62040-55-5

Basic information

• Product Name: 4-Amino-L-phenylalanine hydrochloride
• Synonyms: H-P-AMINO-L-PHE-OH HCL;H-P-AMINO-PHE-OH HCL;H-PHE(4-NH2)-OH HCL;H-PHE(4-NH2)-OH XHCL;H-PHE(4-NH2) XHCL;L-P-AMINOPHENYLALANINE HYDROCHLORIDE SALT;L-4-AMINOPHENYLALANINE HYDROCHLORIDE;4-AMINO-L-PHENYLALANINE HYDROCHLORIDE
• CAS NO: 62040-55-5
• Molecular Formula: C₉H₁₂N₂O₂*ClH
• Molecular Weight: 216.66
• EINECS: 263-388-2
• Product Categories: Amino Acids & Derivatives;Aromatics;Peptide Synthesis;Phenylalanine Derivatives;Unnatural Amino Acid Derivatives;Chiral Reagents;Intermediates & Fine Chemicals;Pharmaceuticals
• Mol File: 62040-55-5.mol

Chemical Properties

• Boiling Point: 383.5 °C at 760 mmHg
• Flash Point: 185.8 °C
• Appearance: Off-White Powder
• Vapor Pressure: 1.44E-06mmHg at 25°C
• Storage Temp.: -15°C
• Solubility: Acetic Acid, Water
• BRN: 3657715
• CAS DataBase Reference: 4-Amino-L-phenylalanine hydrochloride(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Amino-L-phenylalanine hydrochloride(62040-55-5)
• EPA Substance Registry System: 4-Amino-L-phenylalanine hydrochloride(62040-55-5)

Safety Data

• Safety Statements: 22-24/25
• WGK Germany: 3
• F: 10-23
• Hazardous Substances Data: 62040-55-5(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
4-Amino-L-phenylalanine hydrochloride is used as an active pharmaceutical ingredient for the development of drugs targeting various medical conditions. Its structural similarity to L-Phenylalanine allows it to interact with biological systems in a controlled manner, making it a valuable compound for drug discovery and therapeutic applications.
Used in Research and Development:
In the field of research, 4-Amino-L-phenylalanine hydrochloride serves as a valuable tool for studying the role of L-Phenylalanine in biological processes. It can be used to investigate the mechanisms of action, metabolic pathways, and potential therapeutic effects of L-Phenylalanine and its analogs, contributing to a deeper understanding of their applications in medicine.
Used in Dietary Supplements:
4-Amino-L-phenylalanine hydrochloride may be used as a dietary supplement to support the body's natural production of essential compounds, such as neurotransmitters. Its availability in supplemental form can help individuals who may have deficiencies or require additional support for optimal health and well-being.
Used in Cosmetics and Personal Care:
In the cosmetics and personal care industry, 4-Amino-L-phenylalanine hydrochloride can be utilized for its potential skin health benefits. Its role in the synthesis of neurotransmitters and other biologically active molecules may contribute to improved skin appearance, texture, and overall health, making it a valuable ingredient in skincare formulations.

InChI:InChI=1/C9H12N2O2.ClH/c10-7-3-1-6(2-4-7)5-8(11)9(12)13;/h1-4,8H,5,10-11H2,(H,12,13);1H/t8-;/m0./s1

Upstream product

• 949-99-5 4-nitro-3-phenyl-L-alanine 
• 63-91-2 L-phenylalanine 

Downstream Products

• 114422-51-4 C₁₀⁽¹⁴⁾CH₁₆N₂O₂ 
• 1991-81-7 4-iodo-L-phenylalanine 
• 187283-26-7 C₂₀H₃₀N₄O₆ 
• 187283-25-6 Fmoc-p-(N,N'-Boc-guanidino)Phe 
• 1421446-32-3 C₂₇H₃₂N₄O₅S*C₂HF₃O₂ 

Relevant articles and documents

Biosynthesis of the Antibiotic Obafluorin from D-Glucose and p-Aminophenylalanine in Pseudomonas fluorescens

The separate units which are used to construct the antibiotic obafluorin 1 in Pseudomonas fluorescens are defined by the results of D-glucose incorporation.A key intermediate in the biosynthesis of 1 is established to be L-p-aminophenylalanine 8; L-phenylanaline and L-p-nitrophenylalanine are very poor precursors.Results similar to those for obafluorin are obtained for p-nitrophenylacetic acid 20 which along with derivative 4 and 2-(4-nitrophenyl)ethanol 21 are identified as new metabolites of P. fluorescens.Deuteriated samples of 20, 22 and 23 are notprecursors for obafluorin 1. -p-aminophenylalanine 18 is incorporated into 1 with complete loss of deuterium from C-2 but retention of the deuterium present in both diastereotopic positions on C-3.