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Catalog Number:
29657
CAS Number:
159751-46-9, 912354-10-0
S-Fmoc-2-amino-heptanedioic acid-7-tert-butyl ester
Purity:
≥ 98% (HPLC)
Synonym(s):
(S-Fmoc-2-amino-pimelic acid-7-tert-butyl ester
Documents
$208.31 /100MG
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Product Information

(S)-Fmoc-2-amino-heptanedioic acid-7-tert-butyl ester is a versatile compound widely utilized in peptide synthesis and medicinal chemistry. This amino acid derivative features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amines during the synthesis of peptides. Its unique structure not only enhances stability but also facilitates the introduction of various functional groups, making it an invaluable tool for researchers in drug development and biochemistry.

The compound's tert-butyl ester group provides additional hydrophobicity, which can improve solubility and bioavailability in certain applications. Researchers have successfully employed (S)-Fmoc-2-amino-heptanedioic acid-7-tert-butyl ester in the synthesis of complex peptides and bioactive molecules, showcasing its potential in the pharmaceutical industry. Its ability to streamline the synthesis process while maintaining high purity levels makes it a preferred choice for professionals seeking efficiency and reliability in their chemical processes.

Synonyms
(S-Fmoc-2-amino-pimelic acid-7-tert-butyl ester
CAS Number
159751-46-9, 912354-10-0
Purity
≥ 98% (HPLC)
Molecular Formula
C26H31NO6
Molecular Weight
453.54
MDL Number
MFCD08166552
PubChem ID
58500402
Appearance
White powder
Conditions
Store at 0-8 °C
General Information
Synonyms
(S-Fmoc-2-amino-pimelic acid-7-tert-butyl ester
CAS Number
159751-46-9, 912354-10-0
Purity
≥ 98% (HPLC)
Molecular Formula
C26H31NO6
Molecular Weight
453.54
MDL Number
MFCD08166552
PubChem ID
58500402
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

(S)-Fmoc-2-amino-heptanedioic acid-7-tert-butyl ester is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in the synthesis of peptides, allowing for selective reactions without interfering with other functional groups. Its stability under various conditions makes it a preferred choice among chemists.
  • Drug Development: In pharmaceutical research, it is used to create complex molecules that can lead to new drug candidates, particularly in the development of peptide-based therapeutics.
  • Bioconjugation: The compound is employed in bioconjugation processes, enabling the attachment of biomolecules to surfaces or other molecules, which is crucial for creating targeted drug delivery systems.
  • Analytical Chemistry: It is used as a standard in analytical methods to quantify amino acids and peptides, providing reliable results in quality control and research laboratories.
  • Cosmetic Formulations: The compound finds applications in the cosmetic industry, particularly in formulations aimed at improving skin health, due to its ability to enhance the stability and efficacy of active ingredients.

Citations