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47636 Sigma-Aldrich

Fmoc-Pro-OH

≥99.0% (HPLC)

Synonym: N-(9-Fluorenylmethoxycarbonyl)-L-proline, Fmoc-L-proline

  • CAS Number 71989-31-6

  • Empirical Formula (Hill Notation) C20H19NO4

  • Molecular Weight 337.37

  •  Beilstein/REAXYS Number 3596735

  •  EC Number 276-259-0

  •  MDL number MFCD00037122

  •  eCl@ss 32160406

  •  PubChem Substance ID 57651053

  •  NACRES NA.26

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Properties

Related Categories Amino Acids & Derivatives, Chemical Biology, Chemical Synthesis, Peptide Synthesis and Peptide Chemistry, Proline,
InChI Key   ZPGDWQNBZYOZTI-SFHVURJKSA-N
assay   ≥99.0% (HPLC)
optical activity   [α]20/D −32±1°, c = 1% in DMF
mp   117-118 °C (lit.)
storage temp.   2-8°C

Description

Packaging

5, 50 g in glass bottle

Safety & Documentation

Safety Information

RIDADR 
NONH for all modes of transport
WGK Germany 
3

Documents

Certificate of Analysis (COA)

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Certificate of Origin (COO)

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Protocols & Articles

Articles

Natural Amino Acid Building Blocks for Peptide Synthesis

With a growing peptide drug market the fast, reliable and uncomplicated synthesis of peptides is of paramount importance.1 Today, the most common synthetic approaches to medium and even large peptide...
Matthias Junkers
ChemFiles 2008, 8.7, 22.
Keywords: Building blocks, Peptide synthesis, Peptidomimetics, Solid phase peptide synthesis

Proline Derivatives and Analogs

Proline is a non-polar proteinogenic amino acid that forms a tertiary amide when incorporated into peptides. It does not have a hydrogen on the amide group and therefore cannot act as a hydrogen bond...
Chemfiles Volume 5 Article 12
Keywords: Adhesion, Biochemistry, Catalysis, Deposition, Hydroxylations, Isomerizations, Nucleic acid hybridization, Pharmaceutical, Reductions, Substitutions, Type

Peer-Reviewed Papers
15

References

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