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Key Documents

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A16300

Sigma-Aldrich

N-Acetylglycine

ReagentPlus®, 99%

Sinónimos:

Acetamidoacetic acid, Aceturic acid

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About This Item

Fórmula lineal:
CH3CONHCH2CO2H
Número de CAS:
543-24-8
Peso molecular:
117.10
Beilstein/REAXYS Number:
774114
EC Number:
208-839-6
MDL number:
MFCD00004275
UNSPSC Code:
12352209
eCl@ss:
32160406
PubChem Substance ID:
24890569
NACRES:
NA.22

product line

ReagentPlus®

assay

99%

form

powder or crystals

reaction suitability

reaction type: C-H Activation
reaction type: solution phase peptide synthesis
reagent type: ligand
reaction type: Peptide Synthesis

color

white

mp

207-209 °C (lit.)

application(s)

detection
peptide synthesis

functional group

amine
carboxylic acid

SMILES string

CC(=O)NCC(O)=O

InChI

1S/C4H7NO3/c1-3(6)5-2-4(7)8/h2H2,1H3,(H,5,6)(H,7,8)

Inchi Key

OKJIRPAQVSHGFK-UHFFFAOYSA-N

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Legal Information

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

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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Anatoliy Volkov et al.
Journal of computational chemistry, 25(7), 921-934 (2004-03-18)
Accurate and fast evaluation of electrostatic interactions in molecular systems is still one of the most challenging tasks in the rapidly advancing field of macromolecular chemistry, including molecular recognition, protein modeling and drug design. One of the most convenient and
Y Chen et al.
Biochemistry, 37(28), 9976-9982 (1998-07-17)
A general approach to dissecting the complex photophysics of tryptophan is presented and used to elucidate the effects of amino acid functional groups on tryptophan fluorescence. We have definitively identified the amino acid side chains that quench tryptophan fluorescence and
Z Gu et al.
Journal of magnetic resonance (San Diego, Calif. : 1997), 138(2), 193-198 (1999-05-26)
Triple-resonance experiments capable of correlating directly bonded and proximate carbon and nitrogen backbone sites of uniformly 13C- and 15N-labeled peptides in stationary oriented samples are described. The pulse sequences integrate cross-polarization from 1H to 13C and from 13C to 15N
Jamie L Snow et al.
Journal of the American Chemical Society, 129(32), 9910-9917 (2007-07-26)
Both theoretical and experimental studies are reported for the gas-phase reactions of protonated hydroxylamine with acetic and propanoic acids which yield protonated glycine and alanine, GlyH+ and AlaH+, respectively. The key step for these reactions is an insertion of the
H K Ogawa et al.
Journal of chromatography, 612(1), 145-149 (1993-01-29)
A simple and sensitive method for the determination of N-acetylneuraminic acid and N-glycolylneuraminic acid in glycoproteins by high-performance liquid chromatography has been investigated. The best condition to release sialic acid from glycoproteins involved incubation at 80 degrees C for 1
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