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METHYL ACETATE-D6, also known as deuterated methyl acetate, is a chemical compound that is used as a standard for various applications in scientific research and industry. It is characterized by the presence of deuterium (D), a stable isotope of hydrogen, which provides unique properties compared to the regular hydrogen atom.

32113-85-2

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32113-85-2 Usage

Uses

Used in Chemical Detection:
METHYL ACETATE-D6 is used as a detection agent for chemical detection of γ-rays in the presence of slow neutrons. This application is particularly relevant in fields such as radiation detection, nuclear physics, and environmental monitoring, where accurate measurement of radiation levels is crucial for safety and research purposes.
Used in Scientific Research:
In the field of scientific research, METHYL ACETATE-D6 serves as a valuable standard for various analytical techniques, including nuclear magnetic resonance (NMR) spectroscopy and infrared (IR) spectroscopy. The presence of deuterium in the compound allows for improved signal resolution and enhanced sensitivity in these analytical methods, making it a useful tool for studying molecular structures and interactions.
Used in Industrial Applications:
METHYL ACETATE-D6 can also be employed in industrial applications where its unique properties are advantageous. For instance, it can be used as a reference material for the calibration of instruments and equipment that measure radiation levels or detect specific chemical compounds. Additionally, its deuterated nature may provide benefits in certain chemical reactions or processes where the use of deuterated compounds is preferred.

Check Digit Verification of cas no

The CAS Registry Mumber 32113-85-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,1,1 and 3 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 32113-85:
(7*3)+(6*2)+(5*1)+(4*1)+(3*3)+(2*8)+(1*5)=72
72 % 10 = 2
So 32113-85-2 is a valid CAS Registry Number.

32113-85-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name METHYL ACETATE-D6

1.2 Other means of identification

Product number -
Other names N-methylacetamide oxime

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:32113-85-2 SDS

32113-85-2Relevant academic research and scientific papers

Oxidative functionalization of methane in the presence of a homogeneous rhodium-copper-chloride catalytic system: Transformation of acetic and propionic acids as solvent components

Chepaikin,Bezruchenko,Menchikova,Moiseeva,Gekhman,Moiseev

scheme or table, p. 133 - 142 (2012/01/13)

The oxidative functionalization of methane (O2, CO, 95°C, Rh III/CuI, II/Cl- catalytic system) was studied in an aqueous acetic or propionic acid medium. It was shown that oxidative decarbonylation of carboxylic acids takes place along with methanol and methyl carboxylate formation.

INTERMEDIATES IN COBALT-CATALYSED METHANOL HOMOLOGATION: LABELLING STUDIES WITH DEUTERATED METHANOL AND METHYL IODIDE

Roeper, Michael,Loevenich, Heinz

, p. 95 - 102 (2007/10/02)

The cobalt-catalysed homologation of perdeuterated methanol with CO/H2 gives C2 products in which the CD3 group remains intact.GC/MS measurements showed that no H/D exchange unless the methanol conversion exceeded 50percent.These results indicate that methylene species are unlikely to be as catalytic intermediates, and favour methyl species for such intermediates.In the presence of iodine promoters methyl iodide is a likely intermediate since it is much more readily consumed than methanol in carbonylation/hydrocarbonylation reactions.This was shown by treating a 5/1 mixture of CH3OH and CD3I with CO/H2 in the presence of Co2(CO)8; at short reaction times only the carbonylation/hydrocarbonylation products of methyl iodide could be detected by GC/MS.Methyl iodide can be formed from variety of iodine compounds under homologation conditions, as was confirmed by separate experiments.

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