U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C8H19O4P.C6H15NO3
Molecular Weight 359.396
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TRIETHANOLAMINE OCTYLPHOSPHATE

SMILES

OCCN(CCO)CCO.CCCCCCCCOP(O)(O)=O

InChI

InChIKey=QEWABYCCMMQIHS-UHFFFAOYSA-N
InChI=1S/C8H19O4P.C6H15NO3/c1-2-3-4-5-6-7-8-12-13(9,10)11;8-4-1-7(2-5-9)3-6-10/h2-8H2,1H3,(H2,9,10,11);8-10H,1-6H2

HIDE SMILES / InChI

Molecular Formula C6H15NO3
Molecular Weight 149.1882
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C8H19O4P
Molecular Weight 210.2078
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Labeled 3-aryl-4-indolylmaleimide derivatives and their potential as angiogenic PET biomarkers.
2010-01-15
Partition coefficients of some purine derivatives and its application to pharmacokinetics.
2009-12
A novel elsinochrome A derivative: a study of drug delivery and photodynamic activity.
2009-12
Carboxymethylated pyridoindole antioxidants as aldose reductase inhibitors: Synthesis, activity, partitioning, and molecular modeling.
2008-05-01
Synthesis, structure, and X-band (9.5 GHz) EPR characterization of the new series of pH-sensitive spin probes: N,N-disubstituted 4-amino-2,2,5,5-tetramethyl-3-imidazoline 1-oxyls.
2005-11-25
Synthesis, hydrolysis, and intraocular pressure lowering effects of fadolmidine prodrugs.
2005-05-13
Physicochemical properties of neuromuscular blocking agents and their impact on the pharmacokinetic-pharmacodynamic relationship.
2004-08
Fine-tuning the hydrophobicity of a mitochondria-targeted antioxidant.
2004-07-30
Modification of the surface properties of porous nanometric zirconia particles by covalent grafting.
2004-04-13
pH-dependent modification of lipophilicity of porphyrin-type photosensitizers.
2004-03
Preparation and use as spin trapping agents of new ester-nitrones.
2003-02-07
Affinity of isoflavonoids for lipid bilayers evaluated with liposomal systems.
2003
Formation and structure of titanium alkyl phosphates.
2002-10-15
Effect of mono- and di-acylation on the ocular disposition of ganciclovir: physicochemical properties, ocular bioreversion, and antiviral activity of short chain ester prodrugs.
2002-03
N-2-(2-ethoxycarbonyl-propyl) alpha-phenylnitrone: an efficacious lipophilic spin trap for superoxide detection.
2002-01-01
Influences of alkyl group chain length and polar head group on chemical skin permeation enhancement.
2001-08
Patents

Patents

Substance Class Chemical
Created
by admin
on Tue Apr 01 18:45:56 GMT 2025
Edited
by admin
on Tue Apr 01 18:45:56 GMT 2025
Record UNII
U8LMQ4Z428
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TRIETHANOLAMINE OCTYLPHOSPHATE
Common Name English
PHOSPHORIC ACID, MONOOCTYL ESTER, COMPD. WITH 2,2',2''-NITRILOTRIS(ETHANOL) (1:1)
Preferred Name English
2,2',2''-NITRILOTRIETHANOL OCTYL PHOSPHATE
Common Name English
OCTYL PHOSPHATE TRIETHANOLAMINE SALT
Common Name English
Code System Code Type Description
ECHA (EC/EINECS)
250-136-1
Created by admin on Tue Apr 01 18:45:56 GMT 2025 , Edited by admin on Tue Apr 01 18:45:56 GMT 2025
PRIMARY
EPA CompTox
DTXSID1067546
Created by admin on Tue Apr 01 18:45:56 GMT 2025 , Edited by admin on Tue Apr 01 18:45:56 GMT 2025
PRIMARY
FDA UNII
U8LMQ4Z428
Created by admin on Tue Apr 01 18:45:56 GMT 2025 , Edited by admin on Tue Apr 01 18:45:56 GMT 2025
PRIMARY
PUBCHEM
169147
Created by admin on Tue Apr 01 18:45:56 GMT 2025 , Edited by admin on Tue Apr 01 18:45:56 GMT 2025
PRIMARY
CAS
30342-63-3
Created by admin on Tue Apr 01 18:45:56 GMT 2025 , Edited by admin on Tue Apr 01 18:45:56 GMT 2025
PRIMARY