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L-PHENYLALANINE-13C9, 15N is an isotopically labeled analog of L-Phenylalanine, an essential amino acid. L-PHENYLALANINE-13C9, 15N is characterized by the presence of stable isotopes, specifically carbon-13 (13C) in nine of its carbon atoms and nitrogen-15 (15N) in its nitrogen atom. The isotopically labeled nature of L-PHENYLALANINE-13C9, 15N allows for its use in various applications, particularly in research and development, due to its unique properties and behavior compared to the non-isotopically labeled L-Phenylalanine.

29700-34-3

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29700-34-3 Usage

Uses

Used in Research and Development:
L-PHENYLALANINE-13C9, 15N is used as a genetic tool for selectively labeling proteins. The expression is: L-PHENYLALANINE-13C9, 15N is used as a selective protein labeling agent for [application reason], which is to facilitate the study of protein structure, function, and interactions in various biological systems.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, L-PHENYLALANINE-13C9, 15N is used as a tracer molecule for [application reason], which is to track the metabolic pathways and enzyme activities involving L-Phenylalanine. This helps in the development of new drugs and therapies targeting specific metabolic pathways.
Used in Metabolic Studies:
L-PHENYLALANINE-13C9, 15N is used as a metabolic tracer in [application reason], which is to study the metabolism of L-Phenylalanine and its role in various physiological processes. This information can be crucial for understanding the underlying mechanisms of certain diseases and disorders related to amino acid metabolism.
Used in Analytical Chemistry:
In analytical chemistry, L-PHENYLALANINE-13C9, 15N is used as a reference material for [application reason], which is to calibrate and validate analytical instruments and methods for the detection and quantification of L-Phenylalanine and its derivatives. The isotopically labeled nature of the compound provides a reliable and accurate means for quality control and assurance in analytical measurements.
Used in Nutritional Science:
L-PHENYLALANINE-13C9, 15N is used as a research tool in [application reason], which is to investigate the role of L-Phenylalanine in nutrition, metabolism, and overall health. This can help in the development of dietary supplements, functional foods, and personalized nutrition strategies based on individual metabolic needs and responses.

Check Digit Verification of cas no

The CAS Registry Mumber 29700-34-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,7,0 and 0 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 29700-34:
(7*2)+(6*9)+(5*7)+(4*0)+(3*0)+(2*3)+(1*4)=113
113 % 10 = 3
So 29700-34-3 is a valid CAS Registry Number.

29700-34-3 Well-known Company Product Price

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  • Aldrich

  • (490105)  L-Phenylalanine-15N  98 atom % 15N

  • 29700-34-3

  • 490105-500MG

  • 5,243.94CNY

  • Detail

29700-34-3SDS

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 L-Phenylalanine-15N

1.2 Other means of identification

Product number -
Other names L-<15N>phenylalanine

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:29700-34-3 SDS

29700-34-3Upstream product

29700-34-3Downstream Products

29700-34-3Relevant academic research and scientific papers

Stereoselective synthesis of stable isotope-labeled L-α-amino acids: Electrophilic amination of oppolzer's acyl sultams in the synthesis of L-[15N]alanine, L-[15N]valine, L-[15N]leucine, L-[15N]phenylalanine and

Lodwig,Unkefer

, p. 239 - 248 (2007/10/03)

Using 1-chloro-1-[15N]nitrosocyclohexane, we have prepared five L-[α-15N]amino acids. The stereoselective electophillic hydroxyamination of (S)-acylbornane-10,2-sultams, followed by Zn(o)/H+ reduction, and alkaline cleavag

Chemo-Enzymatic Syntheses of Isotopically Labelled L-Amino Acids

Kelly, Nicholas M.,O'Neill, Bridget C.,Probert, John,Reid, Gordon,Stephen, Rosamund,et al.

, p. 6533 - 6536 (2007/10/02)

L-Alanine labelled with carbon-13 and nitrogen-15 has been prepared in good yield and high optical purity from achiral precursors using alanine dehydrogenase.This versatile approach may be simply adapted for the preparation of a range of isotopically labe

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