Open Access

Table C.1

Detected spectral transitions of CH3COCH3, CH3CHO, CH3OH, 13CH3OH, and C2H5CN.

Frequency Transition Sμ2 Eup Note
(MHz) (D2) (K)
CH3COCH3;v=0

342324.944 30(6,25)–29(5,24) AA 2018.37 282.73 1
342324.944 30(5,25)–29(6,24) AA 1211.16 282.73 1
342410.641 17(17,1)–16(16,1) EA 552.43 146.85
342485.234 17(17,0)–16(16,0) EE 2209.99 147.06 *
342553.854 42(3,39)–42(2,40) EE 456.49 484.93
342553.854 42(4,39)–42(3,40) EE 456.49 484.93
342594.888 17(17,1)–16(16,1) EE 2210.27 146.95
342780.035 17(17,1)–16(16,0) AA 828.92 147.05
342780.036 17(17,0)–16(16,1) AA 1381.37 147.05
342836.912 18(12,6)–17(11,7) AE 68.59 141.3 2
342864.593 18(12,6)–17(11,7) AA 208.58 141.24 3
342896.394 18(12,6)–17(11,7) EE 548.97 141.27 3
343023.152 18(12,6)–17(11,7) EA 133.9 141.31 2
343338.876 31(4,27)–30(5,26) EA 881.62 288.66 4
343338.876 31(5,27)–30(4,26) EA 881.62 288.66 4
343338.918 31(5,27)–30(5,26) AE 1322.45 288.66 4
343338.918 31(4,27)–30(4,26) AE 440.84 288.66 4
343386.006 31(4,27)–30(4,26) EE 3176.31 288.63 5
343386.006 31(5,27)–30(5,26) EE 3176.31 288.63 5
343386.006 31(4,27)–30(5,26) EE 349.64 288.63 5
343386.006 31(5,27)–30(4,26) EE 349.64 288.63 5
343433.081 31(4,27)–30(5,26) AA 2203.26 288.61 6
343433.081 31(5,27)–30(4,26) AA 1322.11 288.61 6
344468.948 32(4,29)–31(3,28) EA 955.83 293.77
344468.948 32(3,29)–31(4,28) EA 955.83 293.77
344468.985 32(3,29)–31(3,28) AE 1433.77 293.77
344468.985 32(4,29)–31(4,28) AE 477.95 293.77
344505.598 16(9,7)–15(8,8) EE 183.87 109.49 7
344509.424 32(4,29)–31(3,28) EE 3469.95 293.73 7
344509.424 32(4,29)–31(4,28) EE 353.28 293.73 7
344509.424 32(3,29)–31(3,28) EE 353.28 293.73 7
344509.424 32(3,29)–31(4,28) EE 3469.95 293.73 7
344549.874 32(4,29)–31(3,28) AA 2389.27 293.69
344549.874 32(3,29)–31(4,28) AA 1433.73 293.69
344793.57 18(15,3)–17(14,3) EA 397.32 150.91 8
344803.465 18(15,4)–17(14,3) AE 595.35 150.81 8
344855.635 18(15,3)–17(14,4) AE 198.44 150.81
344866.506 18(15,4)–17(14,4) EA 396.52 150.71 9
345037.5 18(15,3)–17(14,3) EE 1589.87 150.87 10
345073.724 18(15,4)–17(14,4) EE 1588.26 150.77 6
345256.037 18(15,4)–17(14,3) AA 994.36 150.83
345305.365 18(15,3)–17(14,4) AA 596.65 150.83 1
345607.709 33(2,31)–32(2,30) EA 1030.69 298.09 11
345607.709 33(3,31)–32(3,30) EA 1030.69 298.09 11
345607.736 33(3,31)–32(3,30) AE 1545.71 298.09 11
345607.736 33(2,31)–32(2,30) AE 515.26 298.09 11
345639.619 33(3,31)–32(3,30) EE 3529.95 298.03
345639.619 33(3,31)–32(2,30) EE 592.06 298.03
345639.619 33(2,31)–32(2,30) EE 3529.95 298.03
345639.619 33(2,31)–32(3,30) EE 592.06 298.03
345671.524 33(2,31)–32(2,30) AA 1545.65 297.98 1
345671.524 33(3,31)–32(3,30) AA 2575.79 297.98 1
345673.954 15(7,8)–14(6,9) EE 115.74 92.94 1
345875.586 24(12,12)–23(13,11) AE 152.92 235.24 12
345877.896 24(12,12)–23(13,11) EA 305.88 235.24 12
345912.434 15(7,8)–14(6,9) AA 72.39 92.88 13
345973.657 24(12,12)–23(13,11) EE 1221.85 235.24 6

CH3CHO;v=0

343779.382 18(2,17)–17(2,16) E 224.63 166.47 *
343802.725 18(2,17)–17(2,16) A 224.54 166.46 1

CH3OH;v=0

342729.796 13(1,12)–13(0,13) A 97.52 227.47 *
344109.039 18(2,17)–17(3,15) E 21.24 419.40 1
344443.433 19(1,19)–18(2,16) A 23.97 451.23
345903.916 16(1,15)–15(2,14) A 28.52 332.65
345919.260 18(3,15)–17(4,14) E 22.41 459.43 2

13CH3OH;v=0

344040.629 8(3,6)–9(2,8) 2.17 144.49
344671.733 3(3,0)–4(2,2) 0.25 61.55 1
345083.793 2(2,0)–3(1,3) 0.30 44.60
345132.599 4(0,4)–3(1,3) 1.55 35.76

C2H5CN;v=0

342433.950 40(2,38)–39(3,37) 30.09 360.89 1
342651.886 15(5,11)–14(4,10) 9.20 79.39
342677.561 15(5,10)–14(4,11) 9.20 79.39
343194.574 38(5,33)–37(5,32) 553.54 347.41 *
343503.727 41(8,33)–41(7,34) 32.96 441.47 2
343576.364 41(8,34)–41(7,35) 32.96 441.47 3
343888.020 40(8,32)–40(7,33) 32.01 423.82 4
343940.188 40(8,33)–40(7,34) 32.01 423.82 2
344238.762 39(8,31)–39(7,32) 31.06 406.61 4
344275.871 39(8,32)–39(7,33) 31.06 406.61
344278.941 10(6,4)–9(5,5) 8.98 63.67
344278.941 10(6,5)–9(5,4) 8.98 63.67
344558.366 38(8,30)–38(7,31) 30.11 389.82
344584.505 38(8,31)–38(7,32) 30.12 389.82 2
344849.257 37(8,29)–37(7,30) 29.18 373.47
344867.347 37(8,30)–37(7,31) 29.18 373.47 5
345113.287 36(8,28)–36(7,29) 28.25 357.55
345125.723 36(8,29)–36(7,30) 28.25 357.55
345314.812 36(3,34)–35(2,33) 23.96 295.89 2
345352.535 35(8,27)–35(7,28) 27.33 342.06
345361.010 35(8,28)–35(7,29) 27.32 342.06
345568.673 34(8,26)–34(7,27) 26.40 327.00 3
345574.337 34(8,27)–34(7,28) 26.41 327.00 3
345763.372 33(8,25)–33(7,26) 25.49 312.37
345767.098 33(8,26)–33(7,27) 25.49 312.37
345921.198 39(3,37)–38(3,36) 573.72 344.46 6
345938.020 32(8,24)–32(7,25) 24.58 298.17
345940.515 32(8,25)–32(7,26) 24.58 298.17

Notes. Sμ2 is the product of the line strength (S) and the square of the dipole moment (μ). Eup represents the upper level energy. Asterisks mark the transitions of the molecules that are used for Fig. 2.

CH3COCH3 transitions: (1) blended with 34SO2 transition lines; (2) blended with unidentified molecular lines; (3) blended with CS transition lines; (4) blended with H2CS transition lines; (5) blended with H2CCO transition lines; (6) blended with CH3OCHO transition lines; (7) blended with CH3OCH3 transition lines; (8) blended with (CH2OH)2 transition lines; (9) blended with CH2DOH and C2H5CN transition lines; (10) blended with HCOOH transition lines; (11) blended with HCCCN transition lines; (12) blended with H2C18O transition lines; (13) blended with C2H5CN transition lines.

CH3CHO transitions: (1) blended with H2CS transition lines.

CH3OH transitions: (1) blended with CH3OCHO (v=1) transition lines; (2) blended with C2H5CN transition lines. The 13(1,12)–13(0,13)A and 16(1,15)–15(2,14)A transitions of CH3OH are optically thick.

13CH3OH transitions: (1) blended with CH3OCHO transition lines.

C2H5CN transitions: (1) blended with CH2DOH transition lines; (2) blended with unidentified molecular lines; (3) blended with CH3OCHO (v=1) transition lines; (4) blended with CH3OCHO transition lines; (5) blended with CH2DOH and CH3COCH3 transition lines; (6) blended with CH3OH transition lines.

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