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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
Yong Zhou et al.
Journal of the American Chemical Society, 131(7), 2456-2457 (2009-02-10)
In this Communication, we report one-pot, high yield formation of unprecedented 1-D necklace-like chains consisting of hybrid Pd nanocrystals (NCs) embedded in spheres of a peptidic lipid. We employed the synthetic peptidic lipid, 2-(2-tetradecanamidoacetamido)acetic acid (1). We found that in
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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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