
A formaldehyde releaser, formaldehyde donor or formaldehyde-releasing preservative is a chemical compound that slowly releases
formaldehyde. Formaldehyde-releasers are added to prevent microbial growth and extend shelf life. The intent of these compounds is that they release formaldehyde at levels that suppress microbial growth but sufficiently low to not threaten humans. The use of these chemicals in cosmetics has elicited controversy.
Examples
Many compounds have been formulated a formaldehyde-releasers.
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Quaternium-15 (Dowicil 200; Dowicil 75; Dowicil 100; Dowco 184; Dowicide Q). It was used in low concentrations in cosmetics but has been banned in the EU since 2017 and a bill is under consideration in the US.
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DMDM hydantoin
DMDM hydantoin is an antimicrobial formaldehyde releaser preservative with the trade name Glydant. DMDM hydantoin is an organic compound belonging to a class of compounds known as hydantoins. It is used in the cosmetics industry and found in pro ...
* (ethylenedioxy)dimethanol (EDDM)
*(Benzyloxy)methanol (BHF, benzylhemiformal)
* 2,2',2''-(Hexahydro-1,3-5-triazine-1,3,5-triyl-)triethanol (HHT)
* Tetramethylolacetylenediurea (TMAD)
* 1,3-Bis(hydroxymethyl)-5,5-dimethylimidazolidine-2,4-dione (DMDMH)
* 3,3'-Methylenebis
-methyloxazolidine(MBO)
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Imidazolidinyl urea (Germall 115) for cosmetics
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Diazolidinyl urea (Germall II) for cosmetics
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Tris(hydroxymethyl) nitromethane (Tris Nitro) for cosmetics
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tris(N-hydroxyethyl) hexahydrotriazine (Grotan® BK)
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Sodium hydroxymethylglycinate for cosmetics
Unintentional formaldehyde releasers
Some materials release formaldehyde unintentionally. These materials have also elicited considerable controversy, especially when these materials have household applications such as flooring. Examples:
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Delrin or Acetal
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Phenol formaldehyde resin
Phenol formaldehyde resins (PF) or phenolic resins (also infrequently called phenoplasts) are synthetic polymers obtained by the reaction of phenol or substituted phenol with formaldehyde. Used as the basis for Bakelite, PFs were the first comm ...
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Urea formaldehyde resin
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Melamine resin
Melamine resin or melamine formaldehyde (also shortened to melamine) is a resin with melamine rings terminated with multiple hydroxyl groups derived from formaldehyde. This thermosetting plastic material is made from melamine and formaldehyde ...
Uses
They are found in fuels, cosmetics, toiletries, cleaning agents, adhesives, paints, lacquers, fertilizers, and metalworking fluids.
They are found in lysing agent for cells for in vitro diagnostic reagents. Photo-chemicals and press room chemicals also contain these releasers.
Safety
Formaldehyde is dangerous to human health.
In 2011, the US
National Toxicology Program
The National Toxicology Program (NTP) is an inter-agency program run by the United States Department of Health and Human Services
The United States Department of Health and Human Services (HHS) is a cabinet-level executive branch departmen ...
described formaldehyde as "
known to be a human carcinogen".
The danger of formaldehyde is a major reason for the development of formaldehyde releasers which release formaldehyde slowly at lower levels.
Allergic reaction
Levels of 200–300 p.p.m. formaldehyde in cosmetic products can cause
contact dermatitis in short-term use on normal skin.
A patch test study found that DMDM hydantoin in cosmetic products could increase the risk of cosmetic dermatitis.
Some people have a contact allergy to imidazolidinyl urea causing dermatitis.
[Review of toxicological data](_blank)
(NTP NIEHS) Such people are often also allergic to diazolidinyl urea. In 2005–06, it was the 14th-most-prevalent allergen in patch tests (3.7%).
[Zug KA, Warshaw EM, Fowler JF Jr, Maibach HI, Belsito DL, Pratt MD, Sasseville D, Storrs FJ, Taylor JS, Mathias CG, Deleo VA, Rietschel RL, Marks J. Patch-test results of the North American Contact Dermatitis Group 2005–2006. Dermatitis. 2009 May–Jun;20(3):149-60.]
Cancer
Some consumer cosmetics contain quaternium-15 for its antimicrobial properties.
The
American Cancer Society
The American Cancer Society (ACS) is a nationwide voluntary health organization dedicated to eliminating cancer. Established in 1913, the society is organized into six geographical regions of both medical and lay volunteers operating in more tha ...
states that although quaternium-15 releases formaldehyde, a known carcinogen in laboratory test animals at relatively high doses, because the amount of formaldehyde released from these products is low, it is unclear that avoiding quaternium-15 in cosmetics provides any health benefits.
Even so, Johnson & Johnson announced plans to phase out its use of quaternium-15 in cosmetic products by 2015 in response to consumer pressure.
Importance
Formaldehyde in the EU is restricted to a maximum allowed concentration in finished products no greater than 0.2%.
However, there are hidden sources of formaldehyde such as these formaldehyde releasers. As well, patch tests are prone to false positives at even low concentrations and not a reliable test.
Sensitization to formaldehyde has been decreasing since 1980 due in part to the replacement of formaldehyde by these formaldehyde releasers.
As of 2009, frequency of sensitization to formaldehyde is stable at 2–3% in Europe.
It might be as high as 9% in the USA.
Alternatives
There are three groups of broad-spectrum preservatives with the most safety and efficacy.
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Parabens
*Formaldehyde releasers
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Halogenated compounds
The
FDA requires that cosmetics have an effective preservative, and microbial challenge testing is conducted. The EU's Cosmetic Directive 76/768/EEC requires the use of a preservative on an approved list.
Analysis
There are many ways to test and quantify formaldehyde.
However these methods are not suitable for the determination of free formaldehyde in cosmetics with formaldehyde releasers since these methods often accelerate release of formaldehyde.
[{{cite journal , doi=10.1007/s00216-018-1287-0 , pmid=30062513 , title=GDME-based methodology for the determination of free formaldehyde in cosmetics and hygiene products containing formaldehyde releasers , journal=Analytical and Bioanalytical Chemistry , volume=410 , issue=26 , pages=6873–6880 , year=2018 , last1=Brandão , first1=Pedro Francisco , last2=Ramos , first2=Rui Miguel , last3=Rodrigues , first3=José António , s2cid=51880356 ]
The physical method by
13C NMR spectroscopy does not affect the equilibrium between free and donor sources of formaldehyde and might be the best way to test for formaldehyde releasers.
References
Antimicrobials