Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
07142
CAS Number:
166410-32-8
Fmoc-1,2-diaminoetano·HCl
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-NH(CH2)2NH2·HCl
Documents
$43.87 /1G
Tamaño
Request Bulk Quote
Product Information

Fmoc-1,2-diaminoethane·HCl is a versatile compound widely utilized in peptide synthesis and drug development. This hydrochloride salt of Fmoc-1,2-diaminoethane serves as a crucial building block in the formation of peptides, particularly in solid-phase peptide synthesis (SPPS). Its unique Fmoc (9-fluorenylmethoxycarbonyl) protective group allows for selective deprotection, facilitating the stepwise assembly of complex peptide sequences. This compound is particularly advantageous for researchers aiming to create peptides with specific functionalities, as it enhances the stability and solubility of intermediates during synthesis.

In addition to its applications in peptide synthesis, Fmoc-1,2-diaminoethane·HCl is also employed in the development of pharmaceutical compounds and bioconjugates. Its ability to introduce amino groups into various molecular frameworks makes it a valuable tool in medicinal chemistry and biochemistry. Researchers appreciate its ease of use and compatibility with a wide range of reaction conditions, making it an essential reagent for both academic and industrial applications.

Synonyms
Fmoc-NH(CH2)2NH2·HCl
CAS Number
166410-32-8
Purity
≥ 98 % (HPLC)
Molecular Formula
C17H18N2O2 · HCl
Molecular Weight
318.8
MDL Number
MFCD00830741
PubChem ID
2818106
Appearance
Polvo cristalino blanco
Conditions
Conservar a ≤ -18 °C
General Information
Synonyms
Fmoc-NH(CH2)2NH2·HCl
CAS Number
166410-32-8
Purity
≥ 98 % (HPLC)
Molecular Formula
C17H18N2O2 · HCl
Molecular Weight
318.8
MDL Number
MFCD00830741
PubChem ID
2818106
Appearance
Polvo cristalino blanco
Conditions
Conservar a ≤ -18 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-1,2-diaminoethane·HCl is widely utilized in research focused on

  • Peptide Synthesis: This compound serves as a protective group in solid-phase peptide synthesis, allowing for the selective modification of amino acids without interfering with other functional groups.
  • Drug Development: It plays a crucial role in the development of pharmaceutical compounds, particularly in creating peptide-based drugs that require precise amino acid sequences for efficacy.
  • Bioconjugation: Researchers use it to facilitate the attachment of biomolecules, such as proteins or antibodies, to various surfaces or other molecules, enhancing the functionality of diagnostic and therapeutic agents.
  • Material Science: The compound is applied in the development of advanced materials, including hydrogels and coatings, which benefit from its biocompatibility and chemical stability.
  • Research in Molecular Biology: It is utilized in the synthesis of modified nucleotides and other biomolecules, aiding in the study of gene expression and protein interactions.

Citas