Name | Value |
---|---|
Natural Product | |
InChI=1S/C12H22O11/c13-1-4-6(16)8(18)9(19)11(21-4)23-12(3-15)10(20)7(17)5(2-14)22-12/h4-11,13-20H,1-3H2/t4-,5-,6-,7-,8+,9-,10+,11-,12+/m1/s1 | |
CZMRCDWAGMRECN-UGDNZRGBSA-N | |
C12H22O11 | |
342.116211524 | |
OCC1OC(OC2(OC(CO)C(O)C2O)CO)C(O)C(O)C1O |
Name | Value |
---|---|
OUF00467 | |
2016.01.19 (Created 2010.05.20, modified 2013.04.24) | |
Tsujimoto Y, Tsugawa H, Bamba T, Fukusaki E, engineering department, Osaka Univ. | |
CC BY-SA | |
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. | |
342.11621 | |
Pegasus III TOF-MS system, Leco; GC 6890, Agilent Technologies | |
GC-EI-TOF | |
MS1 | |
1 ml/min | |
200 C | |
85-500 | |
CP-SIL 8 CB LOW BLEED/MS | |
230 C | |
80 C (Duration 2 min)-330 C (rate: 15 C/min; Duration 6 min) | |
2605.254 | |
977.543 sec | |
250 C | |
ChromaTOF ver. 2.32 (LECO) | |
positive | |
4.07904352267104 | |
0.7345710805724543 |