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Key Documents

408425

Sigma-Aldrich

Boc-Met-OH

99%

Synonym(s):

N-(tert-Butoxycarbonyl)-L-methionine, Boc-L-methionine

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About This Item

Linear Formula:
CH3SCH2CH2CH(COOH)NHCOOC(CH3)3
CAS Number:
Molecular Weight:
249.33
Beilstein:
1727869
EC Number:
MDL number:
UNSPSC Code:
12352209
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

99%

optical activity

[α]20/D −22°, c = 1 in methanol

reaction suitability

reaction type: Boc solid-phase peptide synthesis

mp

47-50 °C (lit.)

application(s)

peptide synthesis

SMILES string

CSCC[C@H](NC(=O)OC(C)(C)C)C(O)=O

InChI

1S/C10H19NO4S/c1-10(2,3)15-9(14)11-7(8(12)13)5-6-16-4/h7H,5-6H2,1-4H3,(H,11,14)(H,12,13)/t7-/m0/s1

InChI key

IMUSLIHRIYOHEV-ZETCQYMHSA-N

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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

Certificates of Analysis (COA)

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Polymer-lipid hybrid vesicles are an emerging type of nano-assemblies that show potential as artificial organelles among others. Phospholipids and poly(cholesteryl methacrylate)-block-poly(methionine methacryloyloxyethyl ester (METMA)-random-2-carboxyethyl acrylate (CEA)) labeled with a Förster resonance energy transfer (FRET) reporter pair are used for the
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Transporter-related nutrient sensors, called transceptors, mediate nutrient activation of signaling pathways through the plasma membrane. The mechanism of action of transporting and nontransporting transceptors is unknown. We have screened 319 amino acid analogs to identify compounds that act on Gap1

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