Wittig and aldol chemistry. The meta position exerts a more electronically neutral influence on the carbonyl group than the para position does, so aldehyde reactivity remains high. The dodecyl chain lowers the melting point and raises solubility in non-polar solvents, which makes processing and purification more straightforward.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, a building block of this type is typically used in university and institutional research groups working on organic synthesis, materials chemistry, and surfactant or amphiphile design. It suits work where a long-chain aromatic aldehyde is needed as an intermediate for Schiff base ligands, functional molecules, or specialty formulations. Because it is supplied as a catalogue reagent from TCI, it fits research-scale synthesis, method development, and teaching work at the postgraduate level rather than bulk production.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSchiff base and imine synthesis: the reactive aldehyde carbonyl condenses readily with primary amines, while the dodecyl tail keeps the resulting ligand soluble in organic reaction media.\u003c\/li\u003e\n\u003cli\u003eAmphiphile and surfactant research: the molecule already pairs a polar reactive head with a long lipophilic tail, so it serves as a direct scaffold for molecules designed to assemble at interfaces.\u003c\/li\u003e\n\u003cli\u003eMaterials and functional molecule synthesis: the aldehyde group allows attachment to amine-, phosphorus-, or carbonyl-based partners so that a long alkyl chain can be built into a larger target structure.\u003c\/li\u003e\n\u003cli\u003eChain-extension chemistry such as Wittig and aldol reactions: the aldehyde acts as the electrophilic partner, and the meta substitution leaves its reactivity essentially undiminished.\u003c\/li\u003e\n\u003cli\u003eRedox transformation studies: the compound can be reduced to the corresponding benzyl alcohol or oxidised to the carboxylic acid, giving a convenient route to related long-chain aromatic derivatives.\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: 307498-21-1\u003c\/li\u003e\n\u003cli\u003eCatalogue code: D5682\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in standard TCI research-scale packaging; please confirm the pack size when ordering.\u003c\/li\u003e\n\u003cli\u003eStorage note: store in a tightly closed original container in a cool, dry, well-ventilated place, following the manufacturer's safety data sheet.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eKeep the container tightly closed and store it in a cool, dry, well-ventilated area away from direct sunlight, heat sources, and strong oxidising agents. Aromatic aldehydes are generally sensitive to air, so minimise headspace exposure and reseal the container promptly after each use; the original manufacturer container is the most suitable storage vessel. Handle the material in a fume hood using safety glasses, chemical-resistant gloves, and a laboratory coat, and avoid contact with skin and eyes as well as inhalation of vapours. Transfer with clean, dry glassware, label all secondary containers clearly, and consult the manufacturer's safety data sheet before use and for waste disposal.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086774841562,"sku":"TCI2510D568226652","price":11693000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D5682.jpg?v=1767109080"},{"product_id":"tci2510e004227678","title":"TCI E0042 10031-82-0 4-Ethoxybenzaldehyde","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e4-Ethoxybenzaldehyde is a versatile organic compound widely used in laboratory settings for its reactivity and structural versatility. As a building block in organic synthesis, it serves as a key intermediate in the development of more complex chemical structures. Its aldehyde functional group, combined with the ethoxy substituent, makes it a valuable tool for chemists seeking to modify aromatic rings or introduce new functionalities. This compound is commonly employed in research and educational institutions across Indonesia, supporting both academic and industrial chemical innovation.\u003c\/p\u003e\n\u003cp\u003eThe chemical properties of 4-Ethoxybenzaldehyde make it a preferred choice for various synthetic reactions. Its reactivity allows it to participate in condensation, reduction, and substitution reactions, making it adaptable to a wide range of synthetic strategies. However, its sensitivity to moisture and air necessitates careful handling and storage. Despite these challenges, its ability to interact with a variety of reagents makes it an essential component in the synthesis of new compounds. This reactivity and specificity contribute to its importance in organic chemistry research.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 4-Ethoxybenzaldehyde is a fundamental reagent used in the synthesis of target molecules with specific structural requirements. It is frequently utilized in both academic and research environments to explore new chemical pathways and develop novel compounds. Its role in creating complex structures makes it an indispensable resource for chemists working in Indonesia’s scientific community.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis: 4-Ethoxybenzaldehyde is ideal for constructing complex molecules due to its reactive aldehyde group and ethoxy substituent.\u003c\/li\u003e\n\u003cli\u003eAcademic research: It supports teaching and learning in organic chemistry courses, enabling students to practice synthetic techniques.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical development: Its structural versatility makes it suitable for the synthesis of drug-related compounds and derivatives.\u003c\/li\u003e\n\u003cli\u003eIndustrial applications: It is used in the production of specialty chemicals and materials requiring precise molecular design.\u003c\/li\u003e\n\u003cli\u003eAnalytical studies: Its distinct chemical profile allows it to be used as a reference standard in analytical and spectroscopic experiments.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 10031-82-0\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities to meet different laboratory needs\u003c\/li\u003e\n\u003cli\u003ePhysical form: Liquid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and air\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003e4-Ethoxybenzaldehyde should be stored in a cool, dry environment to prevent degradation due to its sensitivity to moisture and air. It is recommended to use airtight containers made of glass or polyethylene to minimize exposure. The compound should be kept away from light and heat sources to maintain its chemical integrity. In laboratory settings, it is essential to handle this material with appropriate personal protective equipment, such as gloves and safety goggles, to ensure safety. Proper labeling and storage conditions are crucial to prevent contamination and ensure safe usage in chemical experiments.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086814884058,"sku":"TCI2510E004227678","price":1013000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48086814916826,"sku":"TCI2510E004227679","price":9557000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510E0042.jpg?v=1769180735"},{"product_id":"tci2510e032528046","title":"TCI E0325 4748-78-1 4-Ethylbenzaldehyde","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e4-Ethylbenzaldehyde is a chemical compound widely used as a foundational material in various laboratory reactions. It serves as a key building block in organic chemistry, enabling the synthesis of more complex molecules. This compound is particularly valued for its ability to participate in multiple chemical reactions, making it a versatile reagent in both academic and industrial research settings. Its role in the laboratory extends beyond mere reactivity, as it is essential for creating compounds with specific molecular structures, such as fragrances, pharmaceuticals, and industrial chemicals.\u003c\/p\u003e\n\u003cp\u003eThe chemical properties of 4-Ethylbenzaldehyde make it a preferred choice for laboratory use. It exhibits a stable molecular structure while maintaining reactivity, allowing it to engage in reactions such as reduction, oxidation, and substitution. Its well-defined physical properties, including a specific boiling point and melting point, ensure predictable behavior during experimental procedures. These characteristics contribute to the accuracy and reproducibility of chemical experiments, which are critical in scientific research.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 4-Ethylbenzaldehyde is commonly used in organic chemistry research, chemical development, and the production of aromatic compounds. Its reliability and consistency in performance make it a trusted material for scientists and researchers working on a wide range of chemical applications. The compound’s availability and compatibility with various laboratory techniques further enhance its utility in both academic and industrial contexts.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis reactions benefit from 4-Ethylbenzaldehyde due to its reactivity and ability to form complex molecular structures.\u003c\/li\u003e\n\u003cli\u003eAroma compound development relies on this compound for creating fragrances and flavoring agents with specific molecular profiles.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research utilizes 4-Ethylbenzaldehyde as a precursor for synthesizing active pharmaceutical ingredients.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical production employs this compound for manufacturing specialty chemicals with tailored properties.\u003c\/li\u003e\n\u003cli\u003eResearch in chemical modification processes uses 4-Ethylbenzaldehyde for its compatibility with various functional group transformations.\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: 4748-78-1\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory supply\u003c\/li\u003e\n\u003cli\u003ePhysical form: Liquid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct sunlight and incompatible materials\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003e4-Ethylbenzaldehyde should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep the compound in a tightly sealed container to prevent exposure to air and moisture. Suitable storage containers include glass or high-density polyethylene bottles that are resistant to chemical degradation. Due to its reactivity, it should be kept away from strong oxidizing agents and incompatible substances. Laboratory personnel should handle the compound with appropriate personal protective equipment, such as gloves and safety goggles, to ensure safe usage. Regular monitoring of storage conditions is essential to preserve the integrity and effectiveness of the compound in experimental applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mL","offer_id":48086835560666,"sku":"TCI2510E032528046","price":1069000.0,"currency_code":"IDR","in_stock":true},{"title":"100mL","offer_id":48086835593434,"sku":"TCI2510E032528047","price":3008000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48086835626202,"sku":"TCI2510E032528048","price":7364000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510E0325.jpg?v=1768818666"},{"product_id":"tci2510f019129909","title":"TCI F0191 459-57-4 4-Fluorobenzaldehyde","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e4-Fluorobenzaldehyde (CAS 459-57-4) is an organic compound belonging to the aromatic aldehyde family, bearing a fluorine atom at the para position relative to the aldehyde group. In the chemistry laboratory, this compound serves as a highly versatile building block and starting material for synthesis, particularly for constructing more complex molecules that contain fluorine. The presence of a reactive aldehyde group allows the compound to undergo a wide range of reactions, including aldol condensation, Grignard reactions, reduction to the corresponding alcohol, and oxidation to the carboxylic acid.\u003c\/p\u003e\n\u003cp\u003eMeanwhile, the fluorine atom imparts unique characteristics to the final products, such as enhanced metabolic stability and increased lipophilicity, which are highly valued in pharmaceutical and materials research. For this reason, 4-Fluorobenzaldehyde is one of the most sought-after starting materials in organic chemistry, medicinal chemistry, and the development of functional materials. The TCI product is recognized for its high purity and consistent quality, making reaction outcomes more reproducible from batch to batch. As a clear to yellowish liquid, the compound is easy to pour and weigh, which simplifies handling on the laboratory bench and reduces the risk of waste during dispensing.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian research laboratories, this reagent is commonly used in organic synthesis projects at universities, research institutes, and pharmaceutical development facilities. It serves as a reliable intermediate for preparing fluorinated drug candidates, agrochemical intermediates, and functional organic molecules. Researchers working on heterocyclic synthesis, cross-coupling chemistry, and structure-activity relationship studies frequently select this product because of its dependable purity and stable supply through AMI Scientific. Its liquid form is convenient for accurate dosing in small-scale reactions, which is typical of academic and early-stage industrial research settings.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAldol condensation: The reactive aldehyde group readily participates in aldol condensations, enabling the construction of fluorinated α,β-unsaturated carbonyl frameworks that are valuable intermediates in target-oriented synthesis.\u003c\/li\u003e\n\u003cli\u003eGrignard and organometallic additions: The aldehyde carbonyl acts as an electrophilic acceptor for Grignard and organolithium reagents, giving secondary alcohols bearing both fluorine and a new carbon framework for further elaboration.\u003c\/li\u003e\n\u003cli\u003eReduction to fluorinated alcohols: Selective reduction of the aldehyde group produces 4-fluorobenzyl alcohol, a useful building block for ester and ether derivatives applied in medicinal chemistry and material functionalization.\u003c\/li\u003e\n\u003cli\u003eOxidation to 4-fluorobenzoic acid: Controlled oxidation converts the aldehyde into 4-fluorobenzoic acid, an important precursor for coordination chemistry, polymer synthesis, and pharmaceutical intermediates.\u003c\/li\u003e\n\u003cli\u003eMedicinal chemistry scaffold assembly: The fluorine atom improves metabolic stability and lipophilicity of drug candidates, making this aldehyde a preferred starting point for structure-activity relationship studies in drug discovery programs.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI (product code F0191)\u003c\/li\u003e\n\u003cli\u003eCAS number: 459-57-4\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Fluorinated Building Blocks\u003c\/li\u003e\n\u003cli\u003ePhysical form: Clear to yellowish liquid\u003c\/li\u003e\n\u003cli\u003ePack sizes: Standard laboratory pack sizes available; contact AMI Scientific for current options\u003c\/li\u003e\n\u003cli\u003eStorage: Store tightly sealed in a cool, dry place away from light and heat\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore 4-Fluorobenzaldehyde in its original, tightly sealed container in a cool, dry, and well-ventilated area, protected from direct sunlight and sources of heat. Suitable containers are the original glass or compatible laboratory bottles that resist attack by aldehydes; avoid prolonged contact with plastics that may degrade. When dispensing, work in a fume hood and use personal protective equipment such as chemical-resistant gloves, safety goggles, and a laboratory coat, since aldehydes can irritate the skin, eyes, and respiratory tract. Keep the container closed when not in use to prevent oxidation and moisture uptake, and label all secondary containers clearly.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mL","offer_id":48086985375962,"sku":"TCI2510F019129909","price":1097000.0,"currency_code":"IDR","in_stock":true},{"title":"250mL","offer_id":48086985408730,"sku":"TCI2510F019129910","price":6325000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510F0191.jpg?v=1768818884"},{"product_id":"tci2510h016632576","title":"TCI H0166 5736-94-7 4-(Hexyloxy)benzaldehyde","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e4-(Hexyloxy)benzaldehyde is an aromatic compound that combines an aldehyde group on a benzene ring with a hexyloxy chain at the para position. This pairing of a highly reactive functional group with a long alkyl chain makes it a particularly useful building block in organic synthesis, especially for assembling elongated, rod-shaped molecules. In the TCI catalogue the product carries the code H0166 and is classified among the non-heterocyclic building blocks. It is supplied as a research chemical for laboratories that construct larger organic frameworks from defined, well-characterised starting materials rather than from crude mixtures.\u003c\/p\u003e\n\u003cp\u003eThe property that makes this material stand out is its aldehyde group, which reacts readily with primary amines, active methylene compounds and organometallic reagents, opening up a wide range of transformations in a single reaction step. The hexyloxy chain, meanwhile, gives good solubility in organic solvents and contributes the mesogenic character that is key to liquid crystalline phase formation in the derivatives made from it. The alkoxy ether group is electron-donating and therefore influences the electron distribution across the aromatic ring, a feature researchers exploit when tuning the electronic behaviour of a target molecule.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories this compound is typically used in organic synthesis groups at universities and research institutes, as well as in materials-oriented work. It appears in liquid crystal synthesis, in the preparation of Schiff bases and chalcones, and in the development of optical materials and functional organic molecules. Because it is a defined catalogue item from TCI, it suits work where reproducibility between batches matters, such as method development, thesis research and repeated preparations that must give consistent results.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eLiquid crystal synthesis: the para-substituted aldehyde and long hexyloxy tail give the elongated molecular shape and mesogenic character required for building compounds that form liquid crystalline phases.\u003c\/li\u003e\n\u003cli\u003eSchiff base preparation: the aldehyde group condenses readily with primary amines, making this a direct and convenient starting material for imine formation in a single reaction step.\u003c\/li\u003e\n\u003cli\u003eChalcone synthesis: the reactive aldehyde couples with active methylene compounds, giving laboratories a straightforward entry point into chalcone frameworks and their many downstream derivatives.\u003c\/li\u003e\n\u003cli\u003eOptical and functional materials development: the electron-donating alkoxy ether influences electron distribution on the aromatic ring, which researchers use when tuning the electronic properties of organic materials.\u003c\/li\u003e\n\u003cli\u003eGeneral organic building block work: reactivity toward organometallic reagents plus good solubility in organic solvents makes it a flexible intermediate for multi-step routes toward larger molecular targets.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI (Tokyo Chemical Industry), catalogue code H0166\u003c\/li\u003e\n\u003cli\u003eCAS number: 5736-94-7\u003c\/li\u003e\n\u003cli\u003eChemical name: 4-(Hexyloxy)benzaldehyde\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in the standard TCI catalogue pack sizes for this item\u003c\/li\u003e\n\u003cli\u003eStorage: keep in the closed original container, following the conditions stated on the product label and Safety Data Sheet\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the compound in its original tightly closed container, kept in a cool, dry and well-ventilated area away from direct sunlight, heat sources and incompatible chemicals. As an aldehyde, it should be protected from prolonged exposure to air and moisture, so the container should be resealed promptly after each use and handled in a fume hood where practicable. Wear a laboratory coat, safety glasses and suitable chemical-resistant gloves during transfer and weighing. Always consult the manufacturer's Safety Data Sheet before use, and dispose of residues and contaminated materials as chemical waste through the laboratory's normal waste-handling procedures rather than into drains.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48087161405658,"sku":"TCI2510H016632576","price":2503000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510H0166.jpg?v=1768360538"},{"product_id":"tci2510h019832626","title":"TCI H0198 123-08-0 4-Hydroxybenzaldehyde","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI H0198 4-Hydroxybenzaldehyde is the para isomer of hydroxybenzaldehyde, bearing a phenolic hydroxyl group and an aldehyde group positioned directly opposite one another on the benzene ring. The compound ranks among the most widely used aromatic building blocks in organic synthesis laboratories because it serves as a starting point toward a broad family of valuable phenolic derivatives, including aroma compounds and pharmaceutical intermediates. At the researcher's bench, this material becomes the reference choice whenever a molecular design calls for a para-hydroxybenzene core that can be elaborated further through established, well-documented routes.\u003c\/p\u003e\n\u003cp\u003eThe property that makes it a frequent selection is its balance between reactivity and stability. The para arrangement places the hydroxyl group in direct conjugation with the aldehyde group, giving the ring a distinctive electronic character so that both substitution and condensation reactions proceed along patterns that are easy to predict. Its crystalline solid form makes accurate weighing straightforward and allows repurification by recrystallization whenever that is required. The compound also dissolves in many common organic solvents available in the laboratory, which simplifies the preparation of reaction systems.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 4-Hydroxybenzaldehyde is typically kept as a standing bench reagent in organic synthesis groups at universities and research institutes, as well as in industrial R\u0026amp;D units developing flavour, fragrance, and fine-chemical routes. Its predictable handling behaviour and wide documentation make it suitable for teaching-scale preparations and method development alike, where reproducible starting material is more important than exotic reactivity.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSynthesis of phenolic derivatives — the free phenolic hydroxyl can be alkylated, acylated, or otherwise protected, giving a direct and well-documented entry into substituted phenol families.\u003c\/li\u003e\n\u003cli\u003ePreparation of pharmaceutical intermediates — its role as a recognised starting point toward valuable derivatives makes it suitable for building intermediate scaffolds in medicinal chemistry programmes.\u003c\/li\u003e\n\u003cli\u003eAroma compound synthesis — the para-hydroxybenzene core is a known precursor to aroma-active phenolic compounds, so the material supports flavour and fragrance route development work.\u003c\/li\u003e\n\u003cli\u003eCondensation reactions — the aldehyde group participates in condensation chemistry with predictable outcomes, which helps researchers plan multi-step sequences with confidence in each stage.\u003c\/li\u003e\n\u003cli\u003eAromatic substitution studies — conjugation between the hydroxyl and aldehyde groups gives the ring a distinctive electronic profile useful for investigating and teaching substitution behaviour.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI (Tokyo Chemical Industry)\u003c\/li\u003e\n\u003cli\u003eCAS Number: 123-08-0\u003c\/li\u003e\n\u003cli\u003eCatalogue Number: H0198\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePhysical form: crystalline solid\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in standard TCI research pack sizes; please confirm the size required when ordering\u003c\/li\u003e\n\u003cli\u003eStorage: keep in a closed container in a cool, dry place away from light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the container tightly closed in a cool, dry, well-ventilated area, away from direct sunlight and sources of heat or ignition. Amber glass bottles or the original manufacturer packaging are suitable, since they limit exposure to light and moisture that can degrade phenolic aldehydes over time. Handle the solid inside a fume hood and wear standard laboratory protection — safety glasses, gloves, and a laboratory coat — to avoid contact with skin, eyes, and inhalation of dust. Weigh out only the quantity needed, close the container promptly after use to reduce moisture uptake, and keep the material separated from strong oxidising agents and strong bases. Consult the manufacturer's Safety Data Sheet before first use and follow institutional waste disposal procedures for residues.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48087167402202,"sku":"TCI2510H019832626","price":536000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48087167434970,"sku":"TCI2510H019832627","price":1631000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48087167467738,"sku":"TCI2510H019832628","price":3740000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510H0198.jpg?v=1769056275"},{"product_id":"tci2510h023832703","title":"TCI H0238 27893-41-0 4-Heptyloxybenzaldehyde","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e4-Heptyloxybenzaldehyde is a chemical compound widely used in organic reactions for the synthesis of complex molecules. This compound plays a crucial role in laboratories by serving as a versatile building block in various synthetic pathways. Its unique molecular structure, consisting of an aldehyde group and a heptyloxy chain, makes it highly reactive and suitable for a range of chemical transformations. In the field of chemistry, it is commonly employed as a precursor for the production of aromatic compounds and their derivatives.\u003c\/p\u003e\n\u003cp\u003eThe stability of its chemical structure and its favorable reactivity make 4-Heptyloxybenzaldehyde a preferred choice for synthetic chemists. Its ability to participate in multiple reaction types, such as Diels-Alder, Friedel-Crafts, and electrophilic substitution reactions, enhances its utility in laboratory settings. This compound is particularly valuable for researchers aiming to develop new compounds or modify existing organic molecules. Its versatility and reliability contribute to its popularity in both academic and industrial research environments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 4-Heptyloxybenzaldehyde is extensively used in organic chemistry research, especially in universities and research institutions. It is a key reagent in projects involving the synthesis of new compounds or the modification of organic structures. Its application is particularly relevant in pharmacological research and the study of heterocyclic compounds. Its widespread use underscores its importance in advancing chemical research in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSynthesis of complex aromatic compounds for pharmacological research due to its reactive aldehyde group and heptyloxy chain.\u003c\/li\u003e\n\u003cli\u003ePreparation of heterocyclic compounds in organic chemistry studies because of its ability to undergo electrophilic substitution reactions.\u003c\/li\u003e\n\u003cli\u003eDevelopment of new organic molecules through its participation in Diels-Alder and Friedel-Crafts reactions.\u003c\/li\u003e\n\u003cli\u003eModification of existing organic structures in synthetic chemistry due to its versatile functional groups.\u003c\/li\u003e\n\u003cli\u003eInvestigation of chemical reactivity in laboratory experiments as a reliable and stable building block.\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: 27893-41-0\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: Not specified\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003e4-Heptyloxybenzaldehyde should be stored in a cool, dry place away from light and moisture to maintain its chemical stability. It is recommended to use airtight containers to prevent exposure to air and humidity. Due to its reactive nature, it should be handled in a well-ventilated area, preferably under a fume hood, to minimize inhalation risks. Avoid contact with skin and eyes, and use appropriate personal protective equipment such as gloves and safety goggles. Ensure that storage conditions are controlled to prevent degradation and maintain the compound’s effectiveness in laboratory applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mL","offer_id":48087174742234,"sku":"TCI2510H023832703","price":4751000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510H0238.jpg?v=1768360547"},{"product_id":"tci2510i061235837","title":"TCI I0612 15164-44-0 4-Iodobenzaldehyde","description":"\u003cp\u003e\u003cstrong\u003e4-Iodobenzaldehyde\u003c\/strong\u003e (CAS 15164-44-0) is a high-quality chemical from TCI, supplied as \u003cstrong\u003eGC Grade \/ for Synthesis\u003c\/strong\u003e.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eApplication:\u003c\/strong\u003e Used as a building block in condensation, reduction, and multicomponent 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4-Octadecyloxybenzaldehyde","description":"\u003cp\u003e\u003cstrong\u003e4-Octadecyloxybenzaldehyde\u003c\/strong\u003e (CAS 4105-95-7) is a high-quality chemical from TCI, supplied as \u003cstrong\u003eGC Grade \/ for Synthesis\u003c\/strong\u003e.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eApplication:\u003c\/strong\u003e Used as a building block in condensation, reduction, and multicomponent reactions.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eSpecifications:\u003c\/strong\u003e\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003eMolecular formula: C25H42O2\u003c\/li\u003e\n\u003cli\u003eCAS number: 4105-95-7\u003c\/li\u003e\n\u003cli\u003ePurity: \u0026gt;95.0%(GC)\u003c\/li\u003e\n\u003cli\u003eTCI product code: O0223\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eAvailable from \u003cstrong\u003eAMI Scientific\u003c\/strong\u003e, the authorised TCI distributor in Indonesia. \u003cstrong\u003eContact us for pricing and stock availability\u003c\/strong\u003e — we ship throughout 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Indonesia.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48088564170970,"sku":"TCI2510T362455281","price":1490000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48088564203738,"sku":"TCI2510T362455282","price":5172000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510T3624.jpg?v=1768819791"},{"product_id":"tci2510a0480678","title":"TCI A0480 123-11-5 p-Anisaldehyde","description":"\u003cp\u003e\u003cstrong\u003ep-Anisaldehyde\u003c\/strong\u003e (CAS 123-11-5) is a high-quality chemical from TCI, supplied as \u003cstrong\u003eHigh Purity Reagent Grade\u003c\/strong\u003e.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eApplication:\u003c\/strong\u003e Used as a building block in condensation, reduction, and multicomponent reactions.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eSpecifications:\u003c\/strong\u003e\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003eMolecular formula: 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Indonesia.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mL","offer_id":48085299953882,"sku":"TCI2510A0480678","price":564000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48085299986650,"sku":"TCI2510A0480679","price":2503000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510A0480.jpg?v=1769179189"}],"url":"https:\/\/amiscientific.com\/en\/collections\/tci-l4-benzaldehydes-liquid-crystal-lc-building-blocks.oembed","provider":"AMI Scientific","version":"1.0","type":"link"}