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About This Item
Empirical Formula (Hill Notation):
C5H9NO2
CAS Number:
Molecular Weight:
115.13
NACRES:
NA.26
PubChem Substance ID:
eCl@ss:
32160406
UNSPSC Code:
12352209
EC Number:
205-702-2
MDL number:
Beilstein/REAXYS Number:
80810
Product Name
L-Proline, ReagentPlus®, ≥99% (HPLC)
InChI key
ONIBWKKTOPOVIA-BYPYZUCNSA-N
InChI
1S/C5H9NO2/c7-5(8)4-2-1-3-6-4/h4,6H,1-3H2,(H,7,8)/t4-/m0/s1
SMILES string
OC(=O)[C@@H]1CCCN1
product line
ReagentPlus®
assay
≥99% (HPLC)
form
powder
impurities
L-Hydroxyproline, free
color
white
mp
228 °C (dec.) (lit.)
application(s)
detection
Quality Level
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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
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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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
Andrew Davison
Eureka: Biochemistry & Metabolism, 2015, 76-76 (2015)
Quantification of extracellular ammonium concentrations and transporter activity in yeast using AmTrac fluorescent sensors.
Ast C, et al.
Bio-protocol, 5, e1372-e1372 (2015)
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