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Catalog Number:
11289
CAS Number:
33545-98-1
Boc-1,4-diaminobutano·HCl
Purity:
≥ 99% (titulación)
Synonym(s):
Boc-NH(CH2)4NH2·HCl
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Tamaño
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Product Information

Boc-1,4-diaminobutane·HCl is a versatile compound widely utilized in the fields of organic synthesis and medicinal chemistry. This hydrochloride salt of tert-butyl N-(4-aminobutyl)carbamate serves as a crucial building block for the synthesis of various pharmaceuticals and biologically active molecules. Its unique structure allows for the introduction of amine functionalities, making it an essential reagent in the development of peptide-based drugs and other complex organic compounds. Researchers appreciate its stability and ease of handling, which facilitate its use in diverse chemical reactions, including coupling reactions and the formation of amide bonds.

In addition to its applications in drug development, Boc-1,4-diaminobutane·HCl is also employed in the preparation of polymeric materials and as a protective group in peptide synthesis. Its ability to selectively protect amine groups enhances its utility in multi-step synthesis processes, allowing for greater efficiency and yield. This compound stands out for its compatibility with various reaction conditions, making it a preferred choice among chemists looking to streamline their synthetic pathways.

Synonyms
Boc-NH(CH2)4NH2·HCl
CAS Number
33545-98-1
Purity
≥ 99% (titulación)
Molecular Formula
C9H20N2O2 · HCl
Molecular Weight
224.73
MDL Number
MFCD02090802
PubChem ID
11287552
Melting Point
148-161 °C
Appearance
Polvo cristalino blanco
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Boc-NH(CH2)4NH2·HCl
CAS Number
33545-98-1
Purity
≥ 99% (titulación)
Molecular Formula
C9H20N2O2 · HCl
Molecular Weight
224.73
MDL Number
MFCD02090802
PubChem ID
11287552
Melting Point
148-161 °C
Appearance
Polvo cristalino blanco
Conditions
Conservar entre 0 y 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-1,4-diaminobutane·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. Its stability under various conditions makes it a preferred choice in organic synthesis.
  • Drug Development: In pharmaceutical research, it is used to create intermediates for drug compounds, particularly in the development of new therapeutics targeting neurological disorders.
  • Polymer Chemistry: The compound can be incorporated into polymers to enhance their properties, such as increasing flexibility and strength, which is beneficial in creating advanced materials for various applications.
  • Bioconjugation: It is employed in bioconjugation techniques, linking biomolecules to drugs or imaging agents, facilitating targeted delivery systems in cancer therapy.
  • Research in Material Science: The compound is used in the formulation of coatings and adhesives, providing improved adhesion and resistance to environmental factors, which is crucial for industrial applications.

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