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Journal of Modern Chemistry & Chemical Technology Cover

Journal of Modern Chemistry & Chemical Technology

E-ISSN: 2229-6999 | P-ISSN: 2321–5208 | Peer-Reviewed Journal (Refereed Journal) | Hybrid Open Access

About the Journal

Journal of Modern Chemistry & Chemical Technology Journal of Modern Chemistry & Chemical Technology [2229-6999(e)] is a peer-reviewed open-access journal of engineering and scientific journals launched in 2010 focused on the rapid publication of fundamental research papers in all areas of Chemistry, Modern Chemistry, Chemical Engineering, and Chemical Technology which are covered under domain Chemical Engineering. .

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Journal Information

Title: Journal of Modern Chemistry & Chemical Technology
Abbreviation: jomcct
Issues Per Year: 3 Issues
P-ISSN: 2321–5208
E-ISSN: 2229-6999
Publisher: STM Journals, An imprint of Consortium e-Learning Network Pvt. Ltd.
DOI: 10.37591/JOMCCT
Starting Year: 2010
Subject: Modern Chemistry & Chemical Technology
Publication Format: Hybrid Open Access
Language: English
Copyright Policy: CC BY-NC-ND
Type: Peer-reviewed Journal (Refereed Journal)

Address:

STM Journals, An imprint of Consortium e-Learning Network Pvt. Ltd. A-118, 1st Floor, Sector-63, Noida, U.P. India, Pin - 201301

Editorial Board

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jomcct maintains an Editorial Board of practicing researchers from around the world, to ensure manuscripts are handled by editors who are experts in the field of study.

Editor in Chief

Editor

Dr. A. Nepolraj, Head and Assistant professor

Annai College of Arts and Science, Tamilnadu, India, 612503

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Latest Articles

Ahead of Print

Microvita as a Fermi-Boson Hybrid Quantum Excitation: A Statistical Pathway Toward Unified Physics, Chemistry, and Biological Organization

This article reformulates Microvita as a hybrid quantum excitation that interpolates continuously between fermionic and bosonic statistical behavior.

Microvita theory; hybrid statistics; fermion-boson unification; quantum field theory; statistical mechanics; vacuum structure; monopole suppression; chemical coherence; biological organization; MATLAB simulation

Looking into new ideas in green chemistry

Green chemistry has become a revolutionary way to change chemical processes such that they have less of an effect on the environment while still being efficient and cost-effective.

Chemical synthesis, circularity, pollution, scalability, thermosets

Thermoacoustic Properties of 1-Propanol-n-Hexane and 1-Propanol-Cyclohexane Binary Mixtures: A Comparative Study at 298.15 K

This study reports the measurement of ultrasonic velocity (U), viscosity (η), and density (ρ) for the binary liquid mixtures 1-propanol–n-hexane and 1-propanol–cyclohexane at 298.15 K over the full composition range (mole fraction 0.1–0.9).

Acoustic impedance, binary liquid mixtures, intermolecular non-covalent interactions, isentropic compressibility, ultrasonic velocity

Modern Chemistry & Chemical Technology in Sensor Formation

The field of sensor formation stands at the vibrant intersection of modern chemistry and chemical technology, driven by an insatiable demand for precise, rapid, and sensitive detection across myriad applications.

Modern chemistry, chemical technology, sensors, nanomaterials, metal-organic frameworks

Nitrosamine Accumulation, Processing Variables, and Indigenous Plant Inhibitors in Nigerian Traditionally Processed Meats

N-nitrosamines are classified as probable or possible human carcinogens by the International Agency for Research on Cancer. Carcinogenic N-nitrosamines — principally N-nitrosodimethylamine (NDMA) and N-nitrosodiethylamine (NDEA) — are formed in abundance during the preparation of widely consumed Nigerian traditional processed meats including suya, kilishi, and balangu.

N-Nitrosamines, N-nitrosodimethylamine (NDMA), N-nitrosodiethylamine (NDEA), Suya, Kilishi, Balangu, Nigerian Processed Meat, NAFDAC, Hibiscus sabdariffa

Progress in the Chemistry of C-Glycosylation in Carbohydrates

Glycosylation is an intricate biochemical process where a glycosyl donor and a glycosyl acceptor are combined to form a glycoside. This process involves the creation of new stereogenic centers at the anomeric site of the glycosyl donor, leading to the formation of a diverse array of products.

Glycosylation, polysaccharides, C-Glycosides, Glycosidic bond formation, Stereoselective synthesis, Carbohydrate chemistry