Fmoc-Phe-OH - ≥98% , CAS No.35661-40-6

CAS: 35661-40-6 Cat. No.: F105472 Peso molecular: 387.43 Beilstein Registry Number: 3597808 Número EC: 252-661-1 PubChem CID: 978331
Disponible para pedir
GRADE & PURITY ≥98%
Synonyms
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-phenylalanine | N-Fmoc-L-phenylalanine | N-(9-Fluorenylmethoxycarbonyl)-L-phenylalanine
Storage
Store at 2-8°C
Shipped In
Wet ice
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
5g
F105472-5g
1

9,90US$

14,90US$
Guardar 5,00 US$ (33.56%)
25g
F105472-25g
3

18,90US$

28,90US$
Guardar 10,00 US$ (34.60%)
100g
F105472-100g
1

58,90US$

88,90US$
Guardar 30,00 US$ (33.75%)
500g
F105472-500g
1

171,90US$

257,90US$
Guardar 86,00 US$ (33.35%)
Enter a quantity for the sizes you want to add.
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Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at 2-8°C Ships Wet ice Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 6 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Sinónimos
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-phenylalanine | N-Fmoc-L-phenylalanine | N-(9-Fluorenylmethoxycarbonyl)-L-phenylalanine
Especificaciones y pureza
≥98%
Condiciones de almacenamiento de almacenamiento
Store at 2-8°C
Enviado en
Wet ice
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Pureza
≥98%
Nombres e identificadores
Pubchem Sid504760338
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504760338
Sonrisas canónicasOC(=O)[C@H](Cc1ccccc1)NC(=O)OCC2c3ccccc3-c4ccccc24
IUPAC Name(2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-phenylpropanoic acid
InChIKeySJVFAHZPLIXNDH-QFIPXVFZSA-N
INCHI1S/C24H21NO4/c26-23(27)22(14-16-8-2-1-3-9-16)25-24(28)29-15-21-19-12-6-4-10-17(19)18-11-5-7-13-20(18)21/h1-13,21-22H,14-15H2,(H,25,28)(H,26,27)/t22-/m0/s1
Isómeros SMILES C1=CC=C(C=C1)C[C@@H](C(=O)O)NC(=O)OCC2C3=CC=CC=C3C4=CC=CC=C24
WGK Alemania 3
PubChem CID 978331
Peso molecular 387.43
Beilstein 3597808

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic acids and derivatives
ClaseCarboxylic acids and derivatives
SubclassAmino acids, peptides, and analogues
Intermediate Tree Nodes Amino acids and derivatives - Alpha amino acids and derivatives
Direct ParentPhenylalanine and derivatives
Alternative Parents Fluorenes  Phenylpropanoic acids  Amphetamines and derivatives  Carbamate esters  Organic carbonic acids and derivatives  Monocarboxylic acids and derivatives  Carboxylic acids  Organopnictogen compounds  Organonitrogen compounds  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAromatic homopolycyclic compounds
Substituents Phenylalanine or derivatives - Fluorene - 3-phenylpropanoic-acid - Amphetamine or derivatives - Monocyclic benzene moiety - Benzenoid - Carbamic acid ester - Carbonic acid derivative - Carboxylic acid - Monocarboxylic acid or derivatives - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Carbonyl group - Organic oxygen compound - Aromatic homopolycyclic compound
DescripciónThis compound belongs to the class of organic compounds known as phenylalanine and derivatives. These are compounds containing phenylalanine or a derivative thereof resulting from reaction of phenylalanine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
Homo sapiens (32628 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
surA Chaperone SurA (18 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

20 results found

Lot NumberCertificate TypeFechaArticulo
D2623354Certificate of AnalysisMar 04, 2026 F105472
D2623355Certificate of AnalysisMar 04, 2026 F105472
D2623356Certificate of AnalysisMar 04, 2026 F105472
D2623357Certificate of AnalysisMar 04, 2026 F105472
A2622065Certificate of AnalysisJan 28, 2026 F105472
K2119196Certificate of AnalysisSep 04, 2025 F105472
B2626060Certificate of AnalysisAug 14, 2024 F105472
H2421523Certificate of AnalysisAug 14, 2024 F105472
H2421524Certificate of AnalysisAug 14, 2024 F105472
H2421525Certificate of AnalysisAug 14, 2024 F105472
H2421526Certificate of AnalysisAug 14, 2024 F105472
D2407228Certificate of AnalysisMar 11, 2024 F105472
D2407230Certificate of AnalysisMar 11, 2024 F105472
B2026094Certificate of AnalysisDec 18, 2023 F105472
J2210466Certificate of AnalysisJul 21, 2022 F105472
J2210467Certificate of AnalysisJul 21, 2022 F105472
J2210468Certificate of AnalysisJul 21, 2022 F105472
J2210326Certificate of AnalysisJul 21, 2022 F105472
L2315050Certificate of AnalysisJul 21, 2022 F105472
L2315051Certificate of AnalysisJul 21, 2022 F105472

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Propiedades químicas y físicas
Rotación específica [α]-36.0 to -40.0 deg(C=1, DMF)
Punto de fusión (°C)180-187°C
Peso molecular387.400 g/mol
XLogP34.600
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count4
Rotatable Bond Count7
Exact Mass387.147 Da
Monoisotopic Mass387.147 Da
Topological Polar Surface Area75.600 Ų
Heavy Atom Count29
Formal Charge0
Complexity551.000
Isotope Atom Count0
Defined Atom Stereocenter Count1
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Preguntas frecuentes y artículos
Citations of This Product
Referencias
1. Li Wan.  (2020)  Supramolecular nanofiber-reinforced Puerarin hydrogels as drug carriers with synergistic controlled release and antibacterial properties.  JOURNAL OF MATERIALS SCIENCE,  55  (15): (6669-6677).  [PMID:] [10.1007/s10853-020-04455-3]
2. Jie Zhou, Chuanan Liao, Limin Zhang, Qigang Wang, Yang Tian.  (2014)  Molecular Hydrogel-Stabilized Enzyme with Facilitated Electron Transfer for Determination of H2O2 Released from Live Cells.  ANALYTICAL CHEMISTRY,      [PMID:24716876] [10.1021/ac500231e]
3. Jianxu Zhou, Taotao Huo, Junxian Miu, Ziyi Wang, Xiaoyu Shan, Jiaqi Song, Yuquan Bai, Shuichu Hao, Chun Zhang, Shichang Liu, Biao Wang, Guanying Li.  (2025)  Bone-Adhesive Peptide Hydrogel Loaded with Cisplatin for Postoperative Treatment of Osteosarcoma.  ACS Applied Materials & Interfaces,      [PMID:39908045] [10.1021/acsami.4c19608]
4. Junwu Wei, Yangyang Qian, Lijun Bao, Wenjie Song, Yunmei Bi.  (2024)  Disulfide bonds as a molecular switch of enzyme-activatable anticancer drug precise release for fluorescence imaging and enhancing tumor therapy.  TALANTA,      [PMID:38924984] [10.1016/j.talanta.2024.126394]
5. CAIYUN DENG, CHANG XU, XIAOMIN ZHANG, JU YAO, YINGXIN ZHANG, BO YU, ROBERT J. LEE, CHENGJUN JIANG.  (2018)  A Novel Paclitaxel-Loaded Polymeric Micelle System with Favorable Biocompatibility and Superior Antitumor Activity.  ANTICANCER RESEARCH,  38  (1): (219-225).  [PMID:29277776] [PMID:29277776]
6. Jiahe Huang, Chunhong Zhang, Jianwei Bai, Yudan Wang, Toshifumi Satoh, Feng-Huei Lin.  (2025)  Self-Assembled Supramolecular Gels for Catalyzing Asymmetric Aldol and Mannich Reactions in Aqueous Media.  ACS Sustainable Chemistry & Engineering,      [PMID:] [10.1021/acssuschemeng.5c00078]
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