MassBank Record: MSBNK-Osaka_Univ-OUF00084
ACCESSION: MSBNK-Osaka_Univ-OUF00084
RECORD_TITLE: 6-Amino-1-MethylUracil; GC-EI-TOF; MS; n TMS; RT:722.008 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$NAME: 6-Amino-1-MethylUracil
CH$COMPOUND_CLASS: Natural Product
CH$FORMULA: C5H7N3O2
CH$EXACT_MASS: 141.05383
CH$SMILES: O=C(C=1)NC(=O)N(C)C(N)1
CH$IUPAC: InChI=1S/C5H7N3O2/c1-8-3(6)2-4(9)7-5(8)10/h2H,6H2,1H3,(H,7,9,10)
CH$LINK: CAS
2434-53-9
CH$LINK: CHEBI
241801
CH$LINK: CHEMSPIDER
68046
CH$LINK: PUBCHEM
CID:75520
CH$LINK: INCHIKEY
GZLZRPNUDBIQBM-UHFFFAOYSA-N
CH$LINK: COMPTOX
DTXSID30179076
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$CHROMATOGRAPHY: RETENTION_INDEX 1874.613
AC$CHROMATOGRAPHY: RETENTION_TIME 722.008 sec
AC$CHROMATOGRAPHY: TRANSFARLINE_TEMPERATURE 250 C
MS$DATA_PROCESSING: WHOLE ChromaTOF ver. 2.32 (LECO)
PK$SPLASH: splash10-0092-3913000000-159775e04f8057fa3afb
PK$NUM_PEAK: 182
PK$PEAK: m/z int. rel.int.
85 196 196
86 60 60
87 25 25
88 17 17
89 3 3
90 20 20
91 18 18
92 3 3
94 4 4
95 1 1
96 9 9
97 11 11
98 38 38
99 999 999
100 205 205
101 63 63
102 21 21
103 3 3
104 1 1
107 1 1
109 1 1
110 6 6
111 29 29
112 13 13
113 56 56
114 47 47
115 194 194
116 54 54
117 14 14
118 3 3
119 2 2
120 3 3
123 1 1
124 8 8
125 30 30
126 21 21
127 14 14
128 7 7
129 18 18
130 180 180
131 39 39
132 18 18
133 3 3
137 2 2
138 2 2
139 69 69
140 41 41
141 107 107
142 25 25
143 13 13
144 7 7
145 1 1
146 7 7
147 1 1
148 13 13
149 3 3
150 1 1
151 7 7
152 4 4
153 4 4
154 3 3
155 100 100
156 130 130
157 115 115
158 28 28
159 9 9
160 2 2
165 1 1
166 1 1
167 37 37
168 10 10
169 7 7
170 6 6
171 926 926
172 202 202
173 80 80
174 12 12
175 2 2
180 5 5
181 212 212
182 56 56
183 42 42
184 10 10
185 30 30
186 17 17
187 23 23
188 11 11
189 4 4
190 1 1
191 1 1
192 1 1
193 1 1
194 1 1
195 9 9
196 6 6
197 247 247
198 50 50
199 25 25
200 4 4
201 1 1
202 2 2
203 1 1
209 3 3
210 1 1
211 25 25
212 25 25
213 183 183
214 39 39
215 17 17
216 2 2
217 1 1
222 6 6
223 2 2
224 1 1
225 1 1
226 2 2
227 21 21
228 12 12
229 6 6
230 2 2
237 1 1
238 22 22
239 116 116
240 26 26
241 10 10
242 2 2
243 1 1
244 15 15
245 4 4
246 2 2
253 14 14
254 6 6
255 9 9
256 3 3
257 1 1
269 14 14
270 8 8
271 4 4
272 1 1
283 1 1
284 1 1
285 109 109
286 42 42
287 46 46
288 15 15
289 6 6
290 1 1
293 1 1
297 1 1
298 1 1
299 1 1
300 1 1
305 1 1
306 1 1
310 10 10
311 13 13
312 6 6
313 2 2
314 1 1
317 1 1
325 3 3
326 12 12
327 563 563
328 237 237
329 104 104
330 28 28
331 7 7
332 2 2
333 2 2
334 2 2
335 2 2
336 2 2
337 2 2
338 2 2
339 1 1
340 2 2
341 31 31
342 264 264
343 97 97
344 43 43
345 11 11
346 2 2
//
system version 2.2.8-SNAPSHOT