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01310

Sigma-Aldrich

N-Acetyl-L-methionine

≥98.5% (T)

Sinônimo(s):

N-acetyl-L-lysine

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About This Item

Fórmula linear:
CH3SCH2CH2CH(NHCOCH3)CO2H
Número CAS:
65-82-7
Peso molecular:
191.25
Beilstein:
1725552
Número CE:
200-617-7
Número MDL:
MFCD00064441
Código UNSPSC:
12352209
ID de substância PubChem:
329747249
NACRES:
NA.22

Nível de qualidade

100

Ensaio

≥98.5% (T)
≥98.5% (TLC)

forma

powder or crystals

atividade óptica

[α]20/D -21.0±1.0°, c = 1% in H2O

adequação da reação

reaction type: solution phase peptide synthesis

pf

103-106 °C (lit.)

solubilidade

methanol: 50 mg/mL, clear to very slightly hazy, colorless

aplicação(ões)

peptide synthesis

cadeia de caracteres SMILES

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

InChI

1S/C7H13NO3S/c1-5(9)8-6(7(10)11)3-4-12-2/h6H,3-4H2,1-2H3,(H,8,9)(H,10,11)/t6-/m0/s1

chave InChI

XUYPXLNMDZIRQH-LURJTMIESA-N

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Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

Eyeshields, Gloves, type N95 (US)

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Certificados de análise (COA)

Lot/Batch Number
BCCG7455
BCCJ4944
BCCF0218
BCCC4556
BCBW4457

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Sigma-Aldrich

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Sigma-Aldrich

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L-Methionine methyl ester hydrochloride 98%

Sigma-Aldrich

860409

L-Methionine methyl ester hydrochloride

N-Acetyl-L-tryptophan

Sigma-Aldrich

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N-Acetyl-L-phenylalanine ReagentPlus®, 99%

Sigma-Aldrich

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L-Metionina European Pharmacopoeia (EP) Reference Standard

M0960000

L-Metionina

L-Metionina BioUltra, ≥99.5% (NT)

Sigma-Aldrich

64319

L-Metionina

Agnieszka Kołodziejczak-Radzimska et al.
Biotechnology progress, 34(3), 767-777 (2018-01-10)
Acylase I from Aspergillus melleus was immobilized on supports consisting of unmodified and modified silica. Modification was performed using 3-aminopropyltriethoxysilane (APTES) and glutaraldehyde (GA). The effectiveness of immobilization was investigated using the standard Bradford method in addition to a number
Rebecca D Sandlin et al.
Journal of inorganic biochemistry, 104(2), 214-216 (2009-11-13)
A bulky platinum triamine complex, [Pt(Me(5)dien)(NO(3))]NO(3) (Me(5)dien=N,N,N',N',N''-pentamethyldiethylenetriamine) has been prepared and reacted in D(2)O with N-acetylmethionine (N-AcMet) and guanosine 5'-monophosphate (5'-GMP); the reactions have been studied using (1)H NMR spectroscopy. Reaction with 5'-GMP leads to two rotamers of [Pt(Me(5)dien)(5'-GMP-N7)](+). Reaction
Arto Liljeblad et al.
Organic & biomolecular chemistry, 8(4), 886-895 (2010-02-06)
Various commercial lyophilized and immobilized preparations of lipase A from Candida antarctica (CAL-A) were studied for their ability to catalyze the hydrolysis of amide bonds in N-acylated alpha-amino acids, 3-butanamidobutanoic acid (beta-amino acid) and its ethyl ester. The activity toward
Christian Schöneich et al.
Journal of the American Chemical Society, 125(45), 13700-13713 (2003-11-06)
The pathogenesis of Alzheimer's disease is strongly associated with the formation and deposition of beta-amyloid peptide (beta AP) in the brain. This peptide contains a methionine (Met) residue in the C-terminal domain, which is important for its neurotoxicity and its
M Mályusz et al.
Renal physiology and biochemistry, 17(6), 307-315 (1994-11-01)
Hippurate is known to be synthesized from benzoate and glycine in the liver and kidney. It takes part in renal ammoniagenesis by modulating the activity of gamma-glutamyl transpeptidase (gamma GT). Due to its chemical structure, however, hippurate might also serve
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