74938-83-3

Basic information

• Product Name: 2,2-BIS(4-HYDROXYPHENYL)HEXAFLUOROPROPANE, DISODIUM SALT
• Synonyms: 2,2-BIS(4-HYDROXYPHENYL)HEXAFLUOROPROPANE, DISODIUM SALT;BIS-AF-SODIUM SALT;2,2-Bis(4-hydroxyphenyl)hexafluoropropane disodium salt 97%;2,2-Bis(4-hydroxyphenyl)hexafluoropropanedisodiumsalt97%;Phenol,4,4'-[2,2,2-trifluoro-1-(trifluoromethyl)ethylidene]bis-, disodium salt;Disodium 4,4'-[2,2,2-trifluoro-1-(trifluoromethyl)ethylidene]diphenolate;BIS-AF-Sodium salt, Disodium 4,4'-(1,1,1,3,3,3-hexafluoropropane-2,2-diyl)diphenolate
• CAS NO: 74938-83-3
• Molecular Formula: C₁₅H₈F₆O₂*2Na
• Molecular Weight: 380.19
• Mol File: 74938-83-3.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2,2-BIS(4-HYDROXYPHENYL)HEXAFLUOROPROPANE, DISODIUM SALT(CAS DataBase Reference)
• NIST Chemistry Reference: 2,2-BIS(4-HYDROXYPHENYL)HEXAFLUOROPROPANE, DISODIUM SALT(74938-83-3)
• EPA Substance Registry System: 2,2-BIS(4-HYDROXYPHENYL)HEXAFLUOROPROPANE, DISODIUM SALT(74938-83-3)

Safety Data

• Hazard Codes: Xi
• HazardClass: IRRITANT
• Hazardous Substances Data: 74938-83-3(Hazardous Substances Data)

Usage

General Description

2,2-BIS(4-HYDROXYPHENYL)HEXAFLUOROPROPANE, DISODIUM SALT is a chemical compound that is used as a flame retardant and heat stabilizer in a variety of plastic materials, including polyesters and polyamides. Its chemical structure includes two hydroxyl groups and six fluorine atoms, giving it a high level of thermal stability and flame resistance. The disodium salt form of this compound helps to improve its solubility and dispersibility in polymers, making it easier to incorporate into plastic materials and improving its overall effectiveness as a flame retardant. Additionally, it is considered to be relatively non-toxic and environmentally friendly, making it a popular choice for use in consumer products.

Upstream product

• 1478-61-1 4,4'-(hexafluoroisopropylidene)diphenol 

Downstream Products

• 128481-73-2 2,2-bis(3-allyl-4-hydroxyphenyl)hexafluoropropane 
• 82986-78-5 2,2-bis(4-allyloxyphenyl)hexafluoropropane 
• 131043-09-9 Dimethyl 3,3'-<<2,2,2-trifluoro-1-(trifluoromethyl)ethylidene>bis(4,1-phenyleneoxy)>bis(2,2,3,3-tetafluoropropionate) 

Relevant articles and documents

Configurationally Chiral SuFEx-Based Polymers

Novel methods to make synthetic chiral polymers are highly desirable given their potential in a rapidly increasing number of bio-inspired applications. The enantiospecific sulfur–fluorine exchange (SuFEx) reaction of chiral di-sulfonimidoyl fluorides (di-SFs) with diphenols, was used to produce high-molecular-weight chiral polymers with configurational backbone chirality. The resulting new class of polymers, polysulfonimidates, can be efficiently produced via this step-growth mechanism for a wide range of di-SFs and diphenols, yielding MnPS up to 283 kDa with a typical dispersity ? around 1.6. The optical activity of the resulting chiral polymers is largely due to the intrinsic asymmetry of the S atoms (configurational chirality). Finally, the enantiospecificity (ee>98 %) of the polymerization reaction was demonstrated by the degradation of a disulfide-containing polysulfonimidate. This novel route towards configurational main-chain chirality opens up new approaches towards tailor-made chiral polymers with precisely defined properties.