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Browsing Retention Index for different Chemical Structures
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RIpred ID
Structure Name
Chemical Structure
Derivatization Type
Base compound Mass
GC Column/Stationary Phase
Retention Index
RI01724101
d-Fucitol,3TBDMS,isomer#3
Jsmol
C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)CO[Si](C)(C)C(C)(C)C
TBDMS
508.3436
Semi standard non polar
2364.5808
RI01724100
d-Fucitol,3TBDMS,isomer#2
Jsmol
C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H](CO)O[Si](C)(C)C(C)(C)C
TBDMS
508.3436
Semi standard non polar
2352.8662
RI01724099
d-Fucitol,3TBDMS,isomer#1
Jsmol
C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)CO
TBDMS
508.3436
Semi standard non polar
2338.2166
RI01724098
d-Fucitol,2TBDMS,isomer#10
Jsmol
C[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C
TBDMS
394.2571
Semi standard non polar
2051.54
RI01724097
d-Fucitol,2TBDMS,isomer#9
Jsmol
C[C@H](O)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)CO[Si](C)(C)C(C)(C)C
TBDMS
394.2571
Semi standard non polar
2042.3933
RI01724096
d-Fucitol,2TBDMS,isomer#8
Jsmol
C[C@H](O)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](CO)O[Si](C)(C)C(C)(C)C
TBDMS
394.2571
Semi standard non polar
2039.9122
RI01724095
d-Fucitol,2TBDMS,isomer#7
Jsmol
C[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)CO[Si](C)(C)C(C)(C)C
TBDMS
394.2571
Semi standard non polar
2064.7327
RI01724094
d-Fucitol,2TBDMS,isomer#6
Jsmol
C[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H](CO)O[Si](C)(C)C(C)(C)C
TBDMS
394.2571
Semi standard non polar
2055.1816
RI01724093
d-Fucitol,2TBDMS,isomer#5
Jsmol
C[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)CO
TBDMS
394.2571
Semi standard non polar
2046.0164
RI01724092
d-Fucitol,2TBDMS,isomer#4
Jsmol
C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H](O)[C@H](O)CO[Si](C)(C)C(C)(C)C
TBDMS
394.2571
Semi standard non polar
2082.8474
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