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1-(Ethylthio)dodecane, also known as 1-(ethylthio)n-dodecane or 1-ethylthio-1-dodecane, is an organic compound with the chemical formula C14H30S. It is a colorless liquid with a molecular weight of 230.46 g/mol. 1-(Ethylthio)dodecane is characterized by a dodecane chain (a 12-carbon alkane) with an ethylthio group (-SCH2CH3) attached to the first carbon atom. 1-(Ethylthio)dodecane is primarily used as a synthetic intermediate in the production of various chemicals, pharmaceuticals, and agrochemicals. It is also employed as a solvent and a fragrance component in the perfume industry. Due to its potential health and environmental risks, proper handling and disposal procedures should be followed when working with this chemical.

2851-83-4

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2851-83-4 Usage

Classification

Organic compound

Subgroup

Thioethers

Characterization

Presence of a sulfur atom bonded to a carbon atom

Physical state

Clear, colorless liquid

Molecular weight

230.45 g/mol

Applications

Flavoring agent and fragrance in the food, beverage, and cosmetic industries

Additional use

Intermediate in the production of various chemicals and pharmaceutical compounds

Toxicity

Low toxicity

Odor

Pleasant odor

Safety

Considered safe for use in consumer products

Check Digit Verification of cas no

The CAS Registry Mumber 2851-83-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,5 and 1 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2851-83:
(6*2)+(5*8)+(4*5)+(3*1)+(2*8)+(1*3)=94
94 % 10 = 4
So 2851-83-4 is a valid CAS Registry Number.

2851-83-4SDS

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 ethyl dodecyl sulfide

1.2 Other means of identification

Product number -
Other names -

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:2851-83-4 SDS

2851-83-4Relevant academic research and scientific papers

Comparing Separation vs. Fresh Start to Assess Reusability of Pd/C Catalyst in Liquid-Phase Hydrogenation

Mironenko, Roman M.,Saybulina, Elina R.,Trenikhin, Mikhail V.,Izmailov, Rinat R.,Lotsman, Kristina A.,Rodygin, Konstantin S.,Ananikov, Valentine P.

, p. 3656 - 3661 (2021)

The reusability of metal catalysts is a key issue for the potential application of new catalysts in research and industrial practice. The most common procedure for testing catalyst reusability in liquid-phase heterogeneous reactions is based on separating a catalyst from a reaction mixture followed by the next run. An alternative procedure called “fresh start” consists of the addition of a new portion of reagents to the reaction mixture without any isolation operation. In this work, we compare both procedures in a model Pd/C-catalyzed hydrogenation with different heteroatoms, e. g., O-, S-, and N-vinyl derivatives. It was shown that regardless of whether the catalyst is stable or potentially poisoned during the reaction, both procedures lead to comparable results. It appears that a much easier implementation of a fresh start procedure may be an option of choice. The possibilities of using both procedures to rationalize the experimental protocol for assessing Pd/C catalyst reusability in liquid-phase hydrogenations are discussed.

Lewis acid-catalyzed reduction of dithioacetals by 1,4-cyclohexadiene

Ikeshita, Kei-ichiro,Kihara, Nobuhiro,Sonoda, Motohiro,Ogawa, Akiya

, p. 3025 - 3028 (2008/02/06)

Dithioacetals were reduced by 1,4-cyclohexadiene in the presence of a catalytic amount of Lewis acid to afford the corresponding sulfides in good yields.

Selective reduction of thioacetal to sulfide by gallium(II) chloride

Ikeshita, Kei-Ichiro,Kihara, Nobuhiro,Ogawa, Akiya

, p. 8773 - 8775 (2007/10/03)

The reaction of dithioacetals with gallium(II) chloride followed by the acid treatment afforded sulfides in good yields.

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