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Chlorhexidine
[CAS# 55-56-1]

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Identification
ClassificationAPI >> Synthetic anti-infective drugs >> Disinfectant antiseptic
NameChlorhexidine
SynonymsBis(5-(p-chlorophenyl)biguanidinio)hexane; Hexamethylenebis(5-(4-chlorophenyl)biguanide); N,N'-Bis(4-chlorophenyl)-3,12-diimino-tetraazatetradecanediimidamide
Molecular StructureCAS # 55-56-1, Chlorhexidine
Molecular FormulaC22H30Cl2N10
Molecular Weight505.45
CAS Registry Number55-56-1
EC Number200-238-7
SMILESC1=CC(=CC=C1N/C(=N/C(=NCCCCCCN=C(/N=C(/NC2=CC=C(C=C2)Cl)N)N)N)/N)Cl
Properties
Melting point134-136 °C (Expl.)
Solubilitywater: soluble 0.08% (20 °C) (Expl.)
Safety Data
Hazard Symbolssymbol symbol symbol symbol   GHS05;GHS07;GHS08;GHS09 Danger  Details
Risk StatementsH302-H315-H318-H319-H334-H335-H373-H400-H410  Details
Safety StatementsP233-P260-P261-P264-P264+P265-P270-P271-P273-P280-P284-P301+P317-P302+P352-P304+P340-P305+P351+P338-P305+P354+P338-P317-P319-P321-P330-P332+P317-P337+P317-P342+P316-P362+P364-P391-P403-P403+P233-P405-P501  Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Chronic hazardous to the aquatic environmentAquatic Chronic1H410
Acute hazardous to the aquatic environmentAquatic Acute1H400
Eye irritationEye Irrit.2H319
Skin irritationSkin Irrit.2H315
Serious eye damageEye Dam.1H318
Respiratory sensitizationResp. Sens.1H334
Specific target organ toxicity - single exposureSTOT SE3H335
Specific target organ toxicity - repeated exposureSTOT RE2H373
Acute toxicityAcute Tox.4H302
Chronic hazardous to the aquatic environmentAquatic Chronic2H411
Skin sensitizationSkin Sens.1H317
Transport InformationUN 3077
SDSAvailable
up Discovery and Applications
Chlorhexidine is a widely used antiseptic and disinfectant belonging to the class of biguanide compounds. Chemically, it is known as 1,1'-hexamethylenebis[5-(4-chlorophenyl)biguanide], with the molecular formula C22H30Cl2N10. Chlorhexidine was first synthesized in the 1950s and introduced into medical practice due to its broad-spectrum antimicrobial activity and relative safety for topical use.

The discovery of chlorhexidine was motivated by the search for effective antiseptics that could combat a wide range of bacteria, fungi, and some viruses. It demonstrated strong bactericidal and bacteriostatic properties by disrupting microbial cell membranes and precipitating cellular contents, leading to cell death. Chlorhexidine’s mechanism involves binding to negatively charged bacterial cell walls and increasing permeability, causing leakage of intracellular components.

Clinically, chlorhexidine is used in various formulations including solutions, gels, mouthwashes, and impregnated dressings. It is commonly applied for skin disinfection before surgery, oral hygiene to reduce dental plaque and gingivitis, wound care, and sterilization of surgical instruments. Its use in dentistry is widespread due to its efficacy in controlling oral biofilms and reducing dental caries and periodontal disease.

Chlorhexidine exhibits activity against Gram-positive and Gram-negative bacteria, yeasts such as Candida species, and some enveloped viruses. However, it has limited effect against bacterial spores and certain non-enveloped viruses. The compound’s antimicrobial spectrum and substantivity—the ability to adhere to surfaces and release slowly—make it valuable for prolonged antiseptic action.

Pharmacokinetically, chlorhexidine is poorly absorbed through intact skin or mucous membranes, minimizing systemic exposure during topical application. However, ingestion or parenteral use is contraindicated due to potential toxicity. Local adverse effects may include skin irritation, allergic reactions, and staining of teeth and oral mucosa with prolonged use in mouthwash formulations.

Resistance to chlorhexidine is relatively uncommon but has been reported, often involving changes in bacterial cell membrane composition or efflux pump activity. Its broad use has prompted studies on appropriate concentrations and exposure times to reduce the risk of resistance development.

Analytical techniques for chlorhexidine include ultraviolet-visible (UV-Vis) spectrophotometry, high-performance liquid chromatography (HPLC), and mass spectrometry (MS), which allow quantification in pharmaceutical products and biological samples. These methods ensure quality control and support pharmacokinetic and safety evaluations.

In summary, chlorhexidine is a synthetic biguanide antiseptic with broad antimicrobial activity used extensively in medical and dental fields. Its mechanism of disrupting microbial membranes underlies its effectiveness, and its versatile formulations enable applications ranging from skin disinfection to oral hygiene. The compound remains an essential antiseptic due to its efficacy, safety, and prolonged action on treated surfaces.

References

1987. The effect on early plaque formation, gingivitis and salivary bacterial counts of mouthwashes containing hexetidine/zinc, aminefluoride/tin or chlorhexidine. Journal of Clinical Periodontology, 14(8).
DOI: 10.1111/j.1600-051x.1987.tb00992.x

1987. Periodic subgingival antimicrobial irrigation of periodontal pockets. II. Microbiological and radiographical observations. Journal of Clinical Periodontology, 14(9).
DOI: 10.1111/j.1600-051x.1987.tb00997.x

1987. Prolonged oral reduction of Streptococcus mutans in humans after chlorhexidine disinfection followed by fluoride treatment. Scandinavian journal of dental research, 95(4).
DOI: 10.1111/j.1600-0722.1987.tb01847.x
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List of Reports Available for Chlorhexidine
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