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Catalog Number:
29743
CAS Number:
2098497-24-4
Fmoc-D-Homoarg(Et)2-OH hydrochloride salt (symmetrical)
Purity:
≥ 95% (HPLC)
Documents
$58.39 /25MG
Pack Size Availability Price
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Product Information

Fmoc-D-Homoarg(Et)2-OH hydrochloride salt (symmetrical) is a specialized amino acid derivative that plays a crucial role in peptide synthesis and drug development. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is widely utilized in solid-phase peptide synthesis due to its stability and ease of removal under mild conditions. The symmetrical structure of this hydrochloride salt enhances its solubility and reactivity, making it an ideal choice for researchers focused on the development of complex peptides and biologically active compounds.

In practical applications, Fmoc-D-Homoarg(Et)2-OH hydrochloride salt is particularly valuable in the synthesis of peptide-based therapeutics, where precise amino acid sequences are critical for biological activity. Its unique properties allow for the incorporation of diethylamino groups, which can enhance the pharmacological profile of the resulting peptides. This compound is also beneficial in the study of protein interactions and the design of novel biomolecules, making it a versatile tool for both academic and industrial research settings.

CAS Number
2098497-24-4
Purity
≥ 95% (HPLC)
Molecular Formula
C26H34N4O4·HCl
Molecular Weight
503.0
MDL Number
MFCD32012111
PubChem ID
138109523
Appearance
White to off-white powder
Conditions
Store at ≤ -4 °C
General Information
CAS Number
2098497-24-4
Purity
≥ 95% (HPLC)
Molecular Formula
C26H34N4O4·HCl
Molecular Weight
503.0
MDL Number
MFCD32012111
PubChem ID
138109523
Appearance
White to off-white powder
Conditions
Store at ≤ -4 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-D-Homoarg(Et)2-OH hydrochloride salt (symmetrical) is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in solid-phase peptide synthesis, where its protective Fmoc group allows for selective deprotection and coupling reactions.
  • Drug Development: It is used in the development of peptide-based therapeutics, offering advantages in stability and bioactivity, which are crucial for creating effective drug candidates.
  • Bioconjugation: The compound can be employed in bioconjugation processes, facilitating the attachment of peptides to various biomolecules, enhancing the specificity and efficacy of targeted therapies.
  • Research in Neuroscience: Its structural properties make it valuable in neuroscience research, particularly in studying neuropeptides and their roles in signaling pathways.
  • Custom Peptide Libraries: Researchers utilize this chemical to create diverse peptide libraries for high-throughput screening, aiding in the discovery of novel bioactive compounds.

Citations