Skip to Content
Merck
All Photos(4)

Documents

P0380

Sigma-Aldrich

L-Proline

ReagentPlus®, ≥99% (HPLC)

Synonym(s):

(S)-Pyrrolidine-2-carboxylic acid

Sign Into View Organizational & Contract Pricing
All Photos(4)

About This Item

Empirical Formula (Hill Notation):
C5H9NO2
CAS Number:
147-85-3
Molecular Weight:
115.13
Beilstein:
80810
EC Number:
205-702-2
MDL number:
MFCD00064318
UNSPSC Code:
12352209
eCl@ss:
32160406
PubChem Substance ID:
24898097
NACRES:
NA.26

Quality Level

200

product line

ReagentPlus®

Assay

≥99% (HPLC)

form

powder

impurities

L-Hydroxyproline, free

color

white

mp

228 °C (dec.) (lit.)

application(s)

detection

SMILES string

OC(=O)[C@@H]1CCCN1

InChI

1S/C5H9NO2/c7-5(8)4-2-1-3-6-4/h4,6H,1-3H2,(H,7,8)/t4-/m0/s1

InChI key

ONIBWKKTOPOVIA-BYPYZUCNSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

Application

L-Proline has been used:
  • As a supplement during the preparation of chondrogenic medium and synthetic dextrose minimal medium (SD).
  • As a standard during the identification of metabolites in serum samples.
  • In a study to prepare L-proline-L-phenylalanine (L-Pro-L-Phe) mixture in aqueous acetonitrile.

Legal Information

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
SLCL3643
SLCH4834
SLCG4938
SLCD1522
SLBZ8461

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Slide 1 of 2

1 of 2

L-Proline Pharmaceutical Secondary Standard; Certified Reference Material

Supelco

PHR1332

L-Proline

L-Proline phyproof® Reference Substance

PHL83414

L-Proline

Natasja Leth Joergensen et al.
BioResearch open access, 4(1), 109-114 (2015-08-27)
Cartilage regeneration is a fast growing field that combines biotechnology and molecular techniques in creating new tissue mimicking the native microenvironment. Human embryonic stem cells (hESCs) are a highly potent cell source for cartilage regeneration owing to their infinite proliferation
Quantification of extracellular ammonium concentrations and transporter activity in yeast using AmTrac fluorescent sensors.
Ast C, et al.
Bio-protocol, 5, e1372-e1372 (2015)
Proline: a multifunctional amino acid
La' szlo' Szabados and Arnould Savoure
Trends in Plant Science, 1-9 (2009)
Mieczysław Sajewicz et al.
Journal of chromatographic science, 53(1), 31-37 (2014-03-05)
We employ the achiral liquid chromatography with diode array, evaporative light scattering and mass spectrometric detection (HPLC-DAD, HPLC-ELSD and LC-MS) to assess structural instability (understood as spontaneous oscillatory chiral conversion and spontaneous oscillatory condensation) of the two pairs of amino
Proline-Dependent Structural and Biological Properties of Peptides and Proteins
Arieh Yaron
Critical Reviews in Biochemistry and Molecular Biology, 28, 31-81 (2008)
View All Related Papers

Related Content

List Group – Professor Product Portal

The List group focuses on the development of new concepts in catalysis. Since 1999, this research group has pioneered the development of organocatalysis as the third pillar of stereoselective catalysis, along side biocatalysis and transition metal catalysis.

Chromatograms

application for HPLC

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service