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01310

Sigma-Aldrich

N-Acetyl-L-methionine

≥98.5% (T)

Sinónimos:

N-acetyl-L-lysine

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About This Item

Fórmula lineal:
CH3SCH2CH2CH(NHCOCH3)CO2H
Número de CAS:
65-82-7
Peso molecular:
191.25
Beilstein/REAXYS Number:
1725552
EC Number:
200-617-7
MDL number:
MFCD00064441
UNSPSC Code:
12352209
PubChem Substance ID:
329747249
NACRES:
NA.22

Quality Level

100

assay

≥98.5% (T)
≥98.5% (TLC)

form

powder or crystals

optical activity

[α]20/D -21.0±1.0°, c = 1% in H2O

reaction suitability

reaction type: solution phase peptide synthesis

mp

103-106 °C (lit.)

solubility

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

application(s)

peptide synthesis

SMILES string

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

InChI key

XUYPXLNMDZIRQH-LURJTMIESA-N

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Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificados de análisis (COA)

Lot/Batch Number
BCCG7455
BCCF0218
BCCC4556
BCBW4457
BCBQ5510V

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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
Mie R Rasmussen et al.
Journal of proteome research, 15(12), 4591-4600 (2016-11-05)
Loss-of-function mutations in the transmembrane ABCC6 transport protein cause pseudoxanthoma elasticum (PXE), an ectopic, metabolic mineralization disorder that affects the skin, eye, and vessels. ABCC6 is assumed to mediate efflux of one or several small molecule compounds from the liver
James B Thoden et al.
Biochemistry, 43(19), 5716-5727 (2004-05-12)
Divergent evolution of enzyme function is commonly explained by a gene duplication event followed by mutational changes that allow the protein encoded by the copy to acquire a new function. An alternate hypothesis is that this process is facilitated when
M J Wick et al.
Biochemical pharmacology, 37(7), 1225-1231 (1988-04-01)
Both N-hydroxy-2-acetamidofluorene (N-OH-AAF) and the heterocyclic analogue, 2-(N-hydroxyacetamido)carbazole (N-OH-AAC), were shown to be mechanism-based irreversible inhibitors (suicide inhibitors) of partially purified rat hepatic N-acetyltransferase (NAT) activity. Although N-OH-AAC exhibited an apparent first-order inactivation rate constant (ki) that was 7-fold lower
Wen-Fang Ji et al.
The journal of physical chemistry. B, 111(2), 485-489 (2007-01-12)
The amino acid oxidation mechanism has been a research focus in recent years. Although various experimental techniques have been employed to address the problem, it is still a great challenge to identify the oxidation intermediates of amino acids. To explore
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