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Catalog Number:
04961
CAS Number:
180181-05-9
Fmoc-4-carboximetil-piperidina
Purity:
≥ 99 % (HPLC)
Synonym(s):
Fmoc-Cmp-OH, Ácido fmoc-4-piperidilacético
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Product Information

Fmoc-4-carboxymethyl-piperidine is a versatile compound widely utilized in the field of peptide synthesis and drug development. This chemical serves as a protective group for amino acids, facilitating the formation of peptide bonds while ensuring stability during synthesis. Its unique structure, featuring a fluorenylmethoxycarbonyl (Fmoc) group, allows for easy removal under mild conditions, making it an ideal choice for researchers aiming to streamline their synthesis processes. The carboxymethyl group enhances solubility, which is particularly beneficial in aqueous environments, thus improving reaction efficiency and yield.

In addition to its role in peptide synthesis, Fmoc-4-carboxymethyl-piperidine is also valuable in the development of pharmaceuticals and biologically active compounds. Its ability to modify piperidine derivatives opens avenues for creating novel therapeutic agents with enhanced efficacy. Researchers in medicinal chemistry and biochemistry will find this compound indispensable for its practicality and effectiveness in various applications, including drug design and biomolecular studies.

Synonyms
Fmoc-Cmp-OH, Ácido fmoc-4-piperidilacético
CAS Number
180181-05-9
Purity
≥ 99 % (HPLC)
Molecular Formula
C22H23NO4
Molecular Weight
365.42
MDL Number
MFCD00273478
PubChem ID
978354
Appearance
Polvo de color blanco a amarillo pálido
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Fmoc-Cmp-OH, Ácido fmoc-4-piperidilacético
CAS Number
180181-05-9
Purity
≥ 99 % (HPLC)
Molecular Formula
C22H23NO4
Molecular Weight
365.42
MDL Number
MFCD00273478
PubChem ID
978354
Appearance
Polvo de color blanco a amarillo pálido
Conditions
Conservar entre 0 y 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-4-carboxymethyl-piperidine 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: Its unique structure aids in the design and synthesis of bioactive compounds, making it valuable in pharmaceutical research for developing new medications.
  • Bioconjugation: Fmoc-4-carboxymethyl-piperidine is used to create stable linkages between biomolecules, enhancing the efficacy of drug delivery systems and targeted therapies.
  • Material Science: This chemical is applied in the development of advanced materials, such as polymers and nanomaterials, which can be tailored for specific applications in electronics and coatings.
  • Analytical Chemistry: It plays a role in the synthesis of standards and reagents used in various analytical techniques, improving the accuracy of chemical analysis in laboratories.