101-90-6 Usage
Description
2,2'-[1,3-Phenylenebis(oxymethylene)]dioxirane, also known as Resorcinol diglycidyl ether, is a clear yellow or straw-yellow viscous liquid with a slight phenolic odor. It is a benzene derivative and is considered a possible carcinogen. 2,2'-[1,3-Phenylenebis(oxymethylene)]dioxirane is miscible with most organic resins and is combustible.
Uses
Used in Epoxy Resin Industry:
2,2'-[1,3-Phenylenebis(oxymethylene)]dioxirane is used as an epoxy resin for its strong binding properties and versatility in various applications.
Used in Stabilizer Industry:
It is used as a stabilizer of organic chemicals, providing stability and enhancing the performance of these chemicals in different environments.
Used in Rubber Industry:
2,2'-[1,3-Phenylenebis(oxymethylene)]dioxirane is used as a curing agent for "Thiokol" rubber, improving the rubber's strength and durability.
Used in Adhesive Industry:
It is used for the solubilizing of protein adhesives, enhancing the adhesive's bonding capabilities and making it more effective for various applications.
Used in Pharmaceutical Industry:
Resorcinol diglycidyl ether is a derivative of Resorcinol, which is used as a keratolytic and antiseborrheic agent. It is also utilized in veterinary medicine as a topical antipruritic and antiseptic.
Environmental Considerations:
Resorcinol diglycidyl ether is listed as an environmental toxin on the US EPA Toxic Release Inventory (TRI) list, indicating the need for careful handling and disposal to minimize environmental impact.
Air & Water Reactions
Insoluble in water.
Reactivity Profile
2,2'-[1,3-Phenylenebis(oxymethylene)]dioxirane is an alkylating agent. Reacts with compounds having a labile hydrogen .
Fire Hazard
2,2'-[1,3-Phenylenebis(oxymethylene)]dioxirane is combustible.
Safety Profile
Confirmed carcinogen with experimental carcinogenic and tumorigenic data. Poison by intraperitoneal route. Moderately toxic by ingestion. Mutation data reported. A skin irritant. When heated to decomposition it emits acrid smoke and irritating fumes. See also ETHERS.
Carcinogenicity
Diglycidyl resorcinol ether is reasonably anticipated to be a human carcinogen based on sufficient evidence of carcinogenicity from studies in experimental animals.
Check Digit Verification of cas no
The CAS Registry Mumber 101-90-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,0 and 1 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 101-90:
(5*1)+(4*0)+(3*1)+(2*9)+(1*0)=26
26 % 10 = 6
So 101-90-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H10O3.C6H6O2/c1(5-3-8-5)7-2-6-4-9-6;7-5-2-1-3-6(8)4-5/h5-6H,1-4H2;1-4,7-8H
101-90-6Relevant articles and documents
Synthesis, characterization, optical and electrochemical properties and antifungal and anticancer activities of ferrocenyl conjugated novel dendrimers
Saravanan, Velautham,Kannan, Ayyavoo,Rajakumar, Perumal
, p. 1714 - 1722 (2017)
A new class of triazoloferrocenyl conjugates (1, 2 and 3) was obtained by copper(i) catalyzed click chemistry, specifically the alkyne azide cycloaddition (CuAAC) of bis(β-hydroxyl)arylalkyneether with suitable ferrocenyl azides. The synthesized bis(β-hydroxyl)arylether linked ferrocenyl conjugates 1, 2 and 3 exhibit antifungal activity against fungal pathogens, viz. Candida albicans, Candida glabrata and Candida crusi, comparable to that of amphotericin B and also show excellent anticancer activity against MCF-7 cell lines.
Synthesis of novel poly(hydroxyether terephthalate) via polyaddition of 2,5-difluoroterephthalic acid with aromatic bis(epoxide)s
Huang, Xiao-Song,Qing, Feng-Ling
experimental part, p. 1076 - 1082 (2009/04/07)
A novel and more reliable synthetic route to 2,5-difluoroterephthalic acid was developed. A series of new poly(hydroxyether terephthalate) were prepared by the polyaddition of 2,5-difluoroterephthalic acid with various aromatic bis(epoxide)s catalyzed by tetrabutyl ammonium bromide.
