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3,5-Pyrazolidinedione, 4-methyl-1,2-diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 42391-32-2 Structure
  • Basic information

    1. Product Name: 3,5-Pyrazolidinedione, 4-methyl-1,2-diphenyl-
    2. Synonyms:
    3. CAS NO:42391-32-2
    4. Molecular Formula: C16H14N2O2
    5. Molecular Weight: 266.299
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 42391-32-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 3,5-Pyrazolidinedione, 4-methyl-1,2-diphenyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3,5-Pyrazolidinedione, 4-methyl-1,2-diphenyl-(42391-32-2)
    11. EPA Substance Registry System: 3,5-Pyrazolidinedione, 4-methyl-1,2-diphenyl-(42391-32-2)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 42391-32-2(Hazardous Substances Data)

42391-32-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 42391-32-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,3,9 and 1 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 42391-32:
(7*4)+(6*2)+(5*3)+(4*9)+(3*1)+(2*3)+(1*2)=102
102 % 10 = 2
So 42391-32-2 is a valid CAS Registry Number.

42391-32-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methyl-1,2-diphenyl-3,5-pyrazolidinedione

1.2 Other means of identification

Product number -
Other names 4-methyl-1,2-diphenyl-pyrazolidine-3,5-dione

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:42391-32-2 SDS

42391-32-2Relevant articles and documents

Ionic Highways from Covalent Assembly in Highly Conducting and Stable Anion Exchange Membrane Fuel Cells

Kim, Yoonseob,Wang, Yanming,France-Lanord, Arthur,Wang, Yichong,Wu, You-Chi Mason,Lin, Sibo,Li, Yifan,Grossman, Jeffrey C.,Swager, Timothy M.

, p. 18152 - 18159 (2019)

A major challenge in the development of anion exchange membranes for fuel cells is the design and synthesis of highly stable (chemically and mechanically) conducting membranes. Membranes that can endure highly alkaline environments while rapidly transporting hydroxides are desired. Herein, we present a design using cross-linked polymer membranes containing ionic highways along charge-delocalized pyrazolium cations and homoconjugated triptycenes. These ionic highway membranes show improved performance. Specifically, a conductivity of 111.6 mS cm-1 at 80 °C was obtained with a low 7.9% water uptake and 0.91 mmol g-1 ion exchange capacity. In contrast to existing materials, ionic highways produce higher conductivities at reduced hydration and ionic exchange capacities. The membranes retain more than 75% of their initial conductivity after 30 days of an alkaline stability test. The formation of ionic highways for ion transport is confirmed by density functional theory and Monte Carlo studies. A single cell with platinum metal catalysts at 80 °C showed a high peak density of 0.73 W cm-2 (0.45 W cm-2 from a silver-based cathode) and stable performance throughout 400 h tests.

Ionic Highways from Covalent Assembly in Highly Conducting and Stable Anion Exchange Membrane Fuel Cells

Kim, Yoonseob,Wang, Yanming,France-Lanord, Arthur,Wang, Yichong,Wu, You-Chi Mason,Lin, Sibo,Li, Yifan,Grossman, Jeffrey C.,Swager, Timothy M.

supporting information, p. 18152 - 18159 (2019/11/14)

A major challenge in the development of anion exchange membranes for fuel cells is the design and synthesis of highly stable (chemically and mechanically) conducting membranes. Membranes that can endure highly alkaline environments while rapidly transporting hydroxides are desired. Herein, we present a design using cross-linked polymer membranes containing ionic highways along charge-delocalized pyrazolium cations and homoconjugated triptycenes. These ionic highway membranes show improved performance. Specifically, a conductivity of 111.6 mS cm-1 at 80 °C was obtained with a low 7.9% water uptake and 0.91 mmol g-1 ion exchange capacity. In contrast to existing materials, ionic highways produce higher conductivities at reduced hydration and ionic exchange capacities. The membranes retain more than 75% of their initial conductivity after 30 days of an alkaline stability test. The formation of ionic highways for ion transport is confirmed by density functional theory and Monte Carlo studies. A single cell with platinum metal catalysts at 80 °C showed a high peak density of 0.73 W cm-2 (0.45 W cm-2 from a silver-based cathode) and stable performance throughout 400 h tests.

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