formaldehyde

formaldehyde, HCHO, the simplest aldehyde. It melts at -92°C;, boils at -21°C;, and is soluble in water, alcohol, and ether; at STP, it is a flammable, poisonous, colorless gas with a suffocating odor. Formaldehyde is used in the preparation of dyes, in the production of Bakelite and other plastics and synthetic resins, and for several other purposes. Pure gaseous formaldehyde is uncommon, since it readily polymerizes into paraformaldehyde, a white crystalline solid. Paraformaldehyde in the form of candles has been used for fumigating rooms, since it yields formaldehyde when heated. Formalin is a 40% by volume solution of formaldehyde in water, usually with a small amount of methanol (methyl alcohol) added to prevent polymerization; it is used as an antiseptic, disinfectant, and preservative for biological materials. Formaldehyde is prepared commercially by passing methanol vapor mixed with air over a catalyst, e.g., hot copper, to cause oxidation of the methanol; it is also prepared by the oxidation of natural gas. It forms formic acid when it is oxidized. The IUPAC name for formaldehyde is methanal.

or methanal

Simplest aldehyde, chemical formula HCHO. Formaldehyde (37percnt) in water solution, called formalin, is used as a preservative, an embalming agent, and a disinfectant. Large amounts of formaldehyde are used in the manufacture of various familiar plastics. Bakelite (the first completely synthetic plastic) is the trademark for formaldehyde and phenol polymer, and Formica is the trademark for formaldehyde and urea polymer. The reaction of formaldehyde with proteins (called amino formylation) leads to its use in the tanning industry and for treating various vegetable proteins to render them fibrous.

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| Section8 = }} Formaldehyde is a chemical compound with the formula H₂CO. It is the simplest aldehyde—an organic compound containing a terminal carbonyl group: it consists of exactly one carbonyl. It was first synthesized by the Russian chemist Aleksandr Butlerov (1828-1886), but was conclusively identified by August Wilhelm von Hofmann. Formaldehyde exists in several forms aside from H₂CO: the cyclic trimer trioxane and the polymer paraformaldehyde. It exists in water as the hydrate H₂C(OH)₂. Aqueous solutions of formaldehyde are referred to as formalin. "100%" formalin consists of a saturated solution of formaldehyde (roughly 40% by mass) in water, with a small amount of stabilizer, usually methanol to limit oxidation and polymerization.

Formaldehyde is an intermediate in the oxidation (or combustion) of methane as well as other carbon compounds, e.g. forest fires, in automobile exhaust, and in tobacco smoke. When produced in the atmosphere by the action of sunlight and oxygen on atmospheric methane and other hydrocarbons, it becomes part of smog. Small amounts of formaldehyde are produced as a metabolic byproduct in most organisms, including humans.

Production

Formaldehyde is produced industrially by the catalytic oxidation of methanol. The most common catalysts are silver metal or a mixture of an iron oxide with molybdenum and vanadium. In the more commonly used FORMOX process methanol and oxygen react at ca 250-400 °C in presence of iron oxide in combination with molybdenum and/or vanadium to produce formaldehyde according to the chemical equation

2 CH₃OH + O₂ → 2 H₂CO + 2 H₂O

The silver-based catalyst is usually operated at a higher temperature, about 650 °C. Two chemical reactions on it simultaneously produce formaldehyde: that shown above and the dehydrogenation reaction

CH₃OH → H₂CO + H₂

Formaldehyde is readily oxidized by atmospheric oxygen to form formic acid. Formic acid is found in ppm levels in commercial formaldehyde.

Formalin can be produced on a smaller scale using a whole range of other methods including conversion from ethanol instead of the normally-fed methanol feedstock. Such methods are of less commercial importance.

Organic chemistry

Formaldehyde is a central building block in the synthesis of many other compounds. It exhibits most of the chemical properties of other aldehydes but is more reactive. Formaldehyde is a good electrophile, participating in electrophilic aromatic substitution reactions with aromatic compounds, and can undergo electrophilic addition reactions with alkenes. Formaldehyde undergoes a Cannizzaro reaction in the presence of basic catalysts to produce formic acid and methanol.

Condensation with acetaldehyde affords pentaerythritol. Condensation with phenols gives phenol-formaldehyde resins. With 4-substituted phenols one obtains calixarenes.

When combined with hydrogen sulfide it forms trithiane.

3 CH₂O + 3 H₂S → (CH₂S)₃ + 3 H₂O

Biology

Formaldehyde solutions are used as a fixative for microscopy and histology. Pure solutions that are free of the oxidation product formic acid and of the stabilizer methanol are often produced by depolymerization of paraformaldehyde in hot water.

Formaldehyde (and its oligomers and hydrates) are rarely encountered in living organisms. Methanogenesis, which can start from many C1 sources, proceeds via the equivalent of formaldehyde, but this one-carbon species is masked as a methylene group carried by methanopterin. The formaldehyde is the primary cause of the methanol's toxicity, since methanol is metabolised into toxic formaldehyde by alcohol dehydrogenase.

Formaldehyde is converted to formic acid in the body, leading to a rise in blood acidity (acidosis).

Applications

As a disinfectant and biocide

An aqueous solution of formaldehyde can be useful as a disinfectant as it kills most bacteria and fungi (including their spores). It is also used as a preservative in vaccines. Formaldehyde solutions are applied topically in medicine to dry the skin, such as in the treatment of warts. Many aquarists use formaldehyde as a treatment for the parasite ichthyophthirius.

Formaldehyde preserves or fixes tissue or cells by irreversibly cross-linking primary amino groups in proteins with other nearby nitrogen atoms in protein or DNA through a -CH₂- linkage. This is exploited in ChIP-on-chip transcriptomics experiments.

Formaldehyde is also used as a denaturing agent in RNA gel electrophoresis, preventing RNA from forming secondary structures.

Industry

Formaldehyde is a common building block for the synthesis of more complex compounds and materials. When reacted with phenol, urea, or melamine formaldehyde produces, respectively, hard thermoset phenol formaldehyde resin, urea formaldehyde resin, and melamine resin. These resins are commonly used in permanent adhesives such as those used in plywood or carpeting. It is used as the wet-strength resin added to sanitary paper products such as (listed in increasing concentrations injected into the paper machine headstock chest) facial tissue, table napkins, and roll towels. They are also foamed to make insulation, or cast into moulded products. Production of formaldehyde resins accounts for more than half of formaldehyde consumption.

Formaldehyde is also a precursor to polyfunctional alcohols such as pentaerythritol, which is used to make paints and explosives. Other formaldehyde derivatives include methylene diphenyl diisocyanate, an important component in polyurethane paints and foams, and hexamine, which is used in phenol-formaldehyde resins as well as the explosive RDX.

Formaldehyde, along with 18 M (concentrated) sulfuric acid (the entire solution often called the Marquis reagent), is used as an MDMA "testing kit" by such groups as Dancesafe as well as MDMA consumers. The solution alone cannot verify the presence of MDMA but reacts with many other chemicals that the MDMA tablet itself may be adulterated with. The reaction itself produces colors that correlate with these components.

The textile industry uses formaldehyde-based resins as finishers to make fabrics crease-resistant.

It is also used as an ingredient by some shampoo manufacturers.

In photography

Formaldehyde is still used in low concentrations for process C-41 (color negative film) stabilizer in the final wash step, as well as in the process E-6 pre-bleach step, to obviate the need for it in the final wash.

Embalming

Formaldehyde-based solutions are used in embalming to disinfect and temporarily preserve human remains. It is the ability of formaldehyde to fix the tissue that produces the tell-tale firmness of flesh in an embalmed body. Whereas other heavier aldehydes produce a similar firming action none approaches the completeness of formaldehyde. Several European countries restrict the use of formaldehyde, including the import of formaldehyde-treated products and embalming, and the European Union is considering a complete ban on formaldehyde usage (including embalming), subject to a review of List 4B of the Technical Annex to the Report from the Commission to the European Parliament and the Council on the Evaluation of the Active Substances of Plant Protection Products by the European Commission Services. Countries with a strong tradition of embalming corpses, such as Ireland and other colder-weather countries, have raised concerns. The European Union decided on September 22, 2007 to ban Formaldehyde use throughout Europe due to its carcinogenic properties.

Safety

Occupational exposure to formaldehyde by inhalation is mainly from three types of sources: thermal or chemical decomposition of formaldehyde-based resins, formaldehyde emission from aqueous solutions (for example, embalming fluids), and the production of formaldehyde resulting from the combustion of a variety of organic compounds (for example, exhaust gases). Formaldehyde can be toxic, allergenic, and carcinogenic. Because formaldehyde resins are used in many construction materials it is one of the more common indoor air pollutants. At concentrations above 0.1 ppm in air formaldehyde can irritate the eyes and mucous membranes, resulting in watery eyes. Formaldehyde inhaled at this concentration may cause headaches, a burning sensation in the throat, and difficulty breathing, as well as triggering or aggravating asthma symptoms.

Formaldehyde is classified as a probable human carcinogen by the U.S. Environmental Protection Agency. The International Agency for Research on Cancer (IARC) has determined that there is "sufficient evidence" that occupational exposure to formaldehyde causes nasopharyngeal cancer in humans. The United States Environmental Protection Agency USEPA allows no more than 0.016 ppm formaldehyde in the air in new buildings constructed for that agency. On April 11th, 2008, FEMA announced that all trailers purchased by that agency in the future must meet the same standard.

Formaldehyde can cause allergies and is part of the standard patch test series. People with formaldehyde allergy are advised to avoid formaldehyde releasers as well (e.g., Quaternium-15, imidazolidinyl urea, and diazolidinyl urea). Formaldehyde has been banned in cosmetics in both Sweden and Japan.

FEMA Trailer Formaldehyde Exposures

The Federal Emergency Management Agency (FEMA) provided travel trailers and mobile homes starting in 2006 for habitation by Gulf Coast residents displaced by Hurricane Katrina and Hurricane Rita. Some of the people who moved into the trailers complained of breathing difficulties, nosebleeds, and persistent headaches. Formaldehyde-catalyzed resins were used in the production of these homes.

The United States Centers For Disease Control and Prevention (CDC) performed indoor air quality testing for formaldehyde in some of the units. On Thursday, February 14, 2008 the CDC announced that potentially hazardous levels of formaldehyde were found in many of the travel trailers and mobile homes provided by the agency. The CDC's preliminary evaluation of a scientifically established random sample of 519 travel trailers and mobile homes tested between Dec. 21, 2007 and Jan. 23, 2008 (2+ years after manufacture) showed average levels of formaldehyde in all units of about 77 parts per billion (ppb). Long-term exposure to levels in this range can be linked to an increased risk of cancer and, at levels above this range, there can also be a risk of respiratory illness. These levels are higher than expected in indoor air, where levels are commonly in the range of 10-20 ppb, and are higher than the Agency for Toxic Substance Disease Registry (ATSDR, division of the CDC) Minimal Risk Level (MRL) of 8 ppb . Levels measured ranged from 3 ppb to 590 ppb.

The Federal Emergency Management Agency, which requested the testing by the CDC, said it would work aggressively to relocate all residents of the temporary housing as soon as possible. Lawsuits are being filed against FEMA as a result of the exposures.

See also

• Aldehyde
• Formic acid
• Paraformaldehyde

References

External links

• (gas)
• (solution)
• "Formaldehyde", IARC Monograph
• Formaldehyde (gas) from the 11th Report on Carcinogens of the U.S. National Toxicology Program (.pdf file)
• Formaldehyde fact sheet from the Australian National Pollutant Inventory
• NIOSH Pocket Guide to Chemical Hazards
• Process C-41 Using KODAK FLEXICOLOR Chemicals Publication Z-131
• Formaldehyde Council
• Formaldehyde Data Sheet, ChemSub Online
• Prevention guide – Formaldehyde in the work place
• National Institute for Occupational Safety and Health - Formaldehyde Page