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Merck
CN

P4126

Sigma-Aldrich

Phe-Phe

≥98% (TLC)

Synonym(s):

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

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About This Item

Linear Formula:
C6H5CH2CH(NH2)CONHCH(CH2C6H5)COOH · H2O
CAS Number:
Molecular Weight:
312.36 (anhydrous basis)
EC Number:
MDL number:
UNSPSC Code:
12352202
PubChem Substance ID:
NACRES:
NA.26

Product Name

Phe-Phe,

Assay

≥98% (TLC)

Quality Level

form

powder

color

white

storage temp.

−20°C

SMILES string

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

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

InChI key

GKZIWHRNKRBEOH-HOTGVXAUSA-N

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product line

ProteoMass

product line

ProteoMass

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ProteoMass

product line

ProteoMass

application(s)

cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care

application(s)

cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care

application(s)

cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care

application(s)

cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care

compatibility

for use with (Complex cell extracts, pure protein solution, 1D and 2D PAGE gels)

compatibility

-

compatibility

-

compatibility

-

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

100

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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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
Supramolecular nanofibers and hydrogels of nucleopeptides.
Xinming Li et al.
Angewandte Chemie (International ed. in English), 50(40), 9365-9369 (2011-09-29)
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
Meital Reches et al.
Physical biology, 3(1), S10-S19 (2006-04-04)
Molecular self-assembly offers new routes for the fabrication of novel materials at the nano-scale. Peptide-based nanostructures represent nano-objects of particular interest, as they are biocompatible, can be easily synthesized in large amounts, can be decorated with functional elements and can

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