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2,2'-[1,4-Phenylenebis(methylidynenitrilo)]bisphenol, commonly referred to as Bisphenol M, is an organic chemical compound with the chemical formula C15H16N2O2. Structurally similar to Bisphenol A (BPA), Bisphenol M is utilized in the production of a variety of plastic products, adhesives, and coatings. It is recognized for its high heat resistance and stability, which makes it an ideal component for applications that require exposure to high temperatures. Despite its widespread use, there is an ongoing discussion about the potential health and environmental risks associated with Bisphenol M due to its endocrine-disrupting properties and the possibility of leaching into food and beverages from containers made with 2,2'-[1,4-Phenylenebis(methylidynenitrilo)]bisphenol.

13060-68-9

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13060-68-9 Usage

Uses

Used in Plastics Industry:
Bisphenol M is used as a key component in the production of various types of plastics for its high heat resistance and stability, making it suitable for manufacturing plastic products that are intended for use in high-temperature environments.
Used in Adhesives Industry:
In the adhesives industry, Bisphenol M serves as an essential ingredient for creating adhesives with enhanced durability and heat resistance, which are crucial for bonding materials under demanding conditions.
Used in Coatings Industry:
Bisphenol M is utilized in the formulation of coatings to provide them with improved heat resistance and stability, ensuring that the coatings maintain their protective qualities even when exposed to high temperatures.
However, due to the concerns regarding the potential health risks and environmental impact of Bisphenol M, there is continuous research being conducted to assess its safety and explore alternative compounds that can offer similar properties without the associated risks.

Check Digit Verification of cas no

The CAS Registry Mumber 13060-68-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,0,6 and 0 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 13060-68:
(7*1)+(6*3)+(5*0)+(4*6)+(3*0)+(2*6)+(1*8)=69
69 % 10 = 9
So 13060-68-9 is a valid CAS Registry Number.
InChI:InChI=1/C20H16N2O2/c23-19-7-3-1-5-17(19)21-13-15-9-11-16(12-10-15)14-22-18-6-2-4-8-20(18)24/h1-14,21,23H/b15-13-,16-14+,22-18+

13060-68-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-[[4-[(2-hydroxyanilino)methylidene]cyclohexa-2,5-dien-1-ylidene]methylimino]cyclohexa-2,4-dien-1-one

1.2 Other means of identification

Product number -
Other names 1,4-Bis-<2-hydroxy-phenyliminomethyl>-benzol

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:13060-68-9 SDS

13060-68-9Relevant academic research and scientific papers

Synthesis, spectral characterization, catalytic and antibacterial studies of new Ru(III) Schiff base complexes containing chloride/bromide and triphenylphosphine/arsine as co-ligands

Arunachalam,Padma Priya,Jayabalakrishnan,Chinnusamy

, p. 591 - 596 (2009)

A new Ru(III) Schiff base complexes of the type [RuX(EPh3)L] (X = Cl/Br; E = P/As; L = dianion of the Schiff bases were derived by the condensation of 1,4-diformylbenzene with o-aminobenzoic acid/o-aminophenol/o-aminothiophenol in the 1:2 stoic

A novel terephthalaldehyde based turn-on fluorescent chemosensor for Cu2+ and its application in imaging of living cells

Torawane, Pritam,Keshav, Karunesh,Kumawat, Mukesh K.,Srivastava, Rohit,Anand, Thangaraj,Sahoo, Suban,Borse, Amulrao,Kuwar, Anil

, p. 1464 - 1470 (2017)

A new terephthaldehyde-based chemosensor 1 bearing an aminophenol recognition unit has been synthesized and applied to the fluorescent sensing of metal ions. Molecular system 1 acts as a highly selective and sensitive fluorescence turn-on sensor for Cusu

Cyanide Boosting Copper Catalysis: A Mild Approach to Fluorescent Benzazole Derivatives from Nonemissive Schiff Bases in Biological Media

Li, Hongjuan,Sun, Shiguo,Wang, Dejia,Xu, Yongqian

supporting information, p. 3361 - 3366 (2020/04/20)

An application of nucleophilic cyclization and oxidation of nonemissive Schiff bases via cyanide boosting copper catalysis to synthesize fluorescent benzazole derivatives in high conversion yield is disclosed. This approach is highlighted by broad substra

Fe3O4@SiO2@Im[Cl]Mn(III)-complex as a highly efficient magnetically recoverable nanocatalyst for selective oxidation of alcohol to imine and oxime

Kazemnejadi, Milad,Alavi, Seyyedeh Ameneh,Rezazadeh, Zinat,Nasseri, Mohammad Ali,Allahresani, Ali,Esmaeilpour, Mohsen

, p. 230 - 249 (2019/03/28)

An efficient and environmentally friendly oxidation process for the one-pot preparation of oxime, imine and carbonyl compounds through alcohol oxidation in the presence of H2O2 and/or O2 have been developed by a melamine-Mn(III) Schiff base complex supported on Fe3O4@SiO2–Cl nanoparticles, named as Fe3O4@SiO2@Im[Cl]Mn(III)-complex nanocomposite, at room temperature. Direct oxidation of alcohol to carboxylic acid was performed using the catalyst in the presence of molecular O2 at room temperature in a different approach. The oxidation products were obtained with excellent yields and high TOFs. The properties of the catalyst were characterized by Fourier transform infrared spectroscopy (FTIR), elemental analysis (C, H, N), X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), dynamic light scattering (DLS), energy dispersive X-ray analysis (EDX), X-ray photoelectron spectroscopy (XPS), inductive coupled plasma (ICP), cyclic voltammetry (CV), nuclear magnetic resonance (1H & 13C NMR), vibration sample magnetometer (VSM), Brunauer– Emmett–Teller (BET) and differential pulse voltammetry (DPV) analyses. The mechanism of the oxidation processes was investigated for the both H2O2 and O2 oxidants. The role of the imidazolium moiety in the catalyst as a secondary functionality was investigated. Chemoselectivity behavior of the catalyst was studied by some combinations. The catalyst could be recycled from the reaction mixture by a simple external magnet and reused for several times without any considerable reactivity loss.

Direct preparation of oximes and Schiff bases by oxidation of primary benzylic or allylic alcohols in the presence of primary amines using Mn(III) complex of polysalicylaldehyde as an efficient and selective heterogeneous catalyst by molecular oxygen

Kazemnejadi, Milad,Shakeri, Alireza,Mohammadi, Mohammad,Tabefam, Marzieh

, p. 1917 - 1933 (2017/08/15)

The present work introduced the new strategy for direct preparation of Schiff base as well as oxime compounds through oxidation of primary benzylic or allylic alcohols in the presence of amines by complexation of Mn(III) to a polymeric Schiff base ligand based on polysalicylaldehyde (PSA-Schiff base-Mn(III) complex). As a new environmentally benign protocol, manganese heterogeneous polymeric catalytic system demonstrated promising oxidation of alcohols in ethanol using molecular oxygen. PSA was synthesized through polycondensation reaction of 2-hydroxy-5-chloromethyl-benzaldehyde and then treated with 2-aminophenol to form polymeric ligand. Average molecular weight of PSA was studied by an analytical method as well as GPC analysis. Formation of the catalyst was characterized step by step by FTIR, UV–Vis, 1H NMR, TGA, CHN and EDX analyses. Loading amounts of metal ions as well as leaching amount of the catalysis were studied by ICP-OES instrument. The catalyst shows up to high yields for oxidation of primary and secondary primary benzylic or allylic alcohols to carbonyl compounds, especially direct imine formation in a mild, inexpensive and efficient method which can be successfully recovered from the reaction mixture and reused for several times without any remarkable reactivity loss. Effect of solvent, temperature, catalyst amount and oxygen donors along with some blank experiments to elucidation of catalyst activity was evaluated in this work. Also chemoselectivity behavior of the catalyst was investigated with some combinations.

Design of a structural framework with potential use to develop balanced multifunctional agents against Alzheimer's disease

Jiang, Neng,Wang, Xiao-Bing,Li, Zhong-Rui,Li, Su-Yi,Xie, Sai-Sai,Huang, Ming,Kong, Ling-Yi

, p. 14242 - 14255 (2015/03/05)

A series of small molecules had been designed, synthesized, and evaluated as multifunctional ligands against Alzheimer's disease (AD). The results of biological activity tests showed that most of the molecules exhibited a significant ability to inhibit se

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