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.

Aliphatic Ketones (including Enols)

Aliphatic ketones and their enol forms are widely used reagents in organic synthesis, polymer chemistry, fragrances, and industrial formulations. Their carbonyl functionality enables nucleophilic addition, condensation, oxidation, Grignard reactions, and metal-catalyzed transformations. Enols and enolates serve as reactive intermediates in carbon–carbon bond formation, aldol reactions, and heterocycle construction. Aliphatic ketones also function as solvents, plasticizer components, and extraction agents. Their volatility, polarity, and predictable reactivity patterns support applications in coatings, adhesives, and chemical manufacturing. With tunable steric and electronic properties, aliphatic ketones remain fundamental tools in fine chemical synthesis and process chemistry.

2-Bromo-1-Phenylhexan-1-One CAS NO 59774-06-0

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CAS No.:59774-06-0

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5-Diethylamino-2-Pentanone CAS NO 105-14-6

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CAS No.:105-14-6

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Allylacetone CAS NO 109-49-9

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CAS No.:109-49-9

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(Z)-12-Henicosene-2,4-Dione CAS NO 112-09-4

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CAS No.:112-09-4

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4-Heptanone CAS NO 123-19-3

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CAS No.:123-19-3

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Dimedone CAS NO 126-81-8

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CAS No.:126-81-8

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Tetrahydrothiophen-3-One CAS NO 1003-04-9

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CAS No.:1003-04-9

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3-Acetyl-1-Propanol CAS NO 1071-73-4

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CAS No.:1071-73-4

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Amides

Amides are essential organic reagents found throughout pharmaceuticals, polymers, agrochemicals, and materials science. Their stability and strong resonance contribute to predictable reactivity in acylation, condensation, reduction, and cyclization processes. Amides serve as backbone structures in peptides, drug molecules, and specialty polymers. They participate in catalytic transformations such as amidation, transamidation, and metal-catalyzed coupling reactions. Industrial applications include nylon production, surfactants, lubricants, and thickening agents. Due to their broad chemical compatibility, amides function as solvents, stabilizers, and reaction media in synthesis. Their structural versatility and biological relevance make amides indispensable across scientific and industrial disciplines.

Diethyl Acetamidomalonate CAS NO 1068-90-2

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CAS No.:1068-90-2

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1-Hydroxybenzotriazole Hydrate CAS NO 123333-53-9

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CAS No.:123333-53-9

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(S)-n-Fmoc-4-Bromophenylalanine CAS NO 198561-04-5

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CAS No.:198561-04-5

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D-Proline CAS NO 344-25-2

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CAS No.:344-25-2

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D-Dopa CAS NO 5796-17-8

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CAS No.:5796-17-8

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(R)-(-)-2-Amino-1-Butanol CAS NO 5856-63-3

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CAS No.:5856-63-3

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D-Phenylalanine CAS NO 673-06-3

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CAS No.:673-06-3

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L-tert-Leucinamide Hydrochloride CAS NO 75158-12-2

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CAS No.:75158-12-2

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Ethers

Ethers are widely used organic reagents known for their stability, low reactivity, and excellent solvation properties. They serve as key solvents in Grignard reactions, organometallic chemistry, extractions, and chromatographic processes. Ethers participate in cleavage, oxidation, alkylation, and polymerization reactions under controlled conditions. Industrially, they are used in fuel additives, refrigerants, and pharmaceutical formulations. Cyclic ethers such as THF and dioxane play major roles in polymer synthesis and coordination chemistry. Their low polarity, volatility, and ability to stabilize reactive intermediates make ethers essential in laboratory and industrial environments. Their versatility ensures broad application across chemical synthesis, energy materials, and processing technologies.

Triethyl Orthoformate CAS NO 122-51-0

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CAS No.:122-51-0

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3-Chloroanisole CAS NO 2845-89-8

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CAS No.:2845-89-8

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3-Hydroxytetrahydrofuran CAS NO 453-20-3

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CAS No.:453-20-3

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2,4,6-Triallyloxy-1,3,5-Triazi CAS NO 101-37-1

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CAS No.:101-37-1

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2-(2-Iodoethyl)-1,3-Dioxolane-4-Methanol CAS NO 104-08-5

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CAS No.:104-08-5

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3,4-Dihydro-2H-Pyran CAS NO 110-87-2

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CAS No.:110-87-2

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2-Butoxyethanol CAS NO 111-76-2

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CAS No.:111-76-2

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4-Methyl-2-Nitroanisole CAS NO 119-10-8

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CAS No.:119-10-8

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Aromatic Hydrocarbons

Aromatic hydrocarbons are fundamental organic reagents consisting of benzene rings that exhibit exceptional stability, distinct electronic resonance, and versatile chemical reactivity. They serve as core building blocks in pharmaceuticals, polymers, petrochemicals, and advanced materials. Aromatic hydrocarbons undergo electrophilic substitution, oxidation, metal-catalyzed coupling, and radical processes, enabling synthesis of dyes, agrochemicals, intermediates, and functional materials. Their π-electron systems contribute to unique optical, conductive, and structural properties essential for organic semiconductors, OLEDs, and specialty coatings. Industrially, aromatic hydrocarbons are key solvents, fuels, and monomer precursors. Their tunable substitution patterns and robust framework make them indispensable to modern chemical synthesis and material innovation.

4-Chlorotolueneforsynthesis CAS NO 106-43-3

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CAS No.:106-43-3

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Toluene (Methyl-D3) CAS NO 1124-18-1

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CAS No.:1124-18-1

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2-Methoxy-7-Methylnaphthalene CAS NO 1131-53-9

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CAS No.:1131-53-9

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1,2-Bis(2-Pyridyl)Ethylene CAS NO 1437-15-6

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CAS No.:1437-15-6

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2-Chloroethynylbenzene CAS NO 1483-82-5

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CAS No.:1483-82-5

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4-Bromo-p-Terphenyl CAS NO 1762-84-1

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CAS No.:1762-84-1

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4-(Chloromethyl)Quinoline Hydrochloride CAS NO 1822-57-7

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CAS No.:1822-57-7

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4-Chloro-1-Methoxynaphthalene CAS NO 10443-43-3

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CAS No.:10443-43-3

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Aromatic Alcohols

Aromatic alcohols contain hydroxyl groups attached to aromatic rings, offering enhanced stability, controlled polarity, and versatile reactivity. These compounds participate in oxidation, esterification, etherification, substitution, and metal-catalyzed reactions. Aromatic alcohols are widely used in pharmaceuticals, fragrances, agrochemicals, and polymer chemistry. Their structural rigidity and tunable electronic properties make them ideal intermediates for synthesizing dyes, antioxidants, monomers, and specialty chemicals. Benzyl alcohols and phenethyl alcohols are important solvents, preservatives, and fragrance components. In medicinal chemistry, aromatic alcohols improve solubility, metabolic profiles, and binding interactions. Their combination of aromatic character and alcohol functionality ensures broad applicability in fine chemical synthesis and industrial formulations.

Benzyl Alcohol CAS NO 100-51-6

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CAS No.:100-51-6

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