Is triethanolamine harmful for skin?
Triethanolamine is safe for the skin and does not have any side effects, as most products keep its concentration between 1% and 3%. At this concentration, triethanolamine is safe for skin application and does not lead to irritation of the skin or any other side effects.
Is triethanolamine a strong base?
Triethanolamine reacts violently with strong oxidizing agents. Since it is a weak base, it reacts with acids, vigorously with concentrated strong acids.
What is triethanolamine used for?
Triethanolamine is used primarily in making surfactants, such as for emulsifier. It is a common ingredient in formulations used for both industrial and consumer products.
Is triethanolamine good for your skin?
The Panel concluded that Triethanolamine and the related TEA-containing ingredients are safe in the present practices of use and concentration when formulated to be non-irritating. They cautioned that ingredients should not be used in cosmetic products in which N-nitroso compounds can be formed.
What is an alternative to triethanolamine?
|TrisBase, pH 7,8||Very good results, as good or better than with the TEA soap. Easy removal without too much mechanical action.|
|Ethomeen C25, pH 7,6||Little to no results, removal is very slow, could be due to the low pH of the soap (7,5).|
Is triethanolamine bad for face?
Triethanolamine: Triethanolamine is used in many cosmetic products to help balance pH levels, as well as to act as a cleansing base. When absorbed into the body over a long period of time, it can become toxic. Even short periods of exposure can cause allergic reactions, including eye problems and dry hair and skin.
What can I use instead of triethanolamine?
What is another name for triethanolamine?
Trade names for triethanolamine include Daltogen, Sterolamide, Sting-Kill, Thio- faco T-35, and Trolamine.
Is triethylamine same as triethanolamine?
The key difference between triethylamine and triethanolamine is that triethylamine contains three ethyl group attached to the same nitrogen atom whereas triethanolamine contains three ethyl alcohol groups attached to the same nitrogen atom.
What can I use instead of dimethicone?
Dimethicone may be replaced by mixtures such as:
- Coco-Caprylate/Caprate (e.g. Cetiol LC, BASF), considered as a medium spreading emollient “for modern cosmetic applications”
- Butylene glycol Dicaprylate/Dicaprate (e.g. Dermofeel BGC, Evonik Dr. Straetmans GmbH)
Is triethanolamine a carcinogen?
There is inadequate evidence in humans for the carcinogenicity of triethanolamine. There is inadequate evidence in experimental animals for the carcinogenicity of triethanolamine. Triethanolamine is not classifiable as to its carcinogenicity to humans (Group 3).
What is paraben made from?
“Parabens are derived from a chemical known as para-hydroxybenzoic acid (PHBA) that occurs naturally in many fruits and vegetables, like blueberries and carrots,” said Kathryn St. John, the communications director at the American Chemistry Council.