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15490 Aldrich

Boc-Pro-OH

≥99.0% (T)

Synonym: N-(tert-Butoxycarbonyl)-L-proline, Boc-L-proline

  • CAS Number 15761-39-4

  • Empirical Formula (Hill Notation) C10H17NO4

  • Molecular Weight 215.25

  •  Beilstein Registry Number 15828

  •  EC Number 239-848-3

  •  MDL number MFCD00037324

  •  PubChem Substance ID 57647368

  •  eCl@ss 32160406

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Properties

Related Categories Amino Acids & Derivatives, Chemical Biology, Chemical Synthesis, Peptide Chemistry, Proline,
InChI Key   ZQEBQGAAWMOMAI-ZETCQYMHSA-N
assay   ≥99.0% (T)
optical activity   [α]20/D −61±2°, c = 2% in acetic acid
mp   133-135 °C(lit.)

Description

Packaging

5, 25, 100 g in glass bottle

Price and Availability


Cross-Coupling Guide
Safety & Documentation

Safety Information

RIDADR 
NONH for all modes of transport
WGK Germany 
3
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
Aldrich ChemFiles 2008, 8.7, 22.
Keywords: Building blocks, Chemfiles, Methods, 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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