Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C3H8O |
| Molecular Weight | 60.095 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(C)O
InChI
InChIKey=KFZMGEQAYNKOFK-UHFFFAOYSA-N
InChI=1S/C3H8O/c1-3(2)4/h3-4H,1-2H3
| Molecular Formula | C3H8O |
| Molecular Weight | 60.095 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
Cmax
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
258 mg/L EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/2914047/ |
21 mL single, oral dose: 21 mL route of administration: Oral experiment type: SINGLE co-administered: |
ISOPROPYL ALCOHOL serum | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FASTED |
|
335 mg/L EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/2914047/ |
21 mL single, oral dose: 21 mL route of administration: Oral experiment type: SINGLE co-administered: |
ACETONE serum | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FASTED |
PubMed
| Title | Date | PubMed |
|---|---|---|
| Translation elongation factor 1A facilitates the assembly of the tombusvirus replicase and stimulates minus-strand synthesis. | 2010-11-04 |
|
| Effects of electrochemical reduction reactions on the biodegradation of recalcitrant organic compounds (ROCs) and bacterial community diversity. | 2010-08 |
|
| Dental DNA fingerprinting in identification of human remains. | 2010-07 |
|
| Enantioselective gel collapsing: a new means of visual chiral sensing. | 2010-06-02 |
|
| Water-soluble polymer-drug conjugates for combination chemotherapy against visceral leishmaniasis. | 2010-04-01 |
|
| A phylogenetic estimate for golden moles (Mammalia, Afrotheria, Chrysochloridae). | 2010-03-09 |
|
| Molecular structure and hydrogen bonding of 2-aminoethanol, 1-amino-2-propanol, 3-amino-1-propanol, and binary mixtures with water studied by Fourier transform near-infrared spectroscopy and density functional theory calculations. | 2010-03 |
|
| Charge-transfer complexes of 4-nitrocatechol with some amino alcohols. | 2010-03 |
|
| Comparative application of microwave, ultrasonication, ultracentrifugation and conventional heating for preparation of sample as dinitrophenyl derivative for direct enantioseparation of certain amino alcohols and 1-amino-2-propanol from vitamin B12 hydrolysate on alpha1-acid glycoprotein and beta-cyclodextrin columns. | 2009-11-06 |
|
| Radioactive labeling of defined HPMA-based polymeric structures using [18F]FETos for in vivo imaging by positron emission tomography. | 2009-07-13 |
|
| Facile fabrication method and characterization of hollow Ag/SiO2 double-shelled spheres. | 2009-07-07 |
|
| N-(2-hydroxypropyl)methacrylamide-amphotericin B (HPMA-AmB) copolymer conjugates as antileishmanial agents. | 2009-05 |
|
| Aqueous two-phase extraction of 2,3-butanediol from fermentation broths by isopropanol/ammonium sulfate system. | 2009-03 |
|
| Photolysis of adenosylcobalamin and radical pair recombination in ethanolamine ammonia-lyase probed on the micro- to millisecond time scale by using time-resolved optical absorption spectroscopy. | 2009-01-13 |
|
| Cloning and expression of the L-1-amino-2-propanol dehydrogenase gene from Rhodococcus erythropolis, and its application to double chiral compound production. | 2008-09 |
|
| Combination chemotherapy and photodynamic therapy with fab' fragment targeted HPMA copolymer conjugates in human ovarian carcinoma cells. | 2008-08-30 |
|
| 2-amino-1-propanol versus 1-amino-2-propanol: valence band and C 1s core-level photoelectron spectra. | 2007-10-14 |
|
| Biomass in the manufacture of industrial products--the use of proteins and amino acids. | 2007-06 |
|
| A novel NADP+-dependent L-1-amino-2-propanol dehydrogenase from Rhodococcus erythropolis MAK154: a promising enzyme for the production of double chiral aminoalcohols. | 2006-10 |
|
| 1,4-Benzodiazepine N-nitrosoamidines: useful intermediates in the synthesis of tricyclic benzodiazepines. | 2006-08-09 |
|
| Stability-indicating methods for the determination of piretanide in presence of the alkaline induced degradates. | 2005-10-04 |
|
| Persistence and biodegradation of monoethanolamine and 2-propanolamine at an abandoned industrial site. | 2005-05-15 |
|
| Chiral ligand exchange capillary electrophoresis using borate anion as a central ion. | 2004-12 |
|
| Cassette dosing pharmacokinetics of a library of 2,6,9-trisubstituted purine cyclin-dependent kinase 2 inhibitors prepared by parallel synthesis. | 2004-03 |
|
| Highly enantioselective ruthenium-catalyzed reduction of ketones employing readily available Peptide ligands. | 2004-01-05 |
|
| Determination of the configuration of 3,6-anhydrogalactose and cyclizable alpha-galactose 6-sulfate units in red seaweed galactans. | 2003-09-26 |
|
| Novel diphenylalkyl piperazine derivatives with high affinities for the dopamine transporter. | 2003-09-01 |
|
| Determination of the enantiomers of ketamine and norketamine in human plasma by enantioselective liquid chromatography-mass spectrometry. | 2003-08-25 |
|
| Composition and structure of agents responsible for development of water repellency in soils following oil contamination. | 2003-07-01 |
|
| Vibrational circular dichroism spectrum of 1-amino-2-propanol. | 2002-09-11 |
|
| Cytotoxicity of amino alcohols to rat hepatoma-derived Fa32 cells. | 2002-07-11 |
|
| Thermal study of simple amino-alcohol solutions. | 2002-04 |
|
| Myotropic effects of new proctolin analogues modified in the position 5 of peptide chain in insects. | 2002-01-12 |
|
| The mechanism of action of ethanolamine ammonia-lyase, an adenosylcobalamin-dependent enzyme. Studies with isopropanolamine, a true substrate. | 1980-08-10 |
Patents
| Substance Class |
Chemical
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by
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on
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Mon Mar 31 19:01:50 GMT 2025
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on
Mon Mar 31 19:01:50 GMT 2025
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| Record UNII |
ND2M416302
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Validated (UNII)
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| Classification Tree | Code System | Code | ||
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CFR |
21 CFR 172.515
Created by
admin on Mon Mar 31 19:01:50 GMT 2025 , Edited by admin on Mon Mar 31 19:01:50 GMT 2025
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Food Contact Sustance Notif, (FCN No.) |
FCN NO. 1028
Created by
admin on Mon Mar 31 19:01:50 GMT 2025 , Edited by admin on Mon Mar 31 19:01:50 GMT 2025
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IARC | Isopropyl alcohol | ||
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WHO-VATC |
QD08AX05
Created by
admin on Mon Mar 31 19:01:50 GMT 2025 , Edited by admin on Mon Mar 31 19:01:50 GMT 2025
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EPA PESTICIDE CODE |
47501
Created by
admin on Mon Mar 31 19:01:50 GMT 2025 , Edited by admin on Mon Mar 31 19:01:50 GMT 2025
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CFR |
21 CFR 862.3040
Created by
admin on Mon Mar 31 19:01:50 GMT 2025 , Edited by admin on Mon Mar 31 19:01:50 GMT 2025
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CFR |
21 CFR 344.12
Created by
admin on Mon Mar 31 19:01:50 GMT 2025 , Edited by admin on Mon Mar 31 19:01:50 GMT 2025
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NCI_THESAURUS |
C218
Created by
admin on Mon Mar 31 19:01:50 GMT 2025 , Edited by admin on Mon Mar 31 19:01:50 GMT 2025
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WHO-ATC |
D08AX05
Created by
admin on Mon Mar 31 19:01:50 GMT 2025 , Edited by admin on Mon Mar 31 19:01:50 GMT 2025
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JECFA EVALUATION |
ISOPROPYL ALCOHOL
Created by
admin on Mon Mar 31 19:01:50 GMT 2025 , Edited by admin on Mon Mar 31 19:01:50 GMT 2025
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CFR |
21 CFR 173.240
Created by
admin on Mon Mar 31 19:01:50 GMT 2025 , Edited by admin on Mon Mar 31 19:01:50 GMT 2025
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| Code System | Code | Type | Description | ||
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200-661-7
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ISOPROPYL ALCOHOL
Created by
admin on Mon Mar 31 19:01:50 GMT 2025 , Edited by admin on Mon Mar 31 19:01:50 GMT 2025
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797541
Created by
admin on Mon Mar 31 19:01:50 GMT 2025 , Edited by admin on Mon Mar 31 19:01:50 GMT 2025
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PRIMARY | RxNorm | ||
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100000092875
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SUB12085MIG
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ND2M416302
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116
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17824
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135801
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67-63-0
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4215
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1570428
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ISOPROPYL ALCOHOL
Created by
admin on Mon Mar 31 19:01:50 GMT 2025 , Edited by admin on Mon Mar 31 19:01:50 GMT 2025
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PRIMARY | Description: A colourless, clear, and mobile liquid; odour, characteristic. Miscibility: Miscible with water, ethanol (~750 g/l) TS and ether R. Category: Solvent; antiseptic. Storage: 2-Propanol should be kept in a tightly closed container. Additional information: 2-Propanol is volatile and flammable. Boiling range, 81-83 ?C. | ||
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DB02325
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admin on Mon Mar 31 19:01:50 GMT 2025 , Edited by admin on Mon Mar 31 19:01:50 GMT 2025
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D019840
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405
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ND2M416302
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m6524
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admin on Mon Mar 31 19:01:50 GMT 2025 , Edited by admin on Mon Mar 31 19:01:50 GMT 2025
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PRIMARY | Merck Index | ||
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3776
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CHEMBL582
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C602
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DTXSID7020762
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| Related Record | Type | Details | ||
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SALT/SOLVATE -> PARENT |
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SALT/SOLVATE -> PARENT |
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SALT/SOLVATE -> PARENT |
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| Related Record | Type | Details | ||
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PARENT -> IMPURITY |
CHROMATOGRAPHIC PURITY (GC)
EP
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| Related Record | Type | Details | ||
|---|---|---|---|---|
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ACTIVE MOIETY |
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