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30043-13-1

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30043-13-1 Usage

Class

Organophosphorus compounds

Use

Fungicide

Function

Inhibits the growth of fungi and other microorganisms by disrupting their metabolic processes

Applications

Agricultural and industrial use to protect crops and materials from fungal infestations

Toxicity

Can be toxic to humans and the environment if not properly managed.

Check Digit Verification of cas no

The CAS Registry Mumber 30043-13-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,0,4 and 3 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 30043-13:
(7*3)+(6*0)+(5*0)+(4*4)+(3*3)+(2*1)+(1*3)=51
51 % 10 = 1
So 30043-13-1 is a valid CAS Registry Number.

30043-13-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-bis(4-ethoxyphenyl)-2,4-bis(sulfanylidene)-1,3,2λ<sup>5</sup>,4λ<sup>5</sup>-dithiadiphosphetane

1.2 Other means of identification

Product number -
Other names phenetylperthiophosphinic acid anhydride dimer

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:30043-13-1 SDS

30043-13-1Upstream product

30043-13-1Relevant articles and documents

Flexible Molecular Precursors for Selective Decomposition to Nickel Sulfide or Nickel Phosphide for Water Splitting and Supercapacitance

Ayom, Gwaza E.,Gupta, Ram K.,Ingsel, Tenzin,Khan, Malik D.,Lin, Wang,Revaprasadu, Neerish,Zamisa, Sizwe J.,van Zyl, Werner E.

, p. 2693 - 2704 (2020/03/04)

Herein, the synthesis of three nickel(II) dithiophosphonate complexes of the type [Ni{S2P(OR)(4-C6H4OMe)}2] [R=H (1), C3H7 (2)] and [Ni{S2P(OR)(4-C6H4OEt}2] [R=(C6H5)2CH (3)] is described; their structures were confirmed by single-crystal X-ray studies. These complexes were subjected to surfactant/solvent reactions at 300 °C for one hour as flexible molecular precursors to prepare either nickel sulfide or nickel phosphide particles. The decomposition of complex 2 in tri-octylphosphine oxide/1-octadecene (TOPO/ODE), TOPO/tri-n-octylphosphine (TOP), hexadecylamine (HDA)/TOP, and HDA/ODE yielded hexagonal NiS, Ni2P, Ni5P4, and rhombohedral NiS, respectively. Similarly, the decomposition of complex 1 in TOPO/TOP and HDA/TOP yielded hexagonal Ni2P and Ni5P4, respectively, and that of complex 3 in similar solvents led to hexagonal Ni5P4, with TOP as the likely phosphorus provider. Hexagonal NiS was prepared from the solvent-less decomposition of complexes 1 and 2 at 400 °C. NiS (rhom) had the best specific supercapacitance of 2304 F g?1 at a scan rate of 2 mV s?1 followed by 1672 F g?1 of Ni2P (hex). Similarly, NiS (rhom) and Ni2P (hex) showed the highest power and energy densities of 7.4 kW kg?1 and 54.16 W kg?1 as well as 6.3 kW kg?1 and 44.7 W kg?1, respectively. Ni5P4 (hex) had the lowest recorded overpotential of 350 mV at a current density of 50 mA cm?2 among the samples tested for the oxygen evolution reaction (OER). NiS (hex) and Ni5P4 (hex) had the lowest overpotentials of 231 and 235 mV to achieve a current density of 50 mA cm?2, respectively, in hydrogen evolution reaction (HER) examinations.

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