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87140

Sigma-Aldrich

Tetradecane

olefin free, ≥99.0% (GC)

Synonym(s):

n-Tetradecane

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About This Item

Linear Formula:
CH3(CH2)12CH3
CAS Number:
629-59-4
Molecular Weight:
198.39
Beilstein:
1733859
EC Number:
211-096-0
MDL number:
MFCD00008986
UNSPSC Code:
12352100
PubChem Substance ID:
57653230
NACRES:
NA.22

vapor density

6.83 (vs air)

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
GHS08

Signal Word

Danger

Hazard Statements

H304

Precautionary Statements

P301 + P310 - P331 - P405 - P501

Hazard Classifications

Asp. Tox. 1

Supplementary Hazards

EUH066

Storage Class Code

10 - Combustible liquids

WGK

WGK 1

Flash Point(F)

215.6 °F - closed cup

Flash Point(C)

102 °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’.

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A shock tube study of the ignition of n-heptane, n-decane, n-dodecane, and n-tetradecane at elevated pressures
Shen HPS, et al.
Energy and Fuels, 23(5), 2482-2489 (2009)
Preparation and characterization of nano-encapsulated n-tetradecane as phase change material for thermal energy storage
Fang G, et al.
Chemical Engineering Journal, 153(1-3), 217-221 (2009)
Vishwakarma Singh et al.
The Journal of organic chemistry, 74(16), 6092-6104 (2009-07-21)
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
Agnieszka Ewa Wiacek et al.
Langmuir : the ACS journal of surfaces and colloids, 24(14), 7413-7420 (2008-06-21)
Zeta potentials and effective diameters of n-tetradecane emulsions in 1 M ethanol were investigated in the presence of 1,2-dipalmitoyl- sn-glycero-3-phosphocholine (DPPC) (1 mg/100 mL), Candida cylindracea lipase (CCL), and phospholipase PLA2 (1 mg/100 mL) at 20, 37, and 45 degrees
Christoph Aeppli et al.
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
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Protocols

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