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47634

Fmoc-Met-OH

Name: Fmoc-Met-OH
Brand: ALDRICH

≥98.0% (HPLC), for peptide synthesis

Synonym(s):

Fmoc-L-methionine

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About This Item

Empirical Formula (Hill Notation):

C₂₀H₂₁NO₄S

CAS Number:

71989-28-1

Molecular Weight:

371.45

NACRES:

NA.26

PubChem Substance ID:

57651052

UNSPSC Code:

12352209

EC Number:

276-258-5

MDL number:

MFCD00037134

Beilstein/REAXYS Number:

4300266

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Properties

Product Name

Fmoc-Met-OH, ≥98.0% (HPLC)

Quality Level

100

assay

≥98.0% (HPLC)

optical activity

[α]20/D -29.5±1.5°, c = 1% in DMF

reaction suitability

reaction type: Fmoc solid-phase peptide synthesis

mp

121-123 °C (lit.)

application(s)

peptide synthesis

functional group

Fmoc

storage temp.

2-8°C

SMILES string

CSCC[C@H](NC(=O)OCC1c2ccccc2-c3ccccc13)C(O)=O

InChI

1S/C20H21NO4S/c1-26-11-10-18(19(22)23)21-20(24)25-12-17-15-8-4-2-6-13(15)14-7-3-5-9-16(14)17/h2-9,17-18H,10-12H2,1H3,(H,21,24)(H,22,23)/t18-/m0/s1

InChI key

BUBGAUHBELNDEW-SFHVURJKSA-N

Description

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Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Repurposing the Pummerer Rearrangement: Determination of Methionine Sulfoxides in Peptides.

Carolyn C Woodroofe et al.

Chembiochem : a European journal of chemical biology, 21(4), 508-516 (2019-08-01)

The reversible oxidation of methionine residues in proteins has emerged as a biologically important post-translational modification. However, detection and quantitation of methionine sulfoxide in proteins is difficult. Our aim is to develop a method for specifically derivatizing methionine sulfoxide residues.

A Cerberus-Inspired Anti-Infective Multicomponent Gatekeeper Hydrogel against Infections with the Emerging "Superbug" Yeast Candida auris.

Dennis Kubiczek et al.

Macromolecular bioscience, 20(4), e2000005-e2000005 (2020-02-28)

The pathogenic yeast Candida auris has received increasing attention due to its ability to cause fatal infections, its resistance toward important fungicides, and its ability to persist on surfaces including medical devices in hospitals. To brace health care systems for

Inhibition of Tau Protein Aggregation by Rhodanine-based Compounds Solubilized Via Specific Formulation Additives to Improve Bioavailability and Cell Viability.

Marcus Pickhardt et al.

Current Alzheimer research, 14(7), 742-752 (2017-02-06)

Anti-aggregation drugs play an important role in therapeutic approaches for Alzheimer's disease. We have previously developed a number of compounds that are able to inhibit the pathological aggregation of Tau protein. One common obstacle to application is the limited penetration

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Global Trade Item Number

SKU	GTIN
47634-25G-F	04061832362380
47634-100G-F	04061832642598
47634-1KG-F	04061826222751
47634-5G-F	04061832642604