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Hexamethyl-d18-disiloxane, with the CAS number 19108-55-5, is an isotopically labeled research compound that is utilized in various scientific studies and experiments. It is a siloxane derivative characterized by its unique molecular structure, which consists of two methyl groups attached to a silicon atom, connected by an oxygen-oxygen bond. HEXAMETHYL-D18-DISILOXANE is known for its stability and specific properties that make it valuable in research applications.

19108-55-5

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19108-55-5 Usage

Uses

Used in Research and Development:
Hexamethyl-d18-disiloxane is used as a research compound for various scientific investigations. Its isotopically labeled nature allows researchers to study its behavior and interactions with other molecules in a controlled manner. HEXAMETHYL-D18-DISILOXANE is particularly useful in the fields of chemistry, materials science, and pharmaceutical research, where understanding molecular interactions and properties is crucial.
Used in Chemical Analysis:
In the field of chemical analysis, HEXAMETHYL-D18-DISILOXANE serves as a valuable tool for identifying and characterizing other compounds. Its unique properties make it an ideal internal standard or reference material in various analytical techniques, such as gas chromatography and mass spectrometry. This helps researchers to accurately determine the concentration and structure of target compounds in complex samples.
Used in Material Science:
Hexamethyl-d18-disiloxane is also employed in material science research, where its properties can be exploited to develop new materials with specific characteristics. For instance, its stability and chemical inertness make it a candidate for use in the development of advanced polymers, coatings, and adhesives with improved performance and durability.
Used in Pharmaceutical Research:
In the pharmaceutical industry, HEXAMETHYL-D18-DISILOXANE is utilized as a research compound to study its potential applications in drug development. Its unique molecular structure and properties may offer insights into the design of new drugs or the modification of existing ones, leading to improved therapeutic outcomes.

Check Digit Verification of cas no

The CAS Registry Mumber 19108-55-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,1,0 and 8 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 19108-55:
(7*1)+(6*9)+(5*1)+(4*0)+(3*8)+(2*5)+(1*5)=105
105 % 10 = 5
So 19108-55-5 is a valid CAS Registry Number.

19108-55-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name HEXAMETHYL-D18-DISILOXANE

1.2 Other means of identification

Product number -
Other names <2H18>Hexamethyldisiloxane

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:19108-55-5 SDS

19108-55-5Upstream product

19108-55-5Downstream Products

19108-55-5Relevant academic research and scientific papers

Mechanism of Molybdenum-Mediated Carbon Monoxide Deoxygenation and Coupling: Mono- and Dicarbyne Complexes Precede C-O Bond Cleavage and C-C Bond Formation

Buss, Joshua A.,Agapie, Theodor

supporting information, p. 16466 - 16477 (2016/12/27)

Deoxygenative coupling of CO to value-added C≥2 products is challenging and mechanistically poorly understood. Herein, we report a mechanistic investigation into the reductive coupling of CO, which provides new fundamental insights into a multielectron bond-breaking and bond-making transformation. In our studies, the formation of a bis(siloxycarbyne) complex precedes C-O bond cleavage. At -78 °C, over days, C-C coupling occurs without C-O cleavage. However, upon warming to 0 °C, C-O cleavage is observed from this bis(siloxycarbyne) complex. A siloxycarbyne/CO species undergoes C-O bond cleavage at lower temperatures, indicating that monosilylation, and a more electron-rich Mo center, favors deoxygenative pathways. From the bis(siloxycarbyne), isotopic labeling experiments and kinetics are consistent with a mechanism involving unimolecular silyl loss or C-O cleavage as rate-determining steps toward carbide formation. Reduction of Mo(IV) CO adducts of carbide and silylcarbyne species allowed for the spectroscopic detection of reduced silylcarbyne/CO and mixed silylcarbyne/siloxycarbyne complexes, respectively. Upon warming, both of these silylcarbynes undergo C-C bond formation, releasing silylated C2O1 fragments and demonstrating that the multiple bonded terminal Mo≡C moiety is an intermediate on the path to deoxygenated, C-C coupled products. The electronic structures of Mo carbide and carbyne species were investigated quantum mechanically. Overall, the present studies establish the elementary reactions steps by which CO is cleaved and coupled at a single metal site.

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