Skip to Content
Merck
CN

P4126

Phe-Phe

≥98% (TLC)

Synonym(s):

L-Phenylalanyl-L-phenylalanine, Di-L-phenylalanine

Sign In to View Organizational & Contract Pricing.

Select a Size


About This Item

Linear Formula:
C6H5CH2CH(NH2)CONHCH(CH2C6H5)COOH · H2O
CAS Number:
Molecular Weight:
312.36 (anhydrous basis)
NACRES:
NA.26
PubChem Substance ID:
UNSPSC Code:
12352202
EC Number:
219-930-5
MDL number:
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Product Name

Phe-Phe,

InChI key

GKZIWHRNKRBEOH-HOTGVXAUSA-N

InChI

1S/C18H20N2O3/c19-15(11-13-7-3-1-4-8-13)17(21)20-16(18(22)23)12-14-9-5-2-6-10-14/h1-10,15-16H,11-12,19H2,(H,20,21)(H,22,23)/t15-,16-/m0/s1

SMILES string

N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc2ccccc2)C(O)=O

assay

≥98% (TLC)

form

powder

color

white

storage temp.

−20°C

Quality Level

Looking for similar products? Visit Product Comparison Guide

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

H Mozsolits et al.
Biophysical journal, 77(3), 1428-1444 (1999-08-31)
The interaction of three bioactive peptides, bombesin, beta-endorphin, and glucagon with a phosphatidylcholine monolayer that was immobilized to porous silica particles and packed into a stainless steel column cartridge, has been studied using dynamic elution techniques. This immobilized lipid monolayer
Dmitriy Berillo et al.
Journal of colloid and interface science, 368(1), 226-230 (2011-12-02)
In this study, it was found that macroporous hydrogels were formed when self-assembly of fluorenyl-9-methoxycarbonyl (Fmoc)-diphenylalanine (Phe-Phe) peptides was induced using glucono-δ-lactone (GdL) in apparently frozen samples. Formed cryogels exhibited a heterogeneous structure with pore walls of densely packed fibres
Robert C Dunbar et al.
Journal of the American Chemical Society, 133(5), 1212-1215 (2011-01-05)
Chirality reversal of a residue in a peptide can change its mode of binding to a metal ion, as shown here experimentally by gas-phase IR spectroscopy of peptide-metal ion complexes. The binding conformations of Li(+), Na(+), and H(+) with the
Gokhan Demirel et al.
Langmuir : the ACS journal of surfaces and colloids, 27(20), 12533-12538 (2011-09-02)
There is an increasing interest for the utilization of biomolecules for fabricating novel nanostructures due to their ability for specific molecular recognition, biocompatibility, and ease of availability. Among these molecules, diphenylalanine (Phe-Phe) dipeptide is considered as one of the simplest
G B Dreyer et al.
Biochemistry, 32(3), 937-947 (1993-01-26)
Potential advantages of C2-symmetric inhibitors designed for the symmetric HIV-1 protease include high selectivity, potency, stability, and bioavailability. Pseudo-C2-symmetric monools and C2-symmetric diols, containing central hydroxymethylene and (R,R)-dihydroxyethylene moieties flanked by a variety of hydrophobic P1/P1' side chains, were studied

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service