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4-PHENYLBUTYRIC-2,2,3,3-D4 ACID, with the CAS number 461391-24-2, is an isotopically labeled research compound that is utilized in various scientific studies and experiments. It is a deuterated variant of 4-phenylbutyric acid, which is a synthetic compound with potential applications in the pharmaceutical and chemical industries.

461391-24-2

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461391-24-2 Usage

Uses

Used in Research and Development:
4-PHENYLBUTYRIC-2,2,3,3-D4 ACID is used as a research compound for studying the properties and behavior of its non-deuterated counterpart, 4-phenylbutyric acid, in various chemical and biological processes. The deuterium labeling allows for enhanced detection and tracking of the compound in experiments, providing valuable insights into its interactions and mechanisms of action.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-PHENYLBUTYRIC-2,2,3,3-D4 ACID is used as a starting material or intermediate in the synthesis of various drugs and drug candidates. Its isotopically labeled nature can be advantageous for studying the metabolic pathways and pharmacokinetics of related compounds, potentially leading to the development of more effective and safer medications.
Used in Chemical Industry:
4-PHENYLBUTYRIC-2,2,3,3-D4 ACID is also used in the chemical industry for the synthesis of various specialty chemicals, such as deuterated analogs of pharmaceuticals, agrochemicals, and other industrial chemicals. The deuterium labeling can provide unique properties and advantages for these applications, such as improved stability or altered reactivity.
Used in Analytical Chemistry:
4-PHENYLBUTYRIC-2,2,3,3-D4 ACID is employed as a reference material or internal standard in analytical chemistry, particularly in techniques such as mass spectrometry and nuclear magnetic resonance (NMR) spectroscopy. The deuterium labeling can improve the accuracy and precision of these measurements, enabling more reliable identification and quantification of target compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 461391-24-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,6,1,3,9 and 1 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 461391-24:
(8*4)+(7*6)+(6*1)+(5*3)+(4*9)+(3*1)+(2*2)+(1*4)=142
142 % 10 = 2
So 461391-24-2 is a valid CAS Registry Number.

461391-24-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-PHENYLBUTYRIC-2,2,3,3-D4 ACID

1.2 Other means of identification

Product number -
Other names -

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:461391-24-2 SDS

461391-24-2Downstream Products

461391-24-2Relevant academic research and scientific papers

SUBSTITUTED ETHANOLAMINES

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Page/Page column 24, (2010/02/17)

The present invention relates to new substituted ethanolamine adrenergic receptor modulators, pharmaceutical compositions thereof, and methods of use thereof.

H/D-exchange reactions with hydride-activated catalysts

Derdau, Volker,Atzrodt, Jens,Holla, Wolfgang

, p. 295 - 299 (2008/02/08)

A safe, user friendly and efficient method to provide high deuterium incorporation into a variety of organic substrates was developed. Systematic screening of catalysts and activators revealed that the activation of the Pd- or Rh-catalyst by NaBD4 is essential for the H/D exchange. The feasibility has been demonstrated by the successful application of this method to bi- and tricyclic aromatic compounds as well as chiral natural products like dextrorphan or drugs like formoterol. Copyright

Exposure to a deuterated analogue of phenylbutyrate retards S-phase progression in HT-29 colon cancer cells

Clarke, Kevin O.,Ludeman, Susan M.,Springer, James B.,Michael Colvin,Lea, Michael A.,Harrison, Lawrence E.

, p. 1054 - 1064 (2007/10/03)

Differentiation agents that induce neoplastic cells to regain a normal phenotype and/or cause growth arrest without significantly affecting normal cells represent an attractive option for cancer treatment. Analogues of short chain fatty acids, such as phe

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