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Phenol, 2,2'-methylenebis[6-methoxy-4-methyl-, also known as Bisphenol S (BPS), is an organic compound that belongs to the class of bisphenols. It is a white crystalline solid with the chemical formula C15H16O4. BPS is structurally similar to Bisphenol A (BPA), a well-known endocrine disruptor. This synthetic compound is primarily used in the production of polycarbonate plastics and epoxy resins, which are commonly found in various consumer products such as food containers, water bottles, and thermal paper receipts. Due to its potential health risks and environmental concerns, BPS has been a subject of ongoing research and debate, with some countries implementing regulations to limit its use.

1620-70-8

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1620-70-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1620-70-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,2 and 0 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1620-70:
(6*1)+(5*6)+(4*2)+(3*0)+(2*7)+(1*0)=58
58 % 10 = 8
So 1620-70-8 is a valid CAS Registry Number.

1620-70-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(2-hydroxy-3-methoxy-5-methylphenyl)methyl]-6-methoxy-4-methylphenol

1.2 Other means of identification

Product number -
Other names Phenol,2,2'-methylenebis[6-methoxy-4-methyl

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:1620-70-8 SDS

1620-70-8Relevant academic research and scientific papers

Reaction of a lignin model dimer sequentially with chlorine and sodium hydroxide

McKague,Reeve

, p. 573 - 576 (1994)

Dimer 9, which is representative of diaryl methane structures reported present in residual lignin, was reacted with aqueous chlorine at 50 °C. The major product was identified as the tetrachloroquinone dimer 13 (x = 2, y = 2). Similar reaction of the tetr

Lignin-based diphenylmethane diisocyanate as well as preparation method and application thereof

-

Paragraph 0093-0096; 0113-0116, (2021/11/21)

The invention discloses a lignin-based diphenylmethane diisocyanate and a preparation method and application thereof. As shown in Formula I, the lignin-based diphenylmethane diisocyanate is prepared by reacting a lignin-cracking monomer compound II with a carbonyl compound to give compound III, compound III reacts with chloroacetyl ammonia to obtain compound IV, compound IV is subjected Smiles rearrangement reaction to obtain compound V, and compound V is reacted with a compound containing carbon-containing acid to obtain the lignin-based diphenylmethane diisocyanate shown in formula I. The product replaces MDI for synthesis of polyurethane materials, and the toughness of the polyurethane material is improved. Thermal stability and glass transition temperature. When being applied to polyurethane waterproof coating, the water absorption rate is obviously reduced, and the stability of the coating is improved.

Renewable polyphenols, thermoplastics, and resins

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Page/Page column 6; 10-11, (2019/04/26)

A series of renewable bisphenols has been synthesized from creosol (2-methoxy-4-methylphenol) through stoichiometric condensation with short chain aldehydes. Creosol can be readily produced from lignin, potentially allowing for the large scale synthesis o

Synthesis, characterization, and cure chemistry of renewable bis(cyanate) esters derived from 2-methoxy-4-methylphenol

Meylemans, Heather A.,Harvey, Benjamin G.,Reams, Josiah T.,Guenthner, Andrew J.,Cambrea, Lee R.,Groshens, Thomas J.,Baldwin, Lawrence C.,Garrison, Michael D.,Mabry, Joseph M.

, p. 771 - 780 (2013/05/09)

A series of renewable bis(cyanate) esters have been prepared from bisphenols synthesized by condensation of 2-methoxy-4-methylphenol (creosol) with formaldehyde, acetaldehyde, and propionaldehyde. The cyanate esters have been fully characterized by infrar

Synthesis of renewable bisphenols from creosol

Meylemans, Heather A.,Groshens, Thomas J.,Harvey, Benjamin G.

experimental part, p. 206 - 210 (2012/06/30)

A series of renewable bisphenols has been synthesized from creosol (2-methoxy-4-methylphenol) through stoichiometric condensation with short-chain aldehydes. Creosol can be readily produced from lignin, potentially allowing for the large scale synthesis o

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