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Octanethioamide, also known as octanamide or caprylamide, is an organic compound with the chemical formula C8H17CONH2. It is a colorless, odorless, and crystalline solid that is soluble in water and various organic solvents. Octanethioamide is primarily used as an intermediate in the synthesis of various chemicals, including surfactants, pharmaceuticals, and agrochemicals. It is also employed as a plasticizer, a lubricant, and a component in the production of synthetic fibers. The compound is derived from the reaction of octanoic acid and ammonia, and its properties include a melting point of around 95-97°C and a boiling point of approximately 300°C. Due to its potential applications and versatility, octanethioamide is an important chemical in the industrial sector.

5813-91-2

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5813-91-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5813-91-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,1 and 3 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5813-91:
(6*5)+(5*8)+(4*1)+(3*3)+(2*9)+(1*1)=102
102 % 10 = 2
So 5813-91-2 is a valid CAS Registry Number.

5813-91-2SDS

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 octanethioamide

1.2 Other means of identification

Product number -
Other names Thiooctansaeureamid

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:5813-91-2 SDS

5813-91-2Relevant academic research and scientific papers

From sulfur-amine solutions to metal sulfide nanocrystals: Peering into the oleylamine-sulfur black box

Thomson, Jordan W.,Nagashima, Kaz,MacDonald, Peter M.,Ozin, Geoffrey A.

experimental part, p. 5036 - 5041 (2011/06/23)

In this Article, we present our findings on the formation of metal sulfide nanocrystals from sulfur-alkylamine solutions. By pulsed field gradient diffusion NMR along with the standard toolbox of 1D and 2D NMR, we determined that sulfur-amine solutions used as a sulfur precursor exist as alkylammonium polysulfides at low temperatures. Upon heating to temperatures used in nanocrystal synthesis, the polysulfide ions react with excess amine to generate H2S, which combines with the metal precursor to form metal sulfide. Four different reaction pathways were found, each of which produced H 2S and the byproducts identified in this Article. Thioamides were identified as an intermediate and were shown to exhibit much more rapid kinetics than sulfur-alkylamine solutions at low temperatures in the synthesis of metal sulfide nanocrystals.

Synthesis of primary thioamides from nitriles and hydrogen sulfide catalyzed by anion-exchange resin

Liboska, Radek,Zyka, Daniel,Bobek, Miroslav

, p. 1649 - 1651 (2007/10/03)

A new method has been developed for converting nitriles into primary thioamides. Treatment of various nitriles (Table 1, entries 1-12) with gaseous hydrogen sulfide in a mixture of methanol-water or ethanol-water and in the presence of anion-exchange resin (Dowex 1X8, SH- form) at room temperature and ambient pressure gave the corresponding thioamides in 25-96% yield.

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