{"title":"C-ProtectedAmino Acids","description":"\u003cp\u003e\u003cstrong\u003eC-ProtectedAmino Acids\u003c\/strong\u003e — menghimpun asam amino yang gugus karboksilnya dilindungi dalam bentuk ester—seperti metil, etil, atau benzil ester—sementara gugus amina dapat berada dalam keadaan bebas atau turut dilindungi dengan gugus Boc maupun asetil. Bentuk terlindungi ini menjaga selektivitas reaksi pada sintesis peptida bertahap.\u003c\/p\u003e\u003cp\u003eC-Protected Amino Acids digunakan kimiawan sintesis peptida untuk mengendalikan reaktivitas gugus karboksil selama pembentukan ikatan amida, sehingga kopling dapat difokuskan pada gugus amina atau posisi lain yang dituju. Turunan seperti ester N-suksinimidil dan ester benzil dalam kategori ini juga dipakai pada strategi sintesis fase larutan maupun fase padat untuk fragmen peptida dan turunan bioaktif.\u003c\/p\u003e\u003cp\u003eContoh produk dalam koleksi ini: \u003ca href=\"\/en\/products\/tci2510a0118191\"\u003eTCI A0118 36546-50-6 N-Acetyl-L-tyrosine Ethyl Ester Monohydrate\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b553712196\"\u003eTCI B5537 96099-84-2 N-(tert-Butoxycarbonyl)-D-threonine Methyl Ester\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510a0094152\"\u003eTCI A0094 1906-82-7 N-Acetylglycine Ethyl Ester\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b568412389\"\u003eTCI B5684 51513-80-5 6-[(tert-Butoxycarbonyl)amino]hexanoic Acid N-Succinimidyl Ester\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510v020756647\"\u003eTCI V0207 16652-76-9 H-Val-OBzlTos-OH\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b605312855\"\u003eTCI B6053 58816-69-6 SB 297006\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510v019656634\"\u003eTCI V0196 21760-98-5 L-Valine Benzyl Ester\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b650413408\"\u003eTCI B6504 15231-41-1 tert-Butyl 3-Aminopropanoate\u003c\/a\u003e.\u003c\/p\u003e\u003cp\u003ePerhatikan jenis ester pelindung (metil, etil, benzil) beserta kompatibilitasnya dengan gugus pelindung amina, konfigurasi stereokimia (L\/D), serta kemurnian enansiomerik yang dibutuhkan untuk sintesis peptida. 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 Amino Acids, sering dipakai bersamaan dalam satu alur kerja laboratorium:\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-biologically-modified-amino-acids\"\u003eBiologically-modified Amino Acids\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-amino-acid-amides\"\u003eAmino Acid Amides\u003c\/a\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eKembali ke \u003ca href=\"\/en\/collections\/tci-l3-amino-acids\"\u003eAmino Acids\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":"tci2510b568412389","title":"TCI B5684 51513-80-5 6-[(tert-Butoxycarbonyl)amino]hexanoic Acid N-Succinimidyl Ester","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B5684, 6-[(tert-Butoxycarbonyl)amino]hexanoic Acid N-Succinimidyl Ester (CAS 51513-80-5), is a bifunctional linker reagent designed for introducing a flexible 6-aminohexanoic acid (Ahx) spacer into peptide sequences. The NHS ester group reacts efficiently with primary amines under mild conditions, while the Boc protecting group allows selective deprotection for subsequent chain elongation. This compound is widely used in solid-phase and solution-phase peptide synthesis, biomolecule conjugation, and the preparation of peptide-drug conjugates.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085895905498,"sku":"TCI2510B568412389","price":2138000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085895938266,"sku":"TCI2510B568412390","price":8208000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5684_4da5edc1-d6c1-4f1a-a6ac-02e24f2955ed.jpg?v=1767862910"},{"product_id":"tci2510b605312855","title":"TCI B6053 58816-69-6 SB 297006","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6053 (CAS 58816-69-6) is a high-quality biochemical compound supplied by Tokyo Chemical Industry, categorized under amino acids and biochemical reagents for life science research. This product is widely used in pharmacological studies involving receptor-ligand interactions, enzyme inhibition assays, and cellular signaling pathway investigations. It serves as a reliable reference standard or research tool in both academic and industrial laboratory settings.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5mg","offer_id":48085916909786,"sku":"TCI2510B605312855","price":3936000.0,"currency_code":"IDR","in_stock":true},{"title":"25mg","offer_id":48085916942554,"sku":"TCI2510B605312856","price":13773000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6053.jpg?v=1768815963"},{"product_id":"tci2510b650413408","title":"TCI B6504 15231-41-1 tert-Butyl 3-Aminopropanoate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6504 tert-Butyl 3-Aminopropanoate (CAS 15231-41-1) is a tert-butyl–protected form of β-alanine that is widely used in peptide chemistry. Its free amine can be acylated selectively while the carboxyl terminus stays protected until acidic deprotection is performed. This makes it a practical unit for building amide bonds, linkers, and spacer segments in conjugation work. Supplied in 200 mg and 1 g pack sizes, it should be kept tightly closed and stored according to the manufacturer's stated conditions.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eGuchhait et al. (2010). ChemInform Abstract: Towards Molecular Diversity: Dealkylation of tert‐Butyl Amine in Ugi‐Type Multicomponent Reaction Product Establishes tert‐Butyl Isocyanide as a Useful Convertible Isonitrile.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.201052125\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.201052125\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eKraehenbuehl et al. (1994). Vapor Pressures of Methyl tert-Butyl Ether, Ethyl tert-Butyl Ether, Isopropyl tert-Butyl Ether, tert-Amyl Methyl Ether, and tert-Amyl Ethyl Ether. \u003cem\u003eJournal of Chemical \u0026amp; Engineering Data\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1021\/je00016a026\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1021\/je00016a026\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eKrossing et al. (2008). Dimeric Di(tert-butyl)haloalanes and a Monomeric Di(tert-butyl)phosphino-di(tert-butyl)alane. \u003cem\u003eZeitschrift für Naturforschung B\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1515\/znb-2008-0905\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1515\/znb-2008-0905\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":"200mg","offer_id":48085943681242,"sku":"TCI2510B650413408","price":2194000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48085943714010,"sku":"TCI2510B650413409","price":7618000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6504_40b5b1a7-bc69-44a4-bc9b-0e8b8a48668e.jpg?v=1767866049"},{"product_id":"tci2510c033314403","title":"TCI C0333 1738-86-9 N-Benzyloxycarbonylglycine 4-Nitrophenyl Ester","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0333 N-Benzyloxycarbonylglycine 4-Nitrophenyl Ester, CAS 1738-86-9, is a Cbz-protected glycine derivative whose carboxyl group is activated as a 4-nitrophenyl ester. This activation allows amide bond formation with free amines without the need for a separate coupling reagent, making it a classic reagent in peptide chemistry. The 4-nitrophenol released during the reaction provides a convenient colorimetric handle, so the compound is also used as a model substrate in enzyme kinetics and protease or esterase assays. AMI Scientific supplies this TCI product in a 1 g pack; keep it tightly closed and protected from moisture, and consult the manufacturer's Safety Data Sheet before use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085990998234,"sku":"TCI2510C033314403","price":816000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0333.jpg?v=1769144565"},{"product_id":"tci2510c233417082","title":"TCI C2334 3496-11-5 N-Carbobenzoxy-L-valine Succinimidyl Ester","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C2334 3496-11-5 N-Carbobenzoxy-L-valine Succinimidyl Ester is a chemical compound widely used in chemical biology and peptide chemistry. This reagent plays a crucial role in laboratory settings by enabling the activation and conjugation of biomolecules such as proteins and amino acids. Its application is essential in the development of new compounds and in biological therapy research. The compound is particularly valued for its ability to selectively bind to amino groups on target molecules, making it a versatile tool in molecular interactions.\u003c\/p\u003e\n\u003cp\u003eOne of the key properties that make this compound a preferred choice is its high specificity in binding reactions. This allows for precise chemical modifications with minimal interference from other molecular components. Additionally, it exhibits good stability under standard laboratory conditions, which simplifies storage and handling. The compound's chemical structure ensures it remains active over extended periods, making it reliable for repeated use in research protocols.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in biomedical, pharmacological, and biochemical research. Researchers from universities and research institutions rely on it for developing new drugs and studying molecular interactions. Its availability in the local market supports ongoing scientific investigations and contributes to the advancement of life sciences in Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePeptide Chemistry: This compound is ideal for peptide conjugation due to its ability to activate and link amino groups, facilitating the synthesis of modified peptides for therapeutic applications.\u003c\/li\u003e\n\u003cli\u003eProtein Modification: It enables the selective modification of protein molecules, allowing researchers to study functional changes and interactions in biological systems.\u003c\/li\u003e\n\u003cli\u003eBioconjugation Research: Its specificity in binding to amino groups makes it a preferred reagent for creating bioconjugates used in diagnostics and drug delivery systems.\u003c\/li\u003e\n\u003cli\u003eMolecular Imaging Studies: The compound is used in labeling biomolecules for imaging techniques, aiding in the visualization of molecular processes within cells.\u003c\/li\u003e\n\u003cli\u003eDrug Development: It supports the development of new therapeutic agents by enabling the attachment of functional groups to target molecules for enhanced efficacy.\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: 3496-11-5\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Peptide Chemistry\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory supply\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid or powder, depending on the specific formulation\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment, away from moisture and direct sunlight to maintain its chemical integrity. It is recommended to use airtight containers to prevent exposure to air and humidity. Laboratory personnel should handle the compound with care, using appropriate personal protective equipment such as gloves and safety goggles. It is important to ensure that the compound is kept in a secure location that is inaccessible to unauthorized individuals. Regular monitoring of storage conditions is advised to ensure the compound remains stable and effective for research purposes.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086121152730,"sku":"TCI2510C233417082","price":1350000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2334.jpg?v=1768204650"},{"product_id":"tci2510c235117108","title":"TCI C2351 2899-60-7 Z-Gly-Osu","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eZ-Gly-Osu (Z-Glycyl-Osu) is a chemical compound widely used in laboratory settings for peptide synthesis and chemical reactions involving molecular binding. This compound plays a crucial role in biochemical and pharmaceutical research by serving as a substrate or reagent in amino acid coupling reactions. Its application is essential for the formation of complex peptide chains, making it a vital component in the development of bioactive molecules. In the context of chemical biology, Z-Gly-Osu is frequently utilized to study the mechanisms of peptide bond formation and the behavior of amino acid derivatives under various reaction conditions.\u003c\/p\u003e\n\u003cp\u003eThe compound is known for its stable chemical structure and appropriate reactivity, which makes it a preferred choice for precise and controlled chemical experiments. Its chemical properties allow it to react effectively with a variety of reagents and catalysts, enabling researchers to achieve specific structural outcomes. This versatility is particularly valuable in high-precision laboratory environments where reproducibility and accuracy are paramount. The reactivity and stability of Z-Gly-Osu make it suitable for applications that require both reliability and consistency.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Z-Gly-Osu is commonly used in biochemical, pharmaceutical, and organic chemistry research. It is especially relevant for institutions focused on drug development, biological compound synthesis, and the study of chemical reaction mechanisms. Its role in these fields underscores its importance as a key reagent in both academic and industrial research settings.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBiochemical research utilizes Z-Gly-Osu for studying amino acid coupling and peptide bond formation in synthetic pathways.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical development benefits from Z-Gly-Osu's role in the synthesis of bioactive peptides and drug candidates.\u003c\/li\u003e\n\u003cli\u003eOrganic chemistry experiments use Z-Gly-Osu to explore reaction mechanisms and molecular interactions in controlled environments.\u003c\/li\u003e\n\u003cli\u003eDrug discovery programs incorporate Z-Gly-Osu to design and test new therapeutic agents with specific molecular structures.\u003c\/li\u003e\n\u003cli\u003ePeptide chemistry studies rely on Z-Gly-Osu as a building block for constructing complex peptide sequences and analyzing their properties.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 2899-60-7\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Peptide Chemistry\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\u003eZ-Gly-Osu should be stored in a cool, dry environment to maintain its chemical stability and reactivity. It is recommended to keep the compound in airtight containers to prevent exposure to moisture and air, which could affect its performance in reactions. Laboratory personnel should handle the compound with care, using appropriate personal protective equipment such as gloves and safety goggles to ensure safe handling. The compound should be stored away from incompatible materials to avoid any potential chemical interactions. Regular monitoring of storage conditions is advised to ensure the integrity of the compound remains intact for experimental use. Proper labeling of storage containers is also essential to prevent accidental misuse or contamination.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086122103002,"sku":"TCI2510C235117108","price":1941000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086122135770,"sku":"TCI2510C235117109","price":6774000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2351.jpg?v=1771058585"},{"product_id":"tci2510c247517250","title":"TCI C2475 482577-59-3 N-(2'-Cyanobiphenyl-4-ylmethyl)-L-valine Methyl Ester Hydrochloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eN-(2'-Cyanobiphenyl-4-ylmethyl)-L-valine Methyl Ester Hydrochloride is a chemical compound widely used in chemical and biochemical experiments. This compound is a key reagent in peptide chemistry and molecular interaction studies due to its unique structural composition, which includes a valine chain and a cyanobiphenyl group. Its molecular structure makes it particularly useful for exploring organic synthesis and molecular recognition processes. This compound is commonly found in research settings where precise chemical reactions and functional group manipulations are required.\u003c\/p\u003e\n\u003cp\u003eThe compound’s chemical stability under controlled conditions makes it a preferred choice for laboratory use. Its ester functionality and hydrochloride group contribute to its reactivity and compatibility with various synthetic protocols. These properties allow for efficient chemical transformations and functional group modifications, making it a versatile tool in chemical biology. The compound’s sensitivity to moisture and air necessitates careful handling to maintain its integrity and ensure consistent experimental results.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is utilized in applied research such as pharmacological compound synthesis and molecular interaction characterization. It is a common choice for institutions and universities engaged in biological chemistry and peptide research. Its application supports the development of new methodologies and insights in organic and biochemical studies.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMolecular Interaction Studies: This compound is ideal for investigating molecular recognition and binding interactions due to its complex structure and functional groups.\u003c\/li\u003e\n\u003cli\u003ePeptide Chemistry Research: Its valine chain and ester functionality make it suitable for peptide synthesis and modification experiments.\u003c\/li\u003e\n\u003cli\u003eOrganic Synthesis Applications: The compound’s reactivity and stability under controlled conditions support its use in organic synthesis protocols.\u003c\/li\u003e\n\u003cli\u003ePharmacological Compound Development: It is used in the synthesis of bioactive compounds and drug candidates due to its structural versatility.\u003c\/li\u003e\n\u003cli\u003eCharacterization of Functional Groups: The presence of hydrochloride and ester groups allows for detailed analysis of functional group behavior in chemical reactions.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 482577-59-3\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Peptide Chemistry\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Requires protection from moisture and air exposure\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment away from moisture and air exposure to maintain its chemical integrity. It is recommended to use airtight containers made of glass or high-density polyethylene to prevent degradation. Due to its sensitivity, it should be handled in a controlled laboratory setting with appropriate safety measures. Avoid prolonged exposure to light and ensure proper ventilation during handling. The compound should be stored in a secure location to prevent contamination and ensure safe usage in research applications. Always follow standard laboratory safety protocols when working with this material.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086128165082,"sku":"TCI2510C247517250","price":1857000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086128197850,"sku":"TCI2510C247517251","price":5707000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2475.jpg?v=1767098389"},{"product_id":"tci2510c271117564","title":"TCI C2711 2886-33-1 1,4-Dibenzyl L-Aspartate p-Toluenesulfonate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1,4-Dibenzyl L-Aspartate p-Toluenesulfonate is a chemical compound widely used in laboratory settings for biochemical and chemical biology research. This compound is particularly valuable in peptide chemistry due to its structural complexity, which allows it to interact with various enzymes and biological receptors. It serves as a key reagent in the synthesis of complex molecules with specific biological activities, making it an essential tool for researchers working in biochemistry and organic synthesis. Its versatility supports a range of experimental applications, from enzyme kinetics studies to the development of new pharmaceutical compounds.\u003c\/p\u003e\n\u003cp\u003eThe compound is preferred for its stability under controlled conditions and its solubility in organic solvents, which facilitates its use in a variety of chemical reactions. These properties make it ideal for experiments requiring high precision and reproducibility. Additionally, its chemical inertness in certain environments ensures that it maintains its structural integrity during synthesis and analysis. This reliability is crucial for maintaining the accuracy of experimental results in both academic and industrial research settings.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 1,4-Dibenzyl L-Aspartate p-Toluenesulfonate is commonly used in biochemical, pharmacological, and organic synthesis research. Researchers and students rely on this compound for experiments that require specific molecular structures and controlled reactivity. Its availability and consistent performance make it a go-to choice for those working on projects involving enzyme interactions, drug development, and advanced chemical synthesis techniques.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBiochemical Research: This compound is ideal for enzyme kinetics studies due to its ability to act as a substrate or modulator in enzymatic reactions, enabling detailed analysis of enzyme activity and inhibition.\u003c\/li\u003e\n\u003cli\u003ePeptide Chemistry: It is frequently used in the synthesis of complex peptides and bioactive molecules, offering structural versatility for designing compounds with targeted biological functions.\u003c\/li\u003e\n\u003cli\u003eOrganic Synthesis: Its solubility in organic solvents and chemical stability make it a preferred reagent for the synthesis of various organic compounds, especially those with functional groups requiring controlled reactivity.\u003c\/li\u003e\n\u003cli\u003ePharmacological Studies: The compound is used to investigate the effects of specific molecular structures on biological systems, aiding in the development of new therapeutic agents.\u003c\/li\u003e\n\u003cli\u003eAnalytical Chemistry: Its well-defined chemical properties allow it to be used as a standard in analytical procedures, ensuring accurate quantification and identification in complex mixtures.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 2886-33-1\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Peptide Chemistry\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its chemical stability and prevent degradation. It is recommended to use airtight containers to minimize exposure to moisture and air, which could affect its purity and reactivity. Due to its organic nature, it should be kept away from incompatible substances such as strong oxidizers or acids. Laboratory personnel should wear appropriate personal protective equipment, including gloves and safety goggles, when handling the compound to ensure safety. Regular monitoring of storage conditions is essential to maintain the integrity of the material for experimental use. Proper labeling of containers is also crucial to prevent accidental misuse or contamination.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086192947418,"sku":"TCI2510C271117564","price":1462000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086192980186,"sku":"TCI2510C271117565","price":5623000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2711.jpg?v=1769144364"},{"product_id":"tci2510c283817716","title":"TCI C2838 1212-53-9 N-Carbobenzoxyglycine Methyl Ester","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eN-Carbobenzoxyglycine Methyl Ester (N-CBZ-Glycine Methyl Ester) is a chemical compound widely used in laboratory settings for its versatility in chemical and biochemical applications. This compound is an ester derived from a carboxylic acid and an amino acid, featuring a complex molecular structure that supports its reactivity in various synthetic processes. Its role in the laboratory is critical for the synthesis of peptides and amino acid analogs, where it acts as a key intermediate. Due to its functional group reactivity, it is also employed in reactions requiring the activation of specific functional groups, making it an essential tool for organic chemists and biochemists.\u003c\/p\u003e\n\u003cp\u003eThe compound's chemical properties, including its stability under certain conditions and reactivity toward hydrolysis and substitution reactions, make it a preferred choice for researchers. Its molecular structure, which includes both ester and carboxylate groups, enables it to participate in a wide range of chemical transformations. These characteristics make it particularly suitable for applications involving the modification of molecules and the synthesis of complex compounds. Its reactivity and structural versatility have made it a staple in many research laboratories, especially those focused on molecular design and drug development.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, N-Carbobenzoxyglycine Methyl Ester is commonly used in research related to chemistry, biochemistry, and pharmacology. It is frequently employed in basic research and development projects by academic institutions and research centers. Its utility in synthesizing complex organic molecules and its role in peptide chemistry make it a valuable resource for scientists working on molecular modifications and drug discovery initiatives.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePeptide Synthesis: This compound is ideal for peptide synthesis due to its ability to activate carboxylate groups, facilitating the formation of peptide bonds in solid-phase peptide synthesis techniques.\u003c\/li\u003e\n\u003cli\u003eAmino Acid Analog Development: It serves as a building block for creating amino acid analogs, which are crucial for studying protein structures and functions in biochemical research.\u003c\/li\u003e\n\u003cli\u003eFunctional Group Activation: Its reactivity toward hydrolysis and substitution reactions makes it suitable for activating specific functional groups in organic synthesis, enhancing reaction efficiency.\u003c\/li\u003e\n\u003cli\u003eMolecular Modification Studies: Researchers use it to modify molecular structures, enabling the study of how structural changes affect biological activity and chemical behavior.\u003c\/li\u003e\n\u003cli\u003eDrug Discovery Research: Its role in synthesizing complex organic compounds makes it a valuable tool in pharmaceutical research, aiding in the development of new therapeutic agents.\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: 1212-53-9\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Peptide Chemistry\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory supply\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid, crystalline powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep it in a tightly sealed container to prevent exposure to moisture and air, which can lead to hydrolysis. Due to its reactivity, it should be handled in a well-ventilated area, and appropriate personal protective equipment such as gloves and safety goggles should be worn. Avoid direct contact with skin and eyes, and ensure that it is stored away from incompatible substances. Regular monitoring of storage conditions is advised to ensure the integrity of the compound during long-term use in laboratory settings.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086199206106,"sku":"TCI2510C283817716","price":816000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086199238874,"sku":"TCI2510C283817717","price":2615000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2838.jpg?v=1768204704"},{"product_id":"tci2510c287317755","title":"TCI C2873 21209-51-8 N-Benzyloxycarbonyl-L-serine Benzyl Ester","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C2873 21209-51-8 N-Benzyloxycarbonyl-L-serine Benzyl Ester is a chemical compound widely used in laboratory settings for its role in peptide synthesis and chemical biology research. As an ester derivative of L-serine protected by a benzyloxycarbonyl group, it serves as a key building block in the creation of complex peptide structures. This compound is particularly valuable in the field of organic chemistry due to its ability to participate in specific chemical reactions that require controlled activation. Its utility extends across various biochemical and pharmaceutical applications, making it an essential tool for researchers aiming to develop new therapeutic agents.\u003c\/p\u003e\n\u003cp\u003eThe compound's chemical properties make it a preferred choice for laboratory use. It exhibits stability under certain conditions, which allows for controlled handling and storage. However, it is sensitive to moisture and air exposure, requiring careful management to maintain its integrity. The presence of the benzyloxycarbonyl group enhances its reactivity in controlled environments, enabling selective chemical transformations. These characteristics make it ideal for applications where precision and specificity are crucial in synthetic processes.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in biochemical and pharmacological research. Scientists rely on it to synthesize complex molecules with potential medicinal applications. Its availability through AMI Scientific ensures that researchers in Indonesia have access to high-quality reagents necessary for advanced chemical and biological studies. The compound's role in drug development and molecular research underscores its importance in modern scientific exploration.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePeptide Synthesis: This compound is ideal for synthesizing complex peptides due to its protected amino group, allowing for controlled and selective chemical reactions.\u003c\/li\u003e\n\u003cli\u003eBiochemical Research: It is frequently used in biochemical studies to investigate protein structures and interactions, supporting molecular-level analysis.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical Development: Its role in creating novel therapeutic agents makes it a valuable tool in drug discovery and development programs.\u003c\/li\u003e\n\u003cli\u003eOrganic Chemistry Experiments: The compound's reactivity and structural specificity make it suitable for a wide range of organic synthesis applications.\u003c\/li\u003e\n\u003cli\u003eMolecular Modeling Studies: Its well-defined structure enables accurate modeling and simulation in computational chemistry and drug design.\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: 21209-51-8\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Peptide Chemistry\u003c\/li\u003e\n\u003cli\u003ePack Sizes: Available in standard laboratory quantities as specified by the supplier\u003c\/li\u003e\n\u003cli\u003ePhysical Form: Solid, typically in crystalline or powder form\u003c\/li\u003e\n\u003cli\u003eStorage Note: Requires protection from moisture and air exposure\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment away from direct sunlight and sources of heat. It is recommended to keep it in airtight containers to prevent exposure to moisture and air, which can degrade its chemical integrity. Due to its sensitivity, it should be handled in a controlled laboratory setting with proper ventilation. Researchers should avoid prolonged exposure to the compound and use appropriate personal protective equipment when handling it. Storage conditions must be strictly maintained to ensure the compound remains stable and suitable for use in chemical and biochemical experiments.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086200746202,"sku":"TCI2510C287317755","price":1997000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086200778970,"sku":"TCI2510C287317756","price":6858000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2873.jpg?v=1768204708"},{"product_id":"tci2510d072620328","title":"TCI D0726 33229-89-9 N,N-Dimethylglycine Ethyl Ester","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eN,N-Dimethylglycine Ethyl Ester (DMG-E), with the CAS number 33229-89-9, is a chemical compound widely used in chemical and biochemical experiments. It is a key reagent in peptide chemistry, where it plays a significant role in the synthesis of various organic compounds. Due to its reactivity and structural versatility, DMG-E is often utilized in complex chemical reactions that require precise molecular interactions. Its role in the laboratory is critical, especially in research areas that demand high chemical reactivity and specificity.\u003c\/p\u003e\n\u003cp\u003eDMG-E is preferred for its stability under controlled conditions and its ability to participate in both substitution and coupling reactions. Its solubility in organic solvents makes it highly convenient for experimental procedures, allowing for easy handling and integration into diverse chemical processes. The compound's molecular structure enables it to interact effectively with a wide range of substrates, making it an essential tool for researchers working in chemical biology and synthetic chemistry. Its reliability and consistent performance contribute to its popularity among scientists.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, DMG-E is commonly used in biochemical and organic chemistry research. Due to its limited availability in the local market, it is often sourced from reliable suppliers like AMI Scientific. This compound is particularly valuable in pharmacological and biomedical studies, where its chemical properties support advanced research and development efforts. Its use is widespread in academic and industrial settings that require high-quality chemical reagents.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePeptide Synthesis: DMG-E is ideal for peptide chemistry due to its reactivity and ability to form stable intermediates in coupling reactions.\u003c\/li\u003e\n\u003cli\u003eOrganic Reaction Mediation: Its solubility in organic solvents makes it suitable for complex organic synthesis processes.\u003c\/li\u003e\n\u003cli\u003eBiochemical Research: The compound is used in biochemical experiments to study molecular interactions and reaction mechanisms.\u003c\/li\u003e\n\u003cli\u003eDrug Development: Its chemical properties support research in pharmaceutical applications, particularly in compound modification.\u003c\/li\u003e\n\u003cli\u003eAnalytical Chemistry: DMG-E is used in analytical procedures to test reactivity and stability under different experimental 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: 33229-89-9\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Peptide Chemistry\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid or liquid, depending on the specific product variant\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eDMG-E 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 moisture and air. Due to its reactivity, it should be handled in a well-ventilated area to minimize potential hazards. Suitable containers for storage include glass or high-density polyethylene vessels that are resistant to chemical degradation. General laboratory precautions include wearing appropriate personal protective equipment, such as gloves and safety goggles, when handling the compound. Proper labeling of containers is essential to ensure safe handling and prevent accidental exposure.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086402760922,"sku":"TCI2510D072620328","price":1715000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48086402793690,"sku":"TCI2510D072620329","price":12872000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D0726.jpg?v=1768204852"},{"product_id":"tci2510d316523420","title":"TCI D3165 77385-90-1 N,N-Dibenzylglycine Ethyl Ester","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eN,N-Dibenzylglycine Ethyl Ester (TCI D3165), with CAS number 77385-90-1, is a chemical compound widely used in laboratory settings, particularly in organic and biochemical research. This compound serves as a key reagent in the synthesis of bioactive molecules and plays a vital role in peptide chemistry. Its structural complexity allows it to participate in various chemical reactions, making it a versatile tool for researchers aiming to develop new compounds with specific biological functions. Due to its chemical stability under controlled conditions, it is a reliable choice for synthetic processes that require precision and consistency.\u003c\/p\u003e\n\u003cp\u003eThe compound's ability to engage in high-reactivity chemical processes makes it a preferred choice for advanced laboratory applications. It exhibits good solubility in organic solvents such as ethyl acetate and chloroform, which simplifies its use in solution-based reactions. Its sensitivity to moisture and air necessitates careful handling, but this also ensures that it remains chemically pure when stored properly. These properties make it an essential component in laboratories where synthetic chemistry and biochemistry are central to research activities.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, N,N-Dibenzylglycine Ethyl Ester is commonly used in peptide synthesis, drug development, and the creation of synthetic chemical compounds. Its role in these fields has grown as the demand for high-quality synthetic materials increases. Researchers in Indonesia rely on this compound for its reliability and effectiveness in producing compounds with specific biological activities, supporting both academic and industrial research efforts.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePeptide Synthesis: This compound is ideal for constructing peptide sequences due to its reactivity and compatibility with standard solid-phase peptide synthesis techniques.\u003c\/li\u003e\n\u003cli\u003eDrug Development: Its use in synthesizing bioactive molecules supports pharmaceutical research aimed at creating new therapeutic agents.\u003c\/li\u003e\n\u003cli\u003eOrganic Chemistry Research: The compound's solubility and reactivity make it suitable for a wide range of organic reactions, enhancing the efficiency of synthetic pathways.\u003c\/li\u003e\n\u003cli\u003eBiochemical Analysis: It serves as a valuable reagent in biochemical assays, aiding in the study of enzyme mechanisms and molecular interactions.\u003c\/li\u003e\n\u003cli\u003eSynthetic Chemistry Projects: Its role as an intermediate in complex molecule synthesis makes it a key component in advanced chemical research and innovation.\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: 77385-90-1\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Peptide Chemistry\u003c\/li\u003e\n\u003cli\u003ePack Sizes: Not specified in the provided data\u003c\/li\u003e\n\u003cli\u003ePhysical Form: Not specified in the provided data\u003c\/li\u003e\n\u003cli\u003eStorage Note: Store in a dry, cool place away from moisture and air exposure\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a dry, cool environment to maintain its chemical stability and prevent degradation. It is recommended to use airtight containers to minimize exposure to moisture and air, which can affect its integrity. Due to its sensitivity, it should be handled with care, ideally in a controlled laboratory setting with proper ventilation. Avoid direct contact with skin and ensure that it is kept away from incompatible substances. Regular monitoring of storage conditions is essential to ensure the compound remains suitable for use in research applications. Proper labeling and storage practices help maintain the safety and effectiveness of this reagent in laboratory settings.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086602285274,"sku":"TCI2510D316523420","price":2447000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086602318042,"sku":"TCI2510D316523421","price":8461000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D3165.jpg?v=1768204961"},{"product_id":"tci2510d330523544","title":"TCI D3305 13515-99-6 Dimethyl DL-Glutamate Hydrochloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eDimethyl DL-Glutamate Hydrochloride (DMG-HCl) is a chemical compound widely used in laboratory settings for its versatility in chemical and biochemical experiments. This compound plays a key role in organic synthesis and the study of biological activities of various substances. It is commonly utilized as a building block for the creation of other compounds or as a substrate in enzymatic reactions. Its stability and reactivity make it an essential tool for researchers working in the fields of chemistry and biochemistry.\u003c\/p\u003e\n\u003cp\u003eDMG-HCl is preferred due to its excellent solubility in water and its ability to react under various chemical conditions. These properties allow it to be used in a wide range of experimental setups, from basic chemical reactions to complex biochemical processes. Its high purity and consistent physical form ensure reliable results in scientific research. Additionally, its stability in controlled laboratory environments enhances its suitability for precise and reproducible experiments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, DMG-HCl is frequently used in research related to chemistry, biochemistry, and pharmaceutical development. Its reliability and availability make it a popular choice among scientists and researchers. The compound is also used in educational institutions for teaching and experimental purposes, supporting both academic and industrial research efforts.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis applications benefit from DMG-HCl’s reactivity and solubility, enabling the creation of complex molecules with high precision.\u003c\/li\u003e\n\u003cli\u003eEnzymatic reaction studies utilize DMG-HCl as a substrate, allowing researchers to investigate enzyme mechanisms and catalytic processes.\u003c\/li\u003e\n\u003cli\u003eBiochemical research relies on DMG-HCl for its role in studying the biological activities of compounds, aiding in drug development and metabolic pathway analysis.\u003c\/li\u003e\n\u003cli\u003eEducational laboratories use DMG-HCl for teaching chemical reactions and biochemical processes, providing hands-on learning experiences for students.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research incorporates DMG-HCl in the development of new drugs, leveraging its chemical properties for compound modification and testing.\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: 13515-99-6\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Peptide Chemistry\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eDMG-HCl should be stored in a cool, dry environment to maintain its stability and prevent degradation. It is recommended to keep the compound in airtight containers to avoid moisture exposure, which can affect its chemical integrity. Proper labeling of storage containers is essential for safety and traceability. In laboratory settings, it is important to handle the compound with appropriate personal protective equipment, such as gloves and safety goggles, to ensure safe handling. Avoid exposure to high temperatures and direct sunlight to preserve its chemical properties. Regular inspection of storage conditions ensures that the compound remains suitable for use in scientific experiments.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086607069402,"sku":"TCI2510D330523544","price":816000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086607102170,"sku":"TCI2510D330523545","price":2559000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D3305.jpg?v=1769143888"},{"product_id":"tci2510d335323604","title":"TCI D3353 23150-65-4 Dimethyl L-Glutamate Hydrochloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eDimethyl L-Glutamate Hydrochloride (DMG-HCl) is a chemical compound widely used in laboratory settings for its versatility in chemical and biochemical experiments. As a key reagent in peptide chemistry, it plays a crucial role in the synthesis and modification of biological molecules. This compound is particularly valuable in research involving molecular interactions, especially in the study of peptides and proteins. Its chemical structure, derived from L-glutamic acid with two methyl groups, makes it a fundamental building block in various synthetic processes.\u003c\/p\u003e\n\u003cp\u003eDMG-HCl is favored for its stability and solubility in polar solvents, which enhances its utility in a wide range of chemical reactions. Being a hydrochloride salt, it maintains its integrity under various experimental conditions, making it a reliable choice for researchers. Its ability to interact with neural systems also makes it a key component in neurochemical studies. These properties ensure that it remains a preferred reagent in laboratories requiring consistent and predictable chemical behavior.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, DMG-HCl is extensively used in chemical, molecular biology, and pharmacological research. It is a common reagent in academic institutions and research centers, supporting experiments that require specific chemical properties and high stability. Its widespread application underscores its importance in advancing scientific understanding in these fields.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePeptide Synthesis: DMG-HCl is essential in the synthesis of peptides due to its ability to participate in chemical reactions that form peptide bonds.\u003c\/li\u003e\n\u003cli\u003eMolecular Modification: It is used to modify biological molecules, enabling the study of structural and functional changes in proteins and peptides.\u003c\/li\u003e\n\u003cli\u003eNeurochemical Research: Its interaction with neural systems makes it valuable for studying neurotransmitter activity and synaptic function.\u003c\/li\u003e\n\u003cli\u003eBiochemical Assays: The compound is commonly used in assays that require stable and soluble reagents for accurate results.\u003c\/li\u003e\n\u003cli\u003eDrug Development: It supports the development of pharmaceutical compounds by providing a reliable chemical intermediate for drug synthesis.\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: 23150-65-4\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Peptide Chemistry\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eDMG-HCl should be stored in a cool, dry environment to maintain its stability and prevent degradation. It is recommended to keep the compound in a sealed container to avoid exposure to moisture and air. Since it is a solid powder, it should be handled with care to prevent inhalation or contact with skin. In laboratory settings, it is important to use appropriate personal protective equipment, such as gloves and safety goggles, when handling this compound. Proper storage conditions ensure the compound remains effective for repeated use in research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086609985754,"sku":"TCI2510D335323604","price":1097000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086610018522,"sku":"TCI2510D335323605","price":3177000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D3353.jpg?v=1769143881"},{"product_id":"tci2510d356023872","title":"TCI D3560 27025-25-8 Dimethyl D-Glutamate Hydrochloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D3560 Dimethyl D-Glutamate Hydrochloride is a diester derivative of D-glutamic acid supplied as the hydrochloride salt. Its role in the laboratory is to provide a D-configured amino acid building block in which both carboxyl groups have already been protected as methyl esters. Because of this, the free amine group can be used directly in acylation reactions, peptide coupling, or Schiff base formation without interference from carboxylic acidity. The material is important for research on non-natural peptides, peptidomimetics, and chiral compounds that require the stereochemistry opposite to that of the natural amino acids.\u003c\/p\u003e\n\u003cp\u003eThe characteristics that make it a widely preferred choice are the stability and the ease of handling of its salt form. As a hydrochloride, the compound is a solid that is far easier to weigh out, store, and keep pure than the free base, which tends to lactamise into pyroglutamate derivatives. The free amine can be liberated by adding a mild base immediately before the reaction. The D configuration gives the material a distinctive value, because peptides containing D residues are generally more resistant to proteolytic attack — a property that is highly sought after in peptide design work.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this building block is typically used in peptide chemistry and chemical biology work where a protected, D-configured glutamate unit is needed as a starting point. Its solid salt form suits routine bench practice, allowing accurate weighing and straightforward storage between experiments. Research groups working on non-natural peptide sequences, peptidomimetic scaffolds, and chiral synthesis draw on it when the opposite stereochemistry to the natural amino acids is required in a target structure.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePeptide coupling reactions: the two carboxyl groups are already masked as methyl esters, so the free amine reacts cleanly without competing carboxylic acidity disturbing the coupling step.\u003c\/li\u003e\n\u003cli\u003eNon-natural peptide research: the D configuration introduces residues that generally resist proteolytic attack, making the material valuable when designing sequences with improved stability.\u003c\/li\u003e\n\u003cli\u003ePeptidomimetic synthesis: it delivers a ready-protected, stereochemically defined glutamate unit that can be built into scaffolds mimicking natural peptides without extra protection chemistry.\u003c\/li\u003e\n\u003cli\u003eAcylation of the free amine: the amine can be liberated with a mild base immediately before reaction, giving a controlled and convenient point of attachment for acyl groups.\u003c\/li\u003e\n\u003cli\u003eSchiff base formation: the unhindered free amine condenses readily with carbonyl partners, while the ester-protected side chain and backbone stay untouched during the transformation.\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: 27025-25-8\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Peptide Chemistry\u003c\/li\u003e\n\u003cli\u003eProduct code: D3560\u003c\/li\u003e\n\u003cli\u003eAvailable pack sizes: 25 g (as listed for this item)\u003c\/li\u003e\n\u003cli\u003ePhysical form: solid hydrochloride salt\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the material in a cool, dry place in its original tightly closed container, protected from moisture, since the hydrochloride salt is a solid that should be kept free of water uptake to preserve its purity. Use clean, dry glass or compatible plastic containers when transferring portions, and reseal promptly after weighing. Handle in a well-ventilated area or fume hood with laboratory gloves, safety glasses, and a lab coat, and avoid generating dust. Prepare the free base only immediately before use, as the free amine tends to lactamise on standing. Follow the manufacturer's safety data sheet and local laboratory waste procedures.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086626468058,"sku":"TCI2510D356023872","price":1799000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086626500826,"sku":"TCI2510D356023873","price":6128000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D3560.jpg?v=1769180612"},{"product_id":"tci2510d442225009","title":"TCI D4422 1791-13-5 Di-tert-butyl L-Aspartate Hydrochloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eDi-tert-butyl L-Aspartate Hydrochloride is a chemical compound widely used in laboratory settings for its versatility in chemical and biochemical experiments. It plays a crucial role in peptide chemistry and the synthesis of complex molecules, where its unique structure enables the creation of bioactive compounds. This compound is particularly valuable in research involving molecular modification and reactions that require stability and reactivity. Its presence in the field of chemical biology makes it an essential reagent for scientists working on advanced synthetic pathways.\u003c\/p\u003e\n\u003cp\u003eThe compound's chemical properties make it a preferred choice for researchers. It exhibits stability under specific conditions, which is vital for maintaining the integrity of chemical reactions. Its hydrochloride group allows it to dissolve easily in organic solvents such as ethyl acetate and acetone, enhancing its utility in various synthetic processes. The solid form of the compound also facilitates precise handling and measurement, making it ideal for high-quality reagent applications. These characteristics ensure its reliability in laboratory environments where precision and consistency are paramount.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Di-tert-butyl L-Aspartate Hydrochloride is commonly used in biochemical, pharmacological, and organic chemistry research. It is a key component in the development of peptides and amino acid analogs, supporting studies that aim to understand biological activity and molecular interactions. Its availability and performance make it a favored material among researchers and academic institutions in Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePeptide Synthesis: This compound is widely used in peptide chemistry due to its ability to participate in solid-phase peptide synthesis, enabling the creation of bioactive peptides with high specificity.\u003c\/li\u003e\n\u003cli\u003eMolecular Modification Studies: Its stable structure and reactivity make it suitable for experiments involving molecular modifications and functional group manipulations.\u003c\/li\u003e\n\u003cli\u003eBioactive Compound Development: Researchers use it as a building block for synthesizing compounds with biological activity, including analogs of amino acids and peptides.\u003c\/li\u003e\n\u003cli\u003eOrganic Reaction Optimization: The compound's solubility in organic solvents makes it ideal for optimizing reaction conditions in organic synthesis protocols.\u003c\/li\u003e\n\u003cli\u003eBiomedical Research: It supports studies in pharmacology and biochemistry, aiding in the investigation of molecular interactions and drug development.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 1791-13-5\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Peptide Chemistry\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory supply\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its chemical stability and prevent degradation. It is recommended to keep it in airtight containers to avoid exposure to moisture and air, which can affect its purity. Since it is a solid, it can be stored in standard laboratory containers, but care should be taken to ensure that the container is properly sealed. Handling should be done with appropriate personal protective equipment to ensure safety. The compound is not hazardous under normal storage conditions but should be handled with care to avoid contamination. Proper labeling and storage practices are essential to maintain its quality and usability in laboratory applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086691348698,"sku":"TCI2510D442225009","price":2475000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086691381466,"sku":"TCI2510D442225010","price":8573000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D4422.jpg?v=1768205056"},{"product_id":"tci2510d475625440","title":"TCI D4756 16115-68-7 Diethyl L-Aspartate Hydrochloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eDiethyl L-Aspartate Hydrochloride is a chemical compound widely used in laboratory settings for its versatility in chemical and biochemical experiments. It belongs to the category of peptide chemistry and is commonly utilized as a building block in the synthesis of complex compounds. This compound plays a crucial role in various chemical reactions where the structure of amino acids or their derivatives is required. Its presence in laboratory research supports the development of new materials, pharmaceuticals, and biochemical processes.\u003c\/p\u003e\n\u003cp\u003eOne of the key attributes that make Diethyl L-Aspartate Hydrochloride a preferred choice is its chemical stability and compatibility with a wide range of molecules. It dissolves well in organic solvents, making it ideal for purification and evaporation processes. This solubility property simplifies experimental procedures and enhances reproducibility in laboratory settings. Additionally, its ability to participate in molecular interactions makes it valuable for studying molecular behavior in different chemical environments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Diethyl L-Aspartate Hydrochloride is commonly used in research related to pure chemistry, biochemistry, and pharmacology. Its availability in practical packaging formats ensures easy access for researchers conducting experiments that require specific chemical compounds. The compound's reliability and consistent performance make it a trusted material for both academic and industrial research applications.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePeptide Synthesis for Pharmacological Research: This compound is ideal for synthesizing peptides, which are essential in drug development and pharmacological studies.\u003c\/li\u003e\n\u003cli\u003eMolecular Interaction Studies in Organic Chemistry: Its ability to interact with various molecules makes it suitable for investigating molecular behavior in organic reactions.\u003c\/li\u003e\n\u003cli\u003eDevelopment of Active Ingredients: It is used in the creation of active compounds for pharmaceutical and cosmetic applications.\u003c\/li\u003e\n\u003cli\u003eBiochemical Analysis in Research Labs: Its stability and solubility support accurate biochemical testing and analysis.\u003c\/li\u003e\n\u003cli\u003eOrganic Reaction Optimization: It assists in the optimization of chemical reactions by acting as a reagent or substrate in specific synthetic pathways.\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: 16115-68-7\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Peptide Chemistry\u003c\/li\u003e\n\u003cli\u003ePack Sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical Form: Solid powder\u003c\/li\u003e\n\u003cli\u003eStorage Note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eDiethyl L-Aspartate Hydrochloride should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep the compound in a sealed container to prevent exposure to moisture and air. Suitable storage containers include glass or plastic vessels with airtight lids. In laboratory settings, it is important to handle the compound with care, using appropriate personal protective equipment such as gloves and safety goggles. Avoid contact with incompatible substances and ensure proper ventilation when working with this material. Regular inspection of storage conditions helps maintain the integrity of the compound for reliable experimental results.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086706487514,"sku":"TCI2510D475625440","price":704000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086706520282,"sku":"TCI2510D475625441","price":2222000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D4756.jpg?v=1768205078"},{"product_id":"tci2510d483925563","title":"TCI D4839 4561-10-8 Dibenzyl L-Glutamate Hydrochloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eDibenzyl L-Glutamate Hydrochloride is a chemical compound widely used in biochemical experiments and life science research. It plays a crucial role in various laboratory applications, particularly in organic synthesis and molecular interaction studies. This compound is valued for its ability to act as a reagent in chemical reactions, supporting the development of new compounds and the analysis of molecular behavior. Its presence in research settings contributes to the advancement of biochemistry, pharmacology, and organic chemistry.\u003c\/p\u003e\n\u003cp\u003eThe compound’s favorable solubility in organic solvents such as ethyl acetate and ethanol makes it a preferred choice for laboratory use. Its stability under specific conditions enhances its reliability in experimental processes. Additionally, its clear structure and high consistency ensure accurate identification and consistent performance in experiments. These properties make it an essential component in both analytical and synthetic procedures.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Dibenzyl L-Glutamate Hydrochloride is commonly used in biochemical, pharmacological, and organic chemistry research. Researchers from universities and research institutions rely on this compound for studies involving biological activity, molecular structure, and chemical reactions. Its availability and performance make it a standard material in many laboratory workflows.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBiochemical Research: This compound is ideal for studying molecular interactions and enzyme activity due to its structural clarity and chemical reactivity.\u003c\/li\u003e\n\u003cli\u003eOrganic Synthesis: It serves as a key reagent in the synthesis of complex organic molecules, offering stability and solubility in organic solvents.\u003c\/li\u003e\n\u003cli\u003eProtein Purification: Its role in molecular interactions makes it useful in the purification and analysis of protein structures.\u003c\/li\u003e\n\u003cli\u003ePharmacological Studies: It is employed in drug development to investigate the effects of compounds on biological systems.\u003c\/li\u003e\n\u003cli\u003eStructural Analysis: Its high consistency and clear structure aid in the identification and analysis of molecular components in various 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: 4561-10-8\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Amino Acids\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eDibenzyl L-Glutamate Hydrochloride should be stored in a cool, dry environment to maintain its chemical integrity. It is recommended to keep the compound in a sealed container to prevent exposure to moisture and air, which may affect its stability. Avoid storing it in areas with high humidity or direct sunlight to prevent degradation. In laboratory settings, it is important to handle the compound with appropriate personal protective equipment, such as gloves and safety goggles, to ensure safe usage. Proper labeling of containers is essential for safe handling and to prevent accidental contamination. Regular inspection of storage conditions ensures the compound remains suitable for use in experiments.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48275698352346,"sku":"TCI2510D483925563","price":1518000.0,"currency_code":"IDR","in_stock":false}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D4839.jpg?v=1768818222"},{"product_id":"tci2510d602627041","title":"TCI D6026 32677-01-3 H-Glu(OtBu)-OtBu.HCl","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D6026 32677-01-3 H-Glu(OtBu)-OtBu.HCl is a chemical compound widely utilized in chemical biology, particularly in peptide chemistry. This compound serves as a key building block in the synthesis of complex peptides, offering researchers a reliable and versatile tool for molecular construction. Its role in laboratory settings is critical for advancing studies in biomedicine, pharmacology, and biotechnology. Due to its chemical stability and reactivity, it enables precise chemical reactions that are essential for developing new therapeutic agents and understanding biological processes.\u003c\/p\u003e\n\u003cp\u003eThe compound's reactivity and ability to form stable bonds with other molecules make it a preferred choice for peptide synthesis. Its chemical structure allows it to participate in various synthetic pathways, enhancing the efficiency and accuracy of laboratory procedures. The compound’s stability under controlled conditions ensures consistent results, which is vital for scientific research. These properties make it a favored material among scientists working on complex molecular structures and drug development projects.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in research related to biological compounds, including the development of new drugs and molecular interaction studies. Its availability in various packaging options makes it convenient for both small-scale and larger research projects. The compound’s reliability and quality have made it a popular choice among researchers in educational and research institutions across Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePeptide Synthesis: This compound is ideal for synthesizing complex peptides due to its reactivity and stability, enabling precise molecular construction.\u003c\/li\u003e\n\u003cli\u003eBiomedical Research: It supports studies on drug development and therapeutic agents by providing a reliable building block for peptide-based compounds.\u003c\/li\u003e\n\u003cli\u003ePharmacological Studies: The compound facilitates the creation of bioactive molecules, aiding in the investigation of drug mechanisms and biological effects.\u003c\/li\u003e\n\u003cli\u003eBiotecnological Applications: It is used in the development of biotechnology products, including enzyme inhibitors and molecular probes.\u003c\/li\u003e\n\u003cli\u003eMolecular Interaction Analysis: Its ability to form stable bonds makes it suitable for studying molecular interactions in biological systems.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 32677-01-3\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Peptide Chemistry\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various packaging options for laboratory use\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its chemical stability and prevent degradation. It is recommended to use airtight containers to protect it from moisture and contaminants. Due to its reactivity, it should be handled in a well-ventilated area, and appropriate personal protective equipment should be worn when working with it. Avoid exposure to high temperatures and direct light, as these can affect its properties. Proper storage ensures the compound remains effective for use in peptide synthesis and other laboratory applications. Always follow standard laboratory safety protocols to ensure safe handling and minimize risks.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086788309210,"sku":"TCI2510D602627041","price":1715000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086788341978,"sku":"TCI2510D602627042","price":5988000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D6026.jpg?v=1768197302"},{"product_id":"tci2510e092428754","title":"TCI E0924 6937-16-2 Ethyl 4-Aminobutyrate Hydrochloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eEthyl 4-Aminobutyrate Hydrochloride is a chemical compound widely used in laboratory experiments across chemistry and biochemical research. As a hydrochloride salt of ethyl 4-aminobutyrate, it plays a key role in various synthetic processes and analytical procedures. This compound is particularly valuable in peptide chemistry due to its ability to participate in complex molecular reactions. Its molecular structure makes it a versatile reagent, supporting both qualitative and quantitative studies in controlled environments.\u003c\/p\u003e\n\u003cp\u003eThe compound's chemical properties, including its stability under specific conditions, make it a preferred choice for researchers. It is highly sensitive to moisture and air exposure, which necessitates careful handling and storage. Despite this sensitivity, its hygroscopic nature allows it to be used effectively in precise chemical syntheses and analytical applications. Its reliability in maintaining chemical integrity under controlled conditions ensures consistent results in laboratory settings.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Ethyl 4-Aminobutyrate Hydrochloride is commonly used in chemical and biochemical research. It is a staple in academic and research institutions, supporting experiments in organic synthesis, peptide chemistry, and biochemistry. Its role in high-precision experiments makes it an essential material for both educational and applied research activities in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePeptide Synthesis: This compound is ideal for peptide chemistry due to its reactivity and compatibility with standard synthetic protocols.\u003c\/li\u003e\n\u003cli\u003eOrganic Synthesis: It serves as a key intermediate in the preparation of various organic compounds, particularly in functional group transformations.\u003c\/li\u003e\n\u003cli\u003eBiochemical Analysis: Its use in biochemical assays allows for the study of molecular interactions and reaction mechanisms.\u003c\/li\u003e\n\u003cli\u003eReagent Testing: It is frequently used to evaluate the reactivity of other compounds in controlled experimental conditions.\u003c\/li\u003e\n\u003cli\u003eQuantitative Analysis: Its stability and known chemical properties make it suitable for use in quantitative analytical procedures.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 6937-16-2\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Peptide Chemistry\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory requirements\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Requires desiccated storage to prevent moisture absorption\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eEthyl 4-Aminobutyrate Hydrochloride should be stored in a cool, dry place away from moisture and direct exposure to air. It is recommended to use airtight containers to prevent hygroscopic absorption, which can affect its chemical integrity. The compound is sensitive to humidity, so maintaining a controlled environment is essential for preserving its properties. Laboratory personnel should handle the material with care, using appropriate personal protective equipment. Proper storage ensures the compound remains effective for use in chemical and biochemical experiments.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086908698842,"sku":"TCI2510E092428754","price":704000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086908731610,"sku":"TCI2510E092428755","price":1857000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510E0924.jpg?v=1768205249"},{"product_id":"tci2510e093728774","title":"TCI E0937 42303-42-4 Ethyl 1-Aminocyclopropanecarboxylate Hydrochloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eEthyl 1-Aminocyclopropanecarboxylate Hydrochloride is a chemical compound widely used in chemical and biochemical experiments. It serves as a key reagent in the synthesis of organic compounds and plays a vital role in biochemical research. This compound is particularly valuable for its ability to participate in various chemical reactions, making it an essential tool in the laboratory. Its unique molecular structure allows it to interact with different functional groups, contributing to the development of new compounds with specific biological activities.\u003c\/p\u003e\n\u003cp\u003eThe compound is preferred due to its stable chemical properties and solubility in organic solvents. These characteristics make it suitable for a wide range of synthetic processes, including peptide chemistry and organic synthesis. Its solubility facilitates efficient separation and purification steps, enhancing the overall effectiveness of laboratory procedures. Additionally, its chemical stability ensures consistent results in repeated experiments, which is crucial for scientific research.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Ethyl 1-Aminocyclopropanecarboxylate Hydrochloride is commonly used in chemical and biochemical research. It is particularly relevant in the development of new compounds with potential medical or industrial applications. Researchers rely on this compound for its versatility and reliability in various synthetic and analytical processes. Its use extends to studies on reaction mechanisms and the optimization of synthesis techniques, supporting advancements in both academic and applied research.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic Synthesis: This compound is ideal for the synthesis of complex organic molecules due to its reactivity and solubility in organic solvents.\u003c\/li\u003e\n\u003cli\u003ePeptide Chemistry: It is frequently used in the synthesis of peptides, as it can participate in amide bond formation and other key reactions.\u003c\/li\u003e\n\u003cli\u003eBiochemical Research: Its role in generating compounds with specific biological activities makes it valuable for studying enzyme mechanisms and protein interactions.\u003c\/li\u003e\n\u003cli\u003eReaction Mechanism Studies: The compound's stability and reactivity make it suitable for investigating the pathways and intermediates in chemical reactions.\u003c\/li\u003e\n\u003cli\u003eIndustrial Compound Development: It is used in the development of new compounds with potential applications in pharmaceuticals and chemical industries.\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: 42303-42-4\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Peptide Chemistry\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory requirements\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep it in a tightly sealed container to prevent moisture absorption. Suitable storage containers include glass or high-density polyethylene vessels. Due to its chemical nature, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. Avoid exposure to heat or direct sunlight to prevent degradation. Proper ventilation is essential when working with this compound to ensure a safe laboratory environment. Always follow standard laboratory safety protocols when handling and storing chemical reagents.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086910763226,"sku":"TCI2510E093728774","price":816000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086910795994,"sku":"TCI2510E093728775","price":2784000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510E0937.jpg?v=1769142261"},{"product_id":"tci2510e094028778","title":"TCI E0940 144978-35-8 Ethyl N-(tert-Butoxycarbonyl)-D-pyroglutamate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eEthyl N-(tert-Butoxycarbonyl)-D-pyroglutamate is a chemical compound widely used in organic and biochemical research, particularly in peptide chemistry. This compound plays a crucial role in the synthesis of peptides and their analogs, serving as a key building block in the creation of bioactive molecules. Its structural complexity and functional group versatility make it an essential tool for chemists and biochemists working on advanced molecular designs. In laboratory settings, it is frequently employed in reactions that require the use of specific functional groups, such as the Boc (tert-butoxycarbonyl) group, which is commonly used in peptide synthesis to protect amino acid residues.\u003c\/p\u003e\n\u003cp\u003eThe compound is valued for its stability under controlled conditions and its reactivity in both acidic and basic environments. These properties allow it to participate in a wide range of chemical transformations, making it a preferred choice for researchers aiming to achieve high reactivity and precision in their synthetic processes. Its ability to undergo selective reactions under specific conditions ensures that it remains a reliable and efficient reagent in the development of complex molecular structures. This makes it particularly useful in applications where controlled chemical reactions are essential.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Ethyl N-(tert-Butoxycarbonyl)-D-pyroglutamate is commonly used by researchers in biochemical, pharmacological, and health sciences. It is especially relevant in drug development and the study of bioactive compounds. Due to its specific properties and versatility, it is a popular choice for applications requiring precise chemical control and high reactivity. Its presence in Indonesian research facilities highlights its importance in advancing scientific knowledge and innovation in the field of chemical biology.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePeptide Synthesis: This compound is ideal for synthesizing peptides and their analogs due to its Boc group, which allows for controlled and efficient peptide chain elongation.\u003c\/li\u003e\n\u003cli\u003eBioactive Compound Development: It is frequently used in the creation of bioactive molecules, supporting research into new therapeutic agents and functional biomolecules.\u003c\/li\u003e\n\u003cli\u003eOrganic Chemistry Reactions: Its reactivity in acidic and basic environments makes it suitable for a variety of organic synthesis reactions requiring functional group manipulation.\u003c\/li\u003e\n\u003cli\u003eDrug Discovery Research: It plays a key role in the development of pharmaceutical compounds by enabling the synthesis of complex molecular structures with high specificity.\u003c\/li\u003e\n\u003cli\u003eMolecular Structure Analysis: Its structural complexity and stability make it a valuable tool for studying molecular interactions and reaction mechanisms in biochemical studies.\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: 144978-35-8\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Peptide Chemistry\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder (as per standard product description)\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment, away from direct sunlight and moisture to maintain its stability and reactivity. It is recommended to use airtight containers to prevent exposure to humidity and contaminants. In laboratory settings, proper personal protective equipment (PPE) such as gloves and safety goggles should be worn when handling the compound to ensure safety. It should be kept in a well-ventilated area to minimize inhalation risks. Avoid contact with incompatible substances, such as strong acids or bases, to prevent unwanted chemical reactions. Proper labeling and storage conditions are essential to ensure the integrity and usability of the compound in research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086911090906,"sku":"TCI2510E094028778","price":536000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086911123674,"sku":"TCI2510E094028779","price":1097000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510E0940.jpg?v=1768205250"},{"product_id":"tci2510e113529034","title":"TCI E1135 144978-12-1 Ethyl N-(tert-Butoxycarbonyl)-L-pyroglutamate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eEthyl N-(tert-Butoxycarbonyl)-L-pyroglutamate is a chemical compound widely used in laboratory settings for peptide synthesis and chemical biology applications. It serves as a key building block in the creation of complex peptide structures, enabling researchers to design and modify amino acid sequences with precision. This compound is particularly valuable in the field of peptide chemistry due to its ability to participate in controlled chemical reactions, making it essential for the development of bioactive molecules. Its role in laboratory research extends to the study of protein structures and the synthesis of therapeutic agents, where its chemical stability and reactivity are critical factors.\u003c\/p\u003e\n\u003cp\u003eThe compound's preference in laboratory settings stems from its controlled reactivity and chemical stability. The tert-butoxycarbonyl (Boc) group attached to the amino acid chain allows for selective chemical modifications, which is crucial in peptide synthesis processes. This controlled reactivity ensures that researchers can manipulate the peptide chain with minimal side reactions, enhancing the efficiency of synthesis protocols. Additionally, the compound's stability under various reaction conditions makes it a reliable choice for long-term storage and repeated use in experimental workflows.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Ethyl N-(tert-Butoxycarbonyl)-L-pyroglutamate is commonly used in academic and industrial research settings. It is frequently found in peptide synthesis laboratories, where it is employed to create custom peptides for drug development and biotechnology applications. Its use is also prevalent in biochemical research, where it contributes to the study of protein structures and enzyme mechanisms. The compound's versatility and reliability make it a staple in many research facilities across Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePeptide Synthesis: This compound is ideal for peptide synthesis due to its controlled reactivity and ability to undergo selective chemical modifications.\u003c\/li\u003e\n\u003cli\u003eBiochemical Research: Its stable chemical properties make it suitable for studying enzyme mechanisms and protein structures in biochemical experiments.\u003c\/li\u003e\n\u003cli\u003eDrug Development: It is used in the creation of bioactive molecules, supporting the development of therapeutic agents and pharmaceutical compounds.\u003c\/li\u003e\n\u003cli\u003eStructural Analysis: The compound's well-defined chemical structure allows for accurate analysis in structural biology and molecular modeling studies.\u003c\/li\u003e\n\u003cli\u003eCustom Peptide Production: It is a key reagent in the production of custom peptides, enabling researchers to design and synthesize specific amino acid sequences.\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: 144978-12-1\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Peptide Chemistry\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eEthyl N-(tert-Butoxycarbonyl)-L-pyroglutamate should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep the compound in a sealed container to prevent exposure to moisture and air, which could affect its reactivity. Suitable storage containers include glass or plastic vessels with airtight closures. In laboratory settings, it is important to handle the compound with care, using appropriate personal protective equipment such as gloves and safety goggles. Avoid direct contact with skin and eyes, and ensure proper ventilation when working with the compound. Due to its chemical nature, it should be stored away from incompatible substances to prevent any potential reactions. Regular monitoring of storage conditions is advised to ensure the compound remains in optimal condition for use in research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086927638746,"sku":"TCI2510E113529034","price":479000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086927671514,"sku":"TCI2510E113529035","price":985000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510E1135.jpg?v=1768205261"},{"product_id":"tci2510e144429467","title":"TCI E1444 946511-97-3 2-Ethylbutyl L-Alaninate Hydrochloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI E1444 with CAS number 946511-97-3 is 2-Ethylbutyl L-Alaninate Hydrochloride, the hydrochloride salt of an L-alanine ester formed with the branched alcohol 2-ethylbutanol. The compound is a very well-recognised molecular building block in phosphoramidate prodrug chemistry, the approach commonly referred to as ProTide technology, in which an amino acid ester is attached to a phosphorus centre in order to improve the absorption and intracellular activation of antiviral compounds. Its role in the laboratory is to supply a chiral amino acid ester fragment in a stable salt form, ready to be coupled at the phosphorus-linking stage.\u003c\/p\u003e\n\u003cp\u003eThe property that makes this material the preferred choice is its hydrochloride salt form. Free amino acid esters tend to be unstable and readily undergo cyclisation to diketopiperazines, whereas the salt form locks the amine group in a protonated state so that the material can be weighed, stored, and handled far more easily. The L configuration at the alanine stereocentre is preserved, which is decisive because the stereochemistry of this fragment has a direct bearing on the enzymatic activation of the resulting prodrug. The branched 2-ethylbutyl chain confers greater lipophilicity than shorter, straight-chain esters.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories this type of reagent is used mainly in medicinal chemistry and synthetic organic research groups working on nucleoside and nucleotide analogues, in university and institutional research facilities, and in pharmaceutical development units exploring prodrug strategies. Because it is a defined chiral building block delivered as a handling-friendly salt, it suits multistep synthesis work where consistency between batches matters and where researchers need a reliable starting fragment rather than one prepared in-house.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePhosphoramidate (ProTide) prodrug synthesis: it supplies the amino acid ester portion that is coupled to a phosphorus centre, which is the defining structural step in this prodrug design approach.\u003c\/li\u003e\n\u003cli\u003eNucleoside and nucleotide analogue research: the fragment is attached to nucleoside phosphate derivatives to improve cellular uptake, a strategy widely applied in antiviral compound development programmes.\u003c\/li\u003e\n\u003cli\u003eChiral building block in multistep organic synthesis: the preserved L configuration at the alanine centre lets researchers carry defined stereochemistry through a synthetic sequence without a separate resolution step.\u003c\/li\u003e\n\u003cli\u003eStructure–activity relationship studies on ester chain variation: the branched 2-ethylbutyl group gives greater lipophilicity than shorter straight-chain esters, making it useful for comparative series work.\u003c\/li\u003e\n\u003cli\u003eMedicinal chemistry method development: as a stable, weighable hydrochloride salt it serves as a dependable reference substrate when optimising coupling conditions, reagents, and reaction workup procedures.\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: 946511-97-3\u003c\/li\u003e\n\u003cli\u003eChemical name: 2-Ethylbutyl L-Alaninate Hydrochloride\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Peptide Chemistry\u003c\/li\u003e\n\u003cli\u003eProduct code: E1444\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in standard TCI research-scale packaging; please confirm the size options when ordering\u003c\/li\u003e\n\u003cli\u003eStorage: store under the conditions stated 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 the material in its original tightly closed container, kept in a cool, dry, and well-ventilated place away from moisture, since amino acid ester hydrochlorides are generally sensitive to humidity. Glass containers with tight-fitting closures are suitable, and the container should be resealed promptly after each use; weighing under reduced exposure to ambient air helps preserve quality. Handle the compound in a fume hood using standard personal protective equipment, including safety glasses, gloves, and a laboratory coat, and avoid inhalation of dust or direct contact with skin and eyes. Keep the product separate from strong bases and strong oxidising agents. Always consult the manufacturer's safety data sheet for the specific storage temperature, hazard classification, and disposal requirements before use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086960734426,"sku":"TCI2510E144429467","price":1434000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086960767194,"sku":"TCI2510E144429468","price":4975000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510E1444.jpg?v=1769142307"},{"product_id":"tci2510e148229520","title":"TCI E1482 60372-77-2 Ethyl Lauroyl Arginate Hydrochloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eEthyl Lauroyl Arginate Hydrochloride is a chemical compound widely used in laboratory settings for its versatile applications in chemical and biochemical experiments. As a derivative of arginine, it plays a crucial role in peptide chemistry and molecular interactions, making it an essential component in research involving proteins and peptides. Its amphoteric nature allows it to function as a surfactant or emulsifier, enhancing the efficiency of various chemical reactions. This compound is particularly valuable in biological chemistry, where it supports the study of molecular interactions and biochemical processes.\u003c\/p\u003e\n\u003cp\u003eThe compound’s stability and physical properties make it a preferred choice for laboratory use. It dissolves well in organic solvents, which simplifies its handling and application in diverse experimental conditions. Its amphoteric character also enables it to act as a pH regulator or emulsifier, offering flexibility in experimental design. These properties contribute to its reliability and effectiveness in a wide range of laboratory applications, ensuring consistent results in research.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Ethyl Lauroyl Arginate Hydrochloride is commonly used in biological chemistry research, especially in institutions focused on molecular interactions and peptide studies. Its availability and performance make it a go-to material for scientists conducting experiments that require surfactant properties or molecular interaction facilitation. Its role in enhancing experimental outcomes underscores its importance in the Indonesian scientific community.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePeptide Chemistry Research – This compound supports the study of peptide interactions and molecular behavior due to its amphoteric nature and surfactant properties.\u003c\/li\u003e\n\u003cli\u003eBiochemical Experiments – Its ability to act as an emulsifier and pH regulator makes it ideal for experiments involving protein and peptide interactions.\u003c\/li\u003e\n\u003cli\u003eMolecular Interaction Studies – The compound facilitates the study of complex molecular interactions, enhancing the accuracy of biochemical analyses.\u003c\/li\u003e\n\u003cli\u003eSurfactant Applications – Its surfactant properties make it suitable for use in emulsification processes and surface-active agent studies.\u003c\/li\u003e\n\u003cli\u003epH Regulation in Reactions – The amphoteric character of Ethyl Lauroyl Arginate Hydrochloride allows it to be used as a pH adjuster in various chemical reactions.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 60372-77-2\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Peptide Chemistry\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eEthyl Lauroyl Arginate Hydrochloride should be stored in a cool, dry environment to maintain its stability and prevent degradation. It is recommended to keep the compound in a sealed container to avoid exposure to moisture and air, which could affect its chemical integrity. Due to its amphoteric nature, it is important to handle it with care to prevent contamination or unintended reactions. In a laboratory setting, it should be stored away from incompatible substances to ensure safety. Proper labeling and storage conditions help maintain the compound’s effectiveness for use in research applications. Always follow standard laboratory safety protocols when handling and storing this material.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086963781850,"sku":"TCI2510E148229520","price":788000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086963814618,"sku":"TCI2510E148229521","price":2306000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510E1482.jpg?v=1767112930"},{"product_id":"tci2510f050330359","title":"TCI F0503 129460-09-9 1-tert-Butyl N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-aspartate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eThis chemical compound, TCI F0503 129460-09-9 1-tert-Butyl N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-aspartate, is a specialized peptide compound used in various chemical and biochemical experiments within laboratory settings. As a complex molecule, it plays a crucial role in organic and peptide synthesis due to its unique molecular structure. Its functional groups allow it to participate in specific chemical reactions, making it an essential tool for researchers working on peptide-related projects. This compound is particularly valuable for its ability to interact with other molecules in controlled environments, enhancing the precision and efficiency of experimental outcomes.\u003c\/p\u003e\n\u003cp\u003eThe compound's chemical stability under specific conditions makes it a preferred choice for laboratory use. Its resistance to unwanted reactions with other reagents ensures that experimental results remain accurate and reliable. The structural complexity of this molecule enables it to form specific interactions with various reagents, which is vital for the synthesis of complex peptides and organic compounds. Additionally, its stability simplifies storage and handling, reducing the risk of degradation during experimental procedures. These properties make it an ideal candidate for applications requiring high precision and reproducibility.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is widely used in biochemical and pharmacological research. It is commonly found in research institutions and universities where scientists are working on peptide synthesis and related biochemical processes. Its role in accelerating the synthesis and testing of bioactive compounds makes it an essential component in the toolkit of biochemists and pharmacologists. The compound's reliability and versatility contribute to its widespread adoption in both academic and applied research settings.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePeptide Synthesis: This compound is ideal for peptide synthesis due to its functional groups that allow for controlled coupling reactions with other amino acids.\u003c\/li\u003e\n\u003cli\u003eBiochemical Research: Its ability to interact with various reagents makes it suitable for biochemical studies involving molecular interactions and enzyme activity.\u003c\/li\u003e\n\u003cli\u003eOrganic Chemistry Experiments: The compound's structural complexity supports its use in the synthesis of complex organic molecules and intermediates.\u003c\/li\u003e\n\u003cli\u003eDrug Development: It is utilized in pharmaceutical research to develop new drugs by facilitating the synthesis of bioactive peptides and derivatives.\u003c\/li\u003e\n\u003cli\u003eAnalytical Chemistry: Its stability and reactivity make it a valuable tool for analytical techniques requiring precise molecular interactions and reaction control.\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: 129460-09-9\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Peptide Chemistry\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified in the provided data\u003c\/li\u003e\n\u003cli\u003ePhysical form: Not specified in the provided data\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its chemical stability and prevent degradation. It is recommended to use airtight containers to protect it from moisture and potential contamination. Due to its chemical complexity, it should be handled with care to avoid unintended reactions with other substances. Proper labeling and storage conditions are essential to ensure the integrity of the compound during experimentation. Laboratory personnel should always wear appropriate personal protective equipment when handling this material to ensure safety and maintain the quality of the compound.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087009263834,"sku":"TCI2510F050330359","price":1406000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48087009296602,"sku":"TCI2510F050330360","price":4526000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510F0503.jpg?v=1768360123"},{"product_id":"tci2510f131831459","title":"TCI F1318 84793-07-7 Fmoc-Glu-OtBu","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI F1318, also known as Fmoc-Glu-OtBu with CAS number 84793-07-7, is a chemical compound widely used in peptide synthesis. This compound is a protected form of glutamic acid, featuring the Fmoc (9-fluorenylmethyloxycarbonyl) group and the OtBu (tert-butoxycarbonyl) group. It plays a crucial role in chemical biology and peptide chemistry by enabling the controlled synthesis of complex peptide structures. Its unique chemical properties make it an essential tool for researchers working in various scientific disciplines.\u003c\/p\u003e\n\u003cp\u003eThe stability and controlled reactivity of Fmoc-Glu-OtBu make it a preferred choice in laboratory settings. The Fmoc group allows for precise coupling and deprotection steps during peptide synthesis, while the OtBu group provides temporary stability during the reaction process. These properties ensure that the compound remains chemically inert until the desired reaction conditions are met. This controlled behavior simplifies the synthesis of peptides with high structural fidelity and functional accuracy.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Fmoc-Glu-OtBu is commonly used in peptide research, including drug development, biological analysis, and biomedical studies. Its role in creating custom peptides with specific sequences and functions makes it a valuable resource for both academic and industrial research. As a key component in peptide synthesis, it supports a wide range of applications that require precise chemical manipulation and controlled reaction environments.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePeptide Synthesis: Fmoc-Glu-OtBu is ideal for solid-phase peptide synthesis due to its controlled reactivity and stability during coupling reactions.\u003c\/li\u003e\n\u003cli\u003eDrug Development: This compound is used in the synthesis of therapeutic peptides, enabling the creation of targeted drug molecules with specific biological activities.\u003c\/li\u003e\n\u003cli\u003eBiological Analysis: It supports the production of peptides for use in assays and diagnostic tests, aiding in the study of biological processes and molecular interactions.\u003c\/li\u003e\n\u003cli\u003eBiomedical Research: Fmoc-Glu-OtBu is essential for developing peptides used in regenerative medicine and therapeutic applications, contributing to advancements in biotechnology.\u003c\/li\u003e\n\u003cli\u003eAcademic Research: Its versatility makes it a preferred choice for researchers exploring new peptide structures and functions in molecular biology and chemistry.\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: 84793-07-7\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Peptide Chemistry\u003c\/li\u003e\n\u003cli\u003ePack Sizes: Available in various quantities as per standard supplier offerings\u003c\/li\u003e\n\u003cli\u003ePhysical Form: Solid powder\u003c\/li\u003e\n\u003cli\u003eStorage Note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment, away from direct light and moisture to maintain its chemical stability. It is recommended to use airtight containers to prevent exposure to humidity and contaminants. Due to its reactivity, it should be handled with care in a well-ventilated laboratory setting. Avoid contact with incompatible substances and ensure proper personal protective equipment is used during handling. The compound is generally stable under standard laboratory conditions when stored correctly. Always follow standard safety protocols when working with chemical reagents to ensure a safe and controlled environment.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48087076077786,"sku":"TCI2510F131831459","price":1771000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48087076110554,"sku":"TCI2510F131831460","price":6184000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510F1318.jpg?v=1768205471"},{"product_id":"tci2510g010231707","title":"TCI G0102 623-33-6 Glycine Ethyl Ester Hydrochloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eGlycine Ethyl Ester Hydrochloride is the hydrochloride salt form of the ethyl ester of glycine, supplied by TCI under catalogue number G0102 and identified by CAS number 623-33-6. In peptide chemistry, this compound serves as a pre-protected carboxyl-terminal component: the carboxylic acid group of glycine has been converted into an ethyl ester so that it does not participate during amide bond formation, while the amino group is held safely in salt form and can be liberated immediately before coupling by the addition of a base. This working pattern is what makes it a foundational reagent for the synthesis of dipeptides, tripeptides, and a wide range of amides and nitrogen-containing heterocycles in the laboratory.\u003c\/p\u003e\n\u003cp\u003eThe principal characteristic that makes this reagent so widely chosen is its stability. As a hydrochloride salt, the compound has a far better shelf life than the corresponding free ester, which readily undergoes self-cyclisation into diketopiperazine, so researchers obtain consistent material from one experiment to the next. It presents as a solid that is easy to weigh out accurately, dissolves well in water and in polar solvents such as methanol as well as dichloromethane once neutralised, and possesses no chiral centre, which removes any concern about racemisation during coupling steps. Together these properties give predictable, reproducible behaviour in routine bench work.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent is typically encountered in university and institutional research settings where peptide and organic synthesis work is carried out, as well as in laboratories developing amide and heterocyclic compounds. Because the material is stable enough to be stored and drawn upon repeatedly, it suits research groups that run synthesis campaigns over extended periods, and its straightforward handling as a weighable solid fits laboratories that prepare reactions on small to moderate scale without specialised transfer equipment.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eDipeptide synthesis — the ethyl ester blocks the glycine carboxyl group so that amide bond formation proceeds selectively at the amine terminus without competing side reactions or the need for additional in-situ protection.\u003c\/li\u003e\n\u003cli\u003eTripeptide and short-chain peptide construction — the protected carboxyl terminus allows stepwise chain extension, with the amino group released by base only at the moment coupling is required for each successive residue.\u003c\/li\u003e\n\u003cli\u003eGeneral amide preparation — the free amine, liberated from the salt by neutralisation, reacts cleanly with activated acids and acyl donors to give glycine-derived amides under standard laboratory conditions.\u003c\/li\u003e\n\u003cli\u003eSynthesis of nitrogen-containing heterocycles — the bifunctional amino-ester framework provides both a nucleophilic nitrogen and an electrophilic ester carbon for ring-forming reactions in heterocyclic chemistry programmes.\u003c\/li\u003e\n\u003cli\u003eChemical biology and peptide-mimetic research — the absence of a chiral centre means glycine-derived fragments can be introduced without any risk of racemisation compromising the stereochemical integrity of the target molecule.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI, supplied under catalogue number G0102\u003c\/li\u003e\n\u003cli\u003eCAS number: 623-33-6\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Peptide Chemistry\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in the standard TCI catalogue pack sizes for this item; please confirm the required quantity when ordering\u003c\/li\u003e\n\u003cli\u003ePhysical form: solid, readily weighed for accurate measurement\u003c\/li\u003e\n\u003cli\u003eStorage note: store as a stable hydrochloride salt in a closed container, protected from moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the material in a tightly closed original container in a cool, dry place away from moisture, since the compound is hygroscopic in character as a hydrochloride salt and is best protected from atmospheric humidity. Glass or the supplier's original packaging is suitable; the container should be resealed promptly after each withdrawal. Weigh the solid using clean, dry spatulas and avoid returning unused material to the stock bottle. Handle in a well-ventilated area or fume hood, wearing gloves, safety glasses, and a laboratory coat, and consult the supplier's safety data sheet before use. Keep separated from strong bases and strong oxidising agents, and allow refrigerated containers to warm to room temperature before opening to prevent condensation on the contents.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48087091052762,"sku":"TCI2510G010231707","price":507000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48087091085530,"sku":"TCI2510G010231708","price":2278000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510G0102.jpg?v=1767114615"},{"product_id":"tci2510g017931786","title":"TCI G0179 1118-89-4 Diethyl L-Glutamate Hydrochloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI G0179 Diethyl L-Glutamate Hydrochloride is the hydrochloride salt form of the diethyl ester of L-glutamic acid, supplied as a white crystalline solid. In this molecule, both carboxyl groups of glutamic acid have been converted into ethyl esters, protecting them from unwanted reactions, while the amino group is bound as a hydrochloride salt so that the material remains stable during storage. This combination makes it a highly useful intermediate in peptide chemistry, because researchers can work directly with the free amino group once it has been neutralised, without first carrying out a separate carboxyl protection step.\u003c\/p\u003e\n\u003cp\u003eThe properties that make this material a preferred choice are its preserved L-configuration and the ease with which its reactivity can be controlled. The amino group, held as a salt, is unreactive during storage, yet it can be liberated immediately by adding a mild base such as triethylamine or N,N-diisopropylethylamine directly in the reaction flask. The ethyl esters at the α and γ positions can be hydrolysed back in a controlled manner using aqueous base whenever the free acid groups need to be restored. The salt form also provides good solubility in polar solvents and reduces the tendency of the material to take up moisture.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is typically used in university and institutional research groups working on peptide synthesis, chemical biology, and organic methodology. It is generally ordered as a supporting building block for multi-step syntheses, where a stable, storable glutamate derivative with both carboxyl groups already masked saves preparation time. Because the material is stable as a salt at ambient handling temperatures, it suits laboratories that need reliable bench chemicals for teaching, method development, and routine synthetic work.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePeptide bond formation: the free amino group released after neutralisation can be coupled directly with activated carboxyl partners, while both ester groups remain masked throughout the coupling step.\u003c\/li\u003e\n\u003cli\u003eMulti-step organic synthesis: serves as a stable, storable glutamate building block that removes the need for a separate carboxyl protection stage before the target sequence is assembled.\u003c\/li\u003e\n\u003cli\u003eChemical biology research: provides an L-configured glutamate derivative for preparing modified amino acid analogues and probe molecules where stereochemical integrity of the starting material must be maintained.\u003c\/li\u003e\n\u003cli\u003eControlled ester hydrolysis studies: the α and γ ethyl esters can be cleaved back to the free acids with aqueous base, allowing staged deprotection strategies to be developed and compared.\u003c\/li\u003e\n\u003cli\u003eSolution-phase reaction work: the hydrochloride salt dissolves well in polar solvents, making it convenient for preparing homogeneous reaction mixtures and stock solutions in synthetic laboratories.\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: 1118-89-4\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Peptide Chemistry\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in standard TCI catalogue pack sizes; please confirm the size required when ordering\u003c\/li\u003e\n\u003cli\u003ePhysical form: white crystalline solid\u003c\/li\u003e\n\u003cli\u003eStorage: keep in a tightly closed container in a cool, dry place away from moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the material in its original tightly closed container in a cool, dry location, protected from moisture and away from direct sunlight. Amber or opaque glass bottles with well-sealing caps are suitable for transferring smaller working quantities, and containers should be resealed promptly after each use to limit exposure to humid air. Handle the solid in a fume hood or well-ventilated area, using gloves, safety glasses, and a laboratory coat, and avoid generating dust during weighing. Use clean, dry spatulas to prevent contamination of the bulk material, and label all secondary containers clearly. Keep the compound separate from strong bases and strong oxidising agents, and follow institutional waste procedures when disposing of residues and rinse solutions.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48087095804122,"sku":"TCI2510G017931786","price":676000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48087095836890,"sku":"TCI2510G017931787","price":2138000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510G0179.jpg?v=1768205484"},{"product_id":"tci2510g024631869","title":"TCI G0246 5680-79-5 Glycine Methyl Ester Hydrochloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eGlycine Methyl Ester Hydrochloride is the hydrochloride salt of the methyl ester of glycine, the simplest amino acid, in which the carboxyl group has been converted into a methyl ester. In peptide chemistry, this material serves as a carboxyl-terminal unit that is already protected, so it can be coupled directly to another amino acid through amide bond formation. The hydrochloride salt form keeps the amino group protonated, which gives a stable solid that is easy to store; the free amine is then released by adding a mild base immediately before the coupling reaction takes place.\u003c\/p\u003e\n\u003cp\u003eThe properties that make this reagent a preferred choice are its good storage stability, consistent purity, and the ease with which the protecting group can be removed. The methyl ester can be hydrolysed back to the free acid using dilute base under mild conditions, so other sensitive groups elsewhere in the target molecule are not damaged in the process. Because glycine has no chiral centre, there is no risk of racemisation during coupling, which makes this material a safe choice for the opening steps of building a peptide chain. The solid also dissolves well in water and in polar solvents such as methanol and dimethylformamide, making it straightforward to prepare homogeneous reaction mixtures.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent is typically used in university and institutional research groups working on peptide synthesis, medicinal chemistry, and chemical biology, as well as in industrial R\u0026amp;D settings where short peptide sequences or amide-containing intermediates are prepared. It is commonly kept as a standard shelf reagent for synthesis work, since its handling requirements are modest and its behaviour in coupling reactions is predictable enough for routine method development and for teaching-level synthetic exercises.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePeptide chain elongation — supplies a ready-protected carboxyl-terminal residue that can be coupled directly with an incoming amino acid without an additional esterification step beforehand.\u003c\/li\u003e\n\u003cli\u003eAmide bond formation studies — the free amine liberated by mild base reacts cleanly with activated carboxyl partners, making it a dependable substrate for coupling reagent comparisons.\u003c\/li\u003e\n\u003cli\u003eRacemisation-free coupling steps — because glycine carries no chiral centre, this reagent lets chemists build the first residues of a sequence without any stereochemical erosion.\u003c\/li\u003e\n\u003cli\u003eMedicinal chemistry intermediate preparation — the methyl ester can be carried through several synthetic steps and then hydrolysed with dilute base to reveal the free acid.\u003c\/li\u003e\n\u003cli\u003eSolution-phase synthesis in polar media — its good solubility in water, methanol, and dimethylformamide allows homogeneous reaction mixtures that are simple to monitor and work up.\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: 5680-79-5\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Peptide Chemistry\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in standard TCI catalogue pack sizes; please confirm the size required when ordering\u003c\/li\u003e\n\u003cli\u003ePhysical form: solid (hydrochloride salt)\u003c\/li\u003e\n\u003cli\u003eStorage: keep in a tightly closed container in a cool, dry place, protected from moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the material in its original tightly closed container in a cool, dry place, away from moisture and direct sunlight. As a hydrochloride salt, the solid is hygroscopic in character and should be weighed out promptly and the container resealed straight away to avoid moisture pickup. Use clean, dry glass or chemically resistant plastic containers for any subaliquots, and label them clearly. Handle the powder in a fume hood or a well-ventilated area, wear gloves, safety glasses, and a laboratory coat, and avoid generating dust or inhaling it. Consult the manufacturer's safety data sheet before first use and follow local institutional waste disposal procedures.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48087100457178,"sku":"TCI2510G024631869","price":760000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48087100489946,"sku":"TCI2510G024631870","price":3092000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510G0246.jpg?v=1769142490"},{"product_id":"tci2510g025431882","title":"TCI G0254 27532-96-3 Glycine tert-Butyl Ester Hydrochloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eGlycine tert-Butyl Ester Hydrochloride is the hydrochloride salt of the tert-butyl ester of glycine, an amino acid derivative in which the carboxyl group is protected as a tert-butyl ester. In peptide synthesis, the tert-butyl protecting group belongs to the acid-labile class of protecting groups, so it can be removed with trifluoroacetic acid without disturbing base-labile protecting groups such as Fmoc. This orthogonal character is precisely what makes the compound an important building block in multi-level protection strategies for the construction of peptide chains and peptidomimetics.\u003c\/p\u003e\n\u003cp\u003eThe property that makes this material a widely preferred choice is its resistance to basic and nucleophilic conditions, which allows a variety of chemical transformations to be carried out on other parts of the molecule while the carboxyl group remains safely protected. The steric hindrance of the tert-butyl group also suppresses side reactions such as diketopiperazine formation or nucleophilic attack on the ester carbonyl. The hydrochloride salt form makes the solid more stable for storage and weighing, while the free amine is readily generated using a tertiary base such as diisopropylethylamine immediately before the coupling reaction.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent is typically used in university and institutional research groups working on peptide chemistry, medicinal chemistry, and chemical biology, as well as in the research and development units of pharmaceutical companies. Because glycine carries no side chain that requires additional protection, it is often chosen as a starting point for method development, for training new researchers in solution-phase coupling, and for the preparation of small peptide fragments and glycine-containing conjugates.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePeptide chain construction: the acid-labile tert-butyl ester serves as a carboxyl-terminal protecting group that survives repeated basic Fmoc-removal steps and is cleaved cleanly at the end of the sequence with trifluoroacetic acid.\u003c\/li\u003e\n\u003cli\u003eOrthogonal protection strategy development: because tert-butyl esters and base-labile groups such as Fmoc are removed under entirely different conditions, this compound allows chemists to design and validate multi-level protection schemes on a simple substrate.\u003c\/li\u003e\n\u003cli\u003ePeptidomimetic synthesis: the protected glycine unit can be incorporated into non-natural backbone architectures while the carboxyl group remains masked, letting modification chemistry proceed selectively at the amine or at other positions.\u003c\/li\u003e\n\u003cli\u003eSolution-phase coupling and fragment preparation: the free amine is liberated in situ with a tertiary base such as diisopropylethylamine, giving a reactive nucleophile for amide bond formation with activated carboxylic acid partners immediately before use.\u003c\/li\u003e\n\u003cli\u003eSide-reaction suppression in dipeptide chemistry: the steric bulk of the tert-butyl group limits diketopiperazine formation and nucleophilic attack on the ester carbonyl, which improves yields in sequences where cyclisation is otherwise a competing pathway.\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: 27532-96-3\u003c\/li\u003e\n\u003cli\u003eCatalogue number: G0254\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Peptide Chemistry\u003c\/li\u003e\n\u003cli\u003ePhysical form: solid (hydrochloride salt)\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in the pack sizes listed by the manufacturer for this catalogue number; please confirm the required size when ordering\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the material in a tightly closed original container in a cool, dry place, protected from moisture and away from direct sunlight, since the hydrochloride salt is hygroscopic in character and the ester group should not be exposed to humid air for extended periods. Keep the container away from strong acids and strong bases, as acidic conditions will cleave the tert-butyl protecting group. Handle the solid in a well-ventilated area or fume hood using appropriate personal protective equipment, including gloves, safety glasses, and a laboratory coat. Weigh out only the quantity required and reseal the container promptly to limit uptake of atmospheric moisture. Always consult the manufacturer's safety data sheet before use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087101210842,"sku":"TCI2510G025431882","price":592000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48087101243610,"sku":"TCI2510G025431883","price":1743000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48087101276378,"sku":"TCI2510G025431884","price":6016000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510G0254.jpg?v=1771058694"},{"product_id":"tci2510h097733748","title":"TCI H0977 7389-87-9 L-Histidine Methyl Ester Dihydrochloride","description":"\u003cp\u003e\u003cstrong\u003eL-Histidine Methyl Ester Dihydrochloride\u003c\/strong\u003e (CAS 7389-87-9) is a high-quality chemical from TCI, supplied as \u003cstrong\u003eHPLC Grade\u003c\/strong\u003e.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eApplication:\u003c\/strong\u003e Synthesis 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