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Catalog Number:
29718
CAS Number:
1217603-41-2
( S -Fmoc-β-hidroxi-valina
Purity:
≥ 99 % (HPLC)
Synonym(s):
(Ácido S -Fmoc-2-amino-3-hidroxi-3-metil-butírico, ( S -Fmoc-β,β-dimetil-serina
Documents
$100.05 /100 mg
Tamaño
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Product Information

(S)-Fmoc-b-hydroxy-valine is a valuable amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amino groups during the synthesis of complex peptides. Its unique structure not only enhances the stability of the amino acid during reactions but also facilitates the formation of peptides with improved solubility and bioavailability. Researchers and industry professionals appreciate its role in the synthesis of therapeutic peptides, particularly in the development of pharmaceuticals targeting various diseases.

In addition to its application in peptide synthesis, (S)-Fmoc-b-hydroxy-valine is also recognized for its potential in the creation of novel biomaterials and drug delivery systems. Its ability to form stable conjugates with other molecules makes it an attractive candidate for enhancing the efficacy of drug formulations. The compound's favorable properties, such as its solubility and compatibility with various solvents, further support its use in diverse research applications, making it a go-to choice for chemists and biochemists alike.

Synonyms
(Ácido S -Fmoc-2-amino-3-hidroxi-3-metil-butírico, ( S -Fmoc-β,β-dimetil-serina
CAS Number
1217603-41-2
Purity
≥ 99 % (HPLC)
Molecular Formula
C20H21Nº 5
Molecular Weight
355.39
MDL Number
MFCD04974410
PubChem ID
46737422
Appearance
Polvo blanco
Optical Rotation
[a] D 20 = -16 ± 2º (C=1 en DMF)
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
(Ácido S -Fmoc-2-amino-3-hidroxi-3-metil-butírico, ( S -Fmoc-β,β-dimetil-serina
CAS Number
1217603-41-2
Purity
≥ 99 % (HPLC)
Molecular Formula
C20H21Nº 5
Molecular Weight
355.39
MDL Number
MFCD04974410
PubChem ID
46737422
Appearance
Polvo blanco
Optical Rotation
[a] D 20 = -16 ± 2º (C=1 en DMF)
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(S)-Fmoc-b-hydroxy-valine 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 structures with high purity.
  • Drug Development: Its unique properties make it valuable in the pharmaceutical industry for developing new drugs, especially in the design of peptide-based therapeutics that target specific biological pathways.
  • Bioconjugation: The compound is used in bioconjugation processes, enabling the attachment of biomolecules to surfaces or other molecules, which is essential in creating targeted drug delivery systems.
  • Research in Protein Engineering: It plays a significant role in protein engineering, helping researchers modify proteins to enhance their stability and activity, which is crucial for various biotechnological applications.
  • Analytical Chemistry: This chemical is also utilized in analytical chemistry for the development of new methods to analyze complex biological samples, improving the accuracy and efficiency of biochemical assays.

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