1979Journal of AOAC INTERNATIONALRequires access

Colorimetric Determination of Carvone in Volatile Oils in the Presence of Menthone and Pulegone

M. Karawya, Mohamed S. Hifnawy, Seham S. El‐Hawary

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Abstract

Abstract Carvone, menthone, and pulegone in volatile oils are determined by measuring at 370 nm the color obtained by their reaction with 3,5-dinitrobenzoic acid (DNBA) or m-dinitrobenzene (DNB). The DNBA method is sensitive to 50—1500 μg carvone or pulegone/10 mL and to 500-1500 μg menthone/10 mL. The DNB method is as sensitive to carvone and menthone as is the DNBA method, but it is less sensitive to pulegone (300—1500 μg/10 mL). Either carvone or pulegone in the presence of menthone can be determined by using the DNBA method at concentrations less than 500 μg menthone/10 mL. Carvone can also be estimated by the DNB method without pulegone and menthone interference when these constituents are present at levels less than 300 and 500 μg/10 mL, respectively. Other ketonic constituents, piperitone, methyl heptenone, and ionone, did not respond to the color reaction except at concentrations above 750 μg/10 mL. The method was successfully used for the estimation of carvone in oils of Mentha viridis, M. crispa, caraway, and dill.

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Abstract Carvone, menthone, and pulegone in volatile oils are determined by measuring at 370 nm the color obtained by their reaction with 3,5-dinitrobenzoic acid (DNBA) or m-dinitrobenzene (DNB). The DNBA method is sensitive to 50—1500 μg carvone or pulegone/10 mL and to 500-1500 μg menthone/10 mL. The DNB method is as sensitive to carvone and menthone as is the DNBA method, but it is less sensitive to pulegone (300—1500 μg/10 mL). Either carvone or pulegone in the presence of menthone can be determined by using the DNBA method at concentrations less than 500 μg menthone/10 mL. Carvone can also be estimated by the DNB method without pulegone and menthone interference when these constituents are present at levels less than 300 and 500 μg/10 mL, respectively. Other ketonic constituents, piperitone, methyl heptenone, and ionone, did not respond to the color reaction except at concentrations above 750 μg/10 mL. The method was successfully used for the estimation of carvone in oils of Mentha viridis, M. crispa, caraway, and dill.

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Available abstract

Abstract Carvone, menthone, and pulegone in volatile oils are determined by measuring at 370 nm the color obtained by their reaction with 3,5-dinitrobenzoic acid (DNBA) or m-dinitrobenzene (DNB). The DNBA method is sensitive to 50—1500 μg carvone or pulegone/10 mL and to 500-1500 μg menthone/10 mL. The DNB method is as sensitive to carvone and menthone as is the DNBA method, but it is less sensitive to pulegone (300—1500 μg/10 mL). Either carvone or pulegone in the presence of menthone can be determined by using the DNBA method at concentrations less than 500 μg menthone/10 mL. Carvone can also be estimated by the DNB method without pulegone and menthone interference when these constituents are present at levels less than 300 and 500 μg/10 mL, respectively. Other ketonic constituents, piperitone, methyl heptenone, and ionone, did not respond to the color reaction except at concentrations above 750 μg/10 mL. The method was successfully used for the estimation of carvone in oils of Mentha viridis, M. crispa, caraway, and dill.

Key concepts: Menthone, Pulegone, Carvone, Chemistry, Monoterpene, Menthol, Stereochemistry, Essential oil

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Colorimetric Determination of Carvone in Volatile Oils in the Presence of Menthone and Pulegone — Research Paper | ScholarLens