Electronic Grade Isopropyl Alcohol (CAS 67-63-0)

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Electronic Grade Isopropyl Alcohol. CAS 67-63-0.

Free, and generated automatically from the sources listed on this page. No person has reviewed it, and it describes the substance in general — not your material, your process or your intended market.

REACH 2020/878
v1 · 02.09.2026

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Data transcribed from regulatory registers and technical literature, with the source and edition stated. It does not replace the supplier's safety data sheet. Fields without a recorded source are marked as such.

Chemical Overview: Isopropanol
Molecular formulaC3H8O[1]
Molecular weight60.1 g/mol[1]
Melting point-89.5 °C[1][2][3]
Boiling point82.3 °C (760 mmHg)[1][2][3][4]
Density0.7855 g/cm³[1][3]
LogP (lipophilicity)0.05[1]
pKa16.5
IUPAC namepropan-2-ol[1]
SMILESCC(C)O[1]
InChIKeyKFZMGEQAYNKOFK-UHFFFAOYSA-N[1]

Synonyms: Isopropyl alcohol · isopropanol · 2-Propanol · Propan-2-ol · 67-63-0

Data sources: PubChem (NLM/NIH), Yaws Handbook 2nd ed. (2014)
Last updated: 2026-09-02

📚 Scientific references (Chicago Author-Date) (4 sources)
  1. PubChem. National Center for Biotechnology Information (NIH/NLM), chemical compound database. dotyczy: Molecular formula · Molecular weight · Melting point · Boiling point · Density · LogP (lipophilicity) · IUPAC name · SMILES · InChIKey
  2. NIST. Chemistry WebBook, SRD 69. National Institute of Standards and Technology. dotyczy: Melting point · Boiling point
  3. Yaws, C.L. Thermophysical Properties of Chemicals and Hydrocarbons. 2nd ed. Amsterdam: Elsevier (Gulf Professional Publishing), 2014. dotyczy: Melting point · Boiling point · Density
  4. DECHEMA, PTB, and BAM. CHEMSAFE - Database of Evaluated Safety Characteristics for the Avoidance of Explosions. Frankfurt am Main: DECHEMA e.V.; Braunschweig/Berlin: Physikalisch-Technische Bundesanstalt and Bundesanstalt fur Materialforschung und -prufung. dotyczy: Boiling point

SCIENTIFIC RESEARCH

[1]Europe PMC2024
et al.. (2024). "Investigation of new 1,2,3-triazolyl-quinolinyl-propan-2-ol derivatives as potential antimicrobial agents: in vitro and in silico approach.". https://doi.org/10.1080/07391102.2023.221
[2]Europe PMC2023
et al.. (2023). "Novel phenoxy-((phenylethynyl) selanyl) propan-2-ol derivatives as potential anticancer agents.". https://doi.org/10.1186/s13065-023-01076-0
[3]Europe PMC2023
et al.. (2023). "Antifungal activity of Co(II) and Cu(II) complexes containing 1,3-bis(benzotriazol-1-yl)-propan-2-ol on the growth and virulence traits of fluconazole-resistant Candida species: synth
[4]Europe PMC2022
et al.. (2022). "Cardioprotective Effects of 1-(3,6-Dibromo-carbazol-9-yl)-3-Phenylamino-Propan-2-Ol in Diabetic Hearts via Nicotinamide Phosphoribosyltransferase Activation.". https://doi.org/10.1124
[5]Europe PMC2020
et al.. (2020). "Enantiodivergent syntheses of (+)- and (-)-1-(2,6-dimethylphenoxy)propan-2-ol: A way to access (+)- and (-)-mexiletine from D-(+)-mannitol.". https://doi.org/10.1016/j.carres.2019.107
[6]Europe PMC2020
et al.. (2020). "Discovery of a multipotent chaperone, 1-(2,6-Difluorobenzylamino)-3-(1,2,3,4-tetrahydrocarbazol-9-yl)-propan-2-ol with the inhibitory effects on the proliferation of prion, cancer as
[7]Europe PMC2019
et al.. (2019). "Isolation of 1-(3',4'-Dihydroxyphenyl)-3-(2″,4″,6″-trihydroxyphenyl)-propan-2-ol from Grape Seed Extract and Evaluation of its Antioxidant and Antispasmodic Potential.". https://doi.o
[8]Europe PMC2019
et al.. (2019). "Effect of Co-Inoculation with Saccharomyces cerevisiae and Lactic Acid Bacteria on the Content of Propan-2-ol, Acetaldehyde and Weak Acids in Fermented Distillery Mashes.". https://do
📚 Scientific references (Chicago Author-Date) 19 refs · 3 baz

MOLECULE Per-CAS bibliography (live from 13+ databases)

Sources: db:Europe PMC (14) · db:arxiv (1) · db:crossref (4)

  1. db:Europe PMC et al.. (2026). "Solvent-driven Radiolytic Transformation of Hcb in Propan-2-ol Under Gamma Irradiation". https://doi.org/10.21203/rs.3.rs-10536593/v1
  2. db:Europe PMC et al.. (2024). "Investigation of new 1,2,3-triazolyl-quinolinyl-propan-2-ol derivatives as potential antimicrobial agents: in vitro and in silico approach.". https://doi.org/10.1080/07391102.2023.2217922
  3. db:Europe PMC et al.. (2023). "Novel phenoxy-((phenylethynyl) selanyl) propan-2-ol derivatives as potential anticancer agents.". https://doi.org/10.1186/s13065-023-01076-0
  4. db:Europe PMC et al.. (2023). "Antifungal activity of Co(II) and Cu(II) complexes containing 1,3-bis(benzotriazol-1-yl)-propan-2-ol on the growth and virulence traits of fluconazole-resistant Candida species: synthesis, DFT calculations, and biological activity.". https://doi.org/10.1186/s13065-023-01037-7
  5. db:Europe PMC et al.. (2022). "Cardioprotective Effects of 1-(3,6-Dibromo-carbazol-9-yl)-3-Phenylamino-Propan-2-Ol in Diabetic Hearts via Nicotinamide Phosphoribosyltransferase Activation.". https://doi.org/10.1124/jpet.122.001122
  6. db:arxiv Szilvia Pothoczki, Ildikó Pethes, László Pusztai et al.. (2020). "Hydrogen bonding and percolation in propan-2-ol -- water liquid mixtures: X-ray diffraction experiments and computer simulations". arXiv (2001.11923v1). https://doi.org/10.1016/j.molliq.2021.115592
  7. db:Europe PMC et al.. (2020). "Enantiodivergent syntheses of (+)- and (-)-1-(2,6-dimethylphenoxy)propan-2-ol: A way to access (+)- and (-)-mexiletine from D-(+)-mannitol.". https://doi.org/10.1016/j.carres.2019.107892
  8. db:Europe PMC et al.. (2020). "Discovery of a multipotent chaperone, 1-(2,6-Difluorobenzylamino)-3-(1,2,3,4-tetrahydrocarbazol-9-yl)-propan-2-ol with the inhibitory effects on the proliferation of prion, cancer as well as influenza virus.". https://doi.org/10.1080/19336896.2020.1714372
  9. db:Europe PMC et al.. (2019). "Isolation of 1-(3',4'-Dihydroxyphenyl)-3-(2″,4″,6″-trihydroxyphenyl)-propan-2-ol from Grape Seed Extract and Evaluation of its Antioxidant and Antispasmodic Potential.". https://doi.org/10.3390/molecules24132466
  10. db:Europe PMC et al.. (2019). "Effect of Co-Inoculation with Saccharomyces cerevisiae and Lactic Acid Bacteria on the Content of Propan-2-ol, Acetaldehyde and Weak Acids in Fermented Distillery Mashes.". https://doi.org/10.3390/ijms20071659
  11. db:Europe PMC et al.. (2019). "A new member of a class of rod-like Mn12 single molecule magnets using 2-(pyridine-2-ly)propan-2-ol.". https://doi.org/10.1039/c9ra06280g
  12. db:Europe PMC (2017). "Crystal structure of naltrexone chloride solvates with ethanol, propan-2-ol, and 2-methyl-propan-2-ol.". https://doi.org/10.1107/s205698901700843x
  13. db:Europe PMC et al.. (2017). "Crystal structure of 1,3-bis-[(E)-benzyl-idene-amino]-propan-2-ol.". https://doi.org/10.1107/s2056989017004741
  14. db:Europe PMC et al.. (2016). "Crystal structure of 1,3-bis-[(E)-4-meth-oxy-benzyl-idene-amino]-propan-2-ol.". https://doi.org/10.1107/s2056989016016947
  15. db:Europe PMC et al.. (2015). "Crystal structure of di-bromido-tetra-kis(propan-2-ol-κO)nickel(II).". https://doi.org/10.1107/s2056989015023555
  16. db:crossref Yihe Wang, Weidong Yan. (2010). "Excess Molar Volumes of 1,3-Diethyl Propanedioate with Methanol, Ethanol, Propan-1-ol, Propan-2-ol, Butan-2-ol, 2-Methyl-propan-1-ol, and Pentan-1-ol at T = (288.15, 298.15, 313.15, and 328.15) K". Journal of Chemical & Engineering Data. https://doi.org/10.1021/je100100n
  17. db:crossref Kazuhiro Tamura, Isamu Nagata. (1991). "Excess molar enthalipies of (propan-1-ol + butan-2-one) and of (propan-1-ol or propan-2-ol + butan-2-one + benzene) at the temperature 298.15 K". The Journal of Chemical Thermodynamics. https://doi.org/10.1016/s0021-9614(05)80090-4
  18. db:crossref Isamu Nagata, Kazuhiro Tamura. (1988). "Excess molar enthalpies of (propan-1-ol or propan-2-ol + acetonitrile), (propan-1-ol or propan-2-ol + chlorobenzene), and (propan-1-ol or propan-2-ol + acetonitrile + chlorobenzene) at 298.15 K". The Journal of Chemical Thermodynamics. https://doi.org/10.1016/0021-9614(88)90212-1
  19. db:crossref DJT Hill, C Malar. (1975). "The enthalpies of solution of ethanol, propan-1-ol, propan-2-ol and butan-1-ol in deuterium oxide". Australian Journal of Chemistry. https://doi.org/10.1071/ch9750007
Regulatory status of the substance
This substance is subject to regulatory requirements: hazardous waste management (BDO register). Details in the \"Regulatory Status (REACH/ECHA/CLP)\" section and on the SDS. Regulatory information — does not restrict purchase in this store.
🧪 Chemical Data
CAS Number
67-63-0
Molecular formula
C3H8O
Molar mass
60.10 g/mol
IUPAC name (EN)
propan-2-ol
SMILES
CC(C)O
InChIKey
KFZMGEQAYNKOFK-UHFFFAOYSA-N
⚗️ Physicochemical properties
Temp. wrzenia
82.4
Temp. topnienia
-87.4
Density
0.785

Source: PubChem, NIST WebBook. Last updated: 2026-09-02

🔍 External identifiers
15 of 16 ID systems94%
DatabaseIdentifierActions
CAS Registry Number67-63-0Open →
PubChem CID3776[1]Open →
InChIKeyKFZMGEQAYNKOFK-UHFFFAOYSA-N[1]Open →
InChIInChI=1S/C3H8O/c1-3(2)4/h3-4H,1-2H3[1]
SMILESCC(C)O[1]
EC Number200-661-7[2]Open →
ChEMBLCHEMBL582[3]Open →
DrugBankDB02325Open →
KEGG CompoundD00137Open →
HMDBHMDB0000863Open →
ChemSpider3644[4]Open →
MeSH UID (NLM)D019840Open →
UNII (FDA)ND2M416302Open →
NSC Number (NCI)135801Open →
WikiData QIDQ16392Open →

Sources: PubChem (NIH), Wikidata SPARQL, KEGG, ChEMBL (EBI), CompTox CTX (EPA).

📚 Scientific references (Chicago Author-Date) (4 sources)
  1. PubChem. National Center for Biotechnology Information (NIH/NLM), chemical compound database. dotyczy: PubChem CID · InChIKey · InChI · SMILES
  2. ECHA. EC Inventory — EINECS, ELINCS, NLP and List Numbers assigned under REACH. Helsinki: European Chemicals Agency. dotyczy: EC Number
  3. ChEMBL. European Bioinformatics Institute (EMBL-EBI), bioactivity database. dotyczy: ChEMBL
  4. ChemSpider. Royal Society of Chemistry, chemical structure database. dotyczy: ChemSpider

Dalsza literatura

Publications topically related to this CAS. They are not the source of any value given on this card.

Extended Bibliography (4)

  1. ★★☆☆☆ CROSSREF 🔓 OPEN ❓ unverified Anonymous. 2026. "Review for "Tuning Ionically Cross-Linked Proton Exchange Membranes to Control Isopropanol Permeability and Ionomer Durability in Direct Isopropanol Fuel Cells.". https://doi.org/10.1039/d6ta04504a/v1/review1. link [accessed: 2026-09-02] CC0 (metadata)
  2. ★★☆☆☆ CROSSREF 🔓 OPEN ❓ unverified Martnez, Sonia, Edwards, Jos. 1981. "Thermodynamics of the isopropanol/n-hexane and isopropanol/n-heptane systems part II. NMR studies." Monatshefte fr Chemie 112 (6-7): 683-695. https://doi.org/10.1007/bf00899771. link [accessed: 2026-09-02] CC0 (metadata)
  3. ★★☆☆☆ CROSSREF 🔓 OPEN ❓ unverified Barraza, Raul, Edwards, Jose. 1981. "Thermodynamics of the isopropanol/n-hexane and isopropanol/n-heptane systems. Part III. Gas/liquid equilibrium." Monatshefte fr Chemie 112 (8-9): 925-933. https://doi.org/10.1007/bf00905064. link [accessed: 2026-09-02] CC0 (metadata)
  4. ★★☆☆☆ CROSSREF 🔓 OPEN ❓ unverified Anonymous. "isoPropyl alcohol (isopropanol).". https://doi.org/10.3403/30307203. link [accessed: 2026-09-02] CC0 (metadata)

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Electronic Grade Isopropyl Alcohol — CAS 67-63-0. Listed by Xilong Scientific. Prepared from the supplier’s public catalogue; not verified against their internal data.

Data from PubChemSource: PubChem (NIH) · ChEMBL