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1,3-Benzenedicarboxamide, N,N'-bis(4-hydroxyphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1245-91-6

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1245-91-6 Usage

Chemical compound

1,3-Benzenedicarboxamide, N,N'-bis(4-hydroxyphenyl)-

Usage

Widely used in the production of polycarbonate plastics and epoxy resins

Endocrine disruptor

Can interfere with hormone function in the body

Health concerns

Linked to increased risk of certain cancers, reproductive issues, and developmental problems in children

Exposure

Can occur through ingestion of food and beverages stored in plastic containers or cans lined with epoxy resin, as well as through contact with certain consumer products

Consumer demand

Growing concern over BPA use in commercial products, leading to increased demand for BPA-free alternatives

Check Digit Verification of cas no

The CAS Registry Mumber 1245-91-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,4 and 5 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1245-91:
(6*1)+(5*2)+(4*4)+(3*5)+(2*9)+(1*1)=66
66 % 10 = 6
So 1245-91-6 is a valid CAS Registry Number.

1245-91-6SDS

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 1-N,3-N-bis(4-hydroxyphenyl)benzene-1,3-dicarboxamide

1.2 Other means of identification

Product number -
Other names 1,3-Benzenedicarboxamide,N,N'-bis(4-hydroxyphenyl)

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:1245-91-6 SDS

1245-91-6Downstream Products

1245-91-6Relevant academic research and scientific papers

How Does the Hydrogen Bonding Interaction Influence the Properties of Polybenzoxazine? An Experimental Study Combined with Computer Simulation

Shen, Xiaobin,Cao, Lijun,Liu, Yuan,Dai, Jinyue,Liu, Xiaoqing,Zhu, Jin,Du, Shiyu

, p. 4782 - 4799 (2018)

The formation of intra- or intermolecular hydrogen bonding and their influences on polybenzoxazine's properties were investigated after the model benzoxazine monomers (o-AB-fbz, o-AF-fbz, o-AP-fbz, p-AB-fbz, p-AF-fbz, p-AP-fbz) were synthesized. Because of the different electron-donating abilities of bridging units (benzene, furan and pyridine) in isophthalic acid (IPA), 2,5-furandicarboxylic acid (2,5-FDCA) and 2,6-pyridinedicarboxylic acid (2,6-PDCA), the strength of intramolecular H-bonding involved with the oxygen atom in oxazine ring in o-AB-fbz, o-AF-fbz and o-AP-fbz followed the order of o-AB-fbz > o-AF-fbz > o-AP-fbz, and the strength of the overall H-bonding was arranged as follows: o-AB-fbz g), and the influence of H-bonding on Tg was revealed by in situ FT-IR analysis. Molecular dynamics (MD) simulation was also applied to investigate the properties of synthesized polybenzoxazines and similar results were obtained. Not only the formation of H-bonding but also their effects on both the curing behaviors of benzoxazine monomers and the thermal properties of cured resins were systematically investigated, which would help us understand polybenzoxazines more deeply and might be a guideline for improving their comprehensive properties only by manipulating the H-bonding.

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