13464-24-9

Basic information

• Product Name: 4-METHYL-2,4-BIS(4-HYDROXYPHENYL)PENT-1-ENE
• Synonyms: 4-Methyl-2,4-bis(4-hydroxyphenyl)-1-pentene;4-Methyl-2,4-bis(p-hydroxyphenyl)-1-pentene;4-Methyl-2,4-bis-(p-hydroxyphenyl)pent-1-ene;C13625;4-METHYL-2,4-BIS(4-HYDROXYPHENYL)PENT-1-ENE;4,4'-(1,1-dimethyl-3-methylene-1,3-propanediyl)bis-Phenol;2,4-Bis(4-hydroxyphenyl)-4-methyl-1-pentene;4,4'-(4-Methyl-1-pentene-2,4-diyl)bisphenol
• CAS NO: 13464-24-9
• Molecular Formula: C₁₈H₂₀O₂
• Molecular Weight: 268.35
• Mol File: 13464-24-9.mol
• Article Data: 2

Chemical Properties

• Melting Point: 128-132 °C
• Boiling Point: 422.5°Cat760mmHg
• Flash Point: 195.6°C
• Appearance: /
• Density: 1.103g/cm³
• Vapor Pressure: 9.74E-08mmHg at 25°C
• Refractive Index: 1.59
• Storage Temp.: -20°C Freezer
• Solubility: Chloroform (Slightly), Dichloromethane (Slightly), Methanol (Slightly)
• PKA: 10.10±0.15(Predicted)
• CAS DataBase Reference: 4-METHYL-2,4-BIS(4-HYDROXYPHENYL)PENT-1-ENE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-METHYL-2,4-BIS(4-HYDROXYPHENYL)PENT-1-ENE(13464-24-9)
• EPA Substance Registry System: 4-METHYL-2,4-BIS(4-HYDROXYPHENYL)PENT-1-ENE(13464-24-9)

Safety Data

• Hazardous Substances Data: 13464-24-9(Hazardous Substances Data)

Usage

Uses

2,4-Bis(4-hydroxyphenyl)-4-methyl-1-pentene is an intermediate in synthesizing 4,4''-(1,3,3-Trimethyl-1-propene-1,3-diyl)bisphenol (T796655), a Bisphenol A (B519495) impurity with estrogenic activity.

InChI:InChI=1/C18H20O2/c1-13(14-4-8-16(19)9-5-14)12-18(2,3)15-6-10-17(20)11-7-15/h4-11,19-20H,1,12H2,2-3H3

Upstream product

• 80-05-7 BPA 

Related news

Toxicity to early life stages and an estrogenic effect of a bisphenol A metabolite, 4-methyl-2,4-bis(4-hydroxyphenyl)pent-1-ene on the medaka (Oryzias latipes)08/06/2019

In a recent study, it was reported that 4-methyl-2,4-bis(4-hydroxyphenyl)pent-1-ene (MBP), a metabolite of bisphenol A (BPA; 2,2-bis(4-hydroxyphenyl)propane), showed estrogenic activity in several in vitro assays, and the estrogenic activity of MBP was higher than that of BPA. In this study, we ...detailed

Relevant articles and documents

Generation and synthetic uses of stable 4-[2-isopropylidene]-phenol carbocation from bisphenol A

(Equation Presented) Stable 4-[2-isopropylidene]-phenol carbocation, IPP cation 1, was generated readily by addition of bisphenol A in concentrated sulfuric acid at ambient temperature, and the cation could be used for facile syntheses of 4-isopropenyl phenol (IPP), IPP dimers, and spiro-bisphenol derivatives.