BOC-D-Phenylalanine
Nanjing Finechem Holdings Co., LTD
Specifications
N/A
Packing & Storage
Packing
Storage Powder -20°C 3 years 4°C 2 years;In solvent -80°C 6 months, -20°C 1 month
Shipping Room temperature in continental US; may vary elsewhere
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General Information
Chemical & Physical Properties
Safety Information
Synthetic Route
Biological Activity
Common Names Boc-D-Phe-OH
Structure
CAS No. 18942-49-9 Boiling Point (℃) 426.6±38.0 °C at 760 mmHg
Molecular Weight 265.305 Melting Point (℃) 85-88ºC
Density 1.2±0.1 g/cm3 Vapor Specific Gravity N/A
Molecular Formula C14H19NO4 Flash Point (℃) 211.8±26.8 °C
Solubility N/A Autoignition Temperature (℃) N/A
Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes T+:Very toxic
Safety Phrases S1-S28-S45
RIDADR NONH for all modes of transport
WGK Germany  3
SYMPTOMS PREVENTION FIRST AID
Inhalation Cough. Sore throat. Use local exhaust or breathing protection. Fresh air, rest.
Skin Redness. Burning sensation. Itching. Protective gloves. Remove contaminated clothes. Rinse and then wash skin with water and soap.
Eyes Redness. Pain. Wear safety goggles. First rinse with plenty of water for several minutes (remove contact lenses if easily possible), then refer for medical attention.
Ingestion Abdominal pain. Nausea. Vomiting. Do not eat, drink, or smoke during work. Wash hands before eating. Rinse mouth. Induce vomiting (ONLY IN CONSCIOUS PERSONS!). Refer for medical attention.
Description Boc-D-Phe-OH is a phenylalanine derivative[1].
Target Km: 100-400 μM (amino acid transporter b0,+)[1]
In Vitro Amino acids and amino acid derivatives have been commercially used as ergogenic supplements. They influence the secretion of anabolic hormones, supply of fuel during exercise, mental performance during stress related tasks and prevent exercise induced muscle damage. They are recognized to be beneficial as ergogenic dietary substances[1].
References [1]. Luckose F, et al. Effects of amino acid derivatives on physical, mental, and physiological activities. Crit Rev Food Sci Nutr. 2015;55(13):1793-884.
Synonyms
Boc-D-Phe-OH
(2R)-2-[(tert-butoxy)carbonylamino]-3-phenylpropanoic acid
N-(t-butyloxycarbonyl)-D-Phenylalanine
Boc-phenylalanine
BOC-D-PHE
Boc-L-Phenylalanine
(2S)-2-({[(2-Methyl-2-propanyl)oxy]carbonyl}amino)-3-phenylpropanoic acid
N-Boc-D-phenylalanine
(S)-2-((tert-Butoxycarbonyl)amino)-3-phenylpropanoic acid
N-(tert-Butoxycarbonyl)-L-phenylalanine
boc-L-Phe
MFCD00063149
L-Phenylalanine, N-[(1,1-dimethylethoxy)carbonyl]-
N-t-Butyloxycarbonyl-L-phenylalanine
N-(t-butoxycarbonyl)-D-phenylalanine
L-Phenylalanine, N-((1,1-dimethylethoxy)carbonyl)-
N-Boc-L-phenylalanine
Product Description
Introduction: BOC-D-Phenylalanine is a vital amino acid protecting agent widely utilized in peptide synthesis. With its ability to safeguard amino groups during peptide chain assembly, BOC-D-Phenylalanine plays a crucial role in peptide synthesis strategies. Its versatility and reliability make it highly sought after by researchers and chemists in the field.

Product Features: Exceptional Purity: BOC-D-Phenylalanine is produced with meticulous attention to purity. Its high-quality standards ensure minimal impurities, allowing for the synthesis of peptides with excellent quality and purity.

Efficient Amine Protection: BOC-D-Phenylalanine acts as a highly effective protective group for amino groups, preventing unwanted side reactions during peptide synthesis. It selectively shields the amino group of phenylalanine, facilitating precise incorporation of phenylalanine residues into the growing peptide chain.

Compatibility with Diverse Synthesis Methods: BOC-D-Phenylalanine demonstrates excellent compatibility with various peptide synthesis methods, including both solution-phase and solid-phase synthesis. Its versatility enables chemists to employ different strategies for efficient peptide assembly.

Applications: Peptide Synthesis: BOC-D-Phenylalanine plays a pivotal role in solid-phase peptide synthesis (SPPS), which is the primary method for peptide assembly. By protecting the amino group of phenylalanine, it ensures controlled incorporation of phenylalanine residues into the peptide chain, allowing for the synthesis of customized peptides.

Medicinal Chemistry: BOC-D-Phenylalanine is extensively utilized in the synthesis of peptide-based drugs and drug candidates. It enables the incorporation of phenylalanine residues into peptides, facilitating the development of therapeutics targeting specific biological pathways or receptors.

Protein Engineering: BOC-D-Phenylalanine finds application in protein engineering studies. By incorporating BOC-D-Phenylalanine into specific positions within the protein sequence, researchers can investigate the impact of phenylalanine mutations on protein structure, function, and stability.

Market Outlook: The demand for BOC-D-Phenylalanine is growing steadily within the peptide synthesis market due to its reliability and compatibility with various synthesis methods. Pharmaceutical companies, academic research institutions, and contract manufacturing organizations (CMOs) rely on BOC-D-Phenylalanine for peptide synthesis projects aimed at drug discovery and development. With the increasing interest in peptide therapeutics and protein engineering, the market for high-quality amino acid protecting agents like BOC-D-Phenylalanine is expanding.

Conclusion: BOC-D-Phenylalanine is a versatile amino acid protecting agent that plays a crucial role in peptide synthesis. Its exceptional purity, efficient amine protection, and compatibility with diverse synthesis methods make it a valuable tool for chemists and researchers in the field. The applications of BOC-D-Phenylalanine in peptide synthesis, medicinal chemistry, and protein engineering contribute to advancements in drug development, therapeutic design, and protein structure-function studies.

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