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Catalog Number:
30476
CAS Number:
349547-09-7
Ácido ( R )-4-(Fmoc-amino)-3-(Z-amino)butírico
Purity:
98 - 101% (Ensayo por titulación)
Synonym(s):
ZL-Dbu(Fmoc)-OH, Ácido N b-Z- N g-Fmoc-R-diaminobutírico
Documents
$120.58 /100 mg
Tamaño
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Product Information

(R)-4-(Fmoc-amino)-3-(Z-amino)butyric acid is a versatile compound widely utilized in peptide synthesis and pharmaceutical research. This amino acid derivative features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amino groups during solid-phase peptide synthesis. Its unique structure allows for the efficient coupling of amino acids, making it an invaluable tool for researchers focused on developing novel peptides and therapeutic agents. The compound's stability and compatibility with various coupling reagents enhance its appeal in the synthesis of complex peptide sequences, facilitating advancements in drug development and biochemistry.

In addition to its role in peptide synthesis, (R)-4-(Fmoc-amino)-3-(Z-amino)butyric acid is also explored for its potential applications in the development of biomaterials and drug delivery systems. Its ability to form stable conjugates with other biomolecules opens avenues for targeted therapies and improved drug efficacy. Researchers appreciate its ease of use and the high purity levels achievable, which are critical for successful experimental outcomes. This compound stands out for its reliability and effectiveness in both academic and industrial settings, making it a preferred choice for professionals in the field.

Synonyms
ZL-Dbu(Fmoc)-OH, Ácido N b-Z- N g-Fmoc-R-diaminobutírico
CAS Number
349547-09-7
Purity
98 - 101% (Ensayo por titulación)
Molecular Formula
C27H26N2O6
Molecular Weight
474.5
MDL Number
MFCD03788647
PubChem ID
3337413
Melting Point
170 - 180 ?C
Appearance
Polvo cristalino blanco
Optical Rotation
[a] D 20 = 6,5 - 8,0 º (C=1 en DMF)
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
ZL-Dbu(Fmoc)-OH, Ácido N b-Z- N g-Fmoc-R-diaminobutírico
CAS Number
349547-09-7
Purity
98 - 101% (Ensayo por titulación)
Molecular Formula
C27H26N2O6
Molecular Weight
474.5
MDL Number
MFCD03788647
PubChem ID
3337413
Melting Point
170 - 180 ?C
Appearance
Polvo cristalino blanco
Optical Rotation
[a] D 20 = 6,5 - 8,0 º (C=1 en DMF)
Conditions
Conservar entre 0 y 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)-4-(Fmoc-amino)-3-(Z-amino)butyric acid is widely utilized in research focused on

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in solid-phase peptide synthesis, allowing for the creation of complex peptide sequences efficiently.
  • Drug Development: It plays a significant role in pharmaceutical research, particularly in the development of peptide-based drugs, where its structure can enhance bioavailability and efficacy.
  • Bioconjugation: The compound is used in bioconjugation processes, facilitating the attachment of biomolecules to surfaces or other molecules, which is crucial in creating targeted therapies and diagnostics.
  • Research in Neuroscience: Its derivatives are explored in neuroscience for studying neuropeptides, helping researchers understand signaling pathways and potential therapeutic targets for neurological disorders.
  • Custom Synthesis Services: Many chemical suppliers offer custom synthesis services for this compound, allowing researchers to obtain tailored derivatives that meet specific experimental needs, enhancing research flexibility.

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