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147966

Sigma-Aldrich

DL-Phenylalanine

99%, for peptide synthesis, ReagentPlus®

Synonym(s):

(±)-2-Amino-3-phenylpropionic acid

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About This Item

Linear Formula:
C6H5CH2CH(NH2)COOH
CAS Number:
150-30-1
Molecular Weight:
165.19
Beilstein:
3198807
EC Number:
205-756-7
MDL number:
MFCD00064225
UNSPSC Code:
12352209
PubChem Substance ID:
24848868
NACRES:
NA.22

product name

DL-Phenylalanine, ReagentPlus®, 99%

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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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 Merck KGaA, Darmstadt, Germany

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

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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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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