Fmoc-L-phenylalanine, 98%

Name: Fmoc-L-phenylalanine, 98% | 35661-40-6
Brand: J&K Chemical
SKU: JK199851_5_G
Price: 18.9 USD
Availability: OutOfStock

Cat. No JK199851_5_G

Vendor: J&K Chemical

Product Information

Product Name

Fmoc-L-phenylalanine, 98%

Brand Name

J&K

Product Number

199851

CAS

35661-40-6

Molecular Formula

C24H21NO4

Molecular Weight

387.43

SDS Document

View/Download

Certificate of Analysis (COA)

COA not found

General Information

Synonyms

N-(9-Fluorenylmethoxycarbonyl)-L-phenylalanine
Fmoc-Phe-OH

PubChem CID

978331

IUPAC Name

(2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-phenylpropanoic acid

InChI Key

SJVFAHZPLIXNDH-QFIPXVFZSA-N

SMILES

C1=CC=C(C=C1)CC@@H(C(=O)O)NC(=O)OCC2C3=CC=CC=C3C4=CC=CC=C24

Properties

Melting Point

181

Optical Activity

-40.5° to -35.5° (C=1, DMF)

Safety Information

Precautionary Statement

P260

P262

References Data Source From Pubchem

Water-based coupling of amino acids for sustainable solid-phase peptide synthesis

Publication Name: Nature Sustainability

Publication Date: 2026-02-03

DOI: 10.1038/s41893-025-01761-z

Identification of small GTPases as potential target proteins of the mycotoxin and renal carcinogen ochratoxin A

Publication Name: Archives of Toxicology

Publication Date: 2025-09-11

DOI: 10.1007/s00204-025-04189-8

Exploring tunable characteristics of anthranilic acid in peptide-based nanostructures

Publication Name: Journal of Materials Research

Publication Date: 2025-09-02

DOI: 10.1557/s43578-025-01683-8

Discordance between in silico and in vitro results on proteolytic stability of milk protein-derived DPP-4 inhibitory peptides

Publication Name: European Food Research and Technology

Publication Date: 2025-07-09

DOI: 10.1007/s00217-025-04833-8

Natural phytochemical-based strategies for antibiofilm applications

Publication Name: Chinese Medicine

Publication Date: 2025-07-01

DOI: 10.1186/s13020-025-01147-5

Fmoc-L-phenylalanine, 98%

Product Information

General Information

Properties

Safety Information

References Data Source From Pubchem

Water-based coupling of amino acids for sustainable solid-phase peptide synthesis

Identification of small GTPases as potential target proteins of the mycotoxin and renal carcinogen ochratoxin A

Exploring tunable characteristics of anthranilic acid in peptide-based nanostructures

Discordance between in silico and in vitro results on proteolytic stability of milk protein-derived DPP-4 inhibitory peptides

Natural phytochemical-based strategies for antibiofilm applications