MassBank Record: MSBNK-Osaka_Univ-OUF00004
ACCESSION: MSBNK-Osaka_Univ-OUF00004
RECORD_TITLE: 1,6-Anhydro-beta-D-glucose; GC-EI-TOF; MS; n TMS; RT:645.412 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$NAME: 1,6-Anhydroglucose
CH$NAME: 1,6-Anhydro-beta-D-glucose
CH$COMPOUND_CLASS: Natural Product
CH$FORMULA: C6H10O5
CH$EXACT_MASS: 162.05282
CH$SMILES: C1[C@@H]2[C@H]([C@@H]([C@H]([C@H](O1)O2)O)O)O
CH$IUPAC: InChI=1S/C6H10O5/c7-3-2-1-10-6(11-2)5(9)4(3)8/h2-9H,1H2/t2-,3-,4+,5-,6-/m1/s1
CH$LINK: CAS
498-07-7
CH$LINK: CHEMSPIDER
71361
CH$LINK: PUBCHEM
CID:2724705
CH$LINK: INCHIKEY
TWNIBLMWSKIRAT-VFUOTHLCSA-N
CH$LINK: COMPTOX
DTXSID90904321
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$CHROMATOGRAPHY: RETENTION_INDEX 1695.580
AC$CHROMATOGRAPHY: RETENTION_TIME 645.412 sec
AC$CHROMATOGRAPHY: TRANSFARLINE_TEMPERATURE 250 C
MS$DATA_PROCESSING: WHOLE ChromaTOF ver. 2.32 (LECO)
PK$SPLASH: splash10-0uxr-0950000000-70ad01d41ff4333eadf9
PK$NUM_PEAK: 176
PK$PEAK: m/z int. rel.int.
85 70 70
86 14 14
87 36 36
88 15 15
89 47 47
90 10 10
91 8 8
92 2 2
93 2 2
94 4 4
95 9 9
96 8 8
97 27 27
98 16 16
99 62 62
100 10 10
101 230 230
102 33 33
103 418 418
104 41 41
105 37 37
106 3 3
107 3 3
108 1 1
109 23 23
110 3 3
111 40 40
112 7 7
113 68 68
114 13 13
115 62 62
116 129 129
117 213 213
118 28 28
119 46 46
120 6 6
121 5 5
122 1 1
123 1 1
124 2 2
125 9 9
126 5 5
127 34 34
128 9 9
129 442 442
130 61 61
131 141 141
132 25 25
133 296 296
134 44 44
135 36 36
136 6 6
137 6 6
138 1 1
139 6 6
140 3 3
141 16 16
142 66 66
143 153 153
144 24 24
145 34 34
146 8 8
147 627 627
148 104 104
149 101 101
150 14 14
151 11 11
152 16 16
153 9 9
154 5 5
155 76 76
156 13 13
157 34 34
158 5 5
159 29 29
160 5 5
161 75 75
162 11 11
163 22 22
164 4 4
165 2 2
167 1 1
168 3 3
169 36 36
170 20 20
171 58 58
172 11 11
173 11 11
174 11 11
175 15 15
176 2 2
177 37 37
178 6 6
179 3 3
181 1 1
182 1 1
183 22 22
184 3 3
185 4 4
186 1 1
187 6 6
188 2 2
189 228 228
190 63 63
191 204 204
192 37 37
193 20 20
194 3 3
195 3 3
196 3 3
197 4 4
198 4 4
199 15 15
200 7 7
201 7 7
202 2 2
203 18 18
204 999 999
205 205 205
206 94 94
207 17 17
208 3 3
209 1 1
213 1 1
214 1 1
215 15 15
216 9 9
217 868 868
218 190 190
219 85 85
220 15 15
221 13 13
222 3 3
223 1 1
227 3 3
229 6 6
230 6 6
231 17 17
232 4 4
233 3 3
234 2 2
239 1 1
241 2 2
242 9 9
243 55 55
244 18 18
245 22 22
246 6 6
247 3 3
249 1 1
255 1 1
257 3 3
259 5 5
260 17 17
261 9 9
262 3 3
263 1 1
265 1 1
271 1 1
273 10 10
274 2 2
275 1 1
291 1 1
304 3 3
305 5 5
306 2 2
317 15 15
318 5 5
319 1 1
331 1 1
332 12 12
333 105 105
334 40 40
335 19 19
336 4 4
363 1 1
//
system version 2.2.8-SNAPSHOT