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Chemical Structure
Chemical Structure
Chemical Structure

L-Proline

CDX-P0446
Chemodex
CAS Number147-85-3
Product group Chemicals
Estimated Purity>98%
Molecular Weight115.13
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Overview

  • Supplier
    Chemodex
  • Product Name
    L-Proline [147-85-3]
  • Delivery Days Customer
    10
  • CAS Number
    147-85-3
  • Certification
    Research Use Only
  • Estimated Purity
    >98%
  • Molecular Formula
    C5H9NO2
  • Molecular Weight
    115.13
  • Scientific Description
    Chemical. CAS: 147-85-3. Formula: C5H9NO2. MW: 115.13. Synthetic. Proline is a proteinogenic amino acid that is used in the biosynthesis of proteins. L-Proline has been found to act as a weak agonist of the glycine receptor and of both NMDA and non-NMDA (AMPA/kainate) ionotropic glutamate receptors. L-proline is essential for induction of hepatocyte proliferation in culture, through its affect on synthesis of intracellular collagen. It has free radical scavenging potential. Induces differentiation of embyonic stem cells and has been studied as regulator of pluripotent cells in culture. Shows cryoprotective properties. L-Proline is used as asymmetric catalysts in organic synthesis and asymmetric aldol cyclization. It is involved in the Michael addition of dimethyl malonate to alfa-beta-unsaturated aldehydes. It finds uses in pharmaceutical, biotechnological applications due to its osmoprotectant property. - Proline is a proteinogenic amino acid that is used in the biosynthesis of proteins. L-Proline has been found to act as a weak agonist of the glycine receptor and of both NMDA and non-NMDA (AMPA/kainate) ionotropic glutamate receptors. L-proline is essential for induction of hepatocyte proliferation in culture, through its affect on synthesis of intracellular collagen. It has free radical scavenging potential. Induces differentiation of embyonic stem cells and has been studied as regulator of pluripotent cells in culture. Shows cryoprotective properties. L-Proline is used as asymmetric catalysts in organic synthesis and asymmetric aldol cyclization. It is involved in the Michael addition of dimethyl malonate to alfa-beta-unsaturated aldehydes. It finds uses in pharmaceutical, biotechnological applications due to its osmoprotectant property.
  • SMILES
    O=C(O)[C@H]1NCCC1
  • Storage Instruction
    RT
  • UNSPSC
    12352200

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