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Details

Stereochemistry ACHIRAL
Molecular Formula C8H19O4P
Molecular Weight 210.2078
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MONOOCTYL PHOSPHATE

SMILES

CCCCCCCCOP(O)(O)=O

InChI

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

HIDE SMILES / InChI

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

Name Type Language
MONOOCTYL PHOSPHATE
HSDB  
Systematic Name English
JAMP 8
Preferred Name English
OCTYL PHOSPHATE ((C8H17O)(HO)2PO)
Common Name English
PHOSPHORIC ACID, MONOOCTYL ESTER
Systematic Name English
MONOOCTYL PHOSPHATE [HSDB]
Common Name English
MONOOCTYLPHOSPHORIC ACID
Systematic Name English
OCTYL DIHYDROGEN PHOSPHATE
Systematic Name English
OCTYLPHOSPHATE
Systematic Name English
Code System Code Type Description
FDA UNII
D076LJ1H9L
Created by admin on Mon Mar 31 22:22:53 GMT 2025 , Edited by admin on Mon Mar 31 22:22:53 GMT 2025
PRIMARY
PUBCHEM
19892
Created by admin on Mon Mar 31 22:22:53 GMT 2025 , Edited by admin on Mon Mar 31 22:22:53 GMT 2025
PRIMARY
ECHA (EC/EINECS)
223-638-3
Created by admin on Mon Mar 31 22:22:53 GMT 2025 , Edited by admin on Mon Mar 31 22:22:53 GMT 2025
PRIMARY
CAS
3991-73-9
Created by admin on Mon Mar 31 22:22:53 GMT 2025 , Edited by admin on Mon Mar 31 22:22:53 GMT 2025
PRIMARY
EPA CompTox
DTXSID4058605
Created by admin on Mon Mar 31 22:22:53 GMT 2025 , Edited by admin on Mon Mar 31 22:22:53 GMT 2025
PRIMARY
HSDB
2610
Created by admin on Mon Mar 31 22:22:53 GMT 2025 , Edited by admin on Mon Mar 31 22:22:53 GMT 2025
PRIMARY