Skip to Content
MilliporeSigma
All Photos(1)

Documents

47636

Sigma-Aldrich

Fmoc-Pro-OH

≥90% (HPLC)

Synonym(s):

N-(9-Fluorenylmethoxycarbonyl)-L-proline, Fmoc-L-proline

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C20H19NO4
CAS Number:
Molecular Weight:
337.37
Beilstein/REAXYS Number:
3596735
EC Number:
MDL number:
UNSPSC Code:
12352209
eCl@ss:
32160406
PubChem Substance ID:
NACRES:
NA.26

assay

≥90% (HPLC)

optical activity

[α]20/D −32±1°, c = 1% in DMF

reaction suitability

reaction type: Fmoc solid-phase peptide synthesis

mp

117-118 °C (lit.)

application(s)

peptide synthesis

functional group

Fmoc

storage temp.

2-8°C

SMILES string

OC(=O)[C@@H]1CCCN1C(=O)OCC2c3ccccc3-c4ccccc24

InChI

1S/C20H19NO4/c22-19(23)18-10-5-11-21(18)20(24)25-12-17-15-8-3-1-6-13(15)14-7-2-4-9-16(14)17/h1-4,6-9,17-18H,5,10-12H2,(H,22,23)/t18-/m0/s1

InChI key

ZPGDWQNBZYOZTI-SFHVURJKSA-N

Looking for similar products? Visit Product Comparison Guide

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

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

Visit the Document Library

Magdalena Rudowska et al.
Journal of the American Society for Mass Spectrometry, 24(6), 846-856 (2013-04-24)
The fragmentation of peptides containing quaternary ammonium group, but lacking easily mobilizable protons, was examined with the aid of deuterium-labeled analogs and quantum-chemical modeling. The fragmentation of oligoproline containing quaternary ammonium group involves the mobilization of hydrogens localized at α-
Jianhao Wang et al.
Nanotechnology, 29(27), 274001-274001 (2018-04-17)
Small molecules with free thiol groups always show high binding affinity to quantum dots (QDs). However, it is still highly challenging to detect the binding capacity between thiol-containing molecules and QDs inside a capillary. To conquer this limitation, a capillary
Barbara Prandi et al.
Food research international (Ottawa, Ont.), 91, 92-102 (2017-03-16)
Coeliac disease is an autoimmune enteropathy that develops in genetically predisposed subjects after the ingestion of gluten or related proteins. Coeliac disease has an increasing incidence in the last years in western countries and it has been suggested that wheat
Rosanna Capparelli et al.
PloS one, 4(9), e7191-e7191 (2009-09-29)
Temporins are antimicrobial peptides secreted by the granular glands of the European red frog (Rana temporaria). They are 10-14 amino acid long polypeptides active prevalently against gram positive bacteria. This study shows that a synthetic temporin B analogue (TB-YK), acquires
Jingwen Song et al.
Small (Weinheim an der Bergstrasse, Germany), 16(8), e1907309-e1907309 (2020-01-30)
There is a real need for new antibiotics against self-evolving bacteria. One option is to use biofriendly broad-spectrum and mechanically tunable antimicrobial hydrogels that can combat multidrug-resistant microbes. Whilst appealing, there are currently limited options. Herein, broad-spectrum antimicrobial biometallohydrogels based

Articles

Proline analogues are promising candidates for tuning the biological, pharmaceutical, or physicochemical properties of naturally occuring, as well as de novo designed, linear, and, cyclic peptides.

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