2011.0.00510.S/2011.0.00510.S_2012-02-24/2011.0.00510.S/sg_ouss_id/group_ouss_id/member_ouss_id1/calibrated

full summary of this dataset can be found here

Spectral setup

SpwIDFrame#chanskyfreq(MHz)Chwid(kHz)BW(MHz)beam("x" deg)
0TOPO3840113625.2 ~ 115499.8488.2811875.0000003.4 x 2.5, -36.2
1TOPO3840111750.2 ~ 113624.8488.2811875.0000003.5 x 2.5, -36.3
2TOPO3840101625.2 ~ 103499.8488.2811875.0000003.8 x 2.8, -35.7
3TOPO384099750.2 ~ 101624.8488.2811875.0000003.9 x 2.9, -36.8

Observed fields

FieldIDFieldNameR.A.DecEpochnRows
0J1329-560813:29:01.144927-56.08.02.66571J2000115080
2Mars10:43:42.059512+10.22.48.92654J200021000
4Boomerang_Nebula12:44:43.188420-54.31.22.27470J200065760
5Boomerang_Nebula12:44:43.235700-54.30.59.78833J200057540
6Boomerang_Nebula12:44:45.401520-54.31.33.87437J200057540
7Boomerang_Nebula12:44:45.448800-54.31.11.38800J200057540
8Boomerang_Nebula12:44:45.496080-54.30.48.90163J200057540
9Boomerang_Nebula12:44:47.661900-54.31.22.98767J200057540
10Boomerang_Nebula12:44:47.709180-54.31.00.50130J200057540
11Mars11:27:03.174714+06.43.46.93651J200030600
12Mars11:27:06.848536+06.43.33.41277J200030600

Spectral window: 0

Lovas recommendation (http://physics.nist.gov/cgi-bin/micro/table5/start.pl)

click table head to collapse/expand

Rest frequency (MHz)Molecular transition
113641.05313CH3CH2CN 13(5,9)-12(5,8)
113641.14213CH3CH2CN 13(5,8)-12(5,7)
113657.635CH2CHCN 12(2,11)-11(2,10)
113691.46013CH3CH2CN 13(4,10)-12(4,9)
113693.000unidentified
113695.000unidentified
113697.36713CH3CH2CN 13(4,9)-12(4,8)
113729.000unidentified
113743.007CH3OCHO 9(3,6)-8(3,5) E
113756.646CH3OCHO 9(3,6)-8(3,5) A
113766.420HCCCHO 12(1,11)-11(1,10)
113818.000unidentified
113820.12029SiC2 5(0,5)-4(0,4)
113831.151CH2CHCN 18(2,16)-18(1,17)
113844.000unidentified
113978.248CH3CH2CN 13(0,13)-12(0,12)
114003.831CH3OCH3 18(2,16)-18(1,17) AE+EA
114005.399CH3OCH3 18(2,16)-18(1,17) EE
114006.968CH3OCH3 18(2,16)-18(1,17) AA
114064.848t-CH3CH2OH 2(2,0)-1(1,1)
114092.61218OCS 10-9
114113.000unidentified
114182.510C4H 12-11 J=25/2-23/2
114221.040C4H 12-11 J=23/2-21/2
114291.000unidentified
114313.000unidentified
114336.000unidentified
114362.21030SiC2 5(2,4)-4(2,3)
114443.946t-CH3CH2OH 17(2,16)-16(3,13)
114485.037HC5N 43-42
114565.381SO2 29(3,27)-28(4,24)
114574.43834SO2 6(3,3)-7(2,6)
114615.021H13CCCN 13-12
114621.567CH2CHCN 12(2,10)-11(2,9)
114650.932CH3OH 18(-2,17)-18(1,17) E
114737.170C4H 2S J=12-11 2v7 L
114793.820C4H 2S J=12-11 2v7 U
114831.084HCCC15N 13-12
114840.000unidentified
114861.000unidentified
114888.234CH3OCHO 23(6,18)-22(7,15) A
114897.372c-H13CCCH 3(0,3)-2(1,2)
114940.177CH3CHO 6(0,6) - 5(0,5) E
114959.909CH3CHO 6(0,6) - 5(0,5) A++
115021.000unidentified
115038.874C6H 23/2 J=83/2-81/2 e
115072.307CH3OCH3 9(2,8)-9(1,9) AE+EA
115075.086CH3OCH3 9(2,8)-9(1,9) EE
115077.864CH3OCH3 9(2,8)-9(1,9) AA
115083.236C6H 23/2 J=83/2-81/2 f
115141.000unidentified
115153.935NS J=5/2-3/2 F=7/2-5/2 e
115156.812NS J=5/2-3/2 F=5/2-3/2 e
115185.411NS J=5/2-3/2 F=3/2-3/2 e
115212.000unidentified
115216.800C4H 23/2 J=25/2-23/2 1v7f
115271.202CO 1-0
115382.375SiC2 5(0,5)-4(0,4)
115455.898CCCO 12-11

Spectral window: 1

Lovas recommendation (http://physics.nist.gov/cgi-bin/micro/table5/start.pl)

click table head to collapse/expand

Rest frequency (MHz)Molecular transition
111755.028SO2 31(3,29)-30(4,26)
111782.596CH3OCH3 7(0,7)-6(1,6) AA
111783.112CH3OCH3 7(0,7)-6(1,6) EE
111783.628CH3OCH3 7(0,7)-6(1,6) EA+AE
111812.238CH3OCH3 18(3,15)-18(2,16) AE+EA
111813.810CH3OCH3 18(3,15)-18(2,16) EE
111815.382CH3OCH3 18(3,15)-18(2,16) AA
111823.024HC5N 42-41
111827.600unidentified
111943.569CH3CH2CN 18(2,17)-18(1,18)
111957.756CH313CH2CN 13(1,13)-12(1,12)
111967.000unidentified
111967.000unidentified
112006.000unidentified
112016.000K37Cl 15-14
112035.000unidentified
112063.440MgCN 11-10 J=21/2-19/2
112078.440MgCN 11-10 J=23/2-21/2
112101.557CH3CH213CN 13(1,13)-12(1,12)
112114.000unidentified
112150.000unidentified
112166.938l-C3H 2S 5-4 J=11/2-9/2 1v4
112248.722CH3CHO 6(1,6) - 5(1,5) A++
112254.512CH3CHO 6(-1,6)-5(-1,5) E
112254.512CH3CHO 6(-1,6) - 5(-1,5) E
112348.000unidentified
112355.48030SiC2 5(0,5)-4(0,4)
112358.780C17O 1-0 F=3/2-5/2
112358.988C17O 1-0 F=7/2-5/2
112360.005C17O 1-0 F=5/2-5/2
112373.548(CH3)2CO 11(0,11)-10(1,10) EE
112373.548(CH3)2CO 11(1,11)-10(0,10) EE
112381.029(CH3)2CO 11(0,11)-10(1,10) AA
112381.029(CH3)2CO 11(1,11)-10(0,10) AA
112432.300HCOOH 5(4,*)-4(4,*)
112459.610HCOOH 5(3,3)-4(3,2)
112467.000HCOOH 5(3,2)-4(3,1)
112532.000unidentified
112585.000unidentified
112593.440Si13CC 5(0,5)-4(0,4)
112646.233CH3CH2CN 13(1,13)-12(1,12)
112654.117NH2CHO 8(3,6)-9(2,7)
112807.096t-CH3CH2OH 2(2,1)-1(1,0)
112840.644CH2CHCN 12(0,12)-11(0,11)
112869.993CH3OCHO 14(3,11)-13(4,10) A
112874.000unidentified
112891.430HCOOH 5(2,3)-4(2,2) n,t
112893.846C6H- 41-40
112922.500C4H 21/2 J=23/2-21/2 1v7e
112997.000unidentified
112999.982CH3OCH3 20(3,17)-20(2,18) AE+EA
113001.218CH3OCH3 20(3,17)-20(2,18) EE
113002.455CH3OCH3 20(3,17)-20(2,18) AA
113032.110CH2CHCN 8(1,8)-7(0,7)
113059.350CH3OCH3 17(3,14)-17(2,15) EE
113061.121CH3OCH3 17(3,14)-17(2,15) AA
113090.13613CH3CH2CN 13(2,12)-12(2,11)
113123.337CN 1-0 J=1/2-1/2 F=1/2-1/2
113136.200N34S J=5/2-3/2 F=3/2-3/2 e
113144.192CN 1-0 J=1/2-1/2 F=1/2-3/2
113159.000unidentified
113170.528CN 1-0 J=1/2-1/2 F=3/2-1/2
113191.317CN 1-0 J=1/2-1/2 F=3/2-3/2
113246.000unidentified
113255.669CH313CH2CN 13(0,13)-12(0,12)
113260.000unidentified
113265.900C4H 21/2 J=23/2-21/2 1v7f
113266.690CH2CHCN 20(2,18)-20(1,19)
113276.031CH3OCH3 10(6,4)-11(5,7) EE
113279.138CH3OCH3 10(6,5)-11(5,6) EE
113279.455CH3OCH3 10(6,4)-11(5,7) AA
113280.593CH3OCH3 10(6,5)-11(5,6) AA
113314.000unidentified
113322.000unidentified
113326.000unidentified
113350.800CH3OD 6(1,5)-6(0,6) E
113410.204CCS N,J=9,8-8,7
113432.872CH3CH213CN 13(0,13)-12(0,12)
113484.722D2CS 4(0,4)-3(0,3)
113488.140CN 1-0 J=3/2-1/2 F=3/2-1/2
113490.982CN 1-0 J=3/2-1/2 F=5/2-3/2
113499.639CN 1-0 J=3/2-1/2 F=1/2-1/2
113508.944CN 1-0 J=3/2-1/2 F=3/2-3/2
113520.414CN 1-0 J=3/2-1/2 F=1/2-3/2
113546.000unidentified
113557.000unidentified
113566.000unidentified
113617.45313CH3CH2CN 13(7,*)-12(7,*)
113621.13313CH3CH2CN 13(6,*)-12(6,*)
113623.000unidentified
113623.39213CH3CH2CN 13(8,*)-12(8,*)

Spectral window: 2

Lovas recommendation (http://physics.nist.gov/cgi-bin/micro/table5/start.pl)

click table head to collapse/expand

Rest frequency (MHz)Molecular transition
101626.822CH3OCHO 9(1,9)-8(0,8) E
101628.167CH3OCHO 9(1,9)-8(0,8) A
101637.231CH2CHCN 11(1,11)-10(1,10)
101659.000unidentified
101668.700unidentified
101677.000unidentified
101688.88033SO2 12(4,8)-12(3,11)
101690.002CH3CH2CN 27(2,25)-27(1,26)
101708.800unidentified
101713.600unidentified
101737.211CH3OH 9(-2,8)-9(1,8) E
101771.892CH3OCHO 24(5,19)-24(4,20) A
101873.641C6H 21/2 J=73/2-71/2 f
101881.306C6H- 37-36
101892.560MgCN 10-9 J=21/2-19/2
101925.513C6H 21/2 J=73/2-71/2 e
101961.512Na37Cl 8-7
101970.000unidentified
101981.426CH2CO 5(1,4)-4(1,3)
102031.87434SO2 3(1,3)-2(0,2)
102031.940Al35Cl 7-6
102043.000unidentified
102064.263NH2CHO 5(1,5)-4(1,4)
102065.856H2COH+ 4(0,4)-3(1,3)
102122.701CH3OH 10(-2,9)-10(1,9) E
102178.82913CH2CHCN 11(2,9)-10(2,8)
102202.490CH3SH 4( 1)-3( 1) A--
102217.571NH2CHO 2(1,2)-1(0,1)
102274.000unidentified
102298.085HCCCHO 11(0,11)-10(0,10)
102319.000unidentified
102375.000unidentified
102399.000unidentified
102405.662C4H- 11-10
102407.000unidentified
102423.000unidentified
102432.000unidentified
102489.386g-CH3CH2OH 11(1,11)-11(0,11) t=1-0
102516.635CH3CCH 6(4)-5(4)
102530.346CH3CCH 6(3)-5(3)
102533.756(CH3)2CO 10(*,10)-9(*,9) EE t=1
102540.143CH3CCH 6(2)-5(2)
102546.023CH3CCH 6(1)-5(1)
102547.983CH3CCH 6(0)-5(0)
102554.696(CH3)2CO 10(0,10)-9(1,9) EE
102562.281(CH3)2CO 10(0,10)-9(1,9) AA
102587.476CF+ 1-0
102636.230C5H 21/2 J=43/2-41/2 e
102640.000unidentified
102642.660C5H 21/2 J=43/2-41/2 f
102644.000unidentified
102650.000unidentified
102658.096CH3OH 11(-2,10)-11(1,10) E
102690.055SO2 33(8,26)-34(7,27)
102734.338CH3OCHO 16(5,11)-16(4,12) E
102736.773CH3OCHO 16(5,11)-16(4,12) A
102807.370H2C34S 3(1,2)-2(1,1)
102916.085SiC3 9(0,9)-8(0,8)
102952.04213CH3CH2CN 12(0,12)-11(0,11)
102957.990CH3OH 15(-2,13)-16(-3,13) E t=1
102992.345H2CCC 5(1,5)-4(1,4)
103028.000unidentified
103040.548H2CS 3(0,3)-2(0,2)
103051.867H2CS 3(2,1)-2(2,0)
103071.000unidentified
103075.000unidentified
103114.824CH3OCHO 21(4,17)-21(3,18) A
103187.375NH2D 8(3,6)-8(2,6) F=8-9 U
103196.000unidentified
103216.600unidentified
103227.000unidentified
103266.000C4H 21/2 J=21/2-19/2 1v7e
103297.000unidentified
103319.287l-C3H 23/2 J=9/2-7/2 F=5-4f
103319.818l-C3H 23/2 J=9/2-7/2 F=4-3f
103328.000unidentified
103329.920C5H 23/2 J=45/2-43/2 f
103372.506l-C3H 23/2 J=9/2-7/2 F=5-4e
103373.129l-C3H 23/2 J=9/2-7/2 F=4-3e
103376.784CH3OCHO 24(6,18)-24(5,17) A
103381.209CH3OH 12(-2,11)-12(1,11) E
103387.227CH3OCHO 24(6,18)-24(5,17) E
103391.283CH2OHCHO 10(0,10)-9(1,9)
103402.000unidentified
103419.673CH313CH2CN 12(1,12)-11(1,11)
103466.479CH3OCHO 8(2,6)-7(2,5) E
103478.699CH3OCHO 8(2,6)-7(2,5) A

Spectral window: 3

Lovas recommendation (http://physics.nist.gov/cgi-bin/micro/table5/start.pl)

click table head to collapse/expand

Rest frequency (MHz)Molecular transition
99774.130H2C34S 3(1,3)-2(1,2)
99866.509CCS N,J=8,7-7,6
99903.000unidentified
99929.540K35Cl 13-12
99953.270NH2CN 5(2,4)-4(2,3)
99956.600NH2CN 5(2,3)-4(2,2)
99972.660NH2CN 5(0,5)-4(0,4)
100029.565SO N,J=5,4-4,4
100076.386HCCCN 11-10
100094.500CH2CO 5(1,5)-4(1,4)
100109.744CH3CH213CN 11(1,10)-10(1,9)
100110.270CH3SH 4(1)-3(1) A++
100122.000unidentified
100155.839CH313CH2CN 11(1,10)-10(1,9)
100157.000unidentified
100173.100CH3SH 7(2)-8(1) A++
100185.000unidentified
100197.200unidentified
100200.400unidentified
100240.584HCCCN 11-10 1v6 =1e
100294.508CH3OCHO 8(3,5)-7(3,4) E
100308.210CH3OCHO 8(3,5)-7(3,4) A
100322.411HCCCN 11-10 1v7 =1e
100332.000unidentified
100365.000unidentified
100373.000unidentified
100421.000unidentified
100436.000unidentified
100452.072g-CH3CH2OH 24(2,23)-24(1,23) t=1-0
100460.412CH3OCH3 6(2,5)-6(1,6) EA+AE
100463.066CH3OCH3 6(2,5)-6(1,6) EE
100465.708CH3OCH3 6(2,5)-6(1,6) AA
100466.175HCCCN 11-10 1v7 =1f
100482.174CH3OCHO 8(1,7)-7(1,6) E
100490.715CH3OCHO 8(1,7)-7(1,6) A
100491.721N2O 4-3
100498.500unidentified
100509.000unidentified
100526.506CH3NC 5-4
100543.246CH2CN 5(2,3)-4(2,2) J=9/2-7/2
100598.067CH2CN 5(0,5)-4(0,4) J=11/2-9/2
100611.012CH2CN 5(0,5)-4(0,4) J=9/2-7/2
100614.291CH3CH2CN 11(1,10)-10(1,9)
100629.500NH2CN 5(1,4)-4(1,3)
100631.499CH2CN 5(2,4)-4(2,3) J=11/2-9/2
100638.870CH3OH 13(2,11)-12(3,9) E
100681.476CH3OCHO 9(0,9)-8(0,8) E
100683.392CH3OCHO 9(0,9)-8(0,8) A
100708.784HCCCN 11-10 2v7 =0
100711.064HCCCN 11-10 2v7 =2 e
100714.395HCCCN 11-10 2v7 =2 f
100841.300unidentified
100855.437CH3COOH 9(-1,9)-8(-1,8) E
100855.437CH3COOH 9(-1,9)-8(0,8) E
100855.437CH3COOH 9(0,9)-8(-1,8) E
100855.437CH3COOH 9(0,9)-8(0,8) E
100856.600unidentified
100864.800unidentified
100866.300unidentified
100878.105SO2 2(2,0)-3(1,3)
100897.459CH3COOH 9(*,9)-8(*,8) A
100898.580CH3SH 7(1)-7(0) E
100911.136CH2CHCH3 6(1,6)-5(1,5) E
100911.401CH2CHCH3 6(1,6)-5(1,5) A
100990.034t-CH3CH2OH 8(2,7)-8(1,8)
101002.355CH2CO 5(3,3)-4(3,2)
101002.360CH2CO 5(3,2)-4(3,1)
101024.438CH2CO 5(2,4)-4(2,3)
101029.750CH3SH 4(-1)-3(-1) E
101036.589CH2CO 5(0,5)-4(0,4)
101139.160CH3SH 4(0)-3(0) A
101139.650CH3SH 4(0)-3(0) E
101159.460CH3SH 4(2)-3(2) A--
101167.150CH3SH 4(-2)-3(-2) E
101168.340CH3SH 4(2)-3(2) E
101174.677HC5N 38-37
101179.760CH3SH 4(2)-3(2) A
101180.347C6H 23/2 J=73/2-71/2 e
101185.367CH3OH 6(-2,5)-6(1,5) E
101200.400unidentified
101211.500unidentified
101215.324C6H 23/2 J=73/2-71/2 f
101243.600unidentified
101253.800unidentified
101272.900unidentified
101278.999CH3OCHO 9(1,9)-8(0,8) E t=1
101279.200unidentified
101284.360CH3SH 4( 1)-3( 1) E
101284.400H2C34S 3(0,3)-2(0,2)
101287.300unidentified
101293.328CH3OH 7(-2,6)-7(1,6) E
101299.309NH2CHO 18(2,16)-18(2,17)
101302.116CH3OCHO 25(6,19)-25(5,20) A
101305.534CH3OCHO 25(6,19)-25(5,20) E
101314.830DCCCN 12-11
101318.600unidentified
101332.993H2CO 6(1,5)-6(1,6)
101343.448CH3CHO 3(-1,3) - 2(0,2) E
101348.800unidentified
101357.000unidentified
101371.000unidentified
101382.335DNCO 5(1,5)-4(1,4)
101408.900unidentified
101414.723CH3OCHO 13(3,11)-13(2,12) A
101426.664(CH3)2CO 9(1,8)-8(2,7) AE
101426.716(CH3)2CO 9(1,8)-8(2,7) AE,EA
101426.759(CH3)2CO 9(1,8)-8(2,7) EA
101427.041(CH3)2CO 9(2,8)-8(1,7) AE
101427.090(CH3)2CO 9(2,8)-8(1,7) AE,EA
101427.130(CH3)2CO 9(2,8)-8(1,7) EA
101435.900unidentified
101451.059(CH3)2CO 9(1,8)-8(2,7) EE
101451.446(CH3)2CO 9(2,8)-8(1,7) EE
101469.719CH3OH 8(-2,7)-8(1,7) E
101477.885H2CS 3(1,3)-2(1,2)
101499.200unidentified
101503.800unidentified
101523.600unidentified
101531.974CH2CN 5(1,4)-4(1,3) J=11/2-9/2
101534.000H13COOH 9(3,6)-10(2,9)
101545.423CH3OCHO 18(3,15)-18(3,16) A
101553.27513CH3CH2CN 12(1,12)-11(1,11)
101559.383CH3OCH3 12(2,10)-11(3,9) AA
101560.26433SO2 17(5,13)-18(4,14)
101562.117CH3OCH3 12(2,10)-11(3,9) EE
101564.832CH3OCH3 12(2,10)-11(3,9) AE
101564.872CH3OCH3 12(2,10)-11(3,9) EA
101575.500unidentified

uv sampling

FieldIDSpwIDuv_min(klambda)uv_max(klambda)
0013.122265.315
0113.115265.358
0213.109265.416
0313.108265.424
2015.655200.949
2115.655200.949
2215.655200.949
2315.655200.949
4014.459264.230
4114.458264.211
4214.458264.191
4314.458264.188
5014.423264.228
5114.423264.208
5214.423264.187
5314.423264.184
6014.431264.258
6114.430264.238
6214.430264.217
6314.430264.214
7014.442264.287
7114.441264.268
7214.441264.247
7314.441264.244
8014.452264.316
8114.452264.297
8214.451264.276
8314.451264.273
9014.471264.332
9114.470264.313
9214.470264.294
9314.470264.291
10014.494264.411
10114.493264.394
10214.493264.375
10314.493264.372
11015.913261.940
11115.913261.940
11215.913261.940
11315.913261.940
12016.485270.153
12116.485270.153
12216.485270.153
12316.485270.153

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