1987
DOI: 10.1016/s0021-9673(00)96129-6
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Chemistry of acrylamide bromination for trace analysis by gas chromatography and gas chromatography—mass spectrometry

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Cited by 59 publications
(21 citation statements)
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“…The laboratory procedure derivatized the AMD with bromine to form 2,3‐dibromopropionamide. The derivative was then extracted with ethyl acetate and converted to the more stable 2‐bromopropenamide before gas chromatographic analysis, which used an electron‐capture detector (Andrawes et al, 1987). The analysis provided an AMD minimum detection limit of 0.5 μg L −1 The AMD recovery was 97% with a precision of ±0.21 μg L −1 for 1 μg L −1 AMD standards and ±0.75 μg L −1 for 10 μg L −1 AMD standards.…”
Section: Methodsmentioning
confidence: 99%
“…The laboratory procedure derivatized the AMD with bromine to form 2,3‐dibromopropionamide. The derivative was then extracted with ethyl acetate and converted to the more stable 2‐bromopropenamide before gas chromatographic analysis, which used an electron‐capture detector (Andrawes et al, 1987). The analysis provided an AMD minimum detection limit of 0.5 μg L −1 The AMD recovery was 97% with a precision of ±0.21 μg L −1 for 1 μg L −1 AMD standards and ±0.75 μg L −1 for 10 μg L −1 AMD standards.…”
Section: Methodsmentioning
confidence: 99%
“…In bromination of acrylamide, the product is 2,3-dibromopropionamide (2,3-DBPA), which is less polar compared to the original compound and is easily soluble in non-polar organic solvents like ethyl acetate and hexane. However, 2,3-DBPA was found unstable and could be converted to 2-bromopropenamide (2-BPA) on the inlet of GC or on the capillary column by dehydrobromination (25). Since the dehydrobromination might yield poor repeatability and accuracy, it was preferable to deliberately convert 2,3-DBPA to the stable 2-BPA prior to GC analysis.…”
Section: Brominationmentioning
confidence: 99%
“…The reaction product is 2,3-dibromopropionamide (Equation 1), which is less polar compared with the original compound and is detected as the final analyte (13,14,16). However, 2,3-dibromopropionamide (2,3-DBPA) has been found unstable under certain conditions and can be converted to the more stable derivative 2-bromopropenamide (Equation 2) on the inlet of GC or on the capillary column by dehydrobromination (25), which may yield poor repeatability and accuracy. Some researchers prefer to deliberately convert 2,3-DBPA to 2-bromopropenamide (2-BPA) by adding 10% of triethylamine to the final extract before injection (15,23,24 No matter whether 2,3-DBPA or 2-BPA is the target analyte, the advantage of acrylamide bromination is that a relative more volatile compound is produced, which improves GC characteristics.…”
Section: Introductionmentioning
confidence: 99%
“…An overview of the reported methodologies for the determination of acrylamide in food samples was shown in Table 3. Historically, one of the first protocols published for the analysis of acrylamide was GC separation using ECD or MS in determining drinking water acrylamide after derivatization (bromination with 2,3dibromopropionamide, 31 although this method has been practiced to complex matrices such as different food matrices. 32 This procedure seems to be very timeconsuming and with confined success in regarding its reproducibility.…”
Section: Methods Comparison Studymentioning
confidence: 99%