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Dibutyldithiocarbamic acid, also known as DBDTC or DBT, is an organic compound with the chemical formula C11H22N2S4. It is a yellowish, oily liquid that is soluble in water and has a strong, unpleasant odor. DBDTC is primarily used as a rubber accelerator, promoting the vulcanization process in rubber manufacturing, and as a fungicide in agriculture to protect crops from various diseases. It is also employed as a corrosion inhibitor in the oil and gas industry and as a flotation agent in the mining sector. Due to its potential health and environmental risks, including its classification as a possible human carcinogen, its use is regulated in many countries.

150-11-8

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150-11-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 150-11-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,5 and 0 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 150-11:
(5*1)+(4*5)+(3*0)+(2*1)+(1*1)=28
28 % 10 = 8
So 150-11-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H19NS2/c1-3-5-7-10(9(11)12)8-6-4-2/h3-8H2,1-2H3,(H,11,12)

150-11-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-dibutyldithiocarbamic acid

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:150-11-8 SDS

150-11-8Relevant academic research and scientific papers

Visible-Light-Induced Photocatalytic Synthesis of β-Keto Dithiocarbamates via Difunctionalization of Styrenes

Vishwakarma, Ramesh Kumar,Kumar, Saurabh,Singh, Krishna Nand

supporting information, p. 4147 - 4151 (2021/05/26)

A facile photocatalyzed strategy for difunctionalization of styrenes in the presence of CS2 and amines providing β-keto dithiocarbamates has been developed. In the case of 4-nitrostyrene and 2-vinylpyridine, however, only 2-arylethylthiocarbamates are interestingly formed without the aid of photoredox catalysis/TBHP.

In situ formation of thermally stable, room-temperature ionic liquids from CS2 and amidine/amine mixtures

Yu, Tao,Yamada, Taisuke,Weiss, Richard G.

experimental part, p. 5492 - 5499 (2011/12/14)

Amidinium dithiocarbamates salts with diverse structures are prepared in situ by adding one equivalent of CS2 to an equimolar mixture of two nonionic molecules, an amidine and an amine. Many of the salts made in this way are room temperature ionic liquids (RTILs) and the others (ILs) melt well below the decomposition temperature of the salts, ca. 80 °C. Unlike the analogous amidinium carbamate RTILs, which are made by adding CO2 to amidine/amine mixtures and decompose near 50 °C, the amidinium dithiocarbamates do not revert to their amidine/amine mixtures when they are heated. The thermal, rheological, conductance, and spectroscopic properties of representative examples from a total of 50 of these ILs and RTILs are reported, comparisons between them and their nonionic phases (as well as with their amidinium carbamates analogues) are made, and the thermolysis pathways of the ammonium dithiocarbamates are investigated.

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