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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 17726 - 17750 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI0001772616-a-Hydroxypregnenolone,3TBDMS,isomer#1JsmolCC(O[Si](C)(C)C(C)(C)C)=C1[C@H](O[Si](C)(C)C(C)(C)C)C[C@H]2[C@@H]3CC=C4C[C@@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3CC[C@]12CTBDMS674.4946Semi standard non polar3627.722
RI0001772716-a-Hydroxypregnenolone,3TBDMS,isomer#2JsmolC=C(O[Si](C)(C)C(C)(C)C)[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)C[C@H]2[C@@H]3CC=C4C[C@@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3CC[C@@]21CTBDMS674.4946Semi standard non polar3649.328
RI0001772816-a-Hydroxypregnenolone,3TMS,isomer#1JsmolCC(O[Si](C)(C)C)=C1[C@H](O[Si](C)(C)C)C[C@H]2[C@@H]3CC=C4C[C@@H](O[Si](C)(C)C)CC[C@]4(C)[C@H]3CC[C@]12CTMS548.3537Standard polar3234.1858
RI0001772916-a-Hydroxypregnenolone,3TMS,isomer#2JsmolC=C(O[Si](C)(C)C)[C@H]1[C@H](O[Si](C)(C)C)C[C@H]2[C@@H]3CC=C4C[C@@H](O[Si](C)(C)C)CC[C@]4(C)[C@H]3CC[C@@]21CTMS548.3537Standard polar3307.5168
RI0001773016-a-Hydroxypregnenolone,3TBDMS,isomer#1JsmolCC(O[Si](C)(C)C(C)(C)C)=C1[C@H](O[Si](C)(C)C(C)(C)C)C[C@H]2[C@@H]3CC=C4C[C@@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3CC[C@]12CTBDMS674.4946Standard polar3528.702
RI0001773116-a-Hydroxypregnenolone,3TBDMS,isomer#2JsmolC=C(O[Si](C)(C)C(C)(C)C)[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)C[C@H]2[C@@H]3CC=C4C[C@@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3CC[C@@]21CTBDMS674.4946Standard polar3567.8506
RI000177322b,3a,7a,12a-Tetrahydroxy-5b-cholanoic acid,1TMS,isomer#1JsmolC[C@@H](CCC(=O)O)C1CCC2C3C(C[C@H](O)[C@@]21C)[C@@]1(C)C[C@H](O)[C@@H](O[Si](C)(C)C)C[C@H]1C[C@H]3OTMS496.322Semi standard non polar3619.3838
RI000177332b,3a,7a,12a-Tetrahydroxy-5b-cholanoic acid,1TMS,isomer#2JsmolC[C@@H](CCC(=O)O)C1CCC2C3C(C[C@H](O)[C@@]21C)[C@@]1(C)C[C@H](O[Si](C)(C)C)[C@@H](O)C[C@H]1C[C@H]3OTMS496.322Semi standard non polar3651.8604
RI000177342b,3a,7a,12a-Tetrahydroxy-5b-cholanoic acid,1TMS,isomer#3JsmolC[C@@H](CCC(=O)O)C1CCC2C3C(C[C@H](O[Si](C)(C)C)[C@@]21C)[C@@]1(C)C[C@H](O)[C@@H](O)C[C@H]1C[C@H]3OTMS496.322Semi standard non polar3614.3877
RI000177352b,3a,7a,12a-Tetrahydroxy-5b-cholanoic acid,1TMS,isomer#4JsmolC[C@@H](CCC(=O)O)C1CCC2C3C(C[C@H](O)[C@@]21C)[C@@]1(C)C[C@H](O)[C@@H](O)C[C@H]1C[C@H]3O[Si](C)(C)CTMS496.322Semi standard non polar3631.0957
RI000177362b,3a,7a,12a-Tetrahydroxy-5b-cholanoic acid,1TMS,isomer#5JsmolC[C@@H](CCC(=O)O[Si](C)(C)C)C1CCC2C3C(C[C@H](O)[C@@]21C)[C@@]1(C)C[C@H](O)[C@@H](O)C[C@H]1C[C@H]3OTMS496.322Semi standard non polar3611.6128
RI000177372b,3a,7a,12a-Tetrahydroxy-5b-cholanoic acid,2TMS,isomer#1JsmolC[C@@H](CCC(=O)O[Si](C)(C)C)C1CCC2C3C(C[C@H](O)[C@@]21C)[C@@]1(C)C[C@H](O)[C@@H](O[Si](C)(C)C)C[C@H]1C[C@H]3OTMS568.3615Semi standard non polar3541.9568
RI000177382b,3a,7a,12a-Tetrahydroxy-5b-cholanoic acid,2TMS,isomer#2JsmolC[C@@H](CCC(=O)O)C1CCC2C3C(C[C@H](O[Si](C)(C)C)[C@@]21C)[C@@]1(C)C[C@H](O)[C@@H](O[Si](C)(C)C)C[C@H]1C[C@H]3OTMS568.3615Semi standard non polar3497.6992
RI000177392b,3a,7a,12a-Tetrahydroxy-5b-cholanoic acid,2TMS,isomer#3JsmolC[C@@H](CCC(=O)O)C1CCC2C3C(C[C@H](O)[C@@]21C)[C@@]1(C)C[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C[C@H]1C[C@H]3OTMS568.3615Semi standard non polar3541.262
RI000177402b,3a,7a,12a-Tetrahydroxy-5b-cholanoic acid,2TMS,isomer#4JsmolC[C@@H](CCC(=O)O)C1CCC2C3C(C[C@H](O)[C@@]21C)[C@@]1(C)C[C@H](O)[C@@H](O[Si](C)(C)C)C[C@H]1C[C@H]3O[Si](C)(C)CTMS568.3615Semi standard non polar3557.5063
RI000177412b,3a,7a,12a-Tetrahydroxy-5b-cholanoic acid,2TMS,isomer#5JsmolC[C@@H](CCC(=O)O[Si](C)(C)C)C1CCC2C3C(C[C@H](O)[C@@]21C)[C@@]1(C)C[C@H](O[Si](C)(C)C)[C@@H](O)C[C@H]1C[C@H]3OTMS568.3615Semi standard non polar3585.9595
RI000177422b,3a,7a,12a-Tetrahydroxy-5b-cholanoic acid,2TMS,isomer#6JsmolC[C@@H](CCC(=O)O)C1CCC2C3C(C[C@H](O[Si](C)(C)C)[C@@]21C)[C@@]1(C)C[C@H](O[Si](C)(C)C)[C@@H](O)C[C@H]1C[C@H]3OTMS568.3615Semi standard non polar3543.506
RI000177432b,3a,7a,12a-Tetrahydroxy-5b-cholanoic acid,2TMS,isomer#7JsmolC[C@@H](CCC(=O)O)C1CCC2C3C(C[C@H](O)[C@@]21C)[C@@]1(C)C[C@H](O[Si](C)(C)C)[C@@H](O)C[C@H]1C[C@H]3O[Si](C)(C)CTMS568.3615Semi standard non polar3561.9648
RI000177442b,3a,7a,12a-Tetrahydroxy-5b-cholanoic acid,2TMS,isomer#8JsmolC[C@@H](CCC(=O)O[Si](C)(C)C)C1CCC2C3C(C[C@H](O[Si](C)(C)C)[C@@]21C)[C@@]1(C)C[C@H](O)[C@@H](O)C[C@H]1C[C@H]3OTMS568.3615Semi standard non polar3541.867
RI000177452b,3a,7a,12a-Tetrahydroxy-5b-cholanoic acid,2TMS,isomer#9JsmolC[C@@H](CCC(=O)O)C1CCC2C3C(C[C@H](O[Si](C)(C)C)[C@@]21C)[C@@]1(C)C[C@H](O)[C@@H](O)C[C@H]1C[C@H]3O[Si](C)(C)CTMS568.3615Semi standard non polar3541.5344
RI000177462b,3a,7a,12a-Tetrahydroxy-5b-cholanoic acid,2TMS,isomer#10JsmolC[C@@H](CCC(=O)O[Si](C)(C)C)C1CCC2C3C(C[C@H](O)[C@@]21C)[C@@]1(C)C[C@H](O)[C@@H](O)C[C@H]1C[C@H]3O[Si](C)(C)CTMS568.3615Semi standard non polar3553.7278
RI000177472b,3a,7a,12a-Tetrahydroxy-5b-cholanoic acid,3TMS,isomer#1JsmolC[C@@H](CCC(=O)O[Si](C)(C)C)C1CCC2C3C(C[C@H](O[Si](C)(C)C)[C@@]21C)[C@@]1(C)C[C@H](O)[C@@H](O[Si](C)(C)C)C[C@H]1C[C@H]3OTMS640.4011Semi standard non polar3415.7192
RI000177482b,3a,7a,12a-Tetrahydroxy-5b-cholanoic acid,3TMS,isomer#2JsmolC[C@@H](CCC(=O)O[Si](C)(C)C)C1CCC2C3C(C[C@H](O)[C@@]21C)[C@@]1(C)C[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C[C@H]1C[C@H]3OTMS640.4011Semi standard non polar3473.4883
RI000177492b,3a,7a,12a-Tetrahydroxy-5b-cholanoic acid,3TMS,isomer#3JsmolC[C@@H](CCC(=O)O[Si](C)(C)C)C1CCC2C3C(C[C@H](O)[C@@]21C)[C@@]1(C)C[C@H](O)[C@@H](O[Si](C)(C)C)C[C@H]1C[C@H]3O[Si](C)(C)CTMS640.4011Semi standard non polar3474.2239
RI000177502b,3a,7a,12a-Tetrahydroxy-5b-cholanoic acid,3TMS,isomer#4JsmolC[C@@H](CCC(=O)O)C1CCC2C3C(C[C@H](O[Si](C)(C)C)[C@@]21C)[C@@]1(C)C[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C[C@H]1C[C@H]3OTMS640.4011Semi standard non polar3450.5464
Displaying retention index compounds 17726 - 17750 of 1722868 in total