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Catalog Number:
16176
CAS Number:
672310-17-7
Fmoc-1,4-trans-diaminocyclohexane hydrochloride
Purity:
≥ 99% (HPLC)
Synonym(s):
Fmoc-trans-1,4-DACH·HCl
Documents
$72.31 /250MG
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Product Information

Fmoc-1,4-trans-diaminocyclohexane hydrochloride is a versatile compound widely utilized in peptide synthesis and drug development. This protected amino acid derivative features a fluorenylmethoxycarbonyl (Fmoc) group, which provides stability and ease of handling during the synthesis process. Its unique structure allows for selective deprotection, making it an ideal choice for researchers focused on creating complex peptides with high purity and yield.

In the pharmaceutical industry, Fmoc-1,4-trans-diaminocyclohexane hydrochloride is particularly valuable for the development of peptide-based therapeutics, including those targeting specific diseases. Its ability to facilitate the formation of cyclic peptides enhances its application in drug design, providing researchers with the tools necessary to explore novel therapeutic avenues. Additionally, its compatibility with various coupling reagents and solid-phase synthesis techniques makes it a preferred choice among professionals seeking efficiency and reliability in their workflows.

Synonyms
Fmoc-trans-1,4-DACH·HCl
CAS Number
672310-17-7
Purity
≥ 99% (HPLC)
Molecular Formula
C21H24N2O2·HCl
Molecular Weight
372.9
MDL Number
MFCD03001746
PubChem ID
2759186
Melting Point
> 160 °C
Appearance
White crystalline powder
Conditions
Store at 0-8 °C
General Information
Synonyms
Fmoc-trans-1,4-DACH·HCl
CAS Number
672310-17-7
Purity
≥ 99% (HPLC)
Molecular Formula
C21H24N2O2·HCl
Molecular Weight
372.9
MDL Number
MFCD03001746
PubChem ID
2759186
Melting Point
> 160 °C
Appearance
White crystalline 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

Fmoc-1,4-trans-diaminocyclohexane hydrochloride is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting 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 design of new pharmaceuticals, particularly in creating compounds with enhanced bioactivity and stability.
  • Bioconjugation: Researchers use it to facilitate the attachment of biomolecules to surfaces or other molecules, improving the efficacy of drug delivery systems.
  • Material Science: It is applied in the development of advanced materials, such as hydrogels and coatings, which benefit from its unique chemical properties.
  • Diagnostics: The compound is utilized in the creation of diagnostic agents, enhancing the detection of diseases through improved binding to target molecules.

Citations