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Isopropanol

Athanor · official

C3H8O · 60.1 g/mol

IUPAC name: propan-2-ol

Also called IPA, isopropyl alcohol, rubbing alcohol, 2-propanol

Open in Athanor
The structure of Isopropanol
Drawn from its SMILES with RDKit310
FlammableHarmful or irritantDangerHighly Flammable liquid and vapor · Causes serious eye irritation · May cause drowsiness or dizziness

Names and identifiers

IUPAC name
propan-2-ol
Synonyms
IPA, isopropyl alcohol, rubbing alcohol
+ 39 more

2-propanol, Isopropyl alcohol, 2-Propanol, Propan-2-ol, 2-Hydroxypropane, Dimethylcarbinol, sec-Propyl alcohol, Alkolave, Avantine, Hartosol, Petrohol, i-Propanol, 1-Methylethanol, Takineocol, Alcojel, Avantin, 2-Propyl alcohol, Alcolo, Isohol, Lavacol, Lutosol, Propol, Alcosolve 2, Imsol A, Alcosolve, Arquad DMCB, Spectrar, 1-Methylethyl alcohol, i-Propylalkohol, Combi-schutz, n-Propan-2-ol, Iso-propylalkohol, Isopropyl alcohol, rubbing, Alcool isopropilico, Alcool isopropylique, Visco 1152, sec-Propanol, Sterisol hand disinfectant, Iso-propyl alcohol

Molecular formula
C3H8O
Empirical formula
C3H8O
Molecular weight
60.1 g/mol
Exact mass
60.05751
CAS number
67-63-0
PubChem CID
3776
Canonical SMILES
CC(C)O
Isomeric SMILES
CC(C)O
InChI
InChI=1S/C3H8O/c1-3(2)4/h3-4H,1-2H3
InChIKey
KFZMGEQAYNKOFK-UHFFFAOYSA-N
Molfile

Names, InChI and the identifiers from PubChem, retrieved 2026-10-14.

Physical properties

TemperaturePressureDensity
Appearance
Colorless liquid[6]
6 values

From Hazardous Substances Data Bank (HSDB), the most authoritative source here.

ValueAs writtenSource
–Volatile, colorless liquid with a sharp musty odor like rubbing alcohol. Flash point of 53 °F. Vapors are heavier than air and mildly irritating to the eyes, nose, and throat. Density approximately 6.5 lb / gal. Used in making cosmetics, skin and hair preparations, pharmaceuticals, perfumes, lacquer formulations, dye solutions, antifreezes, soaps, window cleaners. Sold in 70% aqueous solution as rubbing alcohol.[1] CAMEO Chemicals
–Liquid; Liquid; Other Solid; Gas Vapor; Dry Powder; Other Solid; Wet Solid; Large Crystals; CBI[2] EPA Chemical Data Reporting (CDR)
–COLOURLESS LIQUID.[3] ILO-WHO International Chemical Safety Cards (ICSCs)
–Colorless liquid with the odor of rubbing alcohol.[4] Occupational Safety and Health Administration (OSHA)
–Colorless liquid with the odor of rubbing alcohol.[5] The National Institute for Occupational Safety and Health (NIOSH)
–shownColorless liquid[6] Hazardous Substances Data Bank (HSDB)cites Lewis, R.J. Sr.; Hawley's Condensed Chemical Dictionary 15th Edition. John Wiley & Sons, Inc. New York, NY 2007., p. 715
Odor
Pleasant odor[6]
2 values

From Hazardous Substances Data Bank (HSDB), the most authoritative source here.

ValueAs writtenSource
–shownPleasant odor[6] Hazardous Substances Data Bank (HSDB)cites Lewis, R.J. Sr.; Hawley's Condensed Chemical Dictionary 15th Edition. John Wiley & Sons, Inc. New York, NY 2007., p. 715
–Odor of rubbing alcohol[6] Hazardous Substances Data Bank (HSDB)cites NIOSH. NIOSH Pocket Guide to Chemical Hazards. Department of Health & Human Services, Centers for Disease Prevention & Control. National Institute for Occupational Safety & Health. DHHS (NIOSH) Publication No. 2010-168 (2010). Available from, as of Oct 3, 2011: https://www.cdc.gov/niosh/npg/
Melting point
-88.5 °C (-127.3 °F, NTP 1992)[1]
5 values

5 of 5 sources agree on it (most common value).

ValueAs writtenSource
−88.5 °Cshown-127.3 °F (NTP, 1992)[1] CAMEO Chemicalscites National Toxicology Program, Institute of Environmental Health Sciences, National Institutes of Health (NTP). 1992. National Toxicology Program Chemical Repository Database. Research Triangle Park, North Carolina.
−90 °C-90 °C[3] ILO-WHO International Chemical Safety Cards (ICSCs)
−88 °C-127 °F[4] Occupational Safety and Health Administration (OSHA)
−87.9 °C-87.9 °C[7] PAC Chemical Database, U.S. Department of Energy
−88 °C-127 °F[5] The National Institute for Occupational Safety and Health (NIOSH)
Boiling point
82.5 °C (180.5 °F) at 760 mmHg (NTP, 1992)[1]
5 values

5 of 5 sources agree on it (most common value).

ValueAs writtenSource
82.5 °Cshown180.5 °F at 760 mmHg (NTP, 1992)[1] CAMEO Chemicalscites National Toxicology Program, Institute of Environmental Health Sciences, National Institutes of Health (NTP). 1992. National Toxicology Program Chemical Repository Database. Research Triangle Park, North Carolina.
83 °C83 °C[3] ILO-WHO International Chemical Safety Cards (ICSCs)
83 °C181 °F[4] Occupational Safety and Health Administration (OSHA)
82.3 °C82.3 °C @760 [mm Hg][7] PAC Chemical Database, U.S. Department of Energy
83 °C181 °F[5] The National Institute for Occupational Safety and Health (NIOSH)
Density
0.7809 @25 °C[7]
5 values

5 of 5 sources agree on it (most common value).

ValueAs writtenSource
–0.785 at 68 °F (USCG, 1999) - Less dense than water[1] CAMEO Chemicalscites U.S. Coast Guard. 1999. Chemical Hazard Response Information System (CHRIS) - Hazardous Chemical Data. Commandant Instruction 16465.12C. Washington, D.C.: U.S. Government Printing Office.
–Relative density (water = 1): 0.79[3] ILO-WHO International Chemical Safety Cards (ICSCs)
–0.79[4] Occupational Safety and Health Administration (OSHA)
–shown0.7809 @25 °C[7] PAC Chemical Database, U.S. Department of Energy
–0.79[5] The National Institute for Occupational Safety and Health (NIOSH)

9 more values were reported but failed the checks (unreadable or out of range), so they are not shown.

Solubility in water
Solubility in water: miscible[3]
5 values

From ILO-WHO International Chemical Safety Cards (ICSCs), the most authoritative source here.

ValueAs writtenSource
–greater than or equal to 100 mg/mL at 72 °F (NTP, 1992)[1] CAMEO Chemicalscites National Toxicology Program, Institute of Environmental Health Sciences, National Institutes of Health (NTP). 1992. National Toxicology Program Chemical Repository Database. Research Triangle Park, North Carolina.
–Miscible with most organic solvents[6] Hazardous Substances Data Bank (HSDB)cites Clayton, G. D. and F. E. Clayton (eds.). Patty's Industrial Hygiene and Toxicology: Volume 2A, 2B, 2C: Toxicology. 3rd ed. New York: John Wiley Sons, 1981-1982., p. 4562
–In water, infinitely soluble at 25 °C[6] Hazardous Substances Data Bank (HSDB)cites Riddick, J.A., W.B. Bunger, Sakano T.K. Techniques of Chemistry 4th ed., Volume II. Organic Solvents. New York, NY: John Wiley and Sons., 1985., p. 196
–shownSolubility in water: miscible[3] ILO-WHO International Chemical Safety Cards (ICSCs)
–Miscible[5] The National Institute for Occupational Safety and Health (NIOSH)
log P
0.05[3]
2 values

2 of 2 sources agree on it (most common value).

ValueAs writtenSource
–log Kow = 0.05[6] Hazardous Substances Data Bank (HSDB)cites Hansch, C., Leo, A., D. Hoekman. Exploring QSAR - Hydrophobic, Electronic, and Steric Constants. Washington, DC: American Chemical Society., 1995., p. 7
–shown0.05[3] ILO-WHO International Chemical Safety Cards (ICSCs)
pKa
pKa = 17.10[6]
Vapor pressure
Vapor pressure, kPa at 20 °C: 4.4[3]
5 values

2 of 4 sources agree on it (most common value).

ValueAs writtenSource
33 mmHg33 mmHg at 68 °F[1] CAMEO Chemicalscites National Toxicology Program, Institute of Environmental Health Sciences, National Institutes of Health (NTP). 1992. National Toxicology Program Chemical Repository Database. Research Triangle Park, North Carolina.
40 mmHg40 mmHg at 74.8 °F (NTP, 1992)[1] CAMEO Chemicalscites National Toxicology Program, Institute of Environmental Health Sciences, National Institutes of Health (NTP). 1992. National Toxicology Program Chemical Repository Database. Research Triangle Park, North Carolina.
45.4 mmHg45.4 mm Hg at 25 °C[6] Hazardous Substances Data Bank (HSDB)cites Daubert, T.E., R.P. Danner. Physical and Thermodynamic Properties of Pure Chemicals Data Compilation. Washington, D.C.: Taylor and Francis, 1989.
33 mmHgshownVapor pressure, kPa at 20 °C: 4.4[3] ILO-WHO International Chemical Safety Cards (ICSCs)
75 mmHg75 [mm Hg] @33.6 °C[7] PAC Chemical Database, U.S. Department of Energy

2 more values were reported but failed the checks (unreadable or out of range), so they are not shown.

Flash point
11.7 °C c.c.[3]
6 values

5 of 5 sources agree on it (most common value).

ValueAs writtenSource
12 °C53 °F (NTP, 1992)[1] CAMEO Chemicalscites National Toxicology Program, Institute of Environmental Health Sciences, National Institutes of Health (NTP). 1992. National Toxicology Program Chemical Repository Database. Research Triangle Park, North Carolina.
12 °C12 °C, 53 °F (Closed cup)[6] Hazardous Substances Data Bank (HSDB)cites National Fire Protection Association; Fire Protection Guide to Hazardous Materials. 14TH Edition, Quincy, MA 2010, p. 325-77
24 °C75 °F (open cup) /91% isopropanol/[6] Hazardous Substances Data Bank (HSDB)cites Flick, E.W. Industrial Solvents Handbook. 3rd ed. Park Ridge, NJ: Noyes Publications, 1985., p. 223
11.7 °Cshown11.7 °C c.c.[3] ILO-WHO International Chemical Safety Cards (ICSCs)
12 °C53 °F[4] Occupational Safety and Health Administration (OSHA)
12 °C53 °F[5] The National Institute for Occupational Safety and Health (NIOSH)
Autoignition temperature
399 °C (750 °F)[6]
3 values

2 of 3 sources agree on it (most common value).

ValueAs writtenSource
399 °C750 °F (USCG, 1999)[1] CAMEO Chemicalscites U.S. Coast Guard. 1999. Chemical Hazard Response Information System (CHRIS) - Hazardous Chemical Data. Commandant Instruction 16465.12C. Washington, D.C.: U.S. Government Printing Office.
399 °Cshown399 °C (750 °F)[6] Hazardous Substances Data Bank (HSDB)cites National Fire Protection Association; Fire Protection Guide to Hazardous Materials. 14TH Edition, Quincy, MA 2010, p. 325-77
456 °C456 °C[3] ILO-WHO International Chemical Safety Cards (ICSCs)
Refractive index
index of refraction 1.3769 at 20 °C and sodium light, vapor pressure 4.5 kPa at 20 °C, viscosity 2.1 cp at 20 °C, completely soluble in water /91% isopropanol/[6]

Each value as its source reports it, with the source's number after it (listed under References). Where several sources report a property, the row shows the value most of them agree on, the rule the app uses; open the values to see every one.

Calculated

Heavy atoms
4
Rings
0
Aromatic rings
0
Fraction sp³ carbons (Fsp3)
1
H-bond donors
1
H-bond acceptors
1
Rotatable bonds
0
TPSA (Ų)
20.2
Formal charge
0
XLogP3
0.3 PubChem
Complexity
10 PubChem
Stereocenters
None
Double-bond geometry
None specified
Point group
C1 of one 3D conformer with its hydrogens, by Athanor’s engine (as in the app)

Elemental analysis

  • C59.96%
  • H13.42%
  • O26.62%

Isotope pattern

100%60.0573.4%61.06162.062

Each peak is a nominal mass with its abundance-weighted exact mass, as a percentage of the tallest, from IUPAC natural isotope abundances.

Computed from the structure with RDKit 2026.09 when this page was built, beside PubChem's own computed values from its record; where the two differ, both are shown.

Predicted

log P
0.39 Crippen (Wildman and Crippen 1999)
log S (water solubility)
-0.46 ESOL (Delaney 2004), log mol/L
Synthetic accessibility
1.74 SA score, 1 easy to 10 hard (Ertl and Schuffenhauer 2009)

Drug-likeness: Lipinski’s rule of five

  • Molecular weight ≤ 500: 60.1
  • log P ≤ 5 (Crippen): 0.39
  • H-bond donors ≤ 5: 1
  • H-bond acceptors ≤ 10: 1

Passes all four rules.

¹³C NMR shifts, predicted

Predictions, not measurements; each names its method. A measured log P, where a source reports one, is under Physical properties.

Safety

Danger

Harmonized EU classification (CLP Annex VI). Source [8].

  • Flammable
  • Harmful or irritant
310
NFPA 704[6]
  • H225Highly Flammable liquid and vapor
  • H319Causes serious eye irritation
  • H336May cause drowsiness or dizziness

Precautionary statements: P210, P233, P240, P241, P242, P243, P261, P264+P265, P271, P280, P303+P361+P353, P304+P340, P305+P351+P338, P319, P337+P317, P370+P378, P403+P233, P403+P235, P405, P501

View all classifications (4)
  • [8] Regulation (EC) No 1272/2008 of the European Parliament and of the Council · DangerH225, H319, H336
  • [8] Regulation (EC) No 1272/2008 of the European Parliament and of the Council · DangerH318, H400, H410
  • [9] European Chemicals Agency (ECHA)This chemical does not meet GHS hazard criteria for < 0.1% (3 of 8845) of reports.
  • [9] European Chemicals Agency (ECHA) · 8,845 reports · DangerH336

Exposure limits

  • PEL-TWA (8-Hour Time Weighted Average): 400 ppm (980 mg/m³)[4]
  • PEL: TWA 400 ppm (980 mg/m3) See Appendix G[5]
  • REL-STEL (Short Term Exposure Limit): 500 ppm (1225 mg/m³)[4]
  • REL: TWA 400 ppm (980 mg/m3) ST 500 ppm (1225 mg/m3)[5]
  • TLV: 200 ppm as TWA; 400 ppm as STEL; A4 (not classifiable as a human carcinogen); BEI issued.[3]
  • TLV-TWA (Time Weighted Average): 200 ppm [2001][4]

First aid

  • Eyes: First check the victim for contact lenses and remove if present. Flush victim's eyes with water or normal saline solution for 20 to 30 minutes while simultaneously calling a hospital or poison control center. Do not put any ointments, oils, or medication in the victim's eyes without specific instructions from a physician. Immediately transport the victim after flushing eyes to a hospital even if no symptoms (such as redness or irritation) develop. Skin: Immediately flood affected skin with water while removing and isolating all contaminated clothing.[1]
  • General First Aid: · Call 911 or emergency medical service. · Ensure that medical personnel are aware of the material(s) involved, take precautions to protect themselves and avoid contamination. · Move victim to fresh air if it can be done safely. · Administer oxygen if breathing is difficult. · If victim is not breathing: -- DO NOT perform mouth-to-mouth resuscitation; the victim may have ingested or inhaled the substance. -- If equipped and pulse detected, wash face and mouth, then give artificial respiration using a proper respiratory medical device (bag-valve mask, pocket mask equipped…[10]
  • General First Aid: · Call 911 or emergency medical service. · Ensure that medical personnel are aware of the material(s) involved, take precautions to protect themselves and avoid contamination. · Move victim to fresh air if it can be done safely. · Administer oxygen if breathing is difficult. · If victim is not breathing: -- DO NOT perform mouth-to-mouth resuscitation; the victim may have ingested or inhaled the substance. -- If equipped and pulse detected, wash face and mouth, then give artificial respiration using a proper respiratory medical device (bag-valve mask, pocket mask equipped…[10]
  • General First Aid: · Call 911 or emergency medical service. · Ensure that medical personnel are aware of the material(s) involved, take precautions to protect themselves and avoid contamination. · Move victim to fresh air if it can be done safely. · Administer oxygen if breathing is difficult. · If victim is not breathing: -- DO NOT perform mouth-to-mouth resuscitation; the victim may have ingested or inhaled the substance. -- If equipped and pulse detected, wash face and mouth, then give artificial respiration using a proper respiratory medical device (bag-valve mask, pocket mask equipped…[10]

Storage

  • Fireproof. Separated from strong oxidants. Cool. Well closed.[3]
  • Keep container tightly closed in a dry and well-ventilated place. Store at room temperature in the original container. Sensitive to light. Store in light-resistant containers. Keep away from heat and sources of ignition. Store in a segrated and approved area. Store away from incompatible materials. (isopropyl Alcohol, Reagent, ACS)[6]
  • Store in tightly closed containers in a cool, well ventilated area away from heat.[6]

Incompatibilities

  • During distillation of 2-propanol recovered from the reduction of crotonaldehyde with aluminium isopropoxide, a violent explosion occurred. This was attributed either to peroxidized diisopropyl ether (a possible by-product) or to peroxidized crotonaldehyde.[6]
  • Forms explosive mixtures with trinitromethane; hydrogen peroxide (similar in power and sensitivity to glyceryl nitrate). Reacts with barium perchlorate to form the highly explosive propyl perchlorate.[6]
  • When a stream of hydrogen entrained isopropyl alcohol vapors and palladium particles, the mixture caught fire on exposure to air.[6]
  • Two explosions occurred during laboratory distillation of isopropanol, one with a sample stored for 4 yr. No cause was apparent, but presence of traces of ketone(s) promoting peroxidation is a possibility. Previously, the presence of 0.36 molar peroxide had been reported in a 99.5% pure sample of isopropanol stored for several months in a partially full clear glass bottle in strong daylight.[6]

Safety data sheets on the supplier’s page: Aladdin Scientific, Smolecule, Angene Chemical.

Always read the supplier’s safety data sheet before working with it.

Spectra

Experimental spectra held by these sources; each link opens the source's own record.

Literature

Reading PubChem, OpenAlex and GSRS…

Bioactivity

Reading ChEMBL…

References

  1. [1]CAMEO Chemicals · Public domain (NOAA) · via PubChem · retrieved 2026-10-14
  2. [2]EPA Chemical Data Reporting (CDR) · Public domain (US EPA) · via PubChem · retrieved 2026-10-14
  3. [3]ILO-WHO International Chemical Safety Cards (ICSCs) · CC BY 4.0 · via PubChem · retrieved 2026-10-14
  4. [4]Occupational Safety and Health Administration (OSHA) · Public domain (US DOL) · via PubChem · retrieved 2026-10-14
  5. [5]The National Institute for Occupational Safety and Health (NIOSH) · Public domain (US CDC) · via PubChem · retrieved 2026-10-14
  6. [6]Hazardous Substances Data Bank (HSDB) · Public domain (US NLM) · via PubChem · retrieved 2026-10-14
  7. [7]PAC Chemical Database, U.S. Department of Energy · Public domain (US DOE) · via PubChem · retrieved 2026-10-14
  8. [8]Regulation (EC) No 1272/2008 of the European Parliament and of the Council · EU reuse policy, CC BY 4.0 · via PubChem · retrieved 2026-10-14
  9. [9]European Chemicals Agency (ECHA) · ECHA legal notice: reuse with acknowledgement · via PubChem · retrieved 2026-10-14
  10. [10]Emergency Response Guidebook (ERG) · Public domain (US DOT) · via PubChem · retrieved 2026-10-14
  11. [11]NMRShiftDB · Linked only · via PubChem · retrieved 2026-10-14
  12. [12]Human Metabolome Database (HMDB) · Linked only · via PubChem · retrieved 2026-10-14
  13. [13]SpectraBase · Linked only · via PubChem · retrieved 2026-10-14
  14. [14]MassBank of North America (MoNA) · CC BY 4.0 · via PubChem · retrieved 2026-10-14
  15. [15]NIST Mass Spectrometry Data Center · Linked only · via PubChem · retrieved 2026-10-14
  16. [16]MassBank Europe · Linked only · via PubChem · retrieved 2026-10-14
  17. ·Calculated values: computed by Athanor with RDKit 2026.09 from the structure.
  18. ·Literature on PubChem

Data last updated 2026-10-14.