147966
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:
Molecular Weight:
165.19
Beilstein:
3198807
EC Number:
MDL number:
UNSPSC Code:
12352209
PubChem Substance ID:
NACRES:
NA.22
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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
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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
XRD, thermal and FTIR studies on gel grown DL-Phenylalanine crystals.
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Crystal Research and Technology, 42(6), 617-620 (2007)
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