8.52003

Fmoc-Ala-OH

Novabiochem^®

• Synonym(e): N-α-Fmoc-L-alanine monohydrate
• Empirische Formel (Hill-System): C₁₈H₁₇NO₄
• CAS-Nummer: 35661-39-3
• Molekulargewicht: 311.33
• MDL-Nummer: MFCD00037139
• UNSPSC-Code: 12352209
• EG-Index-Nummer: 252-660-6
• NACRES: NA.22

Eigenschaften

• Qualitätsniveau: 400
• Produktlinie: Novabiochem^®
• Assay: ≥93.0% (acidimetric); ≥98% (TLC); ≥99.0% (HPLC)
• Form: powder
• Eignung der Reaktion: reaction type: Fmoc solid-phase peptide synthesis
• Hersteller/Markenname: Novabiochem^®
• mp (Schmelzpunkt): 140-150 °C
• Anwendung(en): peptide synthesis
• Funktionelle Gruppe: Fmoc
• Lagertemp.: 2-30°C
• 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)
• InChIKey: QWXZOFZKSQXPDC-UHFFFAOYSA-N

Beschreibung

Allgemeine Beschreibung

High purity Fmoc-protected amino acid for research and process production of peptides, with very low levels of dipeptide, free-amino acids and acetic acid impurities.
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

Anwendung

• 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).

Verlinkung

Replaces: 04-12-1006

Hinweis zur Analyse

Farbe (visuell): weiß bis fast weiß
Aussehen der Substanz (visuell): Pulver
Farbzahl (0,5 M in DMF): ≤ 150 Hazen
Identität (IR): entspricht
Enantiomerenreinheit: ≥ 99.8 % (a/a)
Reinheit (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)
Gehalt an freier Aminosäure (GC): ≤ 0.2 %
Reinheit (DC(011A)): ≥ 98 %
Reinheit (DC(0811)): ≥ 98 %
Löslichkeit (25 mmol in 50 ml DMF): klar löslich
Gehalt (acidimetrisch): ≥ 93.0 %
Wasser (K. F.): ≤ 6.0 %
Ethylacetat (HS-GC): ≤ 0.5 %
Acetat (IC): ≤ 0.02 %
DC-Bedingungen gemäß den Angaben unseres Hauptkataloges

Rechtliche Hinweise

Novabiochem is a registered trademark of Merck KGaA, Darmstadt, Germany

Sicherheitshinweise

• Lagerklassenschlüssel: 11 - Combustible Solids
• WGK: WGK 3
• Flammpunkt (°F): Not applicable
• Flammpunkt (°C): Not applicable