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Catalog Number:
06741
CAS Number:
65915-94-8
Boc-1,6-diaminohexane hydrochloride
Synonym(s):
N-Boc-1,6-hexanediamine hydrochloride
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Product Information

Boc-1,6-diaminohexane·HCl is a versatile compound widely utilized in the synthesis of various pharmaceuticals and fine chemicals. With its unique tert-butyl carbamate protecting group, this hydrochloride salt facilitates the introduction of amino functionalities in organic synthesis, making it an essential building block for researchers and industry professionals. Its stability under a range of conditions and ease of handling make it particularly appealing for applications in peptide synthesis and drug development.

This compound is especially valuable in the production of polyamines and can serve as a precursor for the synthesis of more complex molecules, including those used in medicinal chemistry. The ability to selectively modify the amino groups allows for the creation of tailored compounds with specific biological activities, enhancing its relevance in therapeutic applications. Researchers appreciate its efficiency in facilitating reactions that require protected amines, thus streamlining the synthetic process and improving overall yields.

Synonyms
N-Boc-1,6-hexanediamine hydrochloride
CAS Number
65915-94-8
Molecular Formula
C11H24N2O2·HCl
Molecular Weight
252.79
MDL Number
MFCD00039072
PubChem ID
3017638
Melting Point
157 - 165 °C
Appearance
Off-white powder
Conditions
Store at 0-8 °C
General Information
Synonyms
N-Boc-1,6-hexanediamine hydrochloride
CAS Number
65915-94-8
Molecular Formula
C11H24N2O2·HCl
Molecular Weight
252.79
MDL Number
MFCD00039072
PubChem ID
3017638
Melting Point
157 - 165 °C
Appearance
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-1,6-diaminohexane·HCl is widely utilized in research focused on

  • Peptide Synthesis: This compound serves as a protecting group in the synthesis of peptides, allowing researchers to selectively modify amino acids without affecting others, which is crucial for developing new pharmaceuticals.
  • Drug Development: It plays a significant role in the design of drug candidates, particularly in enhancing the solubility and stability of active pharmaceutical ingredients, making it easier to formulate effective medications.
  • Polymer Chemistry: Used in the production of specialty polymers, it contributes to the development of materials with tailored properties for applications in coatings, adhesives, and biomedical devices.
  • Bioconjugation: This chemical is essential in bioconjugation processes, where it helps attach biomolecules to surfaces or other molecules, enhancing the efficacy of diagnostics and therapeutics.
  • Research in Neuroscience: Its derivatives are explored for potential neuroprotective effects, providing insights into treatments for neurodegenerative diseases, which is a growing area of interest in medical research.

Citations