Spectrophotometric Determination of Phenylephrine Macromolecule by Coupling with Diazotized 4‐Bromo Aniline

Abstract The present study outlines a meticulously devised and accurate spectrophotometric method for the determination of phenylephrine hydrochloride (PHEPH) in both its pure drug form and drop formulation. The methodology hinges upon a diazo‐coupling reaction, whereby PHEPH undergoes coupling with diazotized 4‐bromoaniline under alkaline conditions. The resulting yellowish‐orange azo‐dye demonstrates a remarkable sensitivity, quantified by the molar absorptivity value of 4.684 × 10 3 L mol −1 cm −1 . The pinnacle of absorption occurs at 459 nm, and the linearity of the method is impeccably upheld within the concentration range of 3–48 µg 10 mL −1 of PHEPH, as dictated by Beer's law. An aspect of paramount significance is the enduring stability of the product's coloration, evincing minimal alteration in absorbance over duration of up to 60 min. Notably, the recovery percentage stands at an impressive 100.1376%, testifying to the method's accuracy, while the relative standard deviation (RSD%) of a mere 0.310178% underscores its precision. The applicability of this method extends seamlessly to the estimation of PHEPH within nasal drop formulations, yielding results of commendable reliability and consistency.

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Publication Details

Journal
Macromolecular Symposia
Published
2025-02-01
DOI
https://doi.org/10.1002/masy.202400214
Primary Topic
Molecular Sensors and Ion Detection
Type
article
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article

Spectrophotometric Determination of Phenylephrine Macromolecule by Coupling with Diazotized 4‐Bromo Aniline

Asmaa Ahmed Mohammed, Assen N. Sharif
Macromolecular Symposia
Molecular Sensors and Ion Detection
article

Spectrophotometric Determination of Phenylephrine Macromolecule by Coupling with Diazotized 4‐Bromo Aniline

Asmaa Ahmed Mohammed, Assen N. Sharif
article en

Abstract

Abstract The present study outlines a meticulously devised and accurate spectrophotometric method for the determination of phenylephrine hydrochloride (PHEPH) in both its pure drug form and drop formulation. The methodology hinges upon a diazo‐coupling reaction, whereby PHEPH undergoes coupling with diazotized 4‐bromoaniline under alkaline conditions. The resulting yellowish‐orange azo‐dye demonstrates a remarkable sensitivity, quantified by the molar absorptivity value of 4.684 × 10 3 L mol −1 cm −1 . The pinnacle of absorption occurs at 459 nm, and the linearity of the method is impeccably upheld within the concentration range of 3–48 µg 10 mL −1 of PHEPH, as dictated by Beer's law. An aspect of paramount significance is the enduring stability of the product's coloration, evincing minimal alteration in absorbance over duration of up to 60 min. Notably, the recovery percentage stands at an impressive 100.1376%, testifying to the method's accuracy, while the relative standard deviation (RSD%) of a mere 0.310178% underscores its precision. The applicability of this method extends seamlessly to the estimation of PHEPH within nasal drop formulations, yielding results of commendable reliability and consistency.

Macromolecular SymposiaVol. 414(1)
University of Tikrit (IQ)
Openalex Percentile: Top 97%
Molecular Sensors and Ion Detection
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