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62040-55-5

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62040-55-5 Usage

Description

4-Amino-L-phenylalanine hydrochloride is an analog of L-Phenylalanine, a naturally occurring amino acid that plays a crucial role in various biological processes. This synthetic derivative exhibits similar properties to L-Phenylalanine but may offer distinct advantages in specific applications due to its modified structure.

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.

Check Digit Verification of cas no

The CAS Registry Mumber 62040-55-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,0,4 and 0 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 62040-55:
(7*6)+(6*2)+(5*0)+(4*4)+(3*0)+(2*5)+(1*5)=85
85 % 10 = 5
So 62040-55-5 is a valid CAS Registry Number.
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

62040-55-5 Well-known Company Product Price

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  • Sigma-Aldrich

  • (09193)  4-Amino-L-phenylalaninehydrochloride  ≥96.0% (calc. on dry substance, AT)

  • 62040-55-5

  • 09193-500MG

  • 1,083.42CNY

  • Detail

62040-55-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name p-Amino-L-phenylalanine Hydrochloride

1.2 Other means of identification

Product number -
Other names (2S)-2-amino-3-(4-aminophenyl)propanoic acid,hydrochloride

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:62040-55-5 SDS

62040-55-5Relevant articles and documents

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

Herbert, Richard B.,Knaggs, Andrew R.

, p. 103 - 108 (2007/10/02)

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.

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