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Table C.2

Same as Table  C.1 but for APEX spectra.

Molecule Transition Rest frequency (MHz)

30SiO (4–3) 169 486.87
29SiO (4–3) 171 512.80
HC15N (2–1) 172 107.96
H13CN (2–1) 172 677.85
CH3NH2 (2, 1, 5–1, 0, 5) 173 267.80
H13CO+ (2–1) 173 506.70
SiO (4–3) 173 688.24
HN13C (2–1) 174 179.41
gap 174 770–181 380
N2H+ (2–1) 186 344.68
U U 186 850.00
PN (4–3) 187 953.26
13CH3OH (4, Ka, 4–3, Ka, 3) 188 788.03
13CH3OH (4, Ka, 3–3, Ka, 2) 188 836.43
gap 189 320–19.480
AlF (6–5) 197 833.15
gap 201 330–216 820
SiO (5–4) 217 104.92
13CN (2, 1.5 or 2.5, 1 or 2, F–1, 0.5 or 1.5, 1, F) 217 297.72
13CN (2, 2.5, 2 or 3, F–1, 1.5, 1 or 2, F) 217 456.59
13CN (2, 1.5, 1, F–1, 0.5, 1, F) 217 633.04
H2CO (3, 0, 3–2, 0, 2) 218 222.19
CH3OH? (4, 2, 2–3, 1, 2) 218 440.05
C18O (2–1) 219 560.35
C15N? (2, 2.5, F–1, 1.5, F) 219 933.63
13CO (2–1) 220 398.68
gap 220 790–224 750
H2CO (3, 1, 2–2, 1, 1) 225 697.78
CN (2, 1.5, F–1, 0.5, F) 226 658.92
CN (2, 2.5, F–1, 1.5, F) 226 876.39
instr. 227 260–229 180
CO (2–1) 230 538.00
AlF (7–6) 230 793.89
13CS (5–4) 231 220.69
gap 232 540–241 110
CH3OH?? (5, −1, 5–4, −1, 4) 241 767.22
CH3OH?? (5, 0, 5–4, 0, 4) 241 791.43
CS (5–4) 244 935.56
gap 245 100–257 000
29SiO (6–5) 257 255.21
HC15N (3–2) 258 157.00
U U 257 810.00
U U 258 630.00
H13CN (3–2) 259 011.80
H13CO+ (3–2) 260 255.34
SiO (6–5) 260 518.01
HN13C (3–2) 261 263.51
CCH (3, 3.5, 3–2, 2.5, 3) 261 978.12
HCN (3–2) 265 886.43
U U 268 450.00
gap 268 730–270 000
HNC (3–2) 271 981.142
gap 273 970–278 489
N2H+ (3–2) 279 511.75
H2CO (4, 1, 4–3, 1, 3) 281 526.93
SO2 (6, 2, 4–5, 1, 5) 282 036.57
CH2NH? (2, 1, 2,F–1, 0, 1,F) 284 254.50
CS (6–5) 293 912.09
29SiO (7–6) 300 120.48
CH3OH? (1, 1, 0–1, 0, 1) 303 366.89
SiO (7–6) 303 926.81
34SO? (2, 2–1, 2) 308 993.58
gap 310 610–311 160
13CO (3–2) 330 587.97
telluric 332 500–332 900
CN (3, 2.5, F–2, 2.5, F) 339 487.80
CN (3, 2.5, F–2, 1.5, F) 340 031.29
CH3OH? (2, 2, 0, +0–3, 1, 3, +0) 340 141.22
CN (3, 3.5, F–2, 2.5, F) 340 248.80
HC15N (4–3) 344 200.11
H13CN (4–3) 345 339.77
CO (3–2) 345 795.99
H13CO+ (4–3) 346 998.34
SiO (8–7) 347 330.58
HN13C (4–3) 348 340.90
13CH3OH (1, 1, 1–0, 0, 0) 350 103.12
NO? (4, 1, 3.5, 4.5–3, 1, 2.5, 3.5) 352 204.30
HCN (4–3) 354 505.48
HCO+ (4–3) 356 734.22
gap 356 600–390 520
HS? (2, 1, 1–2, 0, 2) 393 725.70
gap 395 720–396 300
gap 400 300–401 100
CH3NH2? (5, –3, 1–5, 2, 0) 402 354.89
U U 402 500.00
telluric 408 240.00
gap 412 300–413 100
gap 417 080–417 970
gap 421 960–426 760
telluric 427 400.00
telluric 429 350.00
telluric 430 300.00
gap 430 750–438 780
telluric 439 400.00
telluric 441 270.00
13CO (4–3) 440 765.17
telluric 442 050.00
gap 442 750–459 050
CO (4–3) 461 040.77
gap 463 050–471 070
telluric 472 850.00
telluric 474 500.00
telluric 474 100–475 000
gap 475 040–477 200
gap 481 200–489 200
C and 13C (1–0) 492 160.651
gap 494 180–690 060
H13CN (8–7) 690 552.08
CO (6–5) 691 473.08
gap 692 880–805 230
gap 808 060–907 730
end 906 600

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