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Key Documents

185388

Sigma-Aldrich

1-Tetradecanol

97%

Synonym(s):

Myristyl alcohol, Tetradecyl alcohol

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About This Item

Linear Formula:
CH3(CH2)13OH
CAS Number:
Molecular Weight:
214.39
Beilstein:
1742652
EC Number:
MDL number:
UNSPSC Code:
12352100
eCl@ss:
39020231
PubChem Substance ID:
NACRES:
NA.22

vapor density

7.4 (vs air)

Quality Level

Assay

97%

form

solid

autoignition temp.

489 °F

bp

289 °C (lit.)

mp

35-39 °C (lit.)

solubility

water: 0.00013 g/L at 23 °C
chloroform: soluble 10%

density

0.823 g/mL at 25 °C (lit.)

functional group

hydroxyl

SMILES string

CCCCCCCCCCCCCCO

InChI

1S/C14H30O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15/h15H,2-14H2,1H3

InChI key

HLZKNKRTKFSKGZ-UHFFFAOYSA-N

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Application

1-Tetradecanol was used for filling the hollow interiors of gold nanocages in the fabrication of new theranostic system having unique feature of photoacoustic imaging. It was used in fabrication of temperature-regulated drug release system based on phase-change materials.

Pictograms

Exclamation markEnvironment

Signal Word

Warning

Hazard Statements

Hazard Classifications

Aquatic Chronic 1 - Eye Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

298.4 °F - closed cup

Flash Point(C)

148 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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A temperature-sensitive drug release system based on phase-change materials.
Sung-Wook Choi et al.
Angewandte Chemie (International ed. in English), 49(43), 7904-7908 (2010-09-15)
Geon Dae Moon et al.
Journal of the American Chemical Society, 133(13), 4762-4765 (2011-03-16)
This communication reports a new theranostic system with a combination of capabilities to both enhance the contrast of photoacoustic (PA) imaging and control the release of a chemical or biological effector by high-intensity focused ultrasound (HIFU). The fabrication of this
B Ahlström et al.
Microbiology (Reading, England), 144 ( Pt 9), 2497-2504 (1998-10-23)
Hydrolysis of tetradecyl betainate (B14), a fast-acting microbicidal amphiphilic quaternary ammonium compound (QAC) being an ester of betaine and tetradecanol, occurred after binding to Salmonella typhimurium, resulting in release of the water-soluble betaine portion and retention of the lipophilic tetradecanol.
Pengyun Zeng et al.
Drug development and industrial pharmacy, 35(1), 12-18 (2008-07-25)
Solid lipid particles were evaluated for their potential as a thermo-activated drug delivery system. Submicron-sized diphenylhexatriene (DPH)/myristyl alcohol particles were produced by an atomization/drying process and the release rate of DPH into sodium dodecyl sulfate (SDS) micellar solutions was measured.
M Lafleur et al.
Biochemistry, 29(36), 8325-8333 (1990-09-11)
The orientational order profile has been determined by using deuterium nuclear magnetic resonance (2H NMR) for POPE in the lamellar liquid-crystalline (L alpha) and the hexagonal (HII) phases and is shown to be sensitive to the symmetry of the lipid

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