Organic Reagents

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Organic Reagents

Organic reagents include a broad range of functional molecules such as acids, bases, solvents, coupling agents, and selective reagents used in synthesis, catalysis, analytical chemistry, and material preparation. They support diverse transformations and serve as essential components in research laboratories and industrial R&D workflows.

Ionic Liquids

Ionic liquids are salts that remain liquid below 100°C, offering unique physicochemical properties such as low volatility, high thermal stability, strong solvating ability, and tunable polarity. They serve as alternative green solvents in catalysis, electrochemistry, separations, and biomass processing. Ionic liquids enhance reaction efficiency, support metal-catalyzed transformations, and stabilize reactive intermediates. Their structural diversity allows optimization of viscosity, conductivity, acidity, and hydrophobicity for specific applications. In materials science, ionic liquids contribute to battery electrolytes, supercapacitors, CO? capture, and polymer processing. Their eco-friendly characteristics and multifunctionality make ionic liquids valuable across sustainable chemistry and advanced technologies.

Tetrabutylphosphonium Hexafluorophosphate CAS NO 111928-21-3

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CAS No.:111928-21-3

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1-Ethyl-3-Methylimidazolium Nitrate CAS NO 143314-14-1

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CAS No.:143314-14-1

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1-Ethyl-3-Methylimidazolium Tetrafluoroborate CAS NO 143314-16-3

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CAS No.:143314-16-3

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1-Ethyl-3-Methylimidazolium Acetate CAS NO 143314-17-4

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CAS No.:143314-17-4

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1-Ethyl-3-Methylimidazolium Trifluoromethanesulfonate CAS NO 145022-44-2

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CAS No.:145022-44-2

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1-Ethyl-3-Methylimidazolium Methanesulfonate CAS NO 145022-45-3

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CAS No.:145022-45-3

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1-Ethyl-3-Methylimidazolium Hexafluorophosphate CAS NO 155371-19-0

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CAS No.:155371-19-0

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1-Butyl-3-Methylimidazolium Hexafluorophosphate CAS NO 174501-64-5

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CAS No.:174501-64-5

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Thiocyanates and Isothiocyanates

Thiocyanates and isothiocyanates are sulfur- and nitrogen-containing reagents widely used in pharmaceuticals, agrochemicals, polymer chemistry, and ligand synthesis. Their strong nucleophilicity and ambident reactivity enable formation of thioamides, thioureas, heterocycles, and organosulfur compounds. Isothiocyanates are essential in peptide chemistry, bioconjugation, and fluorescent labeling due to their selective reaction with amines. Thiocyanates participate in substitution, oxidation, cyclization, and metal coordination processes. Their unique electronic structure supports applications in catalysts, dyes, and functional materials. The versatility and high reactivity of these reagents make them powerful tools in both laboratory synthesis and industrial chemistry.

Phenyl Isothiocyanate CAS NO 103-72-0

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CAS No.:103-72-0

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Alpha,Alpha'-Dithiocyanato-p-Xylene CAS NO 1014-99-9

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CAS No.:1014-99-9

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Dodecyl Isothiocyanate CAS NO 1072-32-8

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CAS No.:1072-32-8

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Cyclohexyl Isothiocyanate CAS NO 1122-82-3

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CAS No.:1122-82-3

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2-Bromoethyl Isothiocyanate CAS NO 1483-41-6

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CAS No.:1483-41-6

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4-Isothiocyanato-1,1'-Biphenyl CAS NO 1510-24-3

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CAS No.:1510-24-3

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3-Biphenyl Isothiocyanate CAS NO 1510-25-4

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CAS No.:1510-25-4

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p-Vinylphenyl Isothiocyanate CAS NO 1520-20-3

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CAS No.:1520-20-3

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Borate Esters

Borate esters are versatile organoboron reagents used in Suzuki–Miyaura coupling, protective-group chemistry, lubrication, and material synthesis. Their stability and reactivity balance make them ideal for transmetallation processes in cross-coupling reactions. Borate esters act as mild Lewis acids and are essential in producing pharmaceuticals, electronic materials, and agrochemicals. They also serve as plasticizers, flame retardants, and additive components in lubricants. Their ability to form reversible B–O bonds enables dynamic covalent chemistry and responsive material design. With broad functional compatibility and synthetic utility, borate esters remain foundational reagents in modern organic and materials chemistry.

Trimethyl Borate CAS NO 121-43-7

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CAS No.:121-43-7

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Sodium Tetraphenylboron CAS NO 143-66-8

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CAS No.:143-66-8

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Pinacolborane CAS NO 25015-63-8

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CAS No.:25015-63-8

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Tris[2-[2-(2-Methoxyethoxy)Ethoxy]Ethyl] Orthoborate CAS NO 30989-05-0

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CAS No.:30989-05-0

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7-Azaindole-5-Boronic Acid Pinacol Ester CAS NO 16-62-6

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CAS No.:16-62-6

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Trihexylene Glycol Biborate CAS NO 100-89-0

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CAS No.:100-89-0

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Triisopropanolamine Cyclic Borate CAS NO 101-00-8

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CAS No.:101-00-8

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Tributoxyboroxin CAS NO 101-36-0

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CAS No.:101-36-0

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Sulfonic Acids and Sulfinic Acids

Sulfonic and sulfinic acids are strong, highly polar Br?nsted acids widely used in catalysis, detergents, polymer chemistry, and organic synthesis. Their strong acidity and excellent solubility make them effective catalysts in esterification, alkylation, and dehydration reactions. Sulfonic acids serve as precursors to sulfonates, surfactants, ion-exchange materials, and pharmaceutical intermediates. Sulfinic acids participate in radical processes, sulfone formation, and nucleophilic addition, providing access to sulfur-containing functional groups. Their stability and functional versatility support applications in dyes, flame retardants, and advanced materials. These acids remain essential tools for constructing reactive and functionalized organic molecules.

5-Sulfosalicylic Acid Dihydrate CAS NO 5965-83-3

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CAS No.:5965-83-3

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6,8-Dianilinonaphthalene-1-Sulphonic Acid CAS NO 129-93-1

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CAS No.:129-93-1

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Benzenesulfonic Acid,4-(1,1-Dimethylethyl)- CAS NO 1133-17-1

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CAS No.:1133-17-1

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2,2'-Dithiobis(5-Nitrobenzoic Acid) CAS NO 1170-38-3

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CAS No.:1170-38-3

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2-[(Carboxymethyl)Sulphonyl]Benzoic Acid CAS NO 1209-81-0

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CAS No.:1209-81-0

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Trifluoromethanesulfonic Acid CAS NO 1493-13-6

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CAS No.:1493-13-6

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3,3''-Bipyridine-5-Sulfonic Acid CAS NO 1625-80-5

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CAS No.:1625-80-5

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2,2,2-Trifluoroethanesulphonicacid CAS NO 1827-97-0

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CAS No.:1827-97-0

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Selenium Compounds

Selenium compounds exhibit unique redox, biological, and catalytic properties, making them important in pharmaceuticals, materials science, electronics, and chemical synthesis. Organoselenium reagents participate in oxidation, reduction, radical chemistry, and electrophilic or nucleophilic substitution. They support construction of selenides, selenoxides, and heterocycles. Selenium-containing materials contribute to semiconductors, photovoltaic devices, and functional coatings due to their tunable optical and electronic characteristics. In biology and medicine, selenium compounds play roles in antioxidants, enzyme cofactors, and therapeutic agents. Their diverse reactivity and structural tunability ensure broad applicability across advanced synthetic and industrial chemistry.