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147966

Sigma-Aldrich

DL-Phenylalanine

ReagentPlus®, 99%

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Synonym(s):
(±)-2-Amino-3-phenylpropionic acid
Linear Formula:
C6H5CH2CH(NH2)COOH
CAS Number:
150-30-1
Molecular Weight:
165.19
Beilstein:
3198807
EC Number:
205-756-7
MDL number:
MFCD00064225
PubChem Substance ID:
24848868

Quality Level

200

product line

ReagentPlus®

Assay

99%

form

powder, crystals or granules

reaction suitability

reaction type: solution phase peptide synthesis

mp

266-267 °C (dec.) (lit.)

application(s)

peptide synthesis

SMILES string

NC(Cc1ccccc1)C(O)=O

InChI

1S/C9H11NO2/c10-8(9(11)12)6-7-4-2-1-3-5-7/h1-5,8H,6,10H2,(H,11,12)

InChI key

COLNVLDHVKWLRT-UHFFFAOYSA-N

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1 of 4

This Item
1.07257857459159492
DL-Phenylalanine ReagentPlus®, 99%

Sigma-Aldrich

147966

DL-Phenylalanine

DL-Phenylalanine for biochemistry

Millipore

1.07257

DL-Phenylalanine

N-Acetyl-L-phenylalanine ReagentPlus®, 99%

Sigma-Aldrich

857459

N-Acetyl-L-phenylalanine

DL-β-Phenylalanine 98%

Sigma-Aldrich

159492

DL-β-Phenylalanine

assay

99%

assay

-

assay

99%

assay

98%

form

powder, crystals or granules

form

solid

form

powder

form

powder

mp

266-267 °C (dec.) (lit.)

mp

271 °C (decomposition)

mp

171-173 °C (lit.)

mp

222 °C (dec.) (lit.)

reaction suitability

reaction type: solution phase peptide synthesis

reaction suitability

-

reaction suitability

reaction type: C-H Activation, reaction type: solution phase peptide synthesis, reagent type: ligand
reaction type: Peptide Synthesis

reaction suitability

reaction type: solution phase peptide synthesis

application(s)

peptide synthesis

application(s)

-

application(s)

peptide synthesis

application(s)

peptide synthesis

General description

Phenylalanine is an amino acid. It participates in the preparation of ternary piroxicam complexes of Fe(II), Fe(III), Co(II), Ni(II), Cu(II) and Zn(II). Characterization of these complexes by elemental analyses, molar conductance, IR, UV-Vis, magnetic moment, diffuse reflectance and X-ray powder diffraction methods has been conducted. Crystalline DL-phenylalanine was prepared by its reduction in silica gel by solubility method.

Application

DL-Phenylalanine may be used in the synthesis of ternary piroxicam (Pir; 4-hydroxy-2-methyl-N-(2-pyridyl)-2H-1,2-benzothiazine-3-carboxamide 1,1-dioxide) complexes of Fe(II), Fe(III), Co(II), Ni(II), Cu(II) and Zn(II).

Legal Information

ReagentPlus is a registered trademark of Sigma-Aldrich Co. LLC

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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XRD, thermal and FTIR studies on gel grown DL-Phenylalanine crystals.
Ramachandran E and Natarajan S.
Crystal Research and Technology, 42(6), 617-620 (2007)
Gehad G Mohamed et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 60(13), 3141-3154 (2004-10-13)
The ternary piroxicam (Pir; 4-hydroxy-2-methyl-N-(2-pyridyl)-2H-1,2-benzothiazine-3-carboxamide 1,1-dioxide) complexes of Fe(II), Fe(III), Co(II), Ni(II), Cu(II) and Zn(II) with various amino acids (AA) such as glycine (Gly) or DL-phenylalanine (PhA) were prepared and characterized by elemental analyses, molar conductance, IR, UV-Vis, magnetic moment
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