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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 19401 - 19425 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI000194013a,17a-Dihydroxy-5b-androstaneJsmolC[C@]12CCC3C(CCC4C[C@H](O)CC[C@]34C)C1CC[C@H]2OUnderivatized292.2402Semi standard non polar2635.3616
RI000194023a,7a-Dihydroxycholanoic acid,1TMS,isomer#1JsmolC[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O)CC1C[C@H]3OTMS464.3322Semi standard non polar3311.5793
RI000194033a,7a-Dihydroxycholanoic acid,1TMS,isomer#2JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O)CC1C[C@H]3O[Si](C)(C)CTMS464.3322Semi standard non polar3324.2007
RI000194043a,7a-Dihydroxycholanoic acid,1TMS,isomer#3JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C)CC1C[C@H]3OTMS464.3322Semi standard non polar3392.9553
RI000194053a,7a-Dihydroxycholanoic acid,2TMS,isomer#1JsmolC[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C)CC1C[C@H]3OTMS536.3717Semi standard non polar3329.4895
RI000194063a,7a-Dihydroxycholanoic acid,2TMS,isomer#2JsmolC[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O)CC1C[C@H]3O[Si](C)(C)CTMS536.3717Semi standard non polar3249.2463
RI000194073a,7a-Dihydroxycholanoic acid,2TMS,isomer#3JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C)CC1C[C@H]3O[Si](C)(C)CTMS536.3717Semi standard non polar3284.9668
RI000194083a,7a-Dihydroxycholanoic acid,3TMS,isomer#1JsmolC[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C)CC1C[C@H]3O[Si](C)(C)CTMS608.4112Semi standard non polar3240.8792
RI000194093a,7a-Dihydroxycholanoic acid,1TBDMS,isomer#1JsmolC[C@H](CCC(=O)O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O)CC1C[C@H]3OTBDMS506.3791Semi standard non polar3575.5947
RI000194103a,7a-Dihydroxycholanoic acid,1TBDMS,isomer#2JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O)CC1C[C@H]3O[Si](C)(C)C(C)(C)CTBDMS506.3791Semi standard non polar3525.1829
RI000194113a,7a-Dihydroxycholanoic acid,1TBDMS,isomer#3JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C(C)(C)C)CC1C[C@H]3OTBDMS506.3791Semi standard non polar3601.2002
RI000194123a,7a-Dihydroxycholanoic acid,2TBDMS,isomer#1JsmolC[C@H](CCC(=O)O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C(C)(C)C)CC1C[C@H]3OTBDMS620.4656Semi standard non polar3810.581
RI000194133a,7a-Dihydroxycholanoic acid,2TBDMS,isomer#2JsmolC[C@H](CCC(=O)O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O)CC1C[C@H]3O[Si](C)(C)C(C)(C)CTBDMS620.4656Semi standard non polar3698.0012
RI000194143a,7a-Dihydroxycholanoic acid,2TBDMS,isomer#3JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C(C)(C)C)CC1C[C@H]3O[Si](C)(C)C(C)(C)CTBDMS620.4656Semi standard non polar3701.286
RI000194153a,7a-Dihydroxycholanoic acid,3TBDMS,isomer#1JsmolC[C@H](CCC(=O)O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C(C)(C)C)CC1C[C@H]3O[Si](C)(C)C(C)(C)CTBDMS734.5521Semi standard non polar3898.7568
RI000194163a,7a-Dihydroxycholanoic acidJsmol[H][C@@]12CC[C@H]([C@H](C)CCC(O)=O)[C@@]1(C)CC[C@@]1([H])[C@@]2([H])[C@H](O)CC2C[C@H](O)CC[C@]12CUnderivatized392.2927Standard polar3643.087
RI000194173a,7a-Dihydroxycholanoic acidJsmol[H][C@@]12CC[C@H]([C@H](C)CCC(O)=O)[C@@]1(C)CC[C@@]1([H])[C@@]2([H])[C@H](O)CC2C[C@H](O)CC[C@]12CUnderivatized392.2927Standard non polar3279.7258
RI000194183a,7a-Dihydroxycholanoic acidJsmol[H][C@@]12CC[C@H]([C@H](C)CCC(O)=O)[C@@]1(C)CC[C@@]1([H])[C@@]2([H])[C@H](O)CC2C[C@H](O)CC[C@]12CUnderivatized392.2927Semi standard non polar3490.608
RI0001941912a-Hydroxy-3-oxocholadienic acid,1TMS,isomer#1JsmolC[C@H](CCC(=O)O[Si](C)(C)C)C1CCC2C3C=CC4=CC(=O)CC[C@]4(C)C3C[C@H](O)[C@@]21CTMS458.2852Semi standard non polar3479.9287
RI0001942012a-Hydroxy-3-oxocholadienic acid,1TMS,isomer#2JsmolC[C@H](CCC(=O)O)C1CCC2C3C=CC4=CC(=O)CC[C@]4(C)C3C[C@H](O[Si](C)(C)C)[C@@]21CTMS458.2852Semi standard non polar3493.2751
RI0001942112a-Hydroxy-3-oxocholadienic acid,1TMS,isomer#3JsmolC[C@H](CCC(=O)O)C1CCC2C3C=CC4=CC(O[Si](C)(C)C)=CC[C@]4(C)C3C[C@H](O)[C@@]21CTMS458.2852Semi standard non polar3533.2925
RI0001942212a-Hydroxy-3-oxocholadienic acid,2TMS,isomer#1JsmolC[C@H](CCC(=O)O[Si](C)(C)C)C1CCC2C3C=CC4=CC(=O)CC[C@]4(C)C3C[C@H](O[Si](C)(C)C)[C@@]21CTMS530.3248Semi standard non polar3444.3022
RI0001942312a-Hydroxy-3-oxocholadienic acid,2TMS,isomer#2JsmolC[C@H](CCC(=O)O[Si](C)(C)C)C1CCC2C3C=CC4=CC(O[Si](C)(C)C)=CC[C@]4(C)C3C[C@H](O)[C@@]21CTMS530.3248Semi standard non polar3469.5708
RI0001942412a-Hydroxy-3-oxocholadienic acid,2TMS,isomer#3JsmolC[C@H](CCC(=O)O)C1CCC2C3C=CC4=CC(O[Si](C)(C)C)=CC[C@]4(C)C3C[C@H](O[Si](C)(C)C)[C@@]21CTMS530.3248Semi standard non polar3487.1272
RI0001942512a-Hydroxy-3-oxocholadienic acid,1TBDMS,isomer#1JsmolC[C@H](CCC(=O)O[Si](C)(C)C(C)(C)C)C1CCC2C3C=CC4=CC(=O)CC[C@]4(C)C3C[C@H](O)[C@@]21CTBDMS500.3322Semi standard non polar3743.8438
Displaying retention index compounds 19401 - 19425 of 1722868 in total