77-40-7

Basic information

• Product Name: 2,2-Bis(4-hydroxyphenyl)butane
• Synonyms: 4,4'-(1-methylpropylidene)bisphenol;2,2-BIS(P-HYDROXYPHENYL)BUTANE;2,2-BIS(4-HYDROXYPHENYL)BUTANE;BISPHENOL B;BISHYDROXYPHENYLBUTANE;P,P'-SEC-BUTYLIDENEDIPHENOL;p,p'-Dihydroxy-2,2-diphenylbutane;4,4'-(1-Methylpropylidene)diphenol
• CAS NO: 77-40-7
• Molecular Formula: C₁₆H₁₈O₂
• Molecular Weight: 242.31
• EINECS: 201-025-1
• Product Categories: Bisphenol A type Compounds (for High-Performance Polymer Research);Functional Materials;Reagent for High-Performance Polymer Research
• Mol File: 77-40-7.mol
• Article Data: 14

Chemical Properties

• Melting Point: 126°C
• Boiling Point: 345.14°C (rough estimate)
• Flash Point: 195.5 °C
• Appearance: white crystal
• Density: 1.0537 (rough estimate)
• Vapor Pressure: 2.2E-07mmHg at 25°C
• Refractive Index: 1.6000 (estimate)
• Storage Temp.: Inert atmosphere,Room Temperature
• Solubility: DMSO (Slightly), Methanol (Slightly)
• PKA: 10.27±0.10(Predicted)
• CAS DataBase Reference: 2,2-Bis(4-hydroxyphenyl)butane(CAS DataBase Reference)
• NIST Chemistry Reference: 2,2-Bis(4-hydroxyphenyl)butane(77-40-7)
• EPA Substance Registry System: 2,2-Bis(4-hydroxyphenyl)butane(77-40-7)

Safety Data

• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• RTECS: SM1210200
• HazardClass: IRRITANT
• Hazardous Substances Data: 77-40-7(Hazardous Substances Data)

Usage

Uses

In the manufacture of phenolic resins.

Preparation

Using phenol and 2-butanone as raw materials, and with sulfuric acid as the catalytic agent, under heating conditions,?through?condensation?reaction, can obtain2,2-Bis(4-hydroxyphenyl)butane.

InChI:InChI=1/C16H18O2/c1-3-16(2,12-4-8-14(17)9-5-12)13-6-10-15(18)11-7-13/h4-11,17-18H,3H2,1-2H3

Upstream product

• 4461-41-0 2-chloro-but-2-ene 
• 108-95-2 phenol 
• 2211-70-3 2-chloro-but-1-ene 
• 78-93-3 butanone 

Downstream Products

• 129928-55-8 4-(sec-butyl)cyclohexan-1-one 
• 1064170-66-6 4-(1-(4-((6-diazo-5-oxo-5,6-dihydro-1-naphthalenyl)sulfonyl)oxyphenyl)-1-methylpropyl)phenyl 6-diazo-5-oxo-5,6-dihydro-1-naphthalenesulfonate 
• 124-04-9 Adipic acid 
• 100-21-0 terephthalic acid 
• 860766-78-5 2,2'-dibromo-6,6'-dinitro-4,4'-sec-butylidene-di-phenol 
• 2316-50-9 2-bromo-4,6-dinitrophenol 
• 99-28-5 2,6-dibromo-4-nitrophenol 
• 17255-98-0 4-Hydroxy-1-(1-methyl-propenyl)-benzol 
• 108-95-2 phenol 
• 89-72-5 2-sec-butylphenol 
• 6526-80-3 2,2-Di<4-phenyl>butan 
• 99-71-8 4-(1-methylpropyl)phenol 
• 6292-20-2 (+/-)-4-Hydroxy-1-sek.-butyl-cyclohexan 
• 108-93-0 cyclohexanol 

Relevant articles and documents

NOVEL DIAZONAPHTHOQUINONESULFONIC ACID BISPHENOL DERIVATIVE USEFUL IN PHOTO LITHOGRAPHIC SUB MICRON PATTERNING AND A PROCESS FOR PREPARATION THEREOF

The present invention provides novel diazonaphthoquinonesulfonic acid bisphenol derivatives. More particularly, the present invention relates to photo restive coating comprising alkali-soluble resin, a photoactive compound and a surfactant. The photoresist film prepared has less then one micron. The photoactive compound is soluble or swellable in aqueous alkaline solutions and is diazonaphthoquinonesulfonic bisphenol esters of the general formula (A), wherein DNQ represents a 2-Diazo-1-naphthoquinone-4-sulfonyl, 2-Diazo-1-naphthoquinone-5-sulfonyl, 1-Diazo-2-naphthoquinone-4-sulfonyl groups and R1 R1 represents an alkyl, aryl and substituted aryl groups. The invention also provides a process for coating and imaging the light-sensitive composition.

Thermosensitive recording material and color developer compound therefor

A thermosensitive recording material has a support and a thermosensitive coloring layer formed thereon containing a leuco dye and a color developer capable of inducing color formation in the leuco dye upon application of heat thereto, with the color developer including at least one compound (A) having in a molecule thereof at least two aromatic ring moieties with specific structures, selected from the group consisting of an aromatic ring moiety having at least one carboxyl group and electron-attracting functional group, an aromatic ring moiety having at least one carboxyl group and electron-donating functional group, and an aromatic ring moiety having at least one carboxyl group, free of the electron-attracting and electron-donating functional groups. An aromatic carboxylic acid compound serving as the above-mentioned compound (A) and the producing method thereof are also disclosed.

Polymer electrolyte and process for producing the same

A polymer electrolyte having, in a main chain, a structural unit represented by the following formula (1):-[Ar1-(SO2-N-(X+)-SO2-Ar2)m-SO2-N-(X+)-SO2-Ar1-O]- wherein Ar1 and Ar2 independently represent a divalent aromatic groups, m represents an integer of 0 to 3, and X+ represents an ion selected from hydrogen ion, an alkali metal ion and ammonium ion, which is excellent in proton conductivity, thermal resistance and strength. The polymer electrolyte is soluble in solvents and has excellent film forming property and recycling efficiency.