29651-54-5

Basic information

• Product Name: Phenol, 4,4'-cyclododecylidenebis-
• Synonyms: Phenol, 4,4'-cyclododecylidenebis-;4,4'-(Cyclododecane-1,1-diyl)diphenol
• CAS NO: 29651-54-5
• Molecular Formula: C₂₄H₃₂O₂
• Molecular Weight: 352.50968
• EINECS: -0
• Mol File: 29651-54-5.mol
• Article Data: 8

Chemical Properties

• Appearance: /
• Storage Temp.: Inert atmosphere,Room Temperature
• CAS DataBase Reference: Phenol, 4,4'-cyclododecylidenebis-(CAS DataBase Reference)
• NIST Chemistry Reference: Phenol, 4,4'-cyclododecylidenebis-(29651-54-5)
• EPA Substance Registry System: Phenol, 4,4'-cyclododecylidenebis-(29651-54-5)

Safety Data

• Hazardous Substances Data: 29651-54-5(Hazardous Substances Data)

Usage

General Description

Phenol, 4,4'-cyclododecylidenebis- is a chemical compound that is used primarily as a component in the production of resins and polymers. It is known for its high resistance to heat and chemicals, making it suitable for use in industrial applications. It is also used as a stabilizer in the production of plastics and rubber. Phenol, 4,4'-cyclododecylidenebis- is considered to be relatively stable and possesses low toxicity, although it is still important to handle it with caution and follow safety guidelines when working with it. Overall, Phenol, 4,4'-cyclododecylidenebis- plays a vital role in the manufacturing of various industrial products due to its unique properties and versatility.

Upstream product

• 830-13-7 cyclododecanone 
• 108-95-2 phenol 

Downstream Products

• 1187462-94-7 bis(allyl ether) of 1,1-bis(4-hydroxyphenyl)cyclododecane 
• 1187462-93-6 1,1-bis(4-cyanatophenyl)cyclododecane 
• 632336-53-9 1,1-bis(4-trifluoromethanesulfonyloxyphenyl)cyclododecane 

Relevant articles and documents

METHOD FOR PRODUCING BISPHENOL DERIVATIVE HAVING CYCLIC HYDROCARBON

PROBLEM TO BE SOLVED: To provide a method for industrially advantageously produce a bisphenol derivative having a cyclic hydrocarbon in which a cyclic ketone has a 7- or more membered ring without using a hydrogen chloride gas having a strong corrosivenes

Design and synthesis of new polymeric materials for organic nonvolatile electrical bistable storage devices: Poly(biphenylmethylene)s

The synthesis of new polymers, poly(biphenylmethylene)s, derived from bistriflates of bisphenol-type monomers, by Ni(0)-mediated polymerization has been presented. These polymers are interesting because of the nature of the polymer backbone that contains

Method for preparing aromatic bischloroformate compositions

Bischloroformate oligomer compositions are prepared by passing phosgene into a heterogeneous aqueous-organic mixture containing at least one dihydroxyaromatic compound, with simultaneous introduction of a base at a rate to maintain a specific pH range and to produce a specific volume ratio of aqueous to organic phase. By this method, it is possible to employ a minimum amount of phosgene. The reaction may be conducted batchwise or continuously. The bischloroformate composition may be employed for the preparation of cyclic polycarbonate oligomers or linear polycarbonate, and linear polycarbonate formation may be integrated with bischloroformate composition formation in a batch or continuous process.