Skip to Content
Merck
All Photos(2)

Documents

H6800

Sigma-Aldrich

1-Hexadecanol

95%

Synonym(s):

Cetyl alcohol, Palmityl alcohol

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
CH3(CH2)15OH
CAS Number:
Molecular Weight:
242.44
Beilstein:
1748475
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

vapor density

8.34 (vs air)

vapor pressure

<0.01 mmHg ( 43 °C)

Assay

95%

form

solid

autoignition temp.

483 °F

expl. lim.

8 %

bp

179-181 °C/10 mmHg (lit.)

mp

48-50 °C (lit.)

density

0.818 g/mL at 25 °C (lit.)

SMILES string

CCCCCCCCCCCCCCCCO

InChI

1S/C16H34O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17/h17H,2-16H2,1H3

InChI key

BXWNKGSJHAJOGX-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Application

  • 1-Hexadecanol can be used as a reactant in the synthesis of self-assembled m-diethynylbenzene macrocycles (DBMs), water-soluble pillar[6]arene for controllable drug release and poly(ethylene glycol)-based polymer for intracellular delivery of anticancer drugs.
  • It is used in building the template for sol-gel synthesis of mesoporous silicates.
  • It can be employed in the synthesis of anionic gemini surfactants which also exhibit antibacterial and antifungal activities.
  • High-chain fatty acid esters of 1-hexadecanol can be used as phase change materials (PCM) for thermal energy storage.

Storage Class Code

11 - Combustible Solids

WGK

nwg

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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

m-Diethynylbenzene macrocycles: syntheses and self-association behavior in solution.
Tobe Y, et al.
Journal of the American Chemical Society, 124(19), 5350-5364 (2002)
Cellular uptake, intracellular trafficking, and antitumor efficacy of doxorubicin-loaded reduction-sensitive micelles.
Cui C, et al.
Biomaterials, 34(15), 3858-3869 (2013)
Characterization, surface properties and biological activity of some synthesized anionic surfactants.
Negm N A and Tawfik S M
Journal of Industrial and Engineering Chemistry, 20(6), 4463-4472 (2014)
A condensable amphiphile with a cleavable tail as a ?lizard? template for the sol? gel synthesis of functionalized mesoporous silica.
Zhang Q, et al.
Journal of the American Chemical Society, 126(4), 988-989 (2004)
Multistimuli-responsive supramolecular vesicles based on water-soluble pillar [6] arene and SAINT complexation for controllable drug release.
Cao Y, et al.
Journal of the American Chemical Society, 136(30), 10762-10769 (2014)

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