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19728-43-9

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19728-43-9 Usage

General Description

2,4-DI-TERT-BUTYLTHIOPHENOL is a chemical compound with the molecular formula C14H22OS. It is a colorless to light yellow liquid with a strong odor. It is commonly used as an antioxidant and stabilizer in the production of polymers, including plastics and rubbers. It is also utilized as a chemical intermediate in the synthesis of pharmaceuticals and agrochemicals. Due to its ability to inhibit the formation of free radicals and prevent degradation of materials, 2,4-DI-TERT-BUTYLTHIOPHENOL is valued for its role in prolonging the lifespan and performance of various industrial products. However, it must be handled and used with caution, as it is toxic if swallowed and can cause skin and eye irritation.

Check Digit Verification of cas no

The CAS Registry Mumber 19728-43-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,7,2 and 8 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 19728-43:
(7*1)+(6*9)+(5*7)+(4*2)+(3*8)+(2*4)+(1*3)=139
139 % 10 = 9
So 19728-43-9 is a valid CAS Registry Number.
InChI:InChI=1/C14H22S/c1-13(2,3)10-7-8-12(15)11(9-10)14(4,5)6/h7-9,15H,1-6H3

19728-43-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-ditert-butylbenzenethiol

1.2 Other means of identification

Product number -
Other names 2,4-Di-tert-butylthiophenol

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:19728-43-9 SDS

19728-43-9Relevant articles and documents

Molecular and electronic structures of one-electron oxidized Ni II-(dithiosalicylidenediamine) complexes: NiIII-thiolate versus NiII-thiyl radical states

Stenson, Philip A.,Board, Ashley,Marin-Becerra, Armando,Blake, Alexander J.,Davies, E. Stephen,Wilson, Claire,McMaster, Jonathan,Schr?der, Martin

experimental part, p. 2564 - 2576 (2009/04/11)

The dithiosalicylidenediamine NiII complexes [Ni(L)] (R = tBu, R′ = CH2C(CH3)2CH2 1, R′=C6H4 2; R = H, R′ = CH2C(CH 3)2CH2 3, R′ = Cs

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