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Chonnam University researchers discover how a century-old solvent can solve efficient amide synthesis

Researchers at Chonnam National University discovered a century-old solvent, dichloromethane, can efficiently synthesize amide bonds. The breakthrough method enables scalable and cost-effective amide synthesis, reducing waste and using benign byproducts.

SourceChonnam National University, The Research Information Management Team, Office of Research Promotion·JournalJournal of the American Chemical Society·TypeExperimental study·DateSep 25, 2026

Schizophrenia-linked genetic variant renders key brain receptor completely unresponsive to both natural and therapeutic compounds

Researchers at Flinders University discover a genetic mutation that silences a brain receptor, rendering it unresponsive to both natural trace amines and clinical drug candidates. The C182F variant eliminates receptor signaling and reduces cell surface expression, with profound implications for emerging psychiatric treatments.

SourceGenomic Press·JournalGenomic Psychiatry·TypeExperimental study·DateJan 6, 2026

Association of exposure to primary aromatic amines with health risks in China

A recent Chinese study analyzed urine samples from 457 residents across 16 cities, revealing significant associations between primary aromatic amine (PAA) exposure and oxidative DNA damage biomarker 8-OHdG. The findings suggest that even low concentrations of PAA may contribute to long-term cancer risks in the general population.

SourceKeAi Communications Co., Ltd.·JournalEnvironmental Chemistry and Ecotoxicology·DateSep 15, 2025

Retinopathy associated with hair dye

A case report describes a woman who experienced bilateral blurry vision after using hair dye with aromatic amines. The incident highlights the potential risk of retinopathy associated with certain hair dyes.

SourceJAMA Network·JournalJAMA Ophthalmology·DateSep 12, 2024

Choosing outcomes: new switchable process for synthesizing 3-aminoindolines and 2’-aminoarylacetic acids from same substrate

Researchers at Okayama University developed a switchable process to synthesize 3-aminoindolines and 2'-aminoaryl acetic acids from a common substrate using Grignard reagents and azide compounds. The new protocol utilizes tautomerism to control chemoselectivity and achieves efficient synthesis with good yields.

SourceOkayama University·JournalChemical Communications·TypeExperimental study·DateJun 24, 2024

Nucleophilic amino acids as a renewable alternative to petrochemically-derived amines in glycerol epoxy resins

Amino acids from lysine, glutamic acid, leucine, and serine exhibit superior curing properties compared to commercial hardeners. This study demonstrates the potential of these bio-based epoxy curing agents as a renewable alternative to petrochemical-derived amines.

SourceJournal of Bioresources and Bioproducts·JournalJournal of Bioresources and Bioproducts·TypeExperimental study·DateMar 14, 2024

A simple and robust method to add functional molecules to peptides

Researchers from Tohoku University developed a unique chemical reaction to attach two distinct functional molecules to the N-terminus of peptides with a glycine amino acid, achieving site-selective modification and stable carbon-carbon bonds. The method shows potential for labeling diverse peptides and larger proteins for purification,...

SourceTohoku University·JournalAngewandte Chemie International Edition·DateMar 11, 2024

CABBI develops eco-friendly enzyme to create key chemical building blocks

Researchers at CABBI develop photoenzymatic system to efficiently synthesize chiral amines, crucial chemical building blocks with wide applications. The team's new method addresses a longstanding challenge in synthetic chemistry and offers a promising platform for biomanufacturing.

Simultaneous synthesis and fixing of covalent organic frameworks

Researchers from Tokyo Institute of Technology have developed a novel synthesis method for imine-based COFs, eliminating the need for long reaction times, high temperatures, and Lewis acid catalysts. The method uses an electrogenerated acid as a catalyst, enabling direct fixation of COF films onto electrodes.

SourceTokyo Institute of Technology·JournalAngewandte Chemie International Edition·TypeExperimental study·DateJul 19, 2023

Pusan National University researchers develop portable color-changing food spoilage sensor

Researchers at Pusan National University have created a portable molecular sensor that detects biogenic amines released from spoiled food using polydiacetylene-based beads. The sensor, which changes color to red upon binding with BAs, can be used for rapid visual detection of spoiled food during storage and distribution.

SourcePusan National University·JournalFood Chemistry·TypeExperimental study·DateMar 21, 2023

Metalloradical catalysis guides new cobalt-based system that exploits unique features of homolytic radical reaction

Researchers at Boston College have developed a new catalytic approach that enables concurrent control of multiple convergences and selectivities in intermolecular amination of allylic carbon-hydrogen bonds in alkenes. The cobalt-based system exploits unique features of homolytic radical reaction to form desired amine products in a high...

SourceBoston College·JournalNature Chemistry·TypeExperimental study·DateFeb 2, 2023

Kobe University and AGC successfully convert dry cleaning solvent into useful chemical compounds

Researchers developed a new photo-oxidation method to efficiently synthesize pharmaceutical intermediates and polyurethane from perchloroethylene, a common dry cleaning solvent. The method yields high-quality compounds with minimal environmental impact, offering a promising alternative for sustainable chemical recycling.

SourceKobe University·JournalACS Omega·TypeExperimental study·DateJan 31, 2023

A simple, cheap material for carbon capture, perhaps from tailpipes

Researchers have created a cheap and energy-efficient way to capture carbon dioxide from smokestacks using porous melamine material. The process is simple to make and requires primarily off-the-shelf melamine powder, making it a promising solution for scaling down carbon emissions from vehicle exhaust or other movable sources.

SourceUniversity of California - Berkeley·JournalScience Advances·TypeExperimental study·DateAug 4, 2022

New hair dyes avoid allergic reactions

Researchers have created a range of permanent hair dyes that avoid the allergenic properties of traditional formulations, producing a range of hues from rosy pinks to deep blacks. The new dyes were found to be less reactive toward proteins and generated a reduced inflammatory response in cells compared to PPD.

SourceAmerican Chemical Society·JournalACS Sustainable Chemistry & Engineering·DateJan 26, 2022

Chemistry breakthrough leads way to more sustainable pharmaceuticals

Scientists at the University of Bath have developed a new method for synthesizing primary amines, used in over half of all pharmaceuticals, significantly reducing energy usage and chemical waste. This breakthrough aims to speed up drug discovery by making it easier to synthesize new chemical structures for testing.

SourceUniversity of Bath·JournalJournal of the American Chemical Society·TypeExperimental study·DateNov 17, 2021

Hydrogen bonds may be key to airborne dicamba

Washington University researchers found that hydrogen bonding functional groups on amines play a key role in controlling dicamba volatility. The team's study suggests that amines with more hydrogen bonding sites decrease dicamba's ability to become airborne, potentially leading to improved formulations and reduced crop damage.

SourceWashington University in St. Louis·JournalEnvironmental Science & Technology·DateNov 4, 2020

Nanocatalyst makes heavy work of formic acid

Researchers at Osaka University have developed a palladium-based alloy nanocatalyst that promotes the selective production of deuterium isotope compounds from formic acid. The catalyst enables a cost-effective and scalable process for producing these gases, which are useful in fine chemical production and research applications.

SourceOsaka University·JournalNature Communications·DateSep 25, 2019

New catalyst achieves unprecedented activities

Researchers have developed a new efficient catalyst to synthesise aromatic amines, which are central building blocks in many drugs and pesticides. The system is more active than conventional catalysts, enabling faster and more efficient production of these compounds.

SourceRuhr-University Bochum·JournalAngewandte Chemie International Edition·DateDec 4, 2018

Approaching an ideal amino acid synthesis using hydrogen

Osaka University researchers have developed a practical and environmentally innocuous method for functionalizing multiply substituted amines. Their reductive alkylation approach uses hydrogen directly, generating only water as a byproduct and efficiently synthesizing a wide variety of amines, including amino acids.

SourceOsaka University·JournalJournal of the American Chemical Society·DateJun 11, 2018