Chemistry:Paraformaldehyde
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| Names | |
|---|---|
| IUPAC name
Polyoxymethylene
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| Identifiers | |
| ChemSpider |
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| EC Number |
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| UNII | |
| Properties | |
| OH(CH2O)nH (n = 8 - 100) | |
| Appearance | white crystalline solid |
| Density | 1.42 g·cm−3 (25 °C) |
| Melting point | 120 °C (248 °F; 393 K) |
| low | |
| Hazards | |
| Safety data sheet | Oxford MSDS |
| GHS pictograms |    
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| GHS Signal word | Danger |
| H228, H302, H315, H317, H318, H332, H334 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
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| Infobox references | |
Paraformaldehyde (PFA) is the smallest polyoxymethylene, the polymerization product of formaldehyde with a typical degree of polymerization of 8–100 units. Paraformaldehyde commonly has a slight odor of formaldehyde due to decomposition. Paraformaldehyde is a poly-acetal.
Synthesis
Paraformaldehyde forms slowly in aqueous formaldehyde solutions as a white precipitate, especially if stored in the cold. Formalin actually contains very little monomeric formaldehyde; most of it forms short chains of polyformaldehyde. A small amount of methanol is often added as a stabilizer to limit the extent of polymerization.
Reactions
Paraformaldehyde can be depolymerized to formaldehyde gas by dry heating[2] and to formaldehyde solution by water in the presence of a base, an acid or heat. The high purity formaldehyde solutions obtained in this way are used as a fixative for microscopy and histology.
The resulting formaldehyde gas from dry heating paraformaldehyde is flammable.
Uses
Once paraformaldehyde is depolymerized, the resulting formaldehyde may be used as a fumigant, disinfectant, fungicide, and fixative. Longer chain-length (high molecular weight) polyoxymethylenes are used as a thermoplastic and are known as polyoxymethylene plastic (POM, Delrin). It was used in the past in the discredited Sargenti method of root canal treatment.[3]
Paraformaldehyde is not a fixative; it must be depolymerized to formaldehyde in solution. In cell culture, a typical formaldehyde fixing procedure would involve using a 4% formaldehyde solution in phosphate buffered saline (PBS) on ice for 10 minutes. In histology and pathology specimens preparation, usually, the fixation step is performed using 10% Neutral Buffered Formalin (4% formaldehyde) for, at least, 24 hours.
Paraformaldehyde is also used to crosslink proteins to DNA, as used in ChIP (chromatin immunoprecipitation) which is a technique to determine which part of DNA certain proteins are binding to.
Paraformaldehyde can be used as a substitute of aqueous formaldehyde to produce the resinous binding material, which is commonly used together with melamine, phenol or other reactive agents in the manufacturing of particle board, medium density fiberboard and plywood.[4]
Toxicity
As a formaldehyde releasing agent, paraformaldehyde is a potential carcinogen.[5] Its acute oral median lethal dose in rats is 592 mg/kg.[6]
See also
- 1,3,5-Trioxane (metaformaldehyde), the cyclic trimer of formaldehyde
References
- ↑ "C&L Inventory". https://echa.europa.eu/information-on-chemicals/cl-inventory-database/-/discli/details/10166.
- ↑ Yates, J (1973). "Adsorption and decomposition of formaldehyde on tungsten (100) and (111) crystal planes". Journal of Catalysis 30 (2): 260. doi:10.1016/0021-9517(73)90073-0.
- ↑ "Be Wary of Sargenti Root Canal Treatment | Quackwatch". May 2018. http://www.dentalwatch.org/questionable/sargenti/overview.html.
- ↑ "Paraformaldehyde - Dover Chemical". http://dovechem.co.id/en/paraformaldehyde-3.
- ↑ Cogliano, Vincent; Grosse, Yann; Baan, Robert; Straif, Kurt; Secretan, Béatrice; Ghissassi, Fatiha El (September 2004). "Advice on formaldehyde and glycol ethers". The Lancet Oncology 5 (9): 528. doi:10.1016/S1470-2045(04)01562-1. PMID 15384217.
- ↑ "MSDS - 158127 SAFETY DATA SHEET - Paraformaldehyde". SIGMA-ALDRICH. https://www.sigmaaldrich.com/US/en/product/sial/158127.
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