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Sigma-Aldrich

Fmoc-Pro-OH

≥90% (HPLC)

Synonym(s):

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

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About This Item

Empirical Formula (Hill Notation):
C20H19NO4
CAS Number:
71989-31-6
Molecular Weight:
337.37
Beilstein:
3596735
EC Number:
276-259-0
MDL number:
MFCD00037122
UNSPSC Code:
12352209
eCl@ss:
32160406
PubChem Substance ID:
57651053
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

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Related Categories

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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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
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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
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