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Catalog Number:
08090
CAS Number:
106864-37-3
Fmoc-O-sulfo-L-tyrosine sodium salt
Purity:
≥ 99% (HPLC)
Synonym(s):
Fmoc-L-Tyr(SO3H)-OH·sodium salt
Documents
$202.60 /100MG
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Product Information

Fmoc-O-sulfo-L-tyrosine sodium salt is a versatile and valuable compound widely utilized in peptide synthesis and bioconjugation applications. This compound features a unique Fmoc (9-fluorenylmethoxycarbonyl) protecting group, which facilitates the selective protection of amino acids during the synthesis of peptides. Its sulfonate group enhances solubility in aqueous solutions, making it particularly advantageous for researchers working in biological contexts. The compound is essential for the development of peptide-based therapeutics and can be employed in the design of novel biomolecules, such as targeted drug delivery systems and enzyme inhibitors.

Moreover, Fmoc-O-sulfo-L-tyrosine sodium salt is recognized for its role in the synthesis of modified peptides that can interact with specific receptors, thereby advancing research in drug discovery and development. Its unique properties allow for improved stability and bioactivity of peptide constructs, making it a preferred choice among professionals in pharmaceutical and biochemical research. This compound not only streamlines the synthesis process but also enhances the overall efficacy of peptide-based applications.

Synonyms
Fmoc-L-Tyr(SO3H)-OH·sodium salt
CAS Number
106864-37-3
Purity
≥ 99% (HPLC)
Molecular Formula
C24H20NNaO8S
Molecular Weight
505.48
MDL Number
MFCD00077078
PubChem ID
76419956
Appearance
White powder
Conditions
Store at 0-8 °C
General Information
Synonyms
Fmoc-L-Tyr(SO3H)-OH·sodium salt
CAS Number
106864-37-3
Purity
≥ 99% (HPLC)
Molecular Formula
C24H20NNaO8S
Molecular Weight
505.48
MDL Number
MFCD00077078
PubChem ID
76419956
Appearance
White powder
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

Fmoc-O-sulfo-L-tyrosine sodium salt 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 (SPPS), allowing for the incorporation of sulfonic acid groups that enhance solubility and stability.
  • Drug Development: It plays a crucial role in the development of pharmaceuticals by modifying the properties of peptides, improving their bioavailability and therapeutic efficacy.
  • Bioconjugation: The sulfonic acid group facilitates bioconjugation reactions, enabling the attachment of peptides to various biomolecules, which is essential in creating targeted drug delivery systems.
  • Research in Neuroscience: Used in studies involving neurotransmitter pathways, this compound can help in understanding the role of modified tyrosine residues in signaling processes.
  • Diagnostic Applications: It can be utilized in the development of diagnostic assays, where the modified peptides can act as specific biomarkers for various diseases.

Citations