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Phenol and its vapors are corrosive to the eyes, the skin, and the respiratory tract. [60] Its corrosive effect on skin and mucous membranes is due to a protein-degenerating effect. [49] Repeated or prolonged skin contact with phenol may cause dermatitis, or even second and third-degree burns. [61] Inhalation of phenol vapor may cause lung ...
“A phenol peel is a deep chemical peel that acts on skin's outer epidermis and the superficial part of the dermis,” explains Patricia Oyetakin, MD, a board-certified dermatologist based in ...
A phenol peel is one of the strongest chemical peels you can get. Here's a rundown of the risks, benefits, according to a dermatologist and two estheticians.
A phenol-croton oil is a type of chemical peel. [7] The term "phenol-croton oil peel" has replaced the vague term "phenol peel" in medical literature. It was originally used on a clandestine basis by early Hollywood stars in the 1920s and was incorporated into mainstream practice in the 1960s by Thomas Baker and Howard Gordon. [8]
In 1834, German chemist Friedlieb Ferdinand Runge discovered a phenol, also known as carbolic acid, which he derived in an impure form from coal tar.In August 1865, Joseph Lister applied a piece of lint dipped in carbolic acid solution to the wound of an eleven-year-old boy at Glasgow Royal Infirmary, who had sustained a compound fracture after a cart wheel had passed over his leg.
Croton oil is used in Phenol-croton oil chemical peels [2] for its caustic exfoliating effects it has on the skin. [3] Used in conjunction with phenol solutions, it results in an intense reaction that leads to initial skin sloughing.
Monobenzone, also called 4-(Benzyloxy)phenol and monobenzyl ether of hydroquinone (MBEH) is an organic chemical in the phenol family with chemical formula C 6 H 5 CH 2 OC 6 H 4 OH. [1] [2] It is used as a topical drug for medical depigmentation. [3] It is a colourless solid that is classified as the monobenzyl ether of hydroquinone.
Chloroxylenol, also known as para-chloro-meta-xylenol (PCMX), is a chlorine substituted phenol with a white to off-white appearance and a phenolic odor.. The discovery of chloroxylenol was the result of efforts to produce improved antiseptics that began at the end of the 1800s, when scientists gradually realized that more substituted and more lipophilic phenols are less toxic, less irritant ...