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3-Pentyl--d5 Alcohol, also known as 3-Pentyl-2,2,3,4,4-d5 Alcohol (CAS# 144032-75-7), is an isotopically labeled research compound that is utilized in various scientific studies and experiments. It is characterized by its unique molecular structure, which includes deuterium atoms (denoted by the "d5") that replace hydrogen atoms in the molecule. This substitution allows for enhanced detection and tracking of the compound in research settings.

144032-75-7

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144032-75-7 Usage

Uses

Used in Research and Development:
3-Pentyl--d5 Alcohol is used as a research compound for the study of various chemical and biological processes. The incorporation of deuterium atoms in the molecule provides a distinct signature that can be easily detected and monitored, making it a valuable tool for tracing chemical reactions and understanding molecular interactions.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3-Pentyl--d5 Alcohol is used as a labeled compound for drug development and optimization. Its unique isotopic signature can help researchers identify and track the compound's metabolic pathways, distribution, and excretion, which are crucial for assessing the safety and efficacy of new drug candidates.
Used in Analytical Chemistry:
3-Pentyl--d5 Alcohol is employed as a labeled internal standard or reference material in analytical chemistry. Its stable isotopic composition allows for accurate quantification and comparison of other compounds in complex mixtures, improving the precision and reliability of analytical measurements.
Used in Environmental Studies:
In environmental science, 3-Pentyl--d5 Alcohol can be used as a labeled tracer to study the fate and transport of pollutants or contaminants in various ecosystems. The compound's unique isotopic signature enables researchers to track its movement and interactions with environmental factors, providing valuable insights into the behavior of similar unlabeled compounds.
Used in Material Science:
3-Pentyl--d5 Alcohol can also be utilized in material science research, where it may serve as a labeled additive or component in the development of new materials with specific properties. The compound's isotopic signature can help researchers understand the effects of its incorporation on the material's performance and behavior under various conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 144032-75-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,0,3 and 2 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 144032-75:
(8*1)+(7*4)+(6*4)+(5*0)+(4*3)+(3*2)+(2*7)+(1*5)=97
97 % 10 = 7
So 144032-75-7 is a valid CAS Registry Number.

144032-75-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2,3,4,4-pentadeuterio-pentan-3-ol

1.2 Other means of identification

Product number -
Other names 3-Pentanol-2,2,3,4,4-d(5)

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:144032-75-7 SDS

144032-75-7Downstream Products

144032-75-7Relevant academic research and scientific papers

The Mechanism of Ethylene Elimination from the Oxonium Ions CH3CH2CH=O+CH2CH3 and (CH3)2C=O+CH2CH3

Bowen, Richard D.,Derrick, Peter J.

, p. 1033 - 1039 (2007/10/02)

The reactions of the metastable oxonium ions CH3CH2CH=O+CH2CH3 and (CH3)2C=O+CH2CH3 are reported and discussed.Various mechanisms for ethylene elimination, which is the principal dissociation route for these ions, are considered.It is shown by means of 2H-labelling experiments and analysis of collision-induced dissociation spectra that routes involving ion-neutral complexes pre-empt 'conventional' mechanisms for these processes.In contrast, the behaviour of the lower homologues CH3CH2CH=OR+ and (CH3)2C=OR+ (R = H, CH3) is consistent with the operation of 'conventional' mechanisms for ethylene expulsion.This contrast is interpreted in energetic terms.The significance of these results for the chemistry of homologous and analogous 'onium' ions containing a Z+-R function (Z = O, S, NH, NCH3; R= CnH2n+1, n 2) is explained.

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