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L-Proline-2,5,5-d3 is a stable, isotopically labeled form of the amino acid L-Proline, specifically deuterated at the 2, 5, and 5 positions, where the hydrogen atoms have been replaced with deuterium. This unique labeling enables the tracking and monitoring of L-Proline's metabolic fate in biological systems, facilitating the study of biochemical and physiological processes involving L-Proline.

65807-22-9

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65807-22-9 Usage

Uses

Used in Research and Medical Studies:
L-Proline-2,5,5-d3 is used as a research tool for investigating the role of L-Proline in various biological processes. Its application aids in understanding L-Proline's function in health and disease, providing valuable insights into its metabolic pathways and interactions within the body.
Used in Biochemical and Physiological Process Studies:
In the field of biochemistry and physiology, L-Proline-2,5,5-d3 is utilized as a tracer compound to study the specific biochemical reactions and physiological mechanisms that involve L-Proline. The isotopically labeled amino acid allows for a clearer observation of these processes, enhancing the accuracy of experimental results.
Used in Metabolic Fate Tracking:
L-Proline-2,5,5-d3 is employed as a metabolic tracer to monitor the fate of L-Proline within biological systems. This application is crucial for mapping out metabolic pathways and understanding how L-Proline is processed, absorbed, and utilized by the body.
Used in Pharmaceutical Development:
In the pharmaceutical industry, L-Proline-2,5,5-d3 may be used in the development of drugs targeting L-Proline-related metabolic pathways. Its ability to mimic the natural amino acid while being easily traceable can help in assessing the efficacy and safety of potential therapeutic agents.
Used in Diagnostic Applications:
L-Proline-2,5,5-d3 can be applied in diagnostic procedures to detect and monitor conditions related to L-Proline metabolism. Its distinctive isotopic signature allows for sensitive and specific detection methods, potentially improving the accuracy of diagnostic tests.

Check Digit Verification of cas no

The CAS Registry Mumber 65807-22-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,8,0 and 7 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 65807-22:
(7*6)+(6*5)+(5*8)+(4*0)+(3*7)+(2*2)+(1*2)=139
139 % 10 = 9
So 65807-22-9 is a valid CAS Registry Number.

65807-22-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name Prolin-d(3)-(α,δ(1),δ(2))

1.2 Other means of identification

Product number -
Other names L-PROLINE-D3

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:65807-22-9 SDS

65807-22-9Upstream product

65807-22-9Downstream Products

65807-22-9Relevant academic research and scientific papers

Development and Scale-Up of Stereoretentive α-Deuteration of Amines

Michelotti, Alessia,Rodrigues, Fabien,Roche, Maxime

, p. 1741 - 1744 (2017)

A stereoretentive deuteration of amino acids and amines has been developed using ruthenium on carbon catalyst, hydrogen gas at atmospheric pressure, and deuterium oxide as a source of deuterium. The process was successfully scaled-up, avoiding the use of expensive and sensitive catalyst and avoiding the use of deuterium gas under pressure. High deuterium incorporation and high yield of labeled compounds were obtained by a simple filtration process.

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