MassBank Record: MSBNK-Osaka_Univ-OUF00404
ACCESSION: MSBNK-Osaka_Univ-OUF00404
RECORD_TITLE: Orotic acid; GC-EI-TOF; MS; n TMS; RT:662.494 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$NAME: Orotic acid
CH$COMPOUND_CLASS: Natural Product
CH$FORMULA: C5H4N2O4
CH$EXACT_MASS: 156.01711
CH$SMILES: O=C(N1)C=C(NC(=O)1)C(O)=O
CH$IUPAC: InChI=1S/C5H4N2O4/c8-3-1-2(4(9)10)6-5(11)7-3/h1H,(H,9,10)(H2,6,7,8,11)
CH$LINK: CAS
65-86-1
CH$LINK: CHEBI
16742 30839
CH$LINK: CHEMSPIDER
942
CH$LINK: KEGG
C00295 D00055
CH$LINK: PUBCHEM
CID:967
CH$LINK: INCHIKEY
PXQPEWDEAKTCGB-UHFFFAOYSA-N
CH$LINK: COMPTOX
DTXSID0025814
AC$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 1734.521
AC$CHROMATOGRAPHY: RETENTION_TIME 662.494 sec
AC$CHROMATOGRAPHY: TRANSFARLINE_TEMPERATURE 250 C
MS$DATA_PROCESSING: WHOLE ChromaTOF ver. 2.32 (LECO)
PK$SPLASH: splash10-0udi-1982000000-b20f2ec9a2f1acc84ae1
PK$NUM_PEAK: 210
PK$PEAK: m/z int. rel.int.
85 21 21
86 80 80
87 23 23
88 7 7
89 7 7
90 2 2
91 1 1
92 6 6
93 22 22
94 4 4
95 13 13
96 6 6
97 34 34
98 17 17
99 65 65
100 371 371
101 45 45
102 26 26
103 26 26
104 5 5
105 12 12
106 2 2
107 2 2
108 3 3
109 6 6
110 9 9
111 8 8
112 11 11
113 14 14
114 24 24
115 28 28
116 13 13
117 43 43
118 8 8
119 14 14
120 3 3
121 2 2
123 12 12
124 10 10
125 12 12
126 13 13
127 8 8
128 7 7
129 10 10
130 16 16
131 138 138
132 35 35
133 115 115
134 17 17
135 10 10
136 1 1
137 5 5
138 4 4
139 5 5
140 34 34
141 9 9
142 14 14
143 9 9
144 11 11
145 10 10
146 5 5
147 371 371
148 61 61
149 36 36
150 5 5
151 3 3
152 2 2
153 4 4
154 7 7
155 10 10
156 25 25
157 19 19
158 32 32
159 10 10
160 18 18
161 7 7
162 2 2
163 1 1
165 2 2
166 1 1
167 28 28
168 8 8
169 6 6
170 10 10
171 9 9
172 11 11
173 15 15
174 130 130
175 24 24
176 12 12
177 2 2
179 2 2
180 6 6
181 15 15
182 11 11
183 6 6
184 7 7
185 8 8
186 5 5
187 2 2
188 5 5
189 7 7
190 4 4
191 3 3
192 1 1
193 1 1
194 1 1
195 18 18
196 6 6
197 9 9
198 9 9
199 6 6
200 4 4
201 9 9
202 2 2
203 1 1
204 3 3
205 6 6
206 2 2
207 4 4
208 1 1
209 3 3
210 3 3
211 11 11
212 6 6
213 8 8
214 30 30
215 8 8
216 4 4
217 1 1
218 1 1
221 2 2
223 1 1
224 2 2
225 11 11
226 12 12
227 7 7
228 6 6
229 2 2
230 2 2
231 3 3
232 3 3
233 1 1
238 2 2
239 49 49
240 17 17
241 9 9
242 4 4
243 1 1
244 1 1
245 8 8
246 4 4
247 4 4
248 1 1
251 2 2
252 6 6
253 126 126
254 999 999
255 270 270
256 108 108
257 20 20
258 5 5
259 2 2
260 1 1
261 5 5
262 2 2
263 1 1
267 2 2
268 4 4
269 107 107
270 54 54
271 19 19
272 5 5
273 1 1
281 1 1
282 21 21
283 11 11
284 5 5
285 5 5
286 2 2
299 3 3
300 1 1
313 5 5
314 1 1
315 1 1
327 11 11
328 8 8
329 19 19
330 9 9
331 4 4
332 1 1
333 1 1
341 2 2
342 1 1
343 7 7
344 4 4
345 2 2
355 7 7
356 18 18
357 280 280
358 95 95
359 46 46
360 10 10
361 3 3
370 1 1
371 18 18
372 25 25
373 10 10
374 5 5
375 1 1
//
system version 2.2.8-SNAPSHOT