MassBank Record: MSBNK-Osaka_Univ-OUF00058
ACCESSION: MSBNK-Osaka_Univ-OUF00058
RECORD_TITLE: 3-Methylglutaric acid; GC-EI-TOF; MS; n TMS; RT:510.525 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$NAME: 3-Methylglutarate
CH$NAME: 3-Methylglutaric acid
CH$COMPOUND_CLASS: Natural Product
CH$FORMULA: C6H10O4
CH$EXACT_MASS: 146.05791
CH$SMILES: OC(=O)CC(C)CC(O)=O
CH$IUPAC: InChI=1S/C6H10O4/c1-4(2-5(7)8)3-6(9)10/h4H,2-3H2,1H3,(H,7,8)(H,9,10)
CH$LINK: CAS
626-51-7
CH$LINK: CHEMSPIDER
11781
CH$LINK: PUBCHEM
CID:12284
CH$LINK: INCHIKEY
XJMMNTGIMDZPMU-UHFFFAOYSA-N
CH$LINK: COMPTOX
DTXSID50211649
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$CHROMATOGRAPHY: RETENTION_INDEX 1418.715
AC$CHROMATOGRAPHY: RETENTION_TIME 510.525 sec
AC$CHROMATOGRAPHY: TRANSFARLINE_TEMPERATURE 250 C
MS$DATA_PROCESSING: WHOLE ChromaTOF ver. 2.32 (LECO)
PK$SPLASH: splash10-0002-0910000000-81203203246ac374e1aa
PK$NUM_PEAK: 100
PK$PEAK: m/z int. rel.int.
85 14 14
86 3 3
87 11 11
88 26 26
89 18 18
90 3 3
91 2 2
92 4 4
93 3 3
95 17 17
96 1 1
97 6 6
98 4 4
99 82 82
100 11 11
101 64 64
102 9 9
103 15 15
104 3 3
105 6 6
109 4 4
110 3 3
111 34 34
112 4 4
113 15 15
114 3 3
115 18 18
116 108 108
117 151 151
118 19 19
119 13 13
120 1 1
125 3 3
127 6 6
128 19 19
129 21 21
130 80 80
131 37 37
132 13 13
133 83 83
134 12 12
135 7 7
141 42 42
142 9 9
143 138 138
144 24 24
145 9 9
146 3 3
147 999 999
148 166 166
149 144 144
150 18 18
151 7 7
156 2 2
157 37 37
158 6 6
159 118 118
160 15 15
161 5 5
162 7 7
163 4 4
169 2 2
171 2 2
172 215 215
173 59 59
174 15 15
175 3 3
185 27 27
186 4 4
187 1 1
189 16 16
190 5 5
191 6 6
192 1 1
199 1 1
200 56 56
201 30 30
202 6 6
203 3 3
204 67 67
205 13 13
206 6 6
215 2 2
217 22 22
218 5 5
219 2 2
231 5 5
232 1 1
233 6 6
234 1 1
235 1 1
247 62 62
248 22 22
249 9 9
250 2 2
275 206 206
276 48 48
277 20 20
278 3 3
290 1 1
//
system version 2.2.8-SNAPSHOT