Mobile/Wechat/WhatsApp: +447394406898
Email:wibson.aris@gmail.com
CasNo: 4065-45-6
Molecular Formula: C14H12O6S
Appearance: white to yellowish powder
Manufacturing Process |
663 g of dichloroethane and 74.6 g 2-hydroxy-4-methoxybenzophenone were charged into a 3-neck flask equipped with stirrer, thermometer, reflux condenser and dropping funnel and a heating mantle. The solution was heated to the reflux temperature (85°C to 86°C) and was dehydrated by distilling off 66.5 g 1,2-dichloroethane. While maintaining at reflux, 30 g chlorosulfonic acid was added slowly over a period of about two hours. The rate of addition was regulated by the speed of evolution of the HCl. After all the chlorosulfonic acid was added, the charge was still maintained at reflux for an additional 15 minutes to remove traces of HCl. It was then cooled to 5°C and filtered. The filter cake was washed with 500 g cold 1,2-dichloroethane and dried. 98 g of product were obtained. |
Flammability and Explosibility |
Nonflammable |
Contact allergens |
BZP-4 is widely used in cosmetics, particularly shampoos and hair products. Cross-reactivity is rarely expected in patients photoallergic to ketoprofen. |
Brand name |
Sungard (Bayer). |
General Description |
Sulisobenzone is a broad spectrum organic UV filter in sunscreen formulations, known to absorb deleterious UV light. |
InChI:InChI=1/C14H12O6S/c1-20-12-8-11(15)10(7-13(12)21(17,18)19)14(16)9-5-3-2-4-6-9/h2-8,15H,1H3,(H,17,18,19)/p-1
The invention provides a preparation met...
The invention discloses a method for syn...
The invention discloses a synthesis proc...
Suggested is a cosmetic compositions com...
Benzophenone-3
2-
5-benzoyl-4-hydroxy-2-methoxy-benzenesulfonyl chloride
C14H11O6S(1-)*C18H12Cl3S(1+)
1-[2-hydroxy-4-methoxy-5-(3-nitrophenylazo)phenyl]-1-phenylmethanone