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Details

Stereochemistry ACHIRAL
Molecular Formula C32H66O
Molecular Weight 466.8658
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DICETYL ETHER

SMILES

CCCCCCCCCCCCCCCCOCCCCCCCCCCCCCCCC

InChI

InChIKey=FDCJDKXCCYFOCV-UHFFFAOYSA-N
InChI=1S/C32H66O/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31-33-32-30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h3-32H2,1-2H3

HIDE SMILES / InChI

Molecular Formula C32H66O
Molecular Weight 466.8658
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
In vitro and in vivo effects of polyethylene glycol (PEG)-modified lipid in DOTAP/cholesterol-mediated gene transfection.
2010-08-09
Membrane plasmalogen composition and cellular cholesterol regulation: a structure activity study.
2010-06-14
Analysis of mixed micellar and interfacial behavior of cationic gemini hexanediyl-1,6-bis(dimethylcetylammonium bromide) with conventional ionic and nonionic surfactants in aqueous medium.
2010-05-13
Time-resolved soft X-ray diffraction reveals transient structural distortions of ternary liquid crystals.
2009-11-04
Characterization of highly stable liposomal and immunoliposomal formulations of vincristine and vinblastine.
2009-09
In vitro biotransformation of surfactants in fish. Part II--Alcohol ethoxylate (C16EO8) and alcohol ethoxylate sulfate (C14EO2S) to estimate bioconcentration potential.
2009-08
Interaction of a cationic gemini surfactant with conventional surfactants in the mixed micelle and monolayer formation in aqueous medium.
2009-05-15
Median knock-down time as a new method for evaluating insecticide-treated textiles for mosquito control.
2008-06-27
Use of alkane monolayer templates to modify the structure of alkyl ether monolayers on highly ordered pyrolytic graphite.
2008-02-05
Mesh phases in a ternary nonionic surfactant, oil, and water system.
2006-12-19
Thermal diffusion behavior of nonionic surfactants in water.
2006-06-08
Two-dimensional facets in Langmuir monolayers of 1-O-hexadecyl-rac-glycerol at the air-water interface.
2006-04-01
Effect of micelle composition on the formation of surfactant-templated polymer films.
2006-03-23
Use of polyoxyethylene surfactants for the extraction of organochlorine pesticides from agricultural soils.
2006-02-03
Molecular characterization of thyroid toxicity: anchoring gene expression profiles to biochemical and pathologic end points.
2005-10
Synthesis of surfactant-templated silica films with orthogonally aligned hexagonal mesophase.
2005-03-03
Surface phase behavior in Langmuir monolayers of diethylene glycol mono-n-hexadecyl ether at the air-water interface.
2004-11-22
Determination of antifungal proteins in soil by liquid chromatography.
2003-07
Evaluation of nonionic and zwitterionic detergents as membrane protein solubilizers in two-dimensional electrophoresis.
2003-03
A limulus amoebocyte lysate activating activity (LAL activity) that lacks biological activities of endotoxin found in biological products.
2002
Monoalkylether phospholipids in the sulfate-reducing bacteria Desulfosarcina variabilis and Desulforhabdus amnigenus.
2001-12
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 20:56:03 GMT 2025
Edited
by admin
on Mon Mar 31 20:56:03 GMT 2025
Record UNII
BZ3TC4IWYY
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DICETYL ETHER
INCI  
INCI  
Official Name English
COSMACOL ETHER 16
Preferred Name English
HEXADECANE, 1-(HEXADECYLOXY)-
Systematic Name English
NSC-77143
Code English
HEXADECYL ETHER
Systematic Name English
DIHEXADECYL ETHER
Systematic Name English
HEXADECANE, 1,1'-OXYBIS-
Systematic Name English
Code System Code Type Description
ECHA (EC/EINECS)
223-900-7
Created by admin on Mon Mar 31 20:56:03 GMT 2025 , Edited by admin on Mon Mar 31 20:56:03 GMT 2025
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CAS
4113-12-6
Created by admin on Mon Mar 31 20:56:03 GMT 2025 , Edited by admin on Mon Mar 31 20:56:03 GMT 2025
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PUBCHEM
77757
Created by admin on Mon Mar 31 20:56:03 GMT 2025 , Edited by admin on Mon Mar 31 20:56:03 GMT 2025
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EPA CompTox
DTXSID30194067
Created by admin on Mon Mar 31 20:56:03 GMT 2025 , Edited by admin on Mon Mar 31 20:56:03 GMT 2025
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FDA UNII
BZ3TC4IWYY
Created by admin on Mon Mar 31 20:56:03 GMT 2025 , Edited by admin on Mon Mar 31 20:56:03 GMT 2025
PRIMARY
NSC
77143
Created by admin on Mon Mar 31 20:56:03 GMT 2025 , Edited by admin on Mon Mar 31 20:56:03 GMT 2025
PRIMARY