Imidurea, Germall ;. N’,N”-methylenebis[3-[1-(hydroxymethyl)- 2,5- dioxoimidazolidinyl]urea];. 1-[1-(hydroxymethyl)-2,5-dioxoimidazolidinyl]-. Contact Dermatitis. May;14(5) Reactions to Quaternium 15, Bronopol and Germall in a standard series. Ford GP, Beck MH. The incidence of. Germall found in: Imidazolidinyl Urea, Imidazolidinyl Urea, also known as Imidurea or Germall , is an antimicrobial preservative used as a.
|Published (Last):||19 February 2006|
|PDF File Size:||10.41 Mb|
|ePub File Size:||18.52 Mb|
|Price:||Free* [*Free Regsitration Required]|
Examples of cosmetic products and toiletries are lotions, creams, germaol, emollients, foundations, powders, concealers, bronzers, self-tanners, makeup removers, sunscreens, eye shadows, and mascaras. It is chemically related to diazolidinyl urea which is used in the same way.
Preservatives Disinfectants Ureas Hydantoins. Company Ashland develops and 1155 a comprehensive line of biofunctionals, fixative and styling polymers, bioadhesives, and rheology and conditioning polymers for the Personal Care industry.
This article needs additional citations for verification. Rinse off products should involve less risk. Where is Imidazolidinyl urea found?
Imidazolidinyl urea is found in cosmetics, shampoos and skin care germapl. This page was last edited on 30 Augustat From Wikipedia, the free encyclopedia.
Urea (Imidazolidinyl/Diazolidinyl commonly known as Germall II and Germall ) – ChemFreeCom
Avoid cosmetics and other personal care products labeled with imidazolidinyl urea or its synonyms, particularly in stay on products. Other sources of exposure include detergents dishwashing liquids, and cleaning agents.
It is also found in liquid soaps, hair conditioners, gels, bubble baths, baby wipes, and over-the-counter and prescription topical medicines. Instead, new data indicate that the hydroxymethyl functional group of each imidazolidine ring is attached to the carbonrather than on the nitrogen atom: Imidurea, Germall ; N’N” -methylenebis[3-[1- hydroxymethyl – 2,5-dioxoimidazolidinyl]urea]; 1-[1- hydroxymethyl -2,5-dioxoimidazolidinyl]- 3-[[[1- hydroxymethyl -2,5-dioxoimidazolidinyl] carbamoylamino]methyl]urea.
Imidazolidinyl urea was poorly characterized until recently and the single Chemical Abstracts Service structure assigned to it is probably not the major one in the commercial material. It acts synergistically with other preservatives. Imidazolidinyl urea is an antimicrobial preservative used in cosmetics [ citation needed ].
February Learn how and when to remove this template message. Back to Be Informed. Ashland makes their documentation available in the regions indicated below: Retrieved from ” https: Products for household use are not yet labelled.
Chemical Free Community – Chemical Info. It is very effective against Gram-positive and Gram-negative bacteria, including Pseudomonas species. This website provides links to other websites owned by third parties.
Therefore if there is a suspicion that a household product is causing dermatitis, then the manufacturer will have to be contacted for specific advice. With parabens, it provides a broad spectrum of activity against bacteria, yeast, and mold. Premium Body Care Unacceptable Ingredients. Views Read Edit View history.
To help formulators create blockbuster innovations, Ashland focuses on breakthrough chemistries that deliver advanced performance properties in hair care, skin care, sun care, and oral germalk products. Login Use a social account for faster login or easy registration. Please help improve this article by adding citations to reliable sources. Imidazolidinyl urea acts as a formaldehyde releaser. It is important to use only ingredient-labeled cosmetics and other skin care products that do not list imidazolidinyl urea or any of its synonyms on the label.
We’re sorry, but the industry you have selected is not currently available in your chosen language. Imidazolidinyl urea is produced by the chemical reaction of allantoin and formaldehyde in the germal of sodium hydroxide solution and heat.