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4,4'-dihydroxy-3,3'-di-(hydroxymethyl)diphenylmethane, also known as bisphenol S (BPS), is a synthetic organic compound that is structurally similar to bisphenol A (BPA). It is primarily used as a building block in the production of various polymers, including epoxy resins and polycarbonate plastics. BPS has gained attention as a potential substitute for BPA in consumer products due to concerns over BPA's potential health effects. However, recent studies have raised concerns about BPS as well, suggesting that it may have similar endocrine-disrupting properties to BPA, potentially affecting the hormonal system and posing risks to human health and the environment. As a result, there is ongoing research and debate about the safety of BPS and its use in consumer products.

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  • 2346-44-3 Structure
  • Basic information

    1. Product Name: 4,4'-dihydroxy-3,3'-di-(hydroxymethyl)diphenylmethane
    2. Synonyms: 4,4'-dihydroxy-3,3'-di-(hydroxymethyl)diphenylmethane;4,4'-Methylenebis(2-(hydroxyMethyl)phenol)
    3. CAS NO:2346-44-3
    4. Molecular Formula: C15H16O4
    5. Molecular Weight: 260.29
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 2346-44-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 458.6°Cat760mmHg
    3. Flash Point: 221.7°C
    4. Appearance: /
    5. Density: 1.346g/cm3
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 4,4'-dihydroxy-3,3'-di-(hydroxymethyl)diphenylmethane(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4,4'-dihydroxy-3,3'-di-(hydroxymethyl)diphenylmethane(2346-44-3)
    11. EPA Substance Registry System: 4,4'-dihydroxy-3,3'-di-(hydroxymethyl)diphenylmethane(2346-44-3)
  • 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: 2346-44-3(Hazardous Substances Data)

2346-44-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2346-44-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,4 and 6 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2346-44:
(6*2)+(5*3)+(4*4)+(3*6)+(2*4)+(1*4)=73
73 % 10 = 3
So 2346-44-3 is a valid CAS Registry Number.

2346-44-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[[4-hydroxy-3-(hydroxymethyl)phenyl]methyl]-2-(hydroxymethyl)phenol

1.2 Other means of identification

Product number -
Other names Benzenemethanol,3,3'-methylenebis(6-hydroxy

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:2346-44-3 SDS

2346-44-3Downstream Products

2346-44-3Relevant articles and documents

Synthesis of new benzylic di-, tri-, and tetraphosphonic acids as potential chelating agents

Aliouane, Nabila,Helesbeux, Jean-Jacques,Douadi, Tahar,Khan, Mustayeen A.,Bouet, Gilles,Chafaa, Salah,Duval, Olivier

experimental part, p. 354 - 364 (2011/04/24)

Chemical Equation Presented New di-, tri-, and tetraphosphonic acids were synthesized starting from four o-hydroxymethyl phenol derivatives and obtained in three steps in good overall yield. The phosphonic acids were isolated and purified using semi-preparative C18 HPLC column. The new compounds were characterized using different spectroscopic methods (1H, 13C, and 31P NMR; ESI MS; and MSn, IR). Copyright Taylor & Francis Group, LLC.

Spectral assignments and reference data: A 13C NMR study of the methylol derivatives of 2,4′- and 4,4′-dihydroxydiphenylmethanes found in resol phenol-formaldehyde resins

Fisher, Thomas H.,Chao, Ping,Upton, Cindy G.,Day, Anthony J.

, p. 747 - 751 (2007/10/03)

A total of 13 of the 16 possible methylol derivatives of 2,4′- and 4,4′-dihydroxydiphenylmethane have been synthesized, isolated, and identified. These compounds are found as intermediates in the cure process of resol phenol-formaldehyde (PF) resins. Analysis of the 13C NMR spectra (in acetone-d6) of these compounds provided a way to evaluate the seven methylolphenol ring types (methylol derivatives of 2-hydroxyphenyl and 4-hydroxyphenyl rings) found in typical resol PF resins using the ipso carbon region from 150 to 160 ppm. A simple diagnostic test was developed using the chemical shift values of the methylol methylene carbon atoms to identify the presence of intermediates containing either a 2-hydroxyphenyl or a 4-hydroxyphenyl ring. Using these data it is now possible to analyze the major components in extracted prepreg PF resins. Copyright

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