106-83-2 Usage
Description
Butyl Epoxystearate, a chemical compound with the molecular formula C22H42O4, is known for its characteristic fatty odor. It is a low toxicity substance that is widely used in various industrial applications, particularly as a plasticizer in different plastic materials. Its versatility and low toxicity make it a valuable component in a range of products.
Uses
Used in Plastic Industry:
Butyl Epoxystearate is used as a plasticizer to enhance the flexibility and workability of plastic materials. Its incorporation into plastics allows for improved processing and performance characteristics, making it a popular choice in the manufacturing of various plastic products.
Used in Coatings Industry:
In the coatings industry, Butyl Epoxystearate is used as an additive to improve the properties of coatings. It helps in achieving better adhesion, flexibility, and durability of the coatings, making it suitable for a wide range of applications, including automotive, architectural, and industrial coatings.
Used in Inks Industry:
Butyl Epoxystearate is utilized as a component in ink formulations to enhance the flow and performance of inks. Its addition to inks contributes to better print quality, improved drying times, and increased resistance to various environmental factors, such as water and chemicals.
Used in Sealants Industry:
In the sealants industry, Butyl Epoxystearate is employed as an additive to improve the sealing properties of sealants. It helps in achieving better adhesion, flexibility, and durability of sealants, making them suitable for various applications, including construction, automotive, and industrial sealing.
However, it is important to note that Butyl Epoxystearate, like many industrial chemicals, should be handled with care to avoid potential skin irritation or more serious health issues associated with chronic exposure. Proper safety measures and precautions should be taken during its use to ensure the well-being of workers and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 106-83-2 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 6 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 106-83:
(5*1)+(4*0)+(3*6)+(2*8)+(1*3)=42
42 % 10 = 2
So 106-83-2 is a valid CAS Registry Number.
InChI:InChI=1/C22H42O3/c1-3-5-7-8-10-13-16-20-21(25-20)17-14-11-9-12-15-18-22(23)24-19-6-4-2/h20-21H,3-19H2,1-2H3
106-83-2Relevant articles and documents
Homogeneous and heterogeneous catalytic (dehydrogenative) oxidation of oleochemical 1,2-diols to α-hydroxyketones
Vu, Nam Duc,Guicheret, Boris,Duguet, Nicolas,Métay, Estelle,Lemaire, Marc
supporting information, p. 3390 - 3399 (2017/07/28)
Herein, the preparation of methyl oleate α-hydroxyketone from the corresponding 1,2-diol was investigated using both homogeneous and heterogeneous systems. Homogeneous conditions using a Pd(OAc)2/neocuproine complex were first developed using oxygen as a sole oxidant under mild conditions (MeOH, 50 °C). Under these conditions, the conversion of diol reached 95%, and α-hydroxyketone was obtained with 97% selectivity. The access to α-hydroxyketone has also been studied by dehydrogenation using a range of heterogeneous catalysts under solvent-free conditions at high temperatures (160-180 °C). Dehydrogenation using activated Ru/C under vacuum provided α-hydroxyketone with 93% conversion and 82% GC yield. The optimized conditions were applied to a range of oleochemical diols, including a vegetable oil derivative, to obtain the corresponding α-hydroxyketones with up to 74% isolated yields.
