MassBank Record: MSBNK-Osaka_Univ-OUF00050
ACCESSION: MSBNK-Osaka_Univ-OUF00050
RECORD_TITLE: 3-HydroxyBenzoic acid; GC-EI-TOF; MS; n TMS; RT:584.461 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$NAME: 3-HydroxyBenzoate
CH$NAME: 3-HydroxyBenzoic acid
CH$COMPOUND_CLASS: Natural Product
CH$FORMULA: C6H6N2O2
CH$EXACT_MASS: 138.04293
CH$SMILES: Nc(c1)ncc(c1)C(O)=O
CH$IUPAC: InChI=1S/C6H6N2O2/c7-5-2-1-4(3-8-5)6(9)10/h1-3H,(H2,7,8)(H,9,10)
CH$LINK: CAS
99-06-9
CH$LINK: CHEMSPIDER
17469
CH$LINK: PUBCHEM
CID:18496
CH$LINK: INCHIKEY
ZCIFWRHIEBXBOY-UHFFFAOYSA-N
CH$LINK: COMPTOX
DTXSID6062882
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$CHROMATOGRAPHY: RETENTION_INDEX 1565.028
AC$CHROMATOGRAPHY: RETENTION_TIME 584.461 sec
AC$CHROMATOGRAPHY: TRANSFARLINE_TEMPERATURE 250 C
MS$DATA_PROCESSING: WHOLE ChromaTOF ver. 2.32 (LECO)
PK$SPLASH: splash10-01bc-2890000000-710aaf1b8bc4ed09d6d4
PK$NUM_PEAK: 158
PK$PEAK: m/z int. rel.int.
85 24 24
86 4 4
87 21 21
88 8 8
89 105 105
90 45 45
91 326 326
92 129 129
93 51 51
94 6 6
95 46 46
96 20 20
97 24 24
98 18 18
99 9 9
100 1 1
101 6 6
102 9 9
103 64 64
104 67 67
105 109 109
106 20 20
107 39 39
108 7 7
109 18 18
110 3 3
111 30 30
112 28 28
113 8 8
114 1 1
115 33 33
116 6 6
117 26 26
118 22 22
119 67 67
120 32 32
121 59 59
122 57 57
123 23 23
124 5 5
125 9 9
126 219 219
127 34 34
128 2 2
129 4 4
130 1 1
131 32 32
132 9 9
133 136 136
134 26 26
135 159 159
136 30 30
137 27 27
138 4 4
139 3 3
141 1 1
143 5 5
144 1 1
145 11 11
146 3 3
147 137 137
148 33 33
149 190 190
150 46 46
151 113 113
152 18 18
153 6 6
154 1 1
155 1 1
157 4 4
158 1 1
159 1 1
161 6 6
162 4 4
163 30 30
164 14 14
165 119 119
166 59 59
167 18 18
168 4 4
169 1 1
175 2 2
176 1 1
177 53 53
178 12 12
179 39 39
180 13 13
181 22 22
182 5 5
183 2 2
184 1 1
190 1 1
191 18 18
192 8 8
193 561 561
194 136 136
195 60 60
196 13 13
197 4 4
198 1 1
205 2 2
206 1 1
207 67 67
208 31 31
209 24 24
210 6 6
211 1 1
219 2 2
220 1 1
221 9 9
222 5 5
223 739 739
224 215 215
225 140 140
226 32 32
227 9 9
228 1 1
237 4 4
238 3 3
239 2 2
240 2 2
241 1 1
242 2 2
243 1 1
244 1 1
245 1 1
246 1 1
247 2 2
248 2 2
249 3 3
250 3 3
251 9 9
252 6 6
253 3 3
254 2 2
255 2 2
256 1 1
257 1 1
265 6 6
266 8 8
267 999 999
268 368 368
269 133 133
270 29 29
271 5 5
272 1 1
273 2 2
274 2 2
275 2 2
276 1 1
277 1 1
278 1 1
281 15 15
282 346 346
283 121 121
284 45 45
285 10 10
286 1 1
//
system version 2.2.8-SNAPSHOT