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Catalog Number:
01327
CAS Number:
6404-29-1
Boc-6-aminohexanoic acid
Purity:
≥ 98% (Assay)
Synonym(s):
Boc-6-aminocaproic acid, Boc-ε-Ahx-OH, Boc-ε-Acp-OH
Documents
$18.53 /1G
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Product Information

Boc-6-aminohexanoic acid is a versatile compound widely utilized in the fields of organic synthesis and peptide chemistry. This amino acid derivative features a Boc (tert-butyloxycarbonyl) protecting group, making it an ideal choice for the synthesis of peptides and other complex organic molecules. Its unique structure allows for enhanced stability during reactions, facilitating the formation of peptide bonds while minimizing side reactions. Researchers often employ Boc-6-aminohexanoic acid in the development of pharmaceuticals, particularly in the design of peptide-based drugs, where its properties can be leveraged to improve bioavailability and efficacy.

In addition to its applications in drug development, Boc-6-aminohexanoic acid serves as a valuable building block in the synthesis of various biomolecules and polymers. Its compatibility with a range of coupling reagents and reaction conditions makes it a preferred choice for chemists seeking reliable and efficient pathways to complex structures. The compound's ability to enhance solubility and stability in formulations further underscores its significance in both research and industrial applications, making it a crucial component for professionals in the chemical and pharmaceutical industries.

Synonyms
Boc-6-aminocaproic acid, Boc-ε-Ahx-OH, Boc-ε-Acp-OH
CAS Number
6404-29-1
Purity
≥ 98% (Assay)
Molecular Formula
C11H21NO4
Molecular Weight
231.3
MDL Number
MFCD00037798
PubChem ID
637602
Melting Point
~ 40 °C (Lit.)
Appearance
White to off-white powder
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Boc-6-aminocaproic acid, Boc-ε-Ahx-OH, Boc-ε-Acp-OH
CAS Number
6404-29-1
Purity
≥ 98% (Assay)
Molecular Formula
C11H21NO4
Molecular Weight
231.3
MDL Number
MFCD00037798
PubChem ID
637602
Melting Point
~ 40 °C (Lit.)
Appearance
White to off-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

Boc-6-aminohexanoic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in the synthesis of peptides, allowing for the selective modification of amino acids without affecting others, which is crucial for creating complex peptide structures.
  • Drug Development: Its unique structure aids in the design of pharmaceuticals, particularly in enhancing the solubility and stability of drug candidates, making it valuable in medicinal chemistry.
  • Bioconjugation: The compound is employed in bioconjugation processes, facilitating the attachment of biomolecules to drugs or imaging agents, which is essential in targeted therapy and diagnostics.
  • Polymer Chemistry: It is used in the synthesis of biodegradable polymers, contributing to the development of environmentally friendly materials, which are increasingly important in various industries.
  • Research in Biochemistry: Researchers utilize it to study protein interactions and modifications, providing insights into biological processes and potential therapeutic targets.

Citations