01180
N-Acetylglycine
puriss., ≥99.0% (T)
Synonym(s):
Acetamidoacetic acid, Aceturic acid
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About This Item
Linear Formula:
CH3CONHCH2CO2H
CAS Number:
Molecular Weight:
117.10
EC Number:
208-839-6
UNSPSC Code:
12352200
PubChem Substance ID:
Beilstein/REAXYS Number:
774114
MDL number:
grade
puriss.
assay
≥99.0% (T)
mp
207-209 °C
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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Storage Class
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Regulatory Information
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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
Bram Boeckx et al.
The journal of physical chemistry. A, 116(8), 1956-1965 (2012-01-26)
Within the structure determination task for peptides, which is of large interest due to the relation between structure and functionality, infrared spectra can provide detailed information on the conformational behavior. The conformational landscape ofN-acetylgycine has been studied by a combined
Liangxing Wu et al.
Journal of the American Chemical Society, 130(12), 4089-4096 (2008-03-07)
Eight B-containing compounds, i.e., 1a-h, were prepared as mimics of the green fluorescent protein (GFP) fluorophore. The underlying concept was that synthetic GFP chromophore analogues are not fluorescent primarily because of free rotation about an aryl-alkene bond (Figure 1b). This
Functionalizing glycine derivatives by direct C-C bond formation.
Liang Zhao et al.
Angewandte Chemie (International ed. in English), 47(37), 7075-7078 (2008-08-02)
S K Mehta et al.
Journal of colloid and interface science, 314(2), 689-698 (2007-06-26)
The well-characterized, monodisperse nature of reverse micelles formed by sodium bis-(2-ethylhexyl)sulfosuccinate/water/isooctane and their usefulness in assimilating compounds of varied interests have been exploited to investigate the effect of acetyl modified amino acids (MAA) viz., N-acetyl-L-glycine (NAG), N-acetyl-L-aspartic acid (NAA) and
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