BOC-DL-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-DL-Phe-OH
Structure
CAS No. 4530-18-1 Boiling Point (℃) 426.6±38.0 °C at 760 mmHg
Molecular Weight 265.305 Melting Point (℃) N/A
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 2-(tert-butoxycarbonylamino)-3-phenylpropanoic acid 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):1793-882.
Synonyms
boc-dl-phe-oh
N-tert-Butyloxycarbonyl-L-phenylalanine
Boc-phenylalanine
N-{[(2-Methyl-2-propanyl)oxy]carbonyl}-L-phenylalanine
(2S)-2-({[(2-Methyl-2-propanyl)oxy]carbonyl}amino)-3-phenylpropanoic acid
N-(tert-Butoxycarbonyl)-L-phenylalanin
N-(tert-Butoxycarbonyl)-L-phenylalanine
boc-L-Phe
L-Phenylalanine, N-[(1,1-dimethylethoxy)carbonyl]-
N-t-Butyloxycarbonyl-L-phenylalanine
L-Phenylalanine, N-((1,1-dimethylethoxy)carbonyl)-
N-α-t-BOC-L-phenylalanine
N-Boc-L-phenylalanine
MFCD00153311
Product Description
Introduction: BOC-DL-Phenylalanine is a highly versatile amino acid protecting agent widely used in peptide synthesis. Derived from phenylalanine, BOC-DL-Phenylalanine plays a crucial role in protecting amino groups during the assembly of peptide chains. Renowned for its exceptional quality and reliability, BOC-DL-Phenylalanine has become the preferred choice among chemists and researchers involved in peptide synthesis.

Product Features: Exceptional Purity: BOC-DL-Phenylalanine is meticulously synthesized to ensure the highest level of purity, surpassing industry standards. Its exceptional purity guarantees minimal impurities, ensuring superior quality results and the synthesis of high-quality peptides.

Effective Amine Protection: BOC-DL-Phenylalanine acts as an efficient shield for amino groups, preventing undesired side reactions during peptide synthesis. By selectively protecting the amino group, it enables controlled and precise incorporation of amino acids into the growing peptide chain.

Stereoisomeric Flexibility: BOC-DL-Phenylalanine offers stereoisomeric flexibility due to its racemic nature, allowing for the synthesis of peptides with both D- and L-phenylalanine residues. This flexibility enhances the diversity and functionality of synthesized peptides for various research and pharmaceutical applications.

Applications: Peptide Synthesis: BOC-DL-Phenylalanine is an essential component in solid-phase peptide synthesis (SPPS), the most widely used method for efficient peptide assembly. Its role as an amino acid protecting agent enables the stepwise addition of amino acids, preserving the integrity and controlled growth of the peptide chain.

Pharmaceutical Research: BOC-DL-Phenylalanine plays a significant role in the development of peptide-based therapeutics and drug discovery. Its usage facilitates the creation of diverse peptide libraries, allowing researchers to explore structure-activity relationships and identify potential drug candidates.

Protein Engineering: BOC-DL-Phenylalanine finds application in protein engineering, enabling the site-specific incorporation of phenylalanine residues in recombinant proteins. This technique allows researchers to study the impact of specific amino acid substitutions on protein structure and function.

Market Outlook: The demand for BOC-DL-Phenylalanine is experiencing steady growth within the peptide synthesis market due to its reliable performance and compatibility with various synthesis methods. Pharmaceutical companies, academic research institutions, and contract manufacturing organizations (CMOs) heavily rely on BOC-DL-Phenylalanine for their peptide synthesis projects. With the increasing focus on peptide-based therapeutics, protein engineering, and drug discovery, there is a growing market for high-quality amino acid protecting agents.

Conclusion: BOC-DL-Phenylalanine stands as a versatile amino acid protecting agent in peptide synthesis. Its exceptional purity, effective amine protection, and stereoisomeric flexibility make it an essential tool for chemists and researchers involved in peptide-based studies. With its wide range of applications in peptide synthesis, pharmaceutical research, and protein engineering, BOC-DL-Phenylalanine continues to drive advancements in therapeutic development and our understanding of protein structure-function relationships.

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