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47636

Sigma-Aldrich

Fmoc-Pro-OH

≥90% (HPLC)

Sinonimo/i:

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

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About This Item

Formula empirica (notazione di Hill):
C20H19NO4
Numero CAS:
71989-31-6
Peso molecolare:
337.37
Beilstein:
3596735
Numero CE:
276-259-0
Numero MDL:
MFCD00037122
Codice UNSPSC:
12352209
eCl@ss:
32160406
ID PubChem:
57651053
NACRES:
NA.26

Saggio

≥90% (HPLC)

Attività ottica

[α]20/D −32±1°, c = 1% in DMF

Impiego in reazioni chimiche

reaction type: Fmoc solid-phase peptide synthesis

Punto di fusione

117-118 °C (lit.)

applicazioni

peptide synthesis

Gruppo funzionale

Fmoc

Temperatura di conservazione

2-8°C

Stringa SMILE

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
ZPGDWQNBZYOZTI-SFHVURJKSA-N

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Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)

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Certificati d'analisi (COA)

Lot/Batch Number
BCCD1997
BCCB3357
BCBW6904
BCBS8503V
BCBR9670V

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Fmoc-Ala-OH 95%

Sigma-Aldrich

531480

Fmoc-Ala-OH

Fmoc-Hyp(tBu)-OH ≥98.0% (HPLC)

Sigma-Aldrich

47517

Fmoc-Hyp(tBu)-OH

Fmoc-Met-OH ≥98.0% (HPLC)

Sigma-Aldrich

47634

Fmoc-Met-OH

Fmoc-Asn(Trt)-OH ≥97.0%

Sigma-Aldrich

47672

Fmoc-Asn(Trt)-OH

Fmoc-Asp(OtBu)-OH ≥98.0% (HPLC)

Sigma-Aldrich

47618

Fmoc-Asp(OtBu)-OH

Fmoc-Arg(Pbf)-OH ≥98.0% (HPLC)

Sigma-Aldrich

47349

Fmoc-Arg(Pbf)-OH

Fmoc-Glu(OtBu)-OH ≥98.0% (HPLC)

Sigma-Aldrich

47625

Fmoc-Glu(OtBu)-OH

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
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-
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
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
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
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