2014Chinese Journal of Analysis LaboratoryRequires access

Simultaneous determination of vanillin,ethyl-vanillin,maltol and ethylmaltol in cigarette additives by high performance liquid chromatography

Ren Hu-b

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Abstract

High performance liquid chromatographic method for simultaneous determination of vanillin,ethylvanillin,maltol and ethylmaltol in cigarette additives was established.After diluted,vibration and filtration,the cigarette additives were separated on a Thermo Scientific C18(4.6 i.d × 250 mm,5 μm) column in isocratic elution mode using acetonitrile:0.1% formic acid(33:67,V /V) as the mobile phase at 1.0 mL /min.The quantification of these cigarette additives was achieved with external standard method on a diode- array detector at 273 nm.Baseline separation of vanillin,ethyl-vanillin,maltol and ethylmaltol was achieved within 9 min.The linear ranges for vanillin,ethyl-vanillin,maltol and ethylmaltol were 0.0139 ~ 264.5 mg /kg,0.0554 ~302.7 mg /kg,4.01 ~ 262.9 mg /kg and 2.32 ~ 258.1 mg /kg,respectively.The linear correlation coefficients for vanillin,ethyl-vanillin,maltol and ethylmaltol were 0.9998,0.9999,0.9999 and 0.9997,respectively.The detection limits(S /N = 3) for vanillin,ethyl-vanillin,maltol and ethylmaltol were 0.00349,0.00554,1.29,and 0.58 mg /kg,respectively.The recoveries and the relative standard deviations(RSD,n = 9) at the spiked concentration of 10.75- 59.14 mg /kg were 96.8%- 102.2% and 0.62%- 1.6%,respectively.The proposed method has the merits of easy operation,short analysis time and accurate results,which is very suitable for the simultaneous determination of vanillin,ethyl-vanillin,maltol and ethylmaltol in cigarette additives.

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High performance liquid chromatographic method for simultaneous determination of vanillin,ethylvanillin,maltol and ethylmaltol in cigarette additives was established.After diluted,vibration and filtration,the cigarette additives were separated on a Thermo Scientific C18(4.6 i.d × 250 mm,5 μm) column in isocratic elution mode using acetonitrile:0.1% formic acid(33:67,V /V) as the mobile phase at 1.0 mL /min.The quantification of these cigarette additives was achieved with external standard method on a diode- array detector at 273 nm.Baseline separation of vanillin,ethyl-vanillin,maltol and ethylmaltol was achieved within 9 min.The linear ranges for vanillin,ethyl-vanillin,maltol and ethylmaltol were 0.0139 ~ 264.5 mg /kg,0.0554 ~302.7 mg /kg,4.01 ~ 262.9 mg /kg and 2.32 ~ 258.1 mg /kg,respectively.The linear correlation coefficients for vanillin,ethyl-vanillin,maltol and ethylmaltol were 0.9998,0.9999,0.9999 and 0.9997,respectively.The detection limits(S /N = 3) for vanillin,ethyl-vanillin,maltol and ethylmaltol were 0.00349,0.00554,1.29,and 0.58 mg /kg,respectively.The recoveries and the relative standard deviations(RSD,n = 9) at the spiked concentration of 10.75- 59.14 mg /kg were 96.8%- 102.2% and 0.62%- 1.6%,respectively.The proposed method has the merits of easy operation,short analysis time and accurate results,which is very suitable for the simultaneous determination of vanillin,ethyl-vanillin,maltol and ethylmaltol in cigarette additives.

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Available abstract

High performance liquid chromatographic method for simultaneous determination of vanillin,ethylvanillin,maltol and ethylmaltol in cigarette additives was established.After diluted,vibration and filtration,the cigarette additives were separated on a Thermo Scientific C18(4.6 i.d × 250 mm,5 μm) column in isocratic elution mode using acetonitrile:0.1% formic acid(33:67,V /V) as the mobile phase at 1.0 mL /min.The quantification of these cigarette additives was achieved with external standard method on a diode- array detector at 273 nm.Baseline separation of vanillin,ethyl-vanillin,maltol and ethylmaltol was achieved within 9 min.The linear ranges for vanillin,ethyl-vanillin,maltol and ethylmaltol were 0.0139 ~ 264.5 mg /kg,0.0554 ~302.7 mg /kg,4.01 ~ 262.9 mg /kg and 2.32 ~ 258.1 mg /kg,respectively.The linear correlation coefficients for vanillin,ethyl-vanillin,maltol and ethylmaltol were 0.9998,0.9999,0.9999 and 0.9997,respectively.The detection limits(S /N = 3) for vanillin,ethyl-vanillin,maltol and ethylmaltol were 0.00349,0.00554,1.29,and 0.58 mg /kg,respectively.The recoveries and the relative standard deviations(RSD,n = 9) at the spiked concentration of 10.75- 59.14 mg /kg were 96.8%- 102.2% and 0.62%- 1.6%,respectively.The proposed method has the merits of easy operation,short analysis time and accurate results,which is very suitable for the simultaneous determination of vanillin,ethyl-vanillin,maltol and ethylmaltol in cigarette additives.

Key concepts: Vanillin, Maltol, Chemistry, Chromatography, High-performance liquid chromatography, Detection limit, Formic acid, Organic chemistry

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