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DIMETHYL CARBONATE-D6, also known as D6-dimethyl carbonate, is a deuterated derivative of dimethyl carbonate characterized by the presence of the stable isotope deuterium in place of hydrogen atoms. This colorless, flammable liquid with a slightly sweet odor is particularly useful for nuclear magnetic resonance (NMR) spectroscopy analysis due to its deuterated nature. Recognized for its low toxicity and low volatile organic compound (VOC) content, it is considered an environmentally friendly alternative to traditional solvents.

108481-44-3

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108481-44-3 Usage

Uses

Used in Pharmaceutical Industry:
DIMETHYL CARBONATE-D6 is used as a solvent for its ability to dissolve a wide range of compounds, facilitating various chemical reactions and processes in drug development and manufacturing.
Used in Coatings Industry:
In the coatings industry, DIMETHYL CARBONATE-D6 is utilized as a solvent to improve the performance and application properties of coatings, providing a more efficient and environmentally conscious option compared to traditional solvents.
Used in Lithium-Ion Battery Production:
DIMETHYL CARBONATE-D6 is employed in the production of lithium-ion batteries, where it serves as a component in electrolytes, contributing to the battery's performance and safety.
Used in Organic Synthesis:
As a reagent in organic synthesis, DIMETHYL CARBONATE-D6 is used to carry out a variety of chemical reactions, including the formation of esters and other organic compounds, due to its reactivity and stability.
Used in Supercapacitors:
DIMETHYL CARBONATE-D6 is used as a component in electrolytes for supercapacitors, enhancing their energy storage capacity and performance.
Used in Nuclear Magnetic Resonance (NMR) Spectroscopy:
DIMETHYL CARBONATE-D6 is used as a deuterated solvent in NMR spectroscopy, providing a clear and accurate analysis of molecular structures by replacing hydrogen atoms with deuterium, which is less likely to interfere with the NMR signals.

Check Digit Verification of cas no

The CAS Registry Mumber 108481-44-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,4,8 and 1 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 108481-44:
(8*1)+(7*0)+(6*8)+(5*4)+(4*8)+(3*1)+(2*4)+(1*4)=123
123 % 10 = 3
So 108481-44-3 is a valid CAS Registry Number.

108481-44-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name bis(trideuteriomethyl) carbonate

1.2 Other means of identification

Product number -
Other names carbonic acid bis-trideuteriomethyl ester

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:108481-44-3 SDS

108481-44-3Downstream Products

108481-44-3Relevant academic research and scientific papers

Activated metallic gold as an agent for direct methoxycarbonylation

Xu, Bingjun,Madix, Robert J.,Friend, Cynthia M.

supporting information; experimental part, p. 20378 - 20383 (2012/02/06)

We have discovered that metallic gold is a highly effective vehicle for the low-temperature vapor-phase carbonylation of methanol by insertion of CO into the O-H bond to form methoxycarbonyl. This reaction contrasts sharply to the carbonylation pathway well known for homogeneously catalyzed carbonylation reactions, such as the synthesis of acetic acid. The methoxycarbonyl intermediate can be further employed in a variety of methoxycarbonylation reactions, without the use or production of toxic chemicals. More generally we observe facile, selective methoxycarbonylation of alkyl and aryl alcohols and secondary amines on metallic gold well below room temperature. A specific example is the synthesis of dimethyl carbonate, which has extensive use in organic synthesis. This work establishes a unique framework for using oxygen-activated metallic gold as a catalyst for energy-efficient, environmentally benign production of key synthetic chemical agents.

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