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id authors name url | ||
0431 Jian Guo, Tao Huan ROASMI_08 10.1021/acs.analchem.9b05135 | ||
id authors name url source method.type | ||
0431 Jian Guo, Tao Huan ROASMI_08 10.1021/acs.analchem.9b05135 Publication - Guo RP |
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id authors name url | ||
0432 Tobias Bruderer , Emmanuel Varesio , Gérard Hopfgartner ROASMI_65 10.1016/j.jchromb.2017.07.016. | ||
id authors name url source method.type | ||
0432 Tobias Bruderer, Emmanuel Varesio, Gérard Hopfgartner ROASMI_65 10.1016/j.jchromb.2017.07.016 Publication - Bruderer RP |
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id authors name url comment | ||
0433 Tobias Bruderer , Emmanuel Varesio , Gérard Hopfgartner ROASMI_66 10.1016/j.jchromb.2017.07.016. mobile phase A was 5 mM ammonium formate in water with an adjusted pH of 3.0 by the addition of formic acid., Submitted by Fangyuan Sun | ||
id authors name url comment source method.type | ||
0433 Tobias Bruderer, Emmanuel Varesio, Gérard Hopfgartner ROASMI_66 10.1016/j.jchromb.2017.07.016 mobile phase A was 5 mM ammonium formate in water with an adjusted pH of 3.0 by the addition of formic acid., Submitted by Fangyuan Sun Publication - Bruderer RP |
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id authors name url comment | ||
0434 Tobias Bruderer , Emmanuel Varesio , Gérard Hopfgartner ROASMI_71 10.1016/j.jchromb.2017.07.016. mobile phase A was 5 mM ammonium formate in water with an adjusted pH of 3.0 by the addition of formic acid, Submitted by Tobias Bruderer , Emmanuel Varesio , Gérard Hopfgartner | ||
id authors name url comment source method.type | ||
0434 Tobias Bruderer, Emmanuel Varesio, Gérard Hopfgartner ROASMI_71 10.1016/j.jchromb.2017.07.016 mobile phase A was 5 mM ammonium formate in water with an adjusted pH of 3.0 by the addition of formic acid, Submitted by Fangyuan Sun Publication - Bruderer RP |
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id authors name url comment | ||
0435 Tobias Bruderer , Emmanuel Varesio , Gérard Hopfgartner ROASMI_77 10.1016/j.jchromb.2017.07.016. Mobile A was 5 mM ammonium acetate in water with an adjusted pH of 8.0 by the addition of ammonium hydroxide., Submitted by Fangyuan Sun | ||
id authors name url comment source method.type | ||
0435 Tobias Bruderer, Emmanuel Varesio, Gérard Hopfgartner ROASMI_77 10.1016/j.jchromb.2017.07.016 Mobile A was 5 mM ammonium acetate in water with an adjusted pH of 8.0 by the addition of ammonium hydroxide, Submitted by Fangyuan Sun Publication - Bruderer RP |
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id authors name comment url | ||
0436 Pablo Gago-Ferrero, Anna A. Bletsou, Dimitrios E. Damalas, Reza Aalizadeh, Nikiforos A.Alygizakis, Heinz P.Singer, Juliane Hollender, Nikolaos S. Thomaidis ROASMI_85 flow rate:0.2-0.48, Submitted by Fangyuan Sun 10.1016/j.jhazmat.2019.121712 | ||
id authors name comment url source method.type | ||
0436 Pablo Gago-Ferrero, Anna A. Bletsou, Dimitrios E. Damalas, Reza Aalizadeh, Nikiforos A.Alygizakis, Heinz P.Singer, Juliane Hollender, Nikolaos S. Thomaidis ROASMI_85 flow rate:0.2-0.48, Submitted by Fangyuan Sun 10.1016/j.jhazmat.2019.121712 Publication - Gago-Ferrero RP |
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---|---|---|
@@ -1,3 +1,3 @@ | ||
t [min] flow rate [ml/min] A [%] B [%] | ||
0 -1 100 0 | ||
100 -1 10 90 | ||
0 100 0 | ||
100 10 90 |
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id authors name url | ||
0437 L. Mark Hall, Dennis W. Hill, Kelly Bugden, Shannon Cawley, Lowell H. Hall, Ming-Hui Chen, David F. Grant ROASMI_86 10.1021/acs.jcim.7b00496 | ||
id authors name url source method.type | ||
0437 L. Mark Hall, Dennis W. Hill, Kelly Bugden, Shannon Cawley, Lowell H. Hall, Ming-Hui Chen, David F. Grant ROASMI_86 10.1021/acs.jcim.7b00496 Publication - Hall RP |
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id column.name column.usp.code column.length column.id column.particle.size column.temperature column.flowrate column.t0 eluent.A.h2o eluent.A.meoh eluent.A.acn eluent.A.iproh eluent.A.acetone eluent.A.hex eluent.A.chcl3 eluent.A.ch2cl2 eluent.A.hept eluent.A.formic eluent.A.formic.unit eluent.A.acetic eluent.A.acetic.unit eluent.A.trifluoroacetic eluent.A.trifluoroacetic.unit eluent.A.phosphor eluent.A.phosphor.unit eluent.A.nh4ac eluent.A.nh4ac.unit eluent.A.nh4form eluent.A.nh4form.unit eluent.A.nh4carb eluent.A.nh4carb.unit eluent.A.nh4bicarb eluent.A.nh4bicarb.unit eluent.A.nh4f eluent.A.nh4f.unit eluent.A.nh4oh eluent.A.nh4oh.unit eluent.A.trieth eluent.A.trieth.unit eluent.A.triprop eluent.A.triprop.unit eluent.A.tribut eluent.A.tribut.unit eluent.A.nndimethylhex eluent.A.nndimethylhex.unit eluent.A.medronic eluent.A.medronic.unit eluent.A.pH eluent.B.h2o eluent.B.meoh eluent.B.acn eluent.B.iproh eluent.B.acetone eluent.B.hex eluent.B.chcl3 eluent.B.ch2cl2 eluent.B.hept eluent.B.formic eluent.B.formic.unit eluent.B.acetic eluent.B.acetic.unit eluent.B.trifluoroacetic eluent.B.trifluoroacetic.unit eluent.B.phosphor eluent.B.phosphor.unit eluent.B.nh4ac eluent.B.nh4ac.unit eluent.B.nh4form eluent.B.nh4form.unit eluent.B.nh4carb eluent.B.nh4carb.unit eluent.B.nh4bicarb eluent.B.nh4bicarb.unit eluent.B.nh4f eluent.B.nh4f.unit eluent.B.nh4oh eluent.B.nh4oh.unit eluent.B.trieth eluent.B.trieth.unit eluent.B.triprop eluent.B.triprop.unit eluent.B.tribut eluent.B.tribut.unit eluent.B.nndimethylhex eluent.B.nndimethylhex.unit eluent.B.medronic eluent.B.medronic.unit eluent.B.pH eluent.C.h2o eluent.C.meoh eluent.C.acn eluent.C.iproh eluent.C.acetone eluent.C.hex eluent.C.chcl3 eluent.C.ch2cl2 eluent.C.hept eluent.C.formic eluent.C.formic.unit eluent.C.acetic eluent.C.acetic.unit eluent.C.trifluoroacetic eluent.C.trifluoroacetic.unit eluent.C.phosphor eluent.C.phosphor.unit eluent.C.nh4ac eluent.C.nh4ac.unit eluent.C.nh4form eluent.C.nh4form.unit eluent.C.nh4carb eluent.C.nh4carb.unit eluent.C.nh4bicarb eluent.C.nh4bicarb.unit eluent.C.nh4f eluent.C.nh4f.unit eluent.C.nh4oh eluent.C.nh4oh.unit eluent.C.trieth eluent.C.trieth.unit eluent.C.triprop eluent.C.triprop.unit eluent.C.tribut eluent.C.tribut.unit eluent.C.nndimethylhex eluent.C.nndimethylhex.unit eluent.C.medronic eluent.C.medronic.unit eluent.C.pH eluent.D.h2o eluent.D.meoh eluent.D.acn eluent.D.iproh eluent.D.acetone eluent.D.hex eluent.D.chcl3 eluent.D.ch2cl2 eluent.D.hept eluent.D.formic eluent.D.formic.unit eluent.D.acetic eluent.D.acetic.unit eluent.D.trifluoroacetic eluent.D.trifluoroacetic.unit eluent.D.phosphor eluent.D.phosphor.unit eluent.D.nh4ac eluent.D.nh4ac.unit eluent.D.nh4form eluent.D.nh4form.unit eluent.D.nh4carb eluent.D.nh4carb.unit eluent.D.nh4bicarb eluent.D.nh4bicarb.unit eluent.D.nh4f eluent.D.nh4f.unit eluent.D.nh4oh eluent.D.nh4oh.unit eluent.D.trieth eluent.D.trieth.unit eluent.D.triprop eluent.D.triprop.unit eluent.D.tribut eluent.D.tribut.unit eluent.D.nndimethylhex eluent.D.nndimethylhex.unit eluent.D.medronic eluent.D.medronic.unit eluent.D.pH gradient.start.A gradient.start.B gradient.start.C gradient.start.D gradient.end.A gradient.end.B gradient.end.C gradient.end.D | ||
0437 Agilent ZORBAX 300 SB-C18 1 150 1 3.5 -1 -1 -0.075 100 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 100 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 100 0 0 0 10 90 0 0 | ||
id column.name column.usp.code column.length column.id column.particle.size column.temperature column.flowrate eluent.A.h2o eluent.A.meoh eluent.A.acn eluent.A.iproh eluent.A.acetone eluent.A.hex eluent.A.chcl3 eluent.A.ch2cl2 eluent.A.hept eluent.A.formic eluent.A.formic.unit eluent.A.acetic eluent.A.acetic.unit eluent.A.trifluoroacetic eluent.A.trifluoroacetic.unit eluent.A.phosphor eluent.A.phosphor.unit eluent.A.nh4ac eluent.A.nh4ac.unit eluent.A.nh4form eluent.A.nh4form.unit eluent.A.nh4carb eluent.A.nh4carb.unit eluent.A.nh4bicarb eluent.A.nh4bicarb.unit eluent.A.nh4f eluent.A.nh4f.unit eluent.A.nh4oh eluent.A.nh4oh.unit eluent.A.trieth eluent.A.trieth.unit eluent.A.triprop eluent.A.triprop.unit eluent.A.tribut eluent.A.tribut.unit eluent.A.nndimethylhex eluent.A.nndimethylhex.unit eluent.A.medronic eluent.A.medronic.unit eluent.A.pH eluent.A.heptafluorobutyric eluent.A.heptafluorobutyric.unit eluent.B.h2o eluent.B.meoh eluent.B.acn eluent.B.iproh eluent.B.acetone eluent.B.hex eluent.B.chcl3 eluent.B.ch2cl2 eluent.B.hept eluent.B.formic eluent.B.formic.unit eluent.B.acetic eluent.B.acetic.unit eluent.B.trifluoroacetic eluent.B.trifluoroacetic.unit eluent.B.phosphor eluent.B.phosphor.unit eluent.B.nh4ac eluent.B.nh4ac.unit eluent.B.nh4form eluent.B.nh4form.unit eluent.B.nh4carb eluent.B.nh4carb.unit eluent.B.nh4bicarb eluent.B.nh4bicarb.unit eluent.B.nh4f eluent.B.nh4f.unit eluent.B.nh4oh eluent.B.nh4oh.unit eluent.B.trieth eluent.B.trieth.unit eluent.B.triprop eluent.B.triprop.unit eluent.B.tribut eluent.B.tribut.unit eluent.B.nndimethylhex eluent.B.nndimethylhex.unit eluent.B.medronic eluent.B.medronic.unit eluent.B.pH eluent.B.heptafluorobutyric eluent.B.heptafluorobutyric.unit eluent.C.h2o eluent.C.meoh eluent.C.acn eluent.C.iproh eluent.C.acetone eluent.C.hex eluent.C.chcl3 eluent.C.ch2cl2 eluent.C.hept eluent.C.formic eluent.C.formic.unit eluent.C.acetic eluent.C.acetic.unit eluent.C.trifluoroacetic eluent.C.trifluoroacetic.unit eluent.C.phosphor eluent.C.phosphor.unit eluent.C.nh4ac eluent.C.nh4ac.unit eluent.C.nh4form eluent.C.nh4form.unit eluent.C.nh4carb eluent.C.nh4carb.unit eluent.C.nh4bicarb eluent.C.nh4bicarb.unit eluent.C.nh4f eluent.C.nh4f.unit eluent.C.nh4oh eluent.C.nh4oh.unit eluent.C.trieth eluent.C.trieth.unit eluent.C.triprop eluent.C.triprop.unit eluent.C.tribut eluent.C.tribut.unit eluent.C.nndimethylhex eluent.C.nndimethylhex.unit eluent.C.medronic eluent.C.medronic.unit eluent.C.pH eluent.C.heptafluorobutyric eluent.C.heptafluorobutyric.unit eluent.D.h2o eluent.D.meoh eluent.D.acn eluent.D.iproh eluent.D.acetone eluent.D.hex eluent.D.chcl3 eluent.D.ch2cl2 eluent.D.hept eluent.D.formic eluent.D.formic.unit eluent.D.acetic eluent.D.acetic.unit eluent.D.trifluoroacetic eluent.D.trifluoroacetic.unit eluent.D.phosphor eluent.D.phosphor.unit eluent.D.nh4ac eluent.D.nh4ac.unit eluent.D.nh4form eluent.D.nh4form.unit eluent.D.nh4carb eluent.D.nh4carb.unit eluent.D.nh4bicarb eluent.D.nh4bicarb.unit eluent.D.nh4f eluent.D.nh4f.unit eluent.D.nh4oh eluent.D.nh4oh.unit eluent.D.trieth eluent.D.trieth.unit eluent.D.triprop eluent.D.triprop.unit eluent.D.tribut eluent.D.tribut.unit eluent.D.nndimethylhex eluent.D.nndimethylhex.unit eluent.D.medronic eluent.D.medronic.unit eluent.D.pH eluent.D.heptafluorobutyric eluent.D.heptafluorobutyric.unit gradient.start.A gradient.start.B gradient.start.C gradient.start.D gradient.end.A gradient.end.B gradient.end.C gradient.end.D eluent.A.h2o.unit eluent.A.acn.unit eluent.B.h2o.unit eluent.B.acn.unit | ||
0437 Agilent ZORBAX 300 SB-C18 L1 150.0 1.0 3.5 100 0 0 0 0 0 0 0 0 0.0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0.01 % 0 0 100 0 0 0 0 0 0 0.0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0.01 % 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 100 0 0 0 10 90 0 0 % % % % |
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@@ -1,15 +1,28 @@ | ||
id: '0437' | ||
column: | ||
name: Agilent ZORBAX 300 SB-C18 | ||
usp.code: 1 | ||
usp.code: L1 | ||
length: 150 | ||
id: 1 | ||
particle.size: 3.5 | ||
temperature: -1 | ||
flowrate: -1 | ||
t0: -0.075 | ||
eluent: | ||
A: | ||
h2o: 100 | ||
heptafluorobutyric: | ||
value: 0.01 | ||
unit: '%' | ||
h2o: | ||
value: 100 | ||
unit: '%' | ||
acn: | ||
value: 0 | ||
unit: '%' | ||
B: | ||
acn: 100 | ||
heptafluorobutyric: | ||
value: 0.01 | ||
unit: '%' | ||
h2o: | ||
value: 0 | ||
unit: '%' | ||
acn: | ||
value: 100 | ||
unit: '%' |
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id authors name url | ||
0431 Jian Guo, Tao Huan ROASMI_08 10.1021/acs.analchem.9b05135 | ||
id authors name url source method.type | ||
0431 Jian Guo, Tao Huan ROASMI_08 10.1021/acs.analchem.9b05135 Publication - Guo RP |
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id authors name url | ||
0432 Tobias Bruderer , Emmanuel Varesio , Gérard Hopfgartner ROASMI_65 10.1016/j.jchromb.2017.07.016. | ||
id authors name url source method.type | ||
0432 Tobias Bruderer, Emmanuel Varesio, Gérard Hopfgartner ROASMI_65 10.1016/j.jchromb.2017.07.016 Publication - Bruderer RP |
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id authors name url comment | ||
0433 Tobias Bruderer , Emmanuel Varesio , Gérard Hopfgartner ROASMI_66 10.1016/j.jchromb.2017.07.016. mobile phase A was 5 mM ammonium formate in water with an adjusted pH of 3.0 by the addition of formic acid., Submitted by Fangyuan Sun | ||
id authors name url comment source method.type | ||
0433 Tobias Bruderer, Emmanuel Varesio, Gérard Hopfgartner ROASMI_66 10.1016/j.jchromb.2017.07.016 mobile phase A was 5 mM ammonium formate in water with an adjusted pH of 3.0 by the addition of formic acid., Submitted by Fangyuan Sun Publication - Bruderer RP |
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@@ -1,2 +1,2 @@ | ||
id authors name url comment | ||
0434 Tobias Bruderer , Emmanuel Varesio , Gérard Hopfgartner ROASMI_71 10.1016/j.jchromb.2017.07.016. mobile phase A was 5 mM ammonium formate in water with an adjusted pH of 3.0 by the addition of formic acid, Submitted by Tobias Bruderer , Emmanuel Varesio , Gérard Hopfgartner | ||
id authors name url comment source method.type | ||
0434 Tobias Bruderer, Emmanuel Varesio, Gérard Hopfgartner ROASMI_71 10.1016/j.jchromb.2017.07.016 mobile phase A was 5 mM ammonium formate in water with an adjusted pH of 3.0 by the addition of formic acid, Submitted by Fangyuan Sun Publication - Bruderer RP |
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@@ -1,2 +1,2 @@ | ||
id authors name url comment | ||
0435 Tobias Bruderer , Emmanuel Varesio , Gérard Hopfgartner ROASMI_77 10.1016/j.jchromb.2017.07.016. Mobile A was 5 mM ammonium acetate in water with an adjusted pH of 8.0 by the addition of ammonium hydroxide., Submitted by Fangyuan Sun | ||
id authors name url comment source method.type | ||
0435 Tobias Bruderer, Emmanuel Varesio, Gérard Hopfgartner ROASMI_77 10.1016/j.jchromb.2017.07.016 Mobile A was 5 mM ammonium acetate in water with an adjusted pH of 8.0 by the addition of ammonium hydroxide, Submitted by Fangyuan Sun Publication - Bruderer RP |
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@@ -1,2 +1,2 @@ | ||
id authors name comment url | ||
0436 Pablo Gago-Ferrero, Anna A. Bletsou, Dimitrios E. Damalas, Reza Aalizadeh, Nikiforos A.Alygizakis, Heinz P.Singer, Juliane Hollender, Nikolaos S. Thomaidis ROASMI_85 flow rate:0.2-0.48, Submitted by Fangyuan Sun 10.1016/j.jhazmat.2019.121712 | ||
id authors name comment url source method.type | ||
0436 Pablo Gago-Ferrero, Anna A. Bletsou, Dimitrios E. Damalas, Reza Aalizadeh, Nikiforos A.Alygizakis, Heinz P.Singer, Juliane Hollender, Nikolaos S. Thomaidis ROASMI_85 flow rate:0.2-0.48, Submitted by Fangyuan Sun 10.1016/j.jhazmat.2019.121712 Publication - Gago-Ferrero RP |
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Original file line number | Diff line number | Diff line change |
---|---|---|
@@ -1,3 +1,3 @@ | ||
t [min] flow rate [ml/min] A [%] B [%] | ||
0 -1 100 0 | ||
100 -1 10 90 | ||
0 100 0 | ||
100 10 90 |
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@@ -1,2 +1,2 @@ | ||
id authors name url | ||
0437 L. Mark Hall, Dennis W. Hill, Kelly Bugden, Shannon Cawley, Lowell H. Hall, Ming-Hui Chen, David F. Grant ROASMI_86 10.1021/acs.jcim.7b00496 | ||
id authors name url source method.type | ||
0437 L. Mark Hall, Dennis W. Hill, Kelly Bugden, Shannon Cawley, Lowell H. Hall, Ming-Hui Chen, David F. Grant ROASMI_86 10.1021/acs.jcim.7b00496 Publication - Hall RP |
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