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Catalog Number:
15041
CAS Number:
1014018-33-7
Acide Fmoc-( R -4-amino-6-méthylthiohexanoïque
Purity:
≥ 98 % (HPLC)
Synonym(s):
Acide Fmoc-( R -4-amino-6-méthylthio-hexanoïque
Documents
$100.05 /100 mg
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Product Information

Fmoc-(R)-4-amino-6-methylthiohexanoic acid is a valuable compound widely utilized in peptide synthesis and drug development. This amino acid derivative features a 9-fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amino groups during solid-phase peptide synthesis. Its unique structure, characterized by a methylthio group, enhances its reactivity and compatibility with various coupling reagents, making it an excellent choice for researchers focused on synthesizing complex peptides and biologically active compounds.

This compound is particularly beneficial in the pharmaceutical industry, where it plays a crucial role in the development of peptide-based therapeutics. Its ability to facilitate the formation of peptide bonds while maintaining stability under various reaction conditions allows for the efficient assembly of peptides with specific biological functions. Researchers appreciate its high purity and reliability, which contribute to successful outcomes in peptide synthesis projects. With its practical applications and unique properties, Fmoc-(R)-4-amino-6-methylthiohexanoic acid stands out as a key reagent for advancing peptide chemistry.

Synonyms
Acide Fmoc-( R -4-amino-6-méthylthio-hexanoïque
CAS Number
1014018-33-7
Purity
≥ 98 % (HPLC)
Molecular Formula
C 22 H 25 NON 4 S
Molecular Weight
399.5
MDL Number
MFCD05663765
Melting Point
119-126 °C
Appearance
Poudre blanche amorphe
Optical Rotation
[a] = -3 ± 2º (C=1 dans DMF)
Conditions
Conserver à 0-8°C
General Information
Synonyms
Acide Fmoc-( R -4-amino-6-méthylthio-hexanoïque
CAS Number
1014018-33-7
Purity
≥ 98 % (HPLC)
Molecular Formula
C 22 H 25 NON 4 S
Molecular Weight
399.5
MDL Number
MFCD05663765
Melting Point
119-126 °C
Appearance
Poudre blanche amorphe
Optical Rotation
[a] = -3 ± 2º (C=1 dans DMF)
Conditions
Conserver à 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Fmoc-(R)-4-amino-6-methylthiohexanoic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in solid-phase peptide synthesis, allowing researchers to create complex peptides efficiently.
  • Drug Development: Its unique structure aids in the design of peptide-based drugs, particularly in targeting specific biological pathways, enhancing therapeutic efficacy.
  • Bioconjugation: The chemical is used in bioconjugation processes, linking peptides to other molecules, which is crucial in developing targeted drug delivery systems.
  • Research in Neuroscience: It plays a role in synthesizing neuropeptides, which are important for studying neurological functions and disorders.
  • Protein Engineering: The compound is valuable in modifying proteins to improve their stability and activity, which is essential in biotechnology applications.

Citations