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87385-39-5

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87385-39-5 Usage

Description

N,N-Di(ethyl-1,1-d2)aniline, with the CAS number 87385-39-5, is an isotopically labeled research compound that is utilized in various scientific studies and experiments. N,N-DI(ETHYL-1,1-D2)ANILINE is characterized by the presence of deuterium atoms (2H or D) in the ethyl groups, which provides unique properties and advantages in research applications.

Uses

Used in Chemical Synthesis:
N,N-Di(ethyl-1,1-d2)aniline is used as a labeled starting material or intermediate in the synthesis of various organic compounds. The incorporation of deuterium atoms allows for the tracking of chemical reactions and the investigation of reaction mechanisms, providing valuable insights into the synthesis process.
Used in Analytical Chemistry:
In analytical chemistry, N,N-di(ethyl-1,1-d2)aniline serves as an internal standard or a reference compound for the quantification and identification of similar compounds. The presence of deuterium atoms enhances the compound's detectability and differentiation from other species, improving the accuracy and reliability of analytical methods.
Used in Pharmaceutical Research:
N,N-Di(ethyl-1,1-d2)aniline is employed as a labeled analog of aniline in pharmaceutical research. This allows researchers to study the metabolism, distribution, and excretion of the compound, as well as its interactions with biological targets. The use of isotopically labeled compounds can help in understanding the pharmacokinetics and pharmacodynamics of drug candidates.
Used in Material Science:
In material science, N,N-di(ethyl-1,1-d2)aniline can be used to investigate the properties of polymers and other materials. The incorporation of deuterium atoms can affect the physical and chemical properties of the materials, such as their stability, solubility, and mechanical strength. This information is crucial for the development of new materials with improved performance.
Used in Environmental Studies:
N,N-Di(ethyl-1,1-d2)aniline can be utilized in environmental studies to trace the fate and transport of pollutants or contaminants in the environment. The use of isotopically labeled compounds enables the differentiation between naturally occurring and anthropogenic sources, providing valuable information for environmental monitoring and remediation efforts.
Used in Nuclear Magnetic Resonance (NMR) Spectroscopy:
In NMR spectroscopy, N,N-di(ethyl-1,1-d2)aniline serves as a labeled compound for the study of molecular structures and dynamics. The deuterium atoms in the compound can be used to probe the chemical environment and interactions of the molecule, offering detailed information about its structure and behavior in various conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 87385-39-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,3,8 and 5 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 87385-39:
(7*8)+(6*7)+(5*3)+(4*8)+(3*5)+(2*3)+(1*9)=175
175 % 10 = 5
So 87385-39-5 is a valid CAS Registry Number.

87385-39-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-DI(ETHYL-1,1-D2)ANILINE

1.2 Other means of identification

Product number -
Other names S-(1-methyl-1-carboxyethyl) N,N-diethyl-dithiocarbamate

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:87385-39-5 SDS

87385-39-5Downstream Products

87385-39-5Relevant articles and documents

Photochemical Desulphurization of Indoline-2-thiones

Nishio, Takehiko,Okuda, Norikazu,Kashima, Choji

, p. 141 - 143 (2007/10/02)

The photochemical reactions of indoline-2-thiones in the presence of amines have been examined.Irradiation of indoline-2-thiones 1 in the presence of triethylamine yielded the desulphurization products, indolines 2, along with N,N-diethylthioacetamide 3.T

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