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2-Propanol

Drugs and Chemicals · NLM MeSH · updated 2026-10-31 · version 1

Citations verified against PubMedNot yet clinician-reviewed10 referencesApproximately 4 min read

An isomer of 1-propanol.

Table of Contents

1. Definition2. Research landscape3. Reading the evidence4. Open-access studies5. Key reviews6. References7. About this article

Definition and research guide

This page combines a MeSH definition, publication statistics and selected research abstracts. It is a starting point for reading the literature, not a medical textbook or a systematic evidence review.

Content available: 4 complete abstracts (853 words), 10 references. Full article text is not stored or reproduced here; follow the PMID, DOI or PMC links to read the original sources and their access terms.

Definition

An isomer of 1-propanol. It is a colorless liquid having disinfectant properties. It is used in the manufacture of acetone and its derivatives and as a solvent. Topically, it is used as an antiseptic.

Definition: NLM Medical Subject Headings (MeSH) scope note (Public domain (U.S. National Library of Medicine); attribution requested). View the MeSH record.

Also known as: 2 Propanol; Isopropanol; Isopropyl Alcohol; Alcohol, Isopropyl; Rubbing Alcohol; Alcohol, Rubbing.

Where it fits in the MeSH classification

Broader topics
Propanols

Related concepts

  • 1-Propanol

Research landscape

PubMed indexes 2,086 records tagged with the MeSH heading “2-Propanol” (counts retrieved 2026-10-31). 454 of them (21.8%) were published from 2020 onward, and the busiest period so far is 2010-2019 with 803 records.

Reviews account for 68 records (3.3%) and meta-analyses for 8. Randomized controlled trials number 95 (4.6%) as a share of all records on the topic.

PubMed records by publication periodthrough 1999: 128 records; 2000-2009: 701 records; 2010-2019: 803 records; 2020 onward: 454 records128through 19997012000-20098032010-20194542020 onward
Records in PubMed indexed with this heading, by publication period. Real counts from NCBI E-utilities; the final period covers only part of the current year. Volume reflects how much has been published, not how strong the evidence is.
Show the data
PeriodRecords
through 1999128
2000-2009701
2010-2019803
2020 onward454
Share of records by publication typeReviews: 3.3 percent; Meta-analyses: 0.4 percent; Randomized controlled trials: 4.6 percentReviews3.3% (68)Meta-analyses0.4% (8)Randomized controlled trials4.6% (95)
Share of all PubMed records on this heading that carry each publication type. Types overlap with other records, so the shares do not sum to 100%.
Publication-type chart data
Publication types among 2,086 PubMed records
TypeRecordsShare
Reviews683.3%
Meta-analyses80.4%
Randomized controlled trials954.6%

Method: PubMed query "2-Propanol"[MeSH Terms] with publication-type and date filters, retrieved 2026-10-31.

Reading the evidence in drugs and chemicals

Studies of a chemical or drug can answer very different questions: what it is and how it behaves in cells and animals, how the body handles it, and whether it changes outcomes in people. Laboratory and animal findings often do not carry over to patients, and observational studies of exposures are confounded by who uses a substance and why. Nothing on this page is a recommendation to use, avoid, start or stop any substance or medicine; talk to a qualified clinician or pharmacist about your own situation. Check the dose, the species, the comparison group and whether a patient-relevant outcome was measured.

Evidence from open-access studies

These open-access studies come from PubMed’s best-match results for this heading (papers whose main topic it is), ranked here by citation count, with one recent addition. Each abstract is reproduced in full under its recorded open licence so that you can read the authors’ own words. They illustrate the literature; they are not a systematic summary of it. Citation counts measure attention, not reliability or clinical benefit.

Study comparison — selected abstracts, not a systematic review
Study / authorsYearSource label / designEurope PMC citationsLicence / source
Alcohol abrogates human norovirus infectivity in a pH-dependent manner
Sato S, Matsumoto N, Hisaie K, Uematsu S
2020Research article
Design not recorded in structured metadata
27cc by
PMID 32985508 · DOI · PMC7522253
How long is enough? Identification of product dry-time as a primary driver of alcohol-based hand rub efficacy
Suchomel M, Leslie RA, Parker AE, Macinga DR
2018Research article
Design not recorded in structured metadata
22cc by
PMID 29796251 · DOI · PMC5956733
Improving isopropanol tolerance and production of Clostridium beijerinckii DSM 6423 by random mutagenesis and genome shuffling
Gérando HM, Fayolle-Guichard F, Rudant L, Millah SK, Monot F, Lopes Ferreira N, et al.
2016Research article
Design not recorded in structured metadata
21cc by
PMID 26852409 · DOI · PMC4875934
Dual-Functional Antenna Sensor for Highly Sensitive and Selective Detection of Isopropanol Gas Using Optimized Molecularly Imprinted Polymers
Hasan MM, Alev O, Cheffena M
2025Research article
Design not recorded in structured metadata
6cc by
PMID 39976381 · DOI · PMC11959604

Alcohol abrogates human norovirus infectivity in a pH-dependent manner [1]

Research article Sato S, Matsumoto N, Hisaie K, Uematsu S · · 2020 · cited 27 times (Europe PMC)

Abstract reading summary — source excerpts
Opening excerpt
Alcohol-based disinfectants are widely used for the sanitization of microorganisms, especially those that cause infectious diseases, including viruses.
Closing excerpt
Therefore, similar to sodium hypochlorite, alcohol-based disinfectants containing electrolytes can be used for HuNoV inactivation.
Interpretation limits
Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (149 words)

Alcohol-based disinfectants are widely used for the sanitization of microorganisms, especially those that cause infectious diseases, including viruses. However, since the germicidal mechanism of alcohol is lipolysis, alcohol-based disinfectants appear to have a minimal effect on non-enveloped viruses, such as noroviruses. Because there is no cultivation method for human norovirus (HuNoV) in vitro, murine norovirus and feline calicivirus have been used as surrogates for HuNoV to analyze the efficacy of disinfectant regents. Therefore, whether these disinfectants and their conditions are effective against HuNoVs remain unknown. In this study, we report that ethanol or isopropanol alone can sufficiently suppress GII.4 genotype HuNoV replication in human iPSC-derived intestinal epithelial cells. Additionally, pH adjustments and salting-out may contribute toward the virucidal effect of alcohol against other HuNoV genotypes and cancel the impediment of organic substance contamination, respectively. Therefore, similar to sodium hypochlorite, alcohol-based disinfectants containing electrolytes can be used for HuNoV inactivation.

Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 32985508 · DOI · PMC7522253

How long is enough? Identification of product dry-time as a primary driver of alcohol-based hand rub efficacy [2]

Research article Suchomel M, Leslie RA, Parker AE, Macinga DR · · 2018 · cited 22 times (Europe PMC)

Abstract reading summary — source excerpts
Opening excerpt
BackgroundThe World Health Organization has called for the development of improved methodologies to evaluate alcohol-based handrub (ABHR) efficacy, including evaluation at "short application times and volumes that reflect actual use in healthcare facilities".
Closing excerpt
ConclusionsWhen keeping other variables such as alcohol type and concentration constant, product dry-time appears to be the primary driver of ABHR efficacy suggesting that dosing should be customized to each individual and focus on achieving a product dry-time delivering adequate efficacy.
Interpretation limits
Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (231 words)

BackgroundThe World Health Organization has called for the development of improved methodologies to evaluate alcohol-based handrub (ABHR) efficacy, including evaluation at "short application times and volumes that reflect actual use in healthcare facilities". The objective of this study was to investigate variables influencing ABHR efficacy, under test conditions reflective of clinical use.MethodsThe test product (60% V/V 2-propanol) was evaluated according to a modified EN 1500 methodology, where application volumes of 1 mL, 2 mL, and 3 mL were rubbed until dry. Statistical analyses were performed to investigate the relative influences of product volume, hand size, and product dry-time on efficacy, and hand size and hand contamination on product dry-time.ResultsMean log10 reduction factors (SD) were 1.99 (0.66), 2.96 (0.84) and 3.28 (0.96); and mean dry-times (SD) were 24 s (7 s), 50 s (14 s), and 67 s (20 s) at application volumes of 1 mL, 2 mL, and 3 mL, respectively (p ≤ 0.030). When data were examined at the individual volunteer level, there was a statistically significant correlation between dry-time and log reduction factor (p p = 0.047), but no correlation between hand surface area and efficacy (p = 0.698).ConclusionsWhen keeping other variables such as alcohol type and concentration constant, product dry-time appears to be the primary driver of ABHR efficacy suggesting that dosing should be customized to each individual and focus on achieving a product dry-time delivering adequate efficacy.

Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 29796251 · DOI · PMC5956733

Improving isopropanol tolerance and production of Clostridium beijerinckii DSM 6423 by random mutagenesis and genome shuffling [3]

Research article Gérando HM, Fayolle-Guichard F, Rudant L, Millah SK, Monot F, Lopes Ferreira N, et al. · · 2016 · cited 21 times (Europe PMC)

Abstract reading summary — source excerpts
Opening excerpt
Random mutagenesis and genome shuffling was applied to improve solvent tolerance and isopropanol/butanol/ethanol (IBE) production in the strictly anaerobic bacteria Clostridium beijerinckii DSM 6423.
Closing excerpt
This tool also offers the possibility of obtaining improved strains of Clostridium species for which targeted genetic engineering approaches have not been described yet.
Interpretation limits
Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (223 words)

Random mutagenesis and genome shuffling was applied to improve solvent tolerance and isopropanol/butanol/ethanol (IBE) production in the strictly anaerobic bacteria Clostridium beijerinckii DSM 6423. Following chemical mutagenesis with N-methyl-N-nitro-N-nitrosoguanidine (NTG), screening of putatively improved strains was done by submitting the mutants to toxic levels of inhibitory chemicals or by screening for their tolerance to isopropanol (>35 g/L). Suicide substrates, such as ethyl or methyl bromobutyrate or alcohol dehydrogenase inhibitors like allyl alcohol, were tested and, finally, 36 mutants were isolated. The fermentation profiles of these NTG mutant strains were characterized, and the best performing mutants were used for consecutive rounds of genome shuffling. Screening of strains with further enhancement in isopropanol tolerance at each recursive shuffling step was then used to spot additionally improved strains. Three highly tolerant strains were finally isolated and able to withstand up to 50 g/L isopropanol on plates. Even if increased tolerance to the desired end product was not always accompanied by higher production capabilities, some shuffled strains showed increased solvent titers compared to the parental strains and the original C. beijerinckii DSM 6423. This study confirms the efficiency of genome shuffling to generate improved strains toward a desired phenotype such as alcohol tolerance. This tool also offers the possibility of obtaining improved strains of Clostridium species for which targeted genetic engineering approaches have not been described yet.

Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 26852409 · DOI · PMC4875934

Dual-Functional Antenna Sensor for Highly Sensitive and Selective Detection of Isopropanol Gas Using Optimized Molecularly Imprinted Polymers [4]

Research article Hasan MM, Alev O, Cheffena M · · 2025 · cited 6 times (Europe PMC)

Abstract reading summary — source excerpts
Opening excerpt
Accurate monitoring of isopropanol (IPA) levels is crucial for safety in industrial and laboratory settings, as high concentrations can lead to serious health issues.
Closing excerpt
Detailed optimization process and the sensing mechanism for a novel MIP-based selective antenna gas sensor, supported by both structural and electrical characterizations could serve as a milestone for future studies and the advancement of next-generation sensors.
Interpretation limits
Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (250 words)

Accurate monitoring of isopropanol (IPA) levels is crucial for safety in industrial and laboratory settings, as high concentrations can lead to serious health issues. In this study, we present, for the first time, a dual-functional antenna sensor capable of high-performance IPA gas detection with concentration estimation and uninterrupted wireless communication, using optimized molecularly imprinted polymer (MIP)/multiwalled carbon nanotube (MWCNT)-based sensing materials. Comprehensive characterization of these materials confirms the successful formation and homogeneity of the composites. Furthermore, the electrical and gas-sensing properties of the sensing materials were evaluated using functionalized interdigitated electrode (IDE)-based sensing structures, optimized for high sensitivity, were functionalized to evaluate the electrical and gas-sensing properties of the materials. These IDE structures, which acted as impedance-varying components during operation, were coupled with a single-port monopole antenna to develop a highly sensitive and selective gas sensor while maintaining uninterrupted communication services. The results showed that the fabricated sensor platform exhibits strong selectivity, sensitivity, and stability for IPA detection at room temperature, effectively distinguishing it from other interference gases. In addition, using the same sensing material, we demonstrated that the antenna-based gas sensor exhibited higher sensitivity than the chemiresistive sensor, achieving a detection limit (18.8 ppm) below the safety thresholds for IPA. Moreover, the antenna's radiation pattern and communication capabilities remained unaffected, ensuring uninterrupted functionality. Detailed optimization process and the sensing mechanism for a novel MIP-based selective antenna gas sensor, supported by both structural and electrical characterizations could serve as a milestone for future studies and the advancement of next-generation sensors.

Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 39976381 · DOI · PMC11959604

Key reviews and meta-analyses

The most cited review-type papers among PubMed’s best-match results for this heading, listed with bibliographic details only. Follow the links for the full text and access terms.

  • Research article Isopropanol poisoning [5]
    Slaughter RJ, Mason RW, Beasley DM, Vale JA, Schep LJ · Clin Toxicol (Phila) · 2014 · cited 93 times (Europe PMC)
  • Research article Ethylene glycol, methanol and isopropyl alcohol intoxication [6]
    Jammalamadaka D, Raissi S · Am J Med Sci · 2010 · cited 58 times (Europe PMC)
  • Research article Aromatherapy for treatment of postoperative nausea and vomiting [7]
    Hines S, Steels E, Chang A, Gibbons K · Cochrane Database Syst Rev · 2018 · cited 56 times (Europe PMC)
  • Research article Treatment of the alcohol intoxications: ethylene glycol, methanol and isopropanol [8]
    Abramson S, Singh AK · Curr Opin Nephrol Hypertens · 2000 · cited 46 times (Europe PMC)
  • Research article Application of a physiologically based pharmacokinetic model for isopropanol in the derivation of a reference dose and reference concentration [9]
    Gentry PR, Covington TR, Andersen ME, Clewell HJ · Regul Toxicol Pharmacol · 2002 · cited 43 times (Europe PMC)
  • Research article Isopropyl alcohol intoxication: a diagnostic challenge [10]
    Zaman F, Pervez A, Abreo K · Am J Kidney Dis · 2002 · cited 39 times (Europe PMC)

References

  1. Sato S, Matsumoto N, Hisaie K, Uematsu S. Alcohol abrogates human norovirus infectivity in a pH-dependent manner. . 2020. PMID 32985508 · DOI · PMC7522253
  2. Suchomel M, Leslie RA, Parker AE, Macinga DR. How long is enough? Identification of product dry-time as a primary driver of alcohol-based hand rub efficacy. . 2018. PMID 29796251 · DOI · PMC5956733
  3. Gérando HM, Fayolle-Guichard F, Rudant L, Millah SK, Monot F, Lopes Ferreira N, et al.. Improving isopropanol tolerance and production of Clostridium beijerinckii DSM 6423 by random mutagenesis and genome shuffling. . 2016. PMID 26852409 · DOI · PMC4875934
  4. Hasan MM, Alev O, Cheffena M. Dual-Functional Antenna Sensor for Highly Sensitive and Selective Detection of Isopropanol Gas Using Optimized Molecularly Imprinted Polymers. . 2025. PMID 39976381 · DOI · PMC11959604
  5. Slaughter RJ, Mason RW, Beasley DM, Vale JA, Schep LJ. Isopropanol poisoning. Clin Toxicol (Phila). 2014. PMID 24815348 · DOI
  6. Jammalamadaka D, Raissi S. Ethylene glycol, methanol and isopropyl alcohol intoxication. Am J Med Sci. 2010. PMID 20090509 · DOI
  7. Hines S, Steels E, Chang A, Gibbons K. Aromatherapy for treatment of postoperative nausea and vomiting. Cochrane Database Syst Rev. 2018. PMID 29523018 · DOI · PMC6494172
  8. Abramson S, Singh AK. Treatment of the alcohol intoxications: ethylene glycol, methanol and isopropanol. Curr Opin Nephrol Hypertens. 2000. PMID 11128434 · DOI
  9. Gentry PR, Covington TR, Andersen ME, Clewell HJ. Application of a physiologically based pharmacokinetic model for isopropanol in the derivation of a reference dose and reference concentration. Regul Toxicol Pharmacol. 2002. PMID 12383718 · DOI
  10. Zaman F, Pervez A, Abreo K. Isopropyl alcohol intoxication: a diagnostic challenge. Am J Kidney Dis. 2002. PMID 12200829 · DOI

About this article

Sources
NLM Medical Subject Headings (definition, synonyms); NCBI PubMed (counts, identifiers); Europe PMC (open-access abstracts and citation counts).
Verification
Every reference was resolved against PubMed on 2026-10-31; title, year and DOI matched.
Review state
automated source verified; no human expert review has been recorded yet.
Version
1, last updated 2026-10-31.

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At a glance

2,086
PubMed records on this heading
22%
published since 2020
68
review articles
95
randomized trials
10
verified references below

Counts come from PubMed on 2026-10-31; they show how much has been written, not how strong the evidence is.

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