Submission Time

( Vol 29 , Issue 05 )

18 May 2025

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Publish On

( Vol 29 , Issue 05 )

31 May 2025

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Research Journal of Chemistry and Environment

Research Journal of Chemistry and Environment (ISSN:0972-0626) is a monthly peer-reviewed scopus-indexed journal from 2007 to Present. The publisher of this journal is the Journal of International Congress of Chemistry and Environment. RJCE is committed to gathering and disseminating excellent research achievements. The journal welcomes all kind of research/review/abstract papers regarding Engineering subjects including Earth and Planetary Sciences, Environmental Science, Chemical Engineering, Agricultural and Biological Sciences, Renewable Energy, Biochemistry.

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Research Journal of Chemistry and Environment

  • RJCE-30-04-2025-1398
  • Research Journal of Chemistry and Environment
FORMULATION AND ASSESSMENT OF ANTIMICROBIAL ACTIVITY OF NATURAL HERBAL BATH SOAP

Synthetic ingredients and chemicals included in the majority of commercial soaps can be disagreeable or even damaging to the skin. The human skin necessitates specialized care for repair, improving skin tone, and attaining a luminous appearance. Natural herbal soaps are an alternative option. Herbal goods possess dual significance: they serve as cosmetics for body care, and their inclusion of phytochemicals and botanicals contributes to naturally healthy skin. The practice of herbalism and the utilization of herbal products have become prevalent trends. Indian herbs are the most prolific resou

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  • RJCE-27-04-2025-1394
  • Research Journal of Chemistry and Environment
Uncovering Resistance Pathways in Escherichia coli: WGS-Based Insights into Human and Animal Isolates from Baghdad

The escalating threat of antimicrobial resistance (AMR) among Escherichia coli populations presents a significant global and regional health challenge, particularly in regions with limited surveillance frameworks such as Iraq. This study employs whole-genome sequencing (WGS) to investigate the resistome and mutational landscapes of four E. coli isolates—two derived from human clinical sources (H13, H41) and two from animals (A13, A45)—collected from Baghdad. The aim was to delineate the genetic determinants underlying resistance and to explore the potential cross-transmission of resistance

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  • RJCE-23-04-2025-1391
  • Research Journal of Chemistry and Environment
Spectrophotometric Determination of Mesalazine via Diazotization and Coupling With M-Aminophenol and Area Under Curve Methods

This study involves the development of an accurate, efficient, and low-cost spectrophotometric method for the determination of mesalazine (MSZE) in its pure state and various formulations. This process involves the coupling of diazotized MSZE with the reagent m-aminophenol (m-AP) in presence of sodium hydroxide (NaOH) medium to form a water-soluble azo dye with a maximum absorbance value at 470 nm. The method follows Beer's law in the concentration range of 0.5 - 10 μg/mL, with an excellent coefficient of determination (R2 = 0.9997), a molar absorptivity of 1.69 × 104 L/mol.cm², and a Sande

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  • RJCE-16-04-2025-1388
  • Research Journal of Chemistry and Environment
Comparative Analysis of Antimicrobial Resistance in Escherichia coli: Insights from Whole Genome Sequencing of Human and Animal Sources in Baghdad

The antimicrobial resistance (AMR) profiles of four Escherichia coli isolates, two from human fecal samples (H13 and H41) and two from animal fecal samples (A13 and A45), were investigated in this study, which were collected from different sites in Baghdad. Resistance genes, functional proteins, and genomic characteristics like contig number, genome length and GC content were determined by whole-genome sequencing (WGS). It confirmed significant differences in virulence and resistance potential of human and animal-derived isolates. The longest genome was A13 (13.4 Mbp), while A45 had th

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  • RJCE-08-03-2025-1382
  • Research Journal of Chemistry and Environment
Synthesis some of new esters derivative from pyrazine carboxylic acids by microwave and study their biological activity

This paper involves synthesized of some new esters by derivative from pyrazine carboxylic acid using as catalyst under microwave irradiation reaction between carboxyclic acids and primary alchohol methanol, ethanol and propanol the new product bio active has gined alot of attention because their mumerous significant medicine and biological use their structures were identified by (FT.IR, HNAR, 13(NM) and were screened in vitro antims crobial for biological activity.

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