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268062 Sigma-Aldrich

D-Pipecolinic acid

99%

Synonym: (R)-(+)-2-Piperidinecarboxylic acid, (R)-Piperidine-2-carboxylic acid, D-Homoproline

  • CAS Number 1723-00-8

  • Empirical Formula (Hill Notation) C6H11NO2

  • Molecular Weight 129.16

  •  Beilstein/REAXYS Number 81094

  •  EC Number 217-024-4

  •  MDL number MFCD00064346

  •  PubChem Substance ID 24856260

  •  NACRES NA.22

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Properties

Related Categories Chemical Biology, Chemical Synthesis, Peptide Synthesis and Peptide Chemistry, Proline Derivatives, Unnatural Amino Acids & Derivatives More...
assay   99%
optical activity   [α]25/D +27°, c = 1 in H2O
application(s)   peptide synthesis: suitable
mp   277 °C (dec.) (lit.)
SMILES string   OC(=O)[C@H]1CCCCN1
InChI   1S/C6H11NO2/c8-6(9)5-3-1-2-4-7-5/h5,7H,1-4H2,(H,8,9)/t5-/m1/s1
InChI key   HXEACLLIILLPRG-RXMQYKEDSA-N

Description

Packaging

100 mg in clear glass bottle

Other Notes

Tandem Mass Spectrometry data independently generated by Scripps Center for Metabolomics is available to view or download in PDF. 268062.pdf Tested metabolites are featured on Scripps Center for Metabolomics METLIN Metabolite Database. To learn more, visit sigma.com/metlin.

Safety & Documentation

Safety Information

Symbol 
GHS07  GHS07
Signal word 
Warning
Hazard statements 
Precautionary statements 
Target organs 
Respiratory system
Personal Protective Equipment 
RIDADR 
NONH for all modes of transport
WGK Germany 
WGK 3
Flash Point(F) 
Not applicable
Flash Point(C) 
Not applicable

Documents

Certificate of Analysis (COA)

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Protocols & Articles

Articles

Proline Derivatives

Proline is a non-polar, natural amino acid that forms a tertiary amide when incorporated into peptides. Thus, it is the only proteinogenic amino acid that does not act as a hydrogen bond donor in a p...
Matthias Junkers
Aldrich ChemFiles 2008, 8.7, 8.
Keywords: Asymmetric synthesis, Chemfiles, Pharmaceutical

Peer-Reviewed Papers
15

References

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