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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 12726 - 12750 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI01711451biliverdin-IX-alpha,1TBDMS,isomer#2JsmolC=CC1=C(C)C(=CC2=NC(=CC3=C(CCC(=O)[O-])C(C)=C(C=C4NC(=O)C(C)=C4C=C)N3[Si](C)(C)C(C)(C)C)C(CCC(=O)[O-])=C2C)NC1=OTBDMS694.3198Semi standard non polar5356.9614
RI01711450biliverdin-IX-alpha,1TBDMS,isomer#1JsmolC=CC1=C(C)C(=CC2=NC(=CC3=C(CCC(=O)[O-])C(C)=C(C=C4C(C=C)=C(C)C(=O)N4[Si](C)(C)C(C)(C)C)[NH]3)C(CCC(=O)[O-])=C2C)NC1=OTBDMS694.3198Semi standard non polar5187.4824
RI01711449biliverdin-IX-alpha,3TMS,isomer#1JsmolC=CC1=C(C)C(=CC2=NC(=CC3=C(CCC(=O)[O-])C(C)=C(C=C4C(C=C)=C(C)C(=O)N4[Si](C)(C)C)N3[Si](C)(C)C)C(CCC(=O)[O-])=C2C)N([Si](C)(C)C)C1=OTMS796.3519Semi standard non polar4661.005
RI01711448biliverdin-IX-alpha,2TMS,isomer#3JsmolC=CC1=C(C)C(=CC2=NC(=CC3=C(CCC(=O)[O-])C(C)=C(C=C4NC(=O)C(C)=C4C=C)N3[Si](C)(C)C)C(CCC(=O)[O-])=C2C)N([Si](C)(C)C)C1=OTMS724.3123Semi standard non polar4935.5454
RI01711447biliverdin-IX-alpha,2TMS,isomer#2JsmolC=CC1=C(C)C(=CC2=NC(=CC3=C(CCC(=O)[O-])C(C)=C(C=C4C(C=C)=C(C)C(=O)N4[Si](C)(C)C)[NH]3)C(CCC(=O)[O-])=C2C)N([Si](C)(C)C)C1=OTMS724.3123Semi standard non polar4648.714
RI01711446biliverdin-IX-alpha,2TMS,isomer#1JsmolC=CC1=C(C)C(=CC2=NC(=CC3=C(CCC(=O)[O-])C(C)=C(C=C4C(C=C)=C(C)C(=O)N4[Si](C)(C)C)N3[Si](C)(C)C)C(CCC(=O)[O-])=C2C)NC1=OTMS724.3123Semi standard non polar5008.914
RI01711445biliverdin-IX-alpha,1TMS,isomer#3JsmolC=CC1=C(C)C(=CC2=NC(=CC3=C(CCC(=O)[O-])C(C)=C(C=C4NC(=O)C(C)=C4C=C)[NH]3)C(CCC(=O)[O-])=C2C)N([Si](C)(C)C)C1=OTMS652.2728Semi standard non polar4984.4375
RI01711444biliverdin-IX-alpha,1TMS,isomer#2JsmolC=CC1=C(C)C(=CC2=NC(=CC3=C(CCC(=O)[O-])C(C)=C(C=C4NC(=O)C(C)=C4C=C)N3[Si](C)(C)C)C(CCC(=O)[O-])=C2C)NC1=OTMS652.2728Semi standard non polar5248.0864
RI01711443biliverdin-IX-alpha,1TMS,isomer#1JsmolC=CC1=C(C)C(=CC2=NC(=CC3=C(CCC(=O)[O-])C(C)=C(C=C4C(C=C)=C(C)C(=O)N4[Si](C)(C)C)[NH]3)C(CCC(=O)[O-])=C2C)NC1=OTMS652.2728Semi standard non polar5023.4185
RI01711442biliverdin-IX-alpha,2TBDMS,isomer#3JsmolC=CC1=C(C)C(=CC2=NC(=CC3=C(CCC(=O)[O-])C(C)=C(C=C4NC(=O)C(C)=C4C=C)N3[Si](C)(C)C(C)(C)C)C(CCC(=O)[O-])=C2C)N([Si](C)(C)C(C)(C)C)C1=OTBDMS808.4062Standard non polar5022.7495
RI01711441biliverdin-IX-alpha,2TBDMS,isomer#2JsmolC=CC1=C(C)C(=CC2=NC(=CC3=C(CCC(=O)[O-])C(C)=C(C=C4C(C=C)=C(C)C(=O)N4[Si](C)(C)C(C)(C)C)[NH]3)C(CCC(=O)[O-])=C2C)N([Si](C)(C)C(C)(C)C)C1=OTBDMS808.4062Standard non polar4797.154
RI01711440biliverdin-IX-alpha,2TBDMS,isomer#1JsmolC=CC1=C(C)C(=CC2=NC(=CC3=C(CCC(=O)[O-])C(C)=C(C=C4C(C=C)=C(C)C(=O)N4[Si](C)(C)C(C)(C)C)N3[Si](C)(C)C(C)(C)C)C(CCC(=O)[O-])=C2C)NC1=OTBDMS808.4062Standard non polar5091.9043
RI01711439biliverdin-IX-alpha,1TBDMS,isomer#3JsmolC=CC1=C(C)C(=CC2=NC(=CC3=C(CCC(=O)[O-])C(C)=C(C=C4NC(=O)C(C)=C4C=C)[NH]3)C(CCC(=O)[O-])=C2C)N([Si](C)(C)C(C)(C)C)C1=OTBDMS694.3198Standard non polar4739.0796
RI01711438biliverdin-IX-alpha,1TBDMS,isomer#2JsmolC=CC1=C(C)C(=CC2=NC(=CC3=C(CCC(=O)[O-])C(C)=C(C=C4NC(=O)C(C)=C4C=C)N3[Si](C)(C)C(C)(C)C)C(CCC(=O)[O-])=C2C)NC1=OTBDMS694.3198Standard non polar5085.6035
RI01711437biliverdin-IX-alpha,1TBDMS,isomer#1JsmolC=CC1=C(C)C(=CC2=NC(=CC3=C(CCC(=O)[O-])C(C)=C(C=C4C(C=C)=C(C)C(=O)N4[Si](C)(C)C(C)(C)C)[NH]3)C(CCC(=O)[O-])=C2C)NC1=OTBDMS694.3198Standard non polar4807.7676
RI01711436biliverdin-IX-alpha,3TMS,isomer#1JsmolC=CC1=C(C)C(=CC2=NC(=CC3=C(CCC(=O)[O-])C(C)=C(C=C4C(C=C)=C(C)C(=O)N4[Si](C)(C)C)N3[Si](C)(C)C)C(CCC(=O)[O-])=C2C)N([Si](C)(C)C)C1=OTMS796.3519Standard non polar4518.725
RI01711435biliverdin-IX-alpha,2TMS,isomer#3JsmolC=CC1=C(C)C(=CC2=NC(=CC3=C(CCC(=O)[O-])C(C)=C(C=C4NC(=O)C(C)=C4C=C)N3[Si](C)(C)C)C(CCC(=O)[O-])=C2C)N([Si](C)(C)C)C1=OTMS724.3123Standard non polar4674.3506
RI01711434biliverdin-IX-alpha,2TMS,isomer#2JsmolC=CC1=C(C)C(=CC2=NC(=CC3=C(CCC(=O)[O-])C(C)=C(C=C4C(C=C)=C(C)C(=O)N4[Si](C)(C)C)[NH]3)C(CCC(=O)[O-])=C2C)N([Si](C)(C)C)C1=OTMS724.3123Standard non polar4414.5225
RI01711433biliverdin-IX-alpha,2TMS,isomer#1JsmolC=CC1=C(C)C(=CC2=NC(=CC3=C(CCC(=O)[O-])C(C)=C(C=C4C(C=C)=C(C)C(=O)N4[Si](C)(C)C)N3[Si](C)(C)C)C(CCC(=O)[O-])=C2C)NC1=OTMS724.3123Standard non polar4731.5215
RI01711432biliverdin-IX-alpha,1TMS,isomer#3JsmolC=CC1=C(C)C(=CC2=NC(=CC3=C(CCC(=O)[O-])C(C)=C(C=C4NC(=O)C(C)=C4C=C)[NH]3)C(CCC(=O)[O-])=C2C)N([Si](C)(C)C)C1=OTMS652.2728Standard non polar4553.944
RI01711431biliverdin-IX-alpha,1TMS,isomer#2JsmolC=CC1=C(C)C(=CC2=NC(=CC3=C(CCC(=O)[O-])C(C)=C(C=C4NC(=O)C(C)=C4C=C)N3[Si](C)(C)C)C(CCC(=O)[O-])=C2C)NC1=OTMS652.2728Standard non polar4898.313
RI01711430biliverdin-IX-alpha,1TMS,isomer#1JsmolC=CC1=C(C)C(=CC2=NC(=CC3=C(CCC(=O)[O-])C(C)=C(C=C4C(C=C)=C(C)C(=O)N4[Si](C)(C)C)[NH]3)C(CCC(=O)[O-])=C2C)NC1=OTMS652.2728Standard non polar4615.5776
RI01711429betanidin quinone,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)N1C(C(=O)[O-])=CC(=CC=[N+]2C3=CC(=O)C(=O)C=C3CC2C(=O)[O-])CC1C(=O)[O-]TBDMS498.1469Standard polar5038.5225
RI01711428betanidin quinone,1TMS,isomer#1JsmolC[Si](C)(C)N1C(C(=O)[O-])=CC(=CC=[N+]2C3=CC(=O)C(=O)C=C3CC2C(=O)[O-])CC1C(=O)[O-]TMS456.1Standard polar4979.384
RI01711427betanidin quinone,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)N1C(C(=O)[O-])=CC(=CC=[N+]2C3=CC(=O)C(=O)C=C3CC2C(=O)[O-])CC1C(=O)[O-]TBDMS498.1469Semi standard non polar3735.761
Displaying retention index compounds 12726 - 12750 of 1722868 in total