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About This Item
Linear Formula:
CH3SO2CH2CH2CH(NH2)COOH
CAS Number:
Molecular Weight:
181.21
UNSPSC Code:
12352209
NACRES:
NA.22
PubChem Substance ID:
EC Number:
212-466-4
Beilstein/REAXYS Number:
2089918
MDL number:
Product Name
DL-Methionine sulfone, ≥99.0% (NT)
InChI key
UCUNFLYVYCGDHP-UHFFFAOYSA-N
InChI
1S/C5H11NO4S/c1-11(9,10)3-2-4(6)5(7)8/h4H,2-3,6H2,1H3,(H,7,8)
SMILES string
CS(=O)(=O)CCC(N)C(O)=O
assay
≥99.0% (NT)
form
solid
reaction suitability
reaction type: solution phase peptide synthesis
mp
~250 °C (dec.)
application(s)
peptide synthesis
Quality Level
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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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Tae Hee Han et al.
Asian-Australasian journal of animal sciences, 30(8), 1150-1159 (2017-02-12)
This study was conducted to evaluate various wheat supplementation levels on growth performance, blood profiles, nutrient digestibility, and pork quality in growing-finishing pigs. A total of 120 growing pigs ([Yorkshire×Landrace]×Duroc), with an average 27.75± 1.319 kg body weight, were used
Vincenza M Coiro et al.
Protein science : a publication of the Protein Society, 13(11), 2979-2991 (2004-10-23)
Glutamate synthase (GltS) is a complex iron-sulfur flavoprotein that catalyzes the reductive transfer of L-glutamine amide group to the C2 carbon of 2-oxoglutarate yielding two molecules of L-glutamate. Molecular dynamics calculations in explicit solvent were carried out to gain insight
C M Parsons et al.
The British journal of nutrition, 46(1), 77-86 (1981-07-01)
1. The relative potencies of three lysine, one tryptophan and six methionine analogues to their corresponding l-amino acids were determined. 2. Male poults, 9 d of age, were used in five 14 d experiments. Experimental diets were formed by adding
M K Unnikrishnan et al.
Agents and actions, 31(1-2), 110-112 (1990-08-01)
The oxidation of methionine in peptides is often associated with the loss of biological activity. Since methionine showed good antiinflammatory activity, its oxidized products methionine sulfoxide and methionine sulfone were tested. The sulfone was more active than the sulfoxide although
F J Cejudo et al.
Biochemical and biophysical research communications, 123(2), 431-437 (1984-09-17)
Addition of NH4Cl at low concentrations to Azotobacter chroococcum cells caused an immediate cessation of nitrogenase activity, which was recovered once the added NH+4 was exhausted from the medium. In the presence of inhibitors of ammonium assimilation, such as L-methionine-DL-sulfoximine
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