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10583-85-4

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10583-85-4 Usage

Compound type

Sulfur-containing heterocyclic compound.

Structure

A butyl group attached to an imidazoline ring.

Industrial applications

Corrosion inhibitor and biocide in metalworking fluids, lubricants, and water treatment.

Functioning

Acts as a chelating agent, effectively binding to metal ions and preventing their oxidation and corrosion.

Antimicrobial properties

Inhibits the growth of bacteria, fungi, and algae in water-based systems.

Toxicity

Low acute toxicity.

Skin irritation

Classified as a mild irritant.

Handling precautions

Handle with caution and proper safety measures.

Check Digit Verification of cas no

The CAS Registry Mumber 10583-85-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,5,8 and 3 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 10583-85:
(7*1)+(6*0)+(5*5)+(4*8)+(3*3)+(2*8)+(1*5)=94
94 % 10 = 4
So 10583-85-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H12N2S/c1-2-3-5-9-6-4-8-7(9)10/h4,6H,2-3,5H2,1H3,(H,8,10)

10583-85-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-butyl-1H-imidazole-2-thione

1.2 Other means of identification

Product number -
Other names Imidazole-2-thiol,1-butyl

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:10583-85-4 SDS

10583-85-4Downstream Products

10583-85-4Relevant articles and documents

Facile conversion of amino acids into 1-alkyl imidazole-2-thiones, and their oxidative desulfurization to imidazoles with benzoyl peroxide

Wolfe, Derek M.,Schreiner, Peter R.

, p. 2002 - 2008 (2008/02/11)

Glycine was acylated with isothiocyanates and condensed to 3-alkyl 2-thiohydantoins, which were reduced with a mixture of sodium borohydride and lithium chloride and dehydrated to 1-alkyl imidazole-2-thiones. These were oxidatively desulfurized to imidazoles with benzoyl peroxide. No chromatography was required for model compounds. The methods developed were used to elaborate tyrosine to 1,4-di(p-methoxybenzyl)imidazole, a common intermediate in the syntheses of three imidazoles from the sponge Leucetta. Georg Thieme Verlag Stuttgart.

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