Direkt zum Inhalt
Merck
Alle Fotos(2)

Dokumente

A16300

Sigma-Aldrich

N-Acetylglycin

ReagentPlus®, 99%

Synonym(e):

Acetursäure

Anmeldenzur Ansicht organisationsspezifischer und vertraglich vereinbarter Preise
Alle Fotos(2)

About This Item

Lineare Formel:
CH3CONHCH2CO2H
CAS-Nummer:
543-24-8
Molekulargewicht:
117.10
Beilstein:
774114
EG-Nummer:
208-839-6
MDL-Nummer:
MFCD00004275
UNSPSC-Code:
12352209
eCl@ss:
32160406
PubChem Substanz-ID:
24890569
NACRES:
NA.22

Produktlinie

ReagentPlus®

Assay

99%

Form

powder or crystals

Eignung der Reaktion

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

Farbe

white

mp (Schmelzpunkt)

207-209 °C (lit.)

Anwendung(en)

detection
peptide synthesis

Funktionelle Gruppe

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)

InChIKey

OKJIRPAQVSHGFK-UHFFFAOYSA-N

Suchen Sie nach ähnlichen Produkten? Aufrufen Leitfaden zum Produktvergleich

Verwandte Kategorien

Rechtliche Hinweise

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

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)

Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

Besitzen Sie dieses Produkt bereits?

In der Dokumentenbibliothek finden Sie die Dokumentation zu den Produkten, die Sie kürzlich erworben haben.

Die Dokumentenbibliothek aufrufen

Kunden haben sich ebenfalls angesehen

Slide 1 of 3

1 of 3

O-Acetyl-L-Carnitin -hydrochlorid ≥99% (titration), powder

Sigma-Aldrich

A6706

O-Acetyl-L-Carnitin -hydrochlorid

4-(Diethylamino)salicylaldehyd 98%

Sigma-Aldrich

225681

4-(Diethylamino)salicylaldehyd

Sarcosin 98%

Sigma-Aldrich

131776

Sarcosin

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
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
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
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
Alle zugehörigen Dokumente anzeigen

Unser Team von Wissenschaftlern verfügt über Erfahrung in allen Forschungsbereichen einschließlich Life Science, Materialwissenschaften, chemischer Synthese, Chromatographie, Analytik und vielen mehr..

Setzen Sie sich mit dem technischen Dienst in Verbindung.