MassBank Record: MSBNK-Osaka_Univ-OUF00400
ACCESSION: MSBNK-Osaka_Univ-OUF00400
RECORD_TITLE: Octacosanoic acid; GC-EI-TOF; MS; n TMS; RT:1148.862 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$NAME: Octacosanoic acid
CH$COMPOUND_CLASS: Natural Product
CH$FORMULA: C28H56O2
CH$EXACT_MASS: 424.42803
CH$SMILES: CCCCCCCCCCCCCCCCCCCCCCCCCCCC(O)=O
CH$IUPAC: InChI=1S/C28H56O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24-25-26-27-28(29)30/h2-27H2,1H3,(H,29,30)
CH$LINK: CAS
506-48-9
CH$LINK: CHEBI
31001 31002
CH$LINK: CHEMSPIDER
10038
CH$LINK: LIPIDMAPS
LMFA01010028
CH$LINK: PUBCHEM
CID:10470
CH$LINK: INCHIKEY
UTOPWMOLSKOLTQ-UHFFFAOYSA-N
CH$LINK: COMPTOX
DTXSID2075051
AC$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 3237.017
AC$CHROMATOGRAPHY: RETENTION_TIME 1148.862 sec
AC$CHROMATOGRAPHY: TRANSFARLINE_TEMPERATURE 250 C
MS$DATA_PROCESSING: WHOLE ChromaTOF ver. 2.32 (LECO)
PK$SPLASH: splash10-015a-1900000000-58c72f07b64a0561338d
PK$NUM_PEAK: 165
PK$PEAK: m/z int. rel.int.
85 93 93
86 15 15
87 12 12
88 6 6
89 38 38
90 6 6
91 15 15
92 3 3
93 26 26
94 6 6
95 90 90
96 21 21
97 127 127
98 79 79
99 37 37
100 5 5
101 14 14
102 4 4
103 7 7
104 1 1
105 26 26
106 2 2
107 17 17
108 2 2
109 39 39
110 8 8
111 63 63
112 24 24
113 12 12
114 2 2
115 12 12
116 61 61
117 999 999
118 106 106
119 46 46
120 2 2
121 22 22
122 3 3
123 17 17
124 5 5
125 20 20
126 6 6
127 11 11
128 6 6
129 518 518
130 72 72
131 128 128
132 586 586
133 209 209
134 43 43
135 25 25
136 3 3
137 8 8
138 2 2
139 7 7
140 4 4
141 6 6
142 4 4
143 57 57
144 7 7
145 441 441
146 61 61
147 23 23
148 2 2
149 8 8
150 1 1
151 2 2
152 1 1
153 4 4
154 8 8
155 5 5
156 1 1
157 11 11
158 2 2
159 35 35
160 5 5
161 1 1
163 3 3
165 1 1
167 3 3
168 2 2
169 2 2
171 27 27
172 4 4
173 8 8
174 9 9
175 1 1
177 1 1
181 1 1
185 48 48
186 11 11
187 34 34
188 16 16
189 3 3
191 1 1
196 1 1
197 1 1
199 8 8
200 1 1
201 91 91
202 18 18
203 5 5
213 5 5
215 7 7
216 1 1
227 10 10
228 1 1
229 4 4
230 1 1
241 7 7
242 2 2
243 11 11
244 4 4
255 5 5
256 1 1
257 13 13
258 2 2
269 4 4
270 1 1
271 2 2
283 5 5
284 1 1
285 2 2
297 4 4
298 1 1
299 2 2
300 1 1
311 2 2
312 1 1
313 2 2
325 2 2
326 1 1
327 1 1
339 1 1
340 1 1
341 1 1
355 1 1
363 1 1
367 1 1
369 1 1
382 1 1
397 2 2
398 1 1
411 1 1
425 1 1
437 5 5
438 6 6
439 3 3
440 1 1
453 5 5
454 4 4
455 4 4
456 1 1
479 2 2
480 19 19
481 71 71
482 56 56
483 21 21
484 4 4
485 1 1
495 5 5
496 36 36
497 33 33
498 13 13
499 2 2
//
system version 2.2.8-SNAPSHOT