MassBank Record: MSBNK-Osaka_Univ-OUF00044
ACCESSION: MSBNK-Osaka_Univ-OUF00044
RECORD_TITLE: 3,4-Dihydroxyphenylacetic acid; GC-EI-TOF; MS; n TMS; RT:700.387 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$NAME: 3,4-Dihydroxyphenyl Acetic acid
CH$NAME: 3,4-Dihydroxyphenylacetic acid
CH$COMPOUND_CLASS: Natural Product
CH$FORMULA: C8H8O4
CH$EXACT_MASS: 168.04226
CH$SMILES: OC(=O)Cc(c1)cc(O)c(O)c1
CH$IUPAC: InChI=1S/C8H8O4/c9-6-2-1-5(3-7(6)10)4-8(11)12/h1-3,9-10H,4H2,(H,11,12)
CH$LINK: CAS
102-32-9
CH$LINK: CHEBI
1386 17612 41941
CH$LINK: CHEMSPIDER
532
CH$LINK: KEGG
C01161
CH$LINK: PUBCHEM
CID:547
CH$LINK: INCHIKEY
CFFZDZCDUFSOFZ-UHFFFAOYSA-N
CH$LINK: COMPTOX
DTXSID9074430
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$CHROMATOGRAPHY: RETENTION_INDEX 1822.516
AC$CHROMATOGRAPHY: RETENTION_TIME 700.387 sec
AC$CHROMATOGRAPHY: TRANSFARLINE_TEMPERATURE 250 C
MS$DATA_PROCESSING: WHOLE ChromaTOF ver. 2.32 (LECO)
PK$SPLASH: splash10-004i-0931000000-c4bb79d921fb42cf1b40
PK$NUM_PEAK: 142
PK$PEAK: m/z int. rel.int.
85 7 7
86 1 1
87 8 8
88 2 2
89 16 16
90 5 5
91 29 29
92 4 4
93 6 6
95 8 8
96 2 2
97 5 5
98 1 1
99 9 9
100 1 1
101 4 4
102 6 6
103 32 32
104 89 89
105 39 39
106 4 4
107 4 4
109 3 3
110 1 1
111 4 4
113 2 2
115 20 20
116 5 5
117 23 23
118 10 10
119 45 45
120 6 6
121 9 9
122 1 1
123 4 4
125 1 1
129 2 2
131 30 30
132 5 5
133 60 60
134 9 9
135 30 30
136 5 5
137 4 4
143 3 3
145 6 6
146 2 2
147 74 74
148 16 16
149 113 113
150 23 23
151 12 12
152 2 2
153 2 2
157 1 1
159 2 2
160 1 1
161 16 16
162 7 7
163 40 40
164 9 9
165 7 7
166 2 2
167 1 1
173 1 1
175 4 4
176 3 3
177 22 22
178 33 33
179 999 999
180 158 158
181 52 52
182 6 6
183 1 1
189 1 1
191 7 7
192 4 4
193 31 31
194 6 6
195 7 7
196 2 2
197 1 1
203 1 1
205 2 2
206 8 8
207 9 9
208 3 3
209 21 21
210 10 10
211 4 4
212 1 1
219 2 2
220 1 1
221 5 5
222 2 2
223 9 9
224 3 3
225 16 16
226 5 5
227 2 2
233 1 1
235 4 4
236 4 4
237 153 153
238 41 41
239 17 17
240 3 3
249 1 1
251 13 13
252 8 8
253 22 22
254 8 8
255 3 3
265 28 28
266 8 8
267 262 262
268 71 71
269 28 28
270 5 5
271 1 1
281 22 22
282 6 6
283 2 2
294 3 3
295 1 1
296 1 1
340 15 15
341 9 9
342 10 10
343 3 3
344 1 1
368 1 1
369 31 31
370 15 15
371 6 6
372 2 2
383 7 7
384 200 200
385 81 81
386 38 38
387 10 10
388 2 2
//
system version 2.2.8-SNAPSHOT