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Catalog Number:
04051
CAS Number:
77302-72-8
Acide boc-L-α-aminoadipique
Purity:
≥ 99 % (HPLC)
Synonym(s):
Boc-L-Aad-OH, Acide boc-L-2-aminohexanedioïque
Documents
$51.18 /250 mg
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Product Information

Boc-L-a-aminoadipic acid is a valuable compound widely utilized in the synthesis of peptides and pharmaceuticals. This amino acid derivative features a tert-butoxycarbonyl (Boc) protecting group, which enhances its stability and reactivity in various chemical reactions. Researchers and industry professionals appreciate its role in solid-phase peptide synthesis, where it serves as a building block for creating complex peptide structures. Its unique properties allow for selective reactions, making it an essential tool in the development of therapeutic peptides and biologically active compounds.

In addition to its applications in peptide synthesis, Boc-L-a-aminoadipic acid is also explored for its potential in drug design and development. Its structural characteristics facilitate the introduction of functional groups, enabling the modification of pharmacological properties. This compound stands out for its versatility and effectiveness, providing researchers with a reliable option for advancing their projects in medicinal chemistry and biochemistry. With its proven utility in various applications, Boc-L-a-aminoadipic acid remains a key asset for professionals in the chemical and pharmaceutical industries.

Synonyms
Boc-L-Aad-OH, Acide boc-L-2-aminohexanedioïque
CAS Number
77302-72-8
Purity
≥ 99 % (HPLC)
Molecular Formula
C 11 H 196
Molecular Weight
261.3
MDL Number
MFCD00063354
PubChem ID
4193443
Melting Point
123 - 127 °C
Appearance
Poudre blanche
Optical Rotation
[a] 20 D = -9 ± 2 ° (C=1 dans AcOH)
Conditions
Conserver à 0 - 8 °C
General Information
Synonyms
Boc-L-Aad-OH, Acide boc-L-2-aminohexanedioïque
CAS Number
77302-72-8
Purity
≥ 99 % (HPLC)
Molecular Formula
C 11 H 196
Molecular Weight
261.3
MDL Number
MFCD00063354
PubChem ID
4193443
Melting Point
123 - 127 °C
Appearance
Poudre blanche
Optical Rotation
[a] 20 D = -9 ± 2 ° (C=1 dans AcOH)
Conditions
Conserver à 0 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Boc-L-a-aminoadipic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group for amino acids during the synthesis of peptides, allowing for the selective modification of specific amino acid residues without affecting others.
  • Drug Development: It plays a crucial role in the design of pharmaceutical compounds, particularly in the development of peptide-based drugs, enhancing their stability and bioavailability.
  • Biotechnology: In the field of biotechnology, it is used to create modified proteins that can improve enzyme activity or specificity, which is essential for various industrial applications.
  • Research in Neuroscience: Boc-L-a-aminoadipic acid is studied for its potential effects on neurotransmitter systems, contributing to the understanding of neurological disorders and the development of new treatments.
  • Cosmetic Formulations: The compound is also explored in cosmetic chemistry for its potential benefits in skin care products, particularly for formulations aimed at enhancing skin elasticity and hydration.

Citations