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mercaptopentanone,2-mercapto-3-pentanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

17042-24-9

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17042-24-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17042-24-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,0,4 and 2 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 17042-24:
(7*1)+(6*7)+(5*0)+(4*4)+(3*2)+(2*2)+(1*4)=79
79 % 10 = 9
So 17042-24-9 is a valid CAS Registry Number.
InChI:InChI=1/C5H10OS/c1-3-5(6)4(2)7/h4,7H,3H2,1-2H3

17042-24-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-mercapto-pentan-3-one

1.2 Other means of identification

Product number -
Other names 2-Mercapto-pentan-3-one

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:17042-24-9 SDS

17042-24-9Relevant academic research and scientific papers

Some Novel Meatlike Aroma Compounds from the Reactions of Alkanediones with Hydrogen Sulfide and Furanthiols

Mottram, Donald S.,Madruga, Marta S.,Whitfield, Frank B.

, p. 189 - 193 (2007/10/02)

The products of reactions of hydrogen sulfide with 2,3-butanedione and with 2,3-pentanedione in dilute ethanolic solution were analyzed by GC-MS and GC-odor port analysis.Components were also collected from the GC column and analyzed by 1H NMR.Mercaptoketones were formed which readily oxidized to the corresponding disulfides with traces of mono- and trisulfides.When 2-methyl-3-furanthiol or 2-furylmethanethiol was added to the reaction mixtures, a series of disulfides containing alkanone, 2-methyl-3-furyl and 2-furanmethyl moieties were formed.Some of these compounds have been found recently in the volatiles of cooked meat and in meatlike model systems.GC-odor port evaluation of the components of the reaction systems showed that disulfides containing the 2-methyl-3-furyl group had meaty aromas, whereas those without this group were sulfurous or onion-like in character.Keywords: Aroma; meat; mercaptoketones; disulfides

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