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Catalog Number:
28833
CAS Number:
211682-15-4
(R)-3-(Fmoc-amino)-2-methylpropionic acid
Purity:
≥ 99% (HPLC)
Synonym(s):
Fmoc-(R)-ampa-OH
Documents
$90.00 /25MG
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Product Information

(R)-3-(Fmoc-amino)-2-methylpropionic acid is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound, known for its protective Fmoc (9-fluorenylmethyloxycarbonyl) group, allows for efficient coupling reactions while safeguarding the amino group during synthesis. Its unique structure not only enhances the stability of peptides but also facilitates the introduction of various functional groups, making it an essential building block in the design of bioactive molecules. Researchers and industry professionals appreciate its role in developing therapeutic peptides, particularly in the fields of pharmaceuticals and biotechnology, where precision and reliability are paramount.

The compound's ability to streamline the synthesis process while maintaining high purity levels sets it apart from similar amino acid derivatives. Its applications extend to the creation of peptide-based drugs, where the incorporation of (R)-3-(Fmoc-amino)-2-methylpropionic acid can lead to improved efficacy and bioavailability. With its favorable properties, this compound is an excellent choice for those looking to enhance their peptide synthesis protocols and achieve superior results in their research and development efforts.

Synonyms
Fmoc-(R)-ampa-OH
CAS Number
211682-15-4
Purity
≥ 99% (HPLC)
Molecular Formula
C19H19NO4
Molecular Weight
325.36
MDL Number
MFCD04040043
PubChem ID
3637390
Appearance
White powder
Optical Rotation
[a]D20 = -10 ± 2 º (C=1 in DMF)
Conditions
Store at 0-8°C
General Information
Synonyms
Fmoc-(R)-ampa-OH
CAS Number
211682-15-4
Purity
≥ 99% (HPLC)
Molecular Formula
C19H19NO4
Molecular Weight
325.36
MDL Number
MFCD04040043
PubChem ID
3637390
Appearance
White powder
Optical Rotation
[a]D20 = -10 ± 2 º (C=1 in DMF)
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(R)-3-(Fmoc-amino)-2-methylpropionic acid is widely utilized in research focused on

  • Peptide Synthesis: This compound is commonly used as a building block in solid-phase peptide synthesis, allowing researchers to create complex peptides efficiently.
  • Drug Development: Its role in modifying peptide structures makes it valuable in pharmaceutical research, particularly in developing new therapeutics targeting specific diseases.
  • Bioconjugation: The chemical's reactive groups facilitate the attachment of peptides to other biomolecules, enhancing the development of targeted drug delivery systems.
  • Research in Neuroscience: It is used in the synthesis of neuropeptides, which are crucial for studying neurological functions and disorders.
  • Custom Synthesis Services: Many chemical suppliers offer custom synthesis of this compound, providing researchers with tailored solutions for their specific experimental needs.

Citations