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ANILINE HYDROGEN PHTHALATE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

50930-79-5

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50930-79-5 Usage

Chemical Properties

almost white crystalline powder

Check Digit Verification of cas no

The CAS Registry Mumber 50930-79-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,9,3 and 0 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 50930-79:
(7*5)+(6*0)+(5*9)+(4*3)+(3*0)+(2*7)+(1*9)=115
115 % 10 = 5
So 50930-79-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H6O4.C6H7N/c9-7(10)5-3-1-2-4-6(5)8(11)12;7-6-4-2-1-3-5-6/h1-4H,(H,9,10)(H,11,12);1-5H,7H2

50930-79-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name ANILINE HYDROGEN PHTHALATE

1.2 Other means of identification

Product number -
Other names Aniline Hydrogen Phthalate

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:50930-79-5 SDS

50930-79-5Downstream Products

50930-79-5Relevant academic research and scientific papers

Gram-scale production of nitrogen doped graphene using a 1,3-dipolar organic precursor and its utilisation as a stable, metal free oxygen evolution reaction catalyst

Bayazit, Mustafa K.,Moniz, Savio J. A.,Coleman, Karl S.

supporting information, p. 7748 - 7751 (2017/07/15)

For the first time, a one-step scalable synthesis of a few-layer ～10% nitrogen doped (N-doped) graphene nanosheets (GNSs) from a stable but highly reactive 1,3-dipolar organic precursor is reported. The utilization of these N-doped GNSs as metal-free electrocatalysts for the oxygen evolution reaction (OER) is also demonstrated. This process may open the path for the scalable production of other heteroatom doped GNSs by using the broad library of well-known, stable 1,3-dipolar organic compounds.

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