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 |
|---|---|---|---|---|
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 |
|
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 |
PubMed
| Title | Date | PubMed |
|---|---|---|
| The mechanism of action of ethanolamine ammonia-lyase, an adenosylcobalamin-dependent enzyme. Studies with isopropanolamine, a true substrate. | 1980 Aug 10 |
|
| Vibrational circular dichroism spectrum of 1-amino-2-propanol. | 2002 Jul-Oct |
|
| Determination of the configuration of 3,6-anhydrogalactose and cyclizable alpha-galactose 6-sulfate units in red seaweed galactans. | 2003 Sep 26 |
|
| Chiral ligand exchange capillary electrophoresis using borate anion as a central ion. | 2004 Dec |
|
| Highly enantioselective ruthenium-catalyzed reduction of ketones employing readily available Peptide ligands. | 2004 Jan 5 |
|
| Cassette dosing pharmacokinetics of a library of 2,6,9-trisubstituted purine cyclin-dependent kinase 2 inhibitors prepared by parallel synthesis. | 2004 Mar |
|
| Persistence and biodegradation of monoethanolamine and 2-propanolamine at an abandoned industrial site. | 2005 May 15 |
|
| Stability-indicating methods for the determination of piretanide in presence of the alkaline induced degradates. | 2005 Oct 4 |
|
| 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 Oct |
|
| Biomass in the manufacture of industrial products--the use of proteins and amino acids. | 2007 Jun |
|
| 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 Jan 13 |
|
| Radioactive labeling of defined HPMA-based polymeric structures using [18F]FETos for in vivo imaging by positron emission tomography. | 2009 Jul 13 |
|
| N-(2-hydroxypropyl)methacrylamide-amphotericin B (HPMA-AmB) copolymer conjugates as antileishmanial agents. | 2009 May |
|
| 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 Nov 6 |
|
| Effects of electrochemical reduction reactions on the biodegradation of recalcitrant organic compounds (ROCs) and bacterial community diversity. | 2010 Aug |
|
| Dental DNA fingerprinting in identification of human remains. | 2010 Jul |
|
| Translation elongation factor 1A facilitates the assembly of the tombusvirus replicase and stimulates minus-strand synthesis. | 2010 Nov 4 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 18:05:06 GMT 2023
by
admin
on
Fri Dec 15 18:05:06 GMT 2023
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| Record UNII |
ND2M416302
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| Record Status |
Validated (UNII)
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| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
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CFR |
21 CFR 172.515
Created by
admin on Fri Dec 15 18:05:06 GMT 2023 , Edited by admin on Fri Dec 15 18:05:06 GMT 2023
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Food Contact Sustance Notif, (FCN No.) |
FCN NO. 1028
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IARC | Isopropyl alcohol | ||
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WHO-VATC |
QD08AX05
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EPA PESTICIDE CODE |
47501
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admin on Fri Dec 15 18:05:06 GMT 2023 , Edited by admin on Fri Dec 15 18:05:06 GMT 2023
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CFR |
21 CFR 862.3040
Created by
admin on Fri Dec 15 18:05:06 GMT 2023 , Edited by admin on Fri Dec 15 18:05:06 GMT 2023
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CFR |
21 CFR 344.12
Created by
admin on Fri Dec 15 18:05:06 GMT 2023 , Edited by admin on Fri Dec 15 18:05:06 GMT 2023
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NCI_THESAURUS |
C218
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admin on Fri Dec 15 18:05:06 GMT 2023 , Edited by admin on Fri Dec 15 18:05:06 GMT 2023
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WHO-ATC |
D08AX05
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admin on Fri Dec 15 18:05:06 GMT 2023 , Edited by admin on Fri Dec 15 18:05:06 GMT 2023
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JECFA EVALUATION |
ISOPROPYL ALCOHOL
Created by
admin on Fri Dec 15 18:05:06 GMT 2023 , Edited by admin on Fri Dec 15 18:05:06 GMT 2023
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CFR |
21 CFR 173.240
Created by
admin on Fri Dec 15 18:05:06 GMT 2023 , Edited by admin on Fri Dec 15 18:05:06 GMT 2023
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| Code System | Code | Type | Description | ||
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200-661-7
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PRIMARY | |||
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ISOPROPYL ALCOHOL
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admin on Fri Dec 15 18:05:06 GMT 2023 , Edited by admin on Fri Dec 15 18:05:06 GMT 2023
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PRIMARY | |||
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797541
Created by
admin on Fri Dec 15 18:05:06 GMT 2023 , Edited by admin on Fri Dec 15 18:05:06 GMT 2023
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PRIMARY | RxNorm | ||
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100000092875
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PRIMARY | |||
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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 Fri Dec 15 18:05:06 GMT 2023 , Edited by admin on Fri Dec 15 18:05:06 GMT 2023
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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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D019840
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405
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ND2M416302
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m6524
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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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PRIMARY |
| 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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