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Hexamethylenedithiocarbamic acid, also known as HMT, is an organic compound with the chemical formula C6H12N2S2. It is a white crystalline solid that is soluble in water and has a strong, pungent odor. HMT is primarily used as a fungicide, herbicide, and metal deactivator in various industrial applications. It is also employed as a vulcanization accelerator in the rubber industry and as a corrosion inhibitor in metalworking fluids. Additionally, HMT has applications in the pharmaceutical and agricultural sectors, where it is used as a pesticide and a plant growth regulator. The compound is synthesized by reacting carbon disulfide with hexamethyleneamine, and its chemical structure consists of a central carbon atom bonded to two nitrogen atoms, each of which is further bonded to a sulfur atom.

874-56-6

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874-56-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 874-56-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,7 and 4 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 874-56:
(5*8)+(4*7)+(3*4)+(2*5)+(1*6)=96
96 % 10 = 6
So 874-56-6 is a valid CAS Registry Number.

874-56-6SDS

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 azepane-1-carbodithioic acid

1.2 Other means of identification

Product number -
Other names Hexamethylenedithiocarbamate

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:874-56-6 SDS

874-56-6Downstream Products

874-56-6Relevant academic research and scientific papers

Synthesis of novel dithiocarbamates and xanthates using dialkyl azodicarboxylates: S–N bond formation

Ziyaei Halimehjani, Azim,Klepetá?ová, Blanka,Beier, Petr

, p. 1850 - 1858 (2018)

A one?pot three?component route for the synthesis of a novel category of dithiocarbamates or xanthates is developed by a reaction of in-situ generated dithiocarbamic acids or xanthates with dialkyl azodicarboxylates under mild and catalyst-free conditions. The reaction is characterized by a wide scope, high efficiency and straightforward isolation protocol. The synthetic utility of the dithiocarbamates and xanthates was demonstrated on the preparation of symmetrical and unsymmetrical thioureas, isothiocyanates, and thiocarbamates.

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