Hypochlorous Acid
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Hypochlorous Acid
Hypochlorous acid
hypochlorous acid bonding
hypochlorous acid space filling
IUPAC name
hypochlorous acid, chloric(I) acid, chloranol, hydroxidochlorine
Other names
Hydrogen hypochlorite, Chlorine hydroxide, hypochloric acid
3D model (JSmol)
ECHA InfoCard 100.029.302 Edit this at Wikidata
EC Number
  • 232-232-5
  • InChI=1S/ClHO/c1-2/h2H checkY
  • InChI=1/ClHO/c1-2/h2H
  • OCl
Molar mass 52.46 g/mol
Appearance Colorless aqueous solution
Density Variable
Acidity (pKa) 7.53[1]
Conjugate base Hypochlorite
Main hazards corrosive, oxidizing agent
NFPA 704 (fire diamond)
Related compounds
Other anions
Hypofluorous acid
Hypobromous acid
Hypoiodous acid
Related compounds
Calcium hypochlorite
Sodium hypochlorite
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkY?N ?)
Infobox references

Hypochlorous acid (HOCl or HClO) is a weak acid that forms when chlorine dissolves in water, and itself partially dissociates, forming hypochlorite, ClO-. HClO and ClO- are oxidizers, and the primary disinfection agents of chlorine solutions.[2] HClO cannot be isolated from these solutions due to rapid equilibration with its precursor. Sodium hypochlorite (NaClO) and calcium hypochlorite (Ca(ClO)2), are bleaches, deodorants, and disinfectants.

Hypochlorous acid is found naturally in white blood cells of mammals, including the human body.[3] It is non-toxic and has been used as a safe wound care solution for many years.[4]

When dissolved in water, hypochlorous acid water has found to have strong disinfection properties, combined with its non-toxicity characteristics, it has been identified as an ideal cleaning agent and sanitizer.[5] It has been identified by the US Environmental Protection Agency as a disinfectant effective against COVID-19,[6] backed by clinical studies.

Because of its ability to penetrate pathogens' membranes it is also used as a commercial deodorizer.


Hypochlorous acid was discovered in 1834 by the French chemist Antoine Jérôme Balard (1802-1876) by adding, to a flask of chlorine gas, a dilute suspension of mercury(II) oxide in water.[7] He also named the acid and its compounds.[8]

Despite being relatively easy to make, it is difficult to maintain a stable hypochlorous acid solution. It is not until recent years that scientists have been able to cost-effectively produce and maintain hypochlorous acid water for stable commercial use.


  • In organic synthesis, HClO converts alkenes to chlorohydrins.[9]
  • In biology, hypochlorous acid is generated in activated neutrophils by myeloperoxidase-mediated peroxidation of chloride ions, and contributes to the destruction of bacteria.[10][11][12]
  • In medical, hypochlorous acid water has been used as a disinfectant and sanitiser.[3][4][5]
  • In wound care,[13][14][15] and as of early 2016 the U.S. Food and Drug Administration has approved products whose main active ingredient is hypochlorous acid for use in treating wounds and various infections in humans and pets. It is also FDA-approved as a preservative for saline solutions.
  • In disinfection, it has been used in the form of liquid spray, wet wipes and aerosolised application. Recent studies have shown hypochlorous acid water to be suitable for fog and aerosolised application for disinfection chambers and suitable for disinfecting indoor settings such as offices, hospitals and healthcare clinics[16]
  • In food service and water distribution, specialized equipment to generate weak solutions of HClO from water and salt is sometimes used to generate adequate quantities of safe (unstable) disinfectant to treat food preparation surfaces and water supplies.[17][18] It is also commonly used in restaurants due to its non-flammable and nontoxic characteristics.
  • In water treatment, hypochlorous acid is the active sanitizer in hypochlorite-based products (e.g. used in swimming pools).[19]
  • Similarly, in ships and yachts, marine sanitation devices[20] use electricity to convert seawater into hypochlorous acid to disinfect macerated faecal waste before discharge into the sea.
  • In deodorization, hypochlorous acid has been tested to remove up to 99% of foul odours including garbage, rotten meat, toilet, stool and urine odours.

Formation, stability and reactions

Addition of chlorine to water gives both hydrochloric acid (HCl) and hypochlorous acid (HOCl):[21]

Cl2 + H2O ? HClO + HCl
Cl2 + 4 OH- ? 2 ClO- + 2 H2O + 2 e-
Cl2 + 2 e- ? 2 Cl-

When acids are added to aqueous salts of hypochlorous acid (such as sodium hypochlorite in commercial bleach solution), the resultant reaction is driven to the left, and chlorine gas is formed. Thus, the formation of stable hypochlorite bleaches is facilitated by dissolving chlorine gas into basic water solutions, such as sodium hydroxide.

The acid can also be prepared by dissolving dichlorine monoxide in water; under standard aqueous conditions, anhydrous hypochlorous acid is currently impossible to prepare due to the readily reversible equilibrium between it and its anhydride:[22]

2 HOCl ? Cl2O + H2O K (at 0 °C) =

The presence of light or transition metal oxides of copper, nickel, or cobalt accelerates the exothermic decomposition into hydrochloric acid and oxygen:[22]

2 Cl2 + 2 H2O -> 4 HCl + O2

Fundamental reactions

In aqueous solution, hypochlorous acid partially dissociates into the anion hypochlorite ClO-:

HOCl ? ClO- + H+

Salts of hypochlorous acid are called hypochlorites. One of the best-known hypochlorites is NaClO, the active ingredient in bleach.

HOCl is a stronger oxidant than chlorine under standard conditions.

2 HClO(aq) + 2 H+ + 2 e- ? Cl2(g) + 2   E = +1.63 V

HClO reacts with HCl to form chlorine:

HOCl + HCl -> H2O + Cl2

HOCl reacts with ammonia to form monochloramine:

NH3 + HOCl -> NH2Cl + H2O

HOCl can also react with organic amines, forming N-chloroamines.

Hypochlorous acid exists in equilibrium with its anhydride; dichlorine monoxide.[22]

2 HOCl ? Cl2O + H2O K (at 0 °C) =

Reactivity of HClO with biomolecules

Hypochlorous acid reacts with a wide variety of biomolecules, including DNA, RNA,[12][23][24][25] fatty acid groups, cholesterol[26][27][28][29][30][31][32][33] and proteins.[29][34][35][36][37][38][39]

Reaction with protein sulfhydryl groups

Knox et al.[37] first noted that HClO is a sulfhydryl inhibitor that, in sufficient quantity, could completely inactivate proteins containing sulfhydryl groups. This is because HClO oxidises sulfhydryl groups, leading to the formation of disulfide bonds[40] that can result in crosslinking of proteins. The HClO mechanism of sulfhydryl oxidation is similar to that of monochloramine, and may only be bacteriostatic, because once the residual chlorine is dissipated, some sulfhydryl function can be restored.[36] One sulfhydryl-containing amino acid can scavenge up to four molecules of HOCl.[39] Consistent with this, it has been proposed that sulfhydryl groups of sulfur-containing amino acids can be oxidized a total of three times by three HClO molecules, with the fourth reacting with the ?-amino group. The first reaction yields sulfenic acid (R-SOH) then sulfinic acid (R-SO2H) and finally R-SO3H. Sulfenic acids form disulfides with another protein sulfhydryl group, causing cross-linking and aggregation of proteins. Sulfinic acid and R-SO3H derivatives are produced only at high molar excesses of HClO, and disulfides are formed primarily at bacteriocidal levels.[25] Disulfide bonds can also be oxidized by HClO to sulfinic acid.[40] Because the oxidation of sulfhydryls and disulfides evolves hydrochloric acid,[25] this process results in the depletion HClO.

Reaction with protein amino groups

Hypochlorous acid reacts readily with amino acids that have amino group side-chains, with the chlorine from HClO displacing a hydrogen, resulting in an organic chloramine.[41] Chlorinated amino acids rapidly decompose, but protein chloramines are longer-lived and retain some oxidative capacity.[11][39] Thomas et al.[11] concluded from their results that most organic chloramines decayed by internal rearrangement and that fewer available NH2 groups promoted attack on the peptide bond, resulting in cleavage of the protein. McKenna and Davies[42] found that 10 mM or greater HClO is necessary to fragment proteins in vivo. Consistent with these results, it was later proposed that the chloramine undergoes a molecular rearrangement, releasing HCl and ammonia to form an aldehyde.[43] The aldehyde group can further react with another amino group to form a Schiff base, causing cross-linking and aggregation of proteins.[29]

Reaction with DNA and nucleotides

Hypochlorous acid reacts slowly with DNA and RNA as well as all nucleotides in vitro.[23][44] GMP is the most reactive because HClO reacts with both the heterocyclic NH group and the amino group. In similar manner, TMP with only a heterocyclic NH group that is reactive with HClO is the second-most reactive. AMP and CMP, which have only a slowly reactive amino group, are less reactive with HClO.[44] UMP has been reported to be reactive only at a very slow rate.[12][23] The heterocyclic NH groups are more reactive than amino groups, and their secondary chloramines are able to donate the chlorine.[25] These reactions likely interfere with DNA base pairing, and, consistent with this, Prütz[44] has reported a decrease in viscosity of DNA exposed to HClO similar to that seen with heat denaturation. The sugar moieties are nonreactive and the DNA backbone is not broken.[44] NADH can react with chlorinated TMP and UMP as well as HClO. This reaction can regenerate UMP and TMP and results in the 5-hydroxy derivative of NADH. The reaction with TMP or UMP is slowly reversible to regenerate HClO. A second slower reaction that results in cleavage of the pyridine ring occurs when excess HClO is present. NAD+ is inert to HClO.[25][44]

Reaction with lipids

Hypochlorous acid reacts with unsaturated bonds in lipids, but not saturated bonds, and the ClO- ion does not participate in this reaction. This reaction occurs by hydrolysis with addition of chlorine to one of the carbons and a hydroxyl to the other. The resulting compound is a chlorohydrin.[26] The polar chlorine disrupts lipid bilayers and could increase permeability.[27] When chlorohydrin formation occurs in lipid bilayers of red blood cells, increased permeability occurs. Disruption could occur if enough chlorohydrin is formed.[26][32] The addition of preformed chlorohydrin to red blood cells can affect permeability as well.[28] Cholesterol chlorohydrin have also been observed,[27][30] but do not greatly affect permeability, and it is believed that Cl2 is responsible for this reaction.[30]

Mode of disinfectant action

E. coli exposed to hypochlorous acid lose viability in less than 0.1 seconds due to inactivation of many vital systems.[21][45][46][47][48] Hypochlorous acid has a reported LD50 of 0.0104-0.156 ppm[49] and 2.6 ppm caused 100% growth inhibition in 5 minutes.[42] However, the concentration required for bactericidal activity is also highly dependent on bacterial concentration.[37]

Inhibition of glucose oxidation

In 1948, Knox et al.[37] proposed the idea that inhibition of glucose oxidation is a major factor in the bacteriocidal nature of chlorine solutions. He proposed that the active agent or agents diffuse across the cytoplasmic membrane to inactivate key sulfhydryl-containing enzymes in the glycolytic pathway. This group was also the first to note that chlorine solutions (HOCl) inhibit sulfhydryl enzymes. Later studies have shown that, at bacteriocidal levels, the cytosol components do not react with HOCl.[50] In agreement with this, McFeters and Camper[51] found that aldolase, an enzyme that Knox et al.[37] proposes would be inactivated, was unaffected by HOCl in vivo. It has been further shown that loss of sulfhydryls does not correlate with inactivation.[36] That leaves the question concerning what causes inhibition of glucose oxidation. The discovery that HOCl blocks induction of ?-galactosidase by added lactose[52] led to a possible answer to this question. The uptake of radiolabeled substrates by both ATP hydrolysis and proton co-transport may be blocked by exposure to HOCl preceding loss of viability.[50] From this observation, it proposed that HOCl blocks uptake of nutrients by inactivating transport proteins.[35][50][51][53] The question of loss of glucose oxidation has been further explored in terms of loss of respiration. Venkobachar et al.[54] found that succinic dehydrogenase was inhibited in vitro by HOCl, which led to the investigation of the possibility that disruption of electron transport could be the cause of bacterial inactivation. Albrich et al.[12] subsequently found that HOCl destroys cytochromes and iron-sulfur clusters and observed that oxygen uptake is abolished by HOCl and adenine nucleotides are lost. It was also observed that irreversible oxidation of cytochromes paralleled the loss of respiratory activity. One way of addressing the loss of oxygen uptake was by studying the effects of HOCl on succinate-dependent electron transport.[55] Rosen et al.[48] found that levels of reductable cytochromes in HOCl-treated cells were normal, and these cells were unable to reduce them. Succinate dehydrogenase was also inhibited by HOCl, stopping the flow of electrons to oxygen. Later studies[46] revealed that Ubiquinol oxidase activity ceases first, and the still-active cytochromes reduce the remaining quinone. The cytochromes then pass the electrons to oxygen, which explains why the cytochromes cannot be reoxidized, as observed by Rosen et al.[48] However, this line of inquiry was ended when Albrich et al.[34] found that cellular inactivation precedes loss of respiration by using a flow mixing system that allowed evaluation of viability on much smaller time scales. This group found that cells capable of respiring could not divide after exposure to HOCl.

Depletion of adenine nucleotides

Having eliminated loss of respiration, Albrich et al.[34] proposes that the cause of death may be due to metabolic dysfunction caused by depletion of adenine nucleotides. Barrette et al.[52] studied the loss of adenine nucleotides by studying the energy charge of HOCl-exposed cells and found that cells exposed to HOCl were unable to step up their energy charge after addition of nutrients. The conclusion was that exposed cells have lost the ability to regulate their adenylate pool, based on the fact that metabolite uptake was only 45% deficient after exposure to HOCl and the observation that HOCl causes intracellular ATP hydrolysis. It was also confirmed that, at bacteriocidal levels of HOCl, cytosolic components are unaffected. So it was proposed that modification of some membrane-bound protein results in extensive ATP hydrolysis, and this, coupled with the cells inability to remove AMP from the cytosol, depresses metabolic function. One protein involved in loss of ability to regenerate ATP has been found to be ATP synthetase.[35] Much of this research on respiration reconfirms the observation that relevant bacteriocidal reactions take place at the cell membrane.[35][52][56]

Inhibition of DNA replication

Recently it has been proposed that bacterial inactivation by HOCl is the result of inhibition of DNA replication. When bacteria are exposed to HOCl, there is a precipitous decline in DNA synthesis that precedes inhibition of protein synthesis, and closely parallels loss of viability.[42][57] During bacterial genome replication, the origin of replication (oriC in E. coli) binds to proteins that are associated with the cell membrane, and it was observed that HOCl treatment decreases the affinity of extracted membranes for oriC, and this decreased affinity also parallels loss of viability. A study by Rosen et al.[58] compared the rate of HOCl inhibition of DNA replication of plasmids with different replication origins and found that certain plasmids exhibited a delay in the inhibition of replication when compared to plasmids containing oriC. Rosen's group proposed that inactivation of membrane proteins involved in DNA replication are the mechanism of action of HOCl.

Protein unfolding and aggregation

HOCl is known to cause post-translational modifications to proteins, the notable ones being cysteine and methionine oxidation. A recent examination of HOCl's bactericidal role revealed it to be a potent inducer of protein aggregation.[59] Hsp33, a chaperone known to be activated by oxidative heat stress, protects bacteria from the effects of HOCl by acting as a holdase, effectively preventing protein aggregation. Strains of Escherichia coli and Vibrio cholerae lacking Hsp33 were rendered especially sensitive to HOCl. Hsp33 protected many essential proteins from aggregation and inactivation due to HOCl, which is a probable mediator of HOCl's bactericidal effects.


Hypochlorites are the salts of hypochlorous acid; commercially important hypochlorites are calcium hypochlorite and sodium hypochlorite.

Production of hypochlorites using electrolysis

Solutions of hypochlorites can be produced in-situ by electrolysis of an aqueous sodium chloride solution in both batch and flow processes.[60] The composition of the resulting solution depends on the pH at the anode. In acid conditions the solution produced will have a high hypochlorous acid concentration, but will also contain dissolved gaseous chlorine, which can be corrosive, at a neutral pH the solution will be around 75% hypochlorous acid and 25% hypochlorite. Some of the chlorine gas produced will dissolve forming hypochlorite ions. Hypochlorites are also produced by the disproportionation of chlorine gas in alkaline solutions.


HOCl is classified as Non-Hazardous by the Environmental Protection Agency in the US. As any oxidising agent it can be corrosive or irritant depending on its concentration and pH.

In a clinical test, hypochlorous acid water was tested for eye irritation, skin irritation, and toxicity, they concluded that it is non-toxic, nonirritating to eye and skin.[61]

In a recent study, a saline hygiene solution preserved with pure hypochlorous acid was shown to reduce the bacterial load significantly without altering the diversity of bacterial species on the eyelids. After 20 minutes of treatment, there was >99% reduction of the Staphylococci bacteria.[62]


For disinfection, despite being discovered a long time ago, hypochlorous acid water's stability is difficult to maintain, in solution the active compounds quickly deteriorate back into salt water, losing its disinfecting capability, therefore it has been difficult to transport for wide use. Despite its stronger disinfecting capabilities due to cost it is not commonly used as a disinfectant compared to bleach and alcohol.

Technological developments have reduced manufacturing costs and allow for manufacturing and bottling of hypochlorous acid water for home and commercial use. However, most hypochlorous acid water has a short shelf life and is not suitable to keep for a long time. Storing away from heat and direct sunlight can help slow down the deterioration. The further development of continuous flow electrochemical cells has been implemented in new products, allowing the commercialisation of domestic and industrial continuous flow devices for the in-situ generation of hypochlorous acid for disinfection purposes.[63]

See also


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