MassBank Record: MSBNK-Osaka_Univ-OUF00015
ACCESSION: MSBNK-Osaka_Univ-OUF00015
RECORD_TITLE: 2,6-Diaminopurine; GC-EI-TOF; MS; n TMS; RT:840.956 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$NAME: 2,6-Diaminopurine
CH$COMPOUND_CLASS: Natural Product
CH$FORMULA: C5H6N6
CH$EXACT_MASS: 150.06539
CH$SMILES: C1=NC2=C(N1)C(=NC(=N2)N)N
CH$IUPAC: InChI=1S/C5H6N6/c6-3-2-4(9-1-8-2)11-5(7)10-3/h1H,(H5,6,7,8,9,10,11)
CH$LINK: CAS
1904-98-9
CH$LINK: CHEMSPIDER
28738
CH$LINK: PUBCHEM
CID:30976
CH$LINK: INCHIKEY
MSSXOMSJDRHRMC-UHFFFAOYSA-N
CH$LINK: COMPTOX
DTXSID0062052
AC$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 2186.720
AC$CHROMATOGRAPHY: RETENTION_TIME 840.956 sec
AC$CHROMATOGRAPHY: TRANSFARLINE_TEMPERATURE 250 C
MS$DATA_PROCESSING: WHOLE ChromaTOF ver. 2.32 (LECO)
PK$SPLASH: splash10-0udi-3938000000-4868e65400e99cbb961f
PK$NUM_PEAK: 238
PK$PEAK: m/z int. rel.int.
85 169 169
86 92 92
87 22 22
88 97 97
89 10 10
90 5 5
91 1 1
92 6 6
93 8 8
94 8 8
95 21 21
96 21 21
97 23 23
98 60 60
99 630 630
100 324 324
101 79 79
102 32 32
103 7 7
104 3 3
106 1 1
107 5 5
108 5 5
109 11 11
110 45 45
111 125 125
112 29 29
113 59 59
114 52 52
115 32 32
116 58 58
117 15 15
118 11 11
119 1 1
120 1 1
121 5 5
122 8 8
123 16 16
124 37 37
125 37 37
126 32 32
127 25 25
128 9 9
129 10 10
130 424 424
131 79 79
132 42 42
133 7 7
134 7 7
135 12 12
136 8 8
137 14 14
138 84 84
139 38 38
140 44 44
141 69 69
142 34 34
143 20 20
144 10 10
145 3 3
146 54 54
147 10 10
148 6 6
149 11 11
150 8 8
151 17 17
152 61 61
153 29 29
154 17 17
155 49 49
156 39 39
157 60 60
158 16 16
159 6 6
160 5 5
161 1 1
162 1 1
163 5 5
164 20 20
165 83 83
166 26 26
167 44 44
168 65 65
169 24 24
170 12 12
171 198 198
172 56 56
173 21 21
174 4 4
176 5 5
177 9 9
178 18 18
179 56 56
180 33 33
181 38 38
182 118 118
183 43 43
184 17 17
185 5 5
186 2 2
187 18 18
188 5 5
189 3 3
190 24 24
191 9 9
192 10 10
193 31 31
194 29 29
195 17 17
196 21 21
197 19 19
198 8 8
199 2 2
200 1 1
202 2 2
203 1 1
204 3 3
205 10 10
206 9 9
207 19 19
208 13 13
209 11 11
210 16 16
211 6 6
212 13 13
213 4 4
214 3 3
215 1 1
218 1 1
219 2 2
220 5 5
221 50 50
222 34 34
223 18 18
224 8 8
225 5 5
226 2 2
231 1 1
233 11 11
234 8 8
235 14 14
236 29 29
237 167 167
238 55 55
239 24 24
240 6 6
241 2 2
242 2 2
243 1 1
244 2 2
245 1 1
246 3 3
247 23 23
248 11 11
249 12 12
250 11 11
251 36 36
252 48 48
253 36 36
254 12 12
255 3 3
261 3 3
262 37 37
263 299 299
264 81 81
265 31 31
266 23 23
267 15 15
268 4 4
269 1 1
270 1 1
276 3 3
277 38 38
278 43 43
279 35 35
280 14 14
281 4 4
291 1 1
292 3 3
293 34 34
294 19 19
295 7 7
296 2 2
297 1 1
304 1 1
307 1 1
308 3 3
309 12 12
310 6 6
311 6 6
312 2 2
319 2 2
320 3 3
321 4 4
322 3 3
323 2 2
324 3 3
325 2 2
326 1 1
333 2 2
334 14 14
335 121 121
336 106 106
337 46 46
338 18 18
339 4 4
340 1 1
341 2 2
342 4 4
343 5 5
344 5 5
345 4 4
346 6 6
347 5 5
348 5 5
349 19 19
350 57 57
351 999 999
352 460 460
353 201 201
354 58 58
355 16 16
356 5 5
357 3 3
358 5 5
359 4 4
360 4 4
361 5 5
362 5 5
363 3 3
364 4 4
365 49 49
366 550 550
367 224 224
368 98 98
369 27 27
370 7 7
371 1 1
//
system version 2.2.8-SNAPSHOT