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2875-96-9

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2875-96-9 Usage

Description

PROPANE-1,1,1,3,3,3-D6 is a deuterated form of propane, a naturally occurring hydrocarbon gas commonly used as a fuel. PROPANE-1,1,1,3,3,3-D6 has six deuterium atoms, a stable isotope of hydrogen, replacing six of the hydrogen atoms in the molecule. It is known for its low toxicity and minimal environmental impact.

Uses

Used in Solvent Applications:
PROPANE-1,1,1,3,3,3-D6 is used as a solvent due to its chemical properties that make it suitable for dissolving various substances without causing unwanted reactions.
Used in Aerosol Propellants:
In the consumer goods industry, PROPANE-1,1,1,3,3,3-D6 is used as a non-flammable propellant in aerosol sprays, providing a safe and effective means of dispensing products such as personal care items and cleaning solutions.
Used in Refrigeration:
PROPANE-1,1,1,3,3,3-D6 serves as a refrigerant in industrial and commercial applications, where it helps maintain low temperatures for preserving perishable goods and regulating indoor environments.
Used in Foam Manufacturing:
As a blowing agent in foam manufacturing, PROPANE-1,1,1,3,3,3-D6 contributes to the production of various types of foams used in insulation, packaging, and other applications.
Used in Calibration Standards:
In the field of analytical chemistry, PROPANE-1,1,1,3,3,3-D6 is utilized as a calibration standard for instruments, ensuring accurate measurements and reliable data in chemical analyses.
Used in Scientific Research and Chemical Analysis:
The deuterated form of propane is employed in scientific research to track the movement and behavior of propane molecules in different environments, aiding in the study of chemical reactions involving propane.

Check Digit Verification of cas no

The CAS Registry Mumber 2875-96-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,7 and 5 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2875-96:
(6*2)+(5*8)+(4*7)+(3*5)+(2*9)+(1*6)=119
119 % 10 = 9
So 2875-96-9 is a valid CAS Registry Number.
InChI:InChI=1/C3H8/c1-3-2/h3H2,1-2H3/i1D3,2D3

2875-96-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,1,3,3,3-hexadeuteriopropane

1.2 Other means of identification

Product number -
Other names 1,1,1,3,3,3-Hexadeuterio-propan

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:2875-96-9 SDS

2875-96-9Relevant articles and documents

Unprecedented double nucleophilic addition of a hydride at a central carbon of an η3-allyl ligand

Minato, Makoto,Sekimizu, Ryoko,Uchida, Daisuke,Ito, Takashi

, p. 3695 - 3698 (2007/10/03)

Treatment of η3-allyl compound [Cp 2Mo(η3-C3H5)]+ (1; Cp = η5-C5H5) with MH (M = Li, Na) resulted in reduction of the allyl ligand to give propane. Deuterium-labeling studies were used to trace the origins and fates of the hydrogen atoms. The mechanism is discussed in light of the HSAB principle. The studies showed that the formation of propane can be explained by 1,2-hydrogen migration from the central to the terminal carbon of the allyl ligand, and the subsequent double nucleophilic addition of the hydride at the central carbon.

Electrolysis of Potassium Butyrate in Acetonitrile. A Deuterium NMR Study

Laurent, Eliane,Thomalla, Marc,Marquet, Bernard,Burger, Ulrich

, p. 4193 - 4198 (2007/10/02)

The anodic oxidation of 2,2-dideuteriobutyrate ion in acetonitrile gives rise to radical-derived and cation-derived C3 products.By 2H FT NMR spectroscopy, the radical-derived propane and propene are found to be formed without scrambling of the label.Similarly, the products derived from the intermediate isopropyl cation, i.e., the remainder of the propene and N-isopropylamides, bear deuterium only at the terminal C-1 and C-3 positions of the C3 fragment.However, the 1:1:1 label distribution found in the N-n-propylamides and the formation of cyclopropane strongly suggest that ring closure of the n-propyl cation to rapidly scrambling pr otonated cyclopropane is an important reaction pathway.Atom scrambling at the level of protonated cyclopropane shows a large H/D isotope effect.

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