All Photos(1)

Documents

330469

N-Phenylglycine

Name: <I>N</I>-Phenylglycine
Brand: ALDRICH

97%

Synonym(s):

(Phenylamino)acetic acid, Anilinoacetic acid

Sign Into View Organizational & Contract Pricing

All Photos(1)

About This Item

Linear Formula:

C₆H₅NHCH₂COOH

CAS Number:

103-01-5

Molecular Weight:

151.16

Beilstein:

509838

EC Number:

203-070-2

MDL number:

MFCD00014009

UNSPSC Code:

12352209

PubChem Substance ID:

24859860

NACRES:

NA.22

Quality Level

200

Assay

97%

reaction suitability

reaction type: solution phase peptide synthesis

mp

121-123 °C (lit.)

application(s)

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)

InChI key

NPKSPKHJBVJUKB-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

Amino Acids, Resins & Reagents for Peptide Synthesis

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Dentin-bonding molar efficiency using N-phenylglycine, N-phenyl-beta-alanine, or N-methyl-N-phenylglycine.

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

N-phenyliminodiacetic acid as an etchant/primer for dentin bonding.

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

High potency dipeptide sweeteners. 1. L-aspartyl-D-phenylglycine esters.

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

Substitutes for N-phenylglycine in adhesive bonding to dentin.

A D Johnston et al.

Journal of dental research, 68(9), 1337-1344 (1989-09-01)

Using bond strength measurements, we investigated a number of related compounds in order to elucidate the role of the surface-active ingredient, N-phenylglycine (NPG), in experimental two-step and three-step bonding protocols resulting in adhesive bonding to dentin. All active compounds identified

Effects of water and carboxylic acid monomer on polymerization of HEMA in the presence of N-phenylglycine.

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

View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service