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Details

Stereochemistry RACEMIC
Molecular Formula C3H9NO.BH3O3
Molecular Weight 136.943
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of (2-HYDROXYPROPYL)AMMONIUM DIHYDROGEN ORTHOBORATE

SMILES

OB(O)O.CC(O)CN

InChI

InChIKey=FWGLAJMZAXEFTA-UHFFFAOYSA-N
InChI=1S/C3H9NO.BH3O3/c1-3(5)2-4;2-1(3)4/h3,5H,2,4H2,1H3;2-4H

HIDE SMILES / InChI
Isopropanolamine (1-Amino-2-propanol) is a colorless to yellowish liquid with an amine-like odor. It is miscible in water. Intermediate used in the production of dyes, lubrification oils, corrosion inhibitor, detergents, cutting fluids.

Approval Year

Cmax

Cmax

ValueDoseCo-administeredAnalytePopulation
335 mg/L
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
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
Sourcing

Sourcing

Vendor/AggregatorIDURL
PubMed

PubMed

TitleDatePubMed
Thermal study of simple amino-alcohol solutions.
2002 Apr
Determination of the enantiomers of ketamine and norketamine in human plasma by enantioselective liquid chromatography-mass spectrometry.
2003 Aug 25
Determination of the configuration of 3,6-anhydrogalactose and cyclizable alpha-galactose 6-sulfate units in red seaweed galactans.
2003 Sep 26
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
Biomass in the manufacture of industrial products--the use of proteins and amino acids.
2007 Jun
2-amino-1-propanol versus 1-amino-2-propanol: valence band and C 1s core-level photoelectron spectra.
2007 Oct 14
Cloning and expression of the L-1-amino-2-propanol dehydrogenase gene from Rhodococcus erythropolis, and its application to double chiral compound production.
2008 Sep
Radioactive labeling of defined HPMA-based polymeric structures using [18F]FETos for in vivo imaging by positron emission tomography.
2009 Jul 13
Facile fabrication method and characterization of hollow Ag/SiO2 double-shelled spheres.
2009 Jul 7
Aqueous two-phase extraction of 2,3-butanediol from fermentation broths by isopropanol/ammonium sulfate system.
2009 Mar
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
Water-soluble polymer-drug conjugates for combination chemotherapy against visceral leishmaniasis.
2010 Apr 1
Enantioselective gel collapsing: a new means of visual chiral sensing.
2010 Jun 2
Patents
Name Type Language
(2-HYDROXYPROPYL)AMMONIUM DIHYDROGEN ORTHOBORATE
Systematic Name English
2-PROPANOL, 1-AMINO-, COMPD. WITH BORIC ACID (H3BO3) (1:1)
Systematic Name English
BORIC ACID (H3BO3), COMPD. WITH 1-AMINO-2-PROPANOL (1:1)
Systematic Name English
BORIC ACID COMPD. WITH 1-AMINO-2-PROPANOL (1:X)
Common Name English
Code System Code Type Description
CAS
68003-13-4
Created by admin on Sat Dec 16 08:12:02 GMT 2023 , Edited by admin on Sat Dec 16 08:12:02 GMT 2023
PRIMARY
PUBCHEM
161513
Created by admin on Sat Dec 16 08:12:02 GMT 2023 , Edited by admin on Sat Dec 16 08:12:02 GMT 2023
PRIMARY
FDA UNII
YK5M7W95MC
Created by admin on Sat Dec 16 08:12:02 GMT 2023 , Edited by admin on Sat Dec 16 08:12:02 GMT 2023
PRIMARY
CAS
26038-90-4
Created by admin on Sat Dec 16 08:12:02 GMT 2023 , Edited by admin on Sat Dec 16 08:12:02 GMT 2023
NON-SPECIFIC STOICHIOMETRY
EPA CompTox
DTXSID10892195
Created by admin on Sat Dec 16 08:12:02 GMT 2023 , Edited by admin on Sat Dec 16 08:12:02 GMT 2023
PRIMARY
ECHA (EC/EINECS)
247-422-3
Created by admin on Sat Dec 16 08:12:02 GMT 2023 , Edited by admin on Sat Dec 16 08:12:02 GMT 2023
PRIMARY