Direkt zum Inhalt
Merck
Alle Fotos(1)

Dokumente

330469

Sigma-Aldrich

N-Phenylglycin

97%

Synonym(e):

Anilinoessigsäure, Phenylaminoessigsäure

Anmeldenzur Ansicht organisationsspezifischer und vertraglich vereinbarter Preise
Alle Fotos(1)

About This Item

Lineare Formel:
C6H5NHCH2COOH
CAS-Nummer:
103-01-5
Molekulargewicht:
151.16
Beilstein:
509838
EG-Nummer:
203-070-2
MDL-Nummer:
MFCD00014009
UNSPSC-Code:
12352209
PubChem Substanz-ID:
24859860
NACRES:
NA.22

Assay

97%

Eignung der Reaktion

reaction type: solution phase peptide synthesis

mp (Schmelzpunkt)

121-123 °C (lit.)

Anwendung(en)

peptide synthesis

SMILES String

OC(=O)CNc1ccccc1

InChI

1S/C8H9NO2/c10-8(11)6-9-7-4-2-1-3-5-7/h1-5,9H,6H2,(H,10,11)

InChIKey

NPKSPKHJBVJUKB-UHFFFAOYSA-N

Suchen Sie nach ähnlichen Produkten? Aufrufen Leitfaden zum Produktvergleich

Verwandte Kategorien

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 2

1 of 2

Borandimethylamin-Komplex 97%

Sigma-Aldrich

180238

Borandimethylamin-Komplex

N-Methyldiethanolamin ≥99%

Sigma-Aldrich

471828

N-Methyldiethanolamin

R E Webb et al.
Journal of dental research, 70(3), 211-214 (1991-03-01)
Three structurally related substituted amino acids (N-compounds) were studied in a three-step dentin-bonding protocol. The first step of an acidic ferric oxalate solution and the third step of a surface-active comonomer were held constant throughout the study. In the second
G E Schumacher et al.
Journal of dental research, 76(1), 602-609 (1997-01-01)
Effective composite-to-dentin bonding has been achieved by the sequential use of dilute aqueous nitric acid (HNO3) and acetone solutions of N-phenylglycine and a carboxylic acid monomer, e.g., p-PMDM. Both the HNO3 pre-treatment and the surface-initiated polymerization that results from reaction
J M Janusz et al.
Journal of medicinal chemistry, 33(3), 1052-1061 (1990-03-01)
Twenty esters of L-aspartyl-D-phenylglycine, as well as two substituted analogues, an o-fluoro and a p-hydroxy-phenylglycine ester, were prepared. The L-aspartyl-D-phenylglycine (-)-alpha- and (+)-beta-fenchyl esters had the highest sweetness potency at 1200 and 3700 times that of sucrose, respectively. The high
G E Schumacher et al.
Dental materials : official publication of the Academy of Dental Materials, 8(4), 278-282 (1992-07-01)
Effective dentin bonding systems based on para-PMDM diadduct of pyromellitic dianhydride and 2-hydroxyethyl methacrylate (HEMA) have been developed (Bowen et al., 1982). Para-PMDM, a solid of limited solubility, is usually applied from an acetone solution to dentin that has been
Y Imai et al.
Dental materials : official publication of the Academy of Dental Materials, 10(4), 275-277 (1994-07-01)
This research was designed to study the effect of water or carboxylic acid monomer on the polymerization of 2-hydroxyethyl methacrylate (HEMA) in order to understand the bonding mechanism of dentin bonding systems using N-phenylglycine (NPG). The polymerization of HEMA in
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.