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H6800

Sigma-Aldrich

1-Hexadecanol

95%

Synonym(s):

Cetyl alcohol, Palmityl alcohol

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About This Item

Linear Formula:
CH3(CH2)15OH
CAS Number:
36653-82-4
Molecular Weight:
242.44
Beilstein:
1748475
EC Number:
253-149-0
MDL number:
MFCD00004760
UNSPSC Code:
12352100
PubChem Substance ID:
57654268
NACRES:
NA.22

vapor density

8.34 (vs air)

Quality Level

200

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

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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.

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’.

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Aikaterini Papadaki et al.
Biomolecules, 10(1) (2020-01-16)
Oleogelation is an emerging technology to structure oils, which can be widely used to substitute saturated and trans fats. Extra virgin olive oil is widely recognized for its high nutritional value, but its utilization in oleogel production is currently limited.
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)
High-chain fatty acid esters of 1-hexadecanol for low temperature thermal energy storage with phase change materials.
Aydin AA and Aydin A.
Solar Energy Mat. and Solar Cells, 96, 93-100 (2012)
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