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Catalog Number:
07106
CAS Number:
1228900-15-9
Ácido N α - Fmoc- N β -(4,4-dimetil-2,6-dioxociclohex-1-ilideno)-3-metilbutil-D-2,3-diaminopropiónico
Purity:
≥ 99% (Ensayo por titulación)
Synonym(s):
Fmoc-D-Dap(ivDde)-OH
Documents
$65.40 /100 mg
Tamaño
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Product Information

Na-Fmoc-Nb-(4,4-dimethyl-2,6-dioxocyclohex-1-ylidene)-3-methylbutyl-D-2,3-diaminopropionic acid is a specialized amino acid derivative that plays a crucial role in peptide synthesis and drug development. This compound is particularly valued for its ability to enhance the stability and solubility of peptides, making it an essential tool for researchers in the fields of medicinal chemistry and biochemistry. Its unique structure, featuring a fluorenylmethoxycarbonyl (Fmoc) protecting group, allows for selective deprotection during synthesis, facilitating the construction of complex peptide sequences with high fidelity.

In practical applications, this compound is utilized in the development of peptide-based therapeutics, where precise control over peptide structure is paramount. Its distinctive properties enable researchers to create more effective drug candidates with improved pharmacological profiles. Additionally, the compound's compatibility with various coupling reagents and its ability to withstand harsh reaction conditions make it a preferred choice for peptide chemists. By incorporating this amino acid derivative into their workflows, professionals can streamline their synthesis processes and achieve higher yields of desired products.

Synonyms
Fmoc-D-Dap(ivDde)-OH
CAS Number
1228900-15-9
Purity
≥ 99% (Ensayo por titulación)
Molecular Formula
C31H36N2O6
Molecular Weight
532.5
MDL Number
MFCD01631664
PubChem ID
136334288
Melting Point
152 - 165 °C
Appearance
Polvo cristalino blanco
Optical Rotation
[a] D 20 = -7 a -9 º (C=1 en MeOH)
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Fmoc-D-Dap(ivDde)-OH
CAS Number
1228900-15-9
Purity
≥ 99% (Ensayo por titulación)
Molecular Formula
C31H36N2O6
Molecular Weight
532.5
MDL Number
MFCD01631664
PubChem ID
136334288
Melting Point
152 - 165 °C
Appearance
Polvo cristalino blanco
Optical Rotation
[a] D 20 = -7 a -9 º (C=1 en MeOH)
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Na-Fmoc-Nb-(4,4-dimethyl-2,6-dioxocyclohex-1-ylidene)-3-methylbutyl-D-2,3-diaminopropionic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, enabling researchers to create complex molecules for drug development.
  • Drug Development: Its unique structure allows for the design of novel therapeutics, particularly in targeting specific biological pathways, enhancing efficacy in pharmaceutical applications.
  • Bioconjugation: The compound can be used to attach biomolecules to surfaces or other molecules, facilitating the development of targeted drug delivery systems.
  • Research in Neuroscience: It aids in the study of neuropeptides, contributing to a better understanding of neurological disorders and potential treatments.
  • Customizable Chemical Libraries: This compound is valuable in creating diverse chemical libraries for screening in various biological assays, promoting innovation in medicinal chemistry.

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