MassBank Record: MSBNK-Osaka_Univ-OUF00014
ACCESSION: MSBNK-Osaka_Univ-OUF00014
RECORD_TITLE: 2,3-Dihydroxybenzoic acid; GC-EI-TOF; MS; n TMS; RT:662.886 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$NAME: 2,3-Dihydroxybenzoate
CH$NAME: 2,3-Dihydroxybenzoic acid
CH$COMPOUND_CLASS: Natural Product
CH$FORMULA: C7H6O4
CH$EXACT_MASS: 154.02661
CH$SMILES: OC(=O)c(c1)c(O)c(O)cc1
CH$IUPAC: InChI=1S/C7H6O4/c8-5-3-1-2-4(6(5)9)7(10)11/h1-3,8-9H,(H,10,11)
CH$LINK: CAS
303-38-8
CH$LINK: CHEBI
18026 36654
CH$LINK: CHEMSPIDER
18
CH$LINK: KEGG
C00196
CH$LINK: PUBCHEM
CID:19
CH$LINK: INCHIKEY
GLDQAMYCGOIJDV-UHFFFAOYSA-N
CH$LINK: COMPTOX
DTXSID70858712
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$CHROMATOGRAPHY: RETENTION_INDEX 1735.419
AC$CHROMATOGRAPHY: RETENTION_TIME 662.886 sec
AC$CHROMATOGRAPHY: TRANSFARLINE_TEMPERATURE 250 C
MS$DATA_PROCESSING: WHOLE ChromaTOF ver. 2.32 (LECO)
PK$SPLASH: splash10-0a4i-0924000000-1ed6156dbe82344d29af
PK$NUM_PEAK: 194
PK$PEAK: m/z int. rel.int.
85 17 17
86 3 3
87 14 14
88 7 7
89 49 49
90 11 11
91 66 66
92 15 15
93 44 44
94 7 7
95 23 23
96 5 5
97 8 8
98 14 14
99 7 7
100 1 1
101 6 6
102 8 8
103 53 53
104 21 21
105 147 147
106 18 18
107 74 74
108 10 10
109 43 43
110 7 7
111 10 10
112 2 2
113 5 5
114 1 1
115 37 37
116 8 8
117 34 34
118 10 10
119 66 66
120 12 12
121 28 28
122 10 10
123 23 23
124 3 3
125 6 6
126 12 12
127 5 5
128 5 5
129 13 13
130 2 2
131 60 60
132 12 12
133 185 185
134 29 29
135 65 65
136 19 19
137 304 304
138 43 43
139 16 16
140 1 1
141 4 4
142 1 1
143 11 11
144 1 1
145 10 10
146 3 3
147 254 254
148 46 46
149 77 77
150 13 13
151 33 33
152 6 6
153 5 5
154 1 1
155 2 2
157 3 3
159 5 5
160 4 4
161 10 10
162 6 6
163 43 43
164 18 18
165 62 62
166 22 22
167 9 9
168 2 2
169 2 2
171 1 1
173 1 1
174 1 1
175 7 7
176 4 4
177 15 15
178 8 8
179 24 24
180 6 6
181 14 14
182 4 4
183 3 3
184 1 1
185 1 1
187 1 1
189 7 7
190 5 5
191 89 89
192 21 21
193 659 659
194 106 106
195 105 105
196 29 29
197 11 11
198 2 2
199 1 1
203 2 2
204 1 1
205 7 7
206 3 3
207 48 48
208 11 11
209 20 20
210 5 5
211 16 16
212 4 4
213 2 2
215 1 1
217 1 1
219 2 2
220 1 1
221 5 5
222 3 3
223 98 98
224 24 24
225 19 19
226 4 4
227 1 1
233 2 2
234 1 1
235 3 3
236 1 1
237 17 17
238 5 5
239 4 4
240 1 1
241 1 1
245 1 1
247 4 4
248 3 3
249 165 165
250 70 70
251 28 28
252 8 8
253 8 8
254 3 3
255 2 2
256 1 1
257 1 1
258 1 1
259 1 1
260 1 1
261 3 3
262 1 1
263 10 10
264 5 5
265 94 94
266 27 27
267 84 84
268 24 24
269 10 10
270 2 2
279 2 2
280 2 2
281 9 9
282 12 12
283 6 6
284 2 2
295 1 1
297 3 3
298 1 1
299 1 1
309 1 1
311 1 1
312 1 1
323 1 1
324 1 1
325 1 1
326 1 1
339 1 1
353 10 10
354 29 29
355 999 999
356 368 368
357 178 178
358 43 43
359 10 10
360 2 2
370 6 6
371 2 2
372 1 1
//
system version 2.2.8-SNAPSHOT