MassBank Record: MSBNK-Osaka_Univ-OUF00125
ACCESSION: MSBNK-Osaka_Univ-OUF00125
RECORD_TITLE: Benzen-1,3-Dicarboxylic acid; GC-EI-TOF; MS; n TMS; RT:673.896 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$NAME: Benzen-1,3-Dicarboxylic acid
CH$COMPOUND_CLASS: Natural Product
CH$FORMULA: C8H6O4
CH$EXACT_MASS: 166.02661
CH$SMILES: OC(=O)c(c1)cc(cc1)C(O)=O
CH$IUPAC: InChI=1S/C8H6O4/c9-7(10)5-2-1-3-6(4-5)8(11)12/h1-4H,(H,9,10)(H,11,12)
CH$LINK: CAS
121-91-5
CH$LINK: CHEBI
30802 30803 30804
CH$LINK: CHEMSPIDER
8182
CH$LINK: PUBCHEM
CID:8496
CH$LINK: INCHIKEY
QQVIHTHCMHWDBS-UHFFFAOYSA-N
CH$LINK: COMPTOX
DTXSID3021485
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$CHROMATOGRAPHY: RETENTION_INDEX 1760.673
AC$CHROMATOGRAPHY: RETENTION_TIME 673.896 sec
AC$CHROMATOGRAPHY: TRANSFARLINE_TEMPERATURE 250 C
MS$DATA_PROCESSING: WHOLE ChromaTOF ver. 2.32 (LECO)
PK$SPLASH: splash10-0f6t-1980000000-1de0f162e8aa1d67e0a9
PK$NUM_PEAK: 187
PK$PEAK: m/z int. rel.int.
85 21 21
86 4 4
87 11 11
88 9 9
89 113 113
90 45 45
91 104 104
92 18 18
93 29 29
94 4 4
95 16 16
96 15 15
97 10 10
98 4 4
99 3 3
100 1 1
101 9 9
102 8 8
103 537 537
104 345 345
105 93 93
106 13 13
107 20 20
108 3 3
109 10 10
110 11 11
111 7 7
112 4 4
113 2 2
114 1 1
115 34 34
116 7 7
117 29 29
118 66 66
119 106 106
120 21 21
121 68 68
122 10 10
123 8 8
124 1 1
125 18 18
126 62 62
127 31 31
128 4 4
129 10 10
130 3 3
131 27 27
132 14 14
133 121 121
134 51 51
135 277 277
136 40 40
137 20 20
138 2 2
139 2 2
140 260 260
141 36 36
142 2 2
143 4 4
144 1 1
145 17 17
146 11 11
147 69 69
148 21 21
149 75 75
150 19 19
151 21 21
152 3 3
153 9 9
154 1 1
155 1 1
157 1 1
159 3 3
160 1 1
161 7 7
162 3 3
163 33 33
164 6 6
165 23 23
166 6 6
167 2 2
173 1 1
175 20 20
176 11 11
177 151 151
178 85 85
179 61 61
180 21 21
181 8 8
182 2 2
183 1 1
185 1 1
189 1 1
191 6 6
192 16 16
193 74 74
194 24 24
195 16 16
196 3 3
197 2 2
203 1 1
204 1 1
205 239 239
206 42 42
207 143 143
208 33 33
209 19 19
210 4 4
211 8 8
212 1 1
213 1 1
217 8 8
218 2 2
219 15 15
220 11 11
221 222 222
222 41 41
223 22 22
224 3 3
225 1 1
233 17 17
234 6 6
235 30 30
236 17 17
237 11 11
238 4 4
239 1 1
241 1 1
242 1 1
243 15 15
244 10 10
245 6 6
246 2 2
247 1 1
249 3 3
250 2 2
251 42 42
252 14 14
253 10 10
254 3 3
255 1 1
256 1 1
257 1 1
259 1 1
260 1 1
261 10 10
262 11 11
263 6 6
264 4 4
265 4 4
266 2 2
267 1 1
268 1 1
269 1 1
270 1 1
271 1 1
272 1 1
273 1 1
277 5 5
278 5 5
279 240 240
280 129 129
281 41 41
282 11 11
283 2 2
284 1 1
285 2 2
286 3 3
287 3 3
288 3 3
289 3 3
290 4 4
291 3 3
292 1 1
293 4 4
294 10 10
295 999 999
296 258 258
297 106 106
298 19 19
299 4 4
308 1 1
309 44 44
310 76 76
311 23 23
312 8 8
313 1 1
//
system version 2.2.8-SNAPSHOT