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330469

Sigma-Aldrich

N-Phenylglycine

97%

Synonym(s):

(Phenylamino)acetic acid, Anilinoacetic acid

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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

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Related Categories

Storage Class Code

11 - Combustible Solids

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’.

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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.
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
L E Wolinsky et al.
Journal of dental research, 72(1), 72-77 (1993-01-01)
The purpose of the present investigation was to determine whether high-resolution carbon-13 nuclear magnetic resonance could be utilized for detection of ionic bonding interactions of NPG and NPG-GMA with selected inorganic cations. The C1-carbonyl carbon of NPG and NPG-GMA were
N J Miniotis et al.
Journal of dental research, 72(6), 1045-1049 (1993-06-01)
This study evaluated and compared the contributions to dentin adhesive bonding of three N-phenylglycine analogues with electron-withdrawing substituents on the aromatic ring. These electron-deficient "N-compounds" included: N-(4-chlorophenyl)-glycine (NCPG), N-methyl-N-(4-chlorophenyl)-glycine (NMNCPG), and N-(3,4-dichlorophenyl)-glycine (NDCPG). An experimental three-step dentin-bonding protocol that consisted
G Kato et al.
Dental materials : official publication of the Academy of Dental Materials, 14(5), 347-352 (1999-06-24)
The purpose of this study was to investigate the influence of remaining non-resin-impregnated, phosphoric acid demineralized dentin upon the long-term durability of specimens that were wet-bonded to bovine dentin substrates. Prepared bovine dentin samples were etched with 65% phosphoric acid
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