FMOC-ALA-ALA-OH Chemical Properties

Melting point:

175-179℃ (ethyl acetate hexane )

Boiling point:

674.2±45.0 °C(Predicted)

Density 

1.280±0.06 g/cm3(Predicted)

storage temp. 

Sealed in dry,2-8°C

form 

solid

pka

3.49±0.10(Predicted)

color 

White

Safety Information

HS Code 

2924297099

FMOC-ALA-ALA-OH Usage And Synthesis

Description

Fmoc-Ala-Ala-OH is a Fmoc-protected alanine derivative for use in proteomics research and solid-phase peptide synthesis techniques. Alanine is one of the simplest amino acids with a methyl side chain. This small side chain is highly flexible (second only to glycine) for incorporation into peptide chains. The Fmoc group is usually removed with a base such as pyridine, a deprotection strategy orthogonal to the acidic Labilie Boc group. It consists of two L-alanine molecules linked together by a peptide bond, with a protecting group (Fmoc) attached to the N-terminal amino acid. The Fmoc group provides stability and protection during peptide synthesis, and can be easily removed, exposing the free amino group for further reactions.

Uses

Fmoc-Ala-Ala-OH is a self-assemble fluorenylmethoxycarbonyl-dipeptide, which is a smaller amphiphilic building blocks consists dipeptides linked to fluore nylmethoxycarbonyl (Fmoc). Fmoc-Ala-Ala-OH can be used as scaffold materials in 3D cell culture.

FMOC-ALA-ALA-OH(87512-31-0)Related Product Information

• β-Alanine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-N-(2-methoxyethyl)-
• β-Alanine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-N-(2-hydroxyethyl)-
• Fmoc-Pro-Pro-OH
• FMOC-ALA-ALA-OH
• Azepino[3,2,1-hi]indole-2-carboxylicacid,1,2,4,5,6,7-hexahydro-5-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-4-oxo-,(2S,9S)-(9CI)
• FMOC-ILE-PRO-OH
• FMOC-PHE-SER(TBU)-OH
• FMOC-LYS(BOC)-LEU-OH
• FMOC-VAL-PRO-OH
• FMOC-LEU-PRO-OH
• FMOC-PRO-PHE-OH
• FMOC-PHE-PRO-OH
• FMOC-SER(TBU)-THR(TBU)-OH
• FMOC-ALA-PRO-OH
• FMOC-NLE-NLE-OH
• FMOC-PHE-PHE-OH
• FMOC-PHE-ARG-OH
• FMOC-LEU-LEU-OH