MassBank Record: MSBNK-Osaka_Univ-OUF00016
ACCESSION: MSBNK-Osaka_Univ-OUF00016
RECORD_TITLE: 2,6-Pyridinedicarboxylic acid; GC-EI-TOF; MS; n TMS; RT:672.786 sec
DATE: 2016.01.19 (Created 2010.05.20, modified 2013.04.24)
AUTHORS: Tsujimoto Y, Tsugawa H, Bamba T, Fukusaki E, engineering department, Osaka Univ.
LICENSE: CC BY-SA
COMMENT: The chemical compound was chemically modified with N-methyl-N-trimethylsilyl-trifluoroacetamide (MSTFA) before GC-MS analysis. When it has two or more functional groups, this modification gave a mixture of the TMS derivatives having different number of TMS groups at different functional groups.
CH$NAME: 2,6-Pyridinedicarboxylic acid
CH$COMPOUND_CLASS: Natural Product
CH$FORMULA: C7H5NO4
CH$EXACT_MASS: 167.02186
CH$SMILES: OC(=O)c(c1)nc(cc1)C(O)=O
CH$IUPAC: InChI=1S/C7H5NO4/c9-6(10)4-2-1-3-5(8-4)7(11)12/h1-3H,(H,9,10)(H,11,12)
CH$LINK: CAS
499-83-2
CH$LINK: CHEBI
215974 46837
CH$LINK: CHEMSPIDER
9940
CH$LINK: PUBCHEM
CID:10367
CH$LINK: INCHIKEY
WJJMNDUMQPNECX-UHFFFAOYSA-N
CH$LINK: COMPTOX
DTXSID7022043
AC$INSTRUMENT: Pegasus III TOF-MS system, Leco; GC 6890, Agilent Technologies
AC$INSTRUMENT_TYPE: GC-EI-TOF
AC$MASS_SPECTROMETRY: MS_TYPE MS
AC$MASS_SPECTROMETRY: ION_MODE POSITIVE
AC$MASS_SPECTROMETRY: HELIUM_FLOW 1 ml/min
AC$MASS_SPECTROMETRY: ION_SOURCE_TEMPERATURE 200 C
AC$MASS_SPECTROMETRY: SCAN_RANGE_M/Z 85-500
AC$CHROMATOGRAPHY: COLUMN_NAME CP-SIL 8 CB LOW BLEED/MS
AC$CHROMATOGRAPHY: INJECTION_TEMPERATURE 230 C
AC$CHROMATOGRAPHY: OVEN_TEMPERATURE 80 C (Duration 2 min)-330 C (rate: 15 C/min; Duration 6 min)
AC$CHROMATOGRAPHY: RETENTION_INDEX 1758.126
AC$CHROMATOGRAPHY: RETENTION_TIME 672.786 sec
AC$CHROMATOGRAPHY: TRANSFARLINE_TEMPERATURE 250 C
MS$DATA_PROCESSING: WHOLE ChromaTOF ver. 2.32 (LECO)
PK$SPLASH: splash10-0002-1950000000-1221ab338705f508fac4
PK$NUM_PEAK: 174
PK$PEAK: m/z int. rel.int.
85 43 43
86 41 41
87 32 32
88 8 8
89 31 31
90 27 27
91 309 309
92 235 235
93 97 97
94 41 41
95 37 37
96 15 15
97 24 24
98 12 12
99 11 11
100 10 10
101 14 14
102 22 22
103 73 73
104 113 113
105 83 83
106 126 126
107 60 60
108 61 61
109 36 36
110 16 16
111 4 4
112 5 5
113 16 16
114 3 3
115 48 48
116 12 12
117 53 53
118 24 24
119 168 168
120 273 273
121 39 39
122 37 37
123 16 16
124 8 8
125 4 4
126 2 2
127 49 49
128 17 17
129 7 7
130 5 5
131 88 88
132 39 39
133 253 253
134 79 79
135 60 60
136 355 355
137 50 50
138 22 22
139 2 2
140 2 2
141 47 47
142 6 6
143 5 5
144 15 15
145 5 5
146 8 8
147 863 863
148 180 180
149 226 226
150 304 304
151 60 60
152 37 37
153 7 7
154 2 2
155 2 2
156 2 2
157 7 7
158 10 10
159 3 3
160 9 9
161 5 5
162 11 11
163 32 32
164 165 165
165 56 56
166 110 110
167 21 21
168 14 14
169 4 4
170 1 1
173 1 1
174 1 1
176 7 7
177 14 14
178 50 50
179 25 25
180 29 29
181 9 9
182 8 8
183 4 4
184 1 1
189 1 1
190 1 1
191 3 3
192 15 15
193 130 130
194 71 71
195 18 18
196 20 20
197 5 5
198 3 3
206 8 8
207 5 5
208 272 272
209 91 91
210 56 56
211 13 13
212 5 5
217 1 1
218 3 3
220 3 3
221 25 25
222 17 17
223 10 10
224 51 51
225 14 14
226 5 5
227 1 1
232 2 2
233 1 1
234 4 4
235 2 2
236 19 19
237 20 20
238 65 65
239 22 22
240 196 196
241 54 54
242 24 24
243 4 4
248 1 1
250 13 13
251 11 11
252 375 375
253 116 116
254 79 79
255 23 23
256 7 7
257 3 3
264 1 1
265 10 10
266 23 23
267 68 68
268 30 30
269 12 12
270 3 3
271 1 1
272 1 1
276 1 1
278 1 1
279 2 2
280 2 2
281 2 2
282 14 14
283 20 20
284 9 9
285 3 3
294 2 2
295 20 20
296 999 999
297 256 256
298 106 106
299 20 20
300 3 3
310 3 3
311 13 13
312 3 3
313 1 1
//
system version 2.2.8-SNAPSHOT