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Catalog Number:
11810
CAS Number:
153086-78-3
Boc-1-amino-3,6-dioxa-8-octanediamine
Purity:
97 - 100% (Assay by titration)
Synonym(s):
N-Boc-2,2'-(ethylenedioxy)diethylamine, Mono-(Boc)-(PEO)3-diamine
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Product Information

Boc-1-amino-3,6-dioxa-8-octanediamine is a versatile compound widely utilized in the synthesis of various pharmaceuticals and fine chemicals. This compound features a unique structure that includes a tert-butyl carbamate protecting group, enhancing its stability and reactivity in chemical reactions. Its ether linkages contribute to its solubility in organic solvents, making it an excellent choice for applications in medicinal chemistry and polymer science. Researchers often employ Boc-1-amino-3,6-dioxa-8-octanediamine in the development of drug delivery systems and as a building block for complex molecules, particularly in the design of peptide-based therapeutics.

The compound's ability to facilitate the formation of amide bonds and its compatibility with various coupling reagents make it an invaluable tool in peptide synthesis. Additionally, its protective group can be easily removed under mild conditions, allowing for further functionalization of the resulting amine. This flexibility positions Boc-1-amino-3,6-dioxa-8-octanediamine as a preferred choice for chemists seeking efficient and effective solutions in their synthetic pathways.

Synonyms
N-Boc-2,2'-(ethylenedioxy)diethylamine, Mono-(Boc)-(PEO)3-diamine
CAS Number
153086-78-3
Purity
97 - 100% (Assay by titration)
Molecular Formula
C11H24N2O4
Molecular Weight
248.3
MDL Number
MFCD03788155
PubChem ID
9881394
Appearance
Light yellow oil
Conditions
Store at 0 - 8 °C
General Information
Synonyms
N-Boc-2,2'-(ethylenedioxy)diethylamine, Mono-(Boc)-(PEO)3-diamine
CAS Number
153086-78-3
Purity
97 - 100% (Assay by titration)
Molecular Formula
C11H24N2O4
Molecular Weight
248.3
MDL Number
MFCD03788155
PubChem ID
9881394
Appearance
Light yellow oil
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-amino-3,6-dioxa-8-octanediamine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in peptide synthesis, allowing chemists to selectively modify amino acids without affecting other functional groups, enhancing the efficiency of complex peptide assembly.
  • Drug Development: Its unique structure makes it valuable in the design of pharmaceutical compounds, particularly in creating drugs that require specific bioavailability and stability profiles.
  • Bioconjugation: The compound is used in bioconjugation techniques, facilitating the attachment of biomolecules to surfaces or other molecules, which is crucial in developing targeted therapies and diagnostics.
  • Polymer Chemistry: It can be incorporated into polymer formulations to enhance properties such as solubility and thermal stability, making it useful in materials science and engineering applications.
  • Research in Drug Delivery Systems: The compound is explored for its potential in drug delivery systems, where its ability to form stable complexes with drugs can improve their delivery and efficacy in therapeutic applications.

Citations