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Sigma-Aldrich

Fmoc-β-Ala-OH

≥99.0% (HPLC)

Synonym(s):

Fmoc-β-alanine

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About This Item

Empirical Formula (Hill Notation):
C18H17NO4
CAS Number:
35737-10-1
Molecular Weight:
311.33
Beilstein:
2302327
MDL number:
MFCD00063328
UNSPSC Code:
12352209
eCl@ss:
32160406
PubChem Substance ID:
57651023
NACRES:
NA.26

Assay

≥99.0% (HPLC)

form

powder or crystals

reaction suitability

reaction type: Fmoc solid-phase peptide synthesis

mp

142-147 °C

application(s)

peptide synthesis

functional group

Fmoc

storage temp.

2-8°C

SMILES string

OC(=O)CCNC(=O)OCC1c2ccccc2-c3ccccc13

InChI

1S/C18H17NO4/c20-17(21)9-10-19-18(22)23-11-16-14-7-3-1-5-12(14)13-6-2-4-8-15(13)16/h1-8,16H,9-11H2,(H,19,22)(H,20,21)

InChI key

LINBWYYLPWJQHE-UHFFFAOYSA-N

General description

Fmoc-β-Ala-OH also known as Fmoc-β-alanine, is a versatile reagent for solid phase peptide synthesis.

Application

Fmoc-β-Ala-OH is used as a linker to synthesize peptides on a monolithic GMA-EDMA (glycidyl methacrylate-co-ethylene dimethacrylate) matrix via Fmoc solid phase peptide synthesis.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Sofie Trier et al.
European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V, 96, 329-337 (2015-09-09)
Acylation of peptide drugs with fatty acid chains has proven beneficial for prolonging systemic circulation, as well as increasing enzymatic stability and interactions with lipid cell membranes. Thus, acylation offers several potential benefits for oral delivery of therapeutic peptides, and

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