8.52003
Fmoc-Ala-OH
Novabiochem®
Synonyme(s) :
Fmoc-Ala-OH, N-α-Fmoc-L-alanine monohydrate
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A propos de cet article
SMILES string
N(C(C)C(=O)O)C(=O)OCC1c2c(cccc2)c3c1cccc3
InChI
1S/C18H17NO4/c1-11(17(20)21)19-18(22)23-10-16-14-8-4-2-6-12(14)13-7-3-5-9-15(13)16/h2-9,11,16H,10H2,1H3,(H,19,22)(H,20,21)
InChI key
QWXZOFZKSQXPDC-UHFFFAOYSA-N
product line
Novabiochem®
assay
≥93.0% (acidimetric), ≥98% (TLC), ≥99.0% (HPLC)
form
powder
reaction suitability
reaction type: Fmoc solid-phase peptide synthesis
manufacturer/tradename
Novabiochem®
mp
140-150 °C
application(s)
peptide synthesis
functional group
Fmoc
storage temp.
2-30°C
Quality Level
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General description
Standard building block for introduction of alanine amino-acid residues by Fmoc SPPS
Associated Protocols and Technical Articles
Fmoc-amino acids for Peptide Production
Cleavage and Deprotection Protocols for Fmoc SPPS
Application
- Interface Passivation of Perovskite Solar Cells by Fmoc-Ala-OH Amino Acids: This study explores the effects of Fmoc-Ala-OH on perovskite solar cells, showing its potential to improve the efficiency and stability of these devices (Song et al., 2023).
- Charge and Sequence Effects on the Self-Assembly and Subsequent Hydrogelation of Fmoc-depsipeptides: Discusses the role of Fmoc-Ala-OH in the self-assembly processes necessary for creating advanced materials, highlighting its utility in material science (Nguyen et al., 2014).
- High-Quality Conjugated Polymers Achieving Ultra-Trace Detection of Cr2O72- in Agricultural Products: Illustrates the application of Fmoc-Ala-OH in the development of sensitive detection systems for environmental monitoring (Li et al., 2022).
- A Liquid-Phase Continuous-Flow Peptide Synthesizer for Preparing C-terminal Free Peptides: Details how Fmoc-Ala-OH is used in innovative peptide synthesis technologies to streamline production processes in pharmaceutical applications (Otake et al., 2023).
- Self-assembled Structures Formed by Fmoc Modified Aliphatic Amino Acids: Examines the use of Fmoc-Ala-OH in the formation of self-assembled structures, which are crucial for developing new materials with tailored properties (Gour et al., 2021).
Analysis Note
Appearance of substance (visual): powder
Colour index (0,5 M in DMF): ≤ 150 Hazen
Identity (IR): passes test
Enantiomeric purity: ≥ 99.8 % (a/a)
Purity (HPLC): ≥ 99.0 % (a/a)
Fmoc-ß-Ala-OH (HPLC): ≤ 0.1 % (a/a)
Fmoc-ß-Ala-Ala-OH (HPLC): ≤ 0.1 % (a/a)
Fmoc-Ala-Ala-OH (HPLC): ≤ 0.1 % (a/a)
Assay free amino acid (GC): ≤ 0.2 %
Purity (TLC(011A)): ≥ 98 %
Purity (TLC(0811)): ≥ 98 %
Solubility (25 mmole in 50 ml DMF): clearly soluble
Assay (acidimetric): ≥ 93.0 %
Water (K. F.): ≤ 6.0 %
Ethyl acetate (HS-GC): ≤ 0.5 %
Acetate (IC): ≤ 0.02 %
To see the solvent systems used for TLC of Novabiochem® products please click here.
Other Notes
Legal Information
Classe de stockage
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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