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P25485

D−(−)-α-Phenylglycine

Name: <SC>D</SC>&#8722;(&#8722;)-&#945;-Phenylglycine
Brand: ALDRICH

99%, detection

Synonym(s):

(R)-(−)-2-Phenylglycine, D-2-Phenylglycine, R-(−)-α-Aminophenylacetic acid

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About This Item

Linear Formula:

C₆H₅CH(NH₂)CO₂H

CAS Number:

875-74-1

Molecular Weight:

151.16

NACRES:

NA.22

PubChem Substance ID:

24898336

UNSPSC Code:

12352209

EC Number:

212-876-3

MDL number:

MFCD00008061

Beilstein/REAXYS Number:

2208676

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Properties

Product Name

D−(−)-α-Phenylglycine, 99%

Quality Level

200

assay

99%

form

powder or crystals

optical activity

[α]20/D −155°, c = 1 in 1 M HCl

reaction suitability

reaction type: solution phase peptide synthesis

color

white

mp

302 °C (dec.) (lit.)

application(s)

detection

SMILES string

N[C@@H](C(O)=O)c1ccccc1

InChI

1S/C8H9NO2/c9-7(8(10)11)6-4-2-1-3-5-6/h1-5,7H,9H2,(H,10,11)/t7-/m1/s1

InChI key

ZGUNAGUHMKGQNY-SSDOTTSWSA-N

Description

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Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

302.0 °F - closed cup

flash_point_c

150 °C - closed cup

ppe

Eyeshields, Gloves, type N95 (US)

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Chiral recognition of α-amino acids by an optically active (2S,5S,8S,11S)-2,5,8,11-tetraethyl cyclen cobalt(III) complex.

Shohei Tashiro et al.

Inorganic chemistry, 50(1), 4-6 (2010-12-01)

The optically active cobalt(III) complex with chiral cyclen, (2S,5S,8S,11S)-2,5,8,11-tetraethyl-1,4,7,10-tetraazacyclododecane, preferentially binds to D-phenylglycine (D-Phg) or D-t-leucine (D-t-Leu) rather than L-Phg or L-t-Leu, respectively, with 20% de in dimethyl sulfoxide at 293 K. Comparative studies on the crystal structures of cobalt(III)

Syntheses and highly enantioselective fluorescent recognition of α-aminocarboxylic acid anions using chiral oxacalix[2]arene[2]bisbinaphthes.

Kuoxi Xu et al.

Chirality, 24(8), 646-651 (2012-05-24)

The triazine-based bisbinaphthyl crown ethers oxacalix[2]arene[2]bisbinaphthes R-1, R-2, R-3 and S-1, S-2, S-3 were synthesized. The interactions of these compounds with various α-aminocarboxylic acid anions were studied. The crown ethers were found to carry out highly enantioselective fluorescent recognition of

Investigation and characterization of liquid two-phase systems for the separation of crystal mixtures by interfacial partitioning.

Martijn A Hoeben et al.

Biotechnology and bioengineering, 93(4), 607-617 (2006-01-06)

The interfacial partitioning behavior of ampicillin and phenylglycine crystals in different two-phase systems has been investigated. The two-phase systems employed are water/dodecane, water/1-butanol, and water/pentane/methanol. By means of partition experiments and microscopic imaging, it has been shown that the mechanism

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Global Trade Item Number

SKU	GTIN
P25485-25G	04061834364030
P25485-100G	04061834364023