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32745-07-6

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32745-07-6 Usage

Description

N-NITROSODIMETHYL-1,1,1-D3-AMINE, with the CAS number 32745-07-6, is an isotopically labeled research compound utilized in various scientific studies and experiments. It is a derivative of dimethylamine, where one of the hydrogen atoms is replaced by a deuterium atom, making it a valuable tool for researchers to investigate the behavior and properties of molecules in different environments.

Uses

Used in Research and Development:
N-NITROSODIMETHYL-1,1,1-D3-AMINE is used as an isotopically labeled compound for [application reason] in the field of research and development. The presence of deuterium in the molecule allows for the study of reaction mechanisms, kinetic isotope effects, and the investigation of metabolic pathways. N-NITROSODIMETHYL-1,1,1-D3-AMINE is particularly useful in the fields of organic chemistry, biochemistry, and pharmaceutical research.
Used in Analytical Chemistry:
In Analytical Chemistry, N-NITROSODIMETHYL-1,1,1-D3-AMINE is used as a labeled reference material for [application reason]. It can be employed to calibrate and validate analytical instruments, such as mass spectrometers and nuclear magnetic resonance (NMR) spectrometers, ensuring accurate and reliable measurements.
Used in Environmental Studies:
In Environmental Studies, N-NITROSODIMETHYL-1,1,1-D3-AMINE is used as a tracer compound for [application reason]. It can help researchers track the movement and distribution of pollutants in the environment, as well as study the behavior of similar compounds in various ecosystems.
Used in Pharmaceutical Industry:
In the Pharmaceutical Industry, N-NITROSODIMETHYL-1,1,1-D3-AMINE is used as a synthetic intermediate for [application reason]. Its unique isotopic labeling can be advantageous in the development of new drugs, as it allows for the study of drug metabolism, pharmacokinetics, and potential side effects.
Used in Material Science:
In Material Science, N-NITROSODIMETHYL-1,1,1-D3-AMINE is used as a component in the synthesis of advanced materials for [application reason]. N-NITROSODIMETHYL-1,1,1-D3-AMINE's unique properties can contribute to the development of novel materials with specific characteristics, such as improved stability or enhanced performance in various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 32745-07-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,7,4 and 5 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 32745-07:
(7*3)+(6*2)+(5*7)+(4*4)+(3*5)+(2*0)+(1*7)=106
106 % 10 = 6
So 32745-07-6 is a valid CAS Registry Number.

32745-07-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-NITROSODIMETHYL-1,1,1-D3-AMINE

1.2 Other means of identification

Product number -
Other names Nitrosomethyl-n-propylamine

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:32745-07-6 SDS

32745-07-6Downstream Products

32745-07-6Relevant articles and documents

Nitrogen Protonation of N-Nitrosodimethylamine

Keefer, Larry K.,Hrabie, Joseph A.,Hilton, Bruce D.,Wilbur, David

, p. 7459 - 7462 (1988)

Evidence for the presence of the Me2N(H)NO+ ion at kinetically significant concentrations in aqueous solutions of N-nitrosodimethylamine (NDMA) at pH =/ E equilibration in the resulting NDMA-d3 was measured by nuclear magnetic resonance spectroscopy as a function of pD.The reaction was first order in +>, with the plot of observed first-order rate constants versus +> having a slope of k/+> =1E-2 M-1 s-1 at 3 deg C and an ionic strength of 0.2 M.The observed rate date were used to estimate Ka for N-protonated NDMA as 1E12-1E13 M by assuming that the rates of rotation about the N-N bond in Me2N(H)NO+ and of its deprotonation are similar to those for the isoelectronic N-protonated carboxamide function.The trisubstituted nitrogen of the nitrosamine thus appears to be several orders of magnitude less basic than that of the carboxamides.

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