Acetaldehyde Chemical Formula
The formula of acetaldehyde is given as CH3CHO or C2H4O. This chemical compound usually contains two carbon atoms with five single bonds and one carbon-oxygen double bond.
|Formula||C2H4O or CH3CHO|
|Molar Mass||44.053 g·mol-1|
|Melting Point||−123.37 °C|
|Boiling Point||20.2 °C|
Acetaldehyde commonly known as ethanal is an organic chemical compound. In addition, it is one of the most important aldehydes that occur in nature widely and produced by industries on a large scale. Naturally, plants produce acetaldehyde and they occur in coffee, bread, and ripe fruit. Commonly, we use it in perfumes and in food as a flavoring agent. Learn Acetaldehyde Formula here.
Acetaldehyde Formula and Structure
The chemical formula of acetaldehyde is CH3CHO or C2H40. The molar mass is 44.053 g mL-1. Also, the acetaldehyde molecule has the usual functional group of an aldehyde H-C=O bound to a methyl group (-CH3), so the acetaldehyde is the second most simple aldehyde after the formaldehyde.
Furthermore, the C atom from the aldehyde has a hybridization sp2, but the methyl group has sp3, thus the molecule has a planar-trigonal together with tetrahedral geometry. Besides, the chemical structure is shown below:
We can find acetaldehyde in many plants and ripe fruits. Also, it is an intermediate in the ethanol metabolism, through the action of enzymes alcohol dehydrogenase that changes ethanol to acetaldehyde.
Preparation of Acetaldehyde
One of the other method today is the hydration of acetylene or ethylene by the Wacker process in which copper or palladium is the catalyst:
2CH2=CH2 + O2 → 2CH3CHO
Before the Wacker process, acetaldehyde was produced by the hydration of acetylene in which mercury (II) salts serve as a catalyst:
C2H2 + Hg2+ + H2O → CH3CHO + Hg
The reaction is conducted at a temperature of 90-95oC, and the formed acetaldehyde is separated from water and mercury and cooled to 25-30oC.
Another method is the oxidation of ethanol, where partial dehydrogenation of ethanol produces acetaldehyde in the presence of copper as a catalyst:
CH3CH2OH → CH3CHO + H2
In this process, ethanol vapor is passed at a temperature of 260-290oC.
Acetaldehyde Physical Properties
Acetaldehyde appears colorless and has a strong odor liquid. In addition, its boiling point is 20.20C and the melting point is -123oC. the density is 0.784 g mL-1. However, acetaldehyde is soluble in miscible water, ethanol, benzene, acetone, and toluene. Also, it is slightly soluble in chloroform.
Chemical Properties of Acetaldehyde
Its properties are similar to formaldehyde, is an important precursor in organic synthesis, especially as an electrophile. Furthermore, by a condensation reaction, we can gain intermediates such as pentaerythritol (intermediate in explosive manufacture) that we can use in organic synthesis.
Also, we use it to produce hydroxyethyl derivatives through a reaction with a Grignard reagent. Apart from that, acetaldehyde is an important building block that we use in the synthesis of heterocycles, such as imines and pyridines.
Uses of Acetaldehyde
In the chemical industry, it has a variety of applications. Largely we use it in the production of dyes, perfumes, acetic acid and as a flavoring agent. Also, we use it in fuel composition and as a solvent in some industrial processes such as the manufacturing of paper, tanning, and rubber.
A useful resin produces when acetaldehyde combines with urea. Acetaldehyde and acetic anhydride react to produce ethylidene diacetate, a predecessor to vinyl acetate that we use to produce polyvinyl acetate. Also, we use it in the production of n-butyraldehyde. But now they use propylene to generate it.
Safety Hazards and Effects on Health
It is a very toxic liquid. Also, it irritates the mucous membrane. Furthermore, large doses can be fatal can cause respiratory paralysis. In addition, it is highly flammable and can form peroxides. Lastly, acetaldehyde is a carcinogen suspected compound.
Solved Example for You
Question: How to prepare acetaldehyde by dehydrogenation of ethanol?
We can prepare acetaldehyde from the dehydrogenation of ethanol by using copper as a catalyst in this reaction. At 260-2800C, the ethanol reacts over the catalyst to form acetaldehyde:
CH3CH2OH + ½ O2 → CH3CHO + H2O
Acetaldehyde was first observed by the Swedish pharmacist/chemist Carl Wilhelm Scheele (1774); it was then investigated by the French chemists Antoine François, comte de Fourcroy and Louis Nicolas Vauquelin (1800), and the German chemists Johann Wolfgang Döbereiner (1821, 1822, 1832) and Justus von Liebig (1835). In 1835, Liebig named it “aldehyde”; the name was later altered to “acetaldehyde”.
In 2003, global production was about 1 million tonnes. Before 1962, ethanol and acetylene were the major sources of acetaldehyde. Since then, ethylene is the dominant feedstock.
The main method of production is the oxidation of ethylene by the Wacker process, which involves oxidation of ethylene using a homogeneous palladium/copper system:
2 CH2=CH2 + O2 → 2 CH3CHO
In the 1970s, the world capacity of the Wacker-Hoechst direct oxidation process exceeded 2 million tonnes annually.
Smaller quantities can be prepared by the partial oxidation of ethanol in an exothermic reaction. This process typically is conducted over a silver catalyst at about 500–650 °C.
CH3CH2OH + 1⁄2 O2 → CH3CHO + H2O
This method is one of the oldest routes for the industrial preparation of acetaldehyde.
Hydration of acetylene
Prior to the Wacker process and the availability of cheap ethylene, acetaldehyde was produced by the hydration of acetylene.This reaction is catalyzed by mercury(II) salts:
C2H2 + Hg2+ + H2O → CH3CHO + Hg
The mechanism involves the intermediacy of vinyl alcohol, which tautomerizes to acetaldehyde. The reaction is conducted at 90–95 °C, and the acetaldehyde formed is separated from water and mercury and cooled to 25–30 °C. In the wet oxidation process, iron(III) sulfate is used to reoxidize the mercury back to the mercury(II) salt. The resulting iron(II) sulfate is oxidized in a separate reactor with nitric acid.
Dehydrogenation of ethanol
Traditionally, acetaldehyde was produced by the partial dehydrogenation of ethanol:
CH3CH2OH → CH3CHO + H2
In this endothermic process, ethanol vapor is passed at 260–290 °C over a copper-based catalyst. The process was once attractive because of the value of the hydrogen coproduct, but in modern times is not economically viable.
Hydroformylation of methanol
The hydroformylation of methanol with catalysts like cobalt, nickel, or iron salts also produces acetaldehyde, although this process is of no industrial importance. Similarly noncompetitive, acetaldehyde arises from synthesis gas with modest selectivity.
Tautomerization of acetaldehyde to vinyl alcohol
Like many other carbonyl compounds, acetaldehyde tautomerizes to give an enol (vinyl alcohol; IUPAC name: ethenol):
CH3CH=O ⇌ CH2=CHOH ∆H298,g = +42.7 kJ/mol
The equilibrium constant is 6×10−7 at room temperature, thus that the relative amount of the enol form in a sample of acetaldehyde is very small. At room temperature, acetaldehyde (CH3CH=O) is more stable than vinyl alcohol (CH2=CHOH) by 42.7 kJ/mol: Overall the keto-enol tautomerization occurs slowly but is catalyzed by acids.
Photo-induced keto-enol tautomerization is viable under atmospheric or stratospheric conditions. This photo-tautomerization is relevant to the earth’s atmosphere, because vinyl alcohol is thought to be a precursor to carboxylic acids in the atmosphere.
Acetaldehyde is a common electrophile in organic synthesis. In condensation reactions, acetaldehyde is prochiral. It is used primarily as a source of the “CH3C+H(OH)” synthon in aldol and related condensation reactions. Grignard reagents and organolithium compounds react with MeCHO to give hydroxyethyl derivatives. In one of the more spectacular condensation reactions, three equivalents of formaldehyde add to MeCHO to give pentaerythritol, C(CH2OH)4.
In a Strecker reaction, acetaldehyde condenses with cyanide and ammonia to give, after hydrolysis, the amino acid alanine. Acetaldehyde can condense with amines to yield imines; for example, with cyclohexylamine to give N-ethylidenecyclohexylamine. These imines can be used to direct subsequent reactions like an aldol condensation.
It is also a building block in the synthesis of heterocyclic compounds. In one example, it converts, upon treatment with ammonia, to 5-ethyl-2-methylpyridine (“aldehyde-collidine”).
Three molecules of acetaldehyde condense to form “paraldehyde”, a cyclic trimer containing C-O single bonds. Similarly condensation of four molecules of acetaldehyde give the cyclic molecule metaldehyde. Paraldehyde can be produced in good yields, using a sulfuric acid catalyst. Metaldehyde is only obtained in a few percent yield and with cooling, often using HBr rather than H2SO4 as the catalyst. At -40 °C in the presence of acid catalysts, polyacetaldehyde is produced.
Acetaldehyde forms a stable acetal upon reaction with ethanol under conditions that favor dehydration. The product, CH3CH(OCH2CH3)2, is formally named 1,1-diethoxyethane but is commonly referred to as “acetal”. This can cause confusion as “acetal” is more commonly used to describe compounds with the functional groups RCH(OR’)2 or RR’C(OR”)2 rather than referring to this specific compound – in fact, 1,1-diethoxyethane is also described as the diethyl acetal of acetaldehyde.
Precursor to vinylphosphonic acid
Acetaldehyde is a precursor to vinylphosphonic acid, which is used to make adhesives and ion conductive membranes. The synthesis sequence begins with a reaction with phosphorus trichloride:
PCl3 + CH3CHO → CH3CH(O−)PCl3+
CH3CH(O−)PCl3+ + 2 CH3CO2H → CH3CH(Cl)PO(OH)2 + 2 CH3COCl
CH3CH(Cl)PO(OH)2 → CH2=CHPO(OH)2 + HCl
In the liver, the enzyme alcohol dehydrogenase oxidizes ethanol into acetaldehyde, which is then further oxidized into harmless acetic acid by acetaldehyde dehydrogenase. These two oxidation reactions are coupled with the reduction of NAD+ to NADH. In the brain, the enzyme catalase is primarily responsible for oxidizing ethanol to acetaldehyde, and alcohol dehydrogenase plays a minor role. The last steps of alcoholic fermentation in bacteria, plants, and yeast involve the conversion of pyruvate into acetaldehyde and carbon dioxide by the enzyme pyruvate decarboxylase, followed by the conversion of acetaldehyde into ethanol. The latter reaction is again catalyzed by an alcohol dehydrogenase, now operating in the opposite direction.
Traditionally, acetaldehyde was mainly used as a precursor to acetic acid. This application has declined because acetic acid is produced more efficiently from methanol by the Monsanto and Cativa processes. Acetaldehyde is an important precursor to pyridine derivatives, pentaerythritol, and crotonaldehyde. Urea and acetaldehyde combine to give a useful resin. Acetic anhydride reacts with acetaldehyde to give ethylidene diacetate, a precursor to vinyl acetate, which is used to produce polyvinyl acetate.
The global market for acetaldehyde is declining. Demand has been impacted by changes in the production of plasticizer alcohols, which has shifted because n-butyraldehyde is less often produced from acetaldehyde, instead being generated by hydroformylation of propylene. Likewise, acetic acid, once produced from acetaldehyde, is made predominantly by the lower-cost methanol carbonylation process. The impact on demand has led to increase in prices and thus slowdown in the market.
Production of Acetaldehyde
Consumption of acetaldehyde (103 t) in 2003
(* Included in others -glyoxal/glyoxalic acid, crotonaldehyde, lactic acid, n-butanol, 2-ethylhexanol)
China is the largest consumer of acetaldehyde in the world, accounting for almost half of global consumption in 2012. Major use has been the production of acetic acid. Other uses such as pyridines and pentaerythritol are expected to grow faster than acetic acid, but the volumes are not large enough to offset the decline in acetic acid. As a consequence, overall acetaldehyde consumption in China may grow slightly at 1.6% per year through 2018. Western Europe is the second-largest consumer of acetaldehyde worldwide, accounting for 20% of world consumption in 2012. As with China, the Western European acetaldehyde market is expected to increase only very slightly at 1% per year during 2012–2018. However, Japan could emerge as a potential consumer for acetaldehyde in next five years due to newfound use in commercial production of butadiene. The supply of butadiene has been volatile in Japan and the rest of Asia. This should provide the much needed boost to the flat market, as of 2013.
The threshold limit value is 25ppm (STEL/ceiling value) and the MAK (Maximum Workplace Concentration) is 50 ppm. At 50 ppm acetaldehyde, no irritation or local tissue damage in the nasal mucosa is observed. When taken up by the organism, acetaldehyde is metabolized rapidly in the liver to acetic acid. Only a small proportion is exhaled unchanged. After intravenous injection, the half-life in the blood is approximately 90 seconds.
No serious cases of acute intoxication have been recorded. Acetaldehyde naturally breaks down in the human body but has been shown to excrete in urine of rats.
Acetaldehyde is an irritant of the skin, eyes, mucous membranes, throat, and respiratory tract. This occurs at concentrations as low as 1000 ppm. Symptoms of exposure to this compound include nausea, vomiting, and headache. These symptoms may not happen immediately. The perception threshold for acetaldehyde in air is in the range between 0.07 and 0.25 ppm. At such concentrations, the fruity odor of acetaldehyde is apparent. Conjunctival irritations have been observed after a 15-minute exposure to concentrations of 25 and 50 ppm, but transient conjunctivitis and irritation of the respiratory tract have been reported after exposure to 200 ppm acetaldehyde for 15 minutes.
Acetaldehyde is carcinogenic in humans. In 1988 the International Agency for Research on Cancer stated, “There is sufficient evidence for the carcinogenicity of acetaldehyde (the major metabolite of ethanol) in experimental animals.” In October 2009 the International Agency for Research on Cancer updated the classification of acetaldehyde stating that acetaldehyde included in and generated endogenously from alcoholic beverages is a Group I human carcinogen. In addition, acetaldehyde is damaging to DNA and causes abnormal muscle development as it binds to proteins.
People with a genetic deficiency for the enzyme responsible for the conversion of acetaldehyde into acetic acid may have a greater risk of Alzheimer’s disease. “These results indicate that the ALDH2 deficiency is a risk factor for LOAD [late-onset Alzheimer’s disease] …”
A study of 818 heavy drinkers found that those exposed to more acetaldehyde than normal through a genetic variant of the gene encoding for alcohol dehydrogenase are at greater risk of developing cancers of the upper gastrointestinal tract and liver.
The drug disulfiram (Antabuse) inhibits acetaldehyde dehydrogenase, an enzyme that oxidizes the compound into acetic acid. Metabolism of ethanol forms acetaldehyde before acetaldehyde dehydrogenase forms acetic acid, but with the enzyme inhibited, acetaldehyde accumulates. If one consumes ethanol while taking disulfiram, the hangover effect of ethanol is felt more rapidly and intensely. As such, disulfiram is sometimes used as a deterrent for alcoholics wishing to stay sober.
Sources of exposure
Acetaldehyde is a potential contaminant in workplace, indoors, and ambient environments. Moreover, the majority of humans spend more than 90% of their time in indoor environments, increasing any exposure and the risk to human health.
In a study in France, the mean indoor concentration of acetaldehydes measured in 16 homes was approximately seven times higher than the outside acetaldehyde concentration. The living room had a mean of 18.1±17.5 μg m−3 and the bedroom was 18.2±16.9 μg m−3, whereas the outdoor air had a mean concentration of 2.3±2.6 μg m−3.
It has been concluded that volatile organic compounds (VOC) such as benzene, formaldehyde, acetaldehyde, toluene, and xylenes have to be considered priority pollutants with respect to their health effects. It has been pointed that in renovated or completely new buildings, the VOCs concentration levels are often several orders of magnitude higher. The main sources of acetaldehydes in homes include building materials, laminate, PVC flooring, varnished wood flooring, and varnished cork/pine flooring (found in the varnish, not the wood). It is also found in plastics, oil-based and water-based paints, in composite wood ceilings, particle-board, plywood, treated pine wood, and laminated chipboard furniture.
The use of acetaldehyde is widespread in different industries, and it may be released into waste water or the air during production, use, transportation and storage. Sources of acetaldehyde include fuel combustion emissions from stationary internal combustion engines and power plants that burn fossil fuels, wood, or trash, oil and gas extraction, refineries, cement kilns, lumber and wood mills and paper mills. Acetaldehyde is also present in automobile and diesel exhaust. As a result, acetaldehyde is “one of the most frequently found air toxics with cancer risk greater than one in a million”.
Natural tobacco polysaccharides, including cellulose, have been shown to be the primary precursors making acetaldehyde a significant constituent of tobacco smoke. It has been demonstrated to have a synergistic effect with nicotine in rodent studies of addiction. Acetaldehyde is also the most abundant carcinogen in tobacco smoke; it is dissolved into the saliva while smoking.
Acetaldehyde has been found in cannabis smoke. This finding emerged through the use of new chemical techniques that demonstrated the acetaldehyde present was causing DNA damage in laboratory settings.
Many microbes produce acetaldehyde from ethanol, but they have a lower capacity to eliminate the acetaldehyde, which can lead to the accumulation of acetaldehyde in saliva, stomach acid, and intestinal contents. Fermented food and many alcoholic beverages can also contain significant amounts of acetaldehyde. Acetaldehyde, derived from mucosal or microbial oxidation of ethanol, tobacco smoke, and diet, appears to act as a cumulative carcinogen in the upper digestive tract of humans. According to European Commission’s Scientific Committee on Consumer Safety’s (SCCS) “Opinion on Acetaldehyde” (2012) the cosmetic products special risk limit is 5 mg/l and acetaldehyde should not be used in mouth-washing products.
Acetaldehyde is also created by thermal degradation or ultraviolet photo-degradation of some thermoplastic polymers during or after manufacture. One common example occurs when a bottle of water is left in a hot car for a few hours on a hot, sunny day, and one notices its strange sweet taste in the water from the breakdown of the polyethylene terephthalate (PETE) container. The water industry generally recognizes 20–40 ppb as the taste/odor threshold for acetaldehyde. The level at which an average consumer could detect acetaldehyde is still considerably lower than any toxicity.
Candida albicans in patients with potentially carcinogenic oral diseases has been shown to produce acetaldehyde in quantities sufficient to cause problems.
✅ Math Formulas ⭐️⭐️⭐️⭐️⭐