Specification
Description
N-(Fmoc-8-amino-3,6-dioxa-octyl)succinamic acid is a synthetic molecule that belongs to the group of succinamic acids. Succinamic acids are organic molecules that have two carboxylic acid groups and an amide group linked to a cyclic structure. N-(Fmoc-8-amino-3,6-dioxa-octyl)succinamic acid is a modified succinamic acid that has an Fmoc (9-fluorenylmethyloxycarbonyl) protecting group attached to the amino group.
The Fmoc group protects the amino group during synthesis, and it can be removed under mild conditions to expose the amino group for further functionalization. This property makes N-(Fmoc-8-amino-3,6-dioxa-octyl)succinamic acid a valuable building block for the synthesis of other molecules, such as peptides and proteins.
Synonyms
N-(Fmoc-8-amino-3,6-dioxa-octyl)succinamic acid, 1-(9H-Fluoren-9-yl)-3,14-dioxo-2,7,10-trioxa-4,13-diazaheptadecan-17-oic acid, Fmoc-PEG-SU
IUPAC Name
4-[2-[2-[2-(9H-fluoren-9-ylmethoxycarbonylamino)ethoxy]ethoxy]ethylamino]-4-oxobutanoic acid
Canonical SMILES
C1=CC=C2C(=C1)C(C3=CC=CC=C32)COC(=O)NCCOCCOCCNC(=O)CCC(=O)O
InChI
1S/C25H30N2O7/c28-23(9-10-24(29)30)26-11-13-32-15-16-33-14-12-27-25(31)34-17-22-20-7-3-1-5-18(20)19-6-2-4-8-21(19)22/h1-8,22H,9-17H2,(H,26,28)(H,27,31)(H,29,30)
InChI Key
OVPIGBISTJOKKI-UHFFFAOYSA-N
Application
N-(Fmoc-8-amino-3,6-dioxa-octyl)succinamic acid has various applications in scientific experiments, particularly in the synthesis of peptides and proteins. The molecule can be used as a building block for the preparation of various peptides and proteins, such as Fmoc-protected peptides, hydrogels, and bioconjugates.
Storage Temperature
Dry, dark and at 0-4 ℃ for short term (days to weeks) or -20 ℃ for long term (months to years).
Type
Unusual Amino Acids, Pegylated Amino Acids & Special Linkers