ChemicalBook--->CAS DataBase List--->2136-72-3

2136-72-3

2136-72-3 Structure

2136-72-3 Structure
IdentificationBack Directory
[Name]

2-(OCTADECYLOXY)ETHANOL
[CAS]

2136-72-3
[Synonyms]

C18E1
OCTADECYLGLYCOL
octadecaoxyethanol
2-Octadecoxyethanol
2-stearyloxyethanol
3-Oxahenicosane-1-ol
2-(OCTADECYLOXY)ETHANOL
ethanol,2-(octadecyloxy)-
2-(Octadecyloxy)ethan-1-ol
ETHYLENE GLYCOL MONOOCTADECYL ETHER
2-(Octadecyloxy)ethanol, C18E1, Octadecylglycol
[EINECS(EC#)]

218-374-0
[Molecular Formula]

C20H42O2
[MDL Number]

MFCD00043351
[MOL File]

2136-72-3.mol
[Molecular Weight]

314.55
Chemical PropertiesBack Directory
[Melting point ]

48-53 °C
[Boiling point ]

413.1±18.0 °C(Predicted)
[density ]

0.867±0.06 g/cm3(Predicted)
[Fp ]

100 °C
[storage temp. ]

Sealed in dry,2-8°C
[solubility ]

Chloroform (Sparingly), Ethyl Acetate (Slightly)
[form ]

Solid
[pka]

14.42±0.10(Predicted)
[color ]

White to Off-White
[InChI]

InChI=1S/C20H42O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-19-22-20-18-21/h21H,2-20H2,1H3
[InChIKey]

ICIDSZQHPUZUHC-UHFFFAOYSA-N
[SMILES]

C(O)COCCCCCCCCCCCCCCCCCC
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P271-P280
[WGK Germany ]

3
[F ]

3
[HazardClass ]

IRRITANT
[HS Code ]

2905190098
Hazard InformationBack Directory
[Uses]

2-(Octadecyloxy)ethanol is used in preparation of fatty alcohol ethoxylates via etherification of fatty alcohol with ethylene glycol.
[Synthesis]

Respectively, to take propylene glycol 680mg, sodium hydrogen 2.5g added to 100 ml round bottom flask,THF was added to 10 ml of a solution and stirred for 30 minutes,Then raise the temperature to reflux for 1 hour,And then weigh the bromo-octadecane dispersed in 10 ml of THF by adding a separatory funnel and dropping into the reaction solution,After refluxing the reaction overnight. After completion of the reaction, a saturated sodium chloride solution was added,Dichloromethane extraction three times, combined extract, filter evaporated solvent, crude column chromatography separation,The second band was collected, the resulting product, 550 mg, yield 17.1%.
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