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Merck

87140

Sigma-Aldrich

Tetradecane

olefin free, ≥99.0% (GC)

Sinónimos:

n-Tetradecane

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About This Item

Fórmula lineal:
CH3(CH2)12CH3
Número de CAS:
Peso molecular:
198.39
Beilstein/REAXYS Number:
1733859
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

vapor density

6.83 (vs air)

Quality Level

vapor pressure

1 mmHg ( 76.4 °C)

assay

≥99.0% (GC)

form

liquid

autoignition temp.

455 °F

refractive index

n20/D 1.429 (lit.)
n20/D 1.429

bp

252-254 °C (lit.)

mp

5.5 °C (lit.)

density

0.762 g/mL at 20 °C (lit.)

SMILES string

CCCCCCCCCCCCCC

InChI

1S/C14H30/c1-3-5-7-9-11-13-14-12-10-8-6-4-2/h3-14H2,1-2H3

InChI key

BGHCVCJVXZWKCC-UHFFFAOYSA-N

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Application

Tetradecane can be used for the synthesis of thermally stable nano-encapsulated phase change materials (NEPCMs), exhibiting thermal energy storage and heat transfer enhancement applications. It can also be used as an n-alkane model for the study of ignition time measurements for larger n-alkanes.

pictograms

Health hazard

signalword

Danger

hcodes

Hazard Classifications

Asp. Tox. 1

supp_hazards

Storage Class

10 - Combustible liquids

wgk_germany

WGK 1

flash_point_f

215.6 °F - closed cup

flash_point_c

102 °C - closed cup

ppe

Eyeshields, Gloves


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Preparation and characterization of nano-encapsulated n-tetradecane as phase change material for thermal energy storage
Fang G, et al.
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A shock tube study of the ignition of n-heptane, n-decane, n-dodecane, and n-tetradecane at elevated pressures
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Energy and Fuels, 23(5), 2482-2489 (2009)
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A general and stereoselective methodology for the synthesis of bridged bicyclic octenones having various types of alkenyl chains and a tricyclic framework of secoatisanes and higher analogues is reported. In situ generation and cycloaddition of 2-allyl-6,6-spiroepoxycyclohexadienones with ethyl acrylate gave
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Nonpareil almonds, Prunus dulcis , account for the largest percentage of almond varieties grown in the Central Valley of California. Several studies have investigated the various nonvolatile and volatile components of various plant parts; however, the volatile organic compound (VOC)
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Environmental science & technology, 43(23), 8813-8820 (2009-12-01)
Mass transfer of organic contaminants from nonaqueous phase liquids to the aqueous phase can significantly modulate the observable carbon isotope fractionation behavior associated with contaminant transformation. We evaluated the effects of kinetic interphase mass transfer between tetradecane and water on

Protocolos

Separation of Decane; Dodecane; Tetradecane; Hexadecane; Octadecane; Eicosane; Docosane; Tetracosane; Hexacosane; Octacosane

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