MassBank Record: MSBNK-Osaka_Univ-OUF00435
ACCESSION: MSBNK-Osaka_Univ-OUF00435
RECORD_TITLE: Pyridoxamine; GC-EI-TOF; MS; n TMS; RT:809.217 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$NAME: Pyridoxamine
CH$COMPOUND_CLASS: Natural Product
CH$FORMULA: C8H12N2O2
CH$EXACT_MASS: 168.08988
CH$SMILES: OCc(c1)c(CN)c(O)c(C)n1
CH$IUPAC: InChI=1S/C8H12N2O2/c1-5-8(12)7(2-9)6(4-11)3-10-5/h3,11-12H,2,4,9H2,1H3
CH$LINK: CAS
85-87-0
CH$LINK: CHEBI
16410
CH$LINK: CHEMSPIDER
1023
CH$LINK: KEGG
C00534
CH$LINK: PUBCHEM
CID:1052
CH$LINK: INCHIKEY
NHZMQXZHNVQTQA-UHFFFAOYSA-N
CH$LINK: COMPTOX
DTXSID6046929
AC$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 2098.736
AC$CHROMATOGRAPHY: RETENTION_TIME 809.217 sec
AC$CHROMATOGRAPHY: TRANSFARLINE_TEMPERATURE 250 C
MS$DATA_PROCESSING: WHOLE ChromaTOF ver. 2.32 (LECO)
PK$SPLASH: splash10-001j-0590000000-a4bf9fe291241c903e3d
PK$NUM_PEAK: 214
PK$PEAK: m/z int. rel.int.
85 14 14
86 42 42
87 13 13
88 6 6
89 8 8
90 3 3
91 13 13
92 7 7
93 8 8
94 5 5
95 9 9
96 4 4
97 12 12
98 6 6
99 8 8
100 52 52
101 12 12
102 14 14
103 19 19
104 12 12
105 13 13
106 15 15
107 8 8
108 4 4
109 9 9
110 5 5
111 6 6
112 2 2
113 14 14
114 11 11
115 12 12
116 15 15
117 24 24
118 14 14
119 17 17
120 15 15
121 9 9
122 6 6
123 7 7
124 6 6
125 4 4
126 2 2
127 2 2
128 2 2
129 4 4
130 125 125
131 80 80
132 34 34
133 94 94
134 21 21
135 14 14
136 13 13
137 7 7
138 5 5
139 2 2
140 2 2
141 2 2
142 2 2
143 5 5
144 5 5
145 6 6
146 136 136
147 281 281
148 63 63
149 36 36
150 14 14
151 8 8
152 5 5
153 2 2
154 1 1
155 2 2
156 2 2
157 3 3
158 4 4
159 3 3
160 7 7
161 8 8
162 17 17
163 9 9
164 28 28
165 11 11
166 9 9
167 4 4
168 2 2
169 2 2
170 1 1
171 2 2
172 4 4
173 2 2
174 14 14
175 7 7
176 14 14
177 9 9
178 32 32
179 27 27
180 27 27
181 8 8
182 4 4
183 2 2
184 1 1
185 1 1
186 2 2
187 3 3
188 7 7
189 10 10
190 13 13
191 11 11
192 43 43
193 18 18
194 23 23
195 8 8
196 10 10
197 2 2
198 1 1
201 1 1
202 3 3
203 6 6
204 13 13
205 30 30
206 40 40
207 33 33
208 21 21
209 6 6
210 3 3
211 1 1
212 1 1
216 1 1
217 2 2
218 4 4
219 7 7
220 15 15
221 48 48
222 27 27
223 9 9
224 5 5
225 1 1
232 1 1
233 2 2
234 4 4
235 4 4
236 9 9
237 5 5
238 6 6
239 2 2
240 1 1
246 1 1
247 2 2
248 3 3
249 6 6
250 18 18
251 12 12
252 28 28
253 12 12
254 6 6
255 2 2
261 1 1
262 2 2
263 7 7
264 13 13
265 14 14
266 11 11
267 6 6
268 5 5
269 1 1
277 9 9
278 10 10
279 34 34
280 999 999
281 378 378
282 135 135
283 31 31
284 8 8
285 3 3
286 4 4
287 4 4
288 4 4
289 4 4
290 4 4
291 5 5
292 5 5
293 47 47
294 28 28
295 419 419
296 134 134
297 51 51
298 11 11
299 2 2
308 1 1
310 1 1
323 4 4
324 2 2
325 1 1
337 3 3
338 5 5
339 2 2
340 1 1
351 5 5
352 3 3
353 8 8
354 4 4
355 1 1
365 1 1
366 1 1
367 7 7
368 5 5
369 3 3
370 1 1
381 1 1
440 6 6
441 31 31
442 21 21
443 10 10
444 4 4
445 1 1
//
system version 2.2.8-SNAPSHOT