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Code Name Synonym
FM-006 Fmoc-ACBC 1-(Fmoc-amino)cyclobutyl-1-carboxylic acid
CAS 885951-77-9 /upload/more_svg/small/small_FM-006.svg
Formula C20H19NO4
MW 337.4
Purity >99%
Storage +2 ... +8 °C
Note Fmoc-ACBC is used in the synthesis of modified peptides and peptidomimetics. JACS (2013), 135(2), 669-682. DOI:10.1021/ja306028q; DOI:10.1021/jm3015298;  J. Med. Chem. (2018), 61(9), 4263-4269. DOI:10.1021/acs.jmedchem.8b00488.
Specification Link
Code Name Synonym
FM-007 Fmoc-ACPA 1-(Fmoc-aminomethyl)cyclopropyl-1-carboxylic acid
CAS 1263045-62-0 /upload/more_svg/small/small_FM-007.svg
Formula C20H19NO4
MW 337.4
Purity >99%
Storage +2 ... +8 °C
Specification Link
Code Name Synonym
FM-008 Fmoc-ACPC 1-(Fmoc-amino)cyclopropane-1-carboxylic acid
CAS 126705-22-4 /upload/more_svg/small/small_FM-008.svg
Formula C19H17NO4
MW 323.3
Purity >99%
Storage +2 ... +8 °C
Specification Link
Code Name Synonym
FM-229 Fmoc-MeACPC 1-​[[(9H-​fluoren-​9-​ylmethoxy)​carbonyl]​methylamino]​-Cyclopropanecarboxyl​ic acid
CAS 1702888-95-6 /upload/more_svg/small/small_fm-229.svg
Formula C20H19NO4
MW 337.4
Purity >99%
Storage +2 ... +8 °C
Note Used in solid phase peptide synthesis as an N-Methylated ACPC analogue. J. Med. Chem. (2018), 61(8), 3745-3751. DOI:10.1021/acs.jmedchem.8b00336.
Code Name Synonym
FM-122 Fmoc-AEA Fmoc-5-amino-3-oxapentanoic acid
CAS 260367-12-2 /upload/more_svg/small/small_FM-122.svg
Formula C19H19NO5
MW 341.4
Purity >98%
Storage +2 ... +8 °C
Note Fmoc-AEA is used as a linker in solid-phase peptide synthesis and in other applications. Angew. Chem. Int. Ed. (2013), 52(1), 325-330. DOI:10.1002/anie.201205721; J. Am. Chem. Soc. (2013), 135(46), 17488-17493. DOI:10.1021/ja408788t; J. Biol. Chem. (2017), 292(11), 4556-4570. DOI:10.1074/jbc.M116.768853; Chem. Comm. (2017), 53(24), 3477-3480. DOI:10.1039/C7CC00931C.
Specification Link
Code Name Synonym
FM-005 Fmoc-AEEA [2-[2-(Fmoc-amino)ethoxy]ethoxy]acetic acid // Fmoc-8-amino-3,6-dioxaoctanoic acid // Fmoc-O2Oc // Fmoc-Ado // Fmoc-Adoa // Fmoc-Doc
CAS 166108-71-0 /upload/more_svg/small/small_FM-005.svg
Formula C21H23NO6
MW 385.4
Purity >99%
Storage +2 ... +8 °C
Note Fmoc-AEEA is used as a linker in various applications. JACS (2011), 133(35), 14098-14108. DOI:10.1021/ja205235m;ACIEE (2009), 48(41), 7695-7700,  DOI:10.1002/anie.200903328; JACS (2018), 140(7), 2426-2429. DOI:10.1021/jacs.7b13275; ACS Chemical Biology (2018), 13(1), 53-59. DOI:10.1021/acschembio.7b00852.
Code Name Synonym
FM-127 Fmoc-AEEA-OPfp [2-[2-(Fmoc-amino)ethoxy]ethoxy]acetic acid pentafluorophenyl ester // Fmoc-8-amino-3,6-dioxaoctanoic acid pentafluorophenyl ester // Fmoc-O2Oc-OPfp // Fmoc-Ado-OPfp // Fmoc-Adoa-OPfp
CAS 1263044-39-8 /upload/more_svg/small/small_FM-127.svg
Formula C27H22F5NO6
MW 551.5
Purity >99%
Storage -15 ... -25 °C
Note Crystalline substance
Code Name Synonym
FM-129 Fmoc-AEEA-AEEA Fmoc-Ado-Ado // Fmoc-O2Oc-O2Oc // Fmoc-8-amino-3,6-dioxaoctanoyl-8-amino-3,6-dioxaoctanoic acid // Fmoc-Adoa-Adoa
CAS 560088-89-3 /upload/more_svg/small/small_FM-129.svg
Formula C27H34N2O9
MW 530.6
Purity >97.5%
Storage -15 ... -25 °C
Note Fmoc-AEEA-AEEA is used to acylate Lysine side-chain in Insulin and other peptides to increase clearance time and protease resistance of peptides in vivo. PCT Int. Appl. (2009), WO 2009115469 A1. This compound is also used as a linker. WO 2006097537 A2.
Specification Link
Code Name Synonym
FM-217 Fmoc-AEEEP Fmoc-12-amino-4,7,10-trioxadodecanoic acid // 1-(9H-fluoren-9-yl)-3-oxo-2,7,10,13-tetraoxa-4-azahexadecan-16-oic acid // alpha-Fmoc-amino-tri(ethylene glycol)-omega-carboxylic acid // 3-(2-(2-(2-(Fmoc-amino)-ethoxy)ethoxy)ethoxy)propanoic acid // Fmoc-AEEEP // Fmoc-NH-PEG(3)-COOH
CAS 867062-95-1 /upload/more_svg/small/small_fm-217.svg
Formula C24H29NO7
MW 443.5
Purity >98%
Storage +2 ... +8 °C
Code Name Synonym
FM-169 Fmoc-AEEP Fmoc-9-Amino-4,7-Dioxanonanoic acid // Fmoc-3-(2-(2-aminoethoxy)ethoxy)propanoic acid
CAS 872679-70-4 /upload/more_svg/small/small_FM-169.svg
Formula C22H25NO6
MW 399.4
Purity >99%
Storage +2 ... +8 °C
Note Fmoc-AEEP is used as a linker in various applications. Nature Chemistry (2013), 5(4), 282-292. DOI:10.1038/nchem.1577; DOI:10.1002/anie.201402831; Org. Biomol. Chem. (2018), Advance Article, DOI:10.1039/c8ob01212a.

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