Briana A. Capistran, Edward Sisco, Dennis Leber, Vincent J. Desiderio. “Understanding reporting variability in fire debris data interpretation through an interlaboratory study.” ChemRxiv (). https://doi.org/10.26434/chemrxiv.15007617/v1

The supporting information is appended to the main paper

Carbon ladder, ASTM D2887 Calibration Mix, 1:1600 in n-hexane (≥95 %)
GC–MS conditions Agilent 8890-5977C with 7693 automatic liquid sampler; DB-1MS column, 30 m × 0.25 mm × 0.25 μm; 40 °C, hold 3 min, 10 °C/min to 280 °C, hold 4 min; inlet 250 °C, split ratio 10:1; 1 μL injection; helium (99.999 %), 1 mL/min; MS transfer line 280 °C; atune; 70 eV electron impact ionization source at 250 °C; quadrupole 150 °C; gain factor 1.0 a.u.; m/z 40–550; threshold 150 counts; A/D samples 2 a.u.; detector off from 4.34 to 4.75 min
GC–MS approximate retention time, n-heptane (C₇) 5.95 min
GC–MS approximate retention time, n-octane (C₈) 7.80 min
GC–MS approximate retention time, n-nonane (C₉) 9.65 min
GC–MS approximate retention time, n-decane (C₁₀) 11.35 min
GC–MS approximate retention time, n-undecane (C₁₁) 12.90 min
GC–MS approximate retention time, n-dodecane (C₁₂) 14.35 min
GC–MS approximate retention time, n-tetradecane (C₁₄) 16.95 min
GC–MS approximate retention time, n-hexadecane (C₁₆) 19.30 min
GC–MS approximate retention time, n-octadecane (C₁₈) 21.40 min
GC–MS approximate retention time, n-eicosane (C₂₀) 23.30 min
GC–MS approximate retention time, n-tetracosane (C₂₄) 26.70 min
Main, pp. 13, 16; SI, p. 44
Positive control, custom mixture in dichloromethane
GC–MS conditions Agilent 8890-5977C with 7693 automatic liquid sampler; DB-1MS column, 30 m × 0.25 mm × 0.25 μm; 40 °C, hold 3 min, 10 °C/min to 280 °C, hold 4 min; inlet 250 °C, split ratio 10:1; 1 μL injection; helium (99.999 %), 1 mL/min; MS transfer line 280 °C; atune; 70 eV electron impact ionization source at 250 °C; quadrupole 150 °C; gain factor 1.0 a.u.; m/z 40–550; threshold 150 counts; A/D samples 2 a.u.; detector off from 3.50 to 4.00 min
GC–MS approximate retention time, toluene, 10 μg/mL 6.90 min
GC–MS approximate retention time, 2,2,4-trimethylhexane, 15 μg/mL 7.60 min
GC–MS approximate retention time, o-xylene, 10 μg/mL 9.30 min
GC–MS approximate retention time, n-nonane (C₉), 15 μg/mL 9.65 min
GC–MS approximate retention time, m-ethyltoluene, 15 μg/mL 10.50 min
GC–MS approximate retention time, o-ethyltoluene, 15 μg/mL 10.80 min
GC–MS approximate retention time, 1,2,4-trimethylbenzene, 10 μg/mL 11.05 min
GC–MS approximate retention time, indane, 10 μg/mL 11.70 min
GC–MS approximate retention time, 1,2,4,5-tetramethylbenzene, 10 μg/mL 13.00 min
GC–MS approximate retention time, naphthalene, 10 μg/mL 13.90 min
GC–MS approximate retention time, 1-dodecene, 15 μg/mL 14.20 min
GC–MS approximate retention time, n-dodecane (C₁₂), 15 μg/mL 14.35 min
GC–MS approximate retention time, 2-methylnaphthalene, 10 μg/mL 15.45 min
GC–MS approximate retention time, 2-ethylnaphthalene, 15 μg/mL 16.75 min
GC–MS approximate retention time, n-hexadecane (C₁₆), 25 μg/mL 19.30 min
GC–MS approximate retention time, n-octadecane (C₁₈), 25 μg/mL 21.40 min
GC–MS approximate retention time, 2,6,10,14-tetramethylhexadecane, 25 μg/mL 21.55 min
GC–MS approximate retention time, n-eicosane (C₂₀), 25 μg/mL 23.30 min
Main, pp. 13, 16; SI, p. 45
Sample D2, 30 % evaporated paint thinner (medium naphthenic-paraffinic) on burned carpet, 1 μL
GC–MS total ion chromatogram The ignitable liquid compounds eluted at similar retention times as the substrate compounds
Main, pp. 27, 36; SI, p. 51
Sample D5, 10 % evaporated lamp oil (heavy n-alkane) on burned carpet, 1 μL
GC–MS total ion chromatogram Dominated by the strong and distinct n-alkane peaks of the lamp oil product, retention time range 17 min to 20 min