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Table 1

CH3OH line data for the observed transitions, adopted from the CDMS (Cologne Database of Molecular Spectroscopy, Müller et al. 2005).

Frequency Eu Transition
MHz D2 K k type

337 969.414 5.55 390.1  −1 A νt = 1
338 124.502 5.65 78.1 0 E
338 344.628 5.55 70.6  −1 E
338 404.580 1.49 243.8 +6 E
338 408.681 5.66 65.0 0 A
338 430.933 1.50 253.9  −6 E
338 442.344 1.49 258.7 +6 A
338 442.344 1.49 258.7  −6 A
338 456.499 2.76 189.0  −5 E
338 475.290 2.76 201.1 +5 E
338 486.337 2.77 202.9 +5 A
338 486.337 2.77 202.9  −5 A
338 504.099 3.80 152.9  −4 E
338 512.627 3.81 145.3  −4 A
338 512.639 3.81 145.3 +4 A
338 512.856 5.23 102.7  −2 A
338 530.249 3.82 161.0 +4 E
338 540.795 4.60 114.8 +3 A
338 543.204 4.60 114.8  −3 A
338 559.928 4.64 127.7  −3 E
338 583.195 4.62 112.7 +3 E
338 614.999 5.68 86.1 +1 E
338 639.939 5.23 102.7 +2 A
338 721.630 5.14 87.3 +2 E
338 722.940 5.20 90.9  −2 E

Notes. All lines are from the J = 7 → 6 band, and throughout the paper a notation like “ − 6 E” refers to the J = 7-6 → 6-6 E transition. Blended lines are indicated by a .

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