V900562
N-Acetyl-DL-methionine
Vetec™, reagent grade, 98%
Synonym(s):
Methionamine
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About This Item
Linear Formula:
CH3SCH2CH2CH(NHCOCH3)CO2H
CAS Number:
Molecular Weight:
191.25
PubChem Substance ID:
UNSPSC Code:
12352200
Beilstein/REAXYS Number:
1867673
MDL number:
grade
reagent grade
product line
Vetec™
assay
98%
form
powder or crystals
reaction suitability
reaction type: solution phase peptide synthesis
color
white
mp
117-119 °C (lit.)
SMILES string
CSCCC(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)
InChI key
XUYPXLNMDZIRQH-UHFFFAOYSA-N
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Legal Information
Vetec is a trademark of Merck KGaA, Darmstadt, Germany
Storage Class
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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X-ray spectroscopic approaches to the investigation and characterization of photochemical processes.
Pierre Kennepohl et al.
Journal of synchrotron radiation, 16(Pt 4), 484-488 (2009-06-19)
Despite a wealth of studies exemplifying the utility of the 2-5 keV X-ray range in speciation and electronic structure elucidation, the exploitation of this energy regime for the study of photochemical processes has not been forthcoming. Herein, a new endstation
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
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
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
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