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Merck
CN

78560

Sigma-Aldrich

N-Phenylglycine

purum, ≥97.0% (T)

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:
12352200
PubChem Substance ID:
329768160

Key Documents

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grade

purum

Assay

≥97.0% (T)

form

powder or crystals

color

faintly yellow to yellow

mp

121-123 °C (lit.)
121-125 °C

application(s)

detection
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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Storage Class Code

13 - Non 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

Regulatory Information

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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
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
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
Roger Hanselmann et al.
The Journal of organic chemistry, 68(22), 8739-8741 (2003-10-25)
Isoxazolidines have been synthesized in diastereomeric excess up to 94% via a MgBr2-induced chelation-controlled 1,3-dipolar cycloaddition reaction with N-hydroxyphenylglycinol as a chiral auxiliary. The diastereomerically pure isoxazolidines were further transformed into cyclic and acyclic beta-amino acid derivatives.
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