9-Fluorenylmethoxycarbonyl (Fmoc) protected amino acid derivatives and Rink amide 4-methylbenzhydrylamine (Rink amide MBHA) resin were purchased from IRIS Biotech GmbH (Marktredwitz, Germany). The reagents for synthesis were N,N’-diisopropylcabodiimide (DIC), N,N-diisopropyl-ethylamine (DIEA), 1-hydroxybenzotriazole (HOBt), 1,8-diazabicyclo-[5.4.0]undec-7-ene (DBU), piperidine, thioanisol, phenol, 1,2-ethanedithiol, 5(6)-carboxyfluorescein (Cf), and they were purchased from Sigma-Aldrich (Budapest, Hungary). Trifluoroacetic acid (TFA) and solvents (N,N-dimethylformamide (DMF) and dichloromethane) (DCM)) for synthesis, as well as HPLC grade acetonitrile, were obtained from Molar Chemicals (Halásztelek, Hungary). Cf-Penetratin was provided by Kata Horváti (MTA-ELTE Research Group of Peptide Chemistry; Eötvös Loránd University, Institute of Chemistry) [17 (link),18 (link)].
9 fluorenylmethoxycarbonyl fmoc protected amino acid derivatives
Manufactured by Iris Biotech
Sourced in Germany
9-Fluorenylmethoxycarbonyl (Fmoc) protected amino acid derivatives are common building blocks used in solid-phase peptide synthesis. They provide a reversible amino protecting group that allows for the sequential coupling of amino acids to form peptides.
Automatically generated - may contain errors
Lab products found in correlation
Rink amide 4 methylbenzhydrylamine rink amide mbha resin, by Iris Biotech (2 mentions)
Trifluoroacetic acid tfa and solvents, by Molar Chemicals (2 mentions)
N n dimethylformamide dmf and dichloromethane dcm for synthesis, by Molar Chemicals (2 mentions)
Hplc grade acetonitrile, by Molar Chemicals (2 mentions)
1 hydroxybenzotriazole, by Merck Group (2 mentions)
5 6 carboxyfluorescein, by Merck Group (2 mentions)
Phenol, by Merck Group (1 mentions)
Piperidine, by Merck Group (1 mentions)
N n diisopropylethylamine, by Merck Group (1 mentions)
1 2 ethanedithiol, by Merck Group (1 mentions)
1 8 diazabicyclo 5.4.0 undec 7 ene dbu, by Merck Group (1 mentions)
Thioanisol, by Merck Group (1 mentions)
Triisopropylsilane, by Merck Group (1 mentions)
N diisopropylethylamine, by Merck Group (1 mentions)
2 protocols using 9 fluorenylmethoxycarbonyl fmoc protected amino acid derivatives
1
Synthesis of Fluorescent Peptide Conjugates
2
Synthesis of Fluorescent Peptides
Check if the same lab product or an alternative is used in the 5 most similar protocols
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9-Fluorenylmethoxycarbonyl (Fmoc) protected amino acid derivatives and Rink amide 4-methylbenzhydrylamine (Rink amide MBHA) resin were purchased from IRIS Biotech GmbH (Marktredwitz, Germany). The reagents for synthesis were N,N’-diisopropylcabodiimide (DIC), N-diisopropyl-ethylamine (DIEA), 1-hydroxybenzotriazole (HOBt), 1,8-diazabicyclo-[5.4.0]undec-7-ene (DBU), piperidine, triisopropylsilane (TIS), and 5(6)-carboxyfluorescein (CF), and they were purchased from Sigma Aldrich (Budapest, Hungary). Trifluoroacetic acid (TFA) and solvents (N,N-dimethylformamide (DMF) and dichloromethane) (DCM)) for synthesis, as well as HPLC grade acetonitrile, were obtained from Molar Chemicals (Halásztelek, Hungary).
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