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Catalog Number:
11710
CAS Number:
127346-48-9
Boc-1,3-diaminopropane·HCl
Purity:
≥ 99% (Titration)
Synonym(s):
Boc-NH(CH2)3NH2·HCl
Documents
$22.03 /1G
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Product Information

Boc-1,3-diaminopropane·HCl is a versatile compound widely utilized in the fields of organic synthesis and medicinal chemistry. This hydrochloride salt of tert-butyl N-(3-aminopropyl)carbamate serves as an essential building block for the development of various pharmaceuticals and agrochemicals. Its unique structure allows for the introduction of amine functionalities, making it particularly valuable in the synthesis of peptide-based drugs and other biologically active molecules. Researchers appreciate its stability and ease of handling, which facilitate its use in complex synthetic pathways.

In addition to its applications in drug development, Boc-1,3-diaminopropane·HCl is also employed in the preparation of polymeric materials and as a reagent in various chemical reactions. Its ability to act as a protecting group for amines enhances its utility in multi-step synthesis, allowing chemists to achieve higher yields and purities. With its broad range of applications and favorable properties, this compound is an indispensable resource for professionals in the pharmaceutical and chemical industries.

Synonyms
Boc-NH(CH2)3NH2·HCl
CAS Number
127346-48-9
Purity
≥ 99% (Titration)
Molecular Formula
C8H18N2O2·HCl
Molecular Weight
210.7
MDL Number
MFCD01076598
PubChem ID
21982912
Melting Point
151-161 °C
Appearance
White powder
Conditions
Store at 0-8°C
General Information
Synonyms
Boc-NH(CH2)3NH2·HCl
CAS Number
127346-48-9
Purity
≥ 99% (Titration)
Molecular Formula
C8H18N2O2·HCl
Molecular Weight
210.7
MDL Number
MFCD01076598
PubChem ID
21982912
Melting Point
151-161 °C
Appearance
White powder
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Boc-1,3-diaminopropane·HCl is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in the synthesis of peptides, allowing for selective reactions and enhancing yield. Its stability under various conditions makes it a preferred choice for researchers in organic chemistry.
  • Drug Development: In pharmaceutical research, it is used to create intermediates for drug compounds, particularly those targeting neurological disorders. Its ability to improve solubility can enhance the bioavailability of new medications.
  • Polymer Chemistry: The compound is employed in the development of specialty polymers, providing functional groups that can be tailored for specific applications, such as drug delivery systems or biodegradable materials.
  • Bioconjugation: It plays a crucial role in bioconjugation techniques, facilitating the attachment of biomolecules to surfaces or other molecules, which is essential in creating targeted therapies and diagnostics.
  • Research in Catalysis: Boc-1,3-diaminopropane·HCl is used in catalytic processes, where it can act as a ligand in metal-catalyzed reactions, improving reaction rates and selectivity in synthetic pathways.

Citations