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P0380

Sigma-Aldrich

L-Prolina

≥99% (HPLC), ReagentPlus®

Sinónimos:

Ácido (S)-pirrolidina-2-carboxílico

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About This Item

Fórmula empírica (notación de Hill):
C5H9NO2
Número de CAS:
147-85-3
Peso molecular:
115.13
Beilstein/REAXYS Number:
80810
EC Number:
205-702-2
MDL number:
MFCD00064318
UNSPSC Code:
12352209
eCl@ss:
32160406
PubChem Substance ID:
24898097
NACRES:
NA.26

product name

L-Prolina, ReagentPlus®, ≥99% (HPLC)

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

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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

11 - Combustible Solids

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificados de análisis (COA)

Lot/Batch Number
0000386629
0000386630
0000369153
0000377016
0000362768

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Andrew Davison
Eureka: Biochemistry & Metabolism, 2015, 76-76 (2015)
Proline: a multifunctional amino acid
La' szlo' Szabados and Arnould Savoure
Trends in Plant Science, 1-9 (2009)
Metabolomic insights into system-wide coordination of vertebrate metamorphosis.
Ichu TA, et al.
BMC Developmental Biology, 14(1), 1-1 (2014)
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
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
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