Key Documents

View All Documentation

47636

Fmoc-Pro-OH

Name: Fmoc-Pro-OH
Brand: ALDRICH

≥90% (HPLC)

Synonym(s):

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

Select a Size

Change View

About This Item

Empirical Formula (Hill Notation):

C₂₀H₁₉NO₄

CAS Number:

71989-31-6

Molecular Weight:

337.37

NACRES:

NA.26

PubChem Substance ID:

57651053

eCl@ss:

32160406

UNSPSC Code:

12352209

EC Number:

276-259-0

MDL number:

MFCD00037122

Beilstein/REAXYS Number:

3596735

Technical Service

Need help? Our team of experienced scientists is here for you.

Let Us Assist

Properties

Quality Level

100

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

Description

Still not finding the right product?

Explore all of our products under Fmoc-Pro-OH

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

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

Articles

Proline Derivatives and Analogs

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.

Gas-phase fragmentation of oligoproline peptide ions lacking easily mobilizable protons.

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-

Synergistic antibacterial and anti-inflammatory activity of temporin A and modified temporin B in vivo.

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

Hydrophobic Tags for Highly Efficient Light-Activated Protein Release.

Karthik Nadendla et al.

Molecular pharmaceutics, 16(7), 2922-2928 (2019-05-24)

We have previously described the photoactivated depot (PAD) approach for the light-stimulated release of therapeutic proteins such as insulin. The aim of this method is to release insulin from a shallow dermal depot in response to blood glucose information, using

View All Related Papers

Global Trade Item Number

SKU	GTIN
47636-5G-F	04061832362441
47636-1KG-F	04061826222768
47636-250G-F	04061832362403
47636-50G-F	04061832362427

Key Documents

Fmoc-Pro-OH

≥90% (HPLC)

Select a Size

About This Item

Quality Level

assay

optical activity

reaction suitability

mp

application(s)

functional group

storage temp.

SMILES string

InChI

InChI key

Still not finding the right product?

Safety Information

Storage Class

wgk

flash_point_f

flash_point_c

ppe

Documentation

Certificates of Analysis (COA)

Already Own This Product?

Protocols and Articles

Articles

Peer Reviewed Papers

Global Trade Item Number