2565-36-8 Usage
Uses
Used in Pharmaceutical Industry:
2,2'-[methylenebis(oxy)]bisethanol is used as a solvent and plasticizer for the production of various pharmaceutical formulations. Its ability to dissolve a wide range of substances and improve the flexibility of materials makes it valuable in the development of medications and other healthcare products.
Used in Cosmetics Industry:
In the cosmetics industry, 2,2'-[methylenebis(oxy)]bisethanol is utilized as a solvent and plasticizer in the formulation of skincare products, makeup, and other beauty products. Its properties help to create stable and effective cosmetic products that are safe for consumer use.
Used in Personal Care Industry:
2,2'-[methylenebis(oxy)]bisethanol is employed as a key ingredient in personal care products, such as shampoos, conditioners, and body lotions. Its solvent and plasticizing capabilities enhance the performance and texture of these products, ensuring they meet consumer expectations.
Used in Chemical Production:
2,2'-[methylenebis(oxy)]bisethanol is used as a solvent, plasticizer, and detergent in the production of resins, coatings, and adhesives. Its versatility in these applications contributes to the creation of high-quality and durable chemical products.
Overall, 2,2'-[methylenebis(oxy)]bisethanol is a valuable chemical compound with a diverse range of applications in various industries, including pharmaceuticals, cosmetics, personal care, and chemical production. Its solvent and plasticizing properties make it an essential component in the development and manufacturing of numerous products.
Check Digit Verification of cas no
The CAS Registry Mumber 2565-36-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,6 and 5 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2565-36:
(6*2)+(5*5)+(4*6)+(3*5)+(2*3)+(1*6)=88
88 % 10 = 8
So 2565-36-8 is a valid CAS Registry Number.
2565-36-8Relevant articles and documents
Ruthenium-Catalyzed Synthesis of Cyclic and Linear Acetals by the Combined Utilization of CO2, H2, and Biomass Derived Diols
Beydoun, Kassem,Klankermayer, Jürgen
supporting information, p. 11412 - 11415 (2019/07/18)
Herein a transition-metal catalyst system for the selective synthesis of cyclic and linear acetals from the combined utilization of carbon dioxide, molecular hydrogen, and biomass derived diols is presented. Detailed investigations on the substrate scope enabled the selectivity of the reaction to be largely guided and demonstrated the possibility of integrating a broad variety of substrate molecules. This approach allowed a change between the favored formation of cyclic acetals and linear acetals, originating from the bridging of two diols with a carbon-dioxide based methylene unit. This new synthesis option paves the way to novel fuels, solvents, or polymer building blocks, by the recently established “bio-hybrid” approach of integrating renewable energy, carbon dioxide, and biomass in a direct catalytic transformation.
