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Organic reagents

From early AD to mid-19 century, people mainly use the natural organic substance (such as animal and plant extracts) for qualitative analysis or quantitative analysis. From the second half of the 19th century to the 1920s, it had begun to appear of artificially synthetic organic reagent such as using potassium acetate xanthan for test of nickel, copper, and molybdenum; using morin for test of aluminum; using diazo coupling reaction for the detection of Nitrite; using α-β-nitroso naphthol for detection of cobalt; using dimethyglyoxime for nickel test. After the proposal of the special-effects group in the 1930s and the proposal of theoretical analysis of functional groups theory in 1950s, people had carried out large-scale screen of organic reagents in search of special-effects analysis groups for different ions and had successfully synthesized a lot of agents of practical value (such as copper reagents, new copper agent, cadmium reagents, beryllium reagent, thorium reagents, etc.). Before the 1950s, the complex compound, in analytic chemistry, is mainly used in the aspects of the precipitation reaction of a binary chelate for the qualitative detection, precipitate isolation and gravimetric separation and other aspects. In the early 1950s and 1960, it is mainly in the form of complexometric titration. From the beginning of the late 1960s, the main focus has been moved to the photometric analysis. Meanwhile, it has been also developed of chelate organic solvent extraction.

α-Methylstyrene dimer (AMSD): Uses, Applications and Advantages

α-Methylstyrene dimer is a non-sulfur-type free-radical polymerization chain transfer agent, widely used in the production of styrene resins, acrylic resins, and synthetic latex.

Sep 29,2026  Organic reagents

Biological Activities and Biosynthesis Production of Bisabolene

Bisabolene is a natural sesquiterpene hydrocarbon which possesses woody citrus aroma, certain antibacterial and anti-inflammatory activity

Sep 28,2026  Organic reagents

6-Carboxyfluorescein (6-FAM): Dye Properties, Synthesis and Applications

6-Carboxyfluorescein(6-FAM), is used in experiments involving nucleic acid labelling, fluorescence in situ hybridisation (FISH), liposome probes and protein interactions,and is one of the most commonl

Sep 23,2026  Organic reagents

Pharmacological Profiles and Research of Physostigmine

Physostigmine is a toxic natural alkaloid, appearing as white crystals, soluble in ethanol and chloroform, slightly soluble in water, and susceptible to oxidative reddening.

Sep 23,2026  Organic reagents

Diallylamine: Characteristics, Toxicity, and Preparation

Diallylamine is N-prop-2-enylprop-2-en-1-amine. Its diallyl structure enables cyclopolymerization. It is an odorous liquid, less dense than water, used in pharmaceuticals, resins, paper, and corrosio

Sep 22,2026  Organic reagents

Photochemical Reactivity of Thiobenzoic Acid

Thiobenzoic acid is an oxidation-prone thiocarboxylic-acid intermediate insoluble in water, applicable for thioester and pharmaceutical preparation.

Sep 12,2026  Organic reagents

Synthesis and Oxidation of 2-Ethylhexanal

2-Ethylhexanal is a flammable aldehyde intermediate for plasticizers and fragrances, susceptible to oxidation, condensation and hydrogenation.

Sep 11,2026  Organic reagents

Applications of DABSO in Organic Synthesis

DABSO, a bench-stable colorless solid, serves as a solid SO? substitute to couple/cyclize diverse organic substrates via convenient one-pot reactions.

Aug 11,2026  Organic reagents

Decrypting the Biodiesel “Model Molecule”—Methyl Decanoate’s Journey into Combustion Chemistry

This article systematically reviews the research progress of Methyl Decanoate from synthesis, detection, pyrolysis/oxidation chemistry to artificial intelligence-assisted mechanism simplification.

Aug 9,2026  Organic reagents

How to draw lewis structure for ethoxy radical?

This article shows the lewis dot structure of ethoxy radical and steps to draw it.

Jul 27,2026  Organic reagents
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