Skip to Content
Merck
All Photos(1)

Documents

O709

Sigma-Aldrich

1-Octadecanol

95%

Synonym(s):

Octadecyl alcohol, Stearyl alcohol

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
CH3(CH2)17OH
CAS Number:
Molecular Weight:
270.49
Beilstein:
1362907
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

vapor density

9.3 (vs air)

vapor pressure

<0.01 mmHg ( 38 °C)

Assay

95%

form

solid

autoignition temp.

842 °F

expl. lim.

~8 %

bp

210 °C/15 mmHg

mp

56-59 °C (lit.)

solubility

H2O: slightly soluble 0.001 g/L at 23 °C

density

0.812 g/mL at 25 °C (lit.)

SMILES string

CCCCCCCCCCCCCCCCCCO

InChI

1S/C18H38O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19/h19H,2-18H2,1H3

InChI key

GLDOVTGHNKAZLK-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Application

  • 1-Octadecanol is used in the synthesis of O-octadecyl-S-trifluorothiolcarbonate, which is a storable crystalline source of trifluoromethanethiol.
  • It can be used to improve solution processability of conjugated polymers used in the organic electronic applications.
  • It induces hydrophobicity to the amphiphiles used in the drug and gene delivery.
  • It is also employed in the synthesis of solid-liquid phase change materials (PCMs), surfactant and stabilizers.

Storage Class Code

11 - Combustible Solids

WGK

nwg

Flash Point(F)

383.0 °F - closed cup

Flash Point(C)

195 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Facile Access to polymeric vesicular nanostructures: Remarkable ?-end group effects in cholesterol and pyrene functional (co) polymers.
Xu J, et al.
Macromolecules, 44(2), 299-312 (2010)
A Convenient Metal-Free Reagent for the Generation and Capture of Trifluoromethanethiol.
Li S G and Zard S Z
Organic Letters, 15(22), 5898-5901 (2013)
Synthesis of novel solid?liquid phase change materials and electrospinning of ultrafine phase change fibers.
Chen C, et al.
Solar Energy Materials and Solar Cells, 96, 202-209 (2012)
Amphiphilic hyperbranched polyglycerols in a new role as highly efficient multifunctional surface active stabilizers for poly (lactic/glycolic acid) nanoparticles.
Kasza G, et al.
Royal Society of Chemistry Advances, 7(8), 4348-4352 (2017)
Host?guest interaction-based self-engineering of nano-sized vesicles for co-delivery of genes and anticancer drugs.
Yang B, et al.
ACS Applied Materials & Interfaces, 7(39), 22084-22094 (2015)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service